t1105

T-1105 是 T-705 的结构类似物，是一种广谱病毒聚合酶抑制剂，在转化为核糖核苷三磷酸代谢物后抑制 RNA 病毒的聚合酶，有抗病毒活性。

Penfluridol (TLP-607) 是一种高效的二苯类抗精神病药物。

Disitertide acetate (P144 acetate) 是转化生长因子 TGFβ1 的多肽抑制剂，特异性的阻断其与受体间的相互作用。Disitertide acetate 也是PI3K 的抑制剂和凋亡 (apoptosis) 诱导剂。

DIQ3 is non-toxic to normal human cell lines and is an effective anti-cancer agent.

DJ001 是一种高度特异性，选择性和非竞争性的蛋白酪氨酸磷酸酶-σ (PTPσ) 抑制剂，IC50 为 1.43 μM。DJ001 对其他磷酸酶无抑制活性，对蛋白质磷酸酶 5 仅有中等抑制活性。DJ001 促进造血干细胞再生。

DL-TBOA 是一种兴奋性氨基酸转运蛋白抑制剂，抑制兴奋性氨基酸转运蛋白 1 (EAAT1)，EAAT2 和 EAAT3，抑制神经元和星形胶质细胞中 [3H]D-天冬氨酸的摄取。DL-TBOA 可用于研究代谢基本疾病和神经系统疾病。

DL-Norvaline (2-Aminopentanoic acid) 是精氨酸酶的非竞争性抑制剂，是L-norvaline 的代谢物。

Dipycecetyl 是止痛及抗炎剂。

Disitertide (P144) is an inhibitor of TGF-β1.

DLK-IN-1 is a selective oral active inhibitor of bisleucine zipper kinase (DLK, MAP3K12) with Ki of 3 nM. DLK-IN-1 is active in the Alzheimer's disease model, retains excellent CNS permeability, and after multiple days of administration, its concentration

DM3-SMe is a maytansine derivative and tubulin inhibitor. It is a cytotoxic part of antibody-drug conjugates (ADCs) and can bind to antibodies via disulfide bonds or stable thioether bonds. DM3-SMe has high cytotoxic activity in vitro with IC50 of 0.0011

DM3 (Maytansinoid DM3) is a maytansine mimic with disulfide or thiol groups, acting as a tubulin inhibitor and serving as the cytotoxic component in antibody-drug conjugates (ADCs).

DM4-SMe is a cytotoxic part of antibody-drug conjugates (ADCs) and a metabolite of antibody-maytansin conjugates (AMCs) and tubulin inhibitors, which can also be stabilized by disulfide bonds or thioether The bond binds to the antibody. The IC50 of DM4-SM