60
11
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。 | |||
T21236 |
Monomethyl sebacate
Decanoic acid, monomethyl ester,Methyl hydrogen sebacate |
||
Monomethyl sebacate is a biochemical. | |||
T19435 |
Monomethyl fumarate-d3
Monomethyl fumarate D3 |
Others | Others |
Monomethyl fumarate D3 is a deuterium labeled Monomethyl fumarate. | |||
T12081 |
MMAF-OMe
Monomethyl auristatin F methyl ester |
||
MMAF-OMe (Monomethyl auristatin F methyl ester) 是一种抗微管蛋白剂,能够抑制 MDAMB435/5T4,MDAMB361DYT2,MDAMB468 和 Raji (5T4-) 这四种肿瘤细胞,IC50值分别为 0.056 nM,0.166 nM,0.183 nM 和 0.449 nM。它也是ADC 细胞毒素。 | |||
T18143 |
m-PEG12-OH
Dodecaethylene Glycol Monomethyl Ether |
Others; PROTAC Linker | Others; PROTAC |
m-PEG12-OH (Dodecaethylene Glycol Monomethyl Ether) 是一种基于 PEG 的 PROTAC 接头,可用于 PROTAC 的合成。它也是一种不可切割的 12 单元 PEG ADC 接头,用于合成抗体-药物偶联物。 | |||
T3256 |
MMAF
一甲基澳瑞他汀 F,MonoMethyl auristatin F |
Others; Microtubule Associated | Cytoskeletal Signaling; Others |
MMAF (MonoMethyl auristatin F) 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,用作抗肿瘤药物和抗体偶联药物的细胞毒性成分。 | |||
T4677 |
MMAD
Monomethylauristatin D,Demethyldolastatin 10,单甲基澳瑞他汀 D,Monomethyl Dolastatin 10 |
Microtubule Associated | Cytoskeletal Signaling |
MMAD (Demethyldolastatin 10) 是一种有效的微管蛋白抑制剂,是抗体药物偶联物中的一种毒素有效载荷。 | |||
T39203 |
Raloxifene 6-Monomethyl Ether
|
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Compound 7, or Raloxifene 6-Monomethyl Ether, is a derivative of Raloxifene that effectively inhibits estrogen receptor α. It also displays the inhibitory effects on MCF-7 cells, with an IC50 of 250 nM and a pIC50 of 6.6. | |||
T39298 |
Raloxifene 4-Monomethyl Ether
|
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Raloxifene 4-Monomethyl Ether (Compound 37) is a derivative of Raloxifene which acts as an inhibitor of estrogen receptor α. It effectively suppresses the activity of MCF-7 cells, exhibiting an IC50 value of 1 μM and a pIC50 value of 6. | |||
T33475 |
Monomethyl adipate
NSC55113,NSC 55113,NSC-55113 |
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Monomethyl adipate is a biochemical. | |||
T38970 |
Hematoporphyrin monomethyl ether
|
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Hematoporphyrin monomethyl ether (HMME), a second-generation porphyrin-related photosensitizer, is a highly selective and low-toxicity compound known for its singular form and high yield of singlet oxygen. It finds extensive application in diagnosing and treating various tumors, including lung cancer, bladder cancer, nevus flammeus, and brain glioma. | |||
T16467 | Pentaethylene glycol monomethyl ether | Others | Others |
Pentaethylene glycol monomethyl ether (PEG-MME) is a PEG-based PROTAC linker, which is employed for the synthesis of PROTACs[1]. | |||
T15475 |
Hexaethylene glycol monomethyl ether
|
Others | Others |
Hexaethylene glycol monomethyl ether, a PEG-based PROTAC linker, facilitates the synthesis of PROTACs[1]. | |||
T17054 |
Tetraethylene glycol monomethyl ether
|
Others | Others |
Tetraethylene glycol monomethyl ether, a PEG-based PROTAC linker, is employed for the synthesis of PROTACs[1]. | |||
T16374 | Octaethylene glycol monomethyl ether | Others | Others |
Octaethylene glycol monomethyl ether, a PEG-based linker, serves as an essential component in the synthesis of PROTACs[1]. | |||
T16336 |
Nonaethylene glycol monomethyl ether
|
Others | Others |
Nonaethylene glycol monomethyl ether, a PEG-based PROTAC linker, facilitates PROTAC synthesis[1]. | |||
T20988 |
Isopropylene glycol monomethyl ether acetate
|
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Isopropylene glycol monomethyl ether acetate is a bioactive chemical. | |||
T18869 |
Vat-Cit-PAB-Monomethyl Dolastatin 10
|
Others | Others |
Vat-Cit-PAB-Monomethyl Dolastatin 10 is an ADC linker-conjugated drug designed to deliver potent antitumor activity. It achieves this through Monomethyl Dolastatin 10, a potent tubulin inhibitor, connected via the Vat-Cit-PAB ADC linker. | |||
T15834 |
m-PEG10-alcohol
Decaethylene glycol monomethyl ether |
Others | Others |
