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  • C07D207/32—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
  • C07D207/33—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals, directly attached to ring carbon atoms
  • C07D207/333—Radicals substituted by oxygen or sulfur atoms
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  • C07D209/04—Indoles; Hydrogenated indoles
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  • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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Definitions

• Adhesion of leukocytes to the endothelium represents a fundamental, early event in a wide variety of inflammatory conditions, autoimmune disorders and bacterial and viral infections.
• Leukocyte recruitment to endothelium is mediated in part by the inducible expression of adhesion molecules on the surface of endothelial cells that interact with counterreceptors on immune cells.
• Endothelial cells determine which types of leukocytes are recruited by selectively expressing specific adhesion molecules, such as vascular cell adhesion molecule- 1 (VCAM-1), intercellular adhesion molecule- 1 (ICAM-1), and E-selectin.
• VCAM-1 vascular cell adhesion molecule- 1
• ICAM-1 intercellular adhesion molecule- 1
• E-selectin E-selectin.
• VCAM-1 binds to the integrin VLA-4 expressed on lymphocytes, monocytes, macrophages, eosinophils, and basophils but not neutrophils. This interaction facilitates the firm adhesion of these leukocytes to the endothelium.
• VCAM-1 is an inducible gene that is not expressed, or expressed at very low levels, in normal tissues.
• VCAM-1 is upregulated in a number of inflammatory diseases, including arthritis (including rheumatoid arthritis), asthma, dermatitis, psoriasis, cystic fibrosis, post transplantation late and chronic solid organ rejection, multiple sclerosis, systemic lupus erythematosis, inflammatory bowel diseases, autoimmune diabetes, diabetic retinopathy, rhinitis, ischemia-reperfusion injury, post-angioplasty restenosis, chronic obstructive pulmonary disease (COPD), glomerulonephritis, Graves disease, gastrointestinal allergies, conjunctivitis, atherosclerosis, coronary artery disease, angina and small artery disease.
• arthritis including rheumatoid arthritis
• asthma including rheumatoid arthritis
• dermatitis including dermatitis, psoriasis, cystic fibrosis, post transplantation late and chronic solid organ rejection
• multiple sclerosis systemic lupus ery
• Coronary heart disease primarily as a result of atherosclerosis, remains the leading cause of death in industrialized countries.
• Atherosclerosis is a disease characterized by vascular inflammation, deposition of lipids in the arterial vessel wall and smooth muscle cell proliferation resulting in a narrowing of the vessel passages.
• atherosclerotic lesions can become unstable resulting in plaque rupture, thrombosis, myocardial infarction and ischemic heart disease.
• VCAM-1 expression has been shown to inhibit atherosclerosis in several animal models (Sundell et al., Circulation, 100: 42, 1999).
• a monoclonal antibody against VCAM-1 has also been shown to inhibit neointimal formation in a mouse model of arterial wall injury (Oguchi, S., et al., Arterioscler. Thromb. Vase. Biol., 20: 1729-1736, 2000).
• Asthma which is increasing in prevalence and morbidity world-wide, is a chronic inflammatory disease characterized by lung eosinophilia and bronchial hyperreactivity.
• Eosinophils have been considered an important effector cell in the pathogenesis of asthma and other allergic diseases.
• Activated eosinophils release proteins such as major basic protein (MBP) that have been demonstrated to induce bronchial hyperreactivity, one of the defining criteria of asthma (Bousquot, et al., N. Engl. J.
• VCAM-1 is markedly upregulated on human bronchial vascular endothelium of subjects with asthma who have air flow limitation, when compared with subjects without asthma (Pilewski, et al., Am. J. Respir. Cell Mol. Biol., 12, 1-3,1995; Ohkawara, Y., et al., Am. J. Respir. Cell Mol. Biol., 12, 4-12, 1995; Gosset, P., et al., Int. Arch. Allergy Immunol. 106: 69-77, 1995; hacken, ⁇ . H., et al., Clin. Exp.
• VCAM-1 knockout mice had fewer eosinophils and VCAM-1 expression than wildtype mice; however, administration of recombinant IL-12 at the time of ova sensitization and challenge restored lung VCAM-1 expression and eosinophilia (Wang, S., et al., J. Immunol., 166:2741-2749, 2001).
• blocking the integrin receptors for VCAM-1 have had positive effects on animal models of asthma (Rabb et al., Am. J. Respir. Care Med.
• VCAM-l/VLA-4 interactions are also important effector cells in allergic rhinitis.
• VCAM-1 has been demonstrated to be upregulated 24 hrs after nasal allergen provocation in patients with seasonal allergic rhinitis but not in normal subjects (Braunstahl, G. J., et al., J. Allergy Clin. Immunol, 107: 469-476, 2001).
• RA Rheumatoid arthritis
• RA Rheumatoid arthritis
• the role of adhesion molecules in the pathogenesis of RA has also been well documented, and VCAM-1 expression on synovial fibroblasts is a clinical hallmark of RA (Li, P., et al., J. Immunol. 164: 5990-7, 2000).
• VLA-4/VCAM-1 interactions may be the predominant mechanism for recruitment of leukocytes to the synovium (Dinther-Janssen, et al., J. Immunol. 147: 4207-4210, 1991; Issekeutz and Issekeutz, Clin. Immunol. Immunopathol. 61 :436-447, 1991; Morales-Ducret et al., J. Immunol. 149:1424-1431, 1992; Postigo et al., J. Clin. Invest. 89:1445-1452, 1992;
• VCAM-1 has been shown to be chemotactic for T cells (Kitani, A., et al., J. Immun. 161 : 4931- 8, 1998), and in addition to being a possible diagnostic marker for RA, may contribute to its pathogenesis by inducing migration and recruitment of T cells.
• VCAM-1 expressed on fibroblast-Iike synoviocytes has also been implicated in enhanced survival of activated synovial fluid B cells (Marinova, Mutafcheia, L., Arthritis Rheum. 43: 638-644, 2000) that may further contribute to RA pathogenesis.
• VCAM-1 plays a role in SLE.
• Expression of VCAM-1 is increased on dermal vessel endothelial cells in patients with active systematic lupus erythematosus (Jones, S. M., British J. Dermatol. 135: 678-686, 1996) and correlates with increased disease severity (Belmont et al., Arthritis Rheum. 37:376- 383, 1994).
• VCAM-1 expression on mesangial cells in vitro can be stimulated by IL-1, TNF- ⁇ , and INF ⁇ exposure as well as by anti-endothelial cell IgG fraction and anti-DNA autoantibodies from SLE patients (Wuthrich, Kidney Int. 42: 903-914, 1992; Papa, N. D., et al., Lupus, 8: 423-429, 1999; Lai, K. N., et al., Clin Immunol Immunopathol,
• soluble VCAM-1 is higher in SLE patients than in normal subjects (Mrowka, C, et al., Clin. Nephrol. 43: 288-296, 1995; Baraczka, K., et al., Ada.
