trans-5-Hydroxyferulic acid 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T126397，CAS号为 110642-42-7。

Nebicapone is a reversible catechol-O-methyltransferase (COMT) inhibitor and is mainly metabolized by glucuronidation. Nebicapone is mainly peripherally acting inhibitor that decreases the biotransformation of L-DOPA to 3-O-methyl-DOPA by inhibition of CO

Ro 41-0960 is used as a reversible and orally-active COMT-inhibitor.

YM-53601 free base is an inhibitor of squalene synthetase which suppresses lipogenic biosynthesis and lipid secretion in rodents.

Uridine diphosphate glucuronic acid (UDP-GlcA) trisodium 是一种在 UDP-葡萄糖脱氢酶催化过程中形成的辅助因子。它含有 Azide 基团，能够与含有 Alkyne 基团的分子进行铜催化的叠氮-炔环加成反应（CuAAc）。此外，它也可以与具有 DBCO 或 BCN 基团的分子进行环张力促进的炔-叠氮环加成反应 (SPAAC)。

PF-07202954是一种具有较长半衰期的DGAT2抑制剂，对人DGAT2和大鼠DGAT2的IC50分别为10 nM和9.1-33 nM，能够降低西方饮食喂养的大鼠肝脏甘油三酯的含量，可用于研究非酒精性脂肪性肝炎（NASH）。

FTI-2153 is a potent and highly selective farnesyltransferase (FTase) inhibitor (IC50: 1.4 nM). FTI-2153 is >3000-fold more potent at blocking H-Ras (IC50, 10 nM) than Rap1A processing.

Genz-123346 blocks the conversion of ceramide to glucosylceramide (GL1) and inhibits GM1 with an IC50 value of 14 nM. Genz-123346 is a potent, orally available glucosylceramide synthase inhibitor.

(+)-D-threo-PDMP is a ceramide analog and is one of the four possible stereoisomers of PDMP . (+)-D-threo-PDMP is an inhibitor of glucosylceramide synthase. It inhibits glucosylceramide synthase by 50% when used at a concentration of 5 μM in an enzyme assay. (+)-D-threo-PDMP is the active component of racemic DL-threo-PDMP .