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Merck
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重要文件

SML3017

Sigma-Aldrich

甲磺酸乐伐替尼

≥98% (HPLC)

同義詞:

4-[3-氯-4-(N’-环丙基脲)苯氧基]-7-甲氧喹啉-6-甲酰胺甲磺酸盐, 4-[3-氯-4-[(环丙基羰基)氨基]苯氧基]-7-甲氧基-6-喹啉甲酰胺甲磺酸盐, 4-[3-氯-4-[[(环丙胺)羰基]氨基]苯氧基]-7-甲氧基-6-喹啉甲酰胺甲基磺酸盐(1:1), E 7080甲磺酸盐, E-7080甲磺酸盐, E7080甲磺酸盐, ER-203492-00甲磺酸盐, 乐伐替尼甲基磺酸盐

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About This Item

經驗公式(希爾表示法):
C21H19ClN4O4 · CH4O3S
CAS號碼:
分子量::
522.96
MDL號碼:
分類程式碼代碼:
12352200
NACRES:
NA.77

品質等級

化驗

≥98% (HPLC)

形狀

powder

顏色

white to beige

溶解度

DMSO: 2 mg/mL, clear

儲存溫度

2-8°C

SMILES 字串

O=C(C1=CC2=C(OC3=CC=C(C(Cl)=C3)NC(NC4CC4)=O)C=CN=C2C=C1OC)N.O=S(O)(C)=O

InChI

1S/C21H19ClN4O4.CH4O3S/c1-29-19-10-17-13(9-14(19)20(23)27)18(6-7-24-17)30-12-4-5-16(15(22)8-12)26-21(28)25-11-2-3-11;1-5(2,3)4/h4-11H,2-3H2,1H3,(H2,23,27)(H2,25,26,28);1H3,(H,2,3,4)

InChI 密鑰

HWLFIUUAYLEFCT-UHFFFAOYSA-N

生化/生理作用

Lenvatinib (E7080)是一种针对多种受体酪氨酸激酶的口服活性抑制剂,包括VEGFR (Flt-1/KDR/Flt-4 IC50 = 22/4.0/5.2 nM)、PDGFR1/2 (IC50 = 39/51 nM)、FGFR1和KIT (IC50分别= 46和100 nM),可抑制体外血管生成(VEGF/ scf诱导HUVEC管形成IC50 = 5.1/5.2 nM)。口服Lenvatinib可导致产生scf的人小细胞肺癌H146细胞的小鼠体内肿瘤生长停滞(30 mg/kg b.i.p.o)甚至退化(100 mg/kg b.i.p.o)。
口服活性受体酪氨酸激酶抑制剂(Flt-1/KDR/Flt-4), PDGFR1/2, FGFR1和KIT具有抗血管生成的体外和体内疗效。

象形圖

Health hazard

訊號詞

Warning

危險聲明

危險分類

Repr. 2 - STOT RE 2

標靶器官

Gastro-intestinal system,Kidney,Bone,Reproductive organs,Adrenal gland

儲存類別代碼

11 - Combustible Solids

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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