(Q27098418)

Gene Ontology release 2020-05-02

Rhea release 113

cholestenone 5-alpha-reductase activity

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

mass

384.339±0 dalton

1 reference

4-Cholesten-3-one (English)

19 October 2016

chemical formula

C₂₇H₄₄O

1 reference

4-Cholesten-3-one (English)

19 November 2016

canonical SMILES

CC(C)CCCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C

1 reference

4-Cholesten-3-one (English)

19 November 2016

isomeric SMILES

C[C@H](CCCC(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=CC(=O)CC[C@]34C)C

1 reference

4-Cholesten-3-one (English)

19 November 2016

melting point

80.0 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Muricea californica

1 reference

Occurrence and seasonal variation of 19-norcholest-4-en-3-one and 3 beta-monohydroxy sterols in the Californian gorgonian, Muricea californica

Cribricellina cribraria

1 reference

New cytotoxic beta-carboline alkaloids from the marine bryozoan, Cribricellina cribraria

Croton hieronymi

3 references

A linear sesterterpene, two squalene derivatives and two peptide derivatives from Croton hieronymi

A linear sesterterpene, two squalene derivatives and two peptide derivatives from Croton hieronymi

A linear sesterterpene, two squalene derivatives and two peptide derivatives from Croton hieronymi

Acanthophora spicifera

1 reference

Lipid constituents of the red alga Acantophora spicifera

Axinella verrucosa

1 reference

Investigations on the ring contraction step in the biosynthesis of A-nor-stanols by the marine sponge Axinella verrucosa

Tetilla

1 reference

ChemInform Abstract: Steroids from Marine Sponges Suberites vestigium and Chrotella australiensis.

Cinachyrella

1 reference

Isolation and synthesis of the first natural 6-hydroximino 4-en-3-one- steroids from the sponges Cinachyrella spp

Dracaena cinnabari

2 references

Sterols and triterpenoids from Dracaena cinnabari

Sterols and triterpenoids from Dracaena cinnabari

Geodia cydonium

1 reference

Steroidal Ketones from the Sponge Geodia cydonium

Neogymnocrinus richeri

1 reference

Sterol composition of the “living fossil” crinoid Gymnocrinus richeri

Salvia tomentosa

1 reference

Terpenoids From the Roots of Salvia Tomentosa

Streptomyces

1 reference

One new anthraquinone from marine Streptomyces sp. FX-58

Phallusia nigra

1 reference

Minor sterols of marine invertebrates 37. Isolation of novel coprostanols and 4 alpha-methyl sterols from the tunicate Ascidia nigra

Bombax anceps

1 reference

CHEMICAL CONSTITUENTS FROM THE ROOTS OF BOMBAX ANCEPS

Dendrophyllia cornigera

1 reference

3-Keto steroids from the marine organisms Dendrophyllia cornigera and Cymodocea nodosa

Amphilectus fucorum

1 reference

Novel sterols from the sponge esperiopsis edwardii

Gymnodinium lunula

1 reference

Sterols of the cultured dinoflagellate Pyrocystis lunula

Pyrocystis lunula

1 reference

Sterols of the cultured dinoflagellate Pyrocystis lunula

Peyssonnelia

1 reference

Structure and biological evaluation of novel cytotoxic sterol glycosides from the marine red alga Peyssonnelia sp.

Venerupis philippinarum

1 reference

Steroids in the feces of a marine bivalve.

Salvia officinalis

1 reference

Terpenoids From the Roots of Salvia Tomentosa

Arabidopsis thaliana

1 reference

Biosynthesis of cholestanol in higher plants

Paracribricellina cribraria

1 reference

New cytotoxic beta-carboline alkaloids from the marine bryozoan, Cribricellina cribraria

Homo sapiens

1 reference

Metabolomic profiling of schizophrenia patients at risk for metabolic syndrome.

Identifiers

InChI

InChI=1S/C27H44O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h17-19,22-25H,6-16H2,1-5H3/t19-,22+,23-,24+,25+,26+,27-/m1/s1

1 reference

4-Cholesten-3-one (English)

19 November 2016

2 references

4-Cholesten-3-one (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

601-57-0

2 references

Global Substance Registration System

UNII

7T94NHD99C

cholesterone (English)

19 November 2016

https://commonchemistry.cas.org/detail?cas_rn=601-57-0

10 April 2021

1 reference

Cholest-4-en-3-one (English)

19 November 2016

2 references

4-Cholesten-3-one (English)

19 November 2016

ChEBI ID

16175

mapping relation type

2 references

4-CHOLESTEN 3-ONE (English)

19 November 2016

International Chemical Identifier

InChI

InChI=1S/C27H44O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h17-19,22-25H,6-16H2,1-5H3/t19-,22+,23-,24+,25+,26+,27-/m1/s1

1 reference

4-CHOLESTEN 3-ONE (English)

19 November 2016

2 references

inferred from InChIKey

splash10-0532-9400000000-d0d60fb4fbca5c06cb01

1 reference

0 references

splash10-001j-9803000000-0041fa800c684344d6f8

0 references

splash10-001i-0009000000-3ba0c0c4f5b64032e969

0 references

DSSTox substance ID

DTXSID90872379

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

0 references

0 references

1 reference

Global Substance Registration System

UNII

7T94NHD99C

cholesterone (English)

ECHA Substance Infocard ID

19 November 2016

100.009.096

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.009.096

27 December 2018

Human Metabolome Database ID

Cholest-4-en-3-one (English)

quotation

CAS no.: 601-57-0 (English)

HMDB0000921

2 references

based on heuristic

inferred from InChIKey

1 reference

Global Substance Registration System

cholest-4-en-3-one (English)

19 October 2016

2 references

UNII

7T94NHD99C

cholesterone (English)

19 November 2016

0 references

0 references

0 references

0 references

1 reference

2YOO (English)

19 October 2016

1 reference

3SN5 (English)

19 October 2016

1 reference

2X5W (English)