Others

1-Palmitoyl-2-arachidoyl-3-oleoyl-rac-glycerol, a triacylglycerol, incorporates palmitic acid, arachidic acid, and oleic acid at the sn-1, sn-2, and sn-3 positions, respectively, and is identified in cod liver oil.

5β,6β-epoxycholestanol 是由胆固醇在 5,6 双键处进行自由基或非自由基氧化后生成的氧化代谢物。在 U937 巨噬细胞样分化细胞中，该化合物可引发乳酸脱氢酶 (LDH) 的释放和诱导细胞凋亡。5β,6β-epoxycholestanol 已在人体脂肪条纹及晚期动脉粥样硬化病变中发现，但在正常主动脉组织中不存在。

Oleandomycin is similar to Erythromycin has antimicrobial activity. Oleandomycin is a macrolide antibiotic structurally closely related to Erythromycin.

Ninhydrin 是一种显色分析探针，可用于氨基酸和蛋白质的定量分析。

L-Theanine (Standard) 是 L-Theanine 的标准品。适用于定量分析、质量控制及生化实验等相关研究。L-Theanine 是一种存在于绿茶叶片中的非蛋白氨基酸物质，能阻断大脑中谷氨酸与谷氨酸受体结合，具有神经保护和抗氧化活性。 它通过口服能抑制皮层神经元兴奋从而产生抗应激作用。

2',3'-O-Isopropylidene-4'-alpha-azido-uridine is a Nucleoside-Azido-nucleoside.

2-O-α-D-Glucopyranosyl-L-ascorbic Acid (ASCORBYL GLUCOSIDE) 是一种抗坏血酸的葡萄糖苷衍生物，可以被酶水解成为抗坏血酸，能够表现出抗癌活性。

Acamprosate (阿坎酸) 是一种口服活性神经调节剂，用于酒精依赖和酒精中毒的研究与治疗。Acamprosate 是氨基酸类神经递质（如牛磺酸和高半胱氨酸）的类似物，通过结合精胺敏感位点以复杂方式调节NMDAR活性。研究表明，Acamprosate 在NMDA受体上发挥“部分共激动剂”作用。

LY88074 Methyl ether is effective in inhibiting conditions associated with estrogen deprivation syndrome, such as osteoporosis and hyperlipidemia, which occur due to various estrogen-deficient states.

PB succinimidyl ester是一种反应性荧光染料，其激发和发射波长峰值分别约为 405 nm 和 455 nm。PB succinimidyl ester 广泛用于生物分子的共价标记，包括蛋白质和多肽，实现基于荧光的高灵敏检测、成像及在生化和细胞实验中的定量分析。

PXYC1 是一种核糖体蛋白 S1 (RpsA) 拮抗剂，对 RpsA-CTD 和 RpsA-CTD Δ438A 的Kd 分别为 0.81 和 0.31 μM。 在结核分枝杆菌 (Mtb)的转译过程中，核糖体蛋白 S1 (RpsA)发挥重要作用。

Thalidomide-NH-C4-NH2 TFA (compound 29c) is a conjugate consisting of an E3 ligase ligand-linker, incorporating the Thalidomide-based cereblon ligand and a linker moiety. This compound, Thalidomide-NH-C4-NH2 TFA, is utilized as a component in PROTAC BRD2/BRD4 degrader-1, which is a highly potent and selective degrader targeting BET proteins BRD4 and BRD2[1].

MNK inhibitor9 是一种有效的选择性的 MNK1/2抑制剂，IC50值分别为 0.003 µM 和 0.003 µM。MNK inhibitor9 具有良好的细胞渗透性。MNK inhibitor9 可用于肿瘤相关研究。

Trimetozine (Sedoxazine) 是一种镇静剂，自 1959 年以来一直在欧洲上市。它具有温和的镇静作用，已用于治疗焦虑症。

Aeroplysinin I is an antibacterial compound from the sponge. It has cytotoxic activity against colon cancer cells by promoting β-catenin degradation.

Melarsonyl dipotassium, also known as melarsonic acid dipotassium, is a potent anthelmintic agent with the ability to effectively inhibit parasites.

