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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 of CYCLOEUCALENOL

SMILES

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

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

PubMed

TitleDatePubMed
Study on cardiac contractility of cycloeucalenol and cycloeucalenone isolated from Tinospora crispa.
2002 Nov
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 Nov
Biotransformation of cycloartane-type triterpenes by the fungus Glomerella fusarioides.
2006 Apr
[Chemical constituents from herb of Alternanthera philoxeroides].
2006 Jul
[Chemical constituents from root barks of Periploca sepium].
2007 Jul
Diterpenoids and triterpenoids from Euphorbia guyoniana.
2007 May
Biological activities of the chemical constituents of Erythrina stricta and Erythrina subumbrans.
2007 Nov
5 alpha-reductase and aromatase inhibitory constituents from Brassica rapa L. pollen.
2009 Apr
Two new triterpenoids from the leaves and stems of Fritillaria hupehensis.
2009 Sep
[A novel azo-type compound from Dendrolobium triangulare].
2009 Sep
[Chemical constituents from fruits of Ailanthus altissima].
2009 Sep
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:18:29 GMT 2023
Edited
by admin
on Fri Dec 15 18:18:29 GMT 2023
Record UNII
7OF1Q9UE9R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
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
3.BETA.-CYCLOEUCALENOL
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
Created by admin on Fri Dec 15 18:18:29 GMT 2023 , Edited by admin on Fri Dec 15 18:18:29 GMT 2023
PRIMARY
MESH
C007198
Created by admin on Fri Dec 15 18:18:29 GMT 2023 , Edited by admin on Fri Dec 15 18:18:29 GMT 2023
PRIMARY
CHEBI
16653
Created by admin on Fri Dec 15 18:18:29 GMT 2023 , Edited by admin on Fri Dec 15 18:18:29 GMT 2023
PRIMARY
FDA UNII
7OF1Q9UE9R
Created by admin on Fri Dec 15 18:18:29 GMT 2023 , Edited by admin on Fri Dec 15 18:18:29 GMT 2023
PRIMARY
PUBCHEM
101690
Created by admin on Fri Dec 15 18:18:29 GMT 2023 , Edited by admin on Fri Dec 15 18:18:29 GMT 2023
PRIMARY
EPA CompTox
DTXSID70963693
Created by admin on Fri Dec 15 18:18:29 GMT 2023 , Edited by admin on Fri Dec 15 18:18:29 GMT 2023
PRIMARY