| Weight | 622.762 g/mol |
|---|---|
| Formula | C38H42N2O6 |
| Hydrogen Acceptors | 8 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 4 |
| Rotatable Bonds | 4 |
tetrandrine (518-34-3, 23495-89-8)
Score:
#1514 in Biochemistry
,
#3532 in Biology
,
#4426 in Chemistry
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- Sigma-Aldrich - tetrandrine168.00 - 172.50 USD
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- The multidrug resistance of tumour cells was reversed by tetrandrine in vitro and in xenografts derived from human breast adenocarcinoma MCF-7/adr cells (European Journal of Cancer, 2002)
- Interaction of tetrandrine with slowly inactivating calcium channels. Characterization of calcium channel modulation by an alkaloid of Chinese medicinal herb origin. (Journal of Biological Chemistry, 1988)
- Characterization of tetrandrine, a potent inhibitor of P-glycoprotein-mediated multidrug resistance (Cancer Chemotherapy and Pharmacology, 2004)
- Lactoferrin-conjugated biodegradable polymersome holding doxorubicin and tetrandrine for chemotherapy of glioma rats. (Molecular Pharmaceutics, 2010)
- Tetrandrine Inhibits Wnt/-Catenin Signaling and Suppresses Tumor Growth of Human Colorectal Cancer (Molecular Pharmacology, 2011)
- Tetrandrine induces apoptosis by activating reactive oxygen species and repressing Akt activity in human hepatocellular carcinoma (International Journal of Cancer, 2011)
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SMILESCN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC
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InChIKeyWVTKBKWTSCPRNU-UHFFFAOYSA-N
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tetrandrine
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