Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6897 |
Monomethyl auristatin E
一甲基澳瑞他汀E,Vedotin,MMAE |
Apoptosis; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
Monomethyl auristatin E (MMAE) 是海兔毒素 10 的合成衍生物,是一种抗有丝分裂剂,通过阻断微管蛋白的聚合来抑制细胞分裂,并且还具有抑制抗体-药物偶联物的活性。 | |||
T10948 |
MMAE-d8
D8-MMAE,D8-Monomethyl auristatin E |
Others | Others |
D8-MMAE (D8-Monomethyl auristatin E) is an effective mitotic inhibitor and tubulin inhibitor, deuterated MMAE. | |||
T18312 |
Mc-MMAE
Maleimidocaproyl-monomethylauristatin E,马来酰亚胺基己酰-单甲基澳瑞他汀 E |
Microtubule Associated | Cytoskeletal Signaling |
Mc-MMAE (Maleimidocaproyl-monomethylauristatin E) 是保护基团 (马来酰亚氨基己酰) 与 MMAE 共轭连接得到的化合物。它是微管蛋白抑制剂,可用于偶联抗体。 | |||
T40568 |
Fmoc-MMAE
|
||
Fmoc-MMAE, a protective group-conjugated variant of monomethyl auristatin E (MMAE), serves as a powerful inhibitor of tubulin. It finds application in the synthesis of antibody-drug conjugates (ADC). | |||
T18736 |
SuO-Val-Cit-PAB-MMAE
|
Others | Others |
SuO-Val-Cit-PAB-MMAE is an ADC (antibody-drug conjugate) linker comprising the anti-mitotic monomethyl auristatin E (MMAE, a tubulin inhibitor) connected through the SuO-Val-Cit-PAB peptide. | |||
T18679 |
SC-VC-PAB-MMAE
|
Others | Others |
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]. | |||
T17817 |
DBCO-(PEG)3-VC-PAB-MMAE
|
Others | Others |
DBCO-(PEG)3-VC-PAB-MMAE is a chemical compound where monomethyl auristatin E (MMAE), a potent tubulin inhibitor acting as a toxin payload in antibody-drug conjugates, is conjugated to a DBCO-(PEG)3-vc-PAB linker. | |||
T39307 |
Azido-PEG4-Val-Cit-PAB-MMAE
Azido-PEG4-Val-Cit-PAB-MMAE |
||
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. | |||
T70958 | Dov-Val-Dil-OH TFA | ||
Dov-Val-Dil-OH is a useful chemical intermediate for synthesis of auristatin-related compounds, such as Monomethyl auristatin E (MMAE), Auristatins are antimitotic agents which inhibits cell division by blocking the polymerisation of tubulin. | |||
T77838 |
Telisotuzumab vedotin
ABBV-399 |
||
Telisotuzumab vedotin (ABBV-399) 是一种靶向c-Met的抗体-药物偶联物(ADCs),由Monomethyl Auristatin E (MMAE)、Telisotuzumab抗体和mc-val-cit-PABC可裂解型linker组合而成,主要用于癌症研究。 | |||
T82384 | Fmoc-Gly3-VC-PAB-MMAE | ||
Fmoc-Gly3-VC-PAB-MMAE 是一款用于 ADC 的药物-连接子偶联物,由 MonomethylauristatinE 和连接子构成。 | |||
T18303 |
Mal-Phe-C4-VC-PAB-MMAE
|
Others | Others |
Mal-Phe-C4-VC-PAB-MMAE is a chemical compound resulting from the conjugation of monomethyl auristatin E (MMAE), a potent tubulin inhibitor serving as a toxin payload in antibody-drug conjugates, with a Mal-Phe-C4-VC-PAB linker. | |||
T81753 | mp-dLAE-PABC-MMAE | ||
mp-dLAE-PABC-MMAE 是构成抗体药物偶联物 (ADC) 活性部分的化合物。它包括微管蛋白抑制剂 Monomethylauristatin E,并用于ADC的合成。 | |||
T82380 |
Fmoc-VAP-MMAE
|
||
Fmoc-VAP-MMAE是一种含有微管蛋白抑制剂MMAE的ADC活性分子-linker偶联物,配备了Fmoc保护基团。该复合物由ADC Linker和MMAE构成。 | |||
