guanabenz
Trade name: wytensin
Approved
Sep 7, 1982
Guanabenz, an antihypertensive agent for oral administration-, is an aminoguanidine derivative, 2,'6-dichlorobenzylideneamina-guanidine acetate. It is white to an almost white powder having not more than a slight odor. Sparingly soluble in water and in 0.1 N hydrochloric acid; soluble in alcohol and in propylene glycol. Guanabenz is an orally active central alpha-2 adrenergic agonist. Its antihypertensive action appears to be mediated via stimulation of central alpha-adrenergic receptors, resulting in a decrease of sympathetic outflow from the brain at the bulbar level to the peripheral circulatory system. In clinical trials, guanabenz acetate, given orally to hypertensive patients, effectively controlled blood pressure without any significant effect on glomerular filtration rate, renal blood flow, body fluid volume or body weight. The Myelin Repair Foundation and the National Institutes of Health (National Institute of Neurological Disorders and Stroke) are developing guanabenz for the treatment of multiple sclerosis. Unlike the currently available treatment for multiple sclerosis that suppresses the immune system, guanabenz, an FDA approved the drug for the treatment of high blood pressure, has a potential to reduce the loss of myelin by protecting and repairing myelin-producing cells in the brain from damage. Phase I development is underway in the US. — NCATS
Clinical trial activity
3 trials · 3 clinical orgs · 5 marketing orgs
Earliest trial started Apr 15, 2015 (NCT02423083)
Timeline
1980s
- Sep 7, 1982
American Home Products — Earliest FDA Approval
- Sep 7, 1982
American Home Products — NDA Organization
- Sep 7, 1982
American Home Products — NDA Secondary Org
1990s
- Feb 28, 1994
Watson Pharmaceuticals — Marketing Organization
- Jun 1, 1994
Ani Pharmaceuticals — Marketing Organization
- Sep 30, 1998
Fosun — Marketing Organization
- Sep 30, 1998
Chartwell Pharmaceuticals — Marketing Organization
2010s
- Jan 1, 2015
Earliest Phase 1 Sponsor(trial)
2020s
- Jan 1, 2021
Earliest Phase 2 Sponsor(trial)
Indications
Approved for
Mechanism of action
Approval history
- approvedSep 7, 1982
Chemistry & pharmacology
SMILES
N=C(N)N/N=C/c1c(Cl)cccc1Cl- Mol. weight
- 231.09 g/mol
- Lipinski Ro5
- Pass
- Rule of 3
- No
- Chirality
- Achiral Molecule
- Inorganic
- No
- Polymer
- No
- Delivery
- Oral
- Availability
- Discontinued
Oral
Yes
Parenteral
No
Topical
No
Sources
- ChEMBLCHEMBL420 ↗
- WikipediaGuanabenz ↗
- NCATSGGD30112WC ↗
- ChEMBLCHEMBL1200560 ↗
Also known as
- guanabenz
- guanabenz
- guanabenz
- guanabenz
- guanabenz
- guanabenz
- guanabenz
- guanabenz
- guanabenz
- guanabenz
- guanabenz acetate
- guanabenz acetate
- guanabenz acetate
- guanabenz acetate
- guanabenz acetate
- guanabenzo
- guanabenzo
- guanabenzum
- guanabenzum
- wy-8678
- wy-8678
- wy-8678 acetate
- wy-8678 acetate
- wytensin
- wytensin
- wytensin
Clinical trials
| NCT ID | Phase | Start date | Sponsor(s) |
|---|---|---|---|
| NCT05084404 | Phase 2 | Oct 14, 2021 | Yokohama City University |
| NCT02443103 | N/A | May 7, 2015 | Indiana University |
| NCT02423083 | Phase 1 | Apr 15, 2015 | National Institute of Neurological Disorders and Stroke (NINDS) |
Organizations
Research & Development (3)
| Organization | Org type | Trials | As lead sponsor | Phases | Earliest year |
|---|---|---|---|---|---|
| Indiana University | Academic/Hospital | 1 | 1 | 1 | 2015 |
| National Institute of Neurological Disorders and Stroke (NINDS) | Government | 1 | 1 | 1 | 2015 |
| Yokohama City University | Academic/Hospital | 1 | 1 | 1 | 2021 |
Marketing (7)
| Organization | Org type | Relationship | Date |
|---|---|---|---|
| American Home Products | For profit | NDA | Sep 7, 1982 |
| American Home Products | For profit | NDA2 | Sep 7, 1982 |
| Ani Pharmaceuticals | For profit | SYN | Jun 1, 1994 |
| Ani Pharmaceuticals | For profit | MKTG | Jun 1, 1994 |
| Chartwell Pharmaceuticals | For profit | MKTG | Sep 30, 1998 |
| Fosun | For profit | MKTG | Sep 30, 1998 |
| Watson Pharmaceuticals | For profit | MKTG | Feb 28, 1994 |