mof

MG 149 (Tip60 HAT inhibitor) 是一种Tip60抑制剂，IC50为 74 μM。它对 MOF 的抑制性较相似，IC50为 47 μM。

Mofarotene (Ro-40-8757) 是一种小分子化合物，在许多癌细胞系中显示出相当大的抗肿瘤活性，可用于治疗肿瘤和呼吸系统疾病。Mofarotene 是一种维甲酸类似物，可结合并激活维甲酸受体(RARs)，从而改变某些基因的表达，导致易感细胞的细胞分化和细胞增殖降低。

Mycophenolate Mofetil (TM-MMF) 是 Mycophenolic acid 的吗啉乙酯前药。它通过抑制肌苷一磷酸脱氢酶抑制从头嘌呤合成，显示出选择性淋巴细胞抗增殖作用。

Carmofur (HCFU) 是 5-氟尿嘧啶的衍生物，是一种抗肿瘤药物。它是一种酸性神经酰胺酶抑制剂，用于治疗乳腺癌和结直肠癌。它抑制 SARS-CoV-2主要蛋白酶，还抑制 Vero E6 细胞 SARS-CoV-2，EC50为 24.3 μM。

Mofegiline hydrochloride is a potent and selective enzyme-activated irreversible MAO-B inhibitor.

Homoferreirin 是一种天然化合物，可作为天然产物对照品。

Timofibrate，一种由Italchemi S.p.A.-Istituto Chimico Farmaceutico专利的噻唑烷衍生物，具有抗动脉粥样硬化、降低胆固醇和保肝作用。

Bromofos is a effective pesticide.

Mycophenolate Mofetil is a non-competitive, selective, and reversible inhibitor of inosine monophosphate dehydrogenase I II (IC50: 39 nM and 27 nM, respectively).

Moflomycin is an anthracycline derivative. It exhibits a higher antileukemic activity compared to other anthracyclines.

11-Deazahomofolic acid is a phosphoribosylglycinamide formyltransferase inhibitor.

11-Oxahomofolic acid is a potential antitumor drug.

5,6,7,8-Tetrahydro-8-deazahomofolic acid is a potential thymidylate synthase (TS) inhibitor and other folate related enzymes inhibitor.

8-Deazahomofolic acid is a potential thymidylate synthase (TS) inhibitor and other folate related enzymes inhibitor.

Dihydrohomofolic acid is a substrate for dihydrofolate reductase that produces tetrahydro-homo folate which in turn suppresses thymidylate synthetase and then DNA synthesis.

Emofolin sodium is the sodium salt of a synthetic antimetabolite analogue of folate with antineoplastic activity，which competes for the folate binding site of the enzyme dihydrofolate reductase, resulting in inhibition of tetrahydrofolate synthesis, deple

Tetrahydrohomofolic acid is a thymidylate synthetase inhibitor, antibacterial, and antimalarial agent.

Homofolic acid is a folic acid analog.

4′-Bromoflavone is a highly effective inducer of phase II detoxification enzymes and has been identified as a potent agent in cancer chemoprevention.

Mofezolac 是一种非甾体类抗炎药，可缓解疼痛并具有抗炎活性，抑制 COX-1和COX-2的IC50为 1.44 和 447 nM。

Eremofortin A 是一种代谢产物，可以从罗氏青霉的培养物中分离出来。

Mofebutazone 抑制前列腺素和白三烯的免疫释放。

Mofebutazone sodium is, a nonsteroidal antiinflammatory drug (NSAID), is used to treat joint and muscular pain.

Eremofortin B是倍半萜类化合物，由Penicillium roqueforti PR毒素（PRT）合成。