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48

Skullcapflavone II SMB00545-1MG

Empirical Formula (Hill Notation):	C₁₉H₁₈O₈
CAS Number:	55084-08-7
Molecular Weight:	374.34
MDL number:	MFCD02258879
PubChem Substance ID:	329824694
NACRES:	NA.25

General description

Natrual product derived from plant source.

Параметры

assay	≥90% (LC/MS-UV)
form	solid
solubility	DMSO: 1 mg/mL
storage temp.	−20°C
SMILES string	OC1=C(C(C=C(C2=C(O)C=CC=C2OC)O3)=O)C3=C(OC)C(OC)=C1OC
InChI	1S/C19H18O8/c1-23-11-7-5-6-9(20)13(11)12-8-10(21)14-15(22)17(24-2)19(26-4)18(25-3)16(14)27-12/h5-8,20,22H,1-4H3
InChI key	GMQFOKBGMKVUQZ-UHFFFAOYSA-N

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Solanesol from tobacco

Empirical Formula (Hill Notation):	C₄₅H₇₄O
CAS Number:	13190-97-1
Molecular Weight:	631.07
MDL number:	MFCD00070279
PubChem Substance ID:	24899813
NACRES:	NA.25

25, 250 mg in poly bottle

Biochem/physiol Actions

This C45 isoprenoid alcohol is the most abundant lipid in tobacco leaves. It may be an important precursor of the tumorigenic polynuclear aromatic hydrocarbons of smoke.

Параметры

Quality Level	200,
assay	≥90% (HPLC)
form	powder
storage temp.	−20°C
SMILES string	C\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CO
InChI	1S/C45H74O/c1-37(2)19-11-20-38(3)21-12-22-39(4)23-13-24-40(5)25-14-26-41(6)27-15-28-42(7)29-16-30-43(8)31-17-32-44(9)33-18-34-45(10)35-36-46/h19,21,23,25,27,29,31,33,35,46H,11-18,20,22,24,26,28,30,32,34,36H2,1-10H3/b38-21+,39-23+,40-25+,41-27+,42-29+,43-31+,44-33+,45-35+
InChI key	AFPLNGZPBSKHHQ-MEGGAXOGSA-N

Safety Information

Personal Protective Equipment	Eyeshields,, Gloves,, type N95 (US),
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Sophoricoside

Empirical Formula (Hill Notation):	C₂₁H₂₀O₁₀
CAS Number:	152-95-4
Molecular Weight:	432.38
PubChem Substance ID:	329825016
NACRES:	NA.25

Sophoricoside is an isoflavone glycoside found in the fruit of Sophora japonica, known as huai hua in Traditional Chinese Medicine.

Packaging

5 mg in glass bottle
25 mg in poly bottle

Biochem/physiol Actions

Sophoricoside has numerous pharmacological effects including anti-inflammatory, anti-cancer and immunosuppressive activities.

Параметры

Quality Level	200,
assay	≥98% (HPLC)
form	powder
storage temp.	2-8°C
SMILES string	OC1=CC(O)=C(C(C(C2=CC=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]3O)C=C2)=CO4)=O)C4=C1
InChI	1S/C21H20O10/c22-7-15-18(26)19(27)20(28)21(31-15)30-11-3-1-9(2-4-11)12-8-29-14-6-10(23)5-13(24)16(14)17(12)25/h1-6,8,15,18-24,26-28H,7H2/t15-,18-,19+,20-,21-/m0/s1
InChI key	ISQRJFLLIDGZEP-JDCPMNFLSA-N

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Soyasapogenol B

Empirical Formula (Hill Notation):	C₃₀H₅₀O₃
CAS Number:	595-15-3
Molecular Weight:	458.72
MDL number:	MFCD00075988
PubChem Substance ID:	329825024

Biochem/physiol Actions

Soyasapogenol B is a constituent of soya bean saponin that belongs to the family of oleanane triterpenes. It is known to have biofunctions in cell signaling, membrane integrity and stability, and fuel and energy storage. Soyasapogenol B may demonstrate hypocholesterolemic effects.

Параметры

Quality Level	200,
assay	≥98% (HPLC)
form	powder
storage temp.	2-8°C
SMILES string	CC1(C)C[C@@H](O)[C@]2(C)CC[C@@]3(C)[C@]4(C)CC[C@@]5([H])[C@](CO)(C)[C@@H](O)CC[C@]5(C)[C@@]4([H])CC=C3[C@]2([H])C1
InChI	1S/C30H50O3/c1-25(2)16-20-19-8-9-22-27(4)12-11-23(32)28(5,18-31)21(27)10-13-30(22,7)29(19,6)15-14-26(20,3)24(33)17-25/h8,20-24,31-33H,9-18H2,1-7H3/t20-,21+,22+,23-,24+,26+,27-,28+,29+,30+/m0/s1
InChI key	YOQAQNKGFOLRGT-UXXABWCISA-N

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Soyasaponin I

Empirical Formula (Hill Notation):	C₄₈H₇₈O₁₈
CAS Number:	51330-27-9
Molecular Weight:	943.12
MDL number:	MFCD02752366

Soyasaponin I is an oleanene-type triterpenoid aglycone and is a group B soyasaponin. It is an amphiphilic molecule and is metabolized by intestinal bacteria into sugars and aglycones.

Application

Soyasaponin I has been used:

to test its effect on migration and invasion of ovarian cancer cell lines
as standard for the quantification of saponins from quinoa and fenugreek samples
as L-15 medium supplement for Zebrafish liver cell lines

Packaging

5 mg in glass bottle
25 mg in poly bottle

Biochem/physiol Actions

Antioxidant and anti-inflammatory saponin found in soybean. Attenuates TNBS-induced colitis in mice. The structure consists of a glycoside moiety and triterpene derivative. Sialytransferase inhibitor and renin inhibitor.

Параметры

biological source	Glycine max (soybean)
Quality Level	200,
assay	94% (HPLC)
form	powder
storage condition	protect from light
solubility	ethanol: 1 mg/mL, clear, colorless
storage temp.	2-8°C
SMILES string	CC1(C)C[C@@H](O)[C@@](CC[C@]2(C)C3=CC[C@@]4([H])[C@@]2(C)CC[C@]5([H])[C@]4(C)CC[C@H](O[C@]6([H])O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]6O[C@@]7([H])[C@H](O[C@]8([H])O[C@@H](C)[C@H](O)[C@@H](O)[C@H]8O)[C@@H](O)[C@@H](O)[C@@H](CO)O7)[C@@]5(CO)C)(C)[C@@]3([H])C
InChI	1S/C48H78O18/c1-21-29(52)31(54)35(58)40(61-21)65-37-32(55)30(53)24(19-49)62-41(37)66-38-34(57)33(56)36(39(59)60)64-42(38)63-28-12-13-45(5)25(46(28,6)20-50)11-14-48(8)26(45)10-9-22-23-17-43(2,3)18-27(51)44(23,4)15-16-47(22,48)7/h9,21,23-38,40-42,49-58H,10-20H2,1-8H3,(H,59,60)/t21-,23-,24+,25+,26+,27+,28-,29-,30-,31+,32-,33-,34-,35+,36-,37+,38+,40-,41-,42+,44+,45-,46+,47+,48+/m0/s1
InChI key	PTDAHAWQAGSZDD-IOVCITQVSA-N

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Sweroside SMB00083-1MG

Empirical Formula (Hill Notation):	C₁₆H₂₂O₉
CAS Number:	14215-86-2
Molecular Weight:	358.34
MDL number:	MFCD09954487
PubChem Substance ID:	329824761
NACRES:	NA.25

General description

Sweroside is an active component of iridoid glycoside, with a molecular weight of 358.344 Da. It is found in variety of plant species.
Natural product derived from plant source.