• Acute transplant rejection occurs when the transplant recipient recognizes the grafted organ as "non-self "and mounts an immune response characterized by massive infiltration of immune cells, edema, and hemorrage that result in the death of the transplanted organ. Acute rejection occurs in a matter of hours or days and has been correlated with increased levels of VCAM-1 in tissues and in plasma (Tanio et al., Circulation, 89:1760-1768, 1994; Cosimi et al., J. Immunol. 144: 4604-4612, 1990; Pelletier, R., et al., Transplantation, 55: 315, 1992).
• VCAM-1 A monoclonal antibody to VCAM-1 has been shown to inhibit cardiac allograft rejection in mice (Pelletier, R., J. Immunol, 149: 2473-2481, 1992; Pelletier, R., et al., Transplantation Proceedings, 25: 839-841, 1993; Orosz, C. G., et al., J. Heart and Lung Transplantation, 16: 889-904, 1997) and when given for 20 days can cause complete inhibition of rejection and long-term graft acceptance (Orosz C. G., et al., Transplantation, 56: 453-460, 1993).
• Chronic graft rejection also known as allograft vasculopathy is distinct from acute transplant rejection and is a leading cause of late graft loss after renal and heart transplantation. ⁇ istologically it is characterized by concentric neointimal growth within vessels that is largely due to smooth muscle migration and proliferation. It is thought to be the result of endothelial damage brought about by several factors including: ischemia-reperfusion injury, immune complexes, hypertension, hyperlipidemia and viruses. All of these factors have been associated with induction of VCAM-1 in endothelial cells. There is also a strong correlation of soluble and tissue VCAM-1 levels with chronic rejection (Boratynska, M.,. Pol. Arch. Med.
• Multiple sclerosis is a common demyelinating disorder of the central nervous system, causing patches of sclerosis (plaques) in the brain and spinal cord. It occurs in young adults and has protean clinical manifestations. It is well documented that VCAM-1 is expressed on brain microvascular endothelial cells in active lesions of multiple sclerosis (Lee S. J., et al., J. Neuroimmunol, 98: 77-88, 1998). Experimental therapy of experimental autoimmune encephalomyelitis, which is an animal model for multiple sclerosis, using antibodies against several adhesion molecules, including VCAM-1, clearly shows that adhesion molecules are critical for the pathogenesis of the disease (Benveniste et al., J. Neuroimmunol.
• Diabetes mellitus is a metabolic disease in which carbohydrate utilization is reduced and that of lipid and protein is enhanced.
• Evidence has accumulated that increased levels of adhesion molecules may play a functional pathophysiological role in diabetes (Wagner and Jilma, Hormone and Metabolic Research, 29: 627-630, 1997; Kado, S., Diabetes Res. Clin. Pract., 46: 143-8, 1999). It is caused by an absolute or relative deficiency of insulin and is characterized by chronic hyperglycemia, glycosuria, water and electrolyte loss, ketoacidosis, and coma.
• Elevated circulating adhesion molecules including VCAM-1 have been detected in patients with diabetes and in experimental models of diabetes in animals (Lorini et al., Hormone Research, 48: 153, 1997; Otsuki et al., Diabetologia, 40: A440, 1997; Hart et al., FASEB J. 1 LA340, 1997; Albertini et al., Diabetologia, 39: A240, 1996; Wagner et al., Diabetologia, 39: A205, 1996; Enghofer et al., Diabetologia, 39: A97, 1996; Koga M., Diabet. Med, 15: 661-667, 1998).
• peripheral vasculopathies such as diabetic retinopathy and diabetic nephropathy. It is believed that adhesion of leukocytes to the peripheral vasculature plays a central role in the vasculopathies often associated with diabetes.
• Crohn's disease also known as regional enteritis, is a subacute chronic inflammatory condition of unknown cause, involving the internal ileum and less frequently other parts of the gastrointestinal tract. It is characterized by patchy deep ulcers that may cause fistulas, and narrowing and thickening of the bowel by fibrosis and lymphocytic infiltration. Ulcerative colitis is a chronic disease of unknown cause characterized by ulceration of the colon and rectum, with rectal bleeding, mucosal crypt abscesses, inflammatory pseudopolyps, abdominal pain, and diarrhea.
• VCAM-1 reflects the grade of intestinal inflammation in patients with Crohn's disease or ulcerative colitis (Jones, et al., Gut, 36: 724- 30, 1995; Goggins et al., Gastroenterology, 108: A825, 1995; Goeke and Manns, Gastroenterology, 106: A689, 1994; Goeke et al., J Gasterokenterol. 32:480-486, 1997; Loftus et al., Gastroenterology, 108: A684, 1995; Tahami et al., Gastroenterology, 118: A344, 2000). Antibodies to VCAM-1 have been shown to ameliorate experimentally-induced colitis in mice (Soriano, A., Lab. Invest. 80: 1541-1551, 2000).
• Psoriasis is a chronic skin disease characterized by erythematous scaling plaques as a result of keratinocyte hyperplasia, influx of immune cells and endothelial activation (Nickoloff, B. J., et al., J. Invest. Dermatol, 127: 871-884, 1991).
• VCAM-1 is upregulated in psoriatic skin as compared to normal skin (Groves, R. W., J. Am. Acad. Dermatol, 29: 67-72, 1993; Uyemura, K., et al., J. Invest. Dermatol. 101: 701-705, 1993) and levels of circulating VCAM- 1 correlate with disease activity (Schopf, R. E., Br. J. Dermatol, 128: 34-7, 1993).
• linoleic acid linolenic acid, arachidonic acid, linoleyl hydroperoxide (13-HPODE) and arachidonic hydroperoxide (15-HPETE) induce cell-surface gene expression of VCAM-1 but not ICAM-1 or E-selectin.
• Saturated fatty acids such as stearic acid
• monounsaturated fatty acids such as oleic acid
• WO 98/51662 filed by AtheroGenics, Inc. and listing as inventors Russell M. Medford, Patricia K. Somers, Lee K. Hoong, and Charles Q. Meng, claims priority to provisional application U.S.S.N. 60/047,020, filed on May 14, 1997.
• This application discloses the use of a broad group of compounds as cardiovascular protectants that exhibit at least one, and sometimes a composite profile, of reducing cholesterol, lowering LDL, and inhibiting the expression of VCAM-1.
• U.S. Patent No. 5,155,250 to Parker, et al. discloses that 2,6-dialkyl-4-silylphenols are antiatherosclerotic agents. The same compounds are disclosed as serum cholesterol lowering agents in PCT Publication No. WO 95/15760, published on June 15, 1995.
• U.S. Patent No. 5,608,095 to Parker, et al. discloses that alkylated-4-silyl-phenols inhibit the peroxidation of LDL, lower plasma cholesterol, and inhibit the expression of VCAM-1, and thus are useful in the treatment of atherosclerosis.
• WO 98/51289 which claims priority to provisional application U.S.S.N. 60/047,020, filed on May 14, 1997 by Emory University listing Patty Somers as sole inventor, discloses the use of a group of compounds as cardiovascular protectants and antiinflammatory agents which exhibit at least one, and sometimes a composite profile, of reducing cholesterol, lowering LDL, and inhibiting the expression of VCAM-1 and thus can be used as antiinflammatory and cardivascular treating agents.
