CA2186224C - Amidino derivatives useful as nitric oxide synthase inhibitors - Google Patents

Abstract

There is disclosed amidino derivatives of formula (I), pharmaceutical compositions containing these derivatives, and their use in therapy, in particular their use as nitric oxide synthase inhibitors wherein: X is alkyl, alkenyl, alkynyl, -(CH2)kQ(CH2)l- where k is 2 or 3, l is 1 or 2 and Q is 0, Se SiY2 where Y is alkyl, S(O)z where z is 0, 1 or 2, NR where R is hydrogen or alkyl, or -(CH2)mA(CH2)n- where m is 0, 1 or 2, n is 0, 1 or 2, A is 3 to 6 membered aromatic hydrocarbon radical or 3 to 6 membered heterocyclic radical wherein 1 to 3 hetero atoms are oxygen, sulfur or nitrogen and wherein all said radicals may optionally be substituted by one or more substituents such as alkyl, alkoxy, hydroxy, halogen, nitro, cyano, trifluoroalkyl and amino; R1 may be a bond to X or hydrogen (when Q is Se), hydroxyalkyl, alkyl, alkenyl, alkynyl or haloalkyl and wherein all said radicals may optionally be substituted by one or more substituents such as alkyl, alkoxy, hydroxy, halogen, nitro, cyano, trifluoroalkyl and amino; R2 is alkyl, alkenyl, alkynyl, aromatic hydrocarbon radical, haloalkyl, hydroxylamine or heterocyclic radical wherein 1 to 3 hetero atoms are oxygen, sulfur or nitrogen and wherein all said radicals may optionally be substituted by one or more substituents such as alkyl, alkoxy, hydroxy, halogen, nitro, cyano, trifluoroalkyl and amino; and R3 is amino, alkylamine, amino acid, hydroxy, alkoxy, tetrazole or tetrazoloamine.

Description

i ! Wo 95a~~1~ 218 6 2 2 4 PCT~TS95103589 Backaro and of th- r_nv n ,on The present invention relates to novel amidino derivates, pharmaceutical compositions containing these novel compounds, and to their use in therapy, in particular their use as nitric oxide synthase inhibitors.
It has been known since the early 1980~s that the vascular relaxation brought about by acetycholine is dependent on the presence of the endothelium and this activity was ascribed to a labile humoral factor termed endothelium-derived relaxing factor (EDRF). The activity of nitric oxide (NO) as a vasodilator has been known for well over 100 years and NO is the active component of amylnitrite, glyceryltrinitrite and other nitrovasodilators. The recent identification of EDRF as NO has coincided with the discovery of a biochemical pathway by which NO is synthesized-from the amino acid L-arginine by the enzyme NO synthase.
NO is the endogenous stimulator of the soluble guanylate cyclase arid is involved in a number of biological actions in addition to endothelium-dependent relaxation including cytotoxicity of phagocytic cells and cell-to-cell communication in the central nervous system (see Moncada et al. B'o h ms~aT pharmacnlOrn,,. '~R, 1709-1715 (1989) and Moncada a . ha~a oloasnal Ravipwa~
a ~, 109-142 (1991). It is now thought that excess No production may be involved in a number of conditions, particularly conditions which involve systemic ~UBSTITL~TE SHEET (RULE 26~

WO 95125717 2 I 8 6 2 2 4 PCT~595/03589 hypertension such as toxic shock and therapy with certain cytokines. -The synthesis of No from-L-arginine can be inhibited by the L-arginin~ analogue, L-N-monomethyl-arginine_(L-NMMA) and the therapeutic use of L-NMMA for the treatment of toxic shock and other types- of systemic hypertension has been proposed-(WO 91/04024 and GB-A-2240041). The therapeutic use of certain-other NO synthase inhibitors apart from L-NMMA for the same purpose has also been proposed in WO 91104024 and in EP-A-0446699.
It has recently become apparent that there- are at-least two types of NO synthase as follows:
(i) a constitutive, Ca++lcalmodulin dependent enzyme that releases NO inresponse to receptor-cr physical stimulation.
(ii) a Ca+f independent-enzyme which is induced after activation -of vascular smooth muscle, macrophages, endothelial cells, and a number of other cells by endotoxin and eytokines. Once expressed this inducible NO synthase synthesizes NO for long periods.
The N0-released by the constitutive enzyme acts as a transduction mechanism underlying several physiologicab responses. The NO produced by the inducible enzyme is a cytotoxic molecule for tumor cells and. invading microorganisms. .It also appears that the adver-se effects of excess N0 production, in particular pathological-vasodilation and tissue damage, may result largely from the effects of NO synthesized by the induci7~le NO -synthase.
Some of the NO synthase inhibitors proposed for .
therapeutic use.so far, and in particular L-NMMA, are non-selective in that they inhibit both the constitutive and the inducible NO synthase_ Use of such a non-BUBST(TUTE SHEET (RUSE Z8~

