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Tivozanib hydrochloride hydrate
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Tivozanib hydrochloride hydrate图片
CAS NO:682745-41-1
包装与价格:
包装价格(元)
5mg电议
10mg电议
50mg电议
100mg电议
200mg电议
500mg电议

产品名称
AV-951 hydrochloride hydrate
KRN951 hydrochloride hydrate
产品介绍
Tivozanib hydrochloride hydrate 是一种有效的、选择性的、具有口服活性的VEGFR 酪氨酸激酶抑制剂,对 VEGFR-1、VEGFR-2、VEGFR-3的IC50值分别为 0.21、0.16、0.24 nM。Tivozanib hydrochloride hydrate 抑制肿瘤组织中的血管生成和血管通透性,并显示出抗肿瘤活性。Tivozanib hydrochloride hydrate 具有研究转移性肾细胞癌 (RCC) 的潜力。
生物活性

Tivozanib hydrochloride hydrate is a potent and selective and orally activeVEGFRtyrosine kinaseinhibitor withIC50of 0.21, 0.16, 0.24 nM forVEGFR-1, VEGFR-2,VEGFR-3, respectively. Tivozanib hydrochloride hydrate inhibits angiogenesis and vascular permeability in tumor tissues and shows antitumor activity. Tivozanib hydrochloride hydrate has the potential for the research of metastatic renal cell carcinoma (RCC)[1][2][3].

IC50& Target[3]

VEGFR-1

0.21 nM (IC50)

VEGFR-2

0.16 nM (IC50)

VEGFR-3

0.24 nM (IC50)

体外研究
(In Vitro)

Tivozanib hydrochloride hydrate inhibits the phosphorylation of VEGFR-1, VEGFR-2 and VEGFR-3[2].

体内研究
(In Vivo)

Tivozanib hydrochloride hydrate (1 mg/kg; p.o.; 14 days) suppresses the development of CNV lesions and leds to a significant regression of established CNV, reducing the affected areas by 67.7%[4].

Clinical Trial
分子量

509.34

性状

Solid

Formula

C22H22Cl2N4O6

CAS 号

682745-41-1

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, sealed storage, away from moisture and light

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

溶解性数据
In Vitro: 

DMSO : 250 mg/mL(490.83 mM;Need ultrasonic)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM1.9633 mL9.8166 mL19.6333 mL
5 mM0.3927 mL1.9633 mL3.9267 mL
10 mM0.1963 mL0.9817 mL1.9633 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month (sealed storage, away from moisture and light)。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。