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_40165 (CHEMBL655960) |
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IC50 | 4000±n/a nM |
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Citation | Hays, SJ; Caprathe, BW; Gilmore, JL; Amin, N; Emmerling, MR; Michael, W; Nadimpalli, R; Nath, R; Raser, KJ; Stafford, D; Watson, D; Wang, K; Jaen, JC 2-amino-4H-3,1-benzoxazin-4-ones as inhibitors of C1r serine protease. J Med Chem41:1060-7 (1998) [PubMed] Article |
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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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