Others

(-)-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).

PARP1-IN-12 是一种有效的PARP1抑制剂，其IC50值为 2.99 nM。PARP1-IN-12 具有较好的抗癌细胞增殖活性，可诱导细胞凋亡并使细胞周期停滞在 G2/M 期。PARP1-IN-12 能在BRCA 缺陷的细胞中诱导 DNA 双链断裂 (DSBs)。

CP-320626 是一种高效性的人肝脏糖原磷酸化酶 (GP) 抑制剂，具有降胆固醇活性，通过直接抑制 CYP51 抑制胆固醇发生，可用于研究 2 型糖尿病。

Lanatoside E is a cyclic triterpene saponin with antitumor activity.

5-Hexen-1-ol是一种不饱和醇类化合物，广泛应用于生物化学实验和药物合成研究。

Bcl-2-IN-9 是新型的、促凋亡的、细胞毒性低的 Bcl-2 抑制剂 (IC50: 2.9 μM)。Bcl-2-IN-9 能够下调 Bcl-2 表达，诱导癌细胞凋亡 (apoptosis)，并对白血病细胞表现出高选择性。

(S)-Tenofovir ((S)-PMPA) 是Tenofovir 的活性较低的S-对映体，Tenofovir 是一种核苷酸逆转录酶抑制剂。

Apoptosisinducer 3 (Compound 3) 是一种能够选择性诱导细胞凋亡(apoptosis)及其后期过程的化合物，对癌细胞表现出特有的毒性。

CSF1R-IN-5 是一种 CSF1R 的有效抑制剂。其中 CSF-1R 表达于巨噬细胞中，巨噬细胞的存活和分化依赖于 CSF-1/CSF-1R 信号通路。CSF1R-IN-5 可以影响 TAM 和胶质瘤细胞之间炎症因子的交换。CSF1R-IN-5 具有潜力进行癌症疾病的研究。

AL-438 is a non-steroidal selective glucocorticoid receptor modulator.

PF-06263276 is an effective and selective inhibitor of pan-JAK. It also has IC50s of 2.2 nM, 23.1 nM, 59.9 nM and 29.7 nM for JAK1, JAK2, JAK3, and TYK2, respectively.

Damulin A 是从 Gynostemma pentaphyllum 中分离出的达玛烷型皂苷，其与结构相关化合物的抗癌结构–活性关系已被深入研究。比较研究表明，C20(21) 与 C20(22) 双键以及 C-2 位羟基修饰显著促进其细胞毒性，在 A549 细胞中表现出显著的增殖抑制作用，突显 Damulin A 在绞股蓝来源抗癌先导化合物中的重要地位。

TH588 hydrochlorid 是创新的 nudix 水解酶家族抑制剂，可选择性的高效结合并抑制MTH1 (NUDT1)，IC50值为 5 nM。

Azido-PEG11-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.

Esomeprazole hemistrontium, also known as (S)-Omeprazole, is a potent and orally active proton pump inhibitor that effectively reduces acid secretion by inhibiting the H+, K+-ATPase in gastric parietal cells. This compound exhibits promising potential for research in symptomatic gastroesophageal reflux disease [1] [2] [3].

Cap-dependent endonuclease-IN-8 是 cap-dependent 核酸内切酶 (CEN) 的有效抑制剂。Cap-dependent endonuclease-IN-8 能够抑制正粘病毒 (包括甲型流感、乙型流感和丙型流感) 的复制。

Atorvastatin acetonide is an impurity of Atorvastatin. Atorvastatin is an HMG-CoA reductase inhibitor and has the ability to effectively decrease blood lipids.

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.

Nucleosides - 3'-O-Methyl nucleoside

Anticancer agent 34 (compound 9) 是一种磺酰脲类衍生物，也是一种有效的抗微生物剂和抗癌剂。Anticancer agent 34 对蕈状芽孢杆菌、大肠杆菌和白色念珠菌的微生物生长表现出抑制作用 (MIC: 0.039-0.156 mg/ml)。Anticancer agent 34 能够抑制 A549 细胞 (IC50: 8.4 μg/ml)、PC3 细胞 (IC50: 7.8 μg/ml) 的生长。

Ald-Ph-PEG24-TFP ester 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.

TX-1123是一种针对Src、eEF2-K、PKA和EGFR-K/PKC的有效蛋白酪氨酸激酶(PTK)抑制剂，同时也是一种环氧合酶(COX)抑制剂，对COX2和COX1的IC50值分别为1.16μM和15.7μM。它具有低线粒体毒性，可用于癌症研究。

mGlu1 receptor antagonist

VA5 is an transamidase inhibitor by direct binding at the transamidase site. VA5 also inhibits GTP-binding activities. It interaction at the transamidase site locks the protein in the extended/open conformation to disorganize/inactivate the GTP binding/GT

Amino-PEG6-amido-C16-COOH, a PEG-based PROTAC linker, facilitates the synthesis of PROTACs[1].

Vibsanin A，作为一种蛋白激酶C (PKC) 激活剂，展现出对人类癌细胞系的抗增殖活性，同时也兼具HSP90抑制剂的功能。

Lipid 14 是一种可电离的氨基脂质，可用于合成脂质纳米粒 (LNPs)。

2’-O-Hexadecanyl guanosine 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 TNU1655，CAS号为 2382942-29-0。

Hydroxy-PEG1-C2-methyl ester is a polyethylene glycol (PEG) derived linker widely employed for the production of PROTACs - proteolysis targeting chimeras. [1]

Flupentixol is a typical antipsychotic drug of the thioxanthene class. Flupentixol is also used in low doses as an antidepressant.

Bis-Biotin-PEG23 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.

Dodecyl gallate 是一种抗氧化剂，普遍用作食品制造及制药和化妆品行业中。它还对动物病毒，如非洲猪瘟病毒 (ASFV)具有作用活性。

Topoisomerase IIα-IN-3 是 DNA 插入型 topoisomerase-Iiα 抑制剂，能够将细胞周期阻滞在 G0/G1 期，并诱导细胞凋亡 (apoptosis)。

Magnesium Sulfate Heptahydrate是一种可用于细胞培养的生化试剂，能够加入培养基中支持微生物的生长。

HS-PEG7-CH2CH2N3 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.

RET-IN-24（Compound 26）为选择性RET酪氨酸激酶抑制剂，具抗肿瘤活性。