| Identification | Back Directory | [Name]
1H-Pyrrole-1-hexanoic acid, 2,5-dihydro-2,5-dioxo-, (4S)-4,11-diethyl-3,4,12,14-tetrahydro-9-hydroxy-3,14-dioxo-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-4-yl ester | [CAS]
1473403-87-0 | [Synonyms]
MC-SN38
1H-Pyrrole-1-hexanoic acid, 2,5-dihydro-2,5-dioxo-, (4S)-4,11-diethyl-3,4,12,14-tetrahydro-9-hydroxy-3,14-dioxo-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-4-yl ester | [Molecular Formula]
C32H31N3O8 | [MOL File]
1473403-87-0.mol | [Molecular Weight]
585.6 |
| Chemical Properties | Back Directory | [Boiling point ]
913.6±65.0 °C(Predicted) | [density ]
1.46±0.1 g/cm3(Predicted) | [form ]
Solid | [pka]
9.12±0.40(Predicted) | [color ]
White to yellow |
| Hazard Information | Back Directory | [Description]
MC-SN38 is a drug-linker conjugate composed of a potent microtubule-disrupting agent SN38 and a non-cleavable MC linker to make antibody drug conjugate (ADC). SN-38, an active metabolite of the Topoisomerase I inhibitor Irinotecan, inhibits DNA synthesis and causes frequent DNA single-strand breaks. | [Uses]
MC-SN38 is a agent-linker conjugate composed of a potent microtubule-disrupting agent SN38 and a non-cleavable MC linker to make antibody agent conjugate (ADC). SN-38, an active metabolite of the Topoisomerase I inhibitor Irinotecan, inhibits DNA synthesis and causes frequent DNA single-strand breaks[1][2]. | [References]
[1] Jensen NF, et al. Characterization of DNA topoisomerase I in three SN-38 resistant human colon cancer cell lines reveals a newpair of resistance-associated mutations. J Exp Clin Cancer Res. 2016 Mar 31;35:56. DOI:10.1186/s13046-016-0335-x
[2] Kawato Y, et al. Intracellular roles of SN-38, a metabolite of the camptothecin derivative CPT-11, in the antitumor effect of CPT-11. Cancer Res. 1991;51(16):4187-4191. PMID:1651156 |
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YJ Pharma
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13962794339 13962794339; |
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YantaiBio
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13758194781 |
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TargetMol
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400-821-0310 15002144251 |
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www.targetmol.cn/ |
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