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ATR-IN-10 是一种有效的、高度选择性的 ATR 激酶的抑制剂 (IC50: 2.978μM)。

(Iso)-WAY-260022 ((Iso)-NRI-022) 是 WAY-260022 的一种立体异构体。WAY-260022 是去甲肾上腺素再摄取抑制剂，也是选择性 5-羟色胺和多巴胺转运蛋白抑制剂。

Potassium isobutyrate是一种羧酸盐，广泛应用于生物化学实验和药物合成研究。

Benzyl-PEG9-THP 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.

HAE (His-Ala-Glu) 由组氨酸、丙氨酸和谷氨酸组成。

Azido-PEG5-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.

Buclizine 是一种口服具有活力的抗组胺、抗过敏化合物。Buclizine 也是一种大鼠的强致畸剂，表现出抗肿瘤作用。

Plantagoside 是α-mannosidase 的非竞争性特异性抑制剂(IC50:5 μM)，分离自Plantago asiatica 种子中。

BI-0252 is an inhibitor of MDM2-p53 (IC50:4 nM). BI-0252 can induce tumor regressions in all animals of a mouse SJSA-1 xenograft. And it concomitant induction of the tumor protein p53 (TP53) target genes and markers of apoptosis.

Anticancer agent 49 (compound 69) 是一种广谱抗癌剂，其表现出抗增殖活性。Anticancer agent 49 对微管蛋白聚合具有抑制作用。Anticancer agent 49 在体内显示抗肿瘤活性。Anticancer agent 49 具有潜力进行实体瘤和血液肿瘤的研究。

β-Methylcrotonyl coenzyme A lithium，作为亮氨酸代谢的中间体，可用于研究β-甲基巴豆酰辅酶 A 羧化酶（MCCase）的特异性及动力学，用作底物。

RSV-IN-7 (example 253) 是一种 RSV 抑制剂 (EC50: < 0.4 μΜ)。

Pimonidazole hydrochloride 通过与大分子共价结合或在其硝基还原后形成还原性代谢物在缺氧细胞中积累。 可用于肿瘤缺氧的定性和定量评估。 它是一种新型的缺氧标志物，用于肿瘤缺氧和肿瘤细胞增殖的互补研究。

SB 224289 is a selective antagonist of 5-HT1B receptor with pKi of 8.2. It is a centrally active following oral administration in vivo. SB 224289 displays 60-fold selectivity over 5-HT1D, 5-HT1A, 5-HT1E, 5-HT1F, 5-HT2A and 5-HT2C receptors in radioligand

DENV-IN-2 is a highly effective inhibitor of dengue viral replication with a potency indicated by an EC 50 of 0.016 nM. It exhibits significant activity against all four serotypes of the Dengue virus, with EC 50 values ranging from 0.013 to 0.029 nM.

Prodipine hydrochloride for purified and plasma Dipeptidyl peptidase IV (DPP IV) from the rabbit (IC50 of 4.5 μM and 30 μM, respectively).

TROX-1 is the activation state-dependent Cav2 channel antagonist.

Rhodiocyanoside A (Multifidin) 是一种可从红景天中提取的红花青甙，对用抗 2,4-二硝基苯基 IgE 致敏的大鼠腹膜渗出物细胞释放的组胺表现出抑制活性。

Antazoline 具有抗组胺和抗胆碱能作用。它用于治疗各种心律失常。

ST4206 is an antagonist of adenosine A2A. For adenosine A2A receptor and adenosine A1 receptor, the Kis values are 12 nM and 197 nM , respectively.

IKKβ-IN-1 是一种有效的、口服具有活力的 IkappaB(IKK-β) 抑制剂 (IC50: 0.20 μM)。IKKβ-IN-1 能够减少抑制小鼠巨噬细胞中 PGE2和 TNF-α的产生。IKKβ-IN-1 对小鼠具有保护作用，使其免受感染性休克诱导的死亡。

Mal-amido-PEG4-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.

5-Methylpyrazin-2(1H)-one是一种吡嗪酮衍生物，广泛应用于生物化学实验和药物合成研究。

JZP-MA-11是一种用于正电子发射断层扫描(PET)的配体，专一性靶向内源性大麻素α/β-水解酶结构域6(ABHD6)酶，并具有126 nM的IC50值，表明其对ABHD6有选择性抑制作用。JZP-MA-11能有效穿过血脑屏障(BBB)。[18F]JZP-MA-11展现出在靶向小鼠及非人灵长类(NHP)大脑ABHD6方面的临床前评估潜力。

(R,R)-Glycopyrrolate is an agent of anticholinergic, has the ability to reduce the frequency of drooling in vivo with developmental disabilities.

SRX246 has no interaction at V1b and V2 receptors. SRX246 shows negligible binding at 64 other receptors classes, including 35 G-proteincoupled receptors. SRX246 is a potent and CNS-penetrant vasopressin 1a (V1a) receptor antagonist (Ki=0.3 nM for human V

DiFMUP (6,8-Difluoro-4-methylumbelliferyl phosphate) 是一种荧光底物，抑制蛋白酪氨酸磷酸酶（PTPs），可用于检测苏氨酸磷酸酶的活性。

DMAPP, also known as Dimethylallyl pyrophosphate, is an isoprenoid precursor found in all life forms. It serves as an isomer of isopentenyl pyrophosphate (IPP).

CETP-IN-3 is an inhibitor of the plasma glycoprotein cholesterol ester transfer protein (CETP), elevating HDL-C through inhibition of CETP.

Ganolactone B is a natural product from Ganoderma lucidum.

3'-dC(Bz)-2'-phosphoramidite is a Nucleoside Phosphoramidite.

Fabomotizole hydrochloride (CM346 hydrochloride) 是一种具有抗焦虑和神经保护作用的化合物。

CAY10444 is an S1P3 specific antagonist.

Ro 09-0680 是从丹参中提取的化合物，是一种由胶原蛋白诱导的兔血小板聚集的有效抑制剂，具有潜在的抗炎活性，可用于研究心血管疾病。

Mesembrine ((+)-Mesembrine) 一种主要的生物碱，具有芳基八氢吲哚骨架。Mesembrine 是一种5-HT 转运蛋白抑制剂，Ki 为 1.4 nM。Mesembrine 还抑制磷酸二酯酶 4B (PDE4B)，IC50为 7.8 μM。

Thrombin inhibitor6为高效的凝血酶抑制剂，IC50值为1 nM，表现出显著的抗凝作用。