Reaction Details |
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Target | Complement C1s subcomponent |
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Ligand | BDBM50063703 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_40178 |
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IC50 | 1250±n/a nM |
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Citation | Gilmore, JL; Hays, SJ; Caprathe, BW; Lee, C; Emmerling, MR; Michael, W; Jaen, JC Synthesis and evaluation of 2-aryl-4H-3,1-benzoxazin-4-ones as C1r serine protease inhibitors Bioorg Med Chem Lett6:679-682 (1996) Article |
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More Info.: | Get all data from this article, Assay Method |
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Complement C1s subcomponent |
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Name: | Complement C1s subcomponent |
Synonyms: | C1 esterase | C1S | C1S_HUMAN | Complement C1s | Complement C1s subcomponent | Complement C1s subcomponent heavy chain | Complement C1s subcomponent light chain | Complement component 1 subcomponent s | Trypsin | complement component 1, s subcomponent |
Type: | Protein |
Mol. Mass.: | 76657.91 |
Organism: | Homo sapiens (Human) |
Description: | P09871 |
Residue: | 688 |
Sequence: | MWCIVLFSLLAWVYAEPTMYGEILSPNYPQAYPSEVEKSWDIEVPEGYGIHLYFTHLDIE
LSENCAYDSVQIISGDTEEGRLCGQRSSNNPHSPIVEEFQVPYNKLQVIFKSDFSNEERF
TGFAAYYVATDINECTDFVDVPCSHFCNNFIGGYFCSCPPEYFLHDDMKNCGVNCSGDVF
TALIGEIASPNYPKPYPENSRCEYQIRLEKGFQVVVTLRREDFDVEAADSAGNCLDSLVF
VAGDRQFGPYCGHGFPGPLNIETKSNALDIIFQTDLTGQKKGWKLRYHGDPMPCPKEDTP
NSVWEPAKAKYVFRDVVQITCLDGFEVVEGRVGATSFYSTCQSNGKWSNSKLKCQPVDCG
IPESIENGKVEDPESTLFGSVIRYTCEEPYYYMENGGGGEYHCAGNGSWVNEVLGPELPK
CVPVCGVPREPFEEKQRIIGGSDADIKNFPWQVFFDNPWAGGALINEYWVLTAAHVVEGN
REPTMYVGSTSVQTSRLAKSKMLTPEHVFIHPGWKLLEVPEGRTNFDNDIALVRLKDPVK
MGPTVSPICLPGTSSDYNLMDGDLGLISGWGRTEKRDRAVRLKAARLPVAPLRKCKEVKV
EKPTADAEAYVFTPNMICAGGEKGMDSCKGDSGGAFAVQDPNDKTKFYAAGLVSWGPQCG
TYGLYTRVKNYVDWIMKTMQENSTPRED
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BDBM50063703 |
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n/a |
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Name | BDBM50063703 |
Synonyms: | 2-(2-Iodo-phenyl)-benzo[d][1,3]oxazin-4-one | CHEMBL10378 |
Type | Small organic molecule |
Emp. Form. | C14H8INO2 |
Mol. Mass. | 349.1233 |
SMILES | Ic1ccccc1-c1nc2ccccc2c(=O)o1 |
Structure |
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