dimeric

BMS-202 (PD1-PDL1 inhibitor 2) 是一种非肽类 PD-1 PD-L 复合物抑制剂，其 IC50为 18 nM，KD 为 8 μM。它与 PD-L1 直接结合并阻断人类 PD-1 PD-L 的相互作用，具有抗肿瘤活性。

Dimeric coniferyl acetate has anti-inflammary activity, it shows strong NO inhibition with IC50 values of 27.1 uM in lipopolysacchalide (LPS)-activated murine macrophage-like J774.1 cells. It exhibits significant inhibitory effects on the nitric oxide pro

Dupilumab (REGN-668) 是一种用于AD 的全身免疫调节剂。Dupilumab 是一种针对白细胞介素-4受体α亚基的完全人类单克隆抗体，可抑制IL-4和IL-13下游信号传导，具有改善特应性皮炎的作用。

Doxapram hydrochloride hydrate (Doxapram HCl) 是 TASK-1，TASK-3和 TASK-1 TASK-3异二聚体通道的抑制剂，EC50分别为410 nM，37 μM 和9 μM。

S 0960 是一种二聚体胆汁酸类似物，是回肠中顶端钠依赖性胆盐转运蛋白的特异性抑制剂，可用于研究代谢疾病。

G-9807 通过稳定活性二聚体单元，充当 RNase 的变构激活，显著提高 IRE1-KR-0P 的 RNase 活性。

Pyrrole-2-carboxaldehyde exhibits distinctive vibrational and electronic properties which serve to validate its dimeric state in the solid phase and monomeric state in the solution phase.

D-Pantethine (Pantomin) 是泛酸的二聚体形式, 是生产辅酶 A 的中间体。D-Pantethine 能够作为膳食补充剂，用于改善血液胆固醇和研究痤疮。

Enpp-1-IN-22 作为一种前药，是一种口服生物可利用性的强效 ENPP1 抑制剂，显示出抗肿瘤活性。

DOTAGA.(SA.FAPi)2 TFA 作为一种高效的二聚体成纤维细胞激活蛋白抑制剂 (FAPi)，展示出在癌症诊断研究中的应用潜力。

ART838是一种具有高效抗白血病活性和良好药理学特性的二聚戊二酸脲。在体外，ART-838对所有白血病细胞系表现出亚微摩尔级的抑制浓度，比青蒿琥酯增强了88倍的抗白血病能力。此化合物在体内保持较长时间，并且能与抗白血病化合物及新型激酶抑制剂协同作用，抑制白血病细胞生长。在免疫缺陷的NOD-SCID-IL2Rgnull (NSG)小鼠中，ART-838的血浆半衰期超过青蒿琥酯，并能在有效抗白血病浓度下维持>8小时。间歇性周期的ART-838处理显著抑制了NSG小鼠中急性白血病异种移植物和原发移植物的生长，其效力高于青蒿琥酯。

ART631是一种具有强大抗白血病活性和良好药理学特性的二聚型青蒿素，其结构通过二碳链相连。

DQ661 是一种高效的PPT1抑制剂，它作为二聚奎纳克林的自噬 (autophagy) 抑制剂也具有显著作用。DQ661 能够抑制mTORC1的活性，并降低 pS6K T389 和 pS6 S240-244 的蛋白表达水平，同时展现出抗癌潜力。

Bis(7)-tacrine dihydrochloride 衍生自 tacrine ，是一种二聚体乙酰胆碱酯酶 (AChE) 抑制剂，具有治疗阿尔茨海默病的潜力。Bis(7)-tacrine dihydrochloride 通过阻断 NMDA 受体防止谷氨酸诱导的神经元凋亡。Bis(7)-tacrine dihydrochloride 是一种有效的 GABAA 受体拮抗剂。

Picrasidine N is a naturally occurring dimeric alkaloid and a PPARβ δ agonist.

Ioforminol, also known as GE-145 and AN-113111, is a new low-osmolar dimeric radiographic contrast agent. GE-145 exhibits similar preclinical properties to other dimeric radiographic contrast media. In addition, the low osmolality enables an iso-osmolar f

Kopsoffine is a new dimeric indole alkaloid of pleiomutine type from kopsia offcinalis.

Maesol is a novel dimeric phenol isolated from seeds of Maesa montana and Maesa indica.

Lys05 是一种有效的水溶性溶酶体自噬抑制剂，具有抗肿瘤活性。在 MTT 试验中，对1205Lu、c8161、LN229 和 HT-29细胞系的IC50值分别为3.6、3.8、6 和7.9 μM。

Dimeric Smac mimetic; potent inhibitor of X-linked (XIAP) and cellular (cIAP) inhibitor of apoptosis protein (IC50 values are 15, 15 and 21 nM for XIAP, cIAP1 and cIAP2 respectively). Binds to the BIR3 domain of XIAP to prevent interaction with caspase-9. Causes degradation of cIAP1 and cIAP2 and induces apoptosis in MDA-MB-231 breast cancer cells. Causes tumor regression in MDA-MB-231 xenograft-bearing mice. Hennessy et al (2013) Discovery of a novel class of dimeric Smac mimetics as potent IAP antagonists resulting in a clinical candidate for the treatment of cancer (AZD5582). J.Med.Chem. 56 9897 PMID:24320998

Remisporine B is a polyketide and derivative of remisporine A that has been found inPenicilliumand has immunosuppressant activity.1,2It inhibits LPS- or concanavalin A-induced proliferation of isolated mouse splenic lymphocytes (IC50s = 30.1 and 32.4 μg/ml, respectively).1 1.Liu, H., Chen, S., Liu, W., et al.Polyketides with immunosuppressive activities from mangrove endophytic fungus Penicillium sp. ZJ-SY2Mar. Drugs14(12)217(2016) 2.Kong, F., and Carter, G.T.Remisporine B, a novel dimeric chromenone derived from spontaneous Diels-Alder reaction of remisporine ATetrahedron Lett.44(15)3119-3122(2003)

Terazosin dimer impurity dihydrochloride, a dimeric form of Terazosin, is a chemical impurity found in Terazosin. Terazosin itself is a derivative of quinazoline and acts as a competitive and orally active α1-adrenoceptor antagonist[1].

LasR-IN-3, a chemical compound, acts as an inhibitor of LasR in Pseudomonas aeruginosa. It induces structural instability in LasR and causes complete dissociation of its functioning dimeric form [1].

IMP-321 is a soluble dimeric recombinant form of LAG-3 and first-in-class antigen presenting cell activator.