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SuO-Glu-Val-Cit-PAB-MMAE
目录号:SY-101244
SuO-Glu-Val-Cit-PAB-MMAE is a chemical compound comprising a cleavable ADC linker, SuO-Glu-Val-Cit-PAB, and a potent tubulin inhibitor known as MMAE. It is utilized in the synthesis of antibody-drug conjugates (ADCs).
¥1920.00
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SC-VC-PAB-MMAE
目录号:SY-101245
SC-VC-PAB-MMAE is a potent antitumor drug-linker conjugate for antibody-drug conjugates (ADCs), comprising the anti-mitotic agent monomethyl auristatin E (MMAE, a tubulin inhibitor) connected through the cleavable linker SC-VC-PAB[1].
¥3135.00
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MC-VC-PABC-Aur0101
目录号:SY-101246
MC-VC-PABC-Aur0101 is a potent anticancer drug-linker conjugate designed for Antibody-Drug Conjugates (ADCs), comprising Aur0101, an auristatin microtubule inhibitor, connected through the MC-VC-PABC linker to enhance antitumor efficacy.
¥1495.00
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SPB
目录号:SY-101247
SPB is a potent anti-inflammatory drug-linker conjugate for Antibody-Drug Conjugates (ADC), utilizing Xanthotoxol connected through the ADC linker.
¥322.00
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AcLys-PABC-VC-Aur0101
目录号:SY-101248
AcLys-PABC-VC-Aur0101 is a drug-linker conjugate for anti-CXCR4 ADC with potent antitumor activity, comprising the auristatin microtubule inhibitor Aur0101, connected through the cleavable linker AcLys-PABC-VC[1].
¥4466.00
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Azido-PEG4-Val-Cit-PAB-MMAE
目录号:SY-101249
Azido-PEG4-Val-Cit-PAB-MMAE is a drug-linker conjugate for antibody-drug conjugates (ADCs), comprising the anti-mitotic agent monomethyl auristatin E (MMAE, a tubulin inhibitor), connected through the cleavable linker Azido-PEG4-Val-Cit-PAB-OH.
¥7475.00
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MC-Val-Cit-PAB-Auristatin E
目录号:SY-101250
MC-Val-Cit-PAB-Auristatin E is an antibody-drug conjugate (ADC) linker compound featuring Auristatin E, a potent cytotoxic tubulin modifier, connected through the MC-Val-Cit-PAB linker, exhibiting significant antitumor activity.
¥1920.00
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Mal-C2-Gly3-EDA-PNU-159682
目录号:SY-101251
Mal-C2-Gly3-EDA-PNU-159682, a drug-linker conjugate for antibody-drug conjugates (ADC), combines the cleavable ADC linker Mal-C2-Gly3-EDA with the potent ADC cytotoxin PNU-159682.
¥4186.00
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DBCO-PEG4-GGFG-Dxd
目录号:SY-101252
DBCO-PEG4-GGFG-Dxd作为一种点击化学试剂,是抗体-活性分子偶联物的关键组成部分,它结合了DNA拓扑异构酶I抑制剂Dxd与可裂解的ADC linker DBCO-PEG4-GGFG。此化合物利用DBCO基团与含Azide基团的分子之间通过菌株促进的炔-叠氮环加成反应(SPAAC)实现快速且特异的连接。
¥3910.00
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