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SB-267268SB 267268 is a selective and nonpeptidic alpha(v)beta3 (v3) and alpha(v)beta5 (v5) integrins antagonist, with Kis of 0. 9, 0. 5 and 0. 7 nM for human v3, monkey v3 and human v5, respectively. SB 267268 inhibits human and mouse v3 with IC50s of 0. 68 and 0. 29 nM, respectively. SB 267268 reduces angiogenesis and VEGF expression. Product information CAS Number: 205678 26 8 Molecular Weight: 451. 44 Formula: C22H24F3N3O4 Chemical Name: 2 [(4S) 3 oxo 8 {3
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SB-267268 is a selective and nonpeptidic alpha(v)beta3 (αvβ3) and alpha(v)beta5 (αvβ5) integrins antagonist, with Kis of 0.9, 0.5 and 0.7 nM for human αvβ3, monkey αvβ3 and human αvβ5, respectively. SB-267268 inhibits human and mouse αvβ3 with IC50s of 0.68 and 0.29 nM, respectively. SB-267268 reduces angiogenesis and VEGF expression.

Product information

CAS Number: 205678-26-8

Molecular Weight: 451.44

Formula: C22H24F3N3O4

Chemical Name: 2-[(4S)-3-oxo-8-{3-[(pyridin-2-yl)amino]propoxy}-2-(2,2,2-trifluoroethyl)-2,3,4,5-tetrahydro-1H-2-benzazepin-4-yl]acetic acid

Smiles: OC(=O)C[C@@H]1CC2=CC=C(C=C2CN(CC(F)(F)F)C1=O)OCCCNC1C=CC=CN=1

InChiKey: PVDGZHKJXXVONO-INIZCTEOSA-N

InChi: InChI=1S/C22H24F3N3O4/c23-22(24,25)14-28-13-17-11-18(32-9-3-8-27-19-4-1-2-7-26-19)6-5-15(17)10-16(21(28)31)12-20(29)30/h1-2,4-7,11,16H,3,8-10,12-14H2,(H,26,27)(H,29,30)/t16-/m0/s1

Technical Data

Appearance: Solid Power

Purity: ≥98% (or refer to the Certificate of Analysis)

Solubility: Soluble in DMSO

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis

Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.

Shelf Life: ≥12 months if stored properly.

Stock Solution Storage: 0 - 4 oC for 1 month or refer to the Certificate of Analysis.

Drug Formulation: To be determined

HS Tariff Code: 382200

How to use

In Vitro:

SB-267268 was much less potent for inhibition of human, mouse, and ratαvβ6 integrin. SB-267268 inhibits the attachment of bothαvβ3-transfected HEK293 cells to microtiter plate wells precoated with arginine-glycine-aspartic acid (RGD)-containing matrix proteins with IC50 values of 12 nM. SB-267268 also inhibits vitronectin-mediated human and rat aortic smooth-muscle-cell (SMC) migration with IC50 values of approximately 12.3 nM and 3.6 nM, respectively.

In Vivo:

SB-267268 (60 mg/kg; bi-daily, i.p.) reduces blood vessel profiles (BVPs) in the inner retina by 50%. In ROP mice treated with SB-267268, VEGF and VEGFR-2 gene expression in the inner nuclear layer (INL) and the ganglion cell layer (GCL) is reduced.

References:

  1. Wilkinson-Berka JL, et al. SB-267268, a nonpeptidic antagonist of alpha(v)beta3 and alpha(v)beta5 integrins, reduces angiogenesis and VEGF expression in a mouse model of retinopathy of prematurity. Invest Ophthalmol Vis Sci. 2006 Apr;47(4):1600-5.

Products are for research use only. Not for human use.

SB-267268

Item no : 18321214766
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