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≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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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.
2-Thiocytidine is a nucleoside base that has been isolated from hydrolyzates of|Escherichia coli|tRNA.
2-thiactidine is a nucleoside base isolated from the hydrolysate of E. coli | tRNA;
2-Thiocytidine is a purine nucleoside analogue. Purine nucleoside analogues have extensive antitumor activity and target malignant tumors of the inert lymphatic system. The anti-cancer mechanism in this process depends on inhibition of DNA synthesis, induction of apoptosis, etc
Application:
2-Thiocytidine is a cytidine analogue. A profiled metabolite in HFD-induced obese mice after oral administration of Huangjinya green tea extract.
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 |
| Class | Pyrimidine nucleosides |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Pyrimidine nucleosides |
| Alternative Parents | Glycosylamines Pentoses Pyrimidinethiones Aminopyrimidines and derivatives Imidolactams Hydropyrimidines Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Organopnictogen compounds Organosulfur compounds Primary alcohols Primary amines |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Aminopyrimidine - Pyrimidinethione - Hydropyrimidine - Monosaccharide - Pyrimidine - Imidolactam - Heteroaromatic compound - Tetrahydrofuran - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Organopnictogen compound - Organic oxygen compound - Primary alcohol - Primary amine - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as pyrimidine nucleosides. These are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety. |
| External Descriptors | cytidines |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Jul 22, 2023 | T339732 | |
| Certificate of Analysis | Jul 22, 2023 | T339732 | |
| Certificate of Analysis | Jul 22, 2023 | T339732 | |
| Certificate of Analysis | Jul 22, 2023 | T339732 | |
| Certificate of Analysis | Jul 22, 2023 | T339732 | |
| Certificate of Analysis | Jul 22, 2023 | T339732 | |
| Certificate of Analysis | Jul 22, 2023 | T339732 | |
| Certificate of Analysis | Jul 22, 2023 | T339732 | |
| Certificate of Analysis | Jul 22, 2023 | T339732 |
| Solubility | Methanol (Slightly);Water (Slightly);DMSO: 1 mg/ml,DMSO:PBS (pH 7.2) (1:6): 0.14 mg/ml,PBS (pH 7.2): slightly soluble |
|---|---|
| Sensitivity | Moisture Sensitive |
| Molecular Weight | 259.279 g/mol |
| XLogP3 | -1.500 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 2 |
| Exact Mass | 259.063 Da |
| Monoisotopic Mass | 259.063 Da |
| Topological Polar Surface Area | 144.000 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 386.000 |
| 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 |