Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C18H26O5 |
Molecular Weight | 322.396 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H]1CCC[C@@H](O)CCCCCC2=C(C(O)=CC(O)=C2)C(=O)O1
InChI
InChIKey=DWTTZBARDOXEAM-JSGCOSHPSA-N
InChI=1S/C18H26O5/c1-12-6-5-9-14(19)8-4-2-3-7-13-10-15(20)11-16(21)17(13)18(22)23-12/h10-12,14,19-21H,2-9H2,1H3/t12-,14-/m0/s1
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/6351181
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6351181
Taleranol (also known as P-1560) a weak estrogen and a minor metabolite and epimer of the drug, zeranol. Zeranol is an anabolic agent that used in animal feed and is intended for human consumption, is noncarcinogenic, nonteratogenic, and nonmutagenic.
Approval Year
PubMed
Title | Date | PubMed |
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Assessment of oestrogenic potency of chemicals used as growth promoter by in-vitro methods. | 2001 May |
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Study of 202 natural, synthetic, and environmental chemicals for binding to the androgen receptor. | 2003 Oct |
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Rapid yeast estrogen bioassays stably expressing human estrogen receptors alpha and beta, and green fluorescent protein: a comparison of different compounds with both receptor types. | 2004 Jul |
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Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods. | 2006 Nov |
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Assessment of estrogenic and anti-androgenic activities of the mycotoxin zearalenone and its metabolites using in vitro receptor-specific bioassays. | 2014 Dec |
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C2182
Created by
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C028226
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HUN219N434
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CHEMBL491510
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DTXSID3022532
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Taleranol
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100000082997
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65434
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C74260
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SUB10803MIG
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42422-68-4
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3691
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ACTIVE MOIETY
PARENT (METABOLITE)