From Wikipedia, the free encyclopedia
Isopropamide |
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MedlinePlus | a694006 |
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Routes of administration | Oral |
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ATC code | |
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Legal status |
- US: ℞-only and Unscheduled
- In general: unscheduled
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4-amino-N,N-diisopropyl-N-methyl-4-oxo-3,3-diphenylbutan-1-aminium
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CAS Number | |
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PubChem CID | |
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DrugBank | |
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ChemSpider | |
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UNII | |
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ChEMBL | |
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CompTox Dashboard (EPA) | |
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ECHA InfoCard | 100.028.470 |
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Formula | C23H33N2O+ |
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Molar mass | 353.52092 g/mol g·mol−1 |
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3D model (JSmol) | |
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O=C(N)C(c1ccccc1)(c2ccccc2)CC[N+](C(C)C)(C(C)C)C
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InChI=1S/C23H32N2O/c1-18(2)25(5,19(3)4)17-16-23(22(24)26,20-12-8-6-9-13-20)21-14-10-7-11-15-21/h6-15,18-19H,16-17H2,1-5H3,(H-,24,26)/p+1 YKey:JTPUMZTWMWIVPA-UHFFFAOYSA-O Y
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NY (what is this?) (verify) |
Isopropamide (R5) is a long-acting anticholinergic drug. It is used in the treatment of peptic ulcers and other gastrointestinal disorders involving hyperacidity (gastrointestinal acidosis) and hypermotility. Chemically, it contains a quaternary ammonium group. It is most often provided as an iodide salt, but is also available as a bromide or chloride salt. It was discovered at Janssen Pharmaceutica in 1954.
References
- Seeherman R, Isopropamide iodide: a long-acting anticholinergic, Del Med J. 1957 Oct;29(10):265-9.
- Boss EG Jr, Buchanan GC, Effect of isopropamide iodide on basal gastric secretion in the human, Gastroenterology. 1957 Nov;33(5):730-6.
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mAChRsTooltip Muscarinic acetylcholine receptors | Agonists | |
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Antagonists |
- 3-Quinuclidinyl benzilate
- 4-DAMP
- Aclidinium bromide (+formoterol)
- Abediterol
- AF-DX 250
- AF-DX 384
- Ambutonium bromide
- Anisodamine
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- CAR-302,368
- CAR-302,537
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- HL-031,120
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- Isopropamide
- J-104,129
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- PD-102,807
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- Umeclidinium bromide (+vilanterol)
- WIN-2299
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Precursors (and prodrugs) | |
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