Application

Sweroside has been used as a standard in MC-high performance liquid chromatography (HPLC)-ultraviolet (UV) experiment.

Biochem/physiol Actions

Sweroside possesses hepatoprotective, antitumor, antibacterial and antifungal properties. It can be used as a potential therapeutic to treat osteoporosis.

Параметры

assay	≥95% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
SMILES string	OC[C@H]1O[C@@H](O[C@@H]2OC=C3[C@@H](CCOC3=O)[C@H]2C=C)[C@H](O)[C@@H](O)[C@@H]1O
InChI	1S/C16H22O9/c1-2-7-8-3-4-22-14(21)9(8)6-23-15(7)25-16-13(20)12(19)11(18)10(5-17)24-16/h2,6-8,10-13,15-20H,1,3-5H2/t7-,8+,10-,11-,12+,13-,15+,16+/m1/s1
InChI key	VSJGJMKGNMDJCI-ZASXJUAOSA-N

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Swertiamarin SMB00080-1MG

Empirical Formula (Hill Notation):	C₁₆H₂₂O₁₀
CAS Number:	17388-39-5
Molecular Weight:	374.34
MDL number:	MFCD07783984
PubChem Substance ID:	329824758
NACRES:	NA.25

General description

Natural product derived from plant source.

Biochem/physiol Actions

Swertiamarin has shown potential as antiatherogenic agent by inhibiting HMG-CoA reductase activity in high cholesterol fed rats. The high cholesterol fed rats treated with Swertiamarin showed prevention of increased serum total cholesterol, triglycerides, LDLs and VLDLs.

Параметры

assay	≥95% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
SMILES string	OC[C@H]1O[C@@H](O[C@@H]2OC=C3C(=O)OCC[C@@]3(O)[C@H]2C=C)[C@H](O)[C@@H](O)[C@@H]1O
InChI	1S/C16H22O10/c1-2-7-14(24-6-8-13(21)23-4-3-16(7,8)22)26-15-12(20)11(19)10(18)9(5-17)25-15/h2,6-7,9-12,14-15,17-20,22H,1,3-5H2/t7-,9+,10+,11-,12+,14-,15-,16+/m0/s1
InChI key	HEYZWPRKKUGDCR-QBXMEVCASA-N

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Tabersonine

Empirical Formula (Hill Notation):	C₂₁H₂₄N₂O₂
CAS Number:	4429-63-4
Molecular Weight:	336.43
MDL number:	MFCD28140545
PubChem Substance ID:	329825021
NACRES:	NA.25

Tabersonine is a terpenoid indole alkaloid (TIA) found in Amsonia elliptica.

Packaging

10 mg in glass bottle

Biochem/physiol Actions

Tabersonine shows hypotensive, anti-tumor, hypoglycemic, and diuretic activity.

Параметры

Quality Level	200,
assay	≥95% (HPLC)
form	powder
storage temp.	2-8°C
SMILES string	COC(C1=C2NC3=CC=CC=C3[C@]24[C@]5([H])[C@](C=CCN5CC4)(CC)C1)=O
InChI	1S/C21H24N2O2/c1-3-20-9-6-11-23-12-10-21(19(20)23)15-7-4-5-8-16(15)22-17(21)14(13-20)18(24)25-2/h4-9,19,22H,3,10-13H2,1-2H3/t19-,20-,21-/m0/s1
InChI key	FNGGIPWAZSFKCN-ACRUOGEOSA-N

Safety Information

pictograms	GHS07
signalword	Warning
hcodes	H302
pcodes	P301 + P312 + P330
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Tephrosin SMB00172-1MG

Empirical Formula (Hill Notation):	C₂₃H₂₂O₇
CAS Number:	76-80-2
Molecular Weight:	410.42
MDL number:	MFCD00238693
PubChem Substance ID:	329824838
NACRES:	NA.25

General description

Natural product derived from plant source.

Biochem/physiol Actions

Tephrosin is a plant-based rotenoid which has known anti-cancer properties. Tephrosin inhibited proliferation in A549 cancer cells in a dose-sependent manner. Tephrosin has been shown to induce capase-independent apoptosis, and internalization and degradation of inactivated EGFR and ErB2 in human colon cancer cells.

Параметры

assay	≥95% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
SMILES string	COc1cc2OC[C@H]3Oc4c(ccc5OC(C)(C)C=Cc45)C(=O)[C@@]3(O)c2cc1OC
InChI	1S/C23H22O7/c1-22(2)8-7-12-15(30-22)6-5-13-20(12)29-19-11-28-16-10-18(27-4)17(26-3)9-14(16)23(19,25)21(13)24/h5-10,19,25H,11H2,1-4H3/t19-,23-/m1/s1
InChI key	AQBZCCQCDWNNJQ-AUSIDOKSSA-N

Safety Information

pictograms	GHS09
signalword	Warning
hcodes	H410
pcodes	P273 - P501
RIDADR	UN 3077 9 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Tetrahydrocurcumin SMB00370-1G

Empirical Formula (Hill Notation):	C₂₁H₂₄O₆
CAS Number:	36062-04-1
Molecular Weight:	372.41
Beilstein/REAXYS Number:	3485469
MDL number:	MFCD04152347
PubChem Substance ID:	329824974
NACRES:	NA.25

General description

Tetrahydrocurcumin is a major metabolite of curcumin.

Packaging

1 g in poly bottle

Biochem/physiol Actions

Tetrahydrocurcumin is being studied for the treatment of cancer and dementia. It has antioxidant and anti-inflammatory properties. Tetrahydrocurcumin has been shown to have protective effects against diabetes and vascular dysfunction via alleviation of oxidative stress.

