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3VUC

Human renin in complex with compound 5

Summary for 3VUC
Entry DOI10.2210/pdb3vuc/pdb
Related3VSX
DescriptorRenin, 2-acetamido-2-deoxy-beta-D-glucopyranose, (2R,4S,5S)-5-amino-6-[4-(2-chlorophenyl)-2,2-dimethyl-5-oxopiperazin-1-yl]-2-ethyl-4-hydroxy-N-[(1R,2S,3S,5S,7S)-5-hydroxytricyclo[3.3.1.1~3,7~]dec-2-yl]hexanamide, ... (4 entities in total)
Functional Keywordsaspartyl protease, ras, hypertension, inhibitor, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight76098.74
Authors
Takahashi, M.,Matsui, Y.,Hanzawa, H. (deposition date: 2012-06-26, release date: 2013-05-15, Last modification date: 2024-10-30)
Primary citationNakamura, Y.,Fujimoto, T.,Ogawa, Y.,Sugita, C.,Miyazaki, S.,Tamaki, K.,Takahashi, M.,Matsui, Y.,Nagayama, T.,Manabe, K.,Mizuno, M.,Masubuchi, N.,Chiba, K.,Nishi, T.
Discovery of DS-8108b, a Novel Orally Bioavailable Renin Inhibitor.
Acs Med.Chem.Lett., 3:754-758, 2012
Cited by
PubMed Abstract: A novel orally bioavailable renin inhibitor, DS-8108b (5), showing potent renin inhibitory activity and excellent in vivo efficacy is described. We report herein the synthesis and pharmacological effects of 5 including renin inhibitory activity in vitro, suppressive effects of ex vivo plasma renin activity (PRA) in cynomolgus monkey, pharmacokinetic data, and blood pressure-lowering effects in an animal model. Compound 5 demonstrated inhibitory activities toward human renin (IC50 = 0.9 nM) and human and monkey PRA (IC50 = 1.9 and 6.3 nM, respectively). Oral administration of single doses of 3 and 10 mg/kg of 5 in cynomolgus monkey on pretreatment with furosemide led to dose-dependent significant reductions in ex vivo PRA and sustained lowering of mean arterial blood pressure for more than 12 h.
PubMed: 24900544
DOI: 10.1021/ml300168e
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

239149

数据于2025-07-23公开中

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