| Weight | 334.221 g/mol |
|---|---|
| Formula | C11H15N2O8P |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 5 |
nicotinamide mononucleotide (1094-61-7)
Score:
#1685 in Biochemistry
,
#3770 in Biology
,
#4747 in Chemistry
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- Nicotinamide mononucleotide activation of a new DNA-dependent polyadenylic acid synthesizing nuclear enzyme (Biochemical and Biophysical Research Communications, 1963)
- Nicotinamide Mononucleotide, a Key NAD+ Intermediate, Treats the Pathophysiology of Diet- and Age-Induced Diabetes in Mice (Cell Metabolism, 2011)
- Subcellular Compartmentation and Differential Catalytic Properties of the Three Human Nicotinamide Mononucleotide Adenylyltransferase Isoforms (Journal of Biological Chemistry, 2005)
- Perivascular adipose tissue-derived visfatin is a vascular smooth muscle cell growth factor: role of nicotinamide mononucleotide (Cardiovascular Research, 2009)
- Nicotinamide Mononucleotide Adenylyl Transferase-Mediated Axonal Protection Requires Enzymatic Activity But Not Increased Levels of Neuronal Nicotinamide Adenine Dinucleotide (The Journal of Neuroscience, 2009)
- ENZYMATIC SYNTHESIS OF NICOTINAMIDE MONONUCLEOTIDE (Journal of Biological Chemistry, 1957)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC1=CC(=C[N+](=C1)C2C(C(C(O2)COP(=O)(O)[O-])O)O)C(=O)N
-
InChIKeyDAYLJWODMCOQEW-UHFFFAOYSA-N
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