Reaction Details Report a problem with these data
Target
Phospholipase A2, membrane associated
Ligand
BDBM50250399
Substrate
n/a
Meas. Tech.
ChEMBL_156362 (CHEMBL761692)
IC50
2000000±n/a nM
Citation
 Teshirogi, I; Matsutani, S; Shirahase, K; Fujii, Y; Yoshida, T; Tanaka, K; Ohtani, M Synthesis and phospholipase A2 inhibitory activity of thielocin B3 derivatives. J Med Chem 39:5183-91 (1997) [PubMed]  Article 
Target
Name:
Phospholipase A2, membrane associated
Synonyms:
PA2GA_RAT | Phospholipase A2 group IIA | Pla2g2a
Type:
PROTEIN
Mol. Mass.:
16307.95
Organism:
Rat
Description:
ChEMBL_537135
Residue:
146
Sequence:
MKVLLLLAVVIMAFGSIQVQGSLLEFGQMILFKTGKRADVSYGFYGCHCGVGGRGSPKDATDWCCVTHDCCYNRLEKRGCGTKFLTYKFSYRGGQISCSTNQDSCRKQLCQCDKAAAECFARNKKSYSLKYQFYPNKFCKGKTPSC
  
Inhibitor
Name:
BDBM50250399
Synonyms:
5-Hydroxy-4-{(R)-6-hydroxy-5-[(E)-4-methyl-6-(2,6,6-trimethyl-cyclohex-1-enyl)-hex-3-enyl]-3,6-dihydro-2H-pyran-2-yl}-5H-furan-2-one | 5-Hydroxy-4-{6-hydroxy-5-[(E)-4-methyl-6-(2,6,6-trimethyl-cyclohex-1-enyl)-hex-3-enyl]-3,6-dihydro-2H-pyran-2-yl}-5H-furan-2-one | CHEMBL463914 | manoalide
Type:
Small organic molecule
Emp. Form.:
C25H36O5
Mol. Mass.:
416.5503
SMILES:
C\C(CCC1=C(C)CCCC1(C)C)=C/CCC1=CC[C@@H](O[C@H]1O)C1=CC(=O)O[C@H]1O |r,c:4,t:17,25|
Structure:
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