| Weight | 283.244 g/mol |
|---|---|
| Formula | C10H13N5O5 |
| Hydrogen Acceptors | 9 |
| Hydrogen Donors | 5 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
guanosine (118-00-3)
Score:
#1123 in Biochemistry
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#2867 in Biology
,
#3589 in Chemistry
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- Nitric oxide-generating vasodilators and 8-bromo-cyclic guanosine monophosphate inhibit mitogenesis and proliferation of cultured rat vascular smooth muscle cells. (Journal of Clinical Investigation, 1989)
- Nitric oxide activates guanylate cyclase and increases guanosine 3:5-cyclic monophosphate levels in various tissue preparations (Proceedings of the National Academy of Sciences of the United States of America, 1977)
- Role of substrates and products of PI 3-kinase in regulating activation of Rac-related guanosine triphosphatases by Vav. (Science, 1998)
- HOW EASILY OXIDIZABLE IS DNA? ONE-ELECTRON REDUCTION POTENTIALS OF ADENOSINE AND GUANOSINE RADICALS IN AQUEOUS SOLUTION (Journal of the American Chemical Society, 1997)
- Cyclic guanosine monophosphate as a mediator of vasodilation. (Journal of Clinical Investigation, 1986)
- Natriuretic peptides, their receptors, and cyclic guanosine monophosphate-dependent signaling functions (Endocrine Reviews, 2006)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N
-
InChIKeyNYHBQMYGNKIUIF-UHFFFAOYSA-N
- Pubchem - guanosine
- Wikipedia - guanosine
Guanosine is a purine nucleoside comprising guanine attached to a ribose (ribofuranose) ring via a -N9-glycosidic bond. Guanosine can be phosphorylated to become guanosine monophosphate (GMP), cyclic guanosine monophosphate (cGMP), guanosine diphosphate (GDP), and guanosine triphosphate (GTP). These forms play important roles in various biochemical processes such as synthesis of nucleic acids and proteins, photosynthesis, muscle contraction, and intracellular signal transduction (cGMP).
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guanosine
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