Others

Tegadifur (40497S) 是一种可口服的抗肿瘤化合物，具有抗新陈代谢作用，常与尿嘧啶林和治疗直肠腺癌。

CL656 is a stimulator of interferon genes (STING) activator.

Nucleoside Derivatives - 7-Deaza-purine nucleosides; 6-De-aminopurine nucleosides

2-Thiothymidine is a Nucleoside Derivative - Thio-nucleoside.

α-Cytidine 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 TNU1636，CAS号为 13913-16-1。

8-Hydroxyadenosine (8-Oxoadenosine) 是一种存在于 Torula 酵母 RNA 中的嘌呤核苷。

2-Amino-6-chloropurine -9-beta-D-(2'-deoxy-3',5'-di-O-benzoyl-2'-fluoro)arabinoriboside is a Fluoro-modified nucleoside; Halo-nucleoside; Arabino-nucleoside.

2-Amino-6-methythio-9-(beta-D-ribofuranosyl)-9H-purine is a Nucleoside Derivative - 6-Modified purine nucleoside; Thio-nucleoside.

2-Chloro-9-[(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)]-9H-purine is a Nucleoside Derivative - Halo-nucleoside, 6-Deaminopurine nucleoside.

9-(2'-O-Acetyl-5'-O-benzoyl-3'-deoxy-beta-D-ribofuranosyl)-6-chloropurine is a Nucleoside Derivative - 3'-Deoxy nucleoside, Halo-nucleoside; Scaffold and Template.

6-Chloro-2-bromo-9-(2,3,5-tri-O-acetyl)-beta-D-ribofuranosyl-9H-purine is a Nucleoside Derivative - Halo-nucleoside; Scaffold and Template.

6-Chloro-9-(2,3,5-tri-O-benzoyl-2-C-methyl-β-D-ribofuranosyl)-9H-purine is a 2'-C-Methyl nucleoside; Halo-nucleoside.

3'-O-(t-Butyldiphenylsilyl)thymidine is a Nucleoside Derivative - Protected nucleoside w/NH2/OH open.

2'-C-Methyl nucleoside; 2/6/8-modified nucleoside

5-(1-Hydroxy)(methoxycarbonyl)methyl uridine is a Nucleoside Derivative - 5-Modified pyrimidine nucleoside; Naturally modified ribo-nucleoside.

Nucleoside Derivatives - LNA-related nucleosides; Nucleoside Phosphoramidites

1-(3’-O-[4,4’-dimethoxytrityl]-alpha-L-threofuranosyl)uridine 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 TNU1627，CAS号为 325683-90-7。

6-Amino-9-[2-deoxy-β-D-ribofuranosyl]-9H-purine is a Nucleoside Derivative - Other modified nucleoside.

2'-O-MOE-rC is a Nucleoside Phosphoramidite; Nucleoside Derivative - 2'-Modified nucleoside.

5'-DMTr-dA(Bz)-Methyl phosphonamidite is a Nucleoside Derivative - phosphonamidite.

IACS-8803 is a potent cyclic dinucleotide STING agonist that exhibits strong systemic antitumor efficacy.

CV-1808 is a coronary vasodilator, antihypertensive, and antipsychotic following systemic administration in vivo. CV-1808 is an adenosine A2 receptor agonist.

Nucleoside Derivatives –Fluoro-modified nucleosides, 6-Modified purine nucleosides, 3'-Modified nucleosides

MESG, a chromophoric substrate, can be used to quantitate inorganic phosphate.

UMP-morpholidate is an intermediate of pharmaceutical synthesis by coupling.

5-Propargylamino-ddCTP 3TEA是一种ddCTP的衍生物和修饰核苷酸，可用于基因测序。ddCTP是Sanger测序中使用的链终止子之一。

N-Acetylpurinomycin is a selective agonist of CB2 receptor.

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

GS-9851, a HCV nonstructural protein 5B (NS5B) inhibitor, is used potentially for the treatment of HCV infection.

MRS 2768 tetrasodium salt is a P2Y2 agonist.

adenosine A2 receptor agonist

pdTp is a highly selective, small-molecule miRNA regulatory complex RISC subunit SND1 inhibitor.

PSB-6426 is the first potent and selective human nucleoside triphosphate diphosphohydrolase-2 inhibitor.

Ara-F-NAD+, an arabino analogue of NAD + , is a potent, slow-binding CD38 NADase inhibitor, with a K i of 169 nM.

Cytarabine triphosphate (Ara-CTP), a competitive inhibitor of DNA synthesis and an active metabolite of Cytarabine, exhibits predictive potential for leukemic blasts' chemosensitivity to Cytarabine through intracellular levels.

MB-11362, a HCV nonstructural protein 5B (NS5B) inhibitor, is used potentially for the treatment of HCV infection.