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

CAS: 19772-78-2 Cat. No.: B668110 Fórmula: C7H8BrN3O4 Peso molecular: 278.06
Disponível para encomenda
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
★
Tamanho
Alemanha (EU)
USA*
Preço
Qtd
1mg
B668110-1mg
Sob encomenda · 8–12 semanas

496,26€

744,43€
Gravar 248,17 € (33.34%)
5mg
B668110-5mg
Sob encomenda · 8–12 semanas

1735,39€

2603,13€
Gravar 867,74 € (33.33%)
Enter a quantity for the sizes you want to add.

Especificações

Sinónimos
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) Show more
Condições de armazenamento de armazenamento
Room temperature
Propriedades do produto
ALogP
-3.5
Nomes e identificadores
Sorrisos canónicos
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
SMILES isoméricas
C1=C(C(=O)NC(=O)N1C[C@@H](C(=O)O)N)Br
Peso molecular
278.06
Reaxy-Rn
7817208
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7817208&ln=

Dados avançados

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
DescriçãoThis 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
Estrutura 3D
Modelo de Estrutura Química Interativa





Alvos associados (humanos)
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
Alvos associados (não humanos)
Gria4 Glutamate receptor ionotropic, AMPA 4 (112 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propriedades químicas e físicas
Peso molecular278.060 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
Calculadoras de soluções
Revisões

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