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187960-08-3

187960-08-3 Structure

187960-08-3 Structure
IdentificationBack Directory
[Name]

Genistein-D4 (4-Hydroxyphenyl-2,3,5,6-D4)
[CAS]

187960-08-3
[Synonyms]

GeniVida-d4
Bonistein-d4
Genisteol-d4
Baichanin A-d4
4',5,7-Trihydroxyisoflavone-d4
Genistein-2',3',5',6'-d4 (Major)
5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one-d4
4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl-2,3,5,6-d4)-
[Molecular Formula]

C15H6D4O5
[MOL File]

187960-08-3.mol
[Molecular Weight]

274.263
Chemical PropertiesBack Directory
[Melting point ]

290-292°C (dec.)
[storage temp. ]

-20°C Freezer
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[color ]

Light Yellow to Yellow
[Stability:]

Light Sensitive - Protect From Light
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P264-P270-P301+P312-P330-P501
Hazard InformationBack Directory
[Chemical Properties]

Yellow Solid
[Uses]

Exhibits specific inhibitory activity against tyrosine kinases,including autophosphorylation of epidermal growth factor receptor kinase (IC50 - 2.6uM). Also inhibits other protein kinases through competitive inhibition of ATP. Inhibits tumor cell proliferation and induces tumor cell differentiation. Produces cell-cycle arrest and apoptosis in Jurat T-leukemia cells. However, it prevents anti-CD3 monoclonal antibody-induced thymic apoptosis. Genistein also inhibits topoisomerase II activity in vitro. Genistein has also been shown to inhibit the action of GABA on recombinant GABAA receptors2. uv(max)ethanol: 262.5 nm (e= 138). moderately sol. in hot alcohol
[storage]

Store at -20°C
[References]

[1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. DOI:10.1177/1060028018797110
[2] Peterson G, et al. Genistein inhibits both estrogen and growth factor-stimulated proliferation of human breast cancer cells. Cell Growth Differ. 1996 Oct;7(10):1345-51. PMID:8891338
[3] Ding S, et al. Environmentally Relevant Dose of Bisphenol A Does Not Affect Lipid Metabolism and Has No Synergetic or Antagonistic Effects on Genistein's Beneficial Roles on Lipid Metabolism. PLoS One. 2016 May 12;11(5):e0155352. DOI:10.1371/journal.pone.0155352
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