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TargetPhospholipase A2
LigandBDBM50183250
Substrate/Competitorn/a
Meas. Tech.ChEMBL_457563 (CHEMBL922763)
IC50>100000±n/a nM
Citation Moon, TCQuan, ZKim, JKim, HPKudo, IMurakami, MPark, HChang, HW Inhibitory effect of synthetic C-C biflavones on various phospholipase A(2)s activity. Bioorg Med Chem15:7138-43 (2007) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Phospholipase A2
Name:Phospholipase A2
Synonyms:PA21B_RAT | Phospholipase A2 group 1B | Pla2g1b
Type:PROTEIN
Mol. Mass.:16427.59
Organism:Rattus norvegicus
Description:ChEMBL_156506
Residue:146
Sequence:
MKLLLLAALLTAGVTAHSISTRAVWQFRNMIKCTIPGSDPLREYNNYGCYCGLGGSGTPV
DDLDRCCQTHDHCYNQAKKLESCKFLIDNPYTNTYSYKCSGNVITCSDKNNDCESFICNC
DRQAAICFSKVPYNKEYKDLDTKKHC
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BDBM50183250
n/a
NameBDBM50183250
Synonyms:2-(3-(4-(5,7-dihydroxy-4-oxo-4H-chromen-2-yl)phenoxy)-4-hydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one | 2-{4-[5-(5,7-dihydroxy-4-oxo-4H-2-chromenyl)-2-hydroxyphenoxy]phenyl}-5,7-dihydroxy-4H-4-chromenone | CHEMBL187504 | OCHNAFLAVONE
TypeSmall organic molecule
Emp. Form.C30H18O10
Mol. Mass.538.4579
SMILESOc1cc2oc(cc(O)c2c(=O)c1)-c1ccc(Oc2cc(ccc2O)-c2cc(O)c3c(cc(O)cc3=O)o2)cc1
Structure
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