dexmecamylamine
Mecamylamine (Inversine), the first orally available antihypertensive agent, is now rarely used. Introduced as a therapeutic agent for the treatment of hypertension in the 1950s, mecamylamine was the first useful ganglionic blocking agent that was not a quarternary ammonium compound. Mecamylamine is indicated for the management of moderately severe to severe essential hypertension and in uncomplicated cases of malignant hypertension. Mecamylamine reduces blood pressure in both normotensive and hypertensive individuals. A small oral dosage often produces a smooth and predictable reduction of blood pressure. Although this antihypertensive effect is predominantly orthostatic, the supine blood pressure is also significantly reduced. Mecamylamine is a nicotinic parasympathetic ganglionic blocker. Mecamylamine administration produces several deleterious side-effects at therapeutically relevant doses. As such, mecamylamine’s use as an antihypertensive agent was phased out, except in severe hypertension. Mecamylamine easily traverses the blood-brain barrier to reach the central nervous system (CNS), where it acts as a nicotinic acetylcholine receptor (nAChR) antagonist, inhibiting all known nAChR subtypes. Since nAChRs play a major role in numerous physiological and pathological processes, it is not surprising that mecamylamine has been evaluated for its potential therapeutic effects in a wide variety of CNS disorders, including addiction. — NCATS
Clinical trial activity
20 trials · 10 clinical orgs · 0 marketing orgs
Earliest trial started Jun 1, 2008 (NCT00692445)
Timeline
Indications
Approved for
Studied for
- Alcoholism · Phase 3
- Depression · Phase 3
- Depressive Disorder · Phase 3
- Healthy Volunteers · Phase 1
- Hyperhidrosis · Phase 2
- Hypertension · Phase 1/Phase 2
- Kidney Failure, Chronic · Phase 1
- Major Depressive Disorder · Phase 3
- Palmar Plate · Phase 2
- Patients · Phase 1
- Pharmacokinetics · Phase 1
- Substance-Related Disorders · Phase 1
- Urinary Bladder, Overactive · Phase 2
Mechanism of action
Neuronal acetylcholine receptor; alpha4/beta2 antagonist
TC-5214 [S-(+)-mecamylamine] was more effective than TC-5213 [R-(-)-mecamylamine] in inhibiting the LS a4ß2 NNRs. TC-5214 potentiated and TC-5213 inhibited agonist-induced activation of HS a4ß2 NNRs.
Chemistry & pharmacology
SMILES
CN[C@@]1(C)[C@@H]2CC[C@@H](C2)C1(C)C- Mol. weight
- 167.3 g/mol
- Lipinski Ro5
- Pass
- Rule of 3
- Yes
- Chirality
- Single Stereoisomer
- Inorganic
- No
- Polymer
- No
Oral
No
Parenteral
No
Topical
No
Sources
- ChEMBLCHEMBL2103881 ↗
- NCATS6EE945D3OK ↗
- ChEMBLCHEMBL2105753 ↗
Also known as
- dexmecamylamine
- dexmecamylamine
- dexmecamylamine
- dexmecamylamine
- dexmecamylamine hcl
- dexmecamylamine hcl
- dexmecamylamine hydrochloride
- dexmecamylamine hydrochloride
- nih-11008
- nih-11008
- tc-5214
- tc-5214
- tc-5214
Clinical trials
| NCT ID | Phase | Start date | Sponsor(s) |
|---|---|---|---|
| NCT04263623 | Phase 2 | Jan 31, 2020 | Atacama Therapeutics |
| NCT03404570 | Phase 2 | Dec 21, 2017 | Atacama Therapeutics |
| NCT01868516 | Phase 2 | May 1, 2013 | Targacept |
| NCT01500018 | Phase 1 | Jan 1, 2012 | AstraZeneca, INC Research |
| NCT01458899 | Phase 1 | Nov 1, 2011 | AstraZeneca, IQVIA |
| NCT01403922 | Phase 1 | Aug 1, 2011 | AstraZeneca, IQVIA |
| NCT01392820 | Phase 1 | Jul 1, 2011 | AstraZeneca, Kyushu Clinical Pharmacolgy Reasearch Clinic |
| NCT01359618 | Phase 1 | Jun 1, 2011 | AstraZeneca, IQVIA |
| NCT01288079 | Phase 2 | Feb 1, 2011 | AstraZeneca |
| NCT01239771 | Phase 1 | Jan 1, 2011 | AstraZeneca, IQVIA |
| NCT01240967 | Phase 1 | Nov 1, 2010 | AstraZeneca, Orlando Clinical Research Center |
| NCT01180400 | Phase 3 | Sep 1, 2010 | AstraZeneca, Targacept, University of Hamburg |
| NCT01197508 | Phase 3 | Sep 1, 2010 | AstraZeneca, Targacept |
| NCT01175564 | Phase 1 | Jul 1, 2010 | AstraZeneca |
| NCT01145768 | Phase 1 | Jun 1, 2010 | AstraZeneca, IQVIA |
| NCT01157078 | Phase 3 | Jun 1, 2010 | AstraZeneca, Midwest Clinical Research Center, Ohio, Targacept |
| NCT01153347 | Phase 3 | Jun 1, 2010 | AstraZeneca, Florida Clinical Research Center, LLC, Targacept |
| NCT01152554 | Phase 3 | Jun 1, 2010 | AstraZeneca, Florida Clinical Research Center, LLC, Targacept |
| NCT00899977 | Phase 1/Phase 2 (Phase 2) | May 1, 2009 | Targacept |
| NCT00692445 | Phase 2 | Jun 1, 2008 | Targacept |
Organizations
Research & Development (10)
| Organization | Org type | Trials | As lead sponsor | Phases | Earliest year |
|---|---|---|---|---|---|
| AstraZeneca | For profit | 15 | 15 | 3 | 2010 |
| Targacept | For profit | 8 | 3 | 2 | 2008 |
| IQVIA | For profit | 5 | 0 | 1 | 2010 |
| Atacama Therapeutics | For profit | 2 | 2 | 1 | 2017 |
| Florida Clinical Research Center, LLC | For profit | 2 | 0 | 1 | 2010 |
| INC Research | For profit | 1 | 0 | 1 | 2012 |
| Kyushu Clinical Pharmacolgy Reasearch Clinic | Academic/Hospital | 1 | 0 | 1 | 2011 |
| Midwest Clinical Research Center, Ohio | For profit | 1 | 0 | 1 | 2010 |
| Orlando Clinical Research Center | For profit | 1 | 0 | 1 | 2010 |
| University of Hamburg | Academic/Hospital | 1 | 0 | 1 | 2010 |