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Ropitoin is a novel drug of antiarrhythmics.

AR-A 2 is a selective 5-HT1B receptor antagonist, with a high affinity to guinea pig cortex 5HT1B/1D and recombinant guinea pig 5-HT1B receptors (Ki: 0.24 and 0.47 nM) and with 10-fold lower affinity to guinea pig 5-HT1D receptor (Ki: 5 nM).

SCH 51344 抑制Ras 诱导的恶性转化。SCH 51344可防止癌基因转化的成纤维细胞的非锚定生长。

Tuberculosis inhibitor 8 (compound 3b) 是 3-甲氧基-2-苯基咪唑并[1,2-b]哒嗪衍生物，具有针对结核分枝杆菌 (MIC90为 0.69 μM) 和海洋分枝杆菌 (MIC90为 0.69 μM) 的高抗菌活性。

Azido-PEG6-C1-Boc 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.

ATX inhibitor 19 是 ATX 的有效抑制剂 (IC50: 156 nM)。

DBCO-PEG6-amine 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.

Benzyl-PEG4-MS 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 T67180，CAS号为 477781-69-4。

Bendazac (Bendazolic acid) 是一种氧乙酸，具有抗过敏、抗炎、利胆和抗血脂作用。它能够阻断蛋白质变性，延缓白内障的发生过程。

MrgprX2 antagonist-4 and compound B-51 E117, is a potent MrgprX2 antagonist. It specifically targets and inhibits the MrgprX2 receptor, making it suitable for investigating various inflammatory skin disorders.

Clofibrin is a kind of hypolipidemic drug, which can reduce Hypertriglyceride and hypercholesterolemia.

FR 901465 is a biochemical.

IGF-1R inhibitor-2 (example 121) is a compound that inhibits the insulin-like growth factor-1 receptor (IGF-1R). By downregulating the IGF-1R, it has the potential to reverse the transformed phenotype of tumor cells and make them more susceptible to apoptosis.

GNF5-amido-Me, the moiety based on GNF5 (ABL inhibitor),binds through a linker to the IAP ligand forming SNIPER[1].

Salvinolone 是一种天然化合物，可作为天然产物对照品。

USP7-IN-10 hydrochloride (compound 1)是一种高效USP7抑制剂，具有13.39 nM的IC50值。

17-phenyl trinor Prostaglandin F2α cyclopropyl amide (17-phenyl trinor PGF2α cyclopropyl amide) is a novel analog of 17-phenyl trinor PGF2α ethyl amide. There are no published reports on the biological activity of 17-phenyl trinor PGF2α cyclopropyl amide.

Isodihydroauroglaucin 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 T124274，CAS号为 74886-31-0。

Sodium Picosulfate (Laxoberal) 可以抑制水和电解质的吸收，促进它们的分泌。

Terbufibrol 降低正常和高胆固醇血症雄性大鼠的血清总胆固醇水平。

β-Cateninmodulator-5 (compound IIa-84) 为一种融合恶唑与噻唑结构的化合物，兼具高效与选择性的β-Catenin调控活性。

GABAA receptor agent 6 (compound 2027) 是一种有效的γ-GABAAR 拮抗剂，具有低细胞膜通透性 (Ki = 0.56 μM)。

N6-Etheno 2'-deoxyadenosine is used as a biomarker to evaluate chronic inflammation and lipid peroxidation in animal or human tissues.

1,2,3,4-Tetramethylbenzene是一种苯衍生物，广泛应用于生物化学实验和药物合成研究。

TDRL-X80 是一种色素性干皮症蛋白 (XPA) 的有效抑制剂。TDRL-X80 能够抑制 XPA 的 DNA 结合活性。TDRL-X80 能够作用于单、双和顺铂损伤的 DNA，在荧光偏振 (FP) 分析中的 IC50 值为 18、20 和 29 μM，而 ELISA 分析中的 IC50为 21、39 和 28。

KVI-020 是一种选择性的、口服具有活力的心房钾通道 Kv1.5 阻滞剂 (IC50: 480 nM)。KVI-020 对 hERG 表现出抑制作用 (IC50: 15100 nM)。 KVI-020 是一种有效的抗心律失常剂 (antiarrhythmic)，能够用于研究房颤 (AF)。

1-Deacetylnimbolinin B is a natural product from Melia toosendan Sieb. et Zucc.

TP-050 是一种口服有效的选择性 NMDAR 激动剂，抑制 GluN2A 和 GluN2D 的 EC50值分别为 0.51 μM 和 9.6 µM。TP-050 可穿过血脑屏障 (BBB)。TP-050 诱导海马区的长期增益效应 (LTP)，增强神经元信号传输。

hDDAH-1-IN-2 is an orally active human dimethylarginine dimethylaminohydrolase-1 (hDDAH-1) inhibitor.

Cimifugin 4'-O-beta-D-glucopyranoside is a natural product

(R)-Necrocide 1（化合物(R)-38）是一种具有抗增殖活性的有效抗癌剂。

2',4',6'-trihydroxy-3'-(3-methyl-2-butenyl)acetophenone是一种天然的苯乙酮衍生物，可用于生物化学实验和药物合成研究。

Pseudoneolinderane是一种发现于Neolitsea aciculata Koidz的倍半萜烯，可用于生物化学实验和药物合成研究。

Orexin 2 Receptor Agonist 2 (ORA-2) is a specific agonist for the orexin 2 receptor.

S-acetyl-PEG4-NHBoc 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.

Light Green SF Yellowish (Acid Green 5) 是一种碱性染色剂，可用于动物组织染色，可用于植物组织学中作细胞质和纤维染色。