16α-hydroxyestrone   Click here for help

GtoPdb Ligand ID: 12965

Synonyms: 16α-OHE1 | 16-hydroxyestrone | 16alpha-hydroxyestrone | 16alpha-OHE1
PDB Ligand
Compound class: Synthetic organic
Comment: 16α-hydroxyestrone is an estrogenic metabolite that is a 16-hydroxylation product generated during the catalytic breakdown of estrone by cytochrome P450 enzymes in the liver (principally CYP3A4 and 3A5).
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Ligand Activity Visualisation Charts

These are box plot that provide a unique visualisation, summarising all the activity data for a ligand taken from ChEMBL and GtoPdb across multiple targets and species. Click on a plot to see the median, interquartile range, low and high data points. A value of zero indicates that no data are available. A separate chart is created for each target, and where possible the algorithm tries to merge ChEMBL and GtoPdb targets by matching them on name and UniProt accession, for each available species. However, please note that inconsistency in naming of targets may lead to data for the same target being reported across multiple charts.

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View interactive charts of activity data across species
2D Structure
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2D Structure

An image of the ligand's 2D structure. For small molecules with SMILES these are drawn using the NCI/CADD Chemical Identifier Resolver. Click on the image to access the chemical structure search tool with the ligand pre-loaded in the structure editor. For other types of ligands, e.g. longer nucleotides and peptides, a manually drawn representation of the molecule may be provided.

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Click here for structure editor
Physico-chemical Properties
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Physico-chemical Properties

Calculated molecular properties are available for small molecules and natural products (not peptides). Properties were generated using the CDK toolkit. All properties were selected to enable the prediction of the Lipinski Rule-of-Five profile or ‘druglikeness’ for each ligand. For more info on each category see the help pages.

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Hydrogen bond acceptors 3
Hydrogen bond donors 2
Rotatable bonds 0
Topological polar surface area 57.53
Molecular weight 286.37
XLogP 2.53
No. Lipinski's rules broken 0
SMILES / InChI / InChIKey
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SMILES / InChI / InChIKey

SMILES (Simplified Molecular Input Line Entry Specification) A specification for unambiguously describing the structure of chemical molecules using short ASCII strings. Canonical SMILES specify a unique representation of the 2D structure without chiral or isotopic specifications. Isomeric SMILES include chiral specification and isotopes.

Standard InChI (IUPAC International Chemical Identifier) and InChIKey InChI is a non-proprietary, standard, textual identifier for chemical substances designed to facilitate linking of information and database searching. An InChIKey is a simplified version of a full InChI, designed for easier web searching.

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Canonical SMILES C[C@@]12CC[C@@H]3C4=CC=C(C=C4CC[C@H]3[C@@H]2C[C@H](C1=O)O)O
Isomeric SMILES C[C@]12CC[C@H]3[C@H]([C@@H]1C[C@H](C2=O)O)CCC4=C3C=CC(=C4)O
InChI InChI=1S/C18H22O3/c1-18-7-6-13-12-5-3-11(19)8-10(12)2-4-14(13)15(18)9-16(20)17(18)21/h3,5,8,13-16,19-20H,2,4,6-7,9H2,1H3/t13-,14-,15+,16-,18+/m1/s1
InChI Key WPOCIZJTELRQMF-QFXBJFAPSA-N
References
1. Fishman J, Martucci C. (1980)
Biological properties of 16 alpha-hydroxyestrone: implications in estrogen physiology and pathophysiology.
J Clin Endocrinol Metab, 51 (3): 611-5. [PMID:7190977]
2. Fishman J, Schneider J, Hershcope RJ, Bradlow HL. (1984)
Increased estrogen-16 alpha-hydroxylase activity in women with breast and endometrial cancer.
J Steroid Biochem, 20 (4B): 1077-81. [PMID:6727352]
3. Martucci C, Fishman J. (1977)
Direction of estradiol metabolism as a control of its hormonal action--uterotrophic activity of estradiol metabolites.
Endocrinology, 101 (6): 1709-15. [PMID:590186]
4. Schneider J, Kinne D, Fracchia A, Pierce V, Anderson KE, Bradlow HL, Fishman J. (1982)
Abnormal oxidative metabolism of estradiol in women with breast cancer.
Proc Natl Acad Sci U S A, 79 (9): 3047-51. [PMID:6953448]
5. Swaneck GE, Fishman J. (1988)
Covalent binding of the endogenous estrogen 16 alpha-hydroxyestrone to estradiol receptor in human breast cancer cells: characterization and intranuclear localization.
Proc Natl Acad Sci U S A, 85 (21): 7831-5. [PMID:3186693]