• WO 98/23581 discloses the use of benzamidoaldehydes and their use as cysteine protease inhibitors.
• WO 97/12613 of Cornicelli et al. discloses compounds for the inhibition of 15- lipogenase to treat and prevent inflammation or atherosclerosis.
• Compounds disclosed include benzopyranoindole, benzimidazole, catacholes, benzoxadiazines, benzo[a]phenothiazine, or related compounds thereof.
• Japanese Patent No. 06092950 to Masahiko et al. discloses preparation of epoxy compounds wherein electron deficient olefins such as acylstyrene derivatives, styrene derivatives, and cyclohexenone derivatives are efficiently oxidized by a hydrogen peroxide derivative in the presence of a primary or secondary amine in an organic solvent to give said epoxides which are useful intermediates for pharmaceutical and flavoring materials.
• WO 99/001 14 discloses the use of certain chalcones, 1,3- bis-aromatic-propan-1-ones (dihydrochalcones), and l,3-bisaromatic-prop-2-yn-l-ones for the preparation of pharmaceutical compositions for the treatment of prophylaxis of a number of serious diseases including i) conditions relating to harmful effects of inflammatory cytokines, ii) conditions involving infection by Helicobacter species, iii) conditions involving infections by viruses, iv) neoplastic disorders, and v) conditions caused by microorganisms or parasites.
• WO 00/47554 filed by Cor Therapeutics describes a broad class of substituted unsaturated compounds for use as antithrombotic agents.
• WO 96/20936 discloses thiazolidin-4-one derivatives of the formula:
• the compounds which act as PAF antagonists or 5-lipoxygenase inhibitors.
• the compounds are used in the prevention and treatment of inflammatory and allergic disorders mediated by platelet-activating factor and /or leukotrienes.
• U.S. Patent No. 4,085,135 discloses 2'-(carboxymethoxy)-chalcones with antigastric and antiduodenal ulcer activities.
• U.S. Patent No. 5,744,614 to Merkle et al. discloses a process for preparing 3,5- diarylpyrazoles and various derivatives thereof by reacting hydrazine hydrate with 1,3- diarylpropenone in the presence of sulfuric acid and an iodine compound.
• U.S. Patent No. 5,951,541 to Wehlage et al. discloses the use of salts of aromatic hydroxy compounds, such as (hydroxyaryl)alkenone salts, as brighteners in aqueous acidic electroplating baths.
• the invention discloses that such compounds have a lower vapor pressure than the known brighteners, as a single substance and in the electroplating baths,in order to avoid losses of substance. They also have high water solubility properties.
• Japanese Patent No. 07330814 to Shigeki et al. discloses benzylacetophenone compounds as photoinitiator compounds.
• Japanese Patent No. 04217621 to Tomomi discloses siloxane chalcone derivatives in sunscreens.
• U.S. Patent No. 4,085,135 to Kyogoku et al. discloses a process for preparation of 2'- (carboxymethoxy)-chalcones having antigastric and anti duodenal activities with low toxicity and high absorptive ratio in the body. This patent suggests that the high absorptive ratio in the body is due to the 2'-carboxymethoxy group attached to the chalcone derivative.
• U.S. Patent No. 4,855,438 discloses the process for preparation of optically active 2- hydroxyethylazole derivatives which have fungicidal and plant growth-regulating action by reacting an ⁇ - ⁇ -unsaturated ketone which could include a chalcone or a chalcone derivative with an enantiomerically pure oxathiolane in the presence of a strongly basic organometallic compound and at temperatures ranging from -80 to 120 °C.
• JP 63010720 to Nippon Kayaku Co., LTD discloses that chalcone derivatives of the following formula (wherein R 1 and R 2 are hydrogen or alkyl, and m and n are 0-3) are 5- lipoxygenase inhibitors and can be used in treating allergies.
• JP 06116206 to Morinaga Milk Industry Co. Ltd, Japan discloses chalcones of the following structure as 5-lipoxygenase inhibitors, wherein R is acyl and R -R are hydrogen lower alkyl, lower alkoxy or halo, and specifically that in which R is acyl and R -R are hydrogen.
• U.S. Patent No. 6,046,212 to Kowa Co. Ltd. discloses heterocyclic ring-containing chalcones of the following formula as antiallergic agents, wherein A represents a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, or a group :
• VCAM-1 is a mediator of chronic inflammatory disorders
• a more general goal is to identify selective compounds and methods for suppressing the expression of redox sensitive genes or activating redox sensitive genes that are suppressed.
• An even more general goal is to identify selective compounds, pharmaceutical compositions and methods of using the compounds for the treatment of inflammatory diseases. It is therefore an object of the present invention to provide new compounds for the treatment of disorders mediated by VCAM-1.
• Another object of the invention is to provide compounds, compositions, and method of treating cardiovascular and inflammatory diseases. It is another object of the invention to provide compounds, compositions and methods to treat arthritis.
• Another object of the invention is to provide compounds, compositions and methods to treat rheumatoid arthritis.
• the inventions compounds, compositions and methods are also suitable as disease modifying anti-rheumatoid arthritis drugs (DMARDs). It is yet another object of the invention to provide compounds, compositions and methods to treat asthma.
• DMARDs disease modifying anti-rheumatoid arthritis drugs
• COPD chronic obstructive pulmonary disease
• VCAM-1 and thus can be used to treat a patient with a disorder mediated by VCAM-1.
• inflammatory disorders that are mediated by VCAM-1 include, but are not limited to arthritis, asthma, dermatitis, cystic fibrosis, post transplantation late and chronic solid organ rejection, multiple sclerosis, systemic lupus erythematosis, inflammatory bowel diseases, autoimmune diabetes, diabetic retinopathy, diabetic nephropathy, diabetic vasculopathy, rhinitis, ischemia-reperfusion injury, post-angioplasty restenosis, chronic obstructive pulmonary disease (COPD), glomerulonephritis, Graves disease, gastrointestinal allergies, conjunctivitis, atherosclerosis, coronary artery disease, angina and small artery disease.
• COPD chronic obstructive pulmonary disease
• the compounds disclosed herein can also be used in the treatment of inflammatory skin diseases that are mediated by VCAM-1, as well as human endothelial disorders that are mediated by VCAM-1, which include, but are not limited to psoriasis, dermatitis, including eczematous dermatitis, Kaposi's sarcoma, multiple sclerosis, as well as proliferative disorders of smooth muscle cells.
• the compounds disclosed herein can be selected to treat anti-inflammatory conditions that are mediated by mononuclear leucocytes.
• the compounds of the present invention are selected for the prevention or treatment of tissue or organ transplant rejection.
• Treatment and prevention of organ or tissue transplant rejection includes, but is not limited to treatment of recipients of heart, lung, combined heart-lung, liver, kidney, pancreatic, skin, spleen, small bowel, or corneal transplants.