WO 951257f7 _, . 21 ~ 6 2 2 4 PCT/US95/03589 selective NO synthase inhibitor reguires that great care be taken in order to avoid the potentially serious consequences of over-inhibition of the constitutive NO-synthase including hypertension and possible thrombosis ,' 5 and tissue damage. In particular, in the case of the therapeutic use of L-NMMA for the treatment of toxic shock it has been recommended-that-the patient must be subject to continuous blood pressure monitoring throughout the treatment. Thus, while non-selective NO
synthase inhibitors have therapeutic utility provided that appropriate precautions are taken, NO synthase inhibitors which are selective in the sense that they inhibit the inducible NO synthase to a considerably greaterextent than the constitutive N0 synthase would be of even greater therapeutic benefit and easier to use.
WO 93/13055, W093/24126 and LT S. Patent No:
5,132,453 disclose compounds that inhibit nitric oxide synthesis and preferentially inhibit the inducible isoform of nitric oxide .synthase.
SUBSTITUTE SHEEP (RW.E ~j WO 95!25717 2 i 8 b 2 2 4 PCT~S95/03589 The present invention provides amidino derivatives of the formula-(I): -R2 p /~ X
HN~N~ R3 H \
H2N R~
(I) salts, pharmaceutically acceptable esters and prodrugs thereof, wherein X is lower alkyl, lower alkenyl, lower alkynyl, -(CH2)kQ(CH2)1- where k is 2 or 3, 1 is 1 or 2 and Q is 0, Se, SiY2 where Y is lower alkyl, S(0)Z where.a is D, 1 or 2, NR where R is hydrogen or lower alkyl, or -(CH2)mA(CH2)n- where m is 0, 1 or 2, n is 0, 1 or 2, A
is a 3 to 6 membered aromatic hydrocarbon radical or 3 to 6 membered heterocyclic radical wherein 1 to 3 hetro atoms are oxygen, sulfur Dr nitrogen and wherein all said radicals may optionally be substituted by one or more-substituents such as lower alkyl, lower alkoxy, hydroxy, halogen, vitro, cyano, trifluoroalkyl and amino;
, R1 maybe a bond tp x, or a radical selected-from the group consisting of hydrogen (when Q is Se), hydroxyalkyl, lower alkyl, lower alkenyl, lower alkynyl, or haloalkyl and-wherein all said radicals may optionally be substituted by one or more substituents such as lower alkyl, lower alkoxy, hydroxy, halogen, vitro, cyano, trifluoroalkyl and amino;
SUBSTITUTE SHEET ~RU~.E 26) W O 951257 f7 218 6 2 2 4 PCT~S95/113589 R2 is lower alkyl, lower-alkenyl, lower alkynyl, aromatic hydrocarbon radical, haloalkyl, hydroxylamine or heterocyclic radical wherein 1 to 3 hetro atoms are oxygen, sulfur-or nitrogen and wherein all said radicals S may optionally be substituted by one or more substituents such as lower alkyl, lower alkoxy, hydroxy, halogen, vitro, cyano, trifluoroalkyl and amino; and R3 is amino, alkylamine, amino acid, hydroxy, lower alkoxy, tetrazole, or tetrazoloamine.
The invention further relates to. pharmaceutical compositions comprising a compound of formula (I).
Compounds and compositions defined_above have usefulness as inhibitors of nitric oxide synthase. These compounds also prefentially inhibit the inducible farm over the constitutive form of nitric oxide synthase and in the most prefered form inhibit the inducible form over the constitutive form of nitric-oxide synthase by at least 3 fold.
Conditions in which there is an advantage in inhibiting NO production from L-arginine include systemic hypotension associated with septic and/or toxic shock induced by a wide variety of agents; therapy with cytokines such as TNF, IL-1 and IL-2; and as an adjuvant to short term immunosuppression in transplant therapy.
Thereis also a growing body of evidence that NO may be involved in the degeneration of cartilage which takes place in certain conditions such as arthritis and it -is ~ also known that NO synthesis is increased in rheumatoid arthritis. Accordingly, further conditions in which there is an advantage in inhibiting NO production from L-arginine include autoimmune and/or inflammatory conditions affecting the joints, for example arthritis.
SUBSTITi UIrE SHEET (RU~.E 28j wo 9sns~ W 218 6 2 2 4 P~~S9s103S89 Still.further conditions in which there is an advantage in inhibiting NO production-from L-arginine include inflammatory bowel disease, cardiovascular -.
ischemia, diabetes, cerebral ischemia and other=CNS
disorders mediated by NO. , A preferred-embodiment of-the present invention is a compound of-the formula (I):
Rz O
/~ X
HN~N~ R3 H \
HzN Ri .. _ -(I) and salts, and pharmaceutically acceptable ester and prodrugs thereof, wherein:
X is lower alkyl, lower alkenyl, lower alkynyl, -(CH2)kQ(CH2)1- where k is 2 or 3, 1 is-1 or 2 and Q is 0, Se, SiY2 where Y is lower alkyl, S(O)Z where--z is-0, 1 or 2, NR where A is hydrogen or lower alkyl, or --(CH2)mA(CH2)n- where m is 0, 1 or-2, n is 0, 1 or 2, A
is a 3 to 6 membered aromatic hydrocarhon radicalor heterocyclic radical wherein-1-to 3 hetro atoms are oxygen, sulfur or-nitrogen andwherein all said-radicals may optionally be substituted by one or more _ substituents such as lower alkyl, lower alkoxy,-=hydroxy, , halogen,- nitro, cyano, trifluoroalkyl and amino;
R1-maybe a bond to X, or -a radical selected from the group consisting of hydrogen (when Q is Se), hydroxyalkyl, lower alkyl or haloalkyl;
~U$STITUTE SHEET (RW.E 26) WO 95125717 - , . ~ ~ g ~ 2 2 ~ PCTlUS95/03589 R2 is lower alkyl, lower alkenyl, lower alkynyl, aromatic hydrocarbon radical , haloalkyl, or hydroxylamine; and R3 is amino, alkylamine, natural amino acid, hydroxy, lower alkoxy, tetrazole, or tetrazoloamine.
Another preferred embodiment of the present invention is a compound of the formula (I) /~ X
HN~N~ R3 H \
H2N Ri (I) and salts, and pharmaceutically acceptable ester and prodrugs thereof, wherein:
X is a lower alkyl of 1 to about 6carbon atoms, lower alkenyl of 1 to about 6 carbon atoms, lower alkynyl of 1 toabout 6carbon atoms, -(CH2)kQ(CH2)1- where k is 2 or 3, 1 is 1 or 2 and Q is 0, Se, SiY2 whereY is lower alkyl, S(O)z where z is 0, 1 or 2, or NR where R is H or lower alkyl; or -(CH2)mA(CH2)n- where m is 0, 1 or 2, n is 0, 1 or 2, A is a 3 to 6 membered aromatic hydrocarbon radical or heterocyclic radical wherein 1 to 3 hetero atoms are oxygen, sulfur or nitrogen and wherein all said radicals may optionally be substituted by one or more substituents such as lower alkyl, lower alkoxy, hydroxy, halogen, nitro, cyano, trifluoroalkyl and amino;
R1 is hydrogen (when Q is Se), a hydroxyalkyl group of 1 to about 4 carbon atoms, a lower alkyl group of 1 to suBS~nr~ sHE~r c~u~.E ~s~