m-PEG10-alcohol, also known as Decaethylene glycol monomethyl ether, is a non-cleavable 10 unit PEG ADC linker utilized in the synthesis of antibody-drug conjugates (ADCs)[1]. Additionally, m-PEG10-alcohol serves as a PEG-based PROTAC linker, enabling its application in the synthesis of PROTACs[1]. | |||
T26277L |
Tilarginine citrate
L-Ng-monomethyl arginine citrate |
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Tilarginine citrate is a competitive nitric oxide synthetase inhibitor. | |||
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. | |||
T24982 |
546C88
L-N(G)-Methylarginine hydrochloride,NG-Monomethyl-L-arginine hydrochloride,L-NMMA |
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546C88 is an inhibitor of nitric oxide synthase. | |||
T10947 |
D8-MMAD
Monomethylauristatin D D8,Demethyldolastatin 10 D8,Monomethyl Dolastatin 10 D8 |
Others | Others |
D8-MMAD is a deuterated form of MMAD, which is a microtubule destroyer. | |||
T71844 |
Methyl potassium malonate
|
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Methyl potassium malonate is a protein advanced glycosylation inhibitor. | |||
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。 | |||
T4271 |
Diroximel fumarate
Diroximel Fumarete |
Others | Others |
Diroximel fumarate (Diroximel Fumarete) 是一种控释制剂,是口服具有活力的富马酸单乙酯的前体药物。它被认为与其活性代谢物富马酸二甲酯的活性等效。它具有良好的安全性和有效性,具有研究多发性硬化的潜力。 | |||
T40568 |
Fmoc-MMAE
|
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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). | |||
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]. | |||
T39307 |
Azido-PEG4-Val-Cit-PAB-MMAE
Azido-PEG4-Val-Cit-PAB-MMAE |
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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. | |||
T18311 |
Mc-MMAD
|
Others | Others |
Mc-MMAD, a drug-linker conjugate for antibody-drug conjugates (ADCs), incorporates the protective group maleimidocaproyl (Mc) conjugated to monomethyl auristatin D (MMAD), a potent inhibitor of tubulin. | |||
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. | |||
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. | |||
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. | |||
T18251 |
MAL-di-EG-Val-Cit-PAB-MMAF
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Others | Others |
MAL-di-EG-Val-Cit-PAB-MMAF refers to a chemical compound that comprises the linker (MAL-di-EG-Val-Cit-PAB) and the potent blocker of tubulin polymerization (MMAF, Monomethyl auristatin F)[1]. | |||
T77838 |
Telisotuzumab vedotin
ABBV-399 |
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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。 | |||
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. | |||
T79039 |
GGGDTDTC-Mc-vc-PAB-MMAE
|
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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。 | |||
T81361 |
PSMA-Val-Cit-PAB-MMAE
|
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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。 | |||
T82384 |
Fmoc-Gly3-VC-PAB-MMAE
|
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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。 | |||
T77883 |
Val-Ala-PAB-MMAE
|
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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。 | |||
T82380 |
Fmoc-VAP-MMAE
|
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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。 | |||
T81133 |
Sofituzumab vedotin
DMUC5754A |
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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。 | |||
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 | |||
T18473 |
N3-PEG3-vc-PAB-MMAE
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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. | |||
T18326 |
MC-Val-Cit-PAB-MMAF
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Others | Others |
MC-Val-Cit-PAB-MMAF is an antibody-drug conjugate (ADC) component that exhibits antitumor properties through the action of the tubulin inhibitor, monomethyl auristatin F (MMAF), which is connected by a cathepsin-cleavable linker, MC-Val-Cit-PAB. | |||
