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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
Structure of TALERANOL

SMILES

C[C@H]1CCC[C@@H](O)CCCCCC2=CC(O)=CC(O)=C2C(=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

HIDE SMILES / InChI

Molecular Formula C18H26O5
Molecular Weight 322.396
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

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

PubMed

TitleDatePubMed
Human sex hormone-binding globulin binding affinities of 125 structurally diverse chemicals and comparison with their binding to androgen receptor, estrogen receptor, and α-fetoprotein.
2015-02
Assessment of estrogenic and anti-androgenic activities of the mycotoxin zearalenone and its metabolites using in vitro receptor-specific bioassays.
2014-12
Selectivity of natural, synthetic and environmental estrogens for zebrafish estrogen receptors.
2014-10-01
Rat α-Fetoprotein binding affinities of a large set of structurally diverse chemicals elucidated the relationships between structures and binding affinities.
2012-11-19
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
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.
2004-07
Study of 202 natural, synthetic, and environmental chemicals for binding to the androgen receptor.
2003-10
Assessment of oestrogenic potency of chemicals used as growth promoter by in-vitro methods.
2001-05
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:32:02 GMT 2025
Edited
by admin
on Mon Mar 31 18:32:02 GMT 2025
Record UNII
HUN219N434
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TALERANOL
INN   USAN  
INN   USAN  
Official Name English
P-1560
Preferred Name English
(3S,7S)-3,4,5,6,7,8,9,10,11,12-Decahydro-7,14,16-trihydroxy-3-methyl-1H-2-benzoxacyclotetradecin-1-one
Systematic Name English
TALERANOL [USAN]
Common Name English
taleranol [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C2182
Created by admin on Mon Mar 31 18:32:02 GMT 2025 , Edited by admin on Mon Mar 31 18:32:02 GMT 2025
Code System Code Type Description
MESH
C028226
Created by admin on Mon Mar 31 18:32:02 GMT 2025 , Edited by admin on Mon Mar 31 18:32:02 GMT 2025
PRIMARY
FDA UNII
HUN219N434
Created by admin on Mon Mar 31 18:32:02 GMT 2025 , Edited by admin on Mon Mar 31 18:32:02 GMT 2025
PRIMARY
ChEMBL
CHEMBL491510
Created by admin on Mon Mar 31 18:32:02 GMT 2025 , Edited by admin on Mon Mar 31 18:32:02 GMT 2025
PRIMARY
EPA CompTox
DTXSID3022532
Created by admin on Mon Mar 31 18:32:02 GMT 2025 , Edited by admin on Mon Mar 31 18:32:02 GMT 2025
PRIMARY
WIKIPEDIA
Taleranol
Created by admin on Mon Mar 31 18:32:02 GMT 2025 , Edited by admin on Mon Mar 31 18:32:02 GMT 2025
PRIMARY
SMS_ID
100000082997
Created by admin on Mon Mar 31 18:32:02 GMT 2025 , Edited by admin on Mon Mar 31 18:32:02 GMT 2025
PRIMARY
PUBCHEM
65434
Created by admin on Mon Mar 31 18:32:02 GMT 2025 , Edited by admin on Mon Mar 31 18:32:02 GMT 2025
PRIMARY
NCI_THESAURUS
C74260
Created by admin on Mon Mar 31 18:32:02 GMT 2025 , Edited by admin on Mon Mar 31 18:32:02 GMT 2025
PRIMARY
EVMPD
SUB10803MIG
Created by admin on Mon Mar 31 18:32:02 GMT 2025 , Edited by admin on Mon Mar 31 18:32:02 GMT 2025
PRIMARY
CAS
42422-68-4
Created by admin on Mon Mar 31 18:32:02 GMT 2025 , Edited by admin on Mon Mar 31 18:32:02 GMT 2025
PRIMARY
INN
3691
Created by admin on Mon Mar 31 18:32:02 GMT 2025 , Edited by admin on Mon Mar 31 18:32:02 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> METABOLITE
Related Record Type Details
ACTIVE MOIETY