WO 95125717 , ~ ~ 4 PCTlU595103589 about 4 carbon atoms or a haloalkyl group of 1 to about 4 carbon atoms;
A2 is lower alkyl of,:1 to about 4- carbon atoms, -lower alkenyl of 1 to about 4 carbon atoms alkynyl of-1 , to about 4 carbon atoms, aromatic hydrocarbon radical of 3 to about 6 carbon atoms and haloalkyl of 1 to about -4-carbon atoms; and R3 is an amino, alkylamine of 1 to about 9 carbon atoms, hydroxy, lower alkoxy of 1 to about 4 carbon atoms, tetrazole, tetrazoloamine, or natural amino acid.
Still another preferred-embodiment-of formula (I) is X is an alkylerie group-having 3 to 5 carbon atoms and which may optionally be substituted by one or more C1-3 alkyl; a group of formula -(CH2)kQ(CH2)1- where:k is 2-or 3, 1 is 1 or 2 and Q is O, Se, S(0)z-where z is 0, 1 or 2; or a group of formula -(CH2)mA(CH2)n- where m is 0, 1 or 2, n us 0;-1 or 2, A is-a-3-to 6 membered carbocyclic or heterocyclic ring;
Rl is hydrogen (when Q is Se), a hydroxyalkyl grog of-1 to.about 4 carbon atoms, a lower alkyl radical of-1 to about 4 carbon atoms; -R2 is lower alkyl radical. of l.to about 4 carbon atoms;
R3 is an amino, alkylamine of 1 to about 4, carbon atoms, hydroxy, lower-alkoxy group of 1 to about 4 carbon -atoms.
The Fresent invention includes compounds of formula (I) in the form of--salts, in-particular acid addition -salts. Suitable--salts include those formed with both organic and inorganic acids. Such acid addition salts.
~UgSTITU'~E SHEET (RULE ~) W 0 95125717 PCT/UB95~03589 will normally be pharmaceutically acceptable although salts of non-phaxinaceutically acceptable salts may be of utility in the preparation and purification of the compound in question. Thus, preferred salts include those formed from hydrochloric, hydrobromic, sulphuric, citric, tartaric, phosphoric, lactic, pyruvic, acetic, succinic, oxalic, fumaric, malefic, oxaloacetic, methanesulphonic, ethanesulphonic, p-toluenesulphonic, benzenesulphonic and isethionic acids. Salts of the compounds of formula (I) can be made by reacting the appropriate compound in the form of the free base with the appropriate acid.
While it may be possible for the compounds of 15-- formula (I) to be administered as the raw chemical, it is pref-_erable to present them as a pharmaceutical formulation. According to a further aspect, the present invention provides a pharmaceutical formulation comprising a compound of formula (I) or a pharmaceutically acceptable salt orsolvate thereof, together with one or more pharmaceutically acceptable carriers thereof and optionally one or more other therapeutic ingredients. The carriers) must be "acceptable" in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.-The formulations include those suitable for aral, parenteral (including subcutaneous, intradermal, intramuscular, intravenous and iiitraarticular), rectal and topical (including dermal, buccal, sublingual and - intraocular) administration although the most suitable route may depend upon for example the condition and disorder of-the recipient. The formulations may conveniently be presented in unit dosage form and may be prepared by any of the methods well known in the art of pharmacy. All methods include the step of bringing into -SUBSTITUTE SHEET' (RULE 28) association a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof -. '.
("active ingredient") with the carrier-which constitutes one or more accessory ingredients. In general,the 5 formulations are prepared by uniformly and,intimately .
bringing into association the active ingredient with liquid carriers. or finely divided solid carriers or both and then, if necessary, shaping the product into the desired-foz'mulation:
Formulations of the present invention-suitable for-oral administration may be presented as discrete units such as capsules, cachets or -tablets--each containing a-:
predetermined amount of the active ingredient; as a powder or granules; as a solution or a suspension in an-aqueousliquid o-r a non-aqueous liquid; or-~s ari oil-in-water liquid emulsion or a water-in-oil liquid emulsion:
The active ingredient may also-be presented as a bolus~_ electuary or paste.
A tablet may be made by comp-ression or-moulding, -optionally with one or more accessory ingredients.
Compressed- tablets may be prepared by compressing- in a suitable machine the active ingredient in a free-flowing form such as a powder,Dr-granules, optionally mixed with a binder, lubricant, inert diluent, lubricating, surface active or dispersing agent. Moulded tablets may be made by moulding in a suitable machine a mixture of the powdered compound moistened with an inert liquid diluent.
The tablets may optionally be coated or scored and may-be formulated so as-~o provide slow or controlled release of the active ingredient therein.
Formulations for parenter-al administration-include aqueous and non-aqueous sterile injection solutions which may contain antioxidants, buffers, bacteriostats and solutes which render the formulation isotonic with the SUBSTITUTE SHEET (RULE 26~

