N-acetil-L-tirosina amida - ≥98% , CAS No.1948-71-6

CAS: 1948-71-6 Cat. No.: N305300 Peso molecular: 222.24 Número EC: 217-756-4

GRADE & PURITY ≥98%

Synonyms

UNII-X315200H5U | Ac-L-Tyr-NH2 | MFCD00002391 | AMY25330 | (S)-2-acetamido-3-(4-hydroxyphenyl)propanamide | 2-(Acetylamino)-3-(4-hydroxyphenyl)propanamide # | Acetyl-L-tyrosinamid | SCHEMBL468899 | N-.alpha.-Acetyl-L-tyrosinamide | AKOS024257969 | Benzene

Storage

Conservar a 2-8°C

Shipped In

Hielo húmedo

Specifications

Sinónimos

UNII-X315200H5U | Ac-L-Tyr-NH2 | MFCD00002391 | AMY25330 | (S)-2-acetamido-3-(4-hydroxyphenyl)propanamide | 2-(Acetylamino)-3-(4-hydroxyphenyl)propanamide # | Acetyl-L-tyrosinamid | SCHEMBL468899 | N-.alpha.-Acetyl-L-tyrosinamide | AKOS024257969 | Benzene

Especificaciones y pureza

≥98%

Mecanismos bioquímicos y fisiológicos

Análogo de la L-tirosina. Muestra espectros de absorción y emisión específicos distintos de la L-tirosina. Estimula el transporte de L-Tyr principalmente por el sistema ASC.

Condiciones de almacenamiento de almacenamiento

Conservar a 2-8°C

Enviado en

Hielo húmedo

Nota

Siempre que sea posible, prepare y utilice las soluciones el mismo día. Sin embargo, si necesita preparar soluciones madre con antelación, le recomendamos que almacene la solución como alícuotas en viales herméticamente cerrados a -20°C. Por lo general, podrán utilizarse durante un mes. Antes de su uso, y antes de abrir el vial, le recomendamos que deje que el producto se equilibre a temperatura ambiente durante al menos 1 hora. ¿Necesita más consejos sobre solubilidad, uso y manipulación? Visite nuestra página de preguntas frecuentes (FAQ) para obtener más información.

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504760034
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504760034
• Sonrisas canónicas: CC(=O)NC(CC1=CC=C(C=C1)O)C(=O)N
• IUPAC Name: (2S)-2-acetamido-3-(4-hydroxyphenyl)propanamide
• InChIKey: RJNKBEQRBIJDNM-JTQLQIEISA-N
• INCHI: 1S/C11H14N2O3/c1-7(14)13-10(11(12)16)6-8-2-4-9(15)5-3-8/h2-5,10,15H,6H2,1H3,(H2,12,16)(H,13,14)/t10-/m0/s1
• Isómeros SMILES: CC(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N
• Peso molecular: 222.24
• Reaxy-Rn: 2809786
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2809786&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 Tyrosine and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives
• Direct Parent: Tyrosine and derivatives
• Alternative Parents: Phenylalanine and derivatives N-acyl-alpha amino acids and derivatives Amphetamines and derivatives 1-hydroxy-2-unsubstituted benzenoids Fatty amides Acetamides Secondary carboxylic acid amides Primary carboxylic acid amides Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Tyrosine or derivatives - Phenylalanine or derivatives - N-acyl-alpha amino acid or derivatives - Amphetamine or derivatives - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Fatty amide - Benzenoid - Fatty acyl - Acetamide - Secondary carboxylic acid amide - Primary carboxylic acid amide - Carboxamide group - Organic nitrogen compound - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as tyrosine and derivatives. These are compounds containing tyrosine or a derivative thereof resulting from reaction of tyrosine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Punto de inflamación (°C): 231.7ºC
• Punto de ebullición (°C): 459.5ºC
• Punto de fusión (°C): 223-225ºC
• Peso molecular: 222.240 g/mol
• XLogP3: -0.900
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 222.1 Da
• Monoisotopic Mass: 222.1 Da
• Topological Polar Surface Area: 92.400 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 260.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1