Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...
Reexamination Certificate
1999-04-14
2001-06-19
Raymond, Richard L. (Department: 1611)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Having -c-, wherein x is chalcogen, bonded directly to...
C544S315000, C544S316000
Reexamination Certificate
active
06248747
ABSTRACT:
BACKGROUND OF THE INVENTION
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.
Benign Prostatic Hyperplasia (BPH), also called Benigr. 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 norepinephrlne, 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;
2
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
, &agr;
1B
, &agr;
1C
, &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;
1C
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;
1C
antagonists may be effective agents for the treatment of BPH with decreased side effects.
This invention is directed to dihydropyrimidine compounds which are selective antagonists for cloned human &agr;
1C
receptors. This invention is also related to uses of these compounds for lowering intraocular pressure (Zhan, et. al.
Ophthalmol. Vis. Sci
., 34 Abst. #1133, 928, 1993), inhibiting cholesterol synthesis (D'Eletto and Javitt,
J. Cardiovascular Pharmacol
., 13 (Suppl. 2) S1-S4, 1989), benign prostatic hyperplasia, impotency (Milne and Wyllie, EP 0 459 666 A2, 1991), sympathetically mediated pain (Campbell, WO 92/14453, 1992), cardiac arrhythmia (Spiers, et. al.,
J. Cardiovascular Pharmacol
., 16, 824-830, 1990) and for the treatment of any disease where antagonism of the &agr;
1C
receptor may be useful.
SUMMARY OF THE INVENTION
This invention is directed to dihydropyrimidine compounds which are selective antagonists for cloned human &agr;
1C
receptors. This invention is also related to uses of these compounds for lowering intraocular pressure, inhibiting cholesterol synthesis, the treatment of benign prosmatic hyperplasia, impotency, cardiac arrhythmia and for the treatment of any disease where antagonism of the &agr;
1C
receptor may be useful. The invention further provides a pharmaceutical composition comprising a therapeutically effective amount of the above-defined compounds and a pharmaceutically acceptable carrier.
DETAILED DESCRIPTION OF THE INVENTION
The present invention is directed to compounds having the structures:
where A is
where each of Y
1
, Y
2
and Y
3
is independently H; straight chained or branched C
1
-C
7
alkyl, monofluoroalkyl or polyfluoroalkyl, C
2
-C
7
alkenyl or alkynyl; C
3
-C
7
cycloalkyl, monofluorocylcoalkyl, polyfluorocycloalkyl or cycloalkenyl; —F, —Cl, —Br, —I, —NO
2
, —N
3
, —CN, —OR
6
, —OCOR
6
, —COR
6
, —CONHR
6
, —CON(R
6
)
2
, —COOR
6
, —CF
3
or together constitute a methylenedioxy group;
where X is S, O or NH;
where R
1
is H; straight chained or branched C
1
-C
7
alkyl, monofluoroalkyl or polyfluoroalkyl, C
2
-C
7
alkenyl or alkynyl; C
3
-C
7
cycloalkyl, monofluorocylcoalkyl, polyfluorocycloalkyl or cycloalkenyl; —NHR
6
, —N(R
6
)
2
or —OR
6
;
where R
2
is H; straight chained or branched C
1
-C
7
alkyl, monofluoroalkyl or polyfluoroalkyl, C
2
-C
7
alkenyl or alkynyl; C
3
-C
7
cycloalkyl, monofluorocylcoalkyl, polyfluorocycloalkyl or cycloalkenyl; C
3
-C
10
cycloalkyl-C
1
-C
10
-alkyl, cycloalkyl-C
1
-C
10
-monofluoroalkyl or cycloalkyl-C
1
-C
10
-polyfluoroalkyl; —CN, —CH
2
XR
6
, —CH
2
X(CH
2
)
n
NHR
6
, —(CH
2
)
n
NHR
6
, —CH
2
X(CH
2
)
n
N(R
6
)
2
, —CH
2
X(CH
2
)
n
N
3
or —CH
2
X(CH
2
)
n
NHCXR
7
;
where n is an integer from 0 to 5 and where X is as defined above;
where R
3
is H; straight chained or branched C
1
-C
7
alkyl, monofluoroalkyl or polyfluoroalkyl, C
2
-C
7
alkenyl or alkynyl; C
3
-C
7
cycloalkyl, monofluorocylcoalkyl, polyfluorocycloalkyl or cycloalkenyl;
where R
4
is
where each R is independently H; F; straight chained or branched C
1
-C
7
alkyl, monofluoroalkyl or polyfluoroalkyl, C
2
-C
7
alkenyl or alkynyl;
where R
5
is H; straight chained or branched C
1
-C
7
alkyl, monofluoroalkyl or polyfluoroalkyl, C
2
-C
7
alkenyl or alkynyl; C
3
-C
7
cycloalkyl, monofluorocylcoalkyl, polyfl
Chiu George
Dhar T. G. Murali
Gluchowski Charles
Marzabadi Mohammad R.
Nagarathnam Dhanapalan
Cooper & Dunham LLP
Rao Deepak R.
Raymond Richard L.
Synaptic Pharmaceutical Corporation
White John P.
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