W O 95/2571'7 218 6 2 2 4 P~~S95/03589 blood of the intended recipient; and aqueous and non-aqueous sterile suspensions which may include suspending ~ agents and thickening agents.., The formulations may be presented in unit-dose or multi-dose containers, for _ 5 example sealed ampoules and vials, and may be stored in a freeze-dried (lyophilized) condition requiring only the addition of the sterile liquid carrier, for example, saline, water-for-injection, immediately prior to use.
Extemporaneous injection so-lutions and suspensions may be prepared from sterile powders, granules and tablets of the kind previously described.
Formulations for rectal administration may be presented as a suppository with the usual carriers such as cocoa butter or polyethylene glycol.
Formulations for topical administration in the mouth, for example buccally or sublingually, include lozenges comprising the active ingredient in a flavored basis such as sucrose and acacia or tragacanth, and pastilles comprising the active ingredient in a basis such as gelatin and glycerin or sucrose and acacia.
Preferred unit dosage formulations are-those containing an effective dose, as hereinbelow recited, or an appropriate fraction thereof, of the active ingredient.
It should be understood that in addition to the ingredients particularly mentioned above, the formulations of this invention may include other agents conventional in the art having regard to the type of formulation in question, for example those suitable for oral administration may include flavoring agents.
The compounds of the invention may be administered ' orally or via injection at a dose of from 0.1 to 500 SUBSTITUTE SHEET (RULE 26) WO 95/25717 218 6 2 2 4 PCT~S95103589 mg/kg per day. The dose xange for-adult humans'is -generally from Smg to 2g/day. :Tablets or other-.forms of presentation provided..in_discrete units may conveniently contain an amount of compound of -the invention which is-effective at su-ch-dosage or as-a multiple of the same,--.
for instance, units containing Smg to 500mg, usually around lOmg to 200mg.
The compounds of formula -(I) are preferably administered orally or by injection (intravenous or subcutaneous). The precise-amount of compound administered to a patient will-be the responsibility of the attendant physician. However, the dose employed will depend on a number of -factors, including the age and sex of-the patient, the precise disorder being treated, and its severity. Also, the route of administration may vary depending on the--condition and its severity.
As utilized herein, the t-erm °lower alkyl", alone or in combination, means an acyclic alkyl radical containing from 1 to about-10, preferably from 1 to about 8 carbon atoms and more-preferably 1-to about 6 carbon atoms.
Examples of such-radicals'incl-ude methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl,tert-butyl, pentyl, isn-amyl, hexyl, octyl and the like.
The term °lower alkenyl~~ refers to an unsaturated acyclic-hydrocarbon radical in so much as it contains at least one double bond. Such radicals containing from -about 2 to about10-carbon atoms, preferably from about Z
to about 8 carbon atoms and morE preferably 2 to about 6 carbon atoms. Examples of-suitable alkenyl radicals -include-propylenyl, buten-1-yl, isobutenyl, pentenylen-1-yl, 2-2-methylbuten-1-yl, 3-methylbuten-1-yl, hexen-1-yl, hepten-1-yl, and octen-1-yl, and the like.
SUBSTITUTE SHEET ~RW.E ~) WO 95125717 ~ PCT/US95/03589 The term "lower alkynyl" refers to an unsaturated acyclic hydrocarbon radicals in so much as it contains one or more triple bonds, such radicals containing about 2 to about 10 carbon atoms, preferably having from about 2 to about 8 carbon atoms and more preferably having 2 to about 6 carbon atoms. Examples of suitable alkynyl radicals include ethynyl, propynyl, butyn-1-yl, butyn-2-yl, pentyn-1-yl, pentyn-2-yl, 3-methylbutyn-1-yl, hexyn-1-yl, hexyn-2-yl, hexyn-3-yl, 3,3-dimethylbutyn-1-yl radicals and the like, The term "aromatic hydrocarbon radical" means 4 to about 16 carbon atoms, preferably 6 to about.l2 carbon atoms, more-preferably 6 to about 10 carbon atoms.
Examples of suitable aromatic hydrocarbon radicals include phenyl,naphthyl, and the like.
The term °heterocyclyl radical-° means a saturated or unsaturated cyclic hydrocarbon radical with 4 to about 10 carbon atoms, preferably about 5 to about 6; wherein 1 to about 3 carbon atoms are replaced by nitrogen, oxygen or sulfur. The "heterocyclic radical" may be fused to an aromatic hydrocarbon radical. Suitable examples include pyrrolyl, pyridinyl, pyrazolyl, triazolyl, pyrimidinyl, pyridazinyl, oxazolyl, thiazolyl, imidazolyl, indolyl, thiophenyl, furanyl, tetrazolyl, 2-pyrrolinyl, 3-pyrrolinyl, pyrrolindinyl, 1,3-dioxolanyl, 2-imidazonlinyl, imidazolidinyl, 2-pyrazolinyl, pyrazolidinyl, isoxazolyl, isothiazolyl, 1,2,3-oxadiazolyl, 1,2,3-triazolyl, 1,3,4-thiadiazolyl, 2H
pyranyl, 4H-pyranyl, piperidinyl, 1,4-dioxanyl, - morpholinyl, 1,4-dithianyl, thiomorpholinyl, pyrazinyl, piperazinyl, 1,3,5-triazinyl, 1,3,5-trithianyl, benzo(b)thiophenyl, benzimidazolyl, quinolinyl, and the like.
~UBSTITUl'E SHEET (RULE ~

