2922-74-9
2922-74-9
Chemical Structure
2′-Deoxyadenosine 5′-monophosphate disodium
- CAS No.: 2922-74-9
- Formula:C10H12N5Na2O6P
- Molecular Weight:375.19
IUPAC Name: sodium ((2R,3S,5R)-5-(6-amino-9H-purin-9-yl)-3-hydroxytetrahydrofuran-2-yl)methyl phosphate
InChIKey: SNYHHRDGEJPLGT-OJSHLMAWSA-L
SMILES: O[C@H]1C[C@H](N2C(N=CN=C3N)=C3N=C2)O[C@@H]1COP(O[Na])(O[Na])=O
Biological Activity: 2′-Deoxyadenosine 5′-monophosphate disodium, a nucleic acid AMP derivative, is a deoxyribonucleotide found in DNA. 2′-Deoxyadenosine 5′-monophosphate disodium can be used to study adenosine-based interactions during DNA synthesis and DNA damage[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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2′-Deoxyadenosine 5′-monophosphate disodium | 99.31% | 2′-Deoxyadenosine 5′-monophosphate disodium, a nucleic acid AMP derivative, is a deoxyribonucleotide found in DNA. 2′-Deoxyadenosine 5′-monophosphate disodium can be used to study adenosine-based interactions during DNA synthesis and DNA damage. | ||||||||||||||||||||
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2′-Deoxyadenosine 5′-monophosphate disodium (Standard) | ≥98% | Halofuginone (Standard) is the analytical standard of Halofuginone. This product is intended for research and analytical applications. Halofuginone (RU-19110), a Febrifugine derivative, is a competitive prolyl-tRNA synthetase inhibitor with a Ki of 18.3 nM. Halofuginone is a specific inhibitor of type-I collagen synthesis and attenuates osteoarthritis (OA) by inhibition of TGF-β activity. Halofuginone is also a potent pulmonary vasodilator by activating Kv channels and blocking voltage-gated, receptor-operated and store-operated Ca2+ channels. Halofuginone has anti-malaria, anti-inflammatory, anti-cancer, anti-fibrosis effects. | ||||||||||||||||||||
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2′-Deoxyadenosine 5′-monophosphate-13C10,15N5 disodium | 2′-Deoxyadenosine 5′-monophosphate-13C10,15N5 (disodium) is the 13C and 15N labeled 2′-Deoxyadenosine 5′-monophosphate disodium. 2′-Deoxyadenosine 5′-monophosphate disodium, a nucleic acid AMP derivative, is a deoxyribonucleotide found in DNA. 2′-Deoxyadenosine 5′-monophosphate disodium can be used to study adenosine-based interactions during DNA synthesis and DNA damage. | |||||||||||||||||||||
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References