• the compounds can also be used in the prevention or treatment of graft-versus- host disease, such as sometimes occurs following bone marrow transplantation.
• the compounds described herein are useful in both the primary and adjunctive medical treatment of cardiovascular disease.
• the compounds are used in primary treatment of, for example, coronary disease states including atherosclerosis, post- angioplasty restenosis, coronary artery diseases and angina.
• the compounds can be administered to treat small vessel disease that is not treatable by surgery or angioplasty, or other vessel disease in which surgery is not an option.
• the compounds can also be used to stabilize patients prior to revascularization therapy.
• VCAM-1 VCAM-1
• VCAM-1 VCAM-1
• These compounds can be administered to a host as monotherapy, or if desired, in combination with another compound of the invention or another biologically active agent, as described in more detail below.
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, ary
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring;
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ , or one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl; and/or wherein when one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ is a carbon-carbon linked heterocyclic or heteroaryl, only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; and/or wherein when one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ is a carbon-carbon linked heterocyclic or heteroaryl, only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; and/or
• R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together form a heterocyclic or heteroaryl optionally substituted by one or more alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl or aminoalkyl and optionally substituted with one or more selected from the group consisting of hydroxy, alkyl, carboxy, hydroxyalkyl, carboxyalkyl, amino, cyano, alkoxy, alkoxycarbonyl, acyl, oxo, -NR 7 R 8 , and halo; and/or
• R 2 ⁇ , R 3 ⁇ , R 4 ", R 5 ⁇ , R ⁇ or one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ ,R 5 ⁇ , R 6 ⁇ must be selected from the group consisting of cyano, tetrazol-5-yl, carboxy, -C(O)OR , -C(O)NH 2 , -C(O)NHR 2 , -C(O)N(R 2 ) 2 , -C(O)NR 7 R 8 , -C(O)NHC(O)NHR 2 ,
• R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4t ⁇ R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 2 C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, alditol, carbohydrate, polyol alkyl, alkoxy, lower alkoxy, -(O(CH ) 2 ) ⁇ .
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring;
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ , or one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl; and/or
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ is a carbon-carbon linked heterocyclic or heteroaryl, only one of R ⁇ , R 3 ⁇ , R 4 ⁇ , R ⁇ or R 6 " can be -OCH 3 ; and/or wherein when one of R 2 ⁇ , R 3 , R 4 ⁇ , R 5 or R 6 ⁇ is a carbon-carbon linked heterocyclic or heteroaryl, only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; and/or
• R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together, or R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together, or R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together form a heterocyclic or heteroaryl optionally substituted by one or more alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl or aminoalkyl and optionally substituted with one or more selected from the group consisting of hydroxy, alkyl, carboxy, hydroxyalkyl, carboxyalkyl, amino, cyano, alkoxy, alkoxycarbonyl, acyl, oxo, -NR 7 R 8 , and halo; and/or
• R ⁇ , R 3 , R 4 ", or one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ must be selected from the group consisting of cyano, tetrazol-5-yl, carboxy, -C(O)OR 2 , -C(O)NH 2 , -C(O)NHR 2 , C(O)N(R 2 ) 2 , -C(O)NR 7 R 8 , -C(O)NHC(O)NHR 2 , -C(O)NHC(O)N(R 2 ) 2 , C(O)NHC(O)NR 7 R 8 , -C(O)NHSO 2 NHR 2 , -C(O)NHSO 2 N(R 2 ), -C(O)NHSO 2 NR 7 R 8 , -
• OC(R 1 ) 2 C(O)NR 7 R 8 amino, -NHR 2 , N(R 2 ) 2 , NR 7 R 8 , -NHC(R') 2 C(O)OH, -NHC(R') 2 C(O)OR 2 , -NHC(O)R 2 , -N(R 2 )C(O)R 2 , -NHC(O)OR 2 , -NHC(O)SR 2 , -NHSO 2 NHR 2 , -NHSO 2 R 2 , - NHSO 2 NR 7 R 8 , -N(C(O)NHR 2 ) 2 , -NR 2 SO 2 R 2 , -NHC(O)NHR 2 , -NHC(O)NR 7 R 8 , and -
• R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, ary
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring;
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; and/or
• R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4ct taken together or R 4 ⁇ and R 5 ⁇ taken together, or R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together form a heterocyclic or heteroaryl optionally substituted by one or more alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl or aminoalkyl and optionally substituted with one or more selected from the group consisting of hydroxy, alkyl, carboxy, hydroxyalkyl, carboxyalkyl, amino, cyano, alkoxy, alkoxycarbonyl, acyl, oxo, -NR 7 R 8 , and halo; and/or
• R 2ct , R 3 ⁇ , R 4 ", R 5 ⁇ , or R 6 must be selected from the group consisting of cyano, tetrazol-5-yl, carboxy, -C(O)OR 2 , -C(O)NH 2 , -C(O)NHR 2 , -C(O)N(R 2 ) 2 , -C(O)NR 7 R 8 , - C(O)NHC(O)NHR 2 , -C(O)NHC(O)N(R 2 ) 2 , -C(O)NHC(O)NR 7 R 8 , -
• NR 7 R 8 -NHC(R') 2 C(O)OH, -NHC(R') 2 C(0)0R 2 , -NHC(O)R 2 , -N(R 2 )C(O)R 2 , -NHC(O)OR 2 , -NHC(O)SR 2 , -NHSO 2 NHR 2 , -NHSO 2 R 2 , -NHSO 2 NR 7 R 8 , -N(C(O)NHR 2 ) 2 , -NR 2 SO 2 R 2 , - NHC(O)NHR 2 , -NHC(O)NR 7 R 8 , and -NHC(O)N(R 2 ) 2 ; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hal
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 2 C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, alditol, carbohydrate, polyol alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ .
