PeptideDB

ABT-510 acetate

CAS: 442526-87-6 F: C48H87N13O13 W: 1054.28

ABT-510 acetate is an anti-angiogenic TSP peptide (Thrombospondin-1 analogue) that induces apoptosis and inhibits ovaria
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Bioactivity ABT-510 acetate is an anti-angiogenic TSP peptide (Thrombospondin-1 analogue) that induces apoptosis and inhibits ovarian tumour growth in an orthotopic, syngeneic model of epithelial ovarian cancer. ABT-510 acetate also reduces angiogenesis and inflammatory responses in a murine model of inflammatory bowel disease. ABT-510 acetate can be used in studies of cancer (particularly epithelial ovarian cancer) and inflammatory bowel disease (IBD)[1][2].
Invitro ABT-510 acetate (1,5,10,20,50 nM;24 h) 诱导 ID 8 细胞凋亡,增加人类上皮性癌症细胞系 SKOV3、OVCAR3 和 CAOV3 的凋亡发生率[1]。ABT-510 acetate (0-10 μM;7 天) 抑制了 NO 刺激的血管细胞向细胞外基质的生长和侵袭。ABT-510 acetate 可阻断肿瘤驱动的血管细胞生长、NO 驱动的 cGMP 通量以及 CD36 介导的脂肪酸吸收。[3]。 Apoptosis Analysis[1] Cell Line:
In Vivo ABT-510 acetate (100 mg/kg;腹腔注射;每天一次,持续90天) 在体内诱导细胞凋亡,使小鼠的上皮卵巢肿瘤大小、腹水量和继发性病变扩散显著减少[1]。ABT-510 acetate (60 mg/kg;皮下渗透微型泵;每天一次,持续7天) 降低炎症性肠病小鼠模型中的血管生成和炎症[2]。 Animal Model:
Name ABT-510 acetate
CAS 442526-87-6
Formula C48H87N13O13
Molar Mass 1054.28
Appearance Solid
Transport Room temperature in continental US; may vary elsewhere.
Storage

Sealed storage, away from moisture and light, under nitrogen

Powder -80°C 2 years
-20°C 1 year

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light, under nitrogen)

Reference [1]. Greenaway J, et.al. ABT-510 induces tumor cell apoptosis and inhibits ovarian tumor growth in an orthotopic, syngeneic model of epithelial ovarian cancer. Mol Cancer Ther. 2009 Jan;8(1):64-74. [2]. Punekar S,et.al. Thrombospondin 1 and its mimetic peptide ABT-510 decrease angiogenesis and inflammation in a murine model of inflammatory bowel disease. Pathobiology. 2008;75(1):9-21. [3]. Isenberg JS, et.al. Differential effects of ABT-510 and a CD36-binding peptide derived from the type 1 repeats of thrombospondin-1 on fatty acid uptake, nitric oxide signaling, and caspase activation in vascular cells. Biochem Pharmacol. 2008 Feb 15;75(4):875-82.