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UC602

Sigma-Aldrich

Phenyl-d5-7-hydroxywarfarin

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About This Item

Empirical Formula (Hill Notation):
C19H11D5O5
CAS Number:
94820-65-2
Molecular Weight:
329.36
MDL number:
MFCD00272675
UNSPSC Code:
12161501
PubChem Substance ID:
329827673
NACRES:
NA.77

form

solid

Quality Level

200

color

white

mp

201-203 °C

mass shift

M+5

storage temp.

2-8°C

SMILES string

[2H]c1c([2H])c([2H])c(c([2H])c1[2H])C(CC(C)=O)C2=C(O)c3ccc(O)cc3OC2=O

InChI

1S/C19H16O5/c1-11(20)9-15(12-5-3-2-4-6-12)17-18(22)14-8-7-13(21)10-16(14)24-19(17)23/h2-8,10,15,21-22H,9H2,1H3/i2D,3D,4D,5D,6D

InChI key

SKFYEJMLNMTTJA-VIQYUKPQSA-N

Application

7-Hydroxywarfarin internal standard.

Biochem/physiol Actions

Labeled metabolite of warfarin.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H318

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Yoshiya Yamamura et al.
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Mika Kosaka et al.
Drug metabolism and disposition: the biological fate of chemicals, 48(8), 655-661 (2020-06-03)
Pyrrolo[2,1-c][1,4]benzodiazepine dimer (PBD) has shown broad antitumor properties and potential as a therapeutic agent for cancers. During a routine drug-drug interaction assessment, it was found that PBD is a reversible inhibitor of CYP2C8 (IC50 = 1.1 µM) but not CYP1A2
Bianca M Liederer et al.
Xenobiotica; the fate of foreign compounds in biological systems, 49(9), 1063-1077 (2018-09-28)
GNE-617 (N-(4-((3,5-difluorophenyl)sulfonyl)benzyl)imidazo[1,2-a]pyridine-6-carboxamide) is a potent, selective nicotinamide phosphoribosyltransferase (NAMPT) inhibitor being explored as a potential treatment for human cancers. Plasma clearance was low in monkeys and dogs (9.14 mL min-1 kg-1 and 4.62 mL min-1 kg-1, respectively) and moderate in mice and rats (36.4 mL

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