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TargetProthrombin
LigandBDBM50093299
Substrate/Competitorn/a
Meas. Tech.ChEMBL_208726 (CHEMBL809417)
IC50 2200±n/a nM
Citation Dudley, DABunker, AMChi, LCody, WLHolland, DRIgnasiak, DPJaniczek-Dolphin, NMcClanahan, TBMertz, TENarasimhan, LSRapundalo, STTrautschold, JAVan Huis, CAEdmunds, JJ Rational design, synthesis, and biological activity of benzoxazinones as novel factor Xa inhibitors. J Med Chem43:4063-70 (2000) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Prothrombin
Name:Prothrombin
Synonyms:Activation peptide fragment 1 | Activation peptide fragment 2 | Coagulation factor II | F2 | Prothrombin precursor | THRB_HUMAN | Thrombin heavy chain | Thrombin light chain
Type:Protein
Mol. Mass.:70029.57
Organism:Homo sapiens (Human)
Description:P00734
Residue:622
Sequence:
MAHVRGLQLPGCLALAALCSLVHSQHVFLAPQQARSLLQRVRRANTFLEEVRKGNLEREC
VEETCSYEEAFEALESSTATDVFWAKYTACETARTPRDKLAACLEGNCAEGLGTNYRGHV
NITRSGIECQLWRSRYPHKPEINSTTHPGADLQENFCRNPDSSTTGPWCYTTDPTVRRQE
CSIPVCGQDQVTVAMTPRSEGSSVNLSPPLEQCVPDRGQQYQGRLAVTTHGLPCLAWASA
QAKALSKHQDFNSAVQLVENFCRNPDGDEEGVWCYVAGKPGDFGYCDLNYCEEAVEEETG
DGLDEDSDRAIEGRTATSEYQTFFNPRTFGSGEADCGLRPLFEKKSLEDKTERELLESYI
DGRIVEGSDAEIGMSPWQVMLFRKSPQELLCGASLISDRWVLTAAHCLLYPPWDKNFTEN
DLLVRIGKHSRTRYERNIEKISMLEKIYIHPRYNWRENLDRDIALMKLKKPVAFSDYIHP
VCLPDRETAASLLQAGYKGRVTGWGNLKETWTANVGKGQPSVLQVVNLPIVERPVCKDST
RIRITDNMFCAGYKPDEGKRGDACEGDSGGPFVMKSPFNNRWYQMGIVSWGEGCDRDGKY
GFYTHVFRLKKWIQKVIDQFGE
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50093299
n/a
NameBDBM50093299
Synonyms:3-[4-(5-Morpholin-4-yl-pentyl)-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-2-yl]-benzamidine | CHEMBL130378
TypeSmall organic molecule
Emp. Form.C24H30N4O3
Mol. Mass.422.52
SMILESNC(=N)c1cccc(c1)C1Oc2ccccc2N(CCCCCN2CCOCC2)C1=O
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: