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7–Ethyl–10–hydroxycamptothecin SN38 CAS 86639-52-3 High purity Pharmaceutical intermediate for Irinotecan
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xAppearance | Light Yellow Crystal Powder | Purity (HPLC) | ≥99.0% |
---|---|---|---|
Solubility | Insoluble In Water | Impurities | ≤0.5% |
Single Impurity | ≤0.1% | Loss On Drying | ≤5.0% |
Highlight | Pharmaceutical intermediate 7–Ethyl–10–hydroxycamptothecin SN38,CAS 86639-52-3 7–Ethyl–10–hydroxycamptothecin SN38,High purity 7–Ethyl–10–hydroxycamptothecin SN38 |
Product name:7-Ethyl-10-hydroxycamptothecin
CAS No.:86639-52-3
Synonyms:7-10-hydroxycamptothecin;(4S)-4,9-Dihydroxy-4,11-diethyl-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione;(4S)-4,9-Dihydroxy-4α,11-diethyl-3,4,12,14-tetrahydro-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14-dione;EHCPT;7-EtChemicalbookhyl-10-hydroxy-CPT(Camptothecine),SN-38;10-Hydroxycamptothecinacetatesalt,99%;IrinotecanRelatedCompoundB(10mg)((S)-4,11-diethyl-4,9-dihydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione);SN38(7-Ethyl-10-hydroxycaMptothecin)
MF:C22H20N2O5
MW:392.4
Properties:
7-ethyl-10-hydroxycamptothecin, light yellow solid at room temperature and pressure, insoluble in water and soluble in strong polar solvents such as methanol, ethanol, DMSO and other organic solvents. 7-ethyl-10-hydroxycamptothecin, a derivative of the plant-based chemotherapeutic drug camptothecin, has extremely high antitumor activity, however, its low solubility, instability at higher pH, p-glycoprotein effection, and severe first-pass effects make its oral bioavailability extremely low. In addition, the compound can also be used in basic biochemical research, including the identification of active molecules, pharmacological experiments, activity screening, etc.
Application:
7-ethyl-10-hydroxycamptothecin is a derivative of camptothecin, which is a cytotoxic alkaloid of pyrroloquinoline. Besides paclitaxel, it is one of the most studied natural anti-tumor drugs. It mainly exists in the fruit or root bark of Camptothecin, a unique plant in the Chinese davirate family. As an active metabolite of topoisomerase I inhibitor irinotecan, 7-ethyl-10-hydroxycamptothecin inhibits DNA synthesis and RNA synthesis with IC50 of 0.077 and 1.3 μM, respectively. 7-ethyl-10-hydroxycamptothecin is a kind of camptothecin molecule with broad-spectrum antitumor activity, but it is difficult to transform in clinic due to solubility problems. Its water-soluble small molecule prodrug irinotecan (CPT-11) has been approved for the treatment of a variety of malignant tumors including colorectal cancer, lung cancer and ovarian cancer.