Reaction Details |
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Target | Phospholipase A2 group V |
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Ligand | BDBM153290 |
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Substrate/Competitor | n/a |
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Meas. Tech. | sPLA2V Activity Assay |
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pH | 7.5±n/a |
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Temperature | 298.15±n/a K |
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IC50 | 1.917e+4± 3.42e+3 nM |
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Comments | extracted |
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Citation | Bukhari, SN; Zhang, X; Jantan, I; Zhu, HL; Amjad, MW; Masand, VH Synthesis, Molecular Modeling, and Biological Evaluation of Novel 1, 3-Diphenyl-2-propen-1-one Based Pyrazolines as Anti-inflammatory Agents. Chem Biol Drug Des85:729-42 (2015) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Phospholipase A2 group V |
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Name: | Phospholipase A2 group V |
Synonyms: | PA2G5_HUMAN | PLA2G5 | Phospholipase A2 group V | Secretory phospholipase A2, group V (sPLA2-V) |
Type: | Protein |
Mol. Mass.: | 15682.61 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 138 |
Sequence: | MKGLLPLAWFLACSVPAVQGGLLDLKSMIEKVTGKNALTNYGFYGCYCGWGGRGTPKDGT
DWCCWAHDHCYGRLEEKGCNIRTQSYKYRFAWGVVTCEPGPFCHVNLCACDRKLVYCLKR
NLRSYNPQYQYFPNILCS
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BDBM153290 |
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n/a |
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Name | BDBM153290 |
Synonyms: | 3-(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-5-(2,3-dimethoxy-naphthalen-1-yl)-4,5-dihydro-pyrazole-1-carbothioic acid amide (5a) |
Type | Small organic molecule |
Emp. Form. | C24H23N3O4S |
Mol. Mass. | 449.522 |
SMILES | COc1cc2ccccc2c(C2CC(=NN2C(N)=S)c2ccc3OCCOc3c2)c1OC |c:14| |
Structure |
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