dp 5

JBP485 is an inhibitor of renal transporters OAT1 and OAT3. JBP485 is an antihepatitis agent as a substrate for intestinal PEPT1.

FLDP-5 为一种可透过血脑屏障的姜黄素类似物，能够诱导活性氧（ROS）产生、DNA损伤及细胞周期S期阻滞。此外，FLDP-5 在抑制LN-18细胞增殖和迁移方面表现出显著的抗肿瘤活性。

BDP5290 是一种有效 ROCK 和 MRCK 抑制剂，对 ROCK1、ROCK2、MRCKα 和 MRCKβ 的 IC50 分别为 5、50 、10 和 100 nM。

Benzoic acid, p-(5-(p-aminophenoxy)pentyloxy)-, hydrochloride is a bioactive chemical.

Delmitide acetate (RDP58) 是一种 d-异构体十肽，具有抗炎活性和口服活性。该化合物能够抑制 TNF-α、IFN-γ 以及白细胞介素 (IL)-12 的生成，同时提高血红素加氧酶 1 的活性，可用于针对溃疡性结肠炎的研究。

NHC-triphosphate triammonium is an active phosphorylated intracellular metabolite of β-d-N4-Hydroxycytidine (NHC) as a triphosphate form[1]. NHC-triphosphate triammonium is a weak alternative substrate for the viral polymerase and can be incorporated into HCV replicon RNA[1][2]. In an intracellular metabolism assay, HCV replicon cells are treated with 10 μM 3H-labeled NHC, and intracellular nucleotide levels are determined after 1, 2 and 8 hours incubations. NHC is rapidly convered into the mono-, di-, and triphosphate forms, and NHC-TP reaches up to 71.12 pM after 8 hours[1].NHC-triphosphate triammonium (NHC-TP) (5-40 μM) absence leads to full-length polymerization products, it can be a weak alternative substrate. In addition, incorporation of NHC-TP instead of CTP increases the molecular weight of the polymerization product by 16 (one extra oxygen) for each event and an obvious electrophoretic shift is observed in cell-free HCV NS5B polymerization reactions[1].Huh-7 cells are incubated with (10-50 μM; 4 h) NHC or a McGuigan phosphoramidate prodrug of NHC. Intracellular levels of the parental compounds and phosphorylated metabolites are measured using LC-MS MS. Small amounts of NHC-monophosphate (MP) and NHC-diphosphate (DP) can be observed, while NHC-triphosphate triammonium remains the most abundant metabolite[2].NHC-triphosphate triammonium (NHC-TP) metabolite may directly target the viral polymerase and behave as a nonobligate chain terminator. It plays a prominent role in inhibiting early negative-strand RNA synthesis, either through chain termination or mutagenesis, which may in turn interfere with correct replicase complex formation. [1]. Stuyver LJ,et al. Ribonucleoside analogue that blocks replication of bovine viral diarrhea and hepatitis C viruses in culture.Antimicrob Agents Chemother. 2003 Jan;47(1):244-54. [2]. Maryam Ehteshami, et al. Characterization of β-d- N4-Hydroxycytidine as a Novel Inhibitor of Chikungunya Virus.

Clofarabine-5'-diphosphate (Clofarabine-DP) 是 Clofarabine 经脱氧胞苷激酶 (dCK) 磷酸化后的代谢产物。Clofarabine-5'-diphosphate 还能继续磷酸化生成 Clofarabine-5'-triphosphate，在癌细胞中通过阻碍 DNA 合成和 DNA 修复展现出细胞毒性。

DP-15 是一种针对 GSPT1 和 BRD4 的降解剂，其 DC50 分别为 5.25 nM 和 0.48 nM。它在 AML 和 NHL 细胞中显示出纳摩尔水平的抗增殖活性，能够在 G1 期阻滞细胞周期，并诱导 MOLM13 细胞凋亡 (apoptosis)。此外，DP-15 在 MOLM-13 异种移植小鼠模型中表现出抗白血病活性。(Pink: ligand for target protein JQ-1 carboxylic acid; Black: linker; Blue: ligand for E3 ligase Cereblon Thalidomide-5-OH)

Clofarabine-5'-diphosphatetrisodium (Clofarabine-DP trisodium) 是 Clofarabine-5'-diphosphate 的钠盐。Clofarabine 经脱氧胞苷激酶 (dCK) 磷酸化后生成 Clofarabine-5'-diphosphate trisodium，这个代谢产物能够进一步被磷酸化为 Clofarabine-5'-triphosphate，并在癌细胞中通过抑制 DNA 合成及 DNA 修复显现细胞毒性。

AGN 210676 is a selective agonist of prostaglandin EP2(EC50 : 5 nM).