beta-Aspartylhydroxamic acid
Grundinformationen
- CAS
1955-68-6- Standard-SMILES
NC(CC(=O)NO)C(=O)O- InChIKey
ZBYVTTSIVDYQSO-UHFFFAOYSA-N- Summenformel
- C4H8N2O4
- Durchschnittliche Molmasse
- 148,12 g/mol
Überblick
RN given refers to (DL)-isomer
Namen und Bezeichner
- Bevorzugter Name
- beta-Aspartylhydroxamic acid
- IUPAC
- 2-amino-4-(hydroxyamino)-4-oxobutanoic acid
- Englischer Name
- L-Aspartic acid beta-hydroxamate
- Summenformel
- C4H8N2O4
- Molmasse
- 148.12
Namen und Synonyme
beta-Aspartylhydroxamic acidDL-Asparagine, N-hydroxy-20154-32-9RefChem:119210beta-Aspartylhydroxamate2-Amino-4-(hydroxyamino)-4-oxobutanoic acidAspartate-beta-hydroxamateAspartic acid beta-hydroxamateNSC 528507D-Aspartic acid beta-hydroxamate3-alaninehydroxamic acidCHEMBL216856
Weitere Namen anzeigen
AAHl-aspartic acid β-hydroxamateHDXN4-Hydroxy-L-asparagineL-Asparagine, N-hydroxy-L-β-Aspartohydroxamic acidL-ASPARTICACIDβ-HYDROXAMATEL-Aspartyl-?-hydroxamic acid3-(Hydroxycarbamoyl)-L-alanine
SCHEMBL9684668ZBYVTTSIVDYQSO-UHFFFAOYSA-NDAHNSC141662NSC528507NSC-141662NSC-528507
Datenbank-Bezeichner
- CAS
1955-68-6、20154-32-9- PubChem CID
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- -3,5
- Polarare Oberfläche (TPSA)
- 113 Ų
- H-Brücken-Donoren
- 4
- H-Brücken-Akzeptoren
- 5
- Frei drehbare Bindungen
- 3
- Schwere Atome
- 10
- Formalladung
- 0
- Komplexität
- 146
Physikochemische Eigenschaften
- Schmelzpunkt
- 171 · 171-172 °C
- Dichte
- 1.532 · 1.532±0.06 g/cm3(Predicted)
- storage temp.
- 20 °C · −20°C
- pka
- 3.02 · 3.02±0.10(Predicted)
- Aggregatzustand
- Solid
- Farbe
- White to off-white
- Major Application
- detection
- InChI
- 1S/C4H8N2O4/c5-2(4(8)9)1-3(7)6-10/h2,10H,1,5H2,(H,6,7)(H,8,9)/t2-/m0/s1
- InChIKey
- ZBYVTTSIVDYQSO-REOHCLBHSA-N
- SMILES
- N[C@@H](CC(=O)NO)C(O)=O
Sicherheit und Regulatorisches
Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
Sicherheitsdaten
- wgk
- 3
- Speicherklasse
- 11 - Combustible Solids
Chemie und Industrie
Pharmakologische Informationen
MeSH Pharmacological Classification
Substances that inhibit or prevent the proliferation of NEOPLASMS.
Agents used in the prophylaxis or therapy of VIRUS DISEASES. Some of the ways they may act include preventing viral replication by inhibiting viral DNA polymerase; binding to specific cell-surface receptors and inhibiting viral penetration or uncoating; inhibiting viral protein synthesis; or blocking late stages of virus assembly.
Anwendungen
BeschreibungHydroxylated lecithin, also known as b-L-aspartylhydroxamate or b-aspartohydroxamic acid, 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. Based on a literature review a small amount of articles have been published on Hydroxylated lecithin.
VerwendenL-ASPARTIC ACID BETA-HYDROXAMATE can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical and pharmaceutical production process.
Anbieter21 Anbieter
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