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AD-2646 具有抗抑郁活性，抑制2-脱氧-D-葡萄糖（2-DG）诱导的胃酸分泌。

AD-2646 FA 具有抗抑郁活性，抑制2-脱氧-D-葡萄糖（2-DG）诱导的胃酸分泌。

AD 0261 is a radical scavenger. It has a strong inhibitory action on the generation of lipid peroxides and superoxide anions.

AD80 是多激酶抑制剂，可抑制 RET、RAF、SRC 和 S6K，并大大降低 mTOR 活性。

AD57是c-Src 和Abl 的有效抑制剂，IC50分别为0.025μM 和0.041μM。

AD-35 is a neuroprotectant for treating Alzheimer’s diseases by significantly inhibiting the production and release of proinflammatory cytokines TNF-α and IL-1β.

AD2765, also known as AD 2845 and Sphingosylphosphoryl​ ​choline, is a novel thiourea derivative of sphingomyelin that inhibits sphingomyelin hydrolysis and synthesis, increases ceramide, and leads to cell death.

AD 5 is a bioactive chemical.

AD 20 is designed to reduce toxicity. It also enhances the activity of anticancer drugs.

AD-1491 is a bioactive chemical.

AD-5584 是一种具有血脑屏障透过性的ACSS2抑制剂。AD-5584 可以显著减少脂质储存，减少集落形成，并增加细胞死亡，具有抗肿瘤活性。

FKBPL (FK506-binding protein like)-based peptide. Binds to and upregulates expression of CD44. Inhibits breast cancer stem cell (BCSC) growth. Decreases pluripotency markers and promotes differentiation of BCSCs. Also inhibits endothelial cell migration a

AD57, as polypharmacological cancer therapeutic, is designed to regulate multiple targets related to cancer blocks the receptor tyrosine kinase RET in Drosophila (IC50: 2 nM). AD57 effectively suppresses tyrosine kinase RET, weakens the activity of numero

Multitarget AD inhibitor-1 is a reversible and selective inhibitor of butyrylcholinesterase (BuChE) with IC50 values of 7.22 μM and 1.55 μM for human BuChE (hBuChE) and equine serum BuChE (eqBuChE), respectively. Additionally, it exhibits inhibitory activity towards β-secretase (IC50 value of 41.60 μM), amyloid β aggregation (IC50 value of 3.09 μM), and tau aggregation. As a diphenylpropylamine derivative, Multitarget AD inhibitor-1 holds promise for research pertaining to the multifunctional, disease-modifying treatment of Alzheimer's disease.

AD-8007 是一种可以穿过血脑屏障的乙酰辅酶 A 合成酶 2 (ACSS2) 抑制剂。在体外模型中，AD-8007 能显著减少脂质储存和细胞集落形成，并增加肿瘤细胞死亡。AD-8007 具有抗癌活性，可用于乳腺癌研究。

AD 2239 is a bioactive chemical.

AD1058 是一种高效、选择性且能够透过血脑屏障的 ATR 抑制剂 (IC50 = 1.6 nM)，具有显著的体内抗癌活性，通过抑制细胞增殖、破坏细胞周期和诱导细胞凋亡，常用于脑转移和中枢神经系统转移的研究中。

AD 1308 is a bioactive chemical.

AD5075 is a bioactive chemical.

AD 8717 在生命科学相关研究中具有广泛的应用。

AD 128 is a bioactive chemical and therapeutic agent.

AD 11 is a bioactive chemical.

AD-5467 is a bioactive chemical.

N-Trifluoroacetyladriamycin is a metabolite of Valrubicin (N-trifluoroacetyladriamycin-14-valerate, trade name Valstar). Valrubicin is a chemotherapy drug utilized to treat bladder cancer. Valrubicin is the anthracycline doxorubicin analog and is administ