CAS 4105-39-9

2-(methylsulfanyl)-9-pentofuranosyl-9H-purin-6-amine

Description:

2-(Methylsulfanyl)-9-pentofuranosyl-9H-purin-6-amine, with the CAS number 4105-39-9, is a purine derivative that features a methylsulfanyl group and a pentofuranosyl moiety. This compound is characterized by its structural complexity, which includes a purine base, a sugar component, and a sulfur-containing substituent. The presence of the methylsulfanyl group can influence the compound's biological activity and solubility, potentially enhancing its interaction with biological targets. As a purine analog, it may play a role in nucleic acid metabolism or serve as a substrate or inhibitor in various biochemical pathways. The compound's properties, such as solubility, stability, and reactivity, are influenced by its functional groups and overall molecular structure. It is important in research contexts, particularly in studies related to nucleoside analogs and their therapeutic applications. Further investigation into its pharmacological properties and mechanisms of action could provide insights into its potential uses in medicinal chemistry.

Formula: C₁₁H₁₅N₅O₄S

InChI: InChI=1/C11H15N5O4S/c1-21-11-14-8(12)5-9(15-11)16(3-13-5)10-7(19)6(18)4(2-17)20-10/h3-4,6-7,10,17-19H,2H2,1H3,(H2,12,14,15)

SMILES: CSc1nc(c2c(n1)n(cn2)C1C(C(C(CO)O1)O)O)N

2-Methylthioadenosine

CAS: 4105-39-9

2-Methylthioadenosine

Purity: 98%

Molecular weight: 313.33g/mol

Ref: 54-OR1032006

2-Methylthioadenosine

CAS: 4105-39-9

Ref: 7W-GN5875

2-Methylthioadenosine

CAS: 4105-39-9

Nucleoside Derivatives - 2-Modified purine nucleosides; Drugs and Inhibitors; Platelet ADP receptor

Formula: C₁₁H₁₅N₅O₄S

Color and Shape: Solid

Molecular weight: 313.33

Ref: TM-TNU0255

Zeatin Impurity 1

CAS: 4105-39-9

Formula: C₁₁H₁₅N₅O₄S

Molecular weight: 313.33

Ref: 4Z-Z-029012

2-Methylthioadenosine

Controlled Product

CAS: 4105-39-9

Formula: C₁₁H₁₅N₅O₄S

Color and Shape: Neat

Molecular weight: 313.333

Ref: TR-M211450

2-Methylthioadenosine

CAS: 4105-39-9

2-Methylthioadenosine is a purine nucleoside which induces necrotic cell death. It is the first of its kind to be shown to have activity against squamous carcinoma cells, and is activated by nucleoside phosphorylase in order to produce its cytotoxic form. 2-Methylthioadenosine also inhibits the transcription-polymerase chain reaction and increases oxidative injury. This drug has been shown to have receptor activity in brain cells, as well as chemotactic activity for gland cells. 2-Methylthioadenosine has been used as a model organism for polymerase chain reactions, and has been shown to inhibit p2y receptors in the human colon cancer cell line HT29.

Formula: C₁₁H₁₅N₅O₄S

Purity: Min. 95%

Color and Shape: White Off-White Powder

Molecular weight: 313.34 g/mol

Ref: 3D-NM09610