194336
5-Aminovaleric acid hydrochloride
99%
Synonym(s):
5-Aminopentanoic acid
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About This Item
Linear Formula:
H2N(CH2)4CO2H · HCl
CAS Number:
Molecular Weight:
153.61
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22
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assay
99%
reaction suitability
reaction type: solution phase peptide synthesis
mp
95-97 °C (lit.)
application(s)
peptide synthesis
SMILES string
Cl[H].NCCCCC(O)=O
InChI
1S/C5H11NO2.ClH/c6-4-2-1-3-5(7)8;/h1-4,6H2,(H,7,8);1H
InChI key
BLOIUFYKQCCAGP-UHFFFAOYSA-N
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Anne Mengel et al.
Bioorganic & medicinal chemistry letters, 18(22), 5975-5977 (2008-08-07)
5-Aminovaleric acid and ornithine were evaluated as linkers for the cyclization of beta-dipeptides. Two linked examples of beta-Ala-beta-Ala were prepared by standard coupling methods and their conformations probed by NMR, CD, and computational means. The data suggest that these non-
Ting Lv et al.
Photodiagnosis and photodynamic therapy, 9(2), 164-169 (2012-05-19)
Topical photodynamic therapy (PDT) mediated by 5-aminolevulinic acid (ALA) has been used for the treatment of age-related skin lesions for therapeutic or cosmetic purposes. The modulation of collagen component and structure might play a significant role in influencing treatment outcomes
Olga Revelles et al.
Journal of bacteriology, 186(11), 3439-3446 (2004-05-20)
Pseudomonas putida KT2440 is a soil microorganism that attaches to seeds and efficiently colonizes the plant's rhizosphere. Lysine is one of the major compounds in root exudates, and P. putida KT2440 uses this amino acid as a source of carbon
A A Azarashvili et al.
Neuroscience and behavioral physiology, 39(2), 127-132 (2009-01-14)
Experiments on Wistar rats addressed the possibility of dissociated learning using drugs acting directly on brain GABA(B) receptors. A previously suggested hypothesis was tested: that the cholinergic system of the brain plays the decisive role in the mechanisms of dissociative
New chemotactic dimeric peptides show high affinity and potency at the human formylpeptide receptor.
Susanna Spisani et al.
European journal of pharmacology, 567(1-2), 171-176 (2007-05-08)
A number of analogues of the prototypical peptide for-Met-Leu-Phe-OMe (fMLP-OMe) have been studied in order to evaluate their ability to interact with formylpeptide receptors and to induce specific biological responses in human neutrophils. In vitro assays were carried out and
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