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Tranylcypromine hydrochloride is a racemic mixture of (±)-Trans-2-phenylcyclopropyl-1-amine (TCP, tPCPA) · HCl that covalently inhibits the LSD and MAO enzymes. Tranylcypromine (2-PCPA) HCl是一种非选择性的不可逆的单胺氧化酶(MAO)抑制剂，用作抗抑郁药和抗焦虑药。
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SB203580, a selective inhibitor of p38MAPK, controls the various inflammatory responses and cellular stresses. SB203580是一种p38 MAPK抑制剂，IC50为0.3-0.5 μM，与SAPK3(106T)和SAPK4(106T)相比选择性低10倍，且抑制PKB磷酸化，IC50为3-5 μM。
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Entinostat (MS-27-275, MS-275, SNDX-275) an orally class I histone deacetylase (HDAC)-specific inhibitor, is currently in clinical trials.
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GW788388, a potent, selective, and orally active inhibitor of TGFβ signaling, shows potent anti-fibrosis effect. GW788388是一种有效的，选择性的ALK5抑制剂，IC50为18 nM，也抑制其他TGF-βI型和II型受体激酶活性，但不抑制BMP II型受体。
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Ricolinostat (ACY-1215) is an oral, first-in-class, selective inhibitor of HDAC6, and inhibits tubulin deacetylase. Rocilinostat (ACY-1215)是高效HDAC6抑制剂，IC50为5 nM，比对HDAC1/2/3的抑制性高10倍以上，对HDAC8有微弱活性，对HDAC4/5/7/9/11，Sirtuin1和Sirtuin2活性最低。
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