Arylsulfatase是一种催化芳基硫酸酯水解的酶，分为A、B和C酶，能够特异性识别并断裂硫酸酯键，可用于研究相关代谢和疾病。

(±)-γ-Tocopherol是一种内源性代谢物和维生素E的一种形式，具有抗氧化和抗炎特性，能减少LPS和IL-1β诱导的前列腺素(PGE2)的合成。

Apigenin triacetate是一种F. graminearum的代谢物，可用于生物化学实验和药物合成研究。

Drimentine B is a terpenylated diketopiperazine antibiotic originally isolated from Actinomycete bacteria. It is active against Gram-positive and Gram-negative bacteria, fungi, and yeast, and has anthelmintic properties. Drimentine B inhibits proliferation of NS-1 murine β lymphocyte myeloma cells by 41 and 59% in vitro when used at concentrations of 50 and 100 μg/ml, respectively.

Ethylenediaminediacetic acid is derived from two molecules of glycine linked by amines.

Isoprostanes are produced by the non-enzymatic, free radical peroxidation of phospholipid-esterified arachidonic acid. They have been used as biomarkers of oxidative stress, but they also have been found to have potent biological activity. ent-8-iso-15(S)-Prostaglandin F2α (ent-8-iso-15(S)-PGF2α) is a potent vasoconstrictor of porcine retinal and brain microvessels with EC50 values of 15 and 24 nM, respectively. This isoprostane is about ten-fold more potent than 8-iso-PGF2α in a whole blood platelet aggregation inhibition assay.

Estriol 3-β-D-glucuronide is a metabolite of estriol . It is formed from estriol by the UDP-glucuronosyltransferase (UGT) isoform UGT1A10. Estriol 3-β-D-glucuronide binds to basolateral and canalicular liver plasma membranes with Kd values of 85 and 164 μM, respectively. It competitively inhibits the hydrolysis of 4-methylumbelliferyl-β-D-glucuronide and is a substrate for hydrolysis by Klotho-human IgG1 Fc protein (KLFc).

Dapagliflozin-3-O-β-D-glucuronide is a metabolite of dapagliflozin . Dapagliflozin is a first generation selective sodium glucose cotransporter (SGLT) 2 inhibitor that blocks glucose transport.[1] Dapagliflozin is metabolized by uridine diphosphate glucuronosyltransferase (UGT) 1A9 to dapagliflozin-3-O-β-D-glucuronide, which is 2,600-fold less potent than the parent compound with regard to SGLT2 inhibition.[2]

1-Palmitoleoyl-2-hydroxy-sn-glycero-3-PC是一种溶血磷脂。它增加人类胰腺β细胞内cAMP的产生，这一效应可被GPR55拮抗剂CID-16020046（Item No.15247）或GPR119拮抗剂C8阻止。1-Palmitoleoyl-2-hydroxy-sn-glycero-3-PC还在相同的细胞类型中增强葡萄糖刺激的胰岛素分泌，而这种效应可被CID-16020046或C8减弱。