Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...
Reexamination Certificate
2001-06-04
2004-01-20
Raymond, Richard L. (Department: 1624)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Having -c-, wherein x is chalcogen, bonded directly to...
C514S275000, C544S278000, C544S316000
Reexamination Certificate
active
06680323
ABSTRACT:
Throughout this application, various references are referred to within parentheses. Disclosures of these publications in their entireties are hereby incorporated by reference into this application to more fully describe the state of the art to which this invention pertains.
BACKGROUND OF THE INVENTION
The designation “&agr;
1A
” is the appellation recently approved by the IUPHAR Nomenclature Committee for the previously designated “&agr;
1C
” cloned subtype as outlined in the 1995 Receptor and Ion Channel Nomenclature Supplement (Watson and Girdlestone, 1995). The designation &agr;
1A
is used throughout this application and the supporting tables and figures to refer to this receptor subtype. At the same time, the receptor formerly designated &agr;
1A
was renamed &agr;
1D
. The new nomenclature is used throughout this application. Stable cell lines expressing these receptors are described herein; however, these cell lines were deposited with the American Type Culture Collection (ATCC) under the old nomenclature (infra).
Benign Prostatic Hyperplasia (BPH), also called Benign Prostatic Hypertrophy, is a progressive condition which is characterized by a nodular enlargement of prostatic tissue resulting in obstruction of the urethra. This results in increased frequency of urination, nocturia, a poor urine stream and hesitancy or delay in starting the urine flow. Chronic consequences of BPH can include hypertrophy of bladder smooth muscle, a decompensated bladder and an increased incidence of urinary tract infection. The specific biochemical, histological and pharmacological properties of the prostate adenoma leading to the bladder outlet obstruction are not yet known. However, the development of BPH is considered to be an inescapable phenomenon for the aging male population. BPH is observed in approximately 70% of males over the age of 70. Currently, in the United States, the method of choice for treating BPH is surgery (Lepor, H.,
Urol. Clinics North Amer.,
17, 651 (1990)). Over 400,000 prostatectomies are performed annually (data from 1986). A medicinal alternative to surgery is clearly very desirable. The limitations of surgery for treating BPH include the morbidity rate of an operative procedure in elderly men, persistence or recurrence of obstructive and irritative symptoms, as well as the significant cost of surgery.
&agr;-Adrenergic receptors (McGrath, et. al.
Med. Res. Rev.,
9, 407-533, 1989) are specific neuroreceptor proteins located in the peripheral and central nervous systems on tissues and organs throughout the body. These receptors are important switches for controlling many physiological functions and, thus, represent important targets for drug development. In fact, many &agr;-adrenergic drugs have been developed over the past 40 years. Examples include clonidine, phenoxybenzamine and prazosin (treatment of hypertension), naphazoline (nasal decongestant), and apraclonidine (treating glaucoma). &agr;-Adrenergic drugs can be broken down into two distinct classes: agonists (clonidine and naphazoline are agonists), which mimic the receptor activation properties of the endogenous neurotransmitter norepinephrine, and antagonists (phenoxybenzamine and prazosin are antagonists), which act to block the effects of norepinephrine. Many of these drugs are effective but also produce unwanted side effects (for example, clonidine produces dry mouth and sedation in addition to its antihypertensive effects).
During the past 15 years a more precise understanding of &agr;-adrenergic receptors and their drugs has evolved through increased scientific scrutiny. Prior to 1977, only one &agr;-adrenergic receptor was known to exist. Between 1977 and 1988, it was accepted by the scientific community that at least two &agr;-adrenergic receptors (&agr;
1
and &agr;
2
) existed in the central and peripheral nervous systems. Since 1988, new techniques in molecular biology have led to the identification of at least six &agr;-adrenergic receptors which exist throughout the central and peripheral nervous systems: &agr;
1A
(new nomenclature) &agr;
1B
, &agr;
1D
, (new nomenclature), &agr;
2A
, &agr;
2B
and &agr;
2C
(Bylund, D. B., FASEB J., 6, 832 (1992)). In many cases, it is not known precisely which physiological responses in the body are controlled by each of these receptors. In addition, current &agr;-adrenergic drugs are not selective for any particular &agr;-adrenergic receptor. Many of these drugs produce untoward side effects which may be attributed to their poor &agr;-adrenergic receptor selectivity.
Since the mid 1970's, nonselective &agr;-antagonists have been prescribed to treat BPH. In 1976, M. Caine, et al. (Brit. J. Urol., 48, 255 (1976)), reported that the nonselective &agr;-antagonist phenoxybenzamine was useful in relieving the symptoms of BPH. This drug may produce its effects by interacting with &agr;-receptors located on the prostate. However, this drug also produces significant side effects such as dizziness and asthenia which severely limit its use in treating patients on a chronic basis. More recently, the &agr;-adrenergic antagonists prazosin and terazosin have also been found to be useful for treating BPH.
However, these drugs also produce untoward side effects. It has recently been discovered that the &agr;
1A
receptor is responsible for mediating the contraction of human prostate smooth muscle (Gluchowski, C. et. al., WO 94/10989, 1994; Forray, C. et. al.,
Mol. Pharmacol.
45, 703, 1994). This discovery indicates that the &agr;
1A
antagonists may be effective agents for the treatment of BPH with decreased side effects. Further studies have indicated that the &agr;
1A
receptor may also be present in other lower urinary tract tissues, such as urethral smooth muscle (Ford et al. Br. J. Pharmacol., 114, 24P, (1995)).
This invention is directed to dihydropyrimidine compounds which are selective antagonists for cloned human &agr;
1A
receptors. This invention is also related to uses of these compounds for treating benign prostatic hyperplasia, and for the treatment of any disease where antagonism of the &agr;
1A
receptor may be useful.
SUMMARY OF THE INVENTION
This invention is directed to compounds having the structure:
wherein R
1
is —OCH
3
or OH;
wherein R
2
is —CH
2
OH, —CH
2
OCH
3
, or —COOH;
wherein R
1
and R
2
together form a 5-membered lactone ring;
wherein R
3
is selected from the group consisting of —(CH
2
)
3
OH,
provided that when R
1
is OH, R
3
cannot be
or a pharmaceutically acceptable salt thereof.
This invention is also directed to a compound having the structure:
This invention provides a pharmaceutical composition comprising a therapeutically effective amount of any one of the compounds described herein and a pharmaceutically acceptable carrier.
This invention also provides a method of treating a subject suffering from benign prostatic hyperplasia which comprises administering to the subject an amount of any one of the compounds described herein effective to treat benign prostatic hyperplasia.
This invention provides a method of relaxing lower urinary tract tissue which comprises contacting the lower urinary tract tissue with an amount of any one of the compounds described herein effective to relax lower urinary tract tissue.
This invention provides a method of inhibiting contraction of prostatic tissue in a subject which comprises administering an amount of any one of the compounds described herein effective to inhibit contraction of prostatic tissue.
This invention provides a method of treating a disease which is susceptible to treatment by antagonism of the &agr;
1A
receptor which comprises administering to the subject an amount of any one of the compounds described herein effective to treat the disease.
This invention provides a pharmaceutical composition comprising a therapeutically effective amount of any one of the compounds described herein in combination with a therapeutically effective amount of finasteride and a pharmaceutically acceptable carrier.
This invention provides a process of making a pharmaceutical composi
Cui Donghui
Davis Margaret R.
Dunn Michael
Evans Ben E.
Kari Hanumath P.
Cooper & Dunham LLP
Raymond Richard L.
Synaptic Pharmaceutical Corporation
White John P.
LandOfFree
Dihydropyrimidines and uses thereof does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Dihydropyrimidines and uses thereof, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Dihydropyrimidines and uses thereof will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-3215339