Параметры

Quality Level	200,
assay	≥96% (HPLC)
form	powder
storage temp.	−20°C
SMILES string	COc1cc(CCC(=O)CC(=O)CCc2ccc(O)c(OC)c2)ccc1O
InChI	1S/C21H24O6/c1-26-20-11-14(5-9-18(20)24)3-7-16(22)13-17(23)8-4-15-6-10-19(25)21(12-15)27-2/h5-6,9-12,24-25H,3-4,7-8,13H2,1-2H3
InChI key	LBTVHXHERHESKG-UHFFFAOYSA-N

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	385.2 °F
Flash Point C	196.2 °C

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Thevetin A SMB00166-1MG

Empirical Formula (Hill Notation):	C₄₂H₆₄O₁₉
CAS Number:	37933-66-7
Molecular Weight:	872.95
EC Number:	253-722-5
PubChem Substance ID:	329824836
NACRES:	NA.25

General description

Thevetin A is one of the cardiac glycosides found in yellow oleander.
Natural product derived from plant source.

Biochem/physiol Actions

Cardiac glycosides found in yellow oleander including thevetin A, have potential to treat patients with heart failure and atrial fibrillation.

Параметры

assay	≥95% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
InChI	1S/C42H64O19/c1-18-35(61-38-33(51)31(49)29(47)26(60-38)16-56-37-32(50)30(48)28(46)25(14-43)59-37)36(54-3)34(52)39(57-18)58-21-6-10-41(17-44)20(13-21)4-5-24-23(41)7-9-40(2)22(8-11-42(24,40)53)19-12-27(45)55-15-19/h12,17-18,20-26,28-39,43,46-53H,4-11,13-16H2,1-3H3/t18-,20+,21-,22+,23-,24+,25-,26+,28+,29+,30-,31-,32+,33+,34-,35-,36-,37+,38-,39-,40+,41+,42-/m0/s1
InChI key	WPNLWBRKPZXVGD-XQNLSVLQSA-N

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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SMB01030-1MG

Theviridoside SMB01030-1MG

Empirical Formula (Hill Notation): C₁₇H₂₄O₁₁

CAS Number: 23407-76-3

Molecular Weight: 404.37

MDL number: MFCD20260837

General description
The iridoid glycoside theviridoside shows activity against DPPH.
Natural product derived from plant source.
Параметры

assay ≥90% (LC/MS-ELSD)

form solid

storage temp. −20°C

Safety Information

WGK Germany WGK 3

Flash Point F Not applicable

Flash Point C Not applicable

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Thielavin B SMB00566-1MG

Empirical Formula (Hill Notation):	C₃₁H₃₄O₁₀
CAS Number:	71950-67-9
Molecular Weight:	566.60
MDL number:	MFCD11111623
PubChem Substance ID:	329824713
NACRES:	NA.25

General description

Natural product derived from fungal source.

Параметры

assay	≥95% (LC/MS-UV)
form	solid
solubility	DMSO: 1 mg/mL
storage temp.	−20°C
SMILES string	O=C(C1=C(OC)C(C)=C(OC(C2=C(O)C(C)=C(O)C=C2C)=O)C(C)=C1C)OC3=C(C)C(C)=C(C(O)=O)C(OC)=C3C
InChI	1S/C31H34O10/c1-12-11-20(32)17(6)24(33)21(12)30(36)40-26-16(5)14(3)23(28(39-10)19(26)8)31(37)41-25-15(4)13(2)22(29(34)35)27(38-9)18(25)7/h11,32-33H,1-10H3,(H,34,35)
InChI key	UULGWGARYDGVBM-UHFFFAOYSA-N

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Thunberginol H SMB00214-1MG

Empirical Formula (Hill Notation):	C₁₇H₁₆O₅
CAS Number:	64847-01-4
Molecular Weight:	300.31
MDL number:	MFCD24849360
PubChem Substance ID:	329824874
NACRES:	NA.25

General description

Natural product derived from plant source.

Параметры

assay	≥90% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
SMILES string	COc1ccc(cc1OC)[C@H]2Cc3cccc(O)c3C(=O)O2
InChI	1S/C17H16O5/c1-20-13-7-6-10(8-15(13)21-2)14-9-11-4-3-5-12(18)16(11)17(19)22-14/h3-8,14,18H,9H2,1-2H3/t14-/m1/s1
InChI key	WKNXOKHAEDTQCX-CQSZACIVSA-N

Safety Information

pictograms	GHS09
signalword	Warning
hcodes	H410
pcodes	P273 - P501
RIDADR	UN 3077 9 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Trachelosperogenin A1 SMB00270-1MG

Empirical Formula (Hill Notation):	C₃₆H₅₆O₁₂
CAS Number:	109750-36-9
Molecular Weight:	680.82
PubChem Substance ID:	329824914
NACRES:	NA.25

General description

Natural product derived from plant source.

Параметры

assay	≥95% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
SMILES string	C[C@@H]1CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)C[C@@H](O)[C@H](O)[C@@](C)([C@@H]5CC[C@@]34C)C(O)=O)[C@@H]2[C@]1(C)O)C(=O)O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O
InChI	1S/C36H56O12/c1-17-9-12-36(30(45)48-28-25(41)24(40)23(39)20(16-37)47-28)14-13-32(3)18(26(36)35(17,6)46)7-8-21-31(2)15-19(38)27(42)34(5,29(43)44)22(31)10-11-33(21,32)4/h7,17,19-28,37-42,46H,8-16H2,1-6H3,(H,43,44)/t17-,19-,20-,21-,22-,23-,24+,25-,26-,27+,28+,31-,32-,33-,34-,35-,36+/m1/s1
InChI key	YXSQSVWHKZZWDD-IWSVBZIKSA-N

Safety Information

pictograms	GHS06
signalword	Danger
hcodes	H301
pcodes	P301 + P310
RIDADR	UN 2811 6.1 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Trifolirhizin SMB00180-1MG

Empirical Formula (Hill Notation):	C₂₂H₂₂O₁₀
CAS Number:	6807-83-6
Molecular Weight:	446.40
MDL number:	MFCD00238700
PubChem Substance ID:	329824846
NACRES:	NA.25

General description

Natural product derived from plant source.

Параметры

assay	≥95% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
SMILES string	OC[C@H]1O[C@@H](Oc2ccc3[C@@H]4Oc5cc6OCOc6cc5[C@@H]4COc3c2)[C@H](O)[C@@H](O)[C@@H]1O
InChI	1S/C22H22O10/c23-6-17-18(24)19(25)20(26)22(32-17)30-9-1-2-10-13(3-9)27-7-12-11-4-15-16(29-8-28-15)5-14(11)31-21(10)12/h1-5,12,17-26H,6-8H2/t12-,17+,18+,19-,20+,21-,22+/m0/s1
InChI key	VGSYCWGXBYZLLE-QEEQPWONSA-N

Safety Information

RIDADR	UN 3077 9 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Triptonide

Empirical Formula (Hill Notation):	C₂₀H₂₂O₆
CAS Number:	38647-11-9
Molecular Weight:	358.39
MDL number:	MFCD00210566
PubChem Substance ID:	329824957
NACRES:	NA.25

Triptonide is a toxic natural compound found in Tripterygium wilfordii.

