Bromo-willardiine , CAS No.19772-78-2

CAS: 19772-78-2 Cat. No.: B668110 Formule: C7H8BrN3O4 Poids moléculaire: 278.06
DISPONIBLE À COMMANDE
Synonyms
BROMO-WILLARDIINE|5-Bromowillardiine|2-AMINO-3-(5-BROMO-2,4-DIOXO-3,4-DIHYDRO-2H-PYRIMIDIN-1-YL)-PROPIONIC ACID|BWD|5-Bromo-S-willardiine|3-(5-bromo-2,4-dioxo-3,4-dihydropyrimidin-1(2h)-yl)-l-alanine|(2S)-2-amino-3-(5-bromo-2,4-dioxopyrimidin-1-yl)propanoic acid|(S)-2-Amino-3-(5-bromo-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-propionic acid|(S)-2-amino-3-(5-bromo-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)propanoic acid|1(2H)-Pyrimidinepropanoic acid, alpha-amino-5-bromo-3,4-dihydro-2,4-dioxo-, (S)-|(2S)-2-AMINO-3-(5-BROMO-2,4-DIOXO-1,2,3,4-TETRAHYDROPYRIMIDIN-1-YL)PROPANOIC ACID|1(2H)-PYRIMIDINEPROPANOIC ACID, .ALPHA.-AMINO-5-BROMO-3,4-DIHYDRO-2,4-DIOXO-, (.ALPHA.S)-
Storage
Room temperature
★
Taille
Allemagne (EU)
USA*
Prix
Qté
1mg
B668110-1mg
Sur commande · 8–12 semaines

496,26€

744,43€
Enregistrer 248,17 € (33.34%)
5mg
B668110-5mg
Sur commande · 8–12 semaines

1 735,39€

2 603,13€
Enregistrer 867,74 € (33.33%)
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Spécifications

Synonymes
BROMO-WILLARDIINE | 5-Bromowillardiine | 2-AMINO-3-(5-BROMO-2,4-DIOXO-3,4-DIHYDRO-2H-PYRIMIDIN-1-YL)-PROPIONIC ACID | BWD | 5-Bromo-S-willardiine | 3-(5-bromo-2,4-dioxo-3,4-dihydropyrimidin-1(2h)-yl)-l-alanine | (2S)-2-amino-3-(5-bromo-2,4-dioxopyrimidin-1-yl)propanoic acid | (S)-2-Amino-3-(5-bromo-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl) Afficher plus
Conditions de stockage de stockage
Room temperature
Propriétés du produit
ALogP
-3.5
Noms et identifiants
Sourires canoniques
C1=C(C(=O)NC(=O)N1CC(C(=O)O)N)Br
IUPAC Name
(2S)-2-amino-3-(5-bromo-2,4-dioxopyrimidin-1-yl)propanoic acid
InChIKey
AEKIJKSVXKWGRJ-BYPYZUCNSA-N
INCHI
1S/C7H8BrN3O4/c8-3-1-11(2-4(9)6(13)14)7(15)10-5(3)12/h1,4H,2,9H2,(H,13,14)(H,10,12,15)/t4-/m0/s1
Isomères SMILES
C1=C(C(=O)NC(=O)N1C[C@@H](C(=O)O)N)Br
Poids moléculaire
278.06
Reaxy-Rn
7817208
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7817208&ln=

Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClasseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids
Direct ParentL-alpha-amino acids
Alternative Parents Pyrimidones  Halopyrimidines  Aryl bromides  Hydropyrimidines  Vinylogous amides  Heteroaromatic compounds  Ureas  Amino acids  Lactams  Azacyclic compounds  Carboxylic acids  Monocarboxylic acids and derivatives  Organic oxides  Organobromides  Carbonyl compounds  Organopnictogen compounds  Hydrocarbon derivatives  Monoalkylamines  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents L-alpha-amino acid - Halopyrimidine - Pyrimidone - Aryl bromide - Aryl halide - Hydropyrimidine - Pyrimidine - Vinylogous amide - Heteroaromatic compound - Lactam - Amino acid - Urea - Azacycle - Carboxylic acid - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organonitrogen compound - Organobromide - Organohalogen compound - Organic oxygen compound - Primary aliphatic amine - Organic nitrogen compound - Organic oxide - Organopnictogen compound - Carbonyl group - Organooxygen compound - Primary amine - Amine - Hydrocarbon derivative - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.
External Descriptors organobromine compound - non-proteinogenic L-alpha-amino acid - L-alanine derivative
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
GRIA4 Tclin Glutamate receptor 4 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRIK5 Tclin Glutamate receptor ionotropic, kainate 5 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRIA2 Tclin Glutamate receptor 2 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRIA1 Tclin Glutamate receptor 1 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRIA3 Tclin Glutamate receptor ionotropic, AMPA 3 (127 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIA1 Tclin Glutamate receptor ionotropic, AMPA 1 (277 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIA2 Tclin Glutamate receptor ionotropic, AMPA 2 (847 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cibles associées (non humaines)
Gria4 Glutamate receptor ionotropic, AMPA 4 (112 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propriétés chimiques et physiques
Poids moléculaire278.060 g/mol
XLogP3-3.500
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count3
Exact Mass276.97 Da
Monoisotopic Mass276.97 Da
Topological Polar Surface Area113.000 Ų
Heavy Atom Count15
Formal Charge0
Complexity354.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculateurs de solution
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