Others

2,7-Dimethylnaphthalene是一种多环芳烃（PAH）衍生物，广泛应用于生物化学实验和药物合成研究。

8-Hydroxyadenosine (8-Oxoadenosine) 是一种存在于 Torula 酵母 RNA 中的嘌呤核苷。

Cis-ACBD (cis-1-aminocyclobutane-1,3-dicarboxylic acid) 是一种有效的选择性 N-甲基-D-天冬氨酸受体激动剂。

Estramustine phosphate can be used to treat prostatic neoplasms; also has radiation protective properties.

L-869298 is a potent and selective inhibitor of PDE4.

ZSET-845 is an enhancer of cognitive which enhances choline acetyltransferase activity in the hippocampus in the rat.

TYK2-IN-12 (compound 30) 是一种选择性的、口服具有活力的 TYK2 (酪氨酸激酶 2) 抑制剂 (Ki: 0.51 nM)。TYK2-IN-12 对 IL-12 诱导的人和小鼠全血中 IFNγ 具有抑制作用，他们的 IC50 值分别为 2.7 和 7.0 μM。TYK2-IN-12 能够用于研究银屑病。

Mal-C6-amine (TFA) is an alkyl chain-based linker employed in the synthesis of PROTACs[1].

Binifibrate is a hyperlipemiant drug used for the treatment of hyperlipidemia.

7-Hydroxy-4-methylcoumarin-3-acetic acid（7-羟基-4-甲基香豆素-3-乙酸）是一种蓝色荧光团，具有pH依赖性和环境敏感性荧光，广泛用于标记肽、核苷酸和碳水化合物，还可用作pH值指示剂。

SAH (Standard) 是一种可用于分析的标准物质，通常用作 SAH 的研究和分析中参考的标准样品。SAH (S-Adenosylhomocysteine) 属于氨基酸衍生物，是腺苷和半胱氨酸合成的中间体。SAH 是一种 METTL3-METTL14 异二聚体复合物的抑制剂 (IC50=0.9 µM)。SAH 是多种代谢途径中的调节剂。

HCVP-IN-1 (compound 1) is a hepatitis C viral polymerase (HCVP) inhibitor.

Adriforant hydrochloride is an antagonist of histamine H4 receptor.

Lobenzarit, an immunomodulator, is most frequently used to treat arthritis. Its chemical scaffold has been repurposed to tryptophan biosynthesis in Mycobacterium tuberculosis

CHD1Li 6.11 是一种致癌 CHD1L 的有效抑制剂，能够作用于 cat-CHD1L 重组蛋白 (IC50: 3.3 μM)。CHD1Li 6.11 是一种口服具有活力的抗肿瘤剂，明显减少由分离的准间充质细胞 (M 表型) 产生的 CRC 异种移植物的肿瘤体积，这些细胞具有增强的致瘤特性。

1,2-Dimethylnaphthalene是一种特定的二甲基萘异构体，其甲基取代基位于萘环系统的 1 位和 2 位。此多环芳烃是多种植物（包括 Phaseolus vulgaris、Nelumbo lutea 和 Magnolia liliiflora）的天然组成成分。

Chymase-IN-1 是一个有效的，有选择性的，口服有活性的人肥大细胞糜蛋白酶抑制剂，IC50 为 29 nM。

Rolusafine 是一种抗真菌剂。

1-Deazaadenosine is a potent Adenosine deaminase inhibitor (Ki: 0.66 μM). It exhibits anti-cancer activities in vitro and has the potential to be a chemotherapy agent for lymphoproliferative disorders.

2-Methylthio-AMP diTEA (2-MeSAMP) is a selective and direct antagonist of the P2Y12 receptor, effectively inhibiting ADP-dependent platelet aggregation[1][2][3].

S-Benzylglutathione为竞争性谷胱甘肽酶抑制剂，能够经大鼠肾微粒体转化为相应的半胱氨酸衍生物。该化合物适用于研究谷胱甘肽酶系统对谷胱甘肽代谢的分解作用。

Stavudine (d4T) sodium 是一种口服活性核苷逆转录酶抑制剂 (NRTI)， 具有抗HIV-1和HIV-2的活性。Stavudine sodium 还抑制线粒体 DNA (mtDNA) 的复制。Stavudine sodium 降低 NLRP3 炎症小体激活并调节淀粉样 β 自噬。Stavudine sodium 诱导细胞凋亡。

锂柠檬酸用于降低卡纳万病患者脑内过量的N-乙酰天冬氨酸含量。

UCM-13207 是一种特异性 ICMT 抑制剂，可改善早衰症。

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.

cis-Indatraline (cis-Lu 19-005) hydrochloride 是一款用于神经退行性疾病研究的活性化合物。

CFI-400437 是一种ATP 竞争性的PLK4抑制剂 (IC50: 0.6 nM)，是一种吲哚醌衍生物。

PF-184 是一种有效的、选择性的 IKK-2抑制剂 (IC50: 37 nM)，选择性优于 rhIKK-1、IKKi， 及 30 多种酪氨酸和丝氨酸/苏氨酸激酶。PF-184 可用于炎症研究，如哮喘和慢性阻塞性肺疾病。

(E/Z)-10-Hydroxy-2-decenoic 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 T124254，CAS号为 765-01-5。

N3-PEG8-CH2COOH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Boc-Aminooxy-PEG3-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

DNA-PK-IN-1 是一种 DNA-PK 的有效抑制剂。DNA 依赖性蛋白激酶 (DNA-PK) 是一种由 Ku70/Ku80 异二聚体和 DNA 依赖性蛋白激酶催化亚基 (DNA-PKcs) 组成的 DNA-PK 酶复合物。DNA-PK-IN-1 具有潜力进行癌症疾病的研究。

Sodium catechol sulfate is a bioactive chemical.

Propylparaben sodium (propyl parahydroxybenzoate) is a naturally occurring antimicrobial preservative found in plants and bacteria. Widely utilized in cosmetics, pharmaceuticals, and foods, this compound impairs antral follicle growth and steroidogenic function by modifying the cell-cycle, apoptosis, and steroidogenesis pathways. Additionally, propylparaben sodium reduces sperm count and motility in rats.

(-)-Rasfonin is a fungal metabolite that has been found in T. terrophilus.1 It inhibits proliferation of mouse splenocytes induced by concanavalin A and LPS (IC50s = 0.7 and 0.5 μg/ml, respectively). References1. Fujimoto, H., Okamoto, Y., Sone, E., et al. Eleven new 2-pyrones from a fungi imperfecti, Trichurus terrophilus, found in a screening study guided by immunomodulatory activity. Chem. Pharm. Bull. (Tokyo) 53(8), 923-929 (2005).