Packaging

10 mg in glass bottle
50 mg in poly bottle

Biochem/physiol Actions

Triptonide has potent antileukemic and antitumor activities.

Параметры

Quality Level	200,
assay	≥98% (HPLC)
form	powder
storage temp.	2-8°C
SMILES string	O=C(OC1)C2=C1[C@]3([H])C[C@H]4[C@@]5(O4)C([C@]6(C(C)C)[C@@H](O6)[C@H](O7)[C@@]57[C@@]3(C)CC2)=O
InChI	1S/C20H22O6/c1-8(2)18-13(25-18)14-20(26-14)17(3)5-4-9-10(7-23-15(9)21)11(17)6-12-19(20,24-12)16(18)22/h8,11-14H,4-7H2,1-3H3/t11-,12-,13-,14-,17-,18-,19+,20+/m0/s1
InChI key	SWOVVKGLGOOUKI-ZHGGVEMFSA-N

Safety Information

pictograms	GHS06,GHS08
signalword	Danger
hcodes	H300 + H330 - H361f
pcodes	P201 - P301 + P310 + P330 - P304 + P340 + P310
RIDADR	UN 2811 6.1 / PGII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Undulatoside A SMB00202-1MG

Empirical Formula (Hill Notation):	C₁₆H₁₈O₉
CAS Number:	58108-99-9
Molecular Weight:	354.31
MDL number:	MFCD24849355
PubChem Substance ID:	329824865
NACRES:	NA.25

General description

Natural product derived from plant source.

Параметры

assay	≥90% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
SMILES string	CC1=CC(=O)c2c(O)cc(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)cc2O1
InChI	1S/C16H18O9/c1-6-2-8(18)12-9(19)3-7(4-10(12)23-6)24-16-15(22)14(21)13(20)11(5-17)25-16/h2-4,11,13-17,19-22H,5H2,1H3/t11-,13-,14+,15-,16-/m1/s1
InChI key	BYYDEEAJCDGLER-YMILTQATSA-N

Safety Information

pictograms	GHS09
signalword	Warning
hcodes	H410
pcodes	P273 - P501
RIDADR	UN 3077 9 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Vernodalol SMB00117-1MG

Empirical Formula (Hill Notation):	C₂₀H₂₄O₈
CAS Number:	65388-17-2
Molecular Weight:	392.40
MDL number:	MFCD24849314
PubChem Substance ID:	329824795
NACRES:	NA.25

General description

Natural product derived from plant source.

Параметры

assay	≥95% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
SMILES string	COC(=O)C(=C)[C@H]1[C@H](O)[C@H]2C(=C)C(=O)OC[C@]2(C[C@@H]1OC(=O)C(=C)CO)C=C
InChI	1S/C20H24O8/c1-6-20-7-13(28-17(23)10(2)8-21)14(11(3)18(24)26-5)16(22)15(20)12(4)19(25)27-9-20/h6,13-16,21-22H,1-4,7-9H2,5H3/t13-,14+,15+,16-,20+/m0/s1
InChI key	FZALQGCQQJLGKE-BBNZOYGDSA-N

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Veronicoside SMB00127-1MG

Empirical Formula (Hill Notation):	C₂₂H₂₆O₁₁
CAS Number:	50981-09-4
Molecular Weight:	466.44
PubChem Substance ID:	329824805
NACRES:	NA.25

General description

Natural product derived from plant source.

Параметры

assay	≥95% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
SMILES string	OC[C@H]1O[C@@H](O[C@@H]2OC=C[C@H]3[C@H](OC(=O)c4ccccc4)[C@@H]5O[C@]5(CO)[C@@H]23)[C@H](O)[C@@H](O)[C@@H]1O
InChI	1S/C22H26O11/c23-8-12-14(25)15(26)16(27)21(30-12)32-20-13-11(6-7-29-20)17(18-22(13,9-24)33-18)31-19(28)10-4-2-1-3-5-10/h1-7,11-18,20-21,23-27H,8-9H2/t11-,12-,13-,14-,15+,16-,17+,18+,20+,21+,22-/m1/s1
InChI key	GOHHRVCULPSXEU-RWORTQBESA-N

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Verproside SMB00115-1MG

Empirical Formula (Hill Notation):	C₂₂H₂₆O₁₃
CAS Number:	50932-20-2
Molecular Weight:	498.43
MDL number:	MFCD02259447
PubChem Substance ID:	329824793
NACRES:	NA.25

General description

Natural product derived from plant source.

Параметры

assay	≥95% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
SMILES string	OC[C@H]1O[C@@H](O[C@@H]2OC=C[C@H]3[C@H](OC(=O)c4ccc(O)c(O)c4)[C@@H]5O[C@]5(CO)[C@@H]23)[C@H](O)[C@@H](O)[C@@H]1O
InChI	1S/C22H26O13/c23-6-12-14(27)15(28)16(29)21(32-12)34-20-13-9(3-4-31-20)17(18-22(13,7-24)35-18)33-19(30)8-1-2-10(25)11(26)5-8/h1-5,9,12-18,20-21,23-29H,6-7H2/t9-,12-,13-,14-,15+,16-,17+,18+,20+,21+,22-/m1/s1
InChI key	DBUOUVZMYWYRRI-YWEKDMGLSA-N

Safety Information

pictograms	GHS07
signalword	Warning
hcodes	H319
pcodes	P305 + P351 + P338
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Vincosamide SMB00122-1MG

Empirical Formula (Hill Notation):	C₂₆H₃₀N₂O₈
CAS Number:	23141-27-7
Molecular Weight:	498.53
MDL number:	MFCD20274589
PubChem Substance ID:	329824800
NACRES:	NA.25

General description

Natural product derived from plant source.

Параметры

assay	≥90% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
SMILES string	OC[C@H]1O[C@@H](O[C@@H]2OC=C3[C@@H](C[C@H]4N(CCc5c4[nH]c6ccccc56)C3=O)[C@H]2C=C)[C@H](O)[C@@H](O)[C@@H]1O
InChI	1S/C26H30N2O8/c1-2-12-15-9-18-20-14(13-5-3-4-6-17(13)27-20)7-8-28(18)24(33)16(15)11-34-25(12)36-26-23(32)22(31)21(30)19(10-29)35-26/h2-6,11-12,15,18-19,21-23,25-27,29-32H,1,7-10H2/t12-,15+,18-,19-,21-,22+,23-,25+,26+/m1/s1
InChI key	LBRPLJCNRZUXLS-AZVRXDBZSA-N

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Viniferin SMB00074-1MG

Empirical Formula (Hill Notation):	C₂₈H₂₂O₆
CAS Number:	129170-22-5
Molecular Weight:	454.47
PubChem Substance ID:	329824753
NACRES:	NA.25

General description

Natural product derived from plant source.

