Others

Lincophenicol is an Escherichia coli ribosomal peptidyltransferase-catalyzed puromycin reaction inhibitor.

D-Cystine, the D-enantiomer of L-Cystine, functions as an inhibitor of L-aspartate-β-semialdehyde dehydrogenase (ASADH) derived from Escherichia coli.

Tetrachloroveratrole, a byproduct of bacterial O-methylation, arises from the biodegradation of Tri- and Tetra chloroguaiacols. These chloroguaiacols emerge as a result of the wood pulp bleaching process within the paper manufacturing industry.

(±)13-HpODE 在生命科学相关研究中具有广泛的应用。

Simufilam (PTI-125) (hydrochloride) 是一种具有口服活性的细丝蛋白 A (FLNA) 激活剂，具有低毒性，可用于阿尔茨海默病研究。Simufilam (hydrochloride) 优先结合改变的细丝蛋白 A 并恢复其天然构象，恢复受体和突触活性，并减少其与 a7nAChR/TLR4 的关联和下游病理作用。

PPZ2 is a novel DAG-activated TRPC3/TRPC6/TRPC7 channels activator.

SNAP-7941 is a selective antagonist of the melanin concentrating hormone receptor MCH1 with promising anxiolytic, antidepressant and anorectic effects in initial animal studies.

RO 23-6152, a new calcium antagonist, can inhibit platelet aggregation in vitro associated with occlusive coronary thrombus formation.

RO-09-4609 is a potent and selective inhibitor of Candida albicans N-myristoyltransferase (CaNmt).

Ro 63-0563 is a potent, 5-HT6 receptors selective antagonist.

S-312d is a calcium channel antagonist. S-312-d can offer marked neuronal protective effects against ischemic injury.

ONO-AE-248 is a selective agonist of EP3 receptor.

Pamiparib is a highly potent and selective PARP inhibitor. BGB-290 selectively binds to PARP and prevents PARP-mediated repair of single-strand DNA breaks via the base-excision repair (BER) pathway. This enhances the accumulation of DNA strand breaks, pro

Org-33628, a progesterone receptor antagonist, is used potentially for female contraception.

Sch 39304 is an oral triazole antifungal.

Sodelglitazar, a PPAR agonist, is used potentially for the treatment of hyperlipidemia and type 2 diabetes.

SKF-97574 is proton pump inhibitor.

Sonepiprazole mesylate is a selective D4 antagonist

Seprilose, prostaglandin E2 inhibitor, inhibits prostaglandin E2 synthesis.

SCH-50910 is an antagonist of GABAB receptor.

SB-423562 is a calcium-sensing receptor antagonist.

T-226296 is a antagonist of melanin concentrating hormone receptor 1 (MCHR1).

Ro 23-7014, a new thiazepinone Ca2+ channel antagonist, has high affinity for peripheral (Type A) receptors.

RDEA-806, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.

Setafrastat is a vascular endothelial growth factor (VEGF) promotor and rotamase inhibitor.

Sezolamide hydrochloride is a potent topical carbonic anhydrase inhibitor.

RG 14467 is an antagonist of epidermal growth factor-urogastrone.

PNU-107484A is a unique GABA(A) receptor ligand.

Proxodolol, a β-adrenergic receptor antagonist, is used potentially for the treatment of glaucoma, hypertension and angina.

Profadol hydrochloride acts as a mixed agonist-antagonist of the μ-opioid receptor with analgesic activity.

Phocaecholic acid是一种在鸭（A. platyrhynchos）胆汁中发现的胆汁酸。

(-)-Lyoniresinol has antioxidant activity.

Schisanhenol B is a natural product from Schisandra chinensis (Turcz.) Baill.

8-Prenyldaidzein has cytotoxic properties against P-388 cells, its IC 50 values 5.82 ug/mL, it also exhibits very high antioxidant activity against DPPH radical scavenging.

5'-O-(4,4'-Dimethoxytrityl)-2'-O-(2-methoxyethyl)-5-methyluridine is a Nucleoside Derivative - 2'-Modified nucleoside; Protected nucleoside with NH2/OH open; Ready for further phosphorylation.

VP-U-6 is a Nucleoside Phosphoramidite; Nucleoside Derivative - Phosphorus-containing nucleotide; 5'-Modified nucleoside.