Chloroethylclonidine
Grundinformationen
- CAS
77472-95-8- Standard-SMILES
CN(CCCl)Cc1cc(Cl)c(NC2=NCCN2)c(Cl)c1- InChIKey
XFDVJGKSQRUEEM-UHFFFAOYSA-N- Summenformel
- C13H17Cl3N4
- Durchschnittliche Molmasse
- 335,7 g/mol
- Monoisotopische Masse
- 334,05188
Überblick
RN refers to 2-chloroethyl derivative
Namen und Bezeichner
- Bevorzugter Name
- Chloroethylclonidine
- IUPAC
- N-[2,6-dichloro-4-[[2-chloroethyl(methyl)amino]methyl]phenyl]-4,5-dihydro-1H-imidazol-2-amine
- Englischer Name
- Chloroethylclonidine
- Summenformel
- C13H17Cl3N4
- Molmasse
- 335.66
Namen und Synonyme
ChloroethylclonidineChlorethylclonidine77472-95-8DTXSID409134633X825O680HNC-171H-Imidazol-2-amine, N-(2,6-dichloro-4-(((2-chloroethyl)methylamino)methyl)phenyl)-4,5-dihydro-RefChem:125409DTXCID90134246898086-36-3UNII-3X825O680HXFDVJGKSQRUEEM-UHFFFAOYSA-N
Weitere Namen anzeigen
N-[2,6-Dichloro-4-[[methyl(2-chloroethyl)amino]methyl]phenyl]-4,5-dihydro-1H-imidazol-2-amine1H-Imidazol-2-amino, N-(2,6-dichloro-4-(((2-chloroethyl)methylamino)methyl)phenyl)-4,5-dihydro-
N-(2,6-Dichloro-4-(((2-chloroethyl)methylamino)methyl)phenyl)-4,5-dihydro-1H-imidazol-2-amineLopac-B-003N-[2,6-dichloro-4-[[2-chloroethyl(methyl)amino]methyl]phenyl]-4,5-dihydro-1H-imidazol-2-amineLopac0_000195CHEMBL326967SCHEMBL4107963SCHEMBL18154646PDSP1_000070
Datenbank-Bezeichner
- CAS
77472-95-8- PubChem CID
- 104973
- DTXSID
DTXSID40913463- ChEMBL
CHEMBL326967- UNII
- 3X825O680H
- Nikkaji
- J277.781I
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 2
- Polarare Oberfläche (TPSA)
- 39,7 Ų
- H-Brücken-Donoren
- 2
- H-Brücken-Akzeptoren
- 2
- Frei drehbare Bindungen
- 6
- Schwere Atome
- 20
- Formalladung
- 0
- Komplexität
- 328
Chemie und Industrie
Pharmakologische Informationen
MeSH Pharmacological Classification
Drugs that bind to but do not activate alpha-adrenergic receptors thereby blocking the actions of endogenous or exogenous adrenergic agonists. Adrenergic alpha-antagonists are used in the treatment of hypertension, vasospasm, peripheral vascular disease, shock, and pheochromocytoma.
Highly reactive chemicals that introduce alkyl radicals into biologically active molecules and thereby prevent their proper functioning. Many are used as antineoplastic agents, but most are very toxic, with carcinogenic, mutagenic, teratogenic, and immunosuppressant actions. They have also been used as components in poison gases.
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