m 2

S-methyl-KE-298 是 KE-298 的活性代谢物。KE-298 抑制类风湿关节炎滑膜细胞产生基质金属蛋白酶。

M2 ion channel blocker ,Antiviral agent, is capable of inhibiting and blocking the activity of M2 ion channel.

Aflatoxin M2 is a major metabolite of Aflatoxin B1 and is a mycotoxin produced by the fungi Aspergillus flavus and Aspergillus parasiticus.

Dacomitinib metabolite M2 is also known as Dacomitinib cysteine conjugate. Dacomitinib inhibits both the wild-type (WT) EGFR and EGFR T790M.

Gomisin M2 is an anti-HIV agent.

Antibiotic MA 144M2 is an anthracycline glycoside that inhibits the growth of gram-positive bacteria, e.g. Staphyococcus aureaus, Bacillus subtilis and Sarcina lutea, and inhibits the growth of animal tumors such as leukemia L 1210, P 388 and sarcoma 180. It's produced by fermentation of MA 144-producing strains of streptomyces and by the chemical or enzymatic conversion of aclacinomycin A or cinerubin A.

Vinclozolin M2, an active metabolite of vinclozolin, is generated through successive esterase activity and decarboxylation in C. elegans, as well as decarboxylation in human liver microsomes. It functions as an antagonist to the mineralocorticoid (IC50= 1,400 nM) and androgen receptors (IC50= 0.17 nM), demonstrated in reporter assays with MCF-7 cells. This compound is exclusively sold for research and analytical purposes, tailored for controlled laboratory use, and is not available in bulk sizes.

化合物 42 (M1/M2/M4 muscarinic agonist 1) 作为一种muscarinic M4/M1/M2激动剂，表现出对M4/M1/M2的EC50值分别为6.5, 26, 以及210 nM。该化合物主要用于精神疾病如精神分裂症、妄想症的研究。

3 (compound 45) 是一种M1/M2/M4 muscarinic agonist，其对mAChRM1/M2/M4 的EC50s 分别为 3.2 nM、32 nM 和 1.7 nM。

MMT3-72-M2, an MMT3-72 metabolite, is a selective JAK1 inhibitor that inhibits JAK1, JAK2, TYK2, and JAK3 with IC50 values of 10.8 nM, 26.3 nM, 91.6 nM, and 328.7 nM, respectively [1].

U-[13C17]-Aflatoxin M2 in Acetonitrile (Standard)(U-[13C17]-黄曲霉毒素 M2 溶于乙腈 (标准品))是全13C同位素标记的黄曲霉毒素M2溶液，可用作分析标准品，测定样品中的黄曲霉毒素M2。

Neoenactin M2 展现出卓越的抗酵母和抗丝状真菌性能。

SCH 57790 是一种新型且具有选择性的毒蕈碱 M（2） 受体拮抗剂，可释放乙酰胆碱并增强实验动物的认知能力，可用于治疗阿尔茨海默病。

Amantadine hydrochloride (CI-719) 是一种抗病毒药物，用于预防或对症治疗甲型流感和帕金森病。它阻断质子流通过 M2 离子通道，从而阻止病毒 RNA 释放到感染细胞的细胞质中。

Amantadine (1-Aminoadamantane) 是抗病毒药物，也是是 NMDA 型谷氨酸受体的弱拮抗剂，能促进高多巴胺的释放，并阻断多巴胺的再摄取。

M2N12 是一种高度选择性的细胞分裂周期蛋白磷酸酶 25C 抑制剂，IC50值为 0.09 μM。它还抑制 Cdc25A 和 Cdc25B 的活性，IC50值分别为 0.53 μM 和 1.39 μM。它具有抗肿瘤活性，可研究癌症。

KGP94 是一种有效的、选择性的和竞争性的溶酶体内肽酶抑制剂。

Regorafénib N-oxyde M2 是 Regorafenib 的活性代谢物。Regorafenib 是多靶点抑制剂，包括VEGFR1/2/3，PDGFRβ，Kit，RET 和 Raf-1 ， IC50分别是 13/4.2/46，22，7，1.5 和 2.5 nM。

m-(2-Phenoxyethoxy)phenol is a biaoctive chemical.

Phenol, m-(2-(methylamino)ethyl)-, hydrochloride is a biaoctive chemical.

Pimethixene (Calmixen) 是抗组胺和抗血清素剂，用作抗偏头疼剂。它是高效多靶点拮抗剂。

Pimethixene maleate (Pimetixene maleate) 是一种高效的 5-HT2B 受体拮抗剂，具有镇静和镇咳活性。Pimethixene maleate 抑制 5-HT1A，5-HT2A，5-HT2B，5-HT2C，组胺 H1，多巴胺 D2 和 D4.4 以及毒蕈碱 M1 和 M2，可用于研究儿童干咳和刺激性咳嗽。

Otenzepad (AF-DX 116) 是 M2 mAChR 的特异性拮抗剂，对大鼠心脏和兔外周肺的 IC50 分别为 386 nM 和 640 nM。

M2e, human, a vaccine candidate for human influenza A, encompasses the 23 extracellular residues of M2 (the third integral membrane protein of influenza A) and exhibits remarkable conservation across all strains, highlighting its potential as a broadly protective option.