Others

CYT296是一种靶向染色质去凝集的化合物，能增强定义因子(OSKM)介导诱导多能干细胞(iPSC)的生成，并通过诱导小鼠胚胎成纤维细胞(MEFs)染色质的开放状态来促进体细胞的重编程，适用于细胞替代治疗和药物筛选的研究领域。

Muvalaplin tetrahydrochloride (LY3473329) 是一种口服活性脂蛋白 (a)Lp (a) 试剂，当前正处于研发阶段。

Indoramin (hydrochloride) is a novel antihypertensive agent that exhibits selectivity for the α1A-adrenergic receptor.

Chloracetophos is a Agricultural Chemical.

VCPIP1-IN-1 是一种 VCPIP1 抑制剂，可用于研究癌症。

Pelcitoclax (APG-1252) is a powerful inhibitor of the Bcl-2 and Bcl-xl proteins, displaying significant antineoplastic and pro-apoptotic properties[1].

W-15 is a biochemical.

BoNT-IN-1(compound 8)是一种高效的A型肉毒杆菌神经毒素轻链(Clostridium botulinum neurotoxin serotype A light chain, BoNT/A LC)抑制剂, IC50=0.9 uM。BoNT/A LC是锌依赖性的金属蛋白酶, BoNT-IN-1通过Zn2+螯合基序起到抑制作用。

Intermediate of Pregabalin 是Pregabalin 中间体。

SCD1/5-IN-1 (Compound 10) 作为一种SCD1/5抑制剂，适用于神经系统疾病的研究。

WRN inhibitor 4 (example 107)，环状乙烯基砜类化合物，作为Werner综合症ATP依赖性解旋酶（WRN）的抑制剂，适用于癌症研究领域。

AKR1B10-IN-1, a powerful AKR1B10 (Aldo-Keto Reductase 1B10) inhibitor, demonstrates an IC50 value of 3.5 nM. This compound effectively curtails the proliferation, metastasis, and Cisplatin (CDDP) resistance of lung cancer cells.

CDK12-IN-6, a pyrazolotriazine compound, is a powerful inhibitor of CDK12. Its inhibitory activity is significant with an IC50 value of 1.19 μM when tested at high ATP concentration (2 mM). Notably, CDK12-IN-6 does not exhibit any inhibitory effect on CDK2/Cyclin E (IC50 >20 μM) and CDK9/Cyclin T1 (IC50 >20 μM) when tested under the same high ATP conditions (2 mM) (WO2021116178A1).

Compound 1, known as Caffeine Orange, serves as a highly selective aqueous-phase fluorescence turn-on sensor specifically for caffeine. When exposed to 532 nm green excitation light, this compound causes caffeinated coffee to turn orange. Caffeine Orange boasts impressive photophysical properties, including a high extinction coefficient, excellent light stability, and a narrow emission bandwidth, making it valuable in the development of caffeine detection devices [1].

BRP-7 is an inhibitor of 5-LO activating protein.

LEK 8829 is a dopamine D2 receptor antagonist and D1 receptor agonist.

JWH-022 is a cannabimimetic indole that is structurally related to JWH 018, a mildly selective agonist.

mGlu1 receptor antagonist

RCB-02-4-8，一种可电离的阳离子脂质，主要用于构建脂质纳米颗粒(LNPs)以传递mRNA，能有效提升小鼠肺部的转染效率。

PTK7/β-catenin-IN-1 (compound 01065)为一种高效的PTK7/β-catenin抑制剂，其对PTK7/β-catenin的IC50值为8.9 μM，对p53/MDM2的IC50值为56.5 μM，显示出在癌症研究中的应用潜力。

Iedaborbactam, as a beta-lactamase inhibitor (WO2015191907, Example 62), can be used for the research of bacterial infections.

Talogreptide mesaroxetan 是具有抗肿瘤功能的诊断成像剂.

MOTS-c为源于线粒体的多肽（MDP），它通过激活AMPK途径并抑制MAP激酶-c-fos信号通路，具有抗损伤和抗炎效应。

Dioleoyl phosphatidylserine是一种正在研究的脂质，主要应用于研究固体支持脂质双层的组装及其在天然和合成脂质混合物中的长期稳定性。

HPI-1 (hydrate) is a Hedgehog (Hh) pathway inhibitor that suppresses signaling through Sonic Hh (IC50= 1.5 μM) without significantly affecting Wnt signaling (IC50≥ 30 μM).1HPI-1 suppresses Hh activation induced by loss of Suppressor of Fused or by Gli overexpression, suggesting action at posttranslational modification of Gli protein or at the interaction of Gli with a co-factor.1HPI-1 (hydrate) also inhibits signaling through the oncogenic Smoothened (Smo) mutant SmoM2 in neuron precursors, preventing cell proliferation.1 1.Hyman, J.M., Firestone, A.J., Heine, V.M., et al.Small-molecule inhibitors reveal multiple strategies for Hedgehog pathway blockadeProceedings of the National Academy of Sciences of the United States of America106(33)14132-14137(2009)

Pimelic Diphenylamide 106 analog is an Pimelic Diphenylamide 106 analog .

