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T17731LCL2A-SN-38 DCA 1279680-68-0(free base)
CL2A-SN-38 is a drug-linker conjugate composed of a potent a DNA Topoisomerase I inhibitor SN-38 and a linker CL2A to make antibody drug conjugate (ADC).. CL2A-SN-38 is composed of a potent a DNA Topoisomerase I inhibitor SN-38 and a linker CL2A to make a
价 格：￥电议型 号：T17731L产 地：中国大陆
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T1703SN-387-乙基-10-羟基喜树碱；伊立替康杂质B；SN 38；NK012；SN38
SN-38 is an active metabolite of CPT-11.
价 格：￥电议型 号：T1703产 地：中国大陆
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T73905SN-38 glucuronide；化合物 SN-38 glucuronideSN-38 glucuronide
SN-38 glucuronide, an inactive metabolite of Irinotecan, serves as a derivative of this cancer-fighting agent. Irinotecan, known for inhibiting topoisomerase I, is utilized in the research of colon and rectal cancer [1].
价 格：￥电议型 号：T73905产 地：中国大陆
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T20871Desmedipham；化合物 T20871SN-38107|||Bentanex|||Desmediphame|||EP 475|||EP-475|||EP475；SN-38107|||Bentan
Desmedipham is a carbamate herbicide.
价 格：￥电议型 号：T20871产 地：中国大陆
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T18722MAC glucuronide α-hydroxy lactone-linked SN-38；化合物 T18722MAC glucuronide α-hydroxy lactone-linked SN
MAC glucuronide α-hydroxy lactone-linked SN-38 (Topoisomerase I inhibitor) is a cytotoxic drug linker that maintains a stabilized lactone form, showing efficacy against L540cy and Ramos cells, with IC50 values of 99 and 105 ng/mL, respectively[1].
价 格：￥电议型 号：T18722产 地：中国大陆
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T18538MAC glucuronide phenol-linked SN-38；化合物 T18538MAC glucuronide phenol-linked SN-38
MAC glucuronide phenol-linked SN-38, a pH-sensitive lactone and DNA topoisomerase I inhibitor drug linker, exhibits cytotoxicity in L540cy and Ramos cells, with IC50 values of 113 ng/mL and 67 ng/mL, respectively[1].
价 格：￥电议型 号：T18538产 地：中国大陆
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T17731LCL2A-SN-38 DCA 1279680-68-0(free base)；化合物CL2A-SN-38 DCACL2A-SN-38 DCA 1279680-68-0(free base)
CL2A-SN-38 is a drug-linker conjugate composed of a potent a DNA Topoisomerase I inhibitor SN-38 and a linker CL2A to make antibody drug conjugate (ADC).. CL2A-SN-38 is composed of a potent a DNA Topoisomerase I inhibitor SN-38 and a linker CL2A to make antibody drug conjugate (ADC). CL2A-SN-38 provides significant and specific antitumor effects against a range of human solid tumor types. CL2A is a noncleavable complicated PEG8- and triazole-containing PABC-peptide-mc linker. CL2A is cleavable t
价 格：￥电议型 号：T17731L产 地：中国大陆
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T17731CL2A-SN-38；化合物CL2A-SN-38CL2A|||CL2A SN 38|||bystander effect|||SN-38|||antitumor|||CL2A-SN-38|||Inhi
CL2A-SN-38 is a drug-linker conjugate consisting of SN-38, a potent DNA topoisomerase I inhibitor, and linker CL2A, for the manufacture of antibody drug conjugates (ADCs). CL2A-SN-38 provides significant and specific antitumor effects against a range of human solid tumor types. CL2A is a nonclaevable complicated PEG8- and triazole-containing PABC-peptide-mc linker. CL2A is cleavable through pH sensitivity, giving rise to bystander effect, and binds the antibody at a cysteine residue via a disulf
价 格：￥电议型 号：T17731产 地：中国大陆
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T1703SN-38；伊立替康杂质BNK012|||SN 38；7-乙基-10-羟基喜树碱|||NK012|||伊立替康杂质B|||SN 38
SN-38 (NK012) is the active metabolite of Irinotecan, a DNA topoisomerase I (Topo I) inhibitor, which inhibits DNA and RNA synthesis (IC50=0.077/1.3 μM). SN-38 has antitumor activity and induces autophagy.
价 格：￥电议型 号：T1703产 地：中国大陆
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T10832CL2-SN-38；化合物 T10832CL-2-SN-38|||CL2-SN-38|||CL2SN38|||CL2 SN 38；CL-2-SN-38|||CL2-SN-38|||CL2SN38|||
CL2-SN-38, a part of the antibody-drug conjugate (ADC), can conjugate with the anti-Trop-2-humanized antibody hRS7. SN-38 is an inhibitor of DNA topoisomerase I.
价 格：￥电议型 号：T10832产 地：中国大陆
