
CAS 78287-27-1: 7-Ethylcamptothecin
Formula:C22H20N2O4
InChI:InChI=1S/C22H20N2O4/c1-3-12-13-7-5-6-8-17(13)23-19-14(12)10-24-18(19)9-16-15(20(24)25)11-28-21(26)22(16,27)4-2/h5-9,27H,3-4,10-11H2,1-2H3/t22-/m0/s1
InChI key:InChIKey=MYQKIWCVEPUPIL-QFIPXVFZSA-N
SMILES:O=C1N2C(C=3C(C2)=C(CC)C=4C(N3)=CC=CC4)=CC5=C1COC(=O)[C@@]5(CC)O
Synonyms:- (4S)-4,11-Diethyl-4-hydroxy-1H-pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione
- (4S)-4,11-diethyl-4-hydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione
- (S)-4,11-Diethyl-4-hydroxy-1H-pyrano(3',4':6,7)indolizino(1,2-b)quinoline-3,14(4H,12H)-dione
- 1H-Pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione, 4,11-diethyl-4-hydroxy-, (4S)-
- 1H-Pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione, 4,11-diethyl-4-hydroxy-, (S)-
- 7-Ethyl Camptothecin
- 7-Ethyl-20(S)-camptothecin
- Sn 22
- 7-Ethylcamptothecin
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Found 14 products.
7-Ethylcamptothecin
CAS:Formula:C22H20N2O4Purity:>98.0%(T)(HPLC)Color and Shape:Light orange to Yellow to Green powder to crystalMolecular weight:376.417-Ethylcamptothecin
CAS:1.Formula:C22H20N2O4Purity:99.08%Color and Shape:Light Pink SolidMolecular weight:376.41Irinotecan EP Impurity F (7-Ethyl Camptothecin)
CAS:Formula:C22H20N2O4Color and Shape:Yellow SolidMolecular weight:376.41(S)-4,11-Diethyl-4-hydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:376.41198730468757-Ethyl camptothecin
CAS:Camptothecin is a natural product that belongs to the ester family of compounds. It has been isolated from the bark of Camptotheca acuminata, a tree native to China. Camptothecin inhibits cancer cell growth by binding to DNA and interrupting DNA replication and transcription. The drug also binds to RNA polymerase II and blocks RNA synthesis. Camptothecins have a low therapeutic index, meaning that the effective dose may be too high for some patients. This drug is not suitable for use in postharvest treatments because it is unstable under these conditions. The anticancer activity of camptothecin was first observed in 1974 when researchers noted that this drug had an inhibitory effect on tumor xenografts in mice. The mechanism by which camptothecin exerts its effects on cells has not been fully elucidated but it is thought that this drug interacts with choline molecules on the surface of cancer cells, inhibiting their repair mechanisms and leading toFormula:C22H20N2O4Purity:Min. 95%Molecular weight:376.41 g/molRef: 3D-FE23038
Discontinued productIrinotecan Related Compound E ((S)-4,11-Diethyl-4-hydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione)
CAS:Vegetable alkaloids, natural or reproduced by synthesis, their salts and other derivatives, nesoiFormula:C22H20N2O4Color and Shape:Light Brown PowderMolecular weight:376.142317-Ethyl Camptothecin
CAS:Impurity Irinotecan USP Related Compound E Applications An anticancer drug, showed strong activity against various murine tumors. A Camptothecin (CPT) derivative as antineoplastic agent against drug-resistant tumors. Irinotecan USP Related Compound E. References Brangi, M., et al.: Cancer Res., 59 5938 (1999), Miyake, K., et al.: Cancer Res., 59, 8 (1999) , Bom, D., et al.: J. Med. Chem., 43, 3970 (2000) , Gamcsik, M., et al.: Mol. Cancer Ther., 1, 11 (2001).Formula:C22H20N2O4Color and Shape:Light YellowMolecular weight:376.41