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring;
• R 4 , R 5 ⁇ or R ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; and/or
• R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 taken together or R 4 ⁇ and R 5 ⁇ taken together, or R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together, or R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together form a heterocyclic or heteroaryl optionally substituted by one or more alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl or aminoalkyl and optionally substituted with one or more selected from the group consisting of hydroxy, alkyl, carboxy, hydroxyalkyl, carboxyalkyl, amino,
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of cyano, tetrazol-5-yl, carboxy, -C(O)OR 2 , -C(O)NH 2 , -C(O)NHR 2 , -C(O)N(R 2 ) 2 , -C(O)NR 7 R 8 , - C(O)NHC(O)NHR 2 , -C(O)NHC(O)N(R 2 ) 2 , -C(O)NHC(O)NR 7 R 8 , -C(O)NHSO 2 NHR 2 , - C(O)NHSO 2 N(R 2 ), -C(O)NHSO 2 NR 7 R 8 , -C(O)NHC(O)R 2 , -C(O)NHSO 2 R 2 , - C(CH 3 ) 2 C(O)OH, -(CH 2 ) y C(O)
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl,
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl,
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of cyano, tetrazol-5-yl, carboxy, -C(O)OR 2 , -C(O)NH 2 , -C(O)NHR 2 , - C(O)N(R 2 ) 2 , -C(O)NR 7 R 8 , -C(O)NHC(O)NHR 2 , -C(O)NHC(O)N(R 2 ) 2 , -C(O)NHC(O)NR 7 R 8 , - C(O)NHSO 2 NHR 2 , -C(O)NHSO 2 N(R 2 ), -C(O)NHSO 2 NR 7 R 8 , -C(O)NHC(O)R 2 , - C(O)NHSO 2 R 2 , -C(CH 3 ) 2 C(O)OH, -(CH 2
• OC(R') 2 C(O)NR 7 R 8 amino, -NHR 2 , N(R 2 ) 2 , NR 7 R 8 , -NHC(R 1 ) 2 C(O)OH, -NHC(R') 2 C(O)OR 2 , -NHC(O)R 2 , -N(R 2 )C(O)R 2 , -NHC(O)OR 2 , -NHC(O)SR 2 , -NHSO 2 NHR 2 , -NHSO 2 R 2 , - NHSO 2 NR 7 R 8 , -N(C(O)NHR 2 ) 2 , -NR 2 SO 2 R 2 , -NHC(O)NHR 2 , -NHC(O)NR 7 R 8 , and -
• R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of cyano, tetrazol-5-yl, carboxy, -C(O)OR 2 , -C(CH 3 ) 2 C(O)OH, (CH 2 ) y C(O)OH, wherein y is 1, 2, 3, 4, 5, or 6; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 .
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and - C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl,
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of cyano, tetrazol-5-yl, carboxy, -C(O)OR 2 , -C(CH 3 ) 2 C(O)OH, (CH 2 ) y C(O)OH, wherein y is 1, 2, 3, 4, 5, or 6; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 .
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, alkyl, lower alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, haloalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, -C(O)R 2 , R C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, polyol alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, polyoxyalkylene,
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, cycloalkyl, aryl, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , oxo, cyano, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, cycloalkyl, aryl, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, - C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of cyano, tetrazol-5-yl, carboxy, -C(O)OR 2 , -C(CH 3 ) 2 C(O)OH, (CH 2 ) y C(O)OH, wherein y is 1 , 2, 3, 4, 5, or 6; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, - C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 .
• the invention is represented by Formula I or its pharmaceutical
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, alkyl, lower alkyl, cycloalkyl, cycloalkylalkyl, haloalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, heterocyclicamino lower alkyl, hydroxyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, polyoxyalkylene, cycloalkyloxy, cycloalkylalkoxy, heteroarylalkoxy, heteroaryl lower alkoxy, heterocyclicoxy, heterocyclicalkoxy, heterocyclic lower alkoxy, dialkylamino, N(R 2 ) 2 , - NR 7 R 8 , tetrazol
• R 7 8 alkyl, cycloalkyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR R , - C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, cycloalkyl, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, lower alkyl, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 and R 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 8-membered monocyclic or benzofused ring
• R , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of tetrazol-5-yl, carboxy, -C(O)OR 2 , -C(CH 3 ) 2 C(O)OH, (CH 2 ) y C(O)OH, wherein y is 1, 2, 3, 4, 5, or 6; wherein all R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, lower alkyl, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, lower alkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) 1-3 -O-lower alkyl, polyoxyalkylene, heteroaryl lower alkoxy, heterocyclicalkoxy, heterocyclic lower alkoxy, carboxy, -C(O)OR 2 , - C(O)N(R 2 ) 2 , and -C(O)NR 7 R 8 , all of which can be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, cycloalkyl, hydroxy, hydroxyalkyl, heterocyclic, -NR 7 R 8 ,
• R 2 is independently selected from the group consisting of alkyl, and lower alkyl, wherein all may be substituted by one or more selected from the group consisting of halo, lower alkyl, - NR 7 R 8 , alkoxy, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 and R 8 are independently alkyl, and linked together forming a 5- to 7-membered monocyclic or benzofused ring; wherein one of R ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• R ⁇ , R , or R ⁇ must be selected from carboxy or- C(O)OR 2 ; 7 8 wherein all R , R and R substituents can be optionally substituted with one or more selected from the group consisting of halo, lower alkyl, -NR 7 R 8 , -C(O)NR 7 R 8 , and - C(O)N(R 2 ) 2 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, -(O(CH ) 2 ) ⁇ . 3 -O-lower alkyl, heteroaryl lower alkoxy, heterocyclic lower alkoxy, and carboxy, all of which can be optionally substituted by one or more selected from the group consisting of hydroxy, hydroxyalkyl, -NR 7 R 8 , -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ; R 2 is lower alkyl;
• R 7 and R 8 are independently alkyl, and linked together forming a 6-membered monocyclic or benzofused ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 °, R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , and R 6 ⁇ are independently selected from the group consisting of hydrogen and carboxy;
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, heteroaryl lower alkoxy, and heterocyclic lower alkoxy, all of which can be optionally substituted by one or more selected from the group consisting of hydroxy, hydroxyalkyl, - NR 7 R 8 , -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is lower alkyl
• R 7 and R 8 are independently alkyl, and linked together forming a 6-membered monocyclic or benzofused ring
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl
• R 2 ⁇ , R 3 , or R 4 ⁇ must be carboxy.
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 , R 5 ⁇ , and R 6 are independently selected from the group consisting of hydrogen and carboxy;
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, heteroaryl lower alkoxy, and heterocyclic lower alkoxy, all of which can be optionally substituted by one or more selected from the group consisting of hydroxy, hydroxyalkyl, -NR 7 R 8 , -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is lower alkyl
• R 7 andR 8 are independently alkyl, and linked together forming a 6-membered monocyclic or benzofused ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heteroaryl
• R 2ct , R 3 ⁇ , or R 4ct must be carboxy.
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein: R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 , and R 6 ⁇ are independently selected from the group consisting of hydrogen and carboxy;
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, fluorine, chlorine, methoxy, ethoxy, propoxy, 3-(l-morpholino) propoxy, 2-(l- morpholino) ethoxy, CH 3 O(CH 2 ) 2 O(CH 2 ) 2 -,
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be selected from the group consisting of thiophen-s- yl, thiophen-3-yl, benzo[b]thiophen-2-yl, benzo[b]thiophen-3-yl, indol-2-yl, indol-3-yl, pyrrol- 2-yl, pyrrol-3-yl, l-methyl-indol-2-yl, l-methyl-indol-3-yl, N-Boc-indol-2-yl, N-Boc-indol-3- yl, N-Boc-pyrrol-2'yl, and N-Boc-pyrrol-3-yl;
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be carboxy.
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , and R 6 ⁇ are independently selected from the group consisting of hydrogen and carboxy;
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, methoxy, 3-(l-morpholino) propoxy, 2-(l-morpholino) ethoxy, andCH 3 O(CH 2 ) 2 O(CH 2 ) 2 ;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be selected from the group consisting of thiophen-s- yl, benzo[b]thiophen-2-yl, indol-2-yl, l-methyl-indol-2-yl, N-Boc-indol-2-yl, N-Boc-pyrrol- 2'yl, and N-Boc-pyrrol-3-yl;
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be carboxy.
• the invention is selected from a compound A compound selected from the group consisting of 4-[3E-(5-Benzo[b]thien-2-yl-2,4-dimethoxyphenyl)-acryloyl]-benzoic acid;
• the invention is a compound selected from the group consisting of 4-[3E-(5-Benzo[b]thien-2-yl-2,4-dimethoxyphenyl)-acryloyl]-benzoic acid;
• the invention is 4-[3E-(5-Benzo[b]thien-2-yl-2,4-dimethoxyphenyl)-acryloyl]-benzoic acid or its pharmaceutically acceptable salt or ester.
• the invention is 4-[3E-(2,4-Dimethoxy-5-thiophen-2-yl-phenyl)- acryloyl]-benzoic acid, or its pharmaceutically acceptable salt or ester.
• the invention is 4-(3E- ⁇ 4-Methoxy-2-[2-(2- methoxyethoxy)ethoxy]-5-thiophen-2-yl-phenyl ⁇ -acryloyl)-benzoic Acid; and,or its pharmaceutically acceptable salt or ester.
• the invention is 4- ⁇ 3E-[4-Methoxy-2-(2-morpholin-4-yl- ethoxy)-5-thiophen-2-yl-phenyl]-acryloyl ⁇ -benzoic acid, hydrochloride,or its pharmaceutically acceptable salt or ester.
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 , R 5 , and R 6 ⁇ are independently selected from the group consisting of hydrogen and carboxy;
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, heteroaryl lower alkoxy, and heterocyclic lower alkoxy, all of which can be optionally substituted by one or more selected from the group consisting of hydroxy, hydroxyalkyl, - NR 7 R 8 , -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is lower alkyl
• R andR are independently alkyl, and linked together forming a 6-membered monocyclic or benzofused ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , and R 6 ⁇ are independently selected from the group consisting of hydrogen and carboxy;
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, heteroaryl lower alkoxy, and heterocyclic lower alkoxy, all of which can be optionally substituted by one or more selected from the group consisting of hydroxy, hydroxyalkyl, - NR 7 R 8 , -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is lower alkyl;
• R 7 andR 8 are independently alkyl, and linked together forming a 6-membered monocyclic or benzofused ring;
• R 4 , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked tetrahydrofurn-2-yl or dihydrofuran-2-yl ;
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be carboxy.
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, ary
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of -C(O)NH 2 , -C(O)NHR 2 , -C(O)N(R 2 ) 2 , -C(O)NR 7 R 8 , -C(O)NHC(O)NHR 2 , - C(O)NHC(O)N(R 2 ) 2 , -C(O)NHC(O)NR 7 R 8 , -C(O)NHSO 2 NHR 2 , -C(O)NHSO 2 N(R 2 ), - C(O)NHSO 2 NR 7 R 8 , -C(O)NHC(O)R 2 , -C(O)NHSO 2 R 2 ; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of -C(O)NH 2 , -C(O)NHR 2 , -C(O)N(R 2 ) 2 , -C(O)NR 7 R 8 , -C(O)NHC(O)NHR 2 , - C(O)NHC(O)N(R 2 ) 2 , -C(O)NHC(O)NR 7 R 8 , -C(O)NHSO 2 NHR 2 , -C(O)NHSO 2 N(R 2 ), - C(O)NHSO 2 NR 7 R 8 , -C(O)NHC(O)R 2 , and -C(O)NHSO 2 R 2 ; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alky
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, alkyl, lower alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, haloalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, -C(O)R 2 , R 2 C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, polyol alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) ) ⁇ -3 -O-lower alkyl, polyoxyalkylene,
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 must be selected from the group consisting of -C(O)NH 2 , -C(O)NHR 2 , -C(O)N(R 2 ) 2 , -C(O)NR 7 R 8 , -C(O)NHC(O)NHR 2 , - C(O)NHC(O)N(R 2 ) 2 , -C(O)NHC(O)NR 7 R 8 , -C(O)NHSO 2 NHR 2 , -C(O)NHSO 2 N(R 2 ), - C(O)NHSO 2 NR 7 R 8 , -C(O)NHC(O)
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, alkyl, lower alkyl, cycloalkyl, cycloalkylalkyl, haloalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, heterocyclicamino lower alkyl, hydroxyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, polyoxyalkylene, cycloalkyloxy, cycloalkylalkoxy, heteroarylalkoxy, heteroaryl lower alkoxy, heterocyclicoxy, heterocyclicalkoxy, heterocyclic lower alkoxy, dialkylamino, N(R 2 ) 2 , -NR 7 R 8 , -N(R 2
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, cycloalkyl, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, lower alkyl, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, -C(O)NR 7 R 8 , and - C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, cycloalkyl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo,
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 8-membered monocyclic or benzofused ring;
• R , R or R ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of -C(O)NH 2 , -C(O)NHR 2 , -C(O)N(R 2 ) 2 , -C(O)NR 7 R 8 , -C(O)NHC(O)R 2 , and - C(O)NHSO 2 R 2 ; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, lower alkyl, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, lower alkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) ) ⁇ - 3 -O-lower alkyl, polyoxyalkylene, heteroaryl lower alkoxy, heterocyclicalkoxy, heterocyclic lower alkoxy, -N(R 2 )C(O)R 2 , - C(O)NH 2 , and -C(O)NHR 2 , all of which can be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino,
• R 1 is independently selected from the group consisting of hydrogen, and lower alkyl which may be optionally substituted by one or more selected from the group consisting of halo, lower alkyl, -NR 7 R 8 , alkoxy, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, heteroaryl, and heterocyclic, wherein all may be substituted by one or more selected from the group consisting of halo, lower alkyl, -NR 7 R 8 , alkoxy, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently alkyl, and linked together forming a 5- to 7-membered monocyclic ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R S ⁇ or R 6 ⁇ can be -OCH 3 ;
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of -C(O)NH 2 , -C(O)NHR 2 , -C(O)NHC(O)R 2 , and -C(O)NHSO 2 R 2 ; wherein all R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, lower alkyl, heterocyclic, amino, aminoalkyl, and - NR 7 R 8 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, heteroaryl lower alkoxy, heterocyclic lower alkoxy, -N(R 2 )C(O)R 2 , -C(O)NH 2 , and - C(O)NHR 2 , all of which can be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, al
• R 1 is hydrogen
• R 2 is lower alkyl
• R 7 andR 8 are independently alkyl, and linked together forming a 6-membered monocyclic ring
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R , R 3 , or R 4 ⁇ must be selected from the group consisting of -C(O)NH 2 , -C(O)NHR 2 , -C(O)NHC(O)R 2 , and -C(O)NHSO 2 R 2 ; wherein all R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of heterocyclic, amino, aminoalkyl, and -NR 7 R 8 .
• the invention is represented by the following compounds:
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 2 C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, alditol, carbohydrate, polyol alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 )j.
