ILIMAQUINONE

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C22H30O4
Molecular Weight	358.4712
Optical Activity	UNSPECIFIED
Defined Stereocenters	4 / 4
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

COC1=CC(=O)C(O)=C(C[C@]2(C)[C@@H](C)CC[C@@]3(C)[C@H]2CCCC3=C)C1=O

InChI

InChIKey=JJWITJNSXCXULM-YVUMSICPSA-N

InChI=1S/C22H30O4/c1-13-7-6-8-18-21(13,3)10-9-14(2)22(18,4)12-15-19(24)16(23)11-17(26-5)20(15)25/h11,14,18,24H,1,6-10,12H2,2-5H3/t14-,18+,21+,22+/m0/s1

HIDE SMILES / InChI

Molecular Formula	C22H30O4
Molecular Weight	358.4712
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	4 / 4
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

Title	Date	PubMed
Ilimaquinone induces death receptor expression and sensitizes human colon cancer cells to TRAIL-induced apoptosis through activation of ROS-ERK/p38 MAPK-CHOP signaling pathways.	2014-09	24930757
Inhibition of HIV-1 protease and RNase H of HIV-1 reverse transcriptase activities by long chain phenols from the sarcotestas of Ginkgo biloba.	2008-04	18543149
Requirement of phospholipase D for ilimaquinone-induced Golgi membrane fragmentation.	2007-11-23	17897952
Illimaquinone, a selective inhibitor of the RNase H activity of human immunodeficiency virus type 1 reverse transcriptase.	1990-10	1705412

Substance Class	Chemical Created by `admin` on `Mon Mar 31 22:44:04 GMT 2025` Edited by `admin` on `Mon Mar 31 22:44:04 GMT 2025`
Record UNII	5U0WAN3N8Q
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

ILIMAQUINONE

Common Name

English

(-)-ILIMAQUINONE

Preferred Name

English

2,5-CYCLOHEXADIENE-1,4-DIONE, 3-(((1R,2S,4AS,8AS)-DECAHYDRO-1,2,4A-TRIMETHYL-5-METHYLENE-1-NAPHTHALENYL)METHYL)-2-HYDROXY-5-METHOXY-

Systematic Name

English

ILIMAQUINONE, (-)-

Common Name

English

ILIMAQUINONE [MI]

Common Name

English

ILLIMAQUINONE

Common Name

English

Code System Code Type Description

FDA UNII

5U0WAN3N8Q