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

Vue d’ensemble

Information

Antineoplaston A10 Antineoplaston A10 is a naturally occurring substance in the human body that that can be potentially used for the treatment of glioma, lymphoma, astrocytoma and breast cancer. The main ingredient active of antineoplaston A10 (Phenylacetylglutamine, PG) inhibits RAS and promotes apoptosis .

Targets

RAS

Spécifications

Synonymes

Spécifications et pureté

≥98%

Mécanismes biochimiques et physiologiques

Antineoplaston A10 is a naturally occurring substance in the human body that that can be potentially used for the treatment of glioma, lymphoma, astrocytoma and breast cancer. The main ingredient active of antineoplaston A10 (Phenylacetylglutamine, PG) in

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.

Pureté

≥98%

Propriétés du produit

ALogP

0.307

hba_count

Nombre de HBD

Liaison rotative

Noms et identifiants

Pubchem Sid

504753690

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504753690

Sourires canoniques

C1CC(=O)NC(=O)C1NC(=O)CC2=CC=CC=C2

IUPAC Name

N-[(3S)-2,6-dioxopiperidin-3-yl]-2-phenylacetamide

InChIKey

OQGRFQCUGLKSAV-JTQLQIEISA-N

INCHI

1S/C13H14N2O3/c16-11-7-6-10(13(18)15-11)14-12(17)8-9-4-2-1-3-5-9/h1-5,10H,6-8H2,(H,14,17)(H,15,16,18)/t10-/m0/s1

Isomères SMILES

C1CC(=O)NC(=O)[C@H]1NC(=O)CC2=CC=CC=C2

Poids moléculaire

246.26

Reaxy-Rn

6145655

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6145655&ln=

Documentation

📋 Fiche de données de sécurité (FDS)

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

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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 N-acyl-alpha amino acids and derivatives

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	N-acyl-alpha amino acids and derivatives
Alternative Parents	Phenylacetamides Piperidinediones Delta lactams N-unsubstituted carboxylic acid imides Dicarboximides Secondary carboxylic acid amides Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	N-acyl-alpha amino acid or derivatives - Phenylacetamide - Piperidinedione - Delta-lactam - Piperidinone - Monocyclic benzene moiety - Piperidine - Benzenoid - Carboxylic acid imide - Dicarboximide - Carboxylic acid imide, n-unsubstituted - Lactam - Carboxamide group - Secondary carboxylic acid amide - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Carbonyl group - Organopnictogen compound - Organic nitrogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. These are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom.
External Descriptors	Not available
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)

ACHN (49357 Activities)

Lot Number	Certificate Type	Date	Article
I2622057	Certificate of Analysis	Oct 13, 2026	A412322
H2213057	Certificate of Analysis	May 12, 2025	A412322
H2213059	Certificate of Analysis	May 12, 2025	A412322
H2213060	Certificate of Analysis	May 12, 2025	A412322
H2213061	Certificate of Analysis	May 12, 2025	A412322
H2213062	Certificate of Analysis	May 12, 2025	A412322

Solubilité	Solubility (25°C) In vitro DMSO: 49 mg/mL (198.97 mM); Water: Insoluble; Ethanol: Insoluble;
DMSO (mg/mL) Solubilité maximale	49
DMSO (mM) Solubilité maximale	198.976691301876
Eau (mg/mL) Solubilité maximale	＜1
Poids moléculaire	246.260 g/mol
XLogP3	0.400
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	3
Exact Mass	246.1 Da
Monoisotopic Mass	246.1 Da
Topological Polar Surface Area	75.300 Å²
Heavy Atom Count	18
Formal Charge	0
Complexity	348.000
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

Antineoplaston A10 - ≥98% , CAS No.91531-30-5

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