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Details

Stereochemistry ACHIRAL
Molecular Formula C13H17Cl3N4
Molecular Weight 335.66
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLORETHYLCLONIDINE

SMILES

CN(CCCl)CC1=CC(Cl)=C(NC2=NCCN2)C(Cl)=C1

InChI

InChIKey=XFDVJGKSQRUEEM-UHFFFAOYSA-N
InChI=1S/C13H17Cl3N4/c1-20(5-2-14)8-9-6-10(15)12(11(16)7-9)19-13-17-3-4-18-13/h6-7H,2-5,8H2,1H3,(H2,17,18,19)

HIDE SMILES / InChI

Molecular Formula C13H17Cl3N4
Molecular Weight 335.66
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
The effect of adrenergic receptor antagonists on cocaine-induced ventricular fibrillation: alpha but not beta adrenergic receptor antagonists prevent malignant arrhythmias independent of heart rate.
1994 Apr
Contribution of peripheral alpha 1A-adrenoceptors to pain induced by formalin or by alpha-methyl-5-hydroxytryptamine plus noradrenaline.
1996 Apr 22
Hypotensive and hypertensive effects of catecholamines intrathecally injected in anesthetized rats.
1996 Jun 10
Sympathetic neurotransmission in the rat testicular capsule: functional characterization and identification of mRNA encoding alpha1-adrenoceptor subtypes.
2006 Aug 14
Estradiol modulation of phenylephrine-induced excitatory responses in ventromedial hypothalamic neurons of female rats.
2008 May 20
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:07:37 GMT 2023
Edited
by admin
on Fri Dec 15 18:07:37 GMT 2023
Record UNII
3X825O680H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHLORETHYLCLONIDINE
Common Name English
1H-IMIDAZOL-2-AMINE, N-(2,6-DICHLORO-4-(((2-CHLOROETHYL)METHYLAMINO)METHYL)PHENYL)-4,5-DIHYDRO-
Systematic Name English
CHLOROETHYLCLONIDINE
Common Name English
CEC
Common Name English
NC-17
Code English
Code System Code Type Description
WIKIPEDIA
CHLOROETHYLCLONIDINE
Created by admin on Fri Dec 15 18:07:37 GMT 2023 , Edited by admin on Fri Dec 15 18:07:37 GMT 2023
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FDA UNII
3X825O680H
Created by admin on Fri Dec 15 18:07:37 GMT 2023 , Edited by admin on Fri Dec 15 18:07:37 GMT 2023
PRIMARY
CAS
98086-36-3
Created by admin on Fri Dec 15 18:07:37 GMT 2023 , Edited by admin on Fri Dec 15 18:07:37 GMT 2023
SUPERSEDED
EPA CompTox
DTXSID40913463
Created by admin on Fri Dec 15 18:07:37 GMT 2023 , Edited by admin on Fri Dec 15 18:07:37 GMT 2023
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PUBCHEM
104973
Created by admin on Fri Dec 15 18:07:37 GMT 2023 , Edited by admin on Fri Dec 15 18:07:37 GMT 2023
PRIMARY
CAS
77472-95-8
Created by admin on Fri Dec 15 18:07:37 GMT 2023 , Edited by admin on Fri Dec 15 18:07:37 GMT 2023
PRIMARY