WO 95/25717 2 ~ PCTIUS95I03589 The term lower alkoxy", alone or in combination, means an alkyl ether radical wherein the term alkyl is as defined above and most preferably containing 1 to about 4 carbon atoms. Examples-of suitable alkyl ether radicals include methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, iso-butoxy, sec-butoxy, tert-butoxy and the like.
The term "halogen" means fluorine, chlorine; bromine or iodine.
The term amino acid-means an amino-alkanoic wherein the amino can be postioned anywhere on the alkyl group.-The alkyl is as is defined above.
The term "prodrug" refers to a compound that is made more -active in vivo.
As used herein, reference to °treatment" af-a patient is intended to include prophylaxis.
All references, patents or applications, U.S. or foreign, cited in the-application are hereby incorporated by reference as if written herein.
Disclosed-i.s a general synthetic processes useful in the preparation of the compounds of the present invention.
SUBSTITUTE SHEEP (RU~.E 26) WO 95125717 218 6 2 ~ 4 PCT~S95/03589 sc~sme x 8aN' ~ ~ ' COaC83 O
Cl H
MgS04 O
C1 ~ ~ ~N

N

1. NaN(Si(CH313y 2 . CHy I
3. HCl HyN CH;
~ \J' 'ox BaN~~/\~ ~~
O
1. C1iC03 2. ethyl acetimidate ~'Ia HaN C8;
~~J OH
H3C' N
H
O
SUBS~'ITUTE SHEET (RU~.E 25j W 0 95/25717 PCTIUS95l03589 16 -.
SCHEME dI
° ~s NaBH4 ~x ,s. ox ~~ aso~oa xo~so v ~~
Na= o 0 HZN-CHZ-CHz-Br ~1 Sa~ OH
HyN v ICI
O
I. L~C03 2. ethyl acetunidate NH NHy ~ se~ oa x3c v ~N
a RUBSTITUTE SHEET (RU~.E 26~

SCHEr~ III
- C (CxHs)zNSi(CH3)y o 82N' x ~ LSi(CH3)x7xN
'~ ~OH ~)2SQ! OSi(CHj)3 mo'pfCF NaNISi(CII;)31x ~ ~ Ri ~a l.Boc-NH(CT-I~aBr C
H N~~~ ~fSiICH3)x7xN
1 OSi(CHj)j O 2. 4N HCl/dioxane g1 ~
1. CuC03 2 ethyl aceiimidate N'IH R'i /NHx 1 ~ J~ -OH
Bj~N~~
H 'I0 ~UBST(TUTE SHEET ~RU~.E 28~

WO 95125717 ~ ~ PCTIUS95103589 SCHEMEIV
O NHS _ p OH
O N
~H O d NaOH
JQ~ HN v O" N~~
H O
AcaO, 90-100 eC
l \ ~ \
0 339' HCHO

pyridine p Q n O
SN HCl ~H I. CuCO; NHz H, CHaOH
C~-~ ~ ~~ N ~ OH
HiN
O 2. ethyl acetimidate H
O
SUBSTITUTE SHEET (RULE 26~

