Others

PF-4778574 is a positive AMPA receptor allosteric modulation (EC50: 45 to 919 nM in different cells).

Kamuvudine-8 （K8）是一种齐多夫定 (AZT) 衍生物，可用于研究糖尿病性黄斑水肿。

C26 Sphingomyelin (d18:1/26:0) 是一种鞘磷脂，可用于研究神经系统疾病。

HLM006474 是光谱的E2F 抑制剂，在 A375 细胞中，可抑制 E2F4 DAN 结合(IC50:29.8 µM)。

Lenperone HCl is a dopamine antagonist and an antipsychotic agent.

MK-2894 sodium salt is a highly potent and selective antagonist of second generation EP4.

The racemic p53 and MDM2 proteins-interaction-inhibitor is an inhibitor of the interaction between p53 and MDM2 proteins.

Z-321 is an inhibitor of prolyl endopeptidase.

Enhanced Green Fluorescent Protein (EGFP) (200-208)是一种与 H2-K 强烈结合的肽，是 H-2Kd 限制性细胞毒性 T 淋巴细胞 （CTL） 表位。

3-(3-Phenoxybenzyl)amino-β-carboline is a highly effective tubulin inhibitor, selectively degrading αβ-tubulin heterodimers. It induces cell cycle arrest and apoptosis in the G2/M phase. Additionally, 3-(3-Phenoxybenzyl)amino-β-carboline displays notable anticancer activity [1].

Non-selective cholecystokinin (CCK) antagonist

CAY10711 is a substituted diamine that produces rapid bactericidal activity against both Gram-positive and Gram-negative bacteria, including methicillin-resistant S. aureus (MRSA) and stationary-phase bacteria. It displays MIC99 values of 2.9, 11.5, 2.9, and 2.9 μM against S. aureus RN4220, P. aeruginosa PAO1, E. coli ANS1, and MRSA 10082B, respectively. CAY10711 reduces biofilm formation and promotes biofilm dispersal in P. aeruginosa. It is synergistic with kanamycin and has limited adverse effects against mammalian cells or C. elegans development, survival, or reproduction.

Anticancer agent 40 (compound 3e) 是一种有效的抗癌剂。Anticancer agent 40 具有抗癌作用，能够作用于 SKBR-3 细胞 (IC50: 0.94 nM)、SKOV-3 细胞 (IC50: 0.98 nM)、PC-3 细胞 (IC50: 0.96 nM)、U-87 细胞 (IC50: 0.95 nM)、HDF 细胞 (IC50: 2.13 nM)。

DEPMPO is a nitrone that is used to spin trap reactive O-, N-, S-, and C-centered radicals and allow their characterization when used in association with electron spin resonance. It is noted for the stability of adducts formed. DEPMPO can be used in vitro or in vivo, as it crosses lipid bilayer membranes and is a good trapping agent in biological systems. DEPMPO-biotin is a biotinylated form of DEPMPO which retains the outstanding persistency of its adducts. The biotin moiety offers an effective means for monitoring biodistribution in cells, tissues, and organs when used with an avidin-conjugated reporter. Importantly, DEPMPO-biotin binds free radicals, such as S-nitroso groups, on proteins, producing adducts that can be analyzed via the biotin tag. This direct labeling of S-nitrosothiols (SNO) thus serves as an effective alternative to the more cumbersome biotin-switch method for monitoring SNO formation.

AA 2379 是一种可口服的抗风湿剂，有抗炎和解热活性，剂量依赖性地抑制由补体介导的大鼠酵母聚糖诱导的爪水肿和小鼠酵母聚糖活化血清诱导的腹膜炎。

8-Br-GTP, an analog of GTP, functions as both a competitive inhibitor of FtsZ polymerization and GTPase activity (with a K i value of 31.8 μM). Moreover, it is capable of facilitating nucleic acid modification.

L-Threonine derivative-1 是乙酰水杨酸-L-苏氨酸酯，具有潜在的镇痛活性。

RIDR-PI-103 是活性氧 (ROS) 诱导的药物释放前药，含有与泛 PI3K 抑制剂 (PI-103) 连接的自环化部分。在 MDA-MB-361 和 MDA-MB-231 细胞中，Doxorubicin 和 RIDR-PI-103 表现出协同的抑制癌细胞增殖作用。

SDZ-MKS 492 is a selective type III isozyme cyclic nucleotide phosphodiesterase inhibitor.

'(S,R,S)-AHPC-Boc (VH032-Boc) 为募集von-Hippel-Lindau (VHL) 蛋白配体的化学化合物，亦应用于PROTAC技术中。'

Xanthinol Nicotinate (Complamin) 是血管扩张剂，可直接作用于小动脉和毛细血管的平滑肌，能够扩大血管，改善血液流变学并降低外周血管阻力。

Luxabendazole is a benzimidazole carbamate broad-spectrum anthelmintic agent. It has proved to be effective against immature and adult stages of the major gastrointestinal nematodes, cestodes, and trematodes.

4α-TPA 在生命科学相关研究中具有广泛的应用。

Topoisomerase I inhibitor 7 (Compound 8) 是有效的Topoisomerase I 抑制剂。Topoisomerase I inhibitor 7 显著抑制肿瘤生长（高达 79%）。在接受 P388 淋巴瘤移植的小鼠模型中，Topoisomerase I inhibitor 7延长了小鼠寿命（153%）。

BMS-767778, a DPP-4 inhibitor, is used potentially for the treatment of type 2 diabetes.

4-Ethylpyridine是一种吡啶衍生物，能够影响(±)-[3H]nicotine对大鼠脑内P2 preparation的亲和力。

Trehalose 6-behenate is a Th1/Th17 skewing vaccine adjuvant.

Imisopasem manganese (M40403) is a manganese superoxide MnSOD non-peptidyl mimetic.

L-Canaline, a nonprotein amino acid found in many leguminous plants, exhibits potent anticancer and antiproliferative effects. It effectively inhibits the growth of the malaria parasite Plasmodium falciparum with an IC50 of 297 nM. Additionally, L-Canaline acts as a cytotoxic metabolite produced from L-canavanine through arginase catalysis and serves as a potent and irreversible inhibitor of ornithine aminotransferase.

PCI-27483 是一种FVIIa/tissue factor 抑制剂，具有抗肿瘤的作用。

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt 对pre-miR-21 RNA 具有抑制活性。HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt 具有研究肿瘤疾病的潜力，例如癌症，尤其是表达 miR-21 的癌症。

4-(Aminomethyl)benzoic acid (PAMBA) 是一种抗溶纤维蛋白药，是一种非天然氨基酸衍生物。

Benserazide is an inhibitor of dopa decarboxylase. It is often given with levodopa in the treatment of Parkinson's to prevent the conversion of levodopa to dopamine in the periphery, thereby increasing the amount that reaches the central nervous system an

Pirlimycin Hydrochloride, a Clindamycin analog, is a semi-synthetic lincosaminide antibiotic.

MAX-40279 hemiadipate 是一种有效的、双重 FLT3 激酶和 FGFR 激酶抑制剂。MAX-40279 hemiadipate 对急性髓性白血病 (AML) 表现出研究潜力。

Imnopitant 是 NK1 受体的拮抗剂。