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl 5 and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group 10 consisting of thiol, -SC(R 1 ) 2 C(O)OH, -SC(R 1 ) 2 C(O)OR 2 , -SCH 2 C(O)OH,
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the 20 group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, ; > : cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-low
• R 2 C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, alditol, carbohydrate, polyol alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, polyoxyalkylene, cycloalkyloxy, cycloalkylalkoxy, haloalkoxy, aryloxy, arylalkoxy, heteroaryloxy, heteroarylalkoxy, heteroaryl lower alkoxy, heterocyclicoxy, heterocyclicalkoxy, heterocyclic lower alkoxy, - OC(R') 2 C(O)OH, -OC(R') 2 C(O)OR 2 , -OC(R') 2 C(O)NH 2 , -OC(R')
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ; R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or
• R , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• R 2 ⁇ , R 3 ⁇ , or R 4 must be selected from the group consisting of thiol, -SC(R 1 ) 2 C(O)OH, -SC(R 1 ) 2 C(O)OR 2 , -SCH 2 C(O)OH, SCF 2 C(O)OH, -SO 2 NH 2 , -SO 2 NHR 2 , -SO 2 N(R 2 ) 2 , SO 2 NR 7 R 8 , -SO 2 NHC(O)R 2 , -SR 2 , -SO 2 NHC(O)NHR 2 , -SO 2 NHC(O)N(R 2 ) 2 , -SO 2 NHC(O)NR 7 R 8 ; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl,
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, -C(O)R 2 , R 2 C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, polyol alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, polyoxy
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, cycloalkyl, arylarylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, cycloalkyl, aryl, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, - C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of -SC ⁇ C ⁇ OH, -SC(R') 2 C(O)OR 2 , -SCH 2 C(O)OH,
• R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, - C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, heterocyclicamino lower alkyl, hydroxyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, polyoxyalkylene, cycloalkyloxy, cycloalkylalkoxy, heteroarylalkoxy, heteroaryl lower alkoxy, heterocyclicoxy, heterocyclicalkoxy, heterocyclic lower alkoxy, dialkylamino, N(R 2 ) 2
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, cycloalkyl, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, lower alkyl, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, -C(O)NR 7 R 8 , and - C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, cycloalkyl, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, lower alkyl, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, -C(O)NR 7 R 8 , and -C
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• R 2 ⁇ , R 3 ⁇ , or R 4 must be selected from the group consisting of -SC(R ] ) 2 C(O)OR 2 , -SCH 2 C(O)OH, -SO 2 NH 2 , -SO 2 NHR 2 , -SO 2 N(R 2 ) 2 ,
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, lower alkyl, alkenyl, alkynyl, carbocycle, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, hydroxyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ .
• R 2 is independently selected from the group consisting of alkyl and lower alkyl, which may be substituted by one or more selected from the group consisting of halo, lower alkyl, - NR 7 R 8 , alkoxy, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 and R 8 are independently alkyl, and linked together forming a 5- to 7-membered monocyclic ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• R 2 , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of -SC(R') 2 C(O)OR 2 , -SCH 2 C(O)OH, -SO 2 NH 2 , -SO 2 NHR 2 , -SO 2 N(R 2 ) 2 , SO 2 NR 7 R 8 , and -SO 2 NHC(O)R 2 ; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, -NR 7 R 8 , -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, alkenyl, alkynyl, carbocycle, heteroaryl, heterocyclic, hydroxyl, lower alkoxy, -(O(CH 2 ) 2 ) )-3 -O-lower alkyl, heteroaryl lower alkoxy, heterocyclic lower alkoxy, -N(R 2 )C(O)R 2 , -SO 2 NH 2 , -SO 2 NHR 2 , SO 2 NHC(O)R 2 , -SR 2 , SO 2 NHC(O)NHR 2 , -SO 2 NHC(O)N(R 2 ) 2 , -SO 2 NHC(O)NR 7 R 8 , and -C(O)NHSO 2 R 2 , all of which can be optionally substituted
• R 1 is hydrogen;
• R 2 is lower;
• R 7 and R 8 are independently alkyl, and linked together forming a 6-membered monocyclic ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• R 2 , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of -SC(R ! ) 2 C(O)OR 2 , -SO 2 NH 2 , - SO 2 NR 7 R 8 , and -SO 2 NHC(O)R 2 .
• the invention is represented by the following compound:
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, ary
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of amino, -NHR 2 , N(R 2 ) 2 , NR 7 R 8 , -NHC(R') 2 C(O)OH, -NHC(R') 2 C(0)0R 2 , - NHC(O)R 2 , -N(R 2 )C(O)R 2 , -NHC(O)OR 2 , -NHC(O)SR 2 , -NHSO 2 NHR 2 , -NHSO 2 R 2 , - NHSO 2 NR 7 R 8 , -N(C(O)NHR 2 ) 2 , -NR 2 SO 2 R 2 , -NHC(O)NHR 2 , -NHC(O)NR 7 R 8 , and - NHC(O)N(R 2 ) 2 ; wherein all R 1 , R 2 , R 7 and R 8 substituent
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, heteroaryl lower alkoxy, heterocyclic lower alkoxy, , all of which can be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is lower alkyl optionally substituted by alkoxycarbonyl.
• R 7 andR 8 are independently alkyl, and linked together forming a 6-membered monocyclic ring
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of amino, -N(C(O)NHR 2 ) 2 , NR 2 SO 2 R 2 and -NR 2 SO 2 R 2 ; wherein all R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl,
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 2 C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, alditol, carbohydrate, polyol alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) )- -O-lower alkyl, polyoxyalkylene, cycloalkyloxy, cycloalkylalkoxy, haloalkoxy, aryloxy, arylalkoxy, heteroaryloxy, heteroarylalkoxy, heteroaryl lower alkoxy, heterocyclicoxy, heterocyclicalkoxy, heterocyclic lower alkoxy, - OC(R') 2 C(O)OH, -OC(R') 2 C(O)OR 2 , -OC(R') 2 C(O)NH 2 , -OC(R')
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 and R 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of -OC(R') 2 C(O)OH, -OC ⁇ ' ⁇ C ⁇ OR 2 , -OC(R') 2 C(O)NH 2 , OC(R') 2 C(O)NHR 2 , -OC(R') 2 C(O)N(R 2 ) 2 , -OC(R 1 ) 2 C(O)NR 7 R 8 ; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cyclo
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ - 3 -O-lower alkyl, heteroaryl lower alkoxy, heterocyclic lower alkoxy, -OC(R') 2 C(O)OH, - OC(R') 2 C(O)N(R 2 ) 2 , -OC(R') 2 C(O)NR 7 R 8 , all of which can be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, ox
• R 1 is hydrogen or lower alkyl optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is lower alkyl optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, - C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ; R 7 and R 8 are independently alkyl, and linked together forming a 6-membered monocyclic ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 , or R 4 ⁇ must be selected from - OC(R') 2 C(O)OH; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl,
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 2 C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, alditol, carbohydrate, polyol alkyl, alkoxy, lower alkoxy, -(O(CH ) 2 ) ⁇ .
