5-iodo-a85380 dihydrochloride

α4β2 and α6β2 nicotinic acetylcholine receptors agonist

SRT 1720 is a selective activator of SIRT1 (EC1.5: 0.16 μM) and shows less potent activities on SIRT2 (EC1.5: 37 μM) and SIRT3 (EC1.5: 300 μM).

5-Iodo-indirubin-3'-monoxime is a potent inhibitor of GSK-3β, CDK5 P25, and CDK1 cyclin B, competing with ATP for binding to the catalytic site of the kinase (IC50s: 9, 20, and 25 nM).

CRT0066101 dihydrochloride is an inhibitor of PKD.

2-Amino-4-chloro-5-iodo-N2-pivaloyl-7-[2-deoxy-3,5-di-O- (4-methylbenzoyl)-b-D-ribofuanosyl]-7H-pyrrolo[2,3-d]pyrimidine is a Nucleoside Derivative - 7-Deazapurine nucleoside; Halo-nucleoside.

Benzamidine, 5-amino-2-(octyloxy)-, dihydrochloride is a bioactive chemical.

N-(4-Chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-2-yl)-2,2-dimethyl propanamide belongs to Heterocyclic Compounds - Purine; Intermediates and Building Blocks - Nucleoside base, Electrophile; Scaffold and Template.

5-Iodo-2'-O-methylcytidine is a Halo-nucleoside; 2'-O-Methyl nucleoside.

Nucleoside Derivatives - Halo-nucleosides, 5’-Modified nucleosides, 2’-Modified nucleosides

5-Iodo-3'-deoxy-3'-fluorouridine is a Nucleoside, fluoro-modified nucleoside, halo-nucleoside.

5-Fluoromethylornithine dihydrochloride (5-FMOrn dihydrochloride) is a selective inhibitor of L-Ornithine:2-oxoacid aminotransferase (OAT) and a specific inactivator of OAT, which can be used to study metabolic diseases and neurological diseases.

5'-O-(Tert-butyldimethylsilyl)-5-iodo-2'-deoxycytidine is a useful organic compound for research related to life sciences. The catalog number is T67323 and the CAS number is 666848-11-9.

Nucleoside Derivatives - 5’-Modified nucleosides, Halo-nucleosides, 2’-Modified nucleosides

4-Chloro-5-iodo-7-(2-deoxy-b-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine is a Nucleoside Derivative - Halo-nucleoside, 7-Deaza-purine nucleoside.

4-Chloro-5-iodo-7-(2-deoxy-3,5-bis-O-(p-toluoyl)-b-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine is a useful organic compound for research related to life sciences and the catalog number is TNU1024.

5'-O-t-Butyldimethylsilyl 2'-deoxy-5-iodo-uridine is a Halo-nucleoside; 2'-deoxy nucleoside.

5'-Deoxy-5'-iodo-2'-O-(2-methoxyethyl)-5-methyluridine is a Nucleoside Derivative - 5'-Modified nucleoside; Halo-nucleoside; 2'-Modified nucleoside.

Heterocyclic compound - purine; Intermediate and building blocks– electrophile and nucleophile; Nucleoside base

5'-Deoxy-5'-iodo-2'-O-(2-methoxyethyl)uridine is a Nucleoside Derivative - 5'-Modified nucleoside; Halo-nucleoside; 2'-Modified nucleoside.

4-Amino-5-iodo-7-(2-b-C-methyl-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine is a nucleoside derivative, specifically a 7-deaza-purine nucleoside with 2'-modifications. It is also categorized as a halo-nucleoside and serves as both a scaffold and template.

AMG-548 dihydrochloride is an orally active and selective p38α inhibitor (Ki: 0.5 nM) and shows slightly selective over p38β (Ki: 36 nM) and >1000 fold selective against p38γ/p38δ. It is also extremely potent in the inhibition of whole blood LPS stimulate

2-Benzyloxy-5-iodo-3-methylpyridine belongs to Heterocyclic Compounds - Pyridine; Intermediates and Building Blocks - Electrophile.

2-(((4-Methyl-1H-imidazol-5-yl)methyl)thio)ethanamine dihydrochloride is a useful organic compound for research related to life sciences. The catalog number is T67105 and the CAS number is 38603-72-4.

5-Iodo-2'-C-methyl cytidine is a 2'-C-Methyl nucleoside; Halo-nucleoside.

5'-Deoxy-5'-iodo-5-methyluridine is a Nucleoside Derivative - 5'-Modified nucleoside, Halo-nucleoside.

5'-O-DMTr-5-Iodo-2'-deoxyuridine is a Halo-nucleoside.

5-Iodo-2'-C-methyl uridine is a 2'-C-Methyl nucleoside; Halo-nucleoside.

Nucleoside Derivatives - 2’,3’-Dideoxy nucleosides; Halo-nucleosides; 5-Modified pyrimidine nucleosides; Drugs and Inhibitors; tracheitis virus test; herpes simplex keratitis drug

PARP1-IN-5 dihydrochloride is an orally active, potent and selective PARP-1 inhibitor (IC50 =14.7 nM). PARP1-IN-5 dihydrochloride can be used for the research of cancer.