CYCLOEUCALENOL

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C30H50O
Molecular Weight	426.7174
Optical Activity	UNSPECIFIED
Defined Stereocenters	10 / 10
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CC(C)C(=C)CC[C@@H](C)[C@H]1CC[C@@]2(C)[C@@H]3CC[C@H]4[C@H](C)[C@@H](O)CC[C@@]45C[C@@]35CC[C@]12C

InChI

InChIKey=HUNLTIZKNQDZEI-PGFZVWMDSA-N

InChI=1S/C30H50O/c1-19(2)20(3)8-9-21(4)23-12-14-28(7)26-11-10-24-22(5)25(31)13-15-29(24)18-30(26,29)17-16-27(23,28)6/h19,21-26,31H,3,8-18H2,1-2,4-7H3/t21-,22+,23-,24+,25+,26+,27-,28+,29-,30+/m1/s1

HIDE SMILES / InChI

Molecular Formula	C30H50O
Molecular Weight	426.7174
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	10 / 10
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

Title	Date	PubMed
Two new triterpenoids from the leaves and stems of Fritillaria hupehensis.	2009-09	20183324
[A novel azo-type compound from Dendrolobium triangulare].	2009-09	20055176
[Chemical constituents from fruits of Ailanthus altissima].	2009-09	19943484
5 alpha-reductase and aromatase inhibitory constituents from Brassica rapa L. pollen.	2009-04	19336936
Biological activities of the chemical constituents of Erythrina stricta and Erythrina subumbrans.	2007-11	18087807
[Chemical constituents from root barks of Periploca sepium].	2007-07	17879730
Diterpenoids and triterpenoids from Euphorbia guyoniana.	2007-05	17337022
[Chemical constituents from herb of Alternanthera philoxeroides].	2006-07	17048605
Biotransformation of cycloartane-type triterpenes by the fungus Glomerella fusarioides.	2006-04	16643035
Mechanism involved in the spasmolytic effect of a mixture of two triterpenes, cycloartenol and cycloeucalenol, isolated from Herissanthia tiubae in the guinea-pig ileum.	2005-11	16320203
Study on cardiac contractility of cycloeucalenol and cycloeucalenone isolated from Tinospora crispa.	2002-11	12413712
Inhibition of the sterol pathway in leek seedlings impairs phosphatidylserine and glucosylceramide synthesis but triggers an accumulation of triacylglycerols.	2002-08-08	12176396

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:10:08 GMT 2025` Edited by `admin` on `Mon Mar 31 19:10:08 GMT 2025`
Record UNII	7OF1Q9UE9R
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

3.BETA.-CYCLOEUCALENOL

Preferred Name

English

CYCLOEUCALENOL

Common Name

English

9,19-CYCLO-5.ALPHA.,9.BETA.-ERGOST-24(28)-EN-3.BETA.-OL, 4.ALPHA.,14-DIMETHYL-

Common Name

English

CYCLOARTANOL, 4.BETA.-DEMETHYL-24-METHYLENE

Common Name

English

4.ALPHA.,14.ALPHA.-DIMETHYL-9,19-CYCLOPROPANE-24(28)-METHYLENECHOLESTAN-3.BETA.-OL

Common Name

English

9,19-CYCLOERGOST-24(28)-EN-3-OL, 4,14-DIMETHYL-, (3.BETA.,4.ALPHA.,5.ALPHA.)-

Common Name

English

Code System Code Type Description

CAS

469-39-6