LL-Z1272.EPISILON.

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C23H32O4
Molecular Weight	372.4978
Optical Activity	UNSPECIFIED
Defined Stereocenters	3 / 3
E/Z Centers	1
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

C[C@@H]1CCC(=O)[C@H](C)[C@@]1(C)CC\C(C)=C\CC2=C(O)C(C=O)=C(C)C=C2O

InChI

InChIKey=JSPPDMSCDGJJOM-YDMRWXCBSA-N

InChI=1S/C23H32O4/c1-14(10-11-23(5)16(3)7-9-20(25)17(23)4)6-8-18-21(26)12-15(2)19(13-24)22(18)27/h6,12-13,16-17,26-27H,7-11H2,1-5H3/b14-6+/t16-,17+,23+/m1/s1

HIDE SMILES / InChI

Molecular Formula	C23H32O4
Molecular Weight	372.4978
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	3 / 3
E/Z Centers	1
Optical Activity	UNSPECIFIED

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
nitric oxide biosynthetic process 17 Target ID: GO:0006809 Sources: https://www.ncbi.nlm.nih.gov/pubmed/19199645	Inhibitor 8504

Substance Class	Chemical Created by `admin` on `Tue Apr 01 19:41:36 GMT 2025` Edited by `admin` on `Tue Apr 01 19:41:36 GMT 2025`
Record UNII	AQD59552Y1
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

LL-Z1272.EPISILON.

Common Name

English

LL-Z 1272.EPSILON.

Preferred Name

English

ANTIBIOTIC LL-Z1272.EPSILON.

Common Name

English

.BETA.-RESORCYLALDEHYDE, 6-METHYL-3-(3-METHYL-5-(1,2,6-TRIMETHYL-3-OXOCYCLOHEXYL)-2-PENTENYL)-, (+)-

Systematic Name

English

BENZALDEHYDE, 2,4-DIHYDROXY-6-METHYL-3-((2E)-3-METHYL-5-((1S,2R,6R)-1,2,6-TRIMETHYL-3-OXOCYCLOHEXYL)-2-PENTEN-1-YL)-

Systematic Name

English

2,4-DIHYDROXY-6-METHYL-3-((2E)-3-METHYL-5-((1S,2R,6R)-1,2,6-TRIMETHYL-3-OXOCYCLOHEXYL)-2-PENTEN-1-YL)BENZALDEHYDE

Systematic Name

English

Code System Code Type Description

CAS

22562-68-1

Created by admin on Tue Apr 01 19:41:36 GMT 2025 , Edited by admin on Tue Apr 01 19:41:36 GMT 2025

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PUBCHEM

10451939

Created by admin on Tue Apr 01 19:41:36 GMT 2025 , Edited by admin on Tue Apr 01 19:41:36 GMT 2025

PRIMARY

FDA UNII

AQD59552Y1

Created by admin on Tue Apr 01 19:41:36 GMT 2025 , Edited by admin on Tue Apr 01 19:41:36 GMT 2025

PRIMARY

Related Record Type Details


					AQD59552Y1

LL-Z1272.EPISILON.

ACTIVE MOIETY

Comments:

LL-Z1272.beta. and epsilon (dechlorinated derivatives) were more active against cytochrome bd while LL-Z1272.gamma., delta, and zeta (chlorinated derivatives) were potent inhibitors of cytochrome bo and trypanosome alternative oxidase.