Reaction Details |
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Target | Complement C1r subcomponent |
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Ligand | BDBM50063745 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_48026 (CHEMBL661599) |
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IC50 | 400±n/a nM |
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Citation | Plummer, JS; Cai, C; Hays, SJ; Gilmore, JL; Emmerling, MR; Michael, W; Narasimhan, LS; Watson, MD; Wang, K; Nath, R; Evans, LM; Jaen, JC Benzenesulfonamide derivatives of 2-substituted 4H-3,1-benzoxazin-4-ones and benzthiazin-4-ones as inhibitors of complement C1r protease. Bioorg Med Chem Lett9:815-20 (1999) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Complement C1r subcomponent |
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Name: | Complement C1r subcomponent |
Synonyms: | C1R | C1R_HUMAN | Complement C1r | Complement C1r subcomponent |
Type: | Enzyme |
Mol. Mass.: | 80113.65 |
Organism: | Homo sapiens (Human) |
Description: | P00736 |
Residue: | 705 |
Sequence: | MWLLYLLVPALFCRAGGSIPIPQKLFGEVTSPLFPKPYPNNFETTTVITVPTGYRVKLVF
QQFDLEPSEGCFYDYVKISADKKSLGRFCGQLGSPLGNPPGKKEFMSQGNKMLLTFHTDF
SNEENGTIMFYKGFLAYYQAVDLDECASRSKSGEEDPQPQCQHLCHNYVGGYFCSCRPGY
ELQEDTHSCQAECSSELYTEASGYISSLEYPRSYPPDLRCNYSIRVERGLTLHLKFLEPF
DIDDHQQVHCPYDQLQIYANGKNIGEFCGKQRPPDLDTSSNAVDLLFFTDESGDSRGWKL
RYTTEIIKCPQPKTLDEFTIIQNLQPQYQFRDYFIATCKQGYQLIEGNQVLHSFTAVCQD
DGTWHRAMPRCKIKDCGQPRNLPNGDFRYTTTMGVNTYKARIQYYCHEPYYKMQTRAGSR
ESEQGVYTCTAQGIWKNEQKGEKIPRCLPVCGKPVNPVEQRQRIIGGQKAKMGNFPWQVF
TNIHGRGGGALLGDRWILTAAHTLYPKEHEAQSNASLDVFLGHTNVEELMKLGNHPIRRV
SVHPDYRQDESYNFEGDIALLELENSVTLGPNLLPICLPDNDTFYDLGLMGYVSGFGVME
EKIAHDLRFVRLPVANPQACENWLRGKNRMDVFSQNMFCAGHPSLKQDACQGDSGGVFAV
RDPNTDRWVATGIVSWGIGCSRGYGFYTKVLNYVDWIKKEMEEED
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BDBM50063745 |
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n/a |
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Name | BDBM50063745 |
Synonyms: | 2-(2-Iodo-phenylamino)-7-trifluoromethyl-benzo[d][1,3]oxazin-4-one | CHEMBL10312 |
Type | Small organic molecule |
Emp. Form. | C15H8F3IN2O2 |
Mol. Mass. | 432.1359 |
SMILES | FC(F)(F)c1ccc2c(c1)nc(Nc1ccccc1I)oc2=O |
Structure |
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