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SI-591
a cathepsin K inhibitor; structure in first source
Also Known As:
N-(1-(((3-((hexahydro-2-oxo-1H-azepin-3-yl)amino)-1-(1-methylethyl)-2,3-dioxopropyl)amino)carbonyl)cyclohexyl)-2-furancarboxamide
Networked:
1
relevant articles (
0
outcomes,
0
trials/studies)
Bio-Agent Context: Research Results
Heterocyclic Compounds: 198
1-Ring Heterocyclic Compounds
Azepines: 11
SI-591: 1
Amino Acids, Peptides, and Proteins: 1
Peptides: 82426
Oligopeptides: 519
Dipeptides: 945
SI-591: 1
Experts
1.
Fujii, Toshiaki
: 1 article (12/2015)
2.
Ishikawa, Mizuho
: 1 article (12/2015)
3.
Kubo, Akiko
: 1 article (12/2015)
4.
Tanaka, Yoshitaka
: 1 article (12/2015)
Related Diseases
1.
Postmenopausal Osteoporosis
12/01/2015 - "
Therefore, SI-591, a novel cathepsin K inhibitor, could be a promising agent for the treatment of postmenopausal osteoporosis.
"
2.
Bone Resorption
12/01/2015 - "
These results suggest that SI-591 inhibits bone resorption without affecting osteoblast maturation.
"
12/01/2015 - "
SI-591 also decreased the level of CTX-I, a bone resorption marker, which was released from osteoclasts in vitro in a dose-dependent manner.
"
12/01/2015 - "
The mobilization of calcium from the bones to the blood stream is known to increase in rats fed with a low calcium diet; SI-591 inhibited this increase in serum calcium level at an oral dose of 3mg/kg. Furthermore, SI-591 significantly decreased the level of CTX-I and DPD, bone resorption markers, at oral doses of 10mg/kg or less in ovariectomized rats, while it did not affect the level of BGP, a bone formation marker.
"
Related Drugs and Biologics
1.
Cathepsin K
2.
Calcium