WO 95!2571T 218 6 2 2 4 PCT~S95/03589 SCH>;ME V
[Si(CH~]zN
. O (C2H5)2NSi(CH3)3 OSi(CH3)3 HZN
~ (NH4)2SOa N[Si(CH~3]z NHz NaN[Si(CH3)312 R~ NHz RtX, THF, 40 ~C
HzN~~OH ~~
I' OSi(CH3)a O
1. CuC03 N[Si(CH~3]z 2. ethyl acetimidate NH Ri NHz ~ OH
H3C' - N
H
O
SUgST(TUTE SHEET (RUtE 28) The invention is further illustrated Y7y the following examples:

a-Methyl-NS-iminoethyl-ornithine HN N ~ OOH
H \
NiiZ ~CH~s 10 a-Methyl-D,L-ornithine hydrochloride (250 mg; 1.37 mmoles purchased from Sigma) was dissolved in 5 ml of water and 0.5 g of cupric carbonate was added. The mixture was stirred at 60 OC for 1 hr and filtered. The pH of the filtrate was adjusted to pH 9.5 with 0.5 N NaOH solution.
15 Ethyl acetimidate hydrochloride (178 mg; 1.45 mmoles) was added and the pH was maintained at 9.0-9.5 for one hour.
The solution was then adjusted to a pH of 7.5 and kept at room temperature for 12 hours. The solution was acidified with 1 N HC1 to pH 4 and applied to a DowexTM 50 20 X 4 (hydrogen form ). The column was washed with water and then with 10 ~ pyridine. a-Methyl-N8-iminoethyl-ornithine was eluted from the column with 1 N NH~OH. The ninhydrin positive fractions were combined and lyophilized. The residue was dissolved in 0.5 N of aqueous hydrochloric acid and re-lyophilized. a-Methyl-N8-iminoethyl-ornithine hydrochloride appears as white solids. (MH+ = 188); 1H-NMR LD20): d 1.4 (s, 3H); 1.45-1.9 (m. 4 H) ; 2.15 (s, 3 H) ; 3 .3 (t, 2 H1 WO 951257f7 2 i 8 6 2 2 4 P~~S95/03589 a-Methyl-NS-iminoethyl-lysine ~ OH
HN' 'N
H I
O
A suspension of lysine ethyl ester dihydrochloride (33 g;
0.14 mole) and MgS04 (34 g; 0.28 moles) in a solution of 4-chloro-benzaldehyde (39 g; 0.28 moles) and acetonitrile 1500 m1) was stirred while N,N-diisopropylethylamine (36 g; 0.28 moles) was added in portions over 1/2 h. The mixture was stirred for 12 h, filtered, concentrated to a sma7.l volume, and diluted with 500 ml of ethyl ether. The .
ether solution was washed with 0.1$ aqueous NaHC03, aqueous 2 N NaOH containing 2g/100 m1 of NH20H.HC1, again with 0.1$ aqueous NaHC03 and saturated aqueous NaCl.
After drying with MgS04 and removal of the solvent in vacuo, ethyl N, N'-di(4-chloro-phenylmethylene)-L-alanine was obtained as a clear liquid. The liquid was triturated with hexanes and the resulting solid was washed with hexanes for several times. This partially purified intermediate was dissolved in 200 ml of THF and stirred in an acetone/dry ice bath. Sodium bis-(trimethylsilyl)amide in THF (11 ml, 1 M solution) was added dropwisely over 30 min. After one hour, methyl iodide (0.8-g; 13 mmoles) in THF was added dropwisely.
The reaction mixture was slowly warmed up to room temperature and stirred overnight. The mixture was diluted with water, and extracted with ethyl ether. The ether extract was iaashed with 0.1~ aqueous NaHC03 and saturated aqueous NaCl and concentrated to yield crude ethyl N.N'-di(4-chloro-phenylmethylene)-a-methyl-D,L-alanine (M + H= 434). This material (4 g) dissolved in SU~ST(TUTE SHEET (RU~.E 2~) ethyl .ether (100 ml) was stirred vigorously with 1 N HC1 (50 ml) fo.r 2 h, the layer :.;as separated and the aqueous phase was washed with ethyl ether. The aqueous solution was further acidified by the addition of concentrated HC1.
to 6 N and was =Bated to ref hax for 15 h. The solut_on was cooled to room temperature, and rotary evaporated to dryness. The residue was dissolved in water and applied to a DowexTM 50 x 4 (hydrogen form). The column was washed with water, and then 10% pyridine. a-Methyl-D,L-lysine.
~0 !MH+ H = 161) :aas eluted from the column with 1 M NH40H.
a-Methyl-D,L-lysine 1300 mg) was dissolved in water and 0.5 g of cupric carbonate was added. The suspension was stirred at 600 C for 1 h and filtered. The filtrate was adjusted to pH °.5 and ethyl acetimidate was added portionwise in 15 min. The pH was maintained at °.0 to 9.5. After 1 h cf stirring at room temperature, the solution was adjusted to pH 7 and the stirring was continued over~ight. a-Methyl-NE-iminoethyl-lysine caas purl f led by DowexTM 50 x 4 'hydrogen f orm ) chromatography similarly described for a-Methyl-N8-iminoethyl-ornithine.
MH+ = 202; 1T_-i-rrMR (D20) : d 1.4 (s, 3H) ; 1.5-1:8 (m, o H) ;
2.05 (s, 3 H) : ~ .1 (t, 2 H) .

