latent

Primaquine diphosphate 是一种合成的 8-氨基喹啉衍生物，具有抗疟特性。它是一种能破坏间日疟原虫和卵形疟原虫肝脏晚期和潜在组织形态的化合物。

CEF19, Epstein-Barr Virus latent NA-3A (458-466), is a peptide epitope, YPLHEQHGM, representing residues 458-466 of the type 1 Epstein-Barr Virus (EBV) nuclear antigen 3A protein (B95.8 strain).

Leucomalachite Green-d6 是 Leucomalachite Green 的氘代化合物。Leucomalachite Green 的 CAS 号为 129-73-7。Leucomalachite green 是孔雀石绿的主要代谢物，是潜在的致癌物、致畸物和诱变剂。它是一种三苯甲烷燃料，可用于检测血液。

17-GMB-APA-GA, a potent HSP90 inhibitor, is an ADC cytotoxin commonly employed for studying latent T. gondii infection.

ONX-0914 (PR-957) TFA 为针对免疫蛋白酶体中的LMP7（低分子量多肽-7）的选择性抑制剂，LMP7为类糜蛋白酶亚单位。该化合物通过抑制细胞因子产生，减缓实验性关节炎进展，并已证实为分枝杆菌蛋白酶体的非竞争性不可逆抑制剂（Ki=5.2 μM）。此外，ONX-0914 TFA 能通过HSF-1介导的p-TEFb活化，激活潜伏的HIV-1。

ELQ316是一种抗寄生虫化合物。在急性和潜伏性弓形虫病的小鼠模型中，ELQ-316显示出高效的功效，并且其体外IC50值处于皮克摩尔级别。

Linavonkibart (SRK181) 是一种靶向 TGFβ1 的人源化抗体，通过特异性结合 latent TGF-β1，可阻止 TGF-β1 蛋白的释放。

Echinatin exerts a protective effect against ischemia reperfusion (I R)-induced myocardial injury on hearts, this effect may be attributed to the antioxidant and anti-inflammatory activities of this compound. Echinatin can inhibit DNP-ATPase activity whil

Ingenol 3-Hexanoate is a novel potent reactivator of latent HIV-1.

SMAPP1 is an activator of protein phosphatase 1 (PP1). SMAPP1 induces PP1 activity in vitro and activates latent HIV-1 provirus in cultured and primary T cells.

Gnidimacrin activated HIV-1 replication and killed persistently-infected cells at picomolar concentrations. In addition to its potential to purge HIV-1 from latently infected cells, gnidimacrin potently inhibited a panel of HIV-1 R5 virus infection of peripheral blood mononuclear cells (PBMCs) at an average concentration lower than 10 pM. These results suggest that gnidimacrin could activate latent HIV-1, specifically kill HIV-1 persistently infected cells, and inhibit R5 viruses at picomolar concentrations

Livmoniplimab (ABBV-151; ARGX-115) 是一种有效的人源化抗 LRRC32 (GARP) TGFβ1 单克隆抗体。Livmoniplimab 阻断 LRRC32 介导的潜在 TGFβ1 激活。Livmoniplimab 具有癌症研究的潜力。

Leuco Malachite Green-d5 是 Leuco Malachite Green 的氘代化合物。Leuco Malachite Green 的 CAS 号为 129-73-7。Leucomalachite green 是孔雀石绿的主要代谢物，是潜在的致癌物、致畸物和诱变剂。它是一种三苯甲烷燃料，可用于检测血液。

IALYLQQNW 为源自 Epstein-Barr 病毒 (EBV) 潜伏膜蛋白1 (LMP1) 的九肽序列,是潜在的 T 细胞表位.该肽段通过激活针对 EBV 的细胞毒性 T 淋巴细胞 (CTLs),使其能够识别并消灭表达 LMP1 的 EBV 感染细胞.IALYLQQNW 在研究霍奇金病和鼻咽癌时,对EBV相关肿瘤的免疫应答有着重要影响.

BRD-6929 是一种选择性的脑渗透性的HDAC1和HDAC2抑制剂 ，IC50值为 1 和 8 nM。它对 HDAC1 和 HDAC2 有高亲和力，Ki 值为  0.2 和 1.5 nM。它可研究情绪相关行为。

HDAC3-IN-T326 is a potent and selective HDAC3 inhibitor that acts by increasing NF-κB acetylation and activating HIV gene expression in latent HIV-infected cells.

Ingenol ((-)-Ingenol) 是一种PKC 激活剂，Ki 值为 30 μM，具有抗肿瘤活性。 从 Ingenol 酯中配制新的衍生物可能是开发新的先导化合物以重新激活潜伏 HIV 的创新方法。Ingenol mebutate 是治疗光化性角化病的有效方法。

Lipid C2 是一种可电离阳离子脂质，广泛用于形成用于体内递送mRNA的脂质纳米颗粒 (LNP)。含有 Lipid C2 并封装mRNA报告基因的LNP在小鼠中选择性集聚于肝脏和脾脏，而不在心脏、肺或肾脏中积累。携带编码Epstein-Barr病毒 (EBV) 蛋白潜伏膜蛋白 2 (LMP-2) 的mRNA的LNP，与抗程序性细胞死亡蛋白 1 (PD-1) 抗体联用，可缩小肿瘤体积，逆转T细胞耗竭，提高CT26小鼠EBV感染结肠癌模型中脾脏中CD3+CD8+中心T细胞和CD3+CD8+效应记忆T细胞的比例，并降低表达Pd-1的CD3+T细胞的比例。

MDG486, an inhibitor of BAF, works by activating latent HIV-1.

Dibrospidium Free Base is a dispirotripiperazine derivative and alkylating agent with potential antineoplastic and anti-inflammatory activities. The duration of DNA synthesis inhibition in tumor cells was found to correlate with spirobromine antitumor activity. Spirobromin is superior to prospidin by the power of the anti-inflammatory effect. Spyrobromin can diminish the latent period of the development of tumours in the experimental rats at intraperitoneal administration. At intragastric administration of the drug no decrease was noted in the latent period and no increase of tumours was observed in the experimental groups of the animals as compared with control. Dibrospidium has been examined for the treatment of bone cancer. The oral route of administration is the most safe with respect to the oncogenic risk. It was noted that spirobromin exerted the most pronounced toxic action on erythrocytes. Dibrospidium is used for the treatment of acute leukemias (mainly in combinatio......

HIV-1 inhibitor-37 (Compound 83) is a highly powerful HIV-1 inhibitor. It exhibits significant potential for use as an innovative latent HIV-1 reactivating agent [1].