喜樹堿是拓?fù)洚悩?gòu)酶I的選擇性抑制劑，IC50值為679 nM [1]。

喜樹堿可以誘導(dǎo)SMMC-7721、MCF-7和HCT-116腫瘤細(xì)胞的死亡。據(jù)報道，喜樹堿通過AMPK-TSC2-mTOR途徑誘導(dǎo)自噬，同時通過ATM-Chk2-p53-p21途徑誘導(dǎo)早衰[2]。 研究表明喜樹堿在非小細(xì)胞肺癌異種移植物中具有抗腫瘤活性。已經(jīng)發(fā)現(xiàn)喜樹堿誘導(dǎo)的DNA損傷導(dǎo)致H2AX (γH2AX)的磷酸化。以前的研究也證明了在用喜樹堿治療的癌細(xì)胞中減少Top1的表達(dá)[3]。

產(chǎn)品性質(zhì)：

Cas No.:7689-03-4

別名:喜樹堿; Campathecin; (S)-(+)-Camptothecin; CPT

化學(xué)名:(S)-4-ethyl-4-hydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione

Canonical SMILES:O=C(N(CC1=CC(C=CC=C2)=C2N=C13)C3=C4)C(CO5)=C4[C@@](O)(CC)C5=O

分子式:C20H16N2O4

分子量:348.35

溶解度:≥ 8.7mg/mL in DMSO

儲存條件:4°C, protect from light

注意事項：

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References:

[1] Luzzio MJ1, Besterman JM, Emerson DL, Evans MG, Lackey K, Leitner PL, McIntyre G, Morton B, Myers PL, Peel M, et al. Synthesis and antitumor activity of novel water soluble derivatives of camptothecin as specific inhibitors of topoisomerase I. J Med Chem. 1995 Feb 3;38(3):395-401.

[2] Zhang JW1, Zhang SS1, Song JR2, Sun K3, Zong C1, Zhao QD1, Liu WT1, Li R1, Wu MC1, Wei LX4. Autophagy inhibition switches low-dose camptothecin-induced premature senescence to apoptosis in human colorectal cancer cells. Biochem Pharmacol. 2014 May 22. pii: S0006-2952(14)00286-X.

[3] Tsakalozou E1, Adane ED, Liang Y, Arnold SM, Leggas M. Protracted dosing of the lipophilic camptothecin analogue AR-67 in non-small cell lung cancer xenografts and humans. Cancer Chemother Pharmacol. 2014 May 8. [Epub ahead of print]