Reaction Details |
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Target | Acidic phospholipase A2 EC-I |
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Ligand | BDBM50148911 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_305580 (CHEMBL828028) |
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IC50 | 2300±n/a nM |
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Citation | Khanum, SA; Murari, SK; Vishwanth, BS; Shashikanth, S Synthesis of benzoyl phenyl benzoates as effective inhibitors for phospholipase A2 and hyaluronidase enzymes. Bioorg Med Chem Lett15:4100-4 (2005) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Acidic phospholipase A2 EC-I |
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Name: | Acidic phospholipase A2 EC-I |
Synonyms: | PA2A1_ECHCA | Phospholipase A2 |
Type: | PROTEIN |
Mol. Mass.: | 15520.08 |
Organism: | Echis carinatus |
Description: | ChEMBL_305580 |
Residue: | 136 |
Sequence: | MKTLWIVAVWLIAVEGNLYQFGRMIWNRTGKLPILSYGSYGCYCGWGGQGPPKDATDRCC
LVHDCCYTRVGDCSPKMTLYSYRFENGDIICDNKDPCKRAVCECDREAAICLGENVNTYD
KKYKSYEDCTEEVQEC
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BDBM50148911 |
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n/a |
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Name | BDBM50148911 |
Synonyms: | (3beta)-3-hydroxyurs-12-en-28-oic acid | 3beta-hydroxyurs-12-en-28-oic acid | CHEMBL169 | Ursolic acid | malol | prunol | urson |
Type | Small organic molecule |
Emp. Form. | C30H48O3 |
Mol. Mass. | 456.7003 |
SMILES | C[C@@H]1CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2[C@H]1C)C(O)=O |r,c:9| |
Structure |
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