T77892 |
Mal-PEG8-Val-Cit-PAB-MMAF
|
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Mal-PEG8-Val-Cit-PAB-MMAF 是一种用于抗体药物偶联体 (ADC) 的药物-连接物复合体 (drug-linker conjugate for ADC)。该化合物由一个可降解的 ADC linker 以及有效的微管蛋白抑制剂 MMAE 组成。 | |||
T81753 |
mp-dLAE-PABC-MMAE
|
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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。 | |||
T27975 |
MAL-PEG4-MMAF
|
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MAL-PEG4-MMAF is a maleimido functionalized derivative of MMAF (Monomethyl auristatin F) with PEG4 linker. The maleimido functional group can be easily conjugated to protein carriers (such as antibody or enzyme). MAL-PEG4-MMAF is a useful precursor for ma | |||
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. | |||
T71768 | CB10-277 | ||
CB10-277 is a synthetic derivative of dimethylphenyl-triazene related to dacarbazine, with antineoplastic properties. Related to the agent dacarbazine, CB10-277 is converted in vivo to a monomethyl triazene form that alkylates DNA, resulting in inhibition of DNA replication and repair; in addition, this agent may act as a purine analogue, resulting in inhibition of DNA synthesis, and may interact with protein sulfhydryl groups. |
Cat. No. | Product Name | Target | Signaling Pathways |
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T12095 |
Monomethyl fumarate
|
GPR; Drug Metabolite | Endocrinology/Hormones; GPCR/G Protein; Metabolism |
Monomethyl fumarate 是 Dimethyl fumarate 的活性代谢产物。Monomethyl fumarate 是一种 GPR109A 激动剂。Monomethyl fumarate 是一种 GPR109A 激动剂具有用于多种神经保护途径和其他视网膜疾病模型的潜力。 | |||
TN3323 |
Monomethyl lithospermate
Lithospermic acid monomethyl ester |
Akt; PI3K | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
Monomethyl lithospermate (Lithospermic acid monomethyl ester) 具有潜在的抗病毒活性,通过激活PI5K/Akt信号传导,减轻体内大脑中动脉闭塞小鼠缺血性中风损伤,并在体外保护氧葡萄糖剥夺/复氧诱导的SHSY-3Y细胞。Monomethyl lithospermate 能提高 SHSY-5Y 细胞的生存能力,抑制线粒体膜电位 (MMOP) 崩溃,抑制细胞凋亡。Monomethyl lithospermate 还降低中动脉闭塞 (MCAO) 大鼠脑组织中的氧化应激水平,改善缺血性中风 (IS) 大鼠神经损伤。 | |||
TN4578 |
Monomethyl kolavate
|
Antifection | Microbiology/Virology |
Monomethyl kolavate is a power Trypanosoma brucei glyceraldehyde-3-phosphate dehydrogenase (TbGAPDH) inhibitor, with an IC50 value of 12uM. | |||
TN4393 |
Koaburaside monomethyl ether
|
Others | Others |
Koaburaside monomethyl ether是一种天然产物,属于大戟科巴豆属,其产品编号为 TN4393,CAS号为 41514-64-1。Koaburaside monomethyl ether可用作对照参考。 | |||
TN4169 | Grifolin monomethyl ether | Others | Others |
Grifolin monomethyl ether 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN4169,CAS号为 64432-04-8。 | |||
T20793 |
Magnesium Lithospermate B
丹參酸B鎂,Monomethyl lithospermate B,丹参酸 B 镁,Lithospermate B |
Others | Others |
Magnesium Lithospermate B 是一种咖啡酸四聚体的衍生物,从Salviae miltiorrhizae 中提取得到。它能够抑制神经炎症并减轻神经变性。它被广泛用于心血管疾病的研究,并且可以防止葡萄糖引起的细胞内氧化损伤。 | |||
TN3907 |
Pinosylvin monomethyl ether
(E)-3-Hydroxy-5-methoxystilbene |
Antifection | Microbiology/Virology |
(E)-3-Hydroxy-5-methoxystilbene possesses inhibitory activity against several Gram-positive bacteria, including isolates of methicillin-resistant Staphylococcus aureus (MRSA), Mycobacterium bovis BCG, and avirulent Bacillusanthracis (Sterne strain), among | |||
TN6976 |
(+)-Pinoresinol monomethyl ether 4-O-β-D-glucoside
|
||
(+)-Pinoresinol monomethyl ether 4-O-β-D-glucoside is a natural product. | |||
TN3403 |
Djalonensone
交链孢霉甲基醚,Alternariol monomethyl ether |
Immunology/Inflammation related | Immunology/Inflammation |
Djalonensone (Alternariol monomethyl ether) 具有强大的 DPPH 自由基清除作用。 | |||
TN4579 |
Monomethylsulochrin
|
Antifection | Microbiology/Virology |
Monomethylsulochrin shows antimicrobial activity against Escherichia coli, Pseudomonas aeruginosa, Bacillus subtilis and Staphylococcus aureus. It shows moderately inhibitory effects on the human bacterial pathogen Helicobacter pylori with the MIC value of 28.9+/-0.1 microM. | |||
T4764 |
5-Methoxy-5-oxopentanoic acid
戊二酸单乙酯,mono-Methyl glutarate,METHYL HYDROGEN GLUTARATE |
Others; Endogenous Metabolite | Metabolism; Others |
5-Methoxy-5-oxopentanoic acid (mono-Methyl glutarate) 是内源性代谢产物的一种。 |