gist-iminoethyl-aminoethylselenocysteine Se OH
HN N
H
O
Seleno-D,L-cystine (117 mg; 0.5 mmoles, purchased from Sigma) was suspended in 15 ml of nitrogen gas-purged water. Sodium borohydride (38 mg; 1 mole) was added. The reaction mixture became clear in a few minutes. After 2 h W0 95f25717 ' PCT/US95/03589 at room temperature, 2-bromoethylamine HC1 (1.2 g; 6 mmoles) was added and the reaction mixture was stirred ~ for 12 h. The reaction was applied on to a Dowex 50 X 4 (hydrogen form)- column. The column was washed with water . ' S and 10~ pyridine. 2-Aminoethyl-D,L-seleno-cysteine was eluted with 1 M NH40H and, subsequently, treated with cupric carbonate and ethyl acetimidate as described for N8-iminoethyl-ornithine. NE-iminoethyl-aminoethylselenocysteine-was obtained as pale yellow solids. MH+ = 254.

cx-Hydroxymethyl-Ne-iminoethyl-lysine NH2 CHpOH
OH
HN N
H
s O
To an ice-cold stirred mixture of Ne-Cbz-L-lysine (14 g;
0.05 moles, purchased from Sigma) in 2.5 N NaOH (24 ml), benzoyl chloride (10 g) was added gradually. The pH of the solution was maintained at.10.5-10.9 by addition of 2 N Na.OH. The mixture was stirred at room temperature for 1 h anal filtered. The filtrate was extracted with a small amount of ethyl acetate and the organic layer was dried over sodium sulfate. The solid was removed by filtration and the filtrate was evaporated to dryness. The remaining crude oily Ns-Cbz-Na-benzoyl-lysine (6 g) was heated at 90-1000 C with acetic anhydride (100 ml) for 30 min. The mixture was then evaporated. The residue was dissolved in pyridine and treated with aqueous formaldehyde (35~
solution, Fisher). The mixture was stirred for 8 hr, then diluted. The reaction mixture was kept at 100C overnight the precipitated crude material was hydrolyzed in boiling SUBSTITUTE SHEEN' (RU~.E

N HC1 during 5 h. The reaction mixture was cooled and filtered before being evaporated. The solid residue was dissolved in water and passed through DowexTM 50 x 4 (hydrogen form) column. a-Hydroxymethyl-D,L-lysine ~MFi+
5 _ 1771 was eluted with 1 N NH40H and, subsec_ruently, treated with cupric carbonate and ethyl acetimidate to form a-hydroxymethyl-NE-iminoethyl-lysine similarly described for a-Methyl-N8-iminoethyl-ornithine. MH+ _ 218. 1H-NMR (D20): d 1.1-1.8 (m, 6H1; 2.1 (s. 3H); 3:1 (t, 2H); 3.6-3.9 (a(a,b), 2H).
The activity of the above listed compounds as NO
synthase inhibitors have been determined in the following assays:
~~rr"lline-Assav fob Nitric Oxide Svnthase Nitric oxide synthase activity was measured by monitoring the conversion of [3H]-arginine to (3H)-citrulline. Mouse inducible nitric oxide synthase (miNOS) was prepared from an extract of LPS-treated RAw 264.7 cells and partially purified by DEAF-SepharoseTM chromatography. Rat brain constitutive nitric oxide synthase lrnNOS) was prepared from an extract of rat cerebellum and partially purified by DEAF-SepharoseTM chromatography. Enzyme and inhibitors were incubated at 37°C for 15 minutes in a reaction volume of 100 ~L with the following components added to start the reaction: 50 mM Tris (pH ~.6), 1 mg/ml bovine s erum a lbumi n , 1 mM DTT , ~ 2 mM C aC 12 , 10 ~.tM FAD , 10 ~t.M
30. tetrahydrobiopterin, 30 ~1M L-arginine containing L-[2,3-3H~-arginine at 300 cpm/pmole and 1 mM NADPH. For constitutive NOS, 50 nM calmodulin was also added. The reaction was terminated by addition of cold stop buffer containing 10 mM EGTA, 100 mM HEPES, pH 5.5 and 1 mM
citrulline. [3H]-Cit~rulline was separated by chromatography on DowexTM 50W X-8 ration exchange resin and W095I25717 ~ ~ PCT/US95/03589 radioactivity determined with a liquid scintillation counter.
Recombinant human inducible nitric oxide synthase (h1N05) 5 was extracted from Sf9 insect cells (infected with recombinant baculoviruses encoding a cDNA for human inducible nitric oxide synthase which has been isolated and purified from a lambda Zapll cDNA library made from RNA isolated from a colon sample from a patient with 10 ulcerative colitis) and partially purified by DEAE-chromatography.
15 RAw 264.7 cells are plated to confluency on a 96-well tissue culture plate grown overnight (17h) in the presence of LPS to induce NOS. A row of 3-6 wells were left untreated and served as controls for subtraction of nonspecific background. The media was removed from each 20 well and the cells are washed twice with Krebs-Ringers-Hepes (25mM, pH 7.4) with 2 mg/ml glucose. The cells are then placed on ice and incubated with 50 ~L of buffer containing L-arginine (30 ELM) +/- inhibitors for 1h. The assay is initiated by warming the plate tc 37°C in a 25 water bath for 1h. Production of nitrite by intracellular -iNOS is linear with time. To terminate the cellular assay, the plate of cells is placed on ice and the nitrite-containing buffer removed and analyzed for nitrite using a previously published fluorescent determination for-nitrite.-All values are the average of triplicate wells and are compared to a background-subtracted induced set of cells (100 value).
LPS is the abbreviation ~or lipopolysaccharide.
~UBSTI'rU'CE SHEET (RU~.E Z~j WO 95/25717 , ~ ~ ~ ~ PCT/US95103589 TABLE I -CompoundhiNOS miNOS rnNOS Raw -Cell _ .. :: __ .._ _._. . . _._ _. . _ __. . _.__ . __. . _ ICSp L~l IC50 LELMI
Example 1 73.5 39.9-- 355.9 25.0 _ Example 2 26.6 7.2 192.8 52.5 Example.3 35.5 5.0 - 229.0 0.37 Example 4 39~ Inh. 8.6~ Inh.
@ 10 ELM @ 10 ELM
From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention, and without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to- various usages and conditions.
sugs~rru~ sHF~r (RUB

