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Reaction Details
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TargetRenin
LigandBDBM50014100
Substrate/Competitorn/a
Meas. Tech.ChEBML_196424
IC50 0.260000±n/a nM
Citation Bundy, GLPals, DTLawson, JACouch, SJLipton, MFMauragis, MA Potent renin inhibitory peptides containing hydrophilic end groups. J Med Chem33:2276-83 (1990) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Renin
Name:Renin
Synonyms:RENI_RAT | Ren | Ren1
Type:PROTEIN
Mol. Mass.:44272.67
Organism:Rattus norvegicus
Description:ChEMBL_222765
Residue:402
Sequence:
MGGRRMPLWALLLLWTSCSFSLPTDTASFGRILLKKMPSVREILEERGVDMTRISAEWGE
FIKKSSFTNVTSPVVLTNYLDTQYYGEIGIGTPSQTFKVIFDTGSANLWVPSTKCGPLYT
ACEIHNLYDSSESSSYMENGTEFTIHYGSGKVKGFLSQDVVTVGGIIVTQTFGEVTELPL
IPFMLAKFDGVLGMGFPAQAVDGVIPVFDHILSQRVLKEEVFSVYYSRESHLLGGEVVLG
GSDPQHYQGNFHYVSISKAGSWQITMKGVSVGPATLLCEEGCMAVVDTGTSYISGPTSSL
QLIMQALGVKEKRANNYVVNCSQVPTLPDISFYLGGRTYTLSNMDYVQKNPFRNDDLCIL
ALQGLDIPPPTGPVWVLGATFIRKFYTEFDRHNNRIGFALAR
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50014100
n/a
NameBDBM50014100
Synonyms:2-(1-{[1-{2-Hydroxy-1-isobutyl-5-methyl-4-[2-methyl-1-(2-methylamino-pyridine-1-carbonyl)-butylcarbamoyl]-hexylcarbamoyl}-2-(1H-imidazol-4-yl)-ethyl]-methyl-carbamoyl}-2-phenyl-ethylcarbamoyl)-pyrrolidine-1-carboxylic acid tert-butyl ester | CHEMBL412950
TypeSmall organic molecule
Emp. Form.C50H75N9O8
Mol. Mass.930.186
SMILESCC[C@H](C)[C@H](NC(=O)[C@H](C[C@H](O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)N(C)C(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)OC(C)(C)C)C(C)C)C(=O)NCc1ccccn1
Structure
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