RBx 6198: A novel α1-adrenoceptor antagonist for the treatment of benign prostatic hyperplasia

K Nanda, KS Naruganahalli, S Gupta… - European journal of …, 2009 - Elsevier
The present study, investigates the effect of RBx 6198, 2-{3-[4-(2-Isopropoxy-phenyl)-
piperazin-1-yl]-propyl}-3a, 4, 7, 7a-tetrahydro-isoindole-1, 3,-dione, a novel α1-adrenoceptor …

In vivo receptor binding of novel α1-adrenoceptor antagonists for treatment of benign prostatic hyperplasia

S Yamada, T Ohkura, R Kimura, K Kawabe - Life sciences, 1998 - Elsevier
New types of α1-adrenoceptor antagonists (tamsulosin, KMD-3213 and JTH-601) are
currently receiving a great deal of attention, especially in terms of developing effective …

Pharmacological characterization of A‐131701, a novel α1‐adrenoceptor antagonist selective for α1A‐ and α1D‐compared to α1B‐adrenoceptors

AA Hancock, SA Buckner, ME Brune… - Drug Development …, 1998 - Wiley Online Library
New compounds selective for α1A‐adrenoceptors in the prostate may offer enhanced
efficacy for benign prostatic hyperplasia (BPH), with fewer side effects than current …

Pharmacological characterization of [3H]-JTH-601, a novel α1-adrenoceptor antagonist: Binding to recombinant human α1-adrenoceptors and human prostates

M Takahashi, T Taniguchi, H Kanamaru, K Okada… - Life sciences, 2000 - Elsevier
Several α1-adrenoceptor (AR) selective antagonists are now widely used to improve lower
urinary tract symptoms in benign prostatic hyperplasia patients. However, these drugs often …

Subtype selective α1-adrenoceptor antagonists for the treatment of benign prostatic hyperplasia

C Forray, SA Noble - Expert Opinion on Investigational Drugs, 1999 - Taylor & Francis
Benign prostatic hyperplasia (BPH) is highly prevalent in the male population beyond the
age of 60. Impairment of urinary flow due to prostate enlargement gives rise to symptoms of …

An investigation of the uroselective properties of four novel α1a-adrenergic receptor subtype-selective antagonists

VL Pulito, X Li, SS Varga, LS Mulcahy, KS Clark… - … of Pharmacology and …, 2000 - ASPET
The development of α 1a-adrenergic receptor (AR) subtype-selective antagonists is likely to
result in uroselective agents that effectively treat benign prostatic hyperplasia (BPH) …

Selective α (1)-Adrenoceptor Antagonists in Benign Prostatic Hyperplasia: Rationale and Clinical Experience

CR Chapple - European urology, 1996 - karger.com
Symptomatic benign prostatic hyperplasia (BPH) is a common condition in older men and
has a significant impact on their daily lives. Transurethral resection of the prostate is …

Effect of JTH-601, a novel α1-adrenoceptor antagonist, on prostate function in dogs

Y Suzuki, A Kanada, Y Okaya, K Aisaka - European journal of …, 2000 - Elsevier
We examined the effect of JTH-601 (3-{N-[2-(4-hydroxy-2-isopropyl-5-methylphenoxy) ethyl]-
N-methylaminomethyl}-4-methoxy-2, 5, 6-trimethylphenol hemifumarate), a new α1L …

Tamsulosin: a review of its pharmacological properties and therapeutic potential in the management of symptomatic benign prostatic hyperplasia

MI Wilde, D McTavish - Drugs, 1996 - Springer
Synopsis Tamsulosin is the first subtype-selective (α 1A) α 1 adrenoceptor antagonist with
specificity for prostatic α 1 adrenoceptors (α 1A adrenoceptors are thought to be involved in …

Actions of A-131701, a Novel, Selective Antagonist forAlpha-1A Compared with Alpha-1B Adrenoceptors on Intraurethral and Blood Pressure Responses in …

AA Hancock, ME Brune, DG Witte, KC Marsh… - … of Pharmacology and …, 1998 - ASPET
A-131701 (3-[2-((3aR, 9bR)-cis-6-methoxy-2, 3, 3a, 4, 5, 9b, hexahydro-[1H]-benz [e]
isoindol-2-yl) ethyl] pyrido [3′, 4′: 4, 5] thieno [3, 2-d] pyrimidine-2, 4 (1H, 3H)-dione) is a …