| MeSH term | MeSH ID | Detail |
|---|---|---|
| Brain Neoplasms | D001932 | 15 associated lipids |
| Leukemia, Erythroblastic, Acute | D004915 | 41 associated lipids |
| Vision Disorders | D014786 | 10 associated lipids |
| Melanoma | D008545 | 69 associated lipids |
| Growth Disorders | D006130 | 5 associated lipids |
| Femoral Fractures | D005264 | 7 associated lipids |
| Hyperemia | D006940 | 25 associated lipids |
| Infection | D007239 | 6 associated lipids |
| Cell Transformation, Neoplastic | D002471 | 126 associated lipids |
| Leukemia P388 | D007941 | 43 associated lipids |
2,5-diaminopentanoic acid
2,5-diaminopentanoic acid is a lipid of Fatty Acyls (FA) class. The involved functions are known as Vasodilation, Intestinal Absorption and Pinocytosis. 2,5-diaminopentanoic acid often locates in Mitochondria, Microfilaments, NADH dehydrogenase complex and respiratory chain complex III location sensu Eukarya. The associated genes with 2,5-diaminopentanoic acid are GAPDH gene and iberiotoxin.
Cross Reference
Introduction
To understand associated biological information of 2,5-diaminopentanoic acid, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.
What diseases are associated with 2,5-diaminopentanoic acid?
There are no associated biomedical information in the current reference collection.
Possible diseases from mapped MeSH terms on references
We collected disease MeSH terms mapped to the references associated with 2,5-diaminopentanoic acid
PubChem Associated disorders and diseases
What pathways are associated with 2,5-diaminopentanoic acid
There are no associated biomedical information in the current reference collection.
PubChem Biomolecular Interactions and Pathways
Link to PubChem Biomolecular Interactions and PathwaysWhat cellular locations are associated with 2,5-diaminopentanoic acid?
Visualization in cellular structure
Associated locations are in red color. Not associated locations are in black.
Related references are published most in these journals:
| Location | Cross reference | Weighted score | Related literatures |
|---|
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What functions are associated with 2,5-diaminopentanoic acid?
Related references are published most in these journals:
| Function | Cross reference | Weighted score | Related literatures |
|---|
What lipids are associated with 2,5-diaminopentanoic acid?
There are no associated biomedical information in the current reference collection.
What genes are associated with 2,5-diaminopentanoic acid?
Related references are published most in these journals:
| Gene | Cross reference | Weighted score | Related literatures |
|---|
What common seen animal models are associated with 2,5-diaminopentanoic acid?
There are no associated biomedical information in the current reference collection.
NCBI Entrez Crosslinks
All references with 2,5-diaminopentanoic acid
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| Dunford LJ et al. | Maternal protein-energy malnutrition during early pregnancy in sheep impacts the fetal ornithine cycle to reduce fetal kidney microvascular development. | 2014 | FASEB J. | pmid:25077559 |
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| Miyake M et al. | Randomised controlled trial of the effects of L-ornithine on stress markers and sleep quality in healthy workers. | 2014 | Nutr J | pmid:24889392 |
| van der Heijden JW et al. | Methotrexate analogues display enhanced inhibition of TNF-α production in whole blood from RA patients. | 2014 | Scand. J. Rheumatol. | pmid:23987246 |
| Braissant O | GAMT deficiency: 20 years of a treatable inborn error of metabolism. | 2014 | Mol. Genet. Metab. | pmid:24275206 |
| Stockler-Ipsiroglu S et al. | Guanidinoacetate methyltransferase (GAMT) deficiency: outcomes in 48 individuals and recommendations for diagnosis, treatment and monitoring. | 2014 | Mol. Genet. Metab. | pmid:24268530 |
| Lee HH et al. | Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome: a treatable genetic liver disease warranting urgent diagnosis. | 2014 | Hong Kong Med J | pmid:24473688 |
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| Katagiri S et al. | OAT mutations and clinical features in two Japanese brothers with gyrate atrophy of the choroid and retina. | 2014 | Doc Ophthalmol | pmid:24429551 |
| Hwang GH and Cho JY | Enhancement of L-ornithine production by disruption of three genes encoding putative oxidoreductases in Corynebacterium glutamicum. | 2014 | J. Ind. Microbiol. Biotechnol. | pmid:24402505 |