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Cité dans 0 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Spécifications

Synonymes

Spécifications et pureté

≥98%

Mécanismes biochimiques et physiologiques

Competitive group I metabotropic glutamate receptor antagonist and inhibitor of phosphoserine phosphatase.

Conditions de stockage de stockage

Store at -20°C

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Type d'action

ANTAGONIST

Pureté

≥98%

Noms et identifiants

Pubchem Sid

504750721

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504750721

Sourires canoniques

C(C(C(=O)O)N)P(=O)(O)O

IUPAC Name

2-amino-3-phosphonopropanoic acid

InChIKey

LBTABPSJONFLPO-UHFFFAOYSA-N

INCHI

1S/C3H8NO5P/c4-2(3(5)6)1-10(7,8)9/h2H,1,4H2,(H,5,6)(H2,7,8,9)

Isomères SMILES

C(C(C(=O)O)N)P(=O)(O)O

CAS alternatif

20263-06-3

Poids moléculaire

169.07

Reaxy-Rn

2253277

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2253277&ln=

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

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Données avancées

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Classe Carboxylic acids and derivatives
    - Subclass Amino acids, peptides, and analogues
      - Level5 Amino acids and derivatives
        Level6 Alpha amino acids and derivatives
        Level7 Alpha amino acids

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Classe	Carboxylic acids and derivatives
Subclass	Amino acids, peptides, and analogues
Intermediate Tree Nodes	Amino acids and derivatives - Alpha amino acids and derivatives
Direct Parent	Alpha amino acids
Alternative Parents	Organic phosphonic acids Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organophosphorus compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Alpha-amino acid - Organophosphonic acid - Organophosphonic acid derivative - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Primary amine - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Primary aliphatic amine - Organic oxygen compound - Carbonyl group - Amine - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).
External Descriptors	non-proteinogenic alpha-amino acid - alanine derivative
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

Structure 3D

Cibles associées (humaines)

ARSA Tbio Cerebroside-sulfatase (655 Activities)

Discover Target: ARSA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

A498 (42825 Activities)

Lot Number	Certificate Type	Date	Article
H2318462	Certificate of Analysis	Aug 02, 2023	D286664
H2318463	Certificate of Analysis	Aug 02, 2023	D286664
H2318464	Certificate of Analysis	Aug 02, 2023	D286664
H2318465	Certificate of Analysis	Aug 02, 2023	D286664
H2318466	Certificate of Analysis	Aug 02, 2023	D286664
H2318467	Certificate of Analysis	Aug 02, 2023	D286664
H2318468	Certificate of Analysis	Aug 02, 2023	D286664
H2318469	Certificate of Analysis	Aug 02, 2023	D286664

Solubilité	Solvent:1eq. NaOH, Max Conc. mg/mL: 16.91, Max Conc. mM: 100
Sensibilité	Miosture sensitive
Poids moléculaire	169.070 g/mol
XLogP3	-5.200
Hydrogen Bond Donor Count	4
Hydrogen Bond Acceptor Count	6
Rotatable Bond Count	3
Exact Mass	169.014 Da
Monoisotopic Mass	169.014 Da
Topological Polar Surface Area	121.000 Å²
Heavy Atom Count	10
Formal Charge	0
Complexity	174.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	1
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

DL-AP3 - ≥98% , CAS No.5652-28-8

Stockage & expédition

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📋 Fiche de données de sécurité (FDS)

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