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N-563 promotes resistance to Candida albicans infection in mice

L-690330 is a competitive inositol monophosphatase inhibitor (Kis: 0.27 and 0.19 μM for recombinant human and bovine IMPase, 0.30 and 0.42 μM for human and bovine frontal cortex IMPase). L-690330 shows 10-fold more sensitive than a mouse and rat IMPase.

Xenalamine is a synthetic compound of antiviral.

N-(m-PEG4)-N'-(PEG4-acid)-Cy5 is a polyethylene glycol (PEG)-based PROTAC linker employed for PROTACs[1] synthesis.

PIN1degrader-1 (Compound 158H9) 是一种脯氨酸顺反异构酶 (Pin1) 抑制剂，具有IC50值21.5 nM。PIN1degrader-1 通过与Pin1的Cys113形成共价键，引起构象变化，降低Pin1稳定性，并导致蛋白酶体依赖的降解。此化合物能抑制多种癌细胞的活力，可应用于癌症研究。

Levobetaxolol, also known as AL-1577A and Betaxon, is a cardioselective β-adrenergic receptor inhibitor. It has been demonstrated to reduce intraocular pressure in patients affected by ocular hypertension and primary open-angle glaucoma.

SMPB crosslinker is a heterobifunctional protein crosslinking reagent that is reactive toward sulfhydryl and amino groups. The SMPB protein crosslinker is an extended chain length analog of MBS crosslinker. SMPB crosslinker's spacer arm is non-cleavable.

Dibenzylideneacetone is a synthetic curcumin analog. It leads to apoptotic cell death in Leishmania donovani.

Propaquizafop, a phenoxyisopropionic acid derivative, is used as a herbicide.

Rezuforimod 是 N-formyl peptide receptor like-1 receptor (FPRL-1) 的激动剂，在 CHO-Ga16 细胞中具有 EC50 为 0.88 nM 的活性。Rezuforimod 展现出抗炎特性。

FXIa-IN-16 (Compound 43) 是一种口服活性和选择性FXIa抑制剂，其IC50为0.19 nM。FXIa-IN-16 在抗凝和抗血栓方面表现出强效，并在小鼠实验中显示出良好的安全性，适用于血栓形成相关研究。

PL 100 could inhibit HIV-1 protease.

APOL1-IN-3 是一种用于研究肾脏疾病的APOL1抑制剂。

Lomerizine, a blocker of diphenylmethylpiperazine Ca2+ channel, is used to prevent migraines.

Cyproterone, an anti-androgen, is used in combination with estrogen for the therapy of hirsutism and severe acne in females and as a palliative in prostatic carcinoma.

non-selective NOS inhibitor

Agonist for group III mGlu receptors

S-Isopropylisothiourea hydrobromide is an iNOS inhibitor.

mGlu4 receptor agonist

L-670,596 is a thromboxane A2/prostaglandin endoperoxide receptor antagonist.

estrogen receptor (ER) β agonist

Coproporphyrin III is a derivative of porphyrin.

Fmoc-N-Me-Ile-OH is a compound utilized in peptide synthesis.

L-hydroxylysine dihydrochloride , is formed by posttranslational hydroxylation of some lysine residues. It is an amino acid, is exclusive to collagen protein.

Ac-Lys-AMC (Hexanamide) is a fluorescent substrate for histone deacetylase HDACs.

PD168,077 is an agonist of dopamine D4 receptor. It has a facilitatory effect on memory consolidation.

Cgp 29287 is a primate-specific renin inhibitor. It also has a prolonged duration of action.

ETNK-IN-2 (Compound 8) 是乙醇胺激酶 (ETNK) 的抑制剂，其IC50值为 ≥ 5 μM，适用于杀虫剂开发方面的研究。

DGKζ-IN-9 (compound 73) 是一种针对DGKζ的抑制剂，其IC50值为 ≤200 nM。

API32 是一种高效的 Pin1 抑制剂，与 Pin1 PPIase 结构域相互作用，能抑制细胞的增殖与迁移，显示出在肝细胞癌 (HCC) 研究中的潜在价值。

Tetraniliprole 是用于研究烟草切虫（TCW）的一种杀虫剂。

Aspirin DL-lysine is a non-steroidal anti-inflammatory drug. It also may inhibit cancer growth. Aspirin DL-lysine is a water-soluble, injectable aspirin derivative.

DGKα-IN-9 (example 298) 属于DGKα抑制剂。

Insecticidal agent 23 (compound 17) 具备抗血吸虫效果并且毒性低。该化合物对日本血吸虫成虫的体外活性强，其LC50 (72 h) 为 25.31 μM。

(-)-trans-Permethrin ((-)-trans-NRDC-143) 是一种拟除虫菊酯，为牛提供良好的防黑蝇效果。

Thiuram disulfide 是一种用于杀虫的化合物，可以在 435 nm 处用光度法测量其吸光度。