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TargetComplement C1r subcomponent
LigandBDBM50063721
Substrate/Competitorn/a
Meas. Tech.ChEMBL_40166 (CHEMBL655961)
IC50 800±n/a nM
Citation Hays, SJCaprathe, BWGilmore, JLAmin, NEmmerling, MRMichael, WNadimpalli, RNath, RRaser, KJStafford, DWatson, DWang, KJaen, JC 2-amino-4H-3,1-benzoxazin-4-ones as inhibitors of C1r serine protease. J Med Chem41:1060-7 (1998) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Complement C1r subcomponent
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
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50063721
n/a
NameBDBM50063721
Synonyms:2-(2-Iodo-phenylamino)-7-nitro-benzo[d][1,3]oxazin-4-one | CHEMBL10065
TypeSmall organic molecule
Emp. Form.C14H8IN3O4
Mol. Mass.409.1355
SMILES[O-][N+](=O)c1ccc2c(c1)nc(Nc1ccccc1I)oc2=O
Structure
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