PtdIns-(3,4,5)-P3 (PIP3) serves as an anchor for the binding of signal transduction proteins bearing pleckstrin homology (PH) domains such as phosphatidylinositol 3-kinase (PI3K) or PTEN. Protein binding to PIP3 is important for cytoskeletal rearrangement and membrane trafficking and initiates an intricate signaling cascade that has been implicated in cancer. 3,5-dimethyl PIT-1 is a dimethyl analog of PIT-1, the selective inhibitor of PIP3/Akt PH domain binding, that is designed for more favorable solubility in vivo. 3,5-dimethyl PIT-1 inhibits PI3K/Akt signaling (IC50 = 27 μM), suppressing PI3K-PDK1-Akt-dependent phosphorylation, which has been shown to reduce cell viability and induce apoptosis in PTEN-deficient U87MG glioblastoma cells (IC50 = 36 μM). 4T1 breast cancer growth is significantly attenuated in BALB/c mice with a dose of 1 mg/kg of 3,5-dimethyl PIT-1 per day.

Phenol-13C6是一种 13C 标记的Phenol (TRF-00198)。Phenol是一种重要的化化工原材料，可用用于制造杀菌剂和除草剂。

CGS8216 是一种苯二氮卓受体拮抗剂，在高剂量时显示出镇痛活性。CGS8216 具有抗焦虑活性，可用于研究免疫系统疾。

PDE4-IN-14 (化合物1)是PDE4抑制剂，适用于研究与PDE4关联的疾病（例如炎症性和免疫性疾病、癌症及代谢性疾病等）。

DGKζ-IN-4是一种inhibitor，可作为药物配方中的active ingredient。该化合物适用于治疗与immune cell activation相关联的cancer types或对抗PD-1 antibody/PD-L1 antibody治疗产生resistance的cancer。

WAY-607695 是一种潜在的 5-HT1A 受体激动剂。

EcGUS-IN-1 (Compound E-9) 作为一种非竞争性β-glucuronidase抑制剂，具有IC50 2.68 μM和Ki值1.64 μM。它通过抑制大肠杆菌的β-glucuronidase活性，有助于缓解大肠杆菌感染导致的胃肠道不良事件 (GIAE)。

ASIC blocker (IC50 values are 0.44, 2.1 μM and no effect at rat ASIC1a, ASIC3 and ASIC2a, respectively: IC50 value = 0.12 μM at human ASIC1a with no effect at ASIC2a or ASIC3). Inhibition was also observed at heteromeric ASIC channels (IC50 values are 0.79, 0.87 and 4.5 uM at rat ASIC1a+3, ASIC1a+2a and ASIC2a+3; IC5O values are 0.33 and 0.69 uM at human ASIC1a+2a and ASIC1a+3, with no effect at ASIC2a+3). Attenuates pathophysiological nociceptive behaviors in CFA-inflamed and CCI rats.

Fasnall, a fatty acid synthase (FASN) inhibitor, exhibits an IC50 of 3.71 μM against the human recombinant enzyme. It halts tritiated acetate incorporation into lipids (IC50= 5.84 μM), boosts ceramide levels, and triggers lipid droplet formation in BT474 HER2+ breast cancer cells. Demonstrating antiproliferative effects on various breast cancer cell lines, including non-tumorigenic MCF-10A and tumorigenic MCF-7, MDA-MB-468, BT474, and SK-BR-3, its efficacy is directly linked to FASN expression in vitro. In murine models of HER2+ breast cancer, particularly the MMTV-Neu model, Fasnall significantly reduces tumor volume and extends survival. Furthermore, it enhances the efficacy of carboplatin in vivo, bolstering the objective response rate of stable disease from 25% with carboplatin alone to 88% when paired with Fasnall.

113-O16B为含有二硫键的可电离阳离子类脂质，已应用于生成携带mRNA的脂质纳米粒子(LNP)。