U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C20H38N4O4
Molecular Weight 398.5401
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIMORPHOLAMINE

SMILES

CCCCN(CCN(CCCC)C(=O)N1CCOCC1)C(=O)N2CCOCC2

InChI

InChIKey=HZTMGWSBSDLALI-UHFFFAOYSA-N
InChI=1S/C20H38N4O4/c1-3-5-7-21(19(25)23-11-15-27-16-12-23)9-10-22(8-6-4-2)20(26)24-13-17-28-18-14-24/h3-18H2,1-2H3

HIDE SMILES / InChI

Description
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/43915 and https://www.drugs.com/international/dimorpholamine.html

Dimorpholamine is reported as an ingredient of Theraptique in Japan. Dimorpholamine stimulates the respiratory and circulatory centers to increase the respiratory volume and blood pressure. It is indicated for the respiratory and circulatory insufficiency due to shock, hypnotic intoxication. drowning, pneumonia, and high fever.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Theraptique

Approved Use

Indications: Respiratory and circulatory insufficiency due to shock, hypnotic intoxication. drowning, pneumonia, and high fever.
PubMed

PubMed

TitleDatePubMed
Measurement of respiratory function using whole-body plethysmography in unanesthetized and unrestrained nonhuman primates.
2010 Dec
Patents

Sample Use Guides

30-60 mg (1-2 ampoules) via the intramuscular route. If necessary, the same dose may be given repeatedly unless the daily dose exceeds 200 mg (6.5 ampoules).
Route of Administration: Intramuscular
In Vitro Use Guide
Low concentrations (about 2 x 10(-5) g/ml) of dimorpholamine potentiate the twitch contraction of frog sartorius muscle. In relatively high concentrations of 10(-4)--10(-3) g/ml, however, the potentiation was followed by depression.
Name Type Language
DIMORPHOLAMINE
MI   WHO-DD  
Common Name English
Dimorpholamine [WHO-DD]
Common Name English
DIMORPHOLAMINE [JAN]
Common Name English
N,N'-1,2-ETHANEDIYLBIS (N-BUTYL-4-MORPHOLINECARBOXAMIDE)
Systematic Name English
DIMORPHOLAMINE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C47795
Created by admin on Fri Dec 15 16:21:59 GMT 2023 , Edited by admin on Fri Dec 15 16:21:59 GMT 2023
Code System Code Type Description
PUBCHEM
3091
Created by admin on Fri Dec 15 16:21:59 GMT 2023 , Edited by admin on Fri Dec 15 16:21:59 GMT 2023
PRIMARY
EPA CompTox
DTXSID5057628
Created by admin on Fri Dec 15 16:21:59 GMT 2023 , Edited by admin on Fri Dec 15 16:21:59 GMT 2023
PRIMARY
EVMPD
SUB13613MIG
Created by admin on Fri Dec 15 16:21:59 GMT 2023 , Edited by admin on Fri Dec 15 16:21:59 GMT 2023
PRIMARY
SMS_ID
100000079211
Created by admin on Fri Dec 15 16:21:59 GMT 2023 , Edited by admin on Fri Dec 15 16:21:59 GMT 2023
PRIMARY
FDA UNII
8YL4JT0L91
Created by admin on Fri Dec 15 16:21:59 GMT 2023 , Edited by admin on Fri Dec 15 16:21:59 GMT 2023
PRIMARY
MERCK INDEX
m699
Created by admin on Fri Dec 15 16:21:59 GMT 2023 , Edited by admin on Fri Dec 15 16:21:59 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
204-328-7
Created by admin on Fri Dec 15 16:21:59 GMT 2023 , Edited by admin on Fri Dec 15 16:21:59 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104294
Created by admin on Fri Dec 15 16:21:59 GMT 2023 , Edited by admin on Fri Dec 15 16:21:59 GMT 2023
PRIMARY
DRUG CENTRAL
3732
Created by admin on Fri Dec 15 16:21:59 GMT 2023 , Edited by admin on Fri Dec 15 16:21:59 GMT 2023
PRIMARY
CAS
119-48-2
Created by admin on Fri Dec 15 16:21:59 GMT 2023 , Edited by admin on Fri Dec 15 16:21:59 GMT 2023
PRIMARY
NCI_THESAURUS
C65410
Created by admin on Fri Dec 15 16:21:59 GMT 2023 , Edited by admin on Fri Dec 15 16:21:59 GMT 2023
PRIMARY
MESH
C100074
Created by admin on Fri Dec 15 16:21:59 GMT 2023 , Edited by admin on Fri Dec 15 16:21:59 GMT 2023
PRIMARY