Application

Viniferin has been used to study its effect on melanin production in melanocyte cultures.

Biochem/physiol Actions

Protein Huntingtin (Htt) mutation, reduces the SIRT3 (sirtuin 3) expression. Viniferin is known to offer protection against Htt mutation by reducing oxidative stress and preventing SIRT3 depletion, which is involved in energy metabolism. In vitro analysis showed that viniferin derivative could prevent amyloid peptide aggregation.

Параметры

Quality Level	200,
assay	≥95% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
InChI	1S/C28H22O6/c29-19-7-2-16(3-8-19)1-4-18-13-22(32)15-25-26(18)27(23-12-11-21(31)14-24(23)33)28(34-25)17-5-9-20(30)10-6-17/h1-15,27-33H/b4-1+/t27-,28+/m0/s1
InChI key	KQXXUMAWOUVEHD-BQYFGGCBSA-N

Safety Information

pictograms	GHS09
signalword	Warning
hcodes	H410
pcodes	P273 - P501
RIDADR	UN 3077 9 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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SMB01022-1MG

Vinylphenol, O-[L-Rhamnopyranosyl-(1-6)--D-glucopyranoside] SMB01022-1MG

Empirical Formula (Hill Notation): C₂₀H₂₈O₁₀

CAS Number: 86849-78-7

Molecular Weight: 428.43

General description
Vinylphenol, O-[L-Rhamnopyranosyl-(1-6)-β-D-glucopyranoside] is a phenolic glycoside.
Natural product derived from plant source.
Параметры

assay ≥90% (LC/MS-ELSD)

form solid

storage temp. −20°C

Safety Information

WGK Germany WGK 3

Flash Point F Not applicable

Flash Point C Not applicable

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Violanthin SMB00557-1MG

Empirical Formula (Hill Notation):	C₂₇H₃₀O₁₄
CAS Number:	40581-17-7
Molecular Weight:	578.52
MDL number:	MFCD29037226
PubChem Substance ID:	329824704
NACRES:	NA.25

General description

Natural product derived from plant source.

Biochem/physiol Actions

Violanthin is a compound that belongs to a class of organic compounds known as flavanoid 8-c-glycosides

Параметры

assay	≥95% (LC/MS-UV)
form	solid
solubility	DMSO: 1 mg/mL
storage temp.	−20°C
SMILES string	O=C1C=C(OC(C([C@@H]2O[C@H]([C@@H]([C@H]([C@H]2O)O)O)C)=C3O)=C1C(O)=C3[C@@H]4O[C@@H]([C@H]([C@@H]([C@H]4O)O)O)CO)C5=CC=C(C=C5)O
InChI	1S/C27H30O14/c1-8-17(31)21(35)23(37)27(39-8)16-20(34)15(26-24(38)22(36)18(32)13(7-28)41-26)19(33)14-11(30)6-12(40-25(14)16)9-2-4-10(29)5-3-9/h2-6,8,13,17-18,21-24,26-29,31-38H,7H2,1H3/t8-,13+,17-,18+,21+,22-,23+,24+,26-,27-/m0/s1
InChI key	MVOUGOXRXQDXDC-RSPRXDBDSA-N

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

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Virginiaebutanolide C SMB00045-1MG

Empirical Formula (Hill Notation):	C₁₁H₂₀O₄
CAS Number:	109075-62-9
Molecular Weight:	216.27
MDL number:	MFCD24849295
PubChem Substance ID:	329824679
NACRES:	NA.25

General description

Natural product derived from fungal source.

Параметры

assay	≥90% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
SMILES string	CCCCC[C@@H](O)[C@H]1[C@H](CO)COC1=O
InChI	1S/C11H20O4/c1-2-3-4-5-9(13)10-8(6-12)7-15-11(10)14/h8-10,12-13H,2-7H2,1H3/t8-,9-,10-/m1/s1
InChI key	ONFPUQOPHZOEKF-OPRDCNLKSA-N

Safety Information

pictograms	GHS05,GHS06
signalword	Danger
hcodes	H301 - H318
pcodes	P280 - P301 + P310 + P330 - P305 + P351 + P338 + P310
RIDADR	UN 2811 6.1 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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SMB01062-1MG

Viscidulin I SMB01062-1MG

Empirical Formula (Hill Notation): C₁₅H₁₀O₇

CAS Number: 92519-95-4

Molecular Weight: 302.24

MDL number: MFCD18450944

General description
Viscidulin I is a flavonoid.
Natural product derived from plant source.
Параметры

assay ≥90% (LC/MS-ELSD)

form solid

storage temp. −20°C

Safety Information

WGK Germany WGK 3

Flash Point F Not applicable

Flash Point C Not applicable

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Visnadine SMB00087-1MG

Empirical Formula (Hill Notation):	C₂₁H₂₄O₇
CAS Number:	477-32-7
Molecular Weight:	388.41
EC Number:	207-515-1
PubChem Substance ID:	329824765
NACRES:	NA.25

General description

Natural product derived from plant source.

Параметры

assay	≥95% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
SMILES string	CC[C@@H](C)C(=O)O[C@@H]1[C@H](OC(C)=O)c2c(OC1(C)C)ccc3C=CC(=O)Oc23
InChI	1S/C21H24O7/c1-6-11(2)20(24)27-19-18(25-12(3)22)16-14(28-21(19,4)5)9-7-13-8-10-15(23)26-17(13)16/h7-11,18-19H,6H2,1-5H3/t11-,18-,19-/m1/s1
InChI key	GVBNSPFBYXGREE-CXWAGAITSA-N

Safety Information

pictograms	GHS07,GHS09
signalword	Warning
hcodes	H302 - H410
pcodes	P273 - P301 + P312 + P330
RIDADR	UN 3077 9 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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SMB01021-1MG

Vitexin 4"-O-Glucoside SMB01021-1MG

Empirical Formula (Hill Notation): C₂₇H₃₀O₁₅

CAS Number: 178468-00-3

Molecular Weight: 594.52

MDL number: MFCD18827497

General description
Natural product derived from plant source.
Параметры

assay ≥85% (LC/MS-ELSD)

form solid

storage temp. −20°C

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Vulgarin SMB00090-1MG

Empirical Formula (Hill Notation):	C₁₅H₂₀O₄
CAS Number:	3162-56-9
Molecular Weight:	264.32
MDL number:	MFCD01726765
PubChem Substance ID:	329824768
NACRES:	NA.25

General description

Natural product derived from plant source.

