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Details

Stereochemistry ACHIRAL
Molecular Formula C22H25NO4.H3O4P
Molecular Weight 465.4334
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIMOXYLINE PHOSPHATE

SMILES

OP(O)(O)=O.CCOC1=CC=C(CC2=C3C=C(OC)C(OC)=CC3=CC(C)=N2)C=C1OC

InChI

InChIKey=YZKZXTBSUSEYQZ-UHFFFAOYSA-N
InChI=1S/C22H25NO4.H3O4P/c1-6-27-19-8-7-15(11-20(19)24-3)10-18-17-13-22(26-5)21(25-4)12-16(17)9-14(2)23-18;1-5(2,3)4/h7-9,11-13H,6,10H2,1-5H3;(H3,1,2,3,4)

HIDE SMILES / InChI

Molecular Formula C22H25NO4
Molecular Weight 367.4382
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula H3O4P
Molecular Weight 97.9952
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including: https://www.ncbi.nlm.nih.gov/pubmed/14936209 | https://www.ncbi.nlm.nih.gov/pubmed/13240796 | https://www.ncbi.nlm.nih.gov/pubmed/13092557

Dimoxyline is the synthetic analogue of papaverine, Acute toxicity studies show it to be less toxic than papaverine. No analgesic action and no tolerance development in experimental animals by repeated administration. But Dimoxyline does not appear to be as potent as papaverine in comparable dosage. Dimoxyline is indicated for the treatment of patients with angina pectoris. Also, significant amount of benefit was claimed in patients with acute or chronic phlebitis, arterial thrombosis or embolism, Raynaud’s phenomena and early thromboangiitis obliterans or arteriosclerosis obliterans. Detected adverse events are: nausea or abdominal cramps.

Originator

Curator's Comment: # Eli Lilly

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
PAVERIL PHOSPHATE

Approved Use

Unknown

Launch Date

1953
Palliative
PAVERIL PHOSPHATE

Approved Use

Unknown

Launch Date

1953
Palliative
PAVERIL PHOSPHATE

Approved Use

Unknown

Launch Date

1953
PubMed

PubMed

TitleDatePubMed
Effects of dioxyline phosphate and enteric-coated khellin on coronary artery insufficiency.
1951 Jul
Studies on the use of dioxyline phosphate in the treatment of angina pectoris.
1952 Jul
Anginal relief with paveril phosphate.
1952 May
Papaverine analogs. 8. Comparative actions of papaverine, ethaverine and dioxyline on the cardiovascular system.
1960 Jul 1
Patents

Patents

Sample Use Guides

200 mg four times daily
Route of Administration: Oral
When the phosphate of the Dimoxyline was added to the Tyrode’s solution in which a strip of rabbit small intestine was suspended, a concentration of 1 :100,000 and 1200,000 caused a slight reduction in tone and a depression in the number of contractions per unit of time.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:11:24 GMT 2023
Edited
by admin
on Fri Dec 15 15:11:24 GMT 2023
Record UNII
9M18MC2SIE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIMOXYLINE PHOSPHATE
MI   WHO-DD  
Common Name English
L-08146
Code English
6,7-DIMETHOXY-1-(4'-ETHOXY-3'-METHOXYBENZYL)-3-METHYLISOQUINOLINE PHOSPHATE
Common Name English
ISOQUINOLINE, 1-((4-ETHOXY-3-METHOXYPHENYL)METHYL)-6,7-DIMETHOXY-3-METHYL-, PHOSPHATE (1:1)
Systematic Name English
DIOXYLINE PHOSPHATE
Common Name English
LIVERA
Brand Name English
Dimoxyline phosphate [WHO-DD]
Common Name English
DIMOXYLINE PHOSPHATE [MI]
Common Name English
ISOQUINOLINE, 1-(4-ETHOXY-3-METHOXYBENZYL)-6,7-DIMETHOXY-3-METHYL-, PHOSPHATE (1:1)
Systematic Name English
PAVERONE
Brand Name English
PAVERIL PHOSPHATE
Brand Name English
Classification Tree Code System Code
NCI_THESAURUS C29707
Created by admin on Fri Dec 15 15:11:24 GMT 2023 , Edited by admin on Fri Dec 15 15:11:24 GMT 2023
Code System Code Type Description
MERCK INDEX
m147
Created by admin on Fri Dec 15 15:11:24 GMT 2023 , Edited by admin on Fri Dec 15 15:11:24 GMT 2023
PRIMARY Merck Index
PUBCHEM
21877
Created by admin on Fri Dec 15 15:11:24 GMT 2023 , Edited by admin on Fri Dec 15 15:11:24 GMT 2023
PRIMARY
FDA UNII
9M18MC2SIE
Created by admin on Fri Dec 15 15:11:24 GMT 2023 , Edited by admin on Fri Dec 15 15:11:24 GMT 2023
PRIMARY
ChEMBL
CHEMBL2108950
Created by admin on Fri Dec 15 15:11:24 GMT 2023 , Edited by admin on Fri Dec 15 15:11:24 GMT 2023
PRIMARY
CAS
5667-46-9
Created by admin on Fri Dec 15 15:11:24 GMT 2023 , Edited by admin on Fri Dec 15 15:11:24 GMT 2023
PRIMARY
SMS_ID
100000087515
Created by admin on Fri Dec 15 15:11:24 GMT 2023 , Edited by admin on Fri Dec 15 15:11:24 GMT 2023
PRIMARY
EPA CompTox
DTXSID40205234
Created by admin on Fri Dec 15 15:11:24 GMT 2023 , Edited by admin on Fri Dec 15 15:11:24 GMT 2023
PRIMARY
EVMPD
SUB01757MIG
Created by admin on Fri Dec 15 15:11:24 GMT 2023 , Edited by admin on Fri Dec 15 15:11:24 GMT 2023
PRIMARY
NCI_THESAURUS
C77073
Created by admin on Fri Dec 15 15:11:24 GMT 2023 , Edited by admin on Fri Dec 15 15:11:24 GMT 2023
PRIMARY
ECHA (EC/EINECS)
227-126-0
Created by admin on Fri Dec 15 15:11:24 GMT 2023 , Edited by admin on Fri Dec 15 15:11:24 GMT 2023
PRIMARY
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ACTIVE MOIETY