Claims (7)

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:

1. A Compound having the formula:

salts, pharmaceutically acceptable esters and prodrugs thereof, wherein X is C1-C10 alkyl, C2-C10 alkenyl, C2-C10 alkynyl, - (CH2)kQ(CH2)1- where k is 2 or 3, l is 1 or 2 and Q is O, Se, SiY2 where Y is C1-C10 alkyl, S (O) z where z is 0, 1 or 2, NR where R is hydrogen or C1-C10 alkyl, and wherein all said radicals may optionally be substituted by one or more substituents selected from Cl-C10 alkyl , halogen, and trifluoroalkyl ;
R1 is hydrogen (when Q is Se) , C1-C10 alkyl or hydroxyalkyl;
R2 is C1-C10 alkyl, C2-C10 alkenyl, C2-C10 alkynyl or haloalkyl; and R3 is amino, alkylamine, amino acid, hydroxy, C1-C4 alkoxy, tetrazole, or tetrazoloamine.

2. The compound as recited in claim 1 wherein X is C1-C10 alkyl, C2-C10 alkenyl; C2-C10 alkynyl, - (CH2) kQ (CH2) 1- where k is 2 or 3 , 1 is 1 or 2 and Q is 0, Se, SiY2 where Y is C1-C10 alkyl, S(O)z where z is O, 1 or 2, NR where R is hydrogen or C1-C10 alkyl;
wherein all said radicals may optionally be substituted by one or more substituents selected from C1-C10 alkyl, halogen and trifluoroalkyl, R1 is methyl ;
R2 is C1-C10 alkyl, C2-C10 alkenyl, C2-C10 alkynyl and haloalkyl; and R3 is amino, alkylamine, natural amino acid, hydroxy, C2-C4 alkoxy, tetrazole, or tetrazoloamine.

3. The compound as recited in claim 1 wherein X is a C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl of 2 to 6 carbon atoms, -(CH2)kQ(CH2)1- where k is 2 or 3, 1 is 1 or 2 and Q is O, Se, SiYz where Y is C1-C10 alkyl, S (O) z where z is 0, 1 or 2, or NR where R is H or C1-C10 alkyl;
wherein all said radicals may optionally be substituted by one or more substituents selected from C1-C10 alkyl, halogen and trifluoroalkyl;
R1 is methyl;
R2 is C1-C4 alkyl , C2-C4 alkenyl , C2-C4 alkynyl , and haloalkyl of 1 to 4 carbon atoms; and R3 is an amino, alkylamine of 1 to 4 carbon atoms, hydroxy, alkoxy of 1 to 4 carbon atoms, tetrazole, tetrazoloamine, or natural amino acid.

4. The compound as recited in claim 1 wherein X is an alkylene group having 3 to 5 carbon atoms and which may optionally be substituted by one or more C1-3 alkyl ; a group of formula - (CH2) kQ (CH2)1- where k i s 2 or 3, l is 1 or 2 and Q is O, Se, S (O) z where z is 0, 1 or 2;
R1 is methyl;
R2 is an alkyl radical of 2 to 4 carbon atoms; and R3 is an amino, alkylamine of 1 to 4 carbon atoms, hydroxy, an alkoxy group of 1 to 4 carbon atoms.

5. The compound as recited in claim 1 selected from the group consisting of .alpha.-Methyl-N.delta.-iminoethyl-ornithine, .alpha.-Methyl-N.epsilon.-iminoethyl-lysine, .alpha.-Methyl-N.epsilon.-iminoethylaminoethyl-selenocysteine and .alpha.-Hydroxymethyl-N.epsilon.-iminoethyl-lysine.

6. A pharmaceutical composition comprising a compound as recited in claims 1 to 5 together with a pharmaceutically acceptable carrier.

7. Use of the compound as is recited in Claim 1, 2, 3, 4 or 5 for preparing a medicament for inhibiting nitric oxide synthesis in a subject in need of such inhibition.