Reaction Details |
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Target | Complement C1r subcomponent |
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Ligand | BDBM50289014 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_40170 |
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IC50 | >62500±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 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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BDBM50289014 |
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n/a |
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Name | BDBM50289014 |
Synonyms: | 2-(4-Iodo-phenyl)-benzo[d][1,3]oxazin-4-one | CHEMBL347904 |
Type | Small organic molecule |
Emp. Form. | C14H8INO2 |
Mol. Mass. | 349.1233 |
SMILES | Ic1ccc(cc1)-c1nc2ccccc2c(=O)o1 |
Structure |
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