Bunazosin
![]() | |
Systematic (IUPAC) name | |
---|---|
1-(4-(4-amino-6,7-dimethoxyquinazolin-2-yl)-1,4-diazepan-1-yl)butan-1-one | |
Clinical data | |
AHFS/Drugs.com | International Drug Names |
Identifiers | |
CAS Number | 80755-51-7 |
ATC code | none |
PubChem | CID 2472 |
ChemSpider |
2378 ![]() |
UNII |
9UUW4V7G2H ![]() |
ChEMBL |
CHEMBL188185 ![]() |
Chemical data | |
Formula | C19H27N5O3 |
Molar mass | 373.44 g/mol |
| |
| |
(verify) |
Bunazosin (INN) is an alpha 1 antagonist. Bunazosin was initially developed to treat benign prostatic hyperplasia (BPH). It has been approved in Japan in a topical form to treat glaucoma. The mechanism of action is a reduction of aqueous outflow through the uveoscleral pathway resulting in lowering the intraocular pressure. It also may act to improve blood flow to the ocular nerve. Systemic Alpha-1 adrenergic receptor antagonists have been implicated in Intraoperative Floppy Iris Syndrome (IFIS). Bunazosin potentially could have the same effect but there has been no research to substantiate this as a risk for cataract surgery.
This article is issued from Wikipedia - version of the Saturday, April 02, 2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.