Параметры

assay	≥90% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
SMILES string	C[C@H]1[C@@H]2CC[C@]3(C)[C@@H]([C@H]2OC1=O)[C@](C)(O)C=CC3=O
InChI	1S/C15H20O4/c1-8-9-4-6-14(2)10(16)5-7-15(3,18)12(14)11(9)19-13(8)17/h5,7-9,11-12,18H,4,6H2,1-3H3/t8-,9-,11-,12+,14-,15+/m0/s1
InChI key	NGPDZEACIWDCKX-WUDKWMPASA-N

Safety Information

pictograms	GHS06
signalword	Danger
hcodes	H301
pcodes	P264 - P270 - P301 + P310 - P405 - P501
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Wogonoside SMB00081-1MG

Empirical Formula (Hill Notation):	C₂₂H₂₀O₁₁
CAS Number:	51059-44-0
Molecular Weight:	460.39
MDL number:	MFCD08704808
PubChem Substance ID:	329824759
NACRES:	NA.25

General description

Natural product derived from plant source.

Biochem/physiol Actions

Wogonoside, a flavanoid, is known for its anti-inflammatory properties. Wogonoside may have therapeutic potential for use in diseases which involve the development of inflammation and angiogenesis through its inhibition of LPS-induced angiogenesis.

Параметры

assay	≥95% (LC/MS-ELSD)
form	solid
storage temp.	−20°C
SMILES string	COc1c(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)cc(O)c3C(=O)C=C(Oc13)c4ccccc4
InChI	1S/C22H20O11/c1-30-18-13(32-22-17(27)15(25)16(26)20(33-22)21(28)29)8-11(24)14-10(23)7-12(31-19(14)18)9-5-3-2-4-6-9/h2-8,15-17,20,22,24-27H,1H3,(H,28,29)/t15-,16-,17+,20-,22+/m0/s1
InChI key	LNOHXHDWGCMVCO-NTKSAMNMSA-N

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Zataroside B SMB00573-1MG

Empirical Formula (Hill Notation):	C₁₆H₂₄O₇
CAS Number:	95645-52-6
Molecular Weight:	328.36
MDL number:	MFCD29037230
PubChem Substance ID:	329825062

General description

Natural product derived from plant source.

Параметры

assay	≥90% (LC/MS-UV)
form	solid
solubility	DMSO: 1 mg/mL
storage temp.	−20°C
SMILES string	O[C@@H]([C@@H](O[C@@H]([C@H]1O)CO)OC2=C(C)C=C(O)C(C(C)C)=C2)[C@H]1O
InChI	1S/C16H24O7/c1-7(2)9-5-11(8(3)4-10(9)18)22-16-15(21)14(20)13(19)12(6-17)23-16/h4-5,7,12-21H,6H2,1-3H3/t12-,13-,14+,15-,16-/m1/s1
InChI key	XFPSRAYOBUHKRV-IBEHDNSVSA-N

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Zinniol SMB00565-1MG

Empirical Formula (Hill Notation):	C₁₅H₂₂O₄
CAS Number:	17811-28-8
Molecular Weight:	266.33
MDL number:	MFCD03273554
PubChem Substance ID:	329824712
NACRES:	NA.25

Biochem/physiol Actions

Antitumor activity
Natural product derived from fungal source.

Параметры

assay	≥90% (LC/MS-UV)
form	solid
solubility	DMSO: 1 mg/mL
storage temp.	−20°C
SMILES string	CC(C)=CCOC1=CC(CO)=C(CO)C(OC)=C1C
InChI	1S/C15H22O4/c1-10(2)5-6-19-14-7-12(8-16)13(9-17)15(18-4)11(14)3/h5,7,16-17H,6,8-9H2,1-4H3
InChI key	DUMQPTRUYCCSEZ-UHFFFAOYSA-N

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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-Nicotinamide adenine dinucleotide 2-phosphate reduced tetrasodium salt

Empirical Formula (Hill Notation):	C₂₁H₂₆N₇Na₄O₁₇P₃
Molecular Weight:	833.35
EC Number:	214-664-6
MDL number:	MFCD00036263
PubChem Substance ID:	24897841
NACRES:	NA.51

-Nicotinamide adenine dinucleotide 2-phosphate (NADP+) and -Nicotinamide adenine dinucleotide 2-phosphate, reduced (NADPH) comprise a coenzyme redox pair (NADP+:NADPH) involved in a wide range of enzyme catalyzed oxidation reduction reactions. The NADP+/NADPH redox pair facilitates electron transfer in anabolic reactions such as lipid and cholesterol biosynthesis and fatty acyl chain elongation. The NADP+/NADPH redox pair is used in a variety of antioxidation mechanism where it protects agains reactive oxidation species accumulation. NADPH is generated in vivio by the pentose phosphate pathway (PPP).
β-Nicotinamide adenine dinucleotide 2′-phosphate reduced tetrasodium salt has been used in the Griess reagent assay of culture medium to reduce nitrate to nitrite and in glutathione peroxidase assay.

Biochem/physiol Actions

Preparation Note

Chemically reduced

Other Notes

Packaged based on NADPH content as determined by UV-Vis.

Параметры

assay	~95%
Quality Level	200,
packaging	vial of 10 mg
InChI	1S/C21H30N7O17P3.4Na/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32;;;;/h1,3-4,7-8,10-11,13-16,20-21,29-31H,2,5-6H2,(H2,23,32)(H,36,37)(H,38,39)(H2,22,24,25)(H2,33,34,35);;;;/q;4*+1/p-4/t10-,11+,13-,14+,15-,16+,20-,21+;;;;/m0..../s1
InChI key	WYWWVJHQDVCHKF-MPUNMZHWSA-J

Safety Information

Personal Protective Equipment	Eyeshields,, Gloves,, type N95 (US),
RIDADR	NONH for all modes of transport
WGK Germany	3

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-Nicotinamide adenine dinucleotide 2-phosphate reduced tetrasodium salt hydrate

Empirical Formula (Hill Notation):	C₂₁H₂₆N₇Na₄O₁₇P₃ · xH₂O
CAS Number:	2646-71-1
Molecular Weight:	833.35 (anhydrous basis)
EC Number:	220-163-3
MDL number:	MFCD00036263
PubChem Substance ID:	24278049
NACRES:	NA.51

25, 100, 250, 500 mg in poly bottle
1 g in poly bottle

Biochem/physiol Actions

NADPH is an electron donor and a cofactor for many redox enzymes including nitric oxide synthetase.
-Nicotinamide adenine dinucleotide 2-phosphate (NADP+) and -Nicotinamide adenine dinucleotide 2-phosphate, reduced (NADPH) comprise a coenzyme redox pair (NADP+:NADPH) involved in a wide range of enzyme catalyzed oxidation reduction reactions. The NADP+/NADPH redox pair facilitates electron transfer in anabolic reactions such as lipid and cholesterol biosynthesis and fatty acyl chain elongation. The NADP+/NADPH redox pair is used in a variety of antioxidation mechanism where it protects agains reactive oxidation species accumulation. NADPH is generated in vivio by the pentose phosphate pathway (PPP).

Features and Benefits

This compound is also offered as part of Sigmas Library of Pharmacologically Active Compounds (LOPAC®1280), a biologically annotated collection of high-quality, ready-to-screen compounds. Click here to learn more.

Preparation Note

Chemically reduced

Other Notes

Packaged based on solid weight.

Legal Information

LOPAC is a registered trademark of Sigma-Aldrich Co. LLC

Параметры

Quality Level	300
assay	≥97% (HPLC), ≥97% (spectrophotometric assay)
solubility	10 mM NaOH: soluble 50 mg/mL, clear
storage temp.	−20°C
SMILES string	[Na+].[Na+].[Na+].[Na+].NC(=O)C1=CN(C=CC1)[C@H]2O[C@@H](COP([O-])(=O)OP([O-])(=O)OC[C@H]3O[C@H]([C@H](OP([O-])([O-])=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@H](O)[C@@H]2O
InChI	1S/C21H30N7O17P3.4Na/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32;;;;/h1,3-4,7-8,10-11,13-16,20-21,29-31H,2,5-6H2,(H2,23,32)(H,36,37)(H,38,39)(H2,22,24,25)(H2,33,34,35);;;;/q;4*+1/p-4/t10-,11+,13-,14+,15-,16+,20-,21+;;;;/m0..../s1
InChI key	WYWWVJHQDVCHKF-MPUNMZHWSA-J

Safety Information

Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable

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-Nicotinamide adenine dinucleotide hydrate

Empirical Formula (Hill Notation):	C₂₁H₂₇N₇O₁₄P₂ · xH₂O
CAS Number:	53-84-9
Molecular Weight:	663.43 (anhydrous basis)
EC Number:	200-184-4
MDL number:	MFCD00036253
eCl@ss:	39200202
PubChem Substance ID:	24897783
NACRES:	NA.55

250 mg in poly bottle
1, 5 g in poly bottle
Packaged by solid weight.

Biochem/physiol Actions

Electron acceptor

Other Notes

This is the common form of NAD.

Параметры

Quality Level	200,
biological source	yeast
product line	BioUltra
assay	98%
form	powder
impurities	0.1% Insoluble matter
color	white to off-white
solubility	H₂O: 0.1 M, clear, colorless to faintly yellow
anion traces	chloride (Cl^-): 0.2%, sulfate (SO₄^2-): 0.05%
cation traces	Al: 0.0005%, Ca: 0.005%, Cu: 0.001%, Fe: 0.001%, K: 0.005%, Mg: 0.0005%, NH₄⁺: 0.05%, Na: 0.005%, Pb: 0.001%, Zn: 0.0005%
storage temp.	20°C
SMILES string	NC1=NC=NC2=C1N=CN2.O[C@@H]3[C@@H](COP(O)(OP(OC[C@@H](O4)[C@@H](O)[C@@H](O)[C@H]4[N+]5=CC=CC(C(N)=O)=C5)([O-])=O)=O)OC[C@@H]3O
InChI	1S/C21H27N7O14P2/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChI key	BAWFJGJZGIEFAR-NNYOXOHSSA-N
Gene Information	human ... ESR1(2099), ESR2(2100)

Safety Information

Personal Protective Equipment	Eyeshields,, Gloves,, type N95 (US),
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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-Nicotinamide adenine dinucleotide phosphate hydrate

Empirical Formula (Hill Notation):	C₂₁H₂₈N₇O₁₇P₃ · xH₂O
CAS Number:	53-59-8
Molecular Weight:	743.41 (anhydrous basis)
MDL number:	MFCD10567218
PubChem Substance ID:	24897747
NACRES:	NA.51

-Nicotinamide adenine dinucleotide phosphate hydrate is suitable for use in:

the measurement of Glucose-6-phosphate dehydrogenase activity
the Cytochrome P450 3A4 assay as a part of NADPH-regenerating system
the Cytochrome P450 2D6 assay as a part of NADPH-regenerating system
the determination of Glucose-6-phosphate content

Packaging

1 g in glass bottle
100, 250, 500 mg in glass bottle

Biochem/physiol Actions

Other Notes

Packaged based on solid weight.
This is a common form of NADP.

Параметры

Quality Level	200,
assay	95% (HPLC), 95% (spectrophotometric assay)
solubility	H₂O: soluble 50 mg/mL, clear, colorless to faintly yellow
cation traces	sodium and potassium: 0.04%
storage temp.	20°C
SMILES string	O.NC(=O)c1ccc[n+](c1)[C@@H]2O[C@H](COP([O-])(=O)OP(O)(=O)OC[C@H]3O[C@H]([C@H](OP(O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
InChI	1S/C21H28N7O17P3.H2O/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32;/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39);1H2/t10-,11-,13-,14-,15-,16-,20-,21-;/m1./s1
InChI key	ZKJOXOJMGXFSPF-QYZPTAICSA-N

Safety Information

pictograms	GHS07
signalword	Warning
hcodes	H315 - H319 - H335
pcodes	P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	dust mask type N95 (US),, Eyeshields,, Gloves,
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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-Nicotinamide adenine dinucleotide phosphate sodium salt hydrate

Empirical Formula (Hill Notation):	C₂₁H₂₇N₇NaO₁₇P₃ · xH₂O
CAS Number:	698999-85-8
Molecular Weight:	765.39 (anhydrous basis)
MDL number:	MFCD00150480
PubChem Substance ID:	24897427
NACRES:	NA.51

100, 500 mg in poly bottle
1, 5 g in poly bottle
Packaged by solid weight.

Biochem/physiol Actions

Electron acceptor

Other Notes

This is the common form of NADP. Do not confuse with 3′−NADP or α-NADP.
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. N0505.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.

Параметры

Quality Level	300
assay	98% (HPLC), 98% (spectrophotometric assay)
mp	175-178 °C (dec.) (lit.)
solubility	H₂O: soluble 50 mg/mL, clear, colorless to faintly yellow
storage temp.	20°C
SMILES string	O[C@H]1[C@@H](O)[C@H]([N+]2=CC(C(N)=O)=CC=C2)O[C@@H]1COP(OP(OC[C@H]3O[C@@H](N(C=N4)C5=C4C(N)=NC=N5)[C@H](OP(O)(O)=O)[C@@H]3O)([O-])=O)([O-])=O.O.[Na+]
InChI	1S/C21H28N7O17P3.Na.H2O/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32;;/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39);;1H2/q;+1;/p-1/t10-,11-,13-,14-,15-,16-,20-,21-;;/m1../s1
InChI key	CYQLUFJYVTUUFN-WUEGHLCSSA-M

Safety Information

Pictograms	GHS07
Signal Word	Warning
Hazard Statements	H319
Precautionary Statements	P280 - P305 + P351 + P338 - P337 + P313
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable

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-Nicotinamide adenine dinucleotide sodium salt

Empirical Formula (Hill Notation):	C₂₁H₂₆N₇NaO₁₄P₂
CAS Number:	20111-18-6
Molecular Weight:	685.41
MDL number:	MFCD00148917
PubChem Substance ID:	24897433
NACRES:	NA.51

1, 5, 25 g in poly bottle

Biochem/physiol Actions

-Nicotinamide adenine dinucleotide (NAD+) and -Nicotinamide adenine dinucleotide, reduced (NADH) comprise a coenzyme redox pair (NAD+:NADH) involved in a wide range of enzyme catalyzed oxidation reduction reactions. In addition to its redox function, NAD+/NADH is a donor of ADP-ribose units in ADP-ribosylaton (ADP-ribosyltransferases; poly(ADP-ribose) polymerases ) reactions and a precursor of cyclic ADP-ribose (ADP-ribosyl cyclases).

