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
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)
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 |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/14824008Curator'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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/14824008
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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/14824008
Curator's Comment: # Eli Lilly
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/14936209
200 mg four times daily
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/14824008
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
Edited
Fri Dec 15 15:11:24 GMT 2023
by
admin
on
Fri Dec 15 15:11:24 GMT 2023
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Record UNII |
9M18MC2SIE
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C29707
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m147
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21877
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9M18MC2SIE
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CHEMBL2108950
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SUB01757MIG
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C77073
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227-126-0
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Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |
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ACTIVE MOIETY |