for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
A selective cAMP-dependent protein kinase (PKA) activator. Vial of 5 μmol.
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Nucleosides, nucleotides, and analogues |
| Classe | Nucleoside and nucleotide analogues |
| Subclass | 3',5'-cyclic purine nucleoside phosphorothioates |
| Intermediate Tree Nodes | Not available |
| Direct Parent | 3',5'-cyclic purine nucleoside phosphorothioates |
| Alternative Parents | Diarylthioethers Glycosylamines 6-aminopurines Thiophenol ethers Thiophosphate diesters Aminopyrimidines and derivatives Chlorobenzenes Aryl chlorides Imidolactams Monosaccharides N-substituted imidazoles Heteroaromatic compounds Oxolanes Secondary alcohols Oxacyclic compounds Sulfenyl compounds Azacyclic compounds Hydrocarbon derivatives Primary amines Organochlorides |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | 3',5'-cyclic purine nucleoside phosphorothioate - Glycosyl compound - N-glycosyl compound - Diarylthioether - 6-aminopurine - Imidazopyrimidine - Purine - Aryl thioether - Thiophenol ether - Aminopyrimidine - Chlorobenzene - Halobenzene - Thiophosphate diester - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Thiophosphoric acid ester - Imidolactam - Pyrimidine - Benzenoid - Organic thiophosphoric acid or derivatives - Azole - Oxolane - Heteroaromatic compound - Imidazole - Secondary alcohol - Sulfenyl compound - Thioether - Oxacycle - Azacycle - Organoheterocyclic compound - Amine - Organic nitrogen compound - Organosulfur compound - Organochloride - Primary amine - Alcohol - Organonitrogen compound - Hydrocarbon derivative - Organohalogen compound - Organooxygen compound - Organic oxygen compound - Aromatic heteropolycyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as 3',5'-cyclic purine nucleoside phosphorothioates. These are 3',5'-cyclic purine nucleoside phosphate analogues, where a phosphate oxygen has been exchanged for sulphur generating a chiral phosphorothioate. In 3',5'-cyclic nucleoside phosphorothioate, the oxygen atoms at the 3'- and 5'-positions of the ribose are part of the phosphorothioate group. |
| External Descriptors | Not available |
| Solubilità | Soluble in water: >1 mg/mL |
|---|---|
| Peso molecolare | 487.900 g/mol |
| XLogP3 | 2.200 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 3 |
| Exact Mass | 486.994 Da |
| Monoisotopic Mass | 486.994 Da |
| Topological Polar Surface Area | 195.000 Ų |
| Heavy Atom Count | 30 |
| Formal Charge | 0 |
| Complexity | 694.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
