Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H14NO.HO |
| Molecular Weight | 157.2102 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[OH-].C[N+](C)(C)CC1=CC=CO1
InChI
InChIKey=GMIGAQJBMBWDJC-UHFFFAOYSA-M
InChI=1S/C8H14NO.H2O/c1-9(2,3)7-8-5-4-6-10-8;/h4-6H,7H2,1-3H3;1H2/q+1;/p-1
Approval Year
Doses
| Dose | Population | Adverse events |
|---|---|---|
10 % 1 times / day multiple, ophthalmic Dose: 10 %, 1 times / day Route: ophthalmic Route: multiple Dose: 10 %, 1 times / day Sources: |
unhealthy |
Disc. AE: Dacryostenosis acquired... AEs leading to discontinuation/dose reduction: Dacryostenosis acquired (71%) Sources: |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Dacryostenosis acquired | 71% Disc. AE |
10 % 1 times / day multiple, ophthalmic Dose: 10 %, 1 times / day Route: ophthalmic Route: multiple Dose: 10 %, 1 times / day Sources: |
unhealthy |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Positive cooperativity of acetylcholine and other agonists with allosteric ligands on muscarinic acetylcholine receptors. | 1997-07 |
|
| Glaucoma treatment by furnethide and diisopropylfluorophosphate. | 1949-07 |
|
| The use of furmethide in comparison with pilocarpine and eserine for the treatment of glaucoma. | 1947-08 |
|
| Further studies on the use of furmethide in the treatment of glaucoma. | 1946-04 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
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Common Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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503-94-6
Created by
admin on Mon Mar 31 23:37:18 GMT 2025 , Edited by admin on Mon Mar 31 23:37:18 GMT 2025
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PRIMARY | |||
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12309970
Created by
admin on Mon Mar 31 23:37:18 GMT 2025 , Edited by admin on Mon Mar 31 23:37:18 GMT 2025
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PRIMARY | |||
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WD01XG801W
Created by
admin on Mon Mar 31 23:37:18 GMT 2025 , Edited by admin on Mon Mar 31 23:37:18 GMT 2025
|
PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD
