Repositioning Candidate Details

Candidate ID: R0431
Source ID: DB01162
Source Type: approved
Compound Type: small molecule
Compound Name: Terazosin
Synonyms: 1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-4-((tetrahydro-2-furanyl)carbonyl)piperazine; Terazosin; Terazosine
Molecular Formula: C19H25N5O4
SMILES: COC1=C(OC)C=C2C(N)=NC(=NC2=C1)N1CCN(CC1)C(=O)C1CCCO1
Structure:
DrugBank Description: Terazosin is a quinazoline derivative alpha-1-selective adrenergic blocking agent indicated for benign prostatic hyperplasia and hypertension. Terazosin blocks adrenaline's action on alpha-1 adrenergic receptors, causing relaxation of smooth muscle in blood vessels and the prostate.
CAS Number: 63590-64-7
Molecular Weight: 387.4329
DrugBank Indication: Terazosin is indicated for use in treating symptomatic benign prostatic hyperplasia and hypertension.
DrugBank Pharmacology: Terazosin is a quinazoline derivative alpha-1-selective adrenergic blocker.
DrugBank MoA: Terazosin is selective for alpha-1-adrenoceptors but not their individual subtypes. Inhibition of these alpha-1-adrenoceptors results in relaxation of smooth muscle in blood vessels and the prostate, lowering blood pressure and improving urinary flow. Smooth muscle cells accounts for roughly 40% of the volume of the prostate and so their relaxation reduces pressure on the urethra. It has also been shown that catecholamines induce factors responsible for mitogenesis and alpha-1-adrenergic receptor blockers inhibit this effect. A final long term mechanism of terazosin and other alpha-1-adrenergic receptor blockers is the induction of apoptosis of prostate cells. Treatment with terazosin enhances the expression of transforming growth factor beta-1 (TGF-beta1), which upregulates p27kip1, and the caspase cascade.
Targets: Alpha-1A adrenergic receptor antagonist; Alpha-1B adrenergic receptor antagonist; Alpha-1D adrenergic receptor antagonist; Potassium voltage-gated channel subfamily H member 2 inhibitor; Potassium voltage-gated channel subfamily H member 6 inhibitor; Potassium voltage-gated channel subfamily H member 7 inhibitor; Transforming growth factor beta-1 inducer
Inclusion Criteria: Therapeutic strategy associated