 Niacinamide
"Niacinamide" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An important compound functioning as a component of the coenzyme NAD. Its primary significance is in the prevention and/or cure of blacktongue and PELLAGRA. Most animals cannot manufacture this compound in amounts sufficient to prevent nutritional deficiency and it therefore must be supplemented through dietary intake.
| Descriptor ID |
D009536
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| MeSH Number(s) |
D03.066.515.530 D03.383.725.547.530
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| Concept/Terms |
Niacinamide- Niacinamide
- Vitamin PP
- Vitamin B 3
- B 3, Vitamin
- Vitamin B3
- B3, Vitamin
- 3-Pyridinecarboxamide
- 3 Pyridinecarboxamide
- Nicotinamide
Papulex- Papulex
- Pharmagenix Brand of Niacinamide
- Niacinamide Pharmagenix Brand
Nicotinsäureamid Jenapharm- Nicotinsäureamid Jenapharm
- Jenapharm, Nicotinsäureamid
- Jenapharm Brand of Niacinamide
- Niacinamide Jenapharm Brand
Nicobion- Nicobion
- Merck Brand of Niacinamide
- Niacinamide Merck Brand
- Astra Brand of Niacinamide
- Niacinamide Astra Brand
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Below are MeSH descriptors whose meaning is more general than "Niacinamide".
Below are MeSH descriptors whose meaning is more specific than "Niacinamide".
This graph shows the total number of publications written about "Niacinamide" by people in this website by year, and whether "Niacinamide" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2008 | 0 | 1 | 1 |
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Below are the most recent publications written about "Niacinamide" by people in Profiles.
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Bi J, Li H, Ye SQ, Ding S. Pre-B-cell colony-enhancing factor exerts a neuronal protection through its enzymatic activity and the reduction of mitochondrial dysfunction in in vitro ischemic models. J Neurochem. 2012 Jan; 120(2):334-46.
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Dumitrescu CE, Kelly MH, Khosravi A, Hart TC, Brahim J, White KE, Farrow EG, Nathan MH, Murphey MD, Collins MT. A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic features. Osteoporos Int. 2009 Jul; 20(7):1273-8.
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