D-Neopterin - ≥98%(HPLC), sum of enantiomers , CAS No.2009-64-5

CAS: 2009-64-5 Cat. No.: D137509 Fórmula: C₉H₁₁N₅O₄ Peso molecular: 253.21 Beilstein Registry Number: 89070 Número EC: 217-924-7

GRADE & PURITY ≥98%(HPLC), sum of enantiomers

Synonyms

4(8H)-pteridinone, 2-amino-6-[(1S,2R)-1,2,3-trihydroxypropyl]- | [S-(R*,S*)]-2-Amino-6-(1,2,3-trihydroxypropyl)-1H-pteridin-4-on | 2-amino-6-[(1S,2R)-1,2,3-trihydroxypropyl]-1H-pteridin-4-one | BMQYVXCPAOLZOK-XINAWCOVSA-N | AS-56644 | 6-(D-erythro-1,2,3-T

Storage

Store at 2-8°C

Shipped In

Wet ice

Descripción general

D-Neopterin is a precursor of tetrahydrobiopterin and can be used as a biochemical marker indicative of cell proliferation. Elevated levels of D-Neopterin are correlated to immune system activation, malignant disease, allograft rejection, and viral infections. Additionally, D-Neopterin serves as a cofactor for pterin in biological systems.

Specifications

Sinónimos

4(8H)-pteridinone, 2-amino-6-[(1S,2R)-1,2,3-trihydroxypropyl]- | [S-(R*,S*)]-2-Amino-6-(1,2,3-trihydroxypropyl)-1H-pteridin-4-on | 2-amino-6-[(1S,2R)-1,2,3-trihydroxypropyl]-1H-pteridin-4-one | BMQYVXCPAOLZOK-XINAWCOVSA-N | AS-56644 | 6-(D-erythro-1,2,3-T

Especificaciones y pureza

≥98%(HPLC), sum of enantiomers

Mecanismos bioquímicos y fisiológicos

Pterin cofactor; precursor of BH4 (tetrahydrobiopterin).Prognostic marker of immunodeficiency. Precursor of biopterin . Synthesized in response to interferon-γ stimulation. Indicates level of activation of T helper cell 1 derived cellular immune activatio

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

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Nota

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Pureza

≥98%(HPLC)

Nombres e identificadores

Pubchem Sid

504773243

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504773243

Sonrisas canónicas

C1=C(N=C2C(=O)NC(=NC2=N1)N)C(C(CO)O)O

IUPAC Name

2-amino-6-[(1S,2R)-1,2,3-trihydroxypropyl]-3H-pteridin-4-one

InChIKey

BMQYVXCPAOLZOK-XINAWCOVSA-N

INCHI

1S/C9H11N5O4/c10-9-13-7-5(8(18)14-9)12-3(1-11-7)6(17)4(16)2-15/h1,4,6,15-17H,2H2,(H3,10,11,13,14,18)/t4-,6+/m1/s1

Isómeros SMILES

C1=C(N=C2C(=O)NC(=NC2=N1)N)[C@@H]([C@@H](CO)O)O

WGK Alemania

3

Peso molecular

253.21

Beilstein

89070

Reaxy-Rn

258082

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=258082&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Pteridines and derivatives
      • Subclass Pterins and derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Pteridines and derivatives
• Subclass: Pterins and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Biopterins and derivatives
• Alternative Parents: Pyrimidones Aminopyrimidines and derivatives Pyrazines Vinylogous amides Heteroaromatic compounds Secondary alcohols Polyols Azacyclic compounds Primary amines Primary alcohols Organopnictogen compounds Organic oxides Hydrocarbon derivatives Aromatic alcohols
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Biopterin - Aminopyrimidine - Pyrimidone - Pyrazine - Pyrimidine - Heteroaromatic compound - Vinylogous amide - Secondary alcohol - Polyol - Azacycle - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Primary amine - Primary alcohol - Alcohol - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Aromatic alcohol - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as biopterins and derivatives. These are coenzymes containing a 2-amino-pteridine-4-one derivative. They are mainly synthesized in several parts of the body, including the pineal gland.
• 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

• Solubilidad: Soluble in DMSO (20 mM, with gentle warming), 0.05M NaOH, 1M HCl, aqueous acid, and water (very slightly). Ultrasonication may improve the dissolution.
• Peso molecular: 253.220 g/mol
• XLogP3: -3.500
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 3
• Exact Mass: 253.081 Da
• Monoisotopic Mass: 253.081 Da
• Topological Polar Surface Area: 154.000 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 363.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• 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