T18473 |
N3-PEG3-vc-PAB-MMAE
|
Others | Others |
N3-PEG3-vc-PAB-MMAE, a drug-linker conjugate designed for Antibody-Drug Conjugates (ADC), features the integration of monomethyl auristatin E (MMAE), a tubulin inhibitor, via a 3-unit polyethylene glycol (PEG) linker. This compound demonstrates significant antitumor activity. | |||
T79039 |
GGGDTDTC-Mc-vc-PAB-MMAE
|
||
GGGDTDTC-Mc-vc-PAB-MMAE为一种ADC药物-连接物偶联物,主要由微管蛋白抑制剂Monomethylauristatin E (MMAE)组成。 | |||
T77883 |
Val-Ala-PAB-MMAE
|
||
Val-Ala-PAB-MMAE是一种用于抗体药物偶联物(ADC)的药物连接物缀合物,由ADC连接子(Val-Ala-PAB)与微管抑制剂MMAE构成。 | |||
T17789 |
DBCO-(PEG2-VC-PAB-MMAE)2
|
Others | Others |
DBCO-(PEG2-VC-PAB-MMAE)2 consists of Monomethyl auristatin E (MMAE), a toxin payload in antibody-drug conjugate [1], conjugated to the cleavable linker DBCO-(PEG2-VC-PAB)2. MMAE, a potent tubulin inhibitor, serves as the cytotoxic component in this formulation. | |||
T77853 |
MC-VA-PABC-MMAE
|
||
MC-VA-PABC-MMAE是一种ADC(Linker为peptide MC-VA-PABC)的活性分子,由Linker与高效微管蛋白抑制剂MMAE通过偶联反应形成。 | |||
T81361 |
PSMA-Val-Cit-PAB-MMAE
|
||
PSMA-Val-Cit-PAB-MMAE是一种靶向前列腺特异性膜抗原(PSMA)的小分子化合物,用MMAE作为药效基团进行前列腺癌治疗。 | |||
T77823 |
Polatuzumab vedotin
|
||
Polatuzumab vedotin是一种抗体药物偶联物,靶向CD79b。该化合物结合了人源化抗CD79b IgG1单克隆抗体和微管抑制剂monomethyl auristatin E (MMAE),展现出针对大B细胞淋巴瘤(LBCL)的治疗潜力。 | |||
T81133 |
Sofituzumab vedotin
DMUC5754A |
||
Sofituzumab vedotin (DMUC5754A) 是一种抗MUC16的ADC,其含有MMAE并配备蛋白酶切割连接子。该化合物主要应用于癌症研究领域。 | |||
T77881 |
Tisotumab vedotin
|
||
Tisotumab vedotin是一种针对组织因子(tissue factor, TF)的抗体-药物偶联物(ADC),由全人源单克隆抗体(TF-011)与Monomethyl Auristatin E (MMAE)耦合而成,具有显著抗肿瘤活性,适用于晚期或转移性实体瘤的治疗研究。 | |||
T15872 |
m-PEG4-Br
|
Others | Others |
m-PEG4-Br is a cleavable ADC linker used in the synthesis of antibody-drug conjugate (ADC) for Trastuzumab. m-PEG4-Br is placed distally from the monomethyl auristatin E (MMAE) payload to yield an ADC with altered hydrophilicity, antigen binding, and in v | |||
T80609 |
Mecbotamab
|
||
Mecbotamab是一款针对AXL受体酪氨酸激酶的人源化IgG1-κ抗体。作为条件活性生物制剂(CAB),Mecbotamab通过一个可降解连接子与MMAE结合,组成ADC(抗体-药物偶联物)产品Mecbotamab vedotin (BA3011)。 | |||
T82582 | Depatuxizumab MMAE | ||
Depatuxizumab MMAE 是抗EGFR抗体 (Depatuxizumab) 与 Monomethylauristatin E (MMAE) 结合形成的抗体-活性分子偶联物 (ADC),能够抑制EGFRvIII突变型以及野生型EGFR在异种移植瘤模型中的生长。 | |||
T77856 |
Ac-Lys-Val-Cit-PABC-MMAE
|
||
Ac-Lys-Val-Cit-PABC-MMAE作为一种抗体偶联药物(ADC)的活性分子部分,由ADC连接子(肽 Ac-Lys-Val-Cit-PABC)与微管蛋白聚合抑制剂MMAE经偶联形成。 | |||
T77857 |
Ac-Lys-Val-Cit-PABC-MMAE formic
|
||
Ac-Lys-Val-Cit-PABC-MMAE (formic) 为一种抗体药物偶联物(ADC)的活性组分。该化合物是由ADC链接子(肽类Ac-Lys-Val-Cit-PABC)与微管蛋白聚合抑制剂Monomethylauristatin E (MMAE) 结合而得。 | |||
T77186 | Zilovertamab vedotin | ||
Zilovertamab vedotin (VLS-101) 是一种抗体-活性分子偶联物 (ADC), 主要由人源化单克隆抗体 zilovertamab 和单甲基 vedotin 组成的抗微管细胞毒素。该药物通过与肿瘤细胞表面的ROR1结合, 触发快速内化及向溶酶体的转运, 进而裂解释放单甲基 vedotin, 诱导细胞凋亡。适用于癌症的研究领域。 |