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760-78-1

760-78-1 structure
760-78-1 structure

Name 2-aminopentanoic acid
Synonyms DL-NORVALINE
DL-alpha-Aminovaleric acid
Dl-n-valine
α-DL-Aminopentanoic acid
DL-2-Aminovaleric acid (T)
a-DL-Aminopentanoic acid
NORVALINE, DL
2-AMINOPENTANOIC ACID
DL-2-AMINOVALERIC ACID
a-Aminovaleric Acid
2-Aminopentanoic acid
EINECS 212-082-7
(n)-2-aminopentanoic acid
DL-α-Aminovaleric acid
H-DL-Nva-OH H-DL-L-Norvaline
UNII:V639KTF2SZ
Norvaline (VAN)
DL-ALPHA-AMINO-N-VALERICACID
2-Aminovaleric acid
DL-NORVAALINE
DL-2-Aminopentanoic acid
(2R)-2-ammoniopentanoate
H-DL-Nval-OH
(+/-)-2-AMINOPENTANOIC ACID
DL-Norvaline //BP
α-DL-aminopentanoicacid
dextro,laevo-norvaline
MFCD00064420
alpha-DL-Aminopentanoic acid
DL-Norvaline>
(R,S)-2-aminopentanoic acid
2-aminopentanoicaci
DL-A-AMINO-N-VALERIC ACID
(±)-2-Aminopentanoic acid
DL-NORVALINE SIGMA ADE
H-DL-Nva-OH
rac-norvaline
Dl-n-valine English name: DL-Norvaline
aminovaleric acid
2-aminopentanoic acid(-1)
dl-alpha-Amino-N-valenic acid
H-DL-NVA-OH
D-Norvaline/L-norvaline,(1:1)
DL-2-Aminovaleric Acid
DL-norVal-OH
DL -Norvaline
DL-2-AMINOPENTANOIC ACID
DL-Norvaline (HPLC)
rac-(2R*)-2-Aminopentanoic acid
APE
Norvaline
NVA
Valeric acid, 2-amino-, DL
NORVALINE, DL-(RG)
(±)-Norvaline
Description DL-Norvaline, a derivative of L-norvaline, L-norvaline is a non-competitive inhibitor of arginase.
Related Catalog
Target

Human Endogenous Metabolite

In Vitro DL-Norvaline, a derivative of L-norvaline[1], L-norvaline is a non-competitive inhibitor of arginase[2].
Cell Assay A murine macrophage cell line (RAW264.7) is used throughout the study, RAW264.7 cells are induced by A. actinomycetemcomitans-lipopolysaccharide, cells are incubated with various concentrations of L-norvaline or DL-norvaline (0.01, 0.1, 1, 10 mM) and 10 μg of A. actinomycetemcomitans-lipopolysaccharide. In other experiments, cells are incubated with antimurine CD14 or antimurine toll-like receptor 2 and 4 antibody at room temperature for 1 h, washed three times, and then stimulated with 10 μg of A. actinomycetemcomitans-lipopolysaccharide. All experiments are repeated three times, each consisting of triplicate cultures[1].
References

[1]. Sosroseno W, et al. Arginase activity in a murine macrophage cell line (RAW264.7) stimulated with lipopolysaccharide from Actinobacillus actinomycetemcomitans. Oral Microbiol Immunol. 2006 Jun;21(3):145-50.

[2]. El-Bassossy HM, et al. Arginase inhibition alleviates hypertension associated with diabetes: effect on endothelial dependent relaxation and NO production. Vascul Pharmacol. 2012 Nov-Dec;57(5-6):194-200.

Density 1.1±0.1 g/cm3
Boiling Point 222.9±23.0 °C at 760 mmHg
Melting Point ≥300 °C (dec.)
Molecular Formula C5H11NO2
Molecular Weight 117.146
Flash Point 88.6±22.6 °C
Exact Mass 117.078979
PSA 63.32000
LogP 0.38
Vapour Pressure 0.0±0.9 mmHg at 25°C
Index of Refraction 1.464
Storage condition Store at RT.
Water Solubility 1 g/10 mL (18 ºC)
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn
Risk Phrases R20/21/22
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 29224995
HS Code 29224995
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