dma

Solimastat is a novel oral, broad-spectrum matrix metalloproteinase inhibitor (MMPI), being >10-fold more active than marimastat in inhibiting the processing of cell-bound TNF-alpha.

D-Lin-MC3-DMA 是一种递送 siRNA 载体，是一种可离子化的氨基脂质类化合物。

DLIN-MC2-DMA (DLin-M-C2-DMA) 是一种脂质膜，是一种潜在的核酸载体。

DLin-KC2-DMA 是一种可用于siRNA 传递的阳离子，也是一种可电离的脂质，DLinKC2-DMA 可以与 LNP结合并可以使siRNA 介导的 GAPDH 基因沉默。

2,6-DMA hydrochloride 是苯丙胺类化合物，作为血清素 5-HT2 受体激动剂，其 pA2 值为 5.09。

2,4-DMA hydrochloride 是一种苯丙胺类型的血清素5-HT2受体激动剂，其表观PA2值为5.6。

DMA-CPPTL is a prodrug of CPPTL which induces apoptosis in a dose-dependent manner via the ROS/JNK pathway in acute myeloid leukemia.

DMA-135 hydrochloride (DMA-135 HCl) 靶向 RNA 的抗病毒活性化合物，抑制肠道病毒 71 型 (EV71)IRES依赖的翻译和复制。DMA-135 hydrochloride 可用于研究肠道病毒感染。

DLin-K-C3-DMA是一种阳离子脂质，能够结合带负电的mRNA和siRNA，常用于合成脂质纳米粒(LNP)从而递送核酸。

DLIN-MC4-DMA 是一种脂质膜，是一种潜在的核酸载体。

DMAPT (Dimethylamino Parthenolide) 是一种具有口服活性的NF-κB 抑制剂，是一种 Parthenolide (PTL) 的类似物，对原发性急性髓性白血病细胞的LD50值为1.7 μM。具有潜在的抗肿瘤和抗转移作用。

3,6-DMAD dihydrochloride 是一种吖啶衍生物，是一种 IRE1α-XBP1s 通路的有效抑制剂。3,6-DMAD dihydrochloride 可以利用 IRE1α-XBP1s 通路，诱导 IL-6 分泌。3,6-DMAD dihydrochloride 对 IRE1α 寡聚化和核糖核酸内切酶 (RNase) 活性具有抑制作用。3,6-DMAD dihydrochloride 能够用于研究癌症。

SDKPDMAEIEKFDKSK acetate 是一种胸腺素 β4 衍生物。 胸腺素 β4 通过阻断 Akt 磷酸化来抑制 PDGF-BB 诱导的 HSC 纤维化、增殖和迁移。

3,6-DMAD hydrochloride is an inhibitor of the IRE1α-XBP1 pathway of the unfolded protein response.

3-O-Acetylpadmatin 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T126544，CAS号为 100595-93-5。

DLinDMA 是一种稳定的核酸脂质颗粒 (SNALPs) 中的关键脂质成分，是一种可电离的阳离子脂质。它可用于siRNA 递送的研究。

DMAC-PDB is a cleavable linker vital in ADC synthesis. DMAC-PDB joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled drug release, optimizing ADC effectiveness.

DMAC-SPP is a cleavable linker vital in ADC synthesis. DMAC-SPP joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled drug release, optimizing ADC effectiveness.

Sulfo-DMAC-SPP is an ADC linker employed for the synthesis of antibody-drug conjugates (ADCs) [1].

AcLysValCit-PABC-DMAE-SW-163D is a drug-linker conjugate for antibody-drug conjugates (ADCs), featuring a natural bis-intercalator, SW-163D, attached through an AcLysValCitPABC-DMAE linker[1].

SDMAp-hydroxyazobenzene-p′-sulfonate 是 SDMA 的对羟基偶氮苯-p′-磺酸盐衍生物，作为内源性一氧化氮合酶 (NO synthase) 的阻断剂。它也是 NF-κB 的激活剂，能够加强 IL-6 和 TNF-α 的表达。在血清和血浆中稳定，该化合物可以作为肝肾功能障碍的生物标志物使用。

2,3-MDMA hydrochloride 是一种抑制去甲肾上腺素转运蛋白 (noradrenalin transporter) 和血清素转运蛋白 (serotonin transporter) 的化合物，其IC50值分别为6.2 μM和82 μM。

DMAB-anabaseine dihydrochloride (N,N-dimethyl-4-[(E)-(6-pyridin-3-yl-3,4-dihydro-2H-pyridin-5-ylidene)methyl]aniline;dihydrochloride) 是一种含有 α7 的神经元烟碱受体部分激动剂和 α4β2 和其他烟碱受体的拮抗剂。

Synthetic and natural alkyl phosphates, also known as phosphoantigens, stimulate the proliferation of γδ-T lymphocytes. Isopentenyl pyrophosphate, and related derivatives including (E)-hydroxy-dimethyl-allyl pyrophosphate ((E)-HDMAPP), are particularly effective activators of γδ-T cells. (E)-C-HDMAPP is the pyrophosphonate form of (E)-HDMAPP. The pyrophosphonate moiety in (E)-C-HDMAPP is much less susceptible to chemical or enzymatic hydrolysis than its pyrophosphate counterpart. As a result, (E)-C-HDMAPP is much more stable in solution and in vascular circulation. (E)-C-HDMAPP possesses comparable activity to (E)-HDMAPP, which is the most potent of the isoprenoid phosphoantigens. (E)-C-HDMAPP stimulates the synthesis of tumor necrosis factor (TNF-α) by γδ-T lymphocytes with an IC50 value of 0.91 nM. (E)-C-HDMAPP also significantly increases the number of circulating γδ-T cells in vivo, in cynomolgus monkeys.