dda

Bis(p-chlorophenyl)acetic acid is a standard for pesticide residue analysis.

DDA-tetracycline, also known CMT-1 and 4-Des-dimethylaminotetracycline, is a Matrix Metalloproteinase Inhibitor.

DDa-1是一种有效的kinase抑制剂，其作用机制是通过（PROTAC）途径促使kinase的降解。

Dendrogenin A (DDA) 作为一种选择性肝X受体(LXR)调节剂(SLiM)、胆固醇环氧水解酶(ChEH; Ki = 120 nM)的抑制剂及胆固醇的活性代谢产物，通过DDA合成酶将5,6α-环氧胆固醇与组胺结合形成。DDA在非癌性人乳腺上皮细胞和上皮黑色素细胞中存在，但在多种乳腺癌细胞或黑色素瘤细胞中未发现，且在分离的人乳腺肿瘤组织中仅以低水平存在。它抑制22(R)-羟基胆固醇诱导的LXRβ和LXRα激活(分别以IC50 = 76和362 nM)，但也是LXR的部分激动剂，在B16/F10小鼠黑色素瘤细胞中增加Nur77、NOR-1、LC3-I和LC3-II的蛋白水平。DDA选择性调节LXRα和LXRβ，而非孕烯X受体(PXR)、芳香烃受体(AhR)、维生素D受体(VDR)、维甲酸X受体γ(RXRγ)、维甲酸受体α(RARα)、过氧化物酶体增殖物激活受体α(PPARα)、PPARγ、糖皮质激素受体、雄激素受体、雌激素受体α(ERα)及ERβ在2.5 µM下。此外，DDA在2.5和5 µM的浓度下增加B16/F10和SK-MEL-28癌细胞中LC3-II的蛋白水平，并在2.5 µM时诱导这些细胞类型的自噬细胞死亡。DDA (0.37 µg/kg)在B16/F10小鼠黑色素瘤模型和TS/A小鼠乳腺癌模型中减缓肿瘤生长，并在体内外诱导癌细胞分化。

ddATP is a dideoxynucleotide, used as a chain extension inhibitor for DNA polymerase, and used for DNA sequencing by the Sanger method.

DDAC (Quaternium 12)，即Didecyldimethylammonium chloride，是一种广泛应用于各种产品中的双烷基季铵化合物，因其具有杀菌、杀病毒和杀真菌的特性而受到重视。

hDDAH-1-IN-2 is an orally active human dimethylarginine dimethylaminohydrolase-1 (hDDAH-1) inhibitor.

hDDAH-1-IN-2 sulfate is an orally active human dimethylarginine dimethylaminohydrolase-1 (hDDAH-1) inhibitor.

hDDAH-1-IN-1 is a selective non-amino acid catalytic site inhibitor of human dimethylarginine dimethylaminohydrolase-1 (hDDAH-1) (Ki: 18 μM).

hDDAH-1-IN-1 TFA is a selective non-amino acid catalytic site inhibitor of human dimethylarginine dimethylaminohydrolase-1 (hDDAH-1) (Ki: 18 μM).

Toddacoumaquinone 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 T125878。

ADDA 5 hydrochloride is a partial non-competitive inhibitor of cytochrome c oxidase (CcO). For purified CcO from human glioma and bovine heart, the IC50s are 18.93 μM and 31.82 μM , respectively.

ddATP (2',3'-Dideoxyadenosine 5'-triphosphate) tetrasodium 是一种 2',3'-二脱氧肌苷的活性代谢物，能够抑制 DNA polymerase 的链延长。ddATP tetrasodium 可用于 Sanger 法 DNA 测序和病毒感染研究。

Ethylenediaminediacetic acid is derived from two molecules of glycine linked by amines.

Niddamycin is a new macrolide antibiotic.

p-DDAP is an anti-invasive agent that acts by significantly suppressing cell invasion, and the activity and mRNA expression of matrix metalloproteinase-9 (MMP-9).

ADDA is a non-proteinogenic amino acid existed in toxins produced by cyanobacteria.

7-Deaza-7-propargylamino-ddATP, an analog of ddATP, serves as a viable option for gene sequencing purposes due to its chemical composition.

Toddalolactone ((+)-Toddalolactone) 是一种Toddalia asiatica 的主要成分，能够抑制重组人纤溶酶原激活物抑制物-1(PAI-1)的活性， IC50=37.31 μM。

hDDAH-1-IN-2 是选择性，口服有效的人二甲基精氨酸二甲基氨基水合-1(hDDAH-1)抑制剂，对细胞毒性 活力良好。

Toddacoumalone 是一种天然PDE4 (磷酸二酯酶 4) 抑制剂，效力中等，活性分子特性不完善。具有研究银屑病等炎症性疾病潜力。

YYRADDA是一种多肽，能够促进皮肤细胞外基质中胶原蛋白的生成，从而改善皮肤外观并促进受损皮肤的恢复。

Toddanone是从积雪草(Toddalia asiatica)的根部分离出的香豆素类化合物。

DDABT1 exhibits anti-CHIKV activity (IC50 of 14.53 μM) and possesses anti-inflammatory and anti-arthritic properties [1].