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3-Nitro-L-tyrosine

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3-Nitro-L-tyrosine manufacturers

3-Nitro-L-tyrosine Basic information
Product Name:3-Nitro-L-tyrosine
Synonyms:(2R)-2-Amino-3-(4-hydroxy-3-nitrophenyl)propanoic acid;L-Tyrosine, 3-nitro-;3-Nitro-L-tyrosine,99%;(S)-2-aMino-3-(4-hydroxy-3-nitrophenyl)propanoic acid;Z-D-Dap(Boc);3-NITRO-L-TYROSINE (RING-13C6);(S)-3-(3-Nitro-4-hydroxyphenyl)alanine;3-Nitro-L-tyrosine≥ 98% (Assay)
CAS:621-44-3
MF:C9H10N2O5
MW:226.19
EINECS:210-688-6
Product Categories:Pharmaceutical Raw Materials;Amino Acids;Tyrosine [Tyr, Y];Unusual Amino Acids;Oxidative Stress Proteins and ReagentsPeptide Synthesis;Cell Stress;Nitric Oxide and Cell Stress;Amino Acids & Derivatives;Aromatics;Peptide Synthesis;Tyrosine Derivatives;Unnatural Amino Acid Derivatives
Mol File:621-44-3.mol
3-Nitro-L-tyrosine Structure
3-Nitro-L-tyrosine Chemical Properties
Melting point 233-235 °C (dec.) (lit.)
alpha 4 º (c=1, 1N HCl)
Boiling point 367.79°C (rough estimate)
density 1.4160 (rough estimate)
refractive index 1.5373 (estimate)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Aqueous Acid (Slightly), Water
pka2.17±0.20(Predicted)
form crystalline
color yellow to green
Water Solubility insoluble
BRN 2813157
InChIInChI=1S/C9H10N2O5/c10-6(9(13)14)3-5-1-2-8(12)7(4-5)11(15)16/h1-2,4,6,12H,3,10H2,(H,13,14)/t6-/m0/s1
InChIKeyFBTSQILOGYXGMD-LURJTMIESA-N
SMILESC(O)(=O)[C@H](CC1=CC=C(O)C([N+]([O-])=O)=C1)N
CAS DataBase Reference621-44-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 24/25-37/39-26-36
WGK Germany 3
HS Code 29225090
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
3-Nitro-L-tyrosine English
SigmaAldrich English
ACROS English
ALFA English
3-Nitro-L-tyrosine Usage And Synthesis
DescriptionNitrotyrosine is formed by peroxynitrite-mediated nitration of protein tyrosine residues. Its presence on proteins can be used as a marker for peroxynitrite formation in vivo. Both free and protein-bound nitrotyrosine are commonly found in mammalian tissues and are increased in pathological conditions. The basal levels of free nitrotyrosine in human plasma is approximately 3 nM as determined by gas chromatography/mass spectrometry.
Chemical Propertiesochre-yellow to yellow-green powder
UsesA marker for peroxynitrite. Oxidant and cytotoxic agent.
Uses3-Nitro-L-tyrosine is used as an indicator of the formation of peroxynitrite by NO-dependent oxidative damage.
DefinitionChEBI: 3-nitro-L-tyrosine is a 3-nitrotyrosine comprising L-tyrosine having a nitro group at the 3-position on the phenyl ring. It is a L-tyrosine derivative, a non-proteinogenic L-alpha-amino acid and a 3-nitrotyrosine. It is an enantiomer of a 3-nitro-D-tyrosine.
Biochem/physiol ActionsOxidant and cytotoxic agent.
References[1] J S BECKMAN  W H K. Nitric oxide, superoxide, and peroxynitrite: the good, the bad, and ugly.[J]. American Journal of Physiology, 1996, 271 5 Pt 1: C1424-37. DOI: 10.1152/ajpcell.1996.271.5.c1424
[2] J S BECKMANN. Extensive nitration of protein tyrosines in human atherosclerosis detected by immunohistochemistry.[J]. Biological chemistry Hoppe-Seyler, 1994, 375 2: 81-88. DOI: 10.1515/bchm3.1994.375.2.81
[3] K ABE. Upregulation of protein-tyrosine nitration in the anterior horn cells of amyotrophic lateral sclerosis.[J]. Neurological Research, 1997, 19 2: 124-128. DOI: 10.1080/01616412.1997.11740784
[4] ROBERT J. FERRANTE PHD.  Leslie A S PhD, MD. Increased 3-nitrotyrosine and oxidative damage in mice with a human copper/zinc superoxide dismutase mutation[J]. Annals of Neurology, 2004, 42 3: 326-334. DOI: 10.1002/ana.410420309
[5] I Y HADDAD. Quantitation of nitrotyrosine levels in lung sections of patients and animals with acute lung injury.[J]. Journal of Clinical Investigation, 1994, 94 6: 2407-2413. DOI: 10.1172/jci117607
[6] M. OHYA. Plasma Nitrotyrosine Concentration Relates to Prognosis in Human Septic Shock[J]. SHOCK, 2002, 18 1: 116-118. DOI: 10.1097/00024382-200208000-00004
[7] DIMITRIOS TSIKAS. Accurate quantification of basal plasma levels of 3-nitrotyrosine and 3-nitrotyrosinoalbumin by gas chromatography–tandem mass spectrometry[J]. Journal of Chromatography B, 2003, 784 1: Pages 77-90. DOI: 10.1016/s1570-0232(02)00751-1
[8] EDZARD SCHWEDHELM. Gas Chromatographic–Tandem Mass Spectrometric Quantification of Free 3-Nitrotyrosine in Human Plasma at the Basal State[J]. Analytical biochemistry, 1999, 276 2: Pages 195-203. DOI: 10.1006/abio.1999.4361
[9] JIAN LIU  Steven G L. High-fat, low-carbohydrate diet alters myocardial oxidative stress and impairs recovery of cardiac function after ischemia and reperfusion in obese rats[J]. Nutrition Research, 2013, 33 4: Pages 311-321. DOI: 10.1016/j.nutres.2013.02.005
3-Nitro-L-tyrosine Preparation Products And Raw materials
Tag:3-Nitro-L-tyrosine(621-44-3) Related Product Information
L-Tyrosine Boc-D-Tyr-OH H-Arg-Arg-Leu-Ile-Glu-Asp-Asn-Glu-Tyr-Thr-Ala-Arg-Gly-OH Nitrogen dioxide N-Acetyl-3,5-dinitro-L-tyrosine 3-Nitro-L-tyrosine ethyl ester hydrochloride Fmoc-3-nitro-L-tyrosine 3,5-Dinitro-L-tyrosine monohydrate 3-Nitro-D-tyrosine 3,5-Dinitro-L-tyrosine monohydrate, 97 Boc-3-nitro-L-tyrosine Ac-3,5-dinitro-Tyr-OEt Abz-Ser-Pro-3-nitro-Tyr-OH N-Acetyl-L-3-nitrotyrosine ethyl ester Boc-Tyr(Bzl, 3-NO2)-OH Fmoc-3,5-dinitro-Tyr-OH (S)-2-Amino-3-(4-hydroxy-3-nitro-phenyl)-propionic acid methyl ester 3,5-Dinitro-L-tyrosine sodium salt