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Merck

SML1400

Sigma-Aldrich

AEE788

≥98% (HPLC)

别名:

6-{4-[(4-Ethyl-1-piperazinyl)methyl]phenyl}-N-[(1R)-1-phenylethyl]-1H-pyrrolo[2,3-d]pyrimidin-4-amine, CID 10297043, NVP-AEE 788, [6-[4-[(4-Ethylpiperazin-1-yl)methyl]phenyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-((R)-1-phenylethyl)amine

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About This Item

经验公式(希尔记法):
C27H32N6
分子量:
440.58
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

化驗

≥98% (HPLC)

形狀

powder

顏色

white to beige

溶解度

H2O: 10 mg/mL, clear

儲存溫度

−20°C

SMILES 字串

C[C@H](C1=CC=CC=C1)NC2=C3C(NC(C4=CC=C(CN5CCN(CC)CC5)C=C4)=C3)=NC=N2

InChI

1S/C27H32N6/c1-3-32-13-15-33(16-14-32)18-21-9-11-23(12-10-21)25-17-24-26(28-19-29-27(24)31-25)30-20(2)22-7-5-4-6-8-22/h4-12,17,19-20H,3,13-16,18H2,1-2H3,(H2,28,29,30,31)/t20-/m1/s1

InChI 密鑰

OONFNUWBHFSNBT-HXUWFJFHSA-N

生化/生理作用

AEE788 is an orally available and potent dual family of human EGFR and VEGFR receptor tyrosine kinase inhibitor that exhibits potent antitumor and antiangiogenic activity.

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Rintu Thomas et al.
International journal of molecular sciences, 20(10) (2019-05-28)
Inhibiting the tyrosine kinase activity of epidermal growth factor receptor (EGFR) using small molecule tyrosine kinase inhibitors (TKIs) is often ineffective in treating cancers harboring wild-type EGFR (wt-EGFR). TKIs are known to cause dimerization of EGFR without altering its expression

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