UCSF

ZINC03777423

Draw Identity 99% 90% 80% 70%

Substance Information

In ZINC since Heavy atoms Benign functionality
December 3rd, 2005 20 Yes

Popular Name: gamma-linolenic acid gamma-linolenic acid

Find On: PubMed — Wikipedia — Google

CAS Numbers: 506-26-3 , [506-26-3]

Other Names:

(6,9,12)-linolenate; (6,9,12)-linolenic acid; (6Z,9Z,12Z)-Octadecatrienoate; (6Z,9Z,12Z)-Octadecatrienoic acid; (Z,Z,Z)-6,9,12-Octadecatrienoate; (Z,Z,Z)-6,9,12-Octadecatrienoic acid; 6(Z),9(Z),12(Z)-Octadecatrienoate; 6(Z),9(Z),12(Z)-Octadecatrienoic aci

(6,9,12)-linolenate; (6,9,12)-linolenoic acid; 6Z,9Z,12Z-octadecatrienoate; 6Z,9Z,12Z-octadecatrienoic acid; CPD-8117; gamma-linolenate; gamma-linolenic acid

(6,9,12)-linolenate; 6-Z,9-Z,12-Z-octadecatrienoate; 6-cis,9-cis,12-cis-octadecatrienoate; all-cis-6,9,12-octadecatrienoate; cis-Delta(6,9,12)-octadecatrienoate; gamolenate

(6,9,12)-linolenate;(6,9,12)-linolenic acid;(6Z,9Z,12Z)-Octadecatrienoate;(6Z,9Z,12Z)-Octadecatrienoic acid;(Z,Z,Z)-6,9,12-Octadecatrienoate;(Z,Z,Z)-6,9,12-Octadecatrienoic acid;6(Z),9(Z),12(Z)-Octadecatrienoate;6(Z),9(Z),12(Z)-Octadecatrienoic acid;6,9,1

(6,9,12)-linolenic acid; (Z,Z,Z)-6,9,12-octadecatrienoic acid; 18:3 (n-6); 6-cis,9-cis,12-cis-octadecatrienoic acid; C18:3 (n-6); C18:3, n-6,9,12 all-cis; GLA; Octadeca-6,9,12-triensaeure; all-cis-6,9,12-octadecatrienoic acid; cis-Delta(6,9,12)-octadecatr

(6Z,9Z,12Z)-Octadeca-6,9,12-trienoic acid

(6Z,9Z,12Z)-Octadecatrienoic acid; 506-26-3; 6,9,12-Octadecatrienoic acid; C06426; Gamolenic acid; gamma-Linolenic acid

(Z,Z,Z)-6,9,12-Octadecatrienoic acid; 6,9,12-Octadecatrienoic acid, (Z,Z,Z)-; Acide gamolenique [French]; Acido gamolenico [Spanish]; Acidum gamolenicum [Latin]; CCRIS 7668; Gamolenic acid [INN:BAN]; LS-97722; gamma-Linolenic acid

.gamma.-Linolenic Acid

506-26-3; D07213; Gamolenic acid (INN)

6Z,9Z,12Z-octadecatrienoic acid

BRD-K18059238-001-02-1

CHEBI:24197; CHEBI:10573

cis-6, cis-9, cis-12-octadecatrienoic acid; C18:3n-6,9,12

Efamast

Epogam

gamma-linolenate

Gamma-LinolenicAcid

Gamolenic acid

Gamolenic Acid (BAN

GLA

INN)

Linoleic Acid (9c,12c) [60-33-3]

LINOLEIC ACID (9c,12c); [506-26-3]

MFCD00065718

Download: MOL2 SDF SMILES Flexibase

Physical Representations

Type pH range xlogP Des A‑Pol Apolar desolvation (kcal/mol) Des Pol Polar desolvation (kcal/mol) H Don H-bond donors H Acc H-bond acceptors Chg Net charge tPSA (Ų) MWT Molecular weight (g/mol) RB Rotatable bonds DL
Ref Reference (pH 7) 6.13 13.66 -43.62 0 2 -1 40 277.428 13 ↓
Lo Low (pH 4.5-6) 6.13 11.68 -5.43 1 2 0 37 278.436 13 ↓

Vendor Notes

Note Type Comments Provided By
Purity 95% Fluorochem
Target Amine oxidase [flavin-containing] A(P21397)&Y+L amino acid transporter 1(Q9UM01)&Serotonin N-acetyltransferase(Q16613)&Melatonin receptor type 1B(P49286)&Disks large homolog 4(P78352)&72 kDa type IV collagenase(P08253)&Metalloproteinase inhibitor 1(P01033 Herbal Ingredients Targets
UniProt Database Links CI2B_CONTE; CKG_CONGE; CT52_CONMR; CT53_CONMR; CX2_CONMR; CXX_CONTE; E13E_TOBAC; FA101_PSETE; FA102_PSETE; FA10_BOVIN; FA10_CHICK; FA10_HUMAN; FA10_MOUSE; FA10_RABIT; FA10_RAT; FA10_TROCA; FA7_BOVIN; FA7_HUMAN; FA7_MOUSE; FA7_PANPA; FA7_PANTR; FA7_RABIT ChEBI
Patent Database Links EP1685834; EP1911358; US2001023259; US2006035350; US2007244192; US2007270494; US2008139649; US2008166781; US2008176956; US2008260929 ChEBI
Reactome Database Links REACT_21408 ChEBI

Activity (Go SEA)

Direct Reactome Annotations (via ChEBI)

Description Species
Free fatty acid receptors
Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1)

Analogs ( Draw Identity 99% 90% 80% 70% )