1217626-02-2
1217626-02-2
Chemical Structure
7-Ethylcamptothecin-d3-1
- CAS No.: 1217626-02-2
- Formula:C22H17D3N2O4
- Molecular Weight:379.42
IUPAC Name: (S)-4-ethyl-11-(ethyl-2,2,2-d3)-4-hydroxy-1,12-dihydro-14H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H)-dione
InChIKey: MYQKIWCVEPUPIL-MVTYLIICSA-N
SMILES: O=C1C2=C(C=C3C4=NC5=CC=CC=C5C(CC([2H])([2H])[2H])=C4CN31)[C@@](CC)(C(OC2)=O)O
Biological Activity: 7-Ethylcamptothecin-d3-1 is the deuterium labeled 7-Ethylcamptothecin (HY-N2108). 7-Ethylcamptothecin is a derivative of Camptothecin (HY-16560) and a key intermediate in the synthesis of SN-38 (HY-13704). 7-Ethylcamptothecin can be used in tumor-related research[1].
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7-Ethylcamptothecin-d3-1 | 7-Ethylcamptothecin-d3-1 is the deuterium labeled 7-Ethylcamptothecin (HY-N2108). 7-Ethylcamptothecin is a derivative of Camptothecin (HY-16560) and a key intermediate in the synthesis of SN-38 (HY-13704). 7-Ethylcamptothecin can be used in tumor-related research. | |||||||||||||||||||||
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7-Ethylcamptothecin (Standard) | ≥98% | 7-Ethylcamptothecin (Standard) is the analytical standard of 7-Ethylcamptothecin (HY-N2108). This product is intended for research and analytical applications. 7-Ethylcamptothecin is a derivative of Camptothecin (HY-16560) and a key intermediate in the synthesis of SN-38 (HY-13704). 7-Ethylcamptothecin can be used in tumor-related research. | ||||||||||||||||||||
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7-Ethylcamptothecin | 99.58% | 7-Ethylcamptothecin is a derivative of Camptothecin (HY-16560) and a DNA topoisomerase I inhibitor that exhibits significant antitumor activity against tumor cells. 7-Ethylcamptothecin serves as a key precursor for the synthesis of 20 (S)-O-substituted benzoyl-7-ethylcamptothecin compounds. 7-Ethylcamptothecin is widely used in various tumor-related scientific studies. | ||||||||||||||||||||
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References