N,N-Dipropyldopamine is a dopamine receptor agonist.1,2,3 It decreases dihydrophenylalanine (DOPA) levels in the limbic forebrain and striatum of reserpinized rats (ED50s = 25 and 20 μmol/kg, respectively), as well as reduces homovanillic acid levels in rat striatum when administered at a dose of 80 μmol/kg.1 N,N-Dipropyldopamine (0.5-16 mg/kg) reduces spontaneous locomotor activity in mice, an effect that can be reversed by the antipsychotic spiroperidol.2,3

Lenalidomide-propargyl-C2-NH2 hydrochloride is a compound that features a cereblon (CRBN) ligand for the E3 ubiquitin ligase, as well as a linker. It is utilized in the development of the PROTAC MD-224[1] system.

Kaurane-3,16,17-triol,ent-kaurane-3-oxo-16α,17-diol,and ent-16α,17-dihydroxyatisan- 3-one are three kinds of toxic diterpenoids isolated from the roots of genus Euphorbia.

Highly potent and selective antagonist of the platelet P2Y1 receptor

Tacitin (Benzoctamine Hydrochloride) 显示出镇静和抗焦虑的特性。Tacitin 能阻断中枢突触后5-羟色胺受体。

Propargyl-PEG12-methane is a polyethylene glycol (PEG)-based linker utilized in PROTAC synthesis, specifically for PEG-based proteolysis-targeting chimeras (PROTACs)[1].

Diazepinomicin is a secondary metabolite produced by Micromonospora sp. It inhibits the EGF-induced Ras-ERK MAPK signaling pathway and induces apoptosis. Diazepinomicin also is an anti-tumor agent for K-Ras mutant models.

Rac)-Tanomastat ((Rac)-BAY 12-9566) 是 Tanomastat 的外消旋体。其中 Tanomastat (BAY 12-9566) 是一种口服具有活力的、含锌羧基的非肽联苯基质金属蛋白酶(MMPs)抑制剂，能够抑制 MMP-2 (Ki: 11 nM)、MMP-3 (Ki: 143 nM)、MMP-9 (Ki: 301 nM)、MMP-13 (Ki: 1470 nM)。在几种实验性肿瘤模型中，Tanomastat 表现出抗侵袭和抗转移作用。

MK-2206 是一种具有口服具有活力的、高效选择性的变构 Akt 抑制剂，能够作用于 Akt1 (IC50: 8 nM)、Akt2 (IC50: 12 nM) 和 Akt3 (IC50: 65 nM)。许多乳腺癌细胞系、PIK3CA 突变体和 PTEN 丢失细胞系对 MK-2206 敏感。MK-2206 具有抗癌作用。

Glycyroside is an isoflavone diglycoside isolated from Glycyrrhiza eurycarpa P. C. Li.

MAO-B-IN-5 是一种有效的、选择性和具有口服活性的MAO-B 抑制剂，IC50值为 0.204 μM。MAO-B-IN-5 在帕金森病 (PD) 中具有研究潜力。

S22153 is an antagonist of melatonin receptor.

group I/group II metabotropic glutamate receptor antagonist

Propanil is a widely used contact herbicide. It is mainly used in rice production.

m-PEG21-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.

Bis-propargyl-PEG13 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.

mTOR/HDAC-IN-1 (Compound 50) 是一个具有选择性的mTOR 和HDAC 双重抑制剂，对mTOR 和HDAC1的IC50分别为0.49和0.91 nM。 mTOR/HDAC-IN-1 可作为抗癌活性分子 （anti-cancer） 进行研究。该化合物的粉末形式不稳定，建议选择其他盐形式产品。

PI3K/mTOR Inhibitor-7 是有效的 PI3K/mTOR 双重抑制剂。PI3K/mTOR Inhibitor-7 的作用比 gedatolisib 高 4.7 倍，他们的 IC50 值分别为 1.4 μM 和 0.3 μM。10 μM 的 PI3K/mTOR Inhibitor-7 能够明显抑制 PI3K/Akt/mTOR 信号通路。PI3K/mTOR Inhibitor-7 对癌症疾病表现出研究潜力。

4-Methyl-2-phenylpyridine是一种吡啶衍生物，广泛应用于生物化学实验和药物合成研究。

5-HT2 receptors agonist