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TargetRenin
LigandBDBM50022859
Substrate/Competitorn/a
Meas. Tech.ChEBML_195773
IC50 10.0±n/a nM
Citation Bühlmayer, PCaselli, AFuhrer, WGöschke, RRasetti, VRüeger, HStanton, JLCriscione, LWood, JM Synthesis and biological activity of some transition-state inhibitors of human renin. J Med Chem31:1839-46 (1988) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Renin
Name:Renin
Synonyms:Angiotensinogenase | REN | RENI_HUMAN
Type:Enzyme
Mol. Mass.:45058.99
Organism:Homo sapiens (Human)
Description:n/a
Residue:406
Sequence:
MDGWRRMPRWGLLLLLWGSCTFGLPTDTTTFKRIFLKRMPSIRESLKERGVDMARLGPEW
SQPMKRLTLGNTTSSVILTNYMDTQYYGEIGIGTPPQTFKVVFDTGSSNVWVPSSKCSRL
YTACVYHKLFDASDSSSYKHNGTELTLRYSTGTVSGFLSQDIITVGGITVTQMFGEVTEM
PALPFMLAEFDGVVGMGFIEQAIGRVTPIFDNIISQGVLKEDVFSFYYNRDSENSQSLGG
QIVLGGSDPQHYEGNFHYINLIKTGVWQIQMKGVSVGSSTLLCEDGCLALVDTGASYISG
STSSIEKLMEALGAKKRLFDYVVKCNEGPTLPDISFHLGGKEYTLTSADYVFQESYSSKK
LCTLAIHAMDIPPPTGPTWALGATFIRKFYTEFDRRNNRIGFALAR
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  Blast E-value cutoff:
BDBM50022859
n/a
NameBDBM50022859
Synonyms:CHEMBL407670 | Pro-His-Pro-Phe-His-Leu[CH2NH]Val-Ile-His-Lys | Pro-His-Prp-Phe-His-Leu(psi)[CH2NH]Val-Ile-His-Lys | Pro-His-Prp-Phe-His-Leu(psi)[CH2NH]Val-Ile-His-Lys(H-142)
TypeSmall organic molecule
Emp. Form.C60H91N17O10
Mol. Mass.1210.4724
SMILESCC[C@H](C)[C@H](NC(=O)[C@@H](NC[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H]1CCCN1)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CCCCN)C(O)=O
Structure
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