Home Aminos Benzeneethanol,b-[[4-[2-(dimethylamino)ethoxy]phenyl]phenylmethylene]-a-methyl-,(bE)-

Benzeneethanol,b-[[4-[2-(dimethylamino)ethoxy]phenyl]phenylmethylene]-a-methyl-,(bE)-

CAS No.:
97151-02-5
Catalog Number:
AG01CBSY
Molecular Formula:
Molecular Weight:
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1mg
≥98%
1 week
United States
$119
- +
5mg
≥98%
1 week
United States
$300
- +
10mg
≥98%
1 week
United States
$439
- +
Product Description
Catalog Number:
AG01CBSY
Chemical Name:
Benzeneethanol,b-[[4-[2-(dimethylamino)ethoxy]phenyl]phenylmethylene]-a-methyl-,(bE)-
CAS Number:
97151-02-5
MDL Number:
MFCD02101152
IUPAC Name:
(E)-4-[4-[2-(dimethylamino)ethoxy]phenyl]-3,4-diphenylbut-3-en-2-ol
InChI:
InChI=1S/C26H29NO2/c1-20(28)25(21-10-6-4-7-11-21)26(22-12-8-5-9-13-22)23-14-16-24(17-15-23)29-19-18-27(2)3/h4-17,20,28H,18-19H2,1-3H3/b26-25-
InChI Key:
BPHFBQJMFWCHGH-QPLCGJKRSA-N
Properties
Complexity:
495  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1  
Exact Mass:
387.22g/mol
Formal Charge:
0
Heavy Atom Count:
29  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
387.523g/mol
Monoisotopic Mass:
387.22g/mol
Rotatable Bond Count:
8  
Topological Polar Surface Area:
32.7A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
5.9  
Literature
Title Journal
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Characterization of the human cytochrome P450 forms involved in metabolism of tamoxifen to its alpha-hydroxy and alpha,4-dihydroxy derivatives. Chemical research in toxicology 20051001
Organ specificity of DNA adduct formation by tamoxifen and alpha-hydroxytamoxifen in the rat: implications for understanding the mechanism(s) of tamoxifen carcinogenicity and for human risk assessment. Mutagenesis 20050701
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UDP-glucuronosyltransferases and clinical drug-drug interactions. Pharmacology & therapeutics 20050401
Interactions of the stereoisomers of alpha-hydroxytamoxifen with human hydroxysteroid sulfotransferase SULT2A1 and rat hydroxysteroid sulfotransferase STa. Drug metabolism and disposition: the biological fate of chemicals 20041201
Stereoselective metabolic activation of alpha-hydroxy-N-desmethyltamoxifen: the R-isomer forms more DNA adducts in rat liver cells. Chemical research in toxicology 20040501
Biotransformation of tamoxifen in a human endometrial explant culture model. Chemico-biological interactions 20031215
Alpha-hydroxylation of tamoxifen and toremifene by human and rat cytochrome P450 3A subfamily enzymes. Chemical research in toxicology 20030901
Identification of human CYP forms involved in the activation of tamoxifen and irreversible binding to DNA. Carcinogenesis 20021101
The mutational signature of alpha-hydroxytamoxifen at Hprt locus in Chinese hamster cells. Carcinogenesis 20021101
Mutations induced by alpha-hydroxytamoxifen in the lacI and cII genes of Big Blue transgenic rats. Carcinogenesis 20021001
Induction of lacI mutations in Big Blue rats treated with tamoxifen and alpha-hydroxytamoxifen. Cancer letters 20020208
Resolution of alpha-hydroxytamoxifen; R-isomer forms more DNA adducts in rat liver cells. Chemical research in toxicology 20010701
Short-term dosing of alpha-hydroxytamoxifen results in DNA damage but does not lead to liver tumours in female Wistar/Han rats. Carcinogenesis 20010401
Properties