Reaction Details |
| Report a problem with these data |
Target | Prothrombin |
---|
Ligand | BDBM50027306 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEBML_207954 |
---|
IC50 | 22000±n/a nM |
---|
Citation | Iwanowicz, EJ; Lau, WF; Lin, J; Roberts, DG; Seiler, SM Derivatives of 5-amidine indole as inhibitors of thrombin catalytic activity Bioorg Med Chem Lett6:1339-1344 (1996) Article |
---|
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
|
|
|
BDBM50027306 |
---|
n/a |
---|
Name | BDBM50027306 |
Synonyms: | 1H-Indole-5-carboxamidine | CHEMBL26490 |
Type | Small organic molecule |
Emp. Form. | C9H9N3 |
Mol. Mass. | 159.1879 |
SMILES | NC(=N)c1ccc2[nH]ccc2c1 |
Structure |
|