(S)-2-(8-(2-(6-(methylamino)pyridin-2-yl)ethoxy)-3-oxo-2-(2,2,2-trifluoroethyl)-2,3,4,5-tetrahydro-1H-benzo[c]azepin-4-yl)acetic acid

(S)-2-(8-(2-(6-(methylamino)pyridin-2-yl)ethoxy)-3-oxo-2-(2,2,2-trifluoroethyl)-2,3,4,5-tetrahydro-1H-benzo[c]azepin-4-yl)acetic acid Suppliers list

MSDS Information

(S)-2-(8-(2-(6-(methylamino)pyridin-2-yl)ethoxy)-3-oxo-2-(2,2,2-trifluoroethyl)-2,3,4,5-tetrahydro-1H-benzo[c]azepin-4-yl)acetic acid Usage And Synthesis

Biological Activity	sb 273005 is a potent nonpeptide antagonist of αvβ3 (vitronectin receptor), with ki values of 1.2 nm and 0.3 nm to two closely related integrins, αvβ3 and αvβ5, respectively [1].αvβ3 belongs to the integrin family of adhesion molecules. it is a heterodimer. it mediates cell adhesion to serum proteins and extracellular matrix via the recognition of the arg-gly-asp (rgd) sequence [1].sb 273005 binds αvβ3 and αvβ5 with low nm affinity, but binds weakly to integrins αiibβ3 and α5β1. sb 273005 inhibits αvβ3-mediated cell adhesion with an ic50 value of 3 nm, endothelial cell migration with an ic50 of 1.8 nm, and osteoclast-mediated bone resorption with an ic50 of 11 nm in vitro [1].the αvβ3 integrin is pivotal in bone resorption [2]. in the chronic ovx and thyroparathyroidectomized bone resorption rat models, sb 273005 as well as other similar vitronectin receptor antagonists, inhibit bone loss. in aia rats, prophylactical treatment with sb 273005 at doses of 60, 30, and 10 mg/kg twice daily significantly normalized bone mineral density (bmd). normalization values of bmd were 69%, 42%, and 44% for doses of 60, 30, and 10 mg/kg twice daily, respectively. a single daily dose of sb 273005 significantly improved bmd (24% normalization) only when sb 273005 was prophylactically administered at 60 mg/kg [1].
in vitro	SB273005 inhibits human osteoclast-mediated bone resorption in vitro with IC50 of 11 nM. In blood containing MDA-MB-231 cells, binding of SB273005 to lamifiban inhibited tumor cell adhesion to the vascular extracellular matrix (ECM).
in vitro	In rat models of bone resorption and osteoporosis, SB273005 (30 mg/kg, po) inhibits parathyroid hormone-stimulated calcium responses and inhibits bone loss. In adjuvant arthritis rats, it significantly reduced adjuvant-induced arthritis symptoms.
target	< td style="border-bottom: 1px dotted #ccc;padding: 5px;"> 0.3 nM Target Value αvβ5 receptor (Cell-free assay) αvβ3 receptor (Cell-free assay) 1.2 nM references [1]. badger am, blake s, kapadia r, et al. disease-modifying activity of sb 273005, an orally active, nonpeptide αvβ3 (vitronectin receptor) antagonist, in rat adjuvant-induced arthritis. arthritis & rheumatism, 2001, 44(1): 128-137. [2]. murphy mg, cerchio k, stoch sa, et al. effect of l-000845704, an αvβ3 integrin antagonist, on markers of bone turnover and bone mineral density in postmenopausal osteoporotic women. the journal of clinical endocrinology & metabolism, 2005, 90(4): 2022-2028. (S)-2-(8-(2-(6-(methylamino)pyridin-2-yl)ethoxy)-3-oxo-2-(2,2,2-trifluoroethyl)-2,3,4,5-tetrahydro-1H-benzo[c]azepin-4-yl)acetic acid Preparation Products And Raw materials
Tag:(S)-2-(8-(2-(6-(methylamino)pyridin-2-yl)ethoxy)-3-oxo-2-(2,2,2-trifluoroethyl)-2,3,4,5-tetrahydro-1H-benzo[c]azepin-4-yl)acetic acid(205678-31-5) Related Product Information
libaotao Urease inhibitor ABT-199 NS-398 Phenoxybenzamine hydrochloride Cilengitide Temozolomide CO-1686

---