Reaction Details |
| Report a problem with these data |
Target | Basic phospholipase A2 1 |
---|
Ligand | BDBM50148911 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_305607 (CHEMBL828145) |
---|
IC50 | 2900±n/a nM |
---|
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 |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Basic phospholipase A2 1 |
---|
Name: | Basic phospholipase A2 1 |
Synonyms: | PA2B1_NAJME | Phospholipase A2 isozyme DE-I |
Type: | PROTEIN |
Mol. Mass.: | 13475.55 |
Organism: | Naja melanoleuca |
Description: | ChEMBL_305607 |
Residue: | 118 |
Sequence: | NLYQFKNMIHCTVPNRPWWHFANYGCYCGRGGKGTPVDDLDRCCQIHDKCYDEAEKISGC
WPYIKTYTYESCQGTLTCKDGGKCAASVCDCDRVAANCFARATYNDKNYNIDFNARCQ
|
|
|
BDBM50148911 |
---|
n/a |
---|
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 |
|