dcα

DC 07090 是一种人肠道病毒 71 3C 蛋白酶抑制剂，具有抗病毒活性，可用于研究核酸病毒感染。

5'-O-DMT-N4-Bz-5-Me-dC (DMT-NBZ-5-METHYL DC) 是一种修饰的核苷，可用于合成核苷磷酰胺。

DC-6-14为一种阳离子脂类，用于合成脂质体，具备基因转染活性。

Di-Val-L-dC, a reverse transcriptase inhibitor, is used potentially for treatment of HBV infection.

The IC50 of DC44SMe for Ramos, Namalwa and HL60 s cancer cells was 2.0 nM, 2.8 nM and 1.9 nM, respectively. DC44SMe can be used for targeted treatment of cancer. DC44SMe is a phosphate prodrug of DC44 and can be used in the synthesis of antibody-drug co

DC-5163 is a potent inhibitor of glyceraldehyde 3-phosphate dehydrogenase (GAPDH) with IC50 of 176.3 nM and Kd of 3.192 μM. DC-5163 selectively inhibits cancer cell proliferation and induces apoptosis, and partially inhibits the glycolysis pathway.

Benzyl DC-81 (Compound 6a) 是一种抗癌化合物，展现对A375和MCF-7细胞线具有显著的抗增殖作用。

Phen-DC3 Trifluoromethanesulfonate is a G-quadruplex (G4) specific ligand. It also can inhibit FANCJ and DinG helicases (IC50s: 65±6 and 50±10 nM, respectively).

2'-F-Bz-dC Phosphoramidite can be used in the synthesis of oligoribonucleotides.

DMT-dC(ac) Phosphoramidite is a phosphoramidite monomer that has been modified for use in oligonucleotide synthesis.

DC1 can be used to synthesize antibody-drug conjugates targeted to the treatment of cancer, is an ADC cytotoxin, similar to the small groove-binding DNA alkylating agent CC-1065.

3'-dC(Bz)-2'-phosphoramidite is a Nucleoside Phosphoramidite.

DC-CPin7, a powerful inhibitor of the bromodomain of CREB-binding protein (CBP), exhibits an IC50 value of 2.5 μM [1].

DC-034 is a potent downregulator of MYC transcription in cancer cells by a G4-dependent mechanism, thereby selectively inhibiting MYC significantly greater than other G4-driven genes.

5’-O-DMTr-2’,2’-difluoro-dC(Bz)-methyl phosphonamidite 是一种广泛具有抗肿瘤活性的嘌呤核苷类似物，主要用于靶向惰性淋巴系统恶性肿瘤。其抗癌机制主要通过抑制 DNA 合成和诱导细胞凋亡 (apoptosis) 来实现。

DC-120 is an ATP competitive AKT kinase inhibitor that suppressed proliferation and induced apoptosis in liver cancer cells both in vitro and in vivo. DC120 blocked the phosphorylation of downstream molecules in the AKT signal pathway in dose- and time-dependent manners both in vitro and in vivo. DC120 inhibits AKT activity in vitro with an EC(50) of 153 nM. DC120 at 20 mg kg day inhibited the CNE2 xenograft tumor growth with a treated group control group ratio of 38.1%, accompanied by increasing terminal deoxynucleotidyl transferasedUTP nick-end labeling-positive cells in the tumor sample.

DC-CPin711, a potent and selective inhibitor of the bromodomain of CREB-binding protein (CBP) with an IC50 of 0.0626 μM, effectively halts the cell cycle at the G1 phase and promotes apoptosis [1].

DC1 is an ADC cytotoxin, similar to the small groove-binding DNA alkylating agent CC-1065. DC1 can be used to synthesize antibody-drug conjugates targeted to the treatment of cancer. DC1Sme is a DC1 derivative with IC50 values of Ramos, Namalwa, HL60 s

AntibioticDC 102,一种新型糖苷吡咯(1,4)苯二氮卓类抗生素,面向枯草芽孢杆菌,具有42 μg mL的最小抑菌浓度(MIC).此外,该化合物在小鼠体内的半致死剂量(LD50)为1.5 mg mL(i.p).

DC271作为RAR激动剂，属于类视黄醇类，能够激发与内源性类视黄醇ATRA及合成类视黄醇EC23相一致的细胞反应。此化合物通过与类视黄醇相关蛋白（例如CRABPII）结合，实现内源性类视黄醇ATRA的细胞核易位作用。

DMT-5Me-dC(Bz)-CE Phosphoramidite 用于生产锁定核酸（LNAs），旨在优化荧光寡核苷酸探针的设计，从而提升其光谱性质和对目标的结合能力。

5'-DMTr-dC (Ac)-methylphosphonamidite is a Nucleoside Derivative - phosphonamidite.

DC-05 是一种DNMT1的抑制剂，IC50和Kd 值分别为 10.3 和 1.09 μM。

DC260126 是一种 GPR40 (FFAR1)拮抗剂，对棕榈酸酯诱导的内质网应激和凋亡有保护作用。它剂量依赖性地抑制亚油酸、油酸、棕榈油酸和月桂酸刺激的 GPR40 介导的 Ca2+升高，IC50分别 6.28、5.96、7.07和4.58 μM。