Other Notes

This is the common form of NAD.

Параметры

Quality Level	300
assay	95% (HPLC), 95% (enzymatic), 95% (spectrophotometric assay)
storage temp.	20°C
SMILES string	[Na].NC(=O)C1=CC=C[N](=C1)C2OC(COP(O)(=O)OP(O)(=O)OCC3OC(C(O)C3O)n4cnc5c(N)ncnc45)C(O)C2O
InChI	1S/C21H28N7O14P2.Na.H/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33;;/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H2,23,33)(H,34,35)(H,36,37)(H2,22,24,25);;
InChI key	GSZRXOXBGUIRAU-UHFFFAOYSA-N
Gene Information	human ... ESR1(2099), ESR2(2100)

Safety Information

Pictograms	GHS07
Signal Word	Warning
Hazard Statements	H315 - H319 - H335
Precautionary Statements	P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable

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-Nicotinamide adenine dinucleotide, reduced dipotassium salt

Empirical Formula (Hill Notation):	C₂₁H₂₇K₂N₇O₁₄P₂
Linear Formula:	C₂₁H₂₇N₇O₁₄P₂K₂
CAS Number:	104809-32-7
Molecular Weight:	741.62
MDL number:	MFCD00079494
PubChem Substance ID:	24897704
NACRES:	NA.51

β-Nicotinamide adenine dinucleotide (NAD+) and β-Nicotinamide adenine dinucleotide, reduced (NADH) comprise a coenzyme redox pair (NAD+:NADH) involved in a wide range of enzyme catalyzed oxidation reduction reactions. In addition to its redox function, NAD+/NADH is a donor of ADP-ribose units in ADP-ribosylaton (ADP-ribosyltransferases; poly(ADP-ribose) polymerases ) reactions and a precursor of cyclic ADP-ribose (ADP-ribosyl cyclases).

Packaging

100, 500 mg in poly bottle
1 g in poly bottle

Biochem/physiol Actions

Electron donor

Параметры

Quality Level	200,
assay	≥95%
storage temp.	−20°C
SMILES string	[K].NC(=O)C1=CN(C=CC1)C2OC(COP(O)(=O)OP(O)(=O)OCC3OC(C(O)C3O)n4cnc5c(N)ncnc45)C(O)C2O
InChI	1S/C21H29N7O14P2.K.H/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33;;/h1,3-4,7-8,10-11,13-16,20-21,29-32H,2,5-6H2,(H2,23,33)(H,34,35)(H,36,37)(H2,22,24,25);;
InChI key	KMRPNNQOKAHXEZ-UHFFFAOYSA-N
Gene Information	human ... IMPDH2(3615)

Safety Information

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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-Nicotinamide adenine dinucleotide, reduced disodium salt hydrate

Empirical Formula (Hill Notation):	C₂₁H₂₇N₇Na₂O₁₄P₂ · xH₂O
CAS Number:	606-68-8
Molecular Weight:	709.40 (anhydrous basis)
EC Number:	210-123-3
MDL number:	MFCD03791273
PubChem Substance ID:	329818676
NACRES:	NA.51

1, 5 g in poly bottle
50, 100, 500 mg in poly bottle
Packaged by solid weight.

Biochem/physiol Actions

NADH is a coenzyme that functions as a regenerating electron donor in catabolic processes including glycolysis, -oxidation and the citric acid cycle (Krebs cycle, TCA cycle). It participates in cell signaling events as well, for example as a substrate for the poly (ADP-ribose) polymerases (PARPs) during the DNA damage response. The NAD+/NADH dependent sirtuins play key roles in stress responses during events involving energy metabolism, with implications in cancer biology, diabetes and neurodegenerative disease.
As a reagent, NADH can be used in enzyme cycling assays to amplify detection of activity of biologically relevant enzymes or metabolites present in low concentrations.

Параметры

Quality Level	300
assay	≥97% (HPLC), ≥97% (spectrophotometric assay)
storage temp.	−20°C
SMILES string	O.[Na+].[Na+].NC(=O)C1=CN(C=CC1)[C@@H]2O[C@H](COP([O-])(=O)OP([O-])(=O)OC[C@H]3O[C@H]([C@H](O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
InChI	1S/C21H29N7O14P2.2Na.H2O/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33;;;/h1,3-4,7-8,10-11,13-16,20-21,29-32H,2,5-6H2,(H2,23,33)(H,34,35)(H,36,37)(H2,22,24,25);;;1H2/q;2*+1;/p-2/t10-,11-,13-,14-,15-,16-,20-,21-;;;/m1.../s1
InChI key	FWBNCIFELNNJCX-UHOVGGJYSA-L

Safety Information

Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

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Отзывы

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Empirical Formula (Hill Notation):	C₃₄H₄₂O₂₂
Molecular Weight:	802.68
NACRES:	NA.25

Empirical Formula (Hill Notation):	C₁₇H₂₄O₁₁
CAS Number:	23407-76-3
Molecular Weight:	404.37
MDL number:	MFCD20260837

Empirical Formula (Hill Notation):	C₁₅H₂₀O₂
CAS Number:	131651-37-1
Molecular Weight:	232.32

Empirical Formula (Hill Notation):	C₃₂H₃₆O₁₃
CAS Number:	150044-49-8
Molecular Weight:	628.62

Empirical Formula (Hill Notation):	C₂₄H₃₀O₃
CAS Number:	23838-17-7
Molecular Weight:	366.49
MDL number:	MFCD01305375

Empirical Formula (Hill Notation):	C₃₅H₅₄O₁₄
CAS Number:	20231-81-6
Molecular Weight:	698.79

Empirical Formula (Hill Notation):	C₂₅H₂₈O₁₃
CAS Number:	36138-58-6
Molecular Weight:	536.48

Empirical Formula (Hill Notation):	C₂₀H₂₈O₁₀
CAS Number:	86849-78-7
Molecular Weight:	428.43

Empirical Formula (Hill Notation):	C₁₅H₁₀O₇
CAS Number:	92519-95-4
Molecular Weight:	302.24
MDL number:	MFCD18450944

Empirical Formula (Hill Notation):	C₂₇H₃₀O₁₅
CAS Number:	178468-00-3
Molecular Weight:	594.52
MDL number:	MFCD18827497

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