CAS 789-61-7
:2′-Deoxy-6-thioguanosine
Description:
2′-Deoxy-6-thioguanosine is a nucleoside analog that features a thiol group at the 6-position of the guanine base, replacing the typical oxygen found in standard nucleosides. This modification imparts unique biochemical properties, making it of interest in various fields, including medicinal chemistry and molecular biology. The compound consists of a deoxyribose sugar linked to a modified guanine base, which can participate in nucleic acid synthesis and potentially interfere with normal cellular processes. Its structure allows it to be incorporated into DNA, where it may affect replication and transcription. 2′-Deoxy-6-thioguanosine has been studied for its potential therapeutic applications, particularly in the context of antiviral and anticancer treatments, as it can mimic natural nucleosides and disrupt the function of nucleic acids in pathogens or cancer cells. Additionally, its unique thiol group can participate in redox reactions, influencing cellular signaling pathways. Overall, this compound represents a significant area of research due to its potential to modulate biological systems.
Formula:C10H13N5O3S
InChI:InChI=1S/C10H13N5O3S/c11-10-13-8-7(9(19)14-10)12-3-15(8)6-1-4(17)5(2-16)18-6/h3-6,16-17H,1-2H2,(H3,11,13,14,19)/t4-,5+,6+/m0/s1
InChI key:InChIKey=SCVJRXQHFJXZFZ-KVQBGUIXSA-N
SMILES:S=C1C2=C(N(C=N2)[C@@H]3O[C@H](CO)[C@@H](O)C3)NC(N)=N1
Synonyms:- 2′-Deoxythioguanosine
- Thioguanine deoxyriboside
- Guanosine, 2′-deoxy-6-thio-
- 2′-Deoxy-6-thioguanosine
- 9H-Purine-6(1H)-thione, 2-amino-9-(2-deoxy-β-D-erythro-pentofuranosyl)-
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Found 10 products.
6-Thio-2'-Deoxyguanosine
CAS:Formula:C10H13N5O3SPurity:98%Color and Shape:SolidMolecular weight:283.30696-Thio-2'-Deoxyguanosine
CAS:6-Thio-2'-Deoxyguanosine (β-TGdR) is a nucleoside analog and telomerase substrate.Formula:C10H13N5O3SPurity:97.52%Color and Shape:SolidMolecular weight:283.312'-Deoxy-6-thio Guanosine
CAS:Controlled Product<p>Applications Guanosine (G837900) derivative with cancer chemotherapeutic properties. It is involved in the inhibition of human RNase H-mediated RNA cleavage from DNA-RNA duplexes via incorporation into DNA.<br>References Momparler, R.L. et al.: Cancer Treat. Rep., 62, 135 (1978); Krynetskaia, N.F. et al.: Mol. Pharmacol., 56, 841 (1999);<br></p>Formula:C10H13N5O3SColor and Shape:NeatMolecular weight:283.312'-Deoxy-6-thioguanosine
CAS:2'-Deoxy-6-thioguanosine is a purine nucleoside analog that inhibits the activation of transcription factors such as nuclear factor kappa-B (NF-κB) and activator protein 1 (AP-1). It also inhibits the synthesis of proinflammatory cytokines, such as IL-1β, IL-6, and TNFα. The matrix effect is an important factor in the prevention of tumor progression. 2'-Deoxy-6-thioguanosine has been shown to inhibit cell proliferation and induce apoptosis in squamous cell carcinoma cells by modulating the expression of HLA class II molecules on tumors. It also prevents invasion by blocking matrix metalloproteinase activity. 2'-Deoxy-6-thioguanosine has been found to be effective against bowel diseases such as ulcerative colitis and Crohn's disease, as well as infectious diseases such as HIV/AIDS.Formula:C10H13N5O3SPurity:Min. 97 Area-%Color and Shape:PowderMolecular weight:283.31 g/mol2'-Deoxy-6-thioguanosine - Bio-X ™
CAS:This product is part of our Bio-X ™ Range. These products are aimed at life science researchers who need high quality ready-to-use products for assay development, screening or other R&D work. With a solubility datasheet and convenient vials, all of our Bio-X ™ products are in stock across our global warehouses for rapid delivery and ease of use.Formula:C10H13N5O3SPurity:Min. 95%Color and Shape:PowderMolecular weight:283.31 g/mol2'-Deoxy-6-thio Guanosine-13C, 15N2
CAS:Controlled Product<p>Applications 2'-Deoxy-6-thio Guanosine-13C, 15N2 is labelled 2'-Deoxy-6-thio Guanosine (D281650) which is a Guanosine (G837900) derivative with cancer chemotherapeutic properties. It is involved in the inhibition of human RNase H-mediated RNA cleavage from DNA-RNA duplexes via incorporation into DNA.<br>References Momparler, R.L. et al.: Cancer Treat. Rep., 62, 135 (1978); Krynetskaia, N.F. et al.: Mol. Pharmacol., 56, 841 (1999)<br></p>Formula:CC9H1315N2N3O3SColor and Shape:NeatMolecular weight:286.286







