CAS NO: | 383392-66-3 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | UC-112 is a novel potent IAP(Inhibitor of apoptosis) inhibitor; potently inhibit cell growth in two human melanoma (A375 and M14) and two human prostate (PC-3 and DU145)cancercell lines(IC50=0.7-3.4 uM). IC50 value: 0.7-3.4 uM (Cell assay) [1] Target:IAP inhibitorin vitro: UC-112 also potently inhibits the growth ofP-glycoprotein(P-gp)-overexpressed multidrug-resistantcancercells, strongly activates caspase-3/7 and caspase-9 activities, and selectively downregulatessurvivinlevel at a concentration as low as 1 μM. Coincubation of UC-112 with a knownproteasome inhibitorZ-Leu-Leu-Leu-CHO (MG-132) rescuedsurvivininhibition, consistent with the anticipated mechanism of action for UC-112 [1]. in vivo: As a single agent, UC-112 strongly inhibits tumor growth and reduces both X chromosome-linkedIAPandsurvivinlevels in an A375 human melanoma xenograft model in vivo [1]. | ||||||||||||||||
分子量 | 348.44 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C22H24N2O2 | ||||||||||||||||
CAS 号 | 383392-66-3 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 33.33 mg/mL(95.65 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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