Grundinformationen
- Standard-SMILES
O=C(O)C1CN(CCCP(=O)(O)O)CCN1- InChIKey
CUVGUPIVTLGRGI-UHFFFAOYSA-N- Summenformel
- C8H17N2O5P
- Durchschnittliche Molmasse
- 252,2 g/mol
- Monoisotopische Masse
- 252,08750827
Überblick
structure given in first source; NMDA receptor antagonist
Namen und Bezeichner
- Bevorzugter Name
- 3-(2-Carboxypiperazin-4-yl)propyl-1-phosphonic acid
- IUPAC
- 4-(3-phosphonopropyl)piperazine-2-carboxylic acid
- Englischer Name
- CARBOXYPEPTIDASE P
- Molmasse
- 0
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
100828-16-8、9075-64-3- PubChem CID
- 1228
- DTXSID
DTXSID10905774- ChEMBL
CHEMBL22304- UNII
- 98Y1I8ZD4M
- EC Number
- 624-824-0、634-473-5
- Nikkaji
- J260.391H、J377.332I
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- -6,8
- Polarare Oberfläche (TPSA)
- 110 Ų
- H-Brücken-Donoren
- 4
- H-Brücken-Akzeptoren
- 7
- Frei drehbare Bindungen
- 5
- Schwere Atome
- 16
- Formalladung
- 0
- Komplexität
- 292
Physikochemische Eigenschaften
- storage temp.
- 20 °C · −20°C
- Aggregatzustand
- powder
- Farbe
- white
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
P233, P260, P264, P264+P265, P271, P280, P284, P302+P352, P304+P340, P305+P351+P338, P321, P332+P317, P337+P317, P342+P316, P362+P364, P403, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 39 reports by companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Warning
H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
Gefahrenhinweise
Hazard Classes and Categories
Skin Irrit. 2 (100%)
Skin Irrit. 2 (100%)
Sicherheitsdaten
- F
- 9
- wgk
- 1
- risk_code
- 36/37/38-42
- hazard_code
- Xn
- safety_code
- 22-24-26-36/37
Chemie und Industrie
Pharmakologische Informationen
MeSH Pharmacological Classification
Drugs used to prevent SEIZURES or reduce their severity.
Drugs that bind to but do not activate excitatory amino acid receptors, thereby blocking the actions of agonists.
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