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 ; and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; and/or R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together, or R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together form a heterocyclic or heteroaryl optionally substituted by one or more alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl or aminoalkyl and optionally substituted with one or more selected from the group consisting of hydroxy, alkyl, carboxy, hydroxyalkyl, carboxyalkyl, amino, cyano, alkoxy, alkoxycarbonyl, acyl, oxo, -NR 7 R 8 , and halo; and/or
• At least one of R 2 ⁇ , R 3 , or R 4ct must be selected from the group consisting of cyano, tetrazol-5-yl, carboxy, -C(O)OR 2 , -C(O)NH 2 , -C(O)NHR 2 , -C(O)N(R 2 ) 2 , -
• R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R ta , R 2 ⁇ , R 3 ⁇ , R ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, (O(CH 2 ) 2 )i- 3 -O-lower alkyl, heteroaryl lower alkoxy, heterocyclic lower alkoxy, all of which can be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ; R 2 is independently al
• R 7 andR 8 are independently selected from the group consisting of alkyl, linked together forming a 6-membered monocyclic ring;
• R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; and/or
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl,
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl,
• R 7 8 heterocyclic, amino, aminoalkyl, -NR R , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring;
• R , R ⁇ or R ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; and/or
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of cyano, tetrazol-5-yl, carboxy, -C(O)OR 2 , -C(O)NH 2 , -C(O)NHR 2 , -C(O)N(R 2 ) 2 , - C(O)NR 7 R 8 , -C(O)NHC(O)NHR 2 , -C(O)NHC(O)N(R 2 ) 2 , --
• R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, (O(CH 2 ) 2 ) 1-3 -O-lower alkyl, heteroaryl lower alkoxy, heterocyclic lower alkoxy, all of which can be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently al
• R 7 andR 8 are independently selected from the group consisting of alkyl, linked together forming a 6-membered monocyclic ring;
• R 4 ⁇ , R s ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; and/or
• R 4 and R 5 ⁇ taken together form a 5-membered ring containing one nitrogen, which may optionally be substituted with one or more selected from the group consisting of alkyl, lower alkyl, cycloalkyl, hydroxyalkyl, aminoalkyl, carboxyalkyl, alkoxycarbonyl; provided that R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ cannot be -OC(R ] ) 2 COOH.
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring; wherein one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ , or one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl; and/or wherein when one of R 2 ⁇ , R 3 ⁇ , R 4 ", R 5 ⁇ or R 6 ⁇ is a carbon-carbon linked heterocyclic or heteroaryl, only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; and/or wherein when one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ is a carbon-carbon linked heterocyclic or heteroaryl, only one of
• R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together, or R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together, or R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together form a heterocyclic or heteroaryl optionally substituted by one or more alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl or aminoalkyl and optionally substituted with one or more selected from the group consisting of hydroxy, alkyl, carboxy, hydroxyalkyl, carboxyalkyl, amino, cyano, alkoxy, alkoxycarbonyl, acyl, oxo, -NR 7 R 8 , and halo; and/or
• R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ cannot be -OC(R') 2 C(O)OH; and/or at least one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , or one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ must be selected from the group consisting of cyano, tetrazol-5-yl, carboxy, -C(O)OR 2 , -C(O)NH 2 , -C(O)NHR 2 , C(O)N(R 2 ) 2 , -C(O)NR 7 R 8 , -C(O)NHC(O)NHR 2 , -C(O)NHC(O)N(R 2 ) 2 , C(O)NHC(O)NR 7 R 8 , -C(O)NHSO 2 NHR 2 , -C(O)NHSO 2 N(
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ ; R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, ary
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring; wherein one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together, or R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together form a heterocyclic or heteroaryl optionally substituted by one or more alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl or aminoalkyl and optionally substituted with one or more
• R , R , R and R substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 2 C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, alditol, carbohydrate, polyol alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) t .
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl,
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R andR are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R S ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together, or R 2 ⁇ and R 3 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together form a heterocyclic or heteroaryl optionally substituted by one or more alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl or aminoalkyl and optionally substituted with one or more selected from the group consisting of hydroxy, al
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein: R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalthio lower alkyl
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of cyano, tetrazoI-5-yl, carboxy, -C(O)OR 2 , -C(O)NH 2 , -C(O)NHR 2 , -
• R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 2 C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, alditol, carbohydrate, polyol alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ .
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl,
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of cyano, tetrazol-5-yl, carboxy, -C(O)OR 2 , -C(CH 3 ) 2 C(O)OH, (CH 2 ) y C(O)OH, wherein y is 1 , 2, 3, 4, 5, or 6; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and - C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl,
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of cyano, tetrazol-5-yl, carboxy, -C(O)OR 2 , -C(CH 3 ) 2 C(O)OH, (CH 2 ) y C(O)OH, wherein y is 1, 2, 3, 4, 5, or 6; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein: R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, alkyl, lower alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, haloalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, -C(O)R 2 , R 2 C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, polyol alkyl, alkoxy, lower alkoxy, -(O(O(O))
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, cycloalkyl, aryl, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, - C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of cyano, tetrazol-5-yl, carboxy, -C(O)OR 2 , -C(CH 3 ) 2 C(O)OH, (CH 2 ) y C(O)OH, wherein y is 1, 2, 3, 4, 5, or 6; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein: R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, alkyl, lower alkyl, cycloalkyl, cycloalkylalkyl, haloalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, heterocyclicamino lower alkyl, hydroxyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, polyoxyalkylene, cycloalkyloxy, cycloalkylalkoxy, heteroarylalkoxy, heteroaryl lower alkoxy, heterocyclicoxy, heterocyclicalkoxy, heterocyclic lower alkoxy, dial
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, cycloalkyl, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, lower alkyl, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 8-membered monocyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of tetrazol-5-yl, carboxy, -C(O)OR 2 , -C(CH 3 ) 2 C(O)OH, (CH 2 ) y C(O)OH, wherein y is 1, 2, 3, 4, 5, or 6; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 " are independently selected from the group consisting of hydrogen, halogen, lower alkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, polyoxyalkylene, heteroaryl lower alkoxy, heterocyclicalkoxy, heterocyclic lower alkoxy, carboxy, -C(O)OR 2 , - C(O)N(R 2 ) 2 , and -C(O)NR 7 R 8 , all of which can be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, cycloalkyl, hydroxy, hydroxyalkyl, heterocyclic, -NR 7 R 8
• R 2 is independently selected from the group consisting of alkyl, and lower alkyl, wherein all may be substituted by one or more selected from the group consisting of halo, lower alkyl, - NR 7 R 8 , alkoxy, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently alkyl, and linked together forming a 5- to 7-membered monocyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from carboxy or -
• R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, lower alkyl, -NR 7 R 8 , -C(O)NR 7 R 8 , and - C(O)N(R 2 ) 2 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, -(O(CH 2 ) 2 )i -3 -O-lower alkyl, heteroaryl lower alkoxy, heterocyclic lower alkoxy, and carboxy, all of which can be optionally substituted by one or more selected from the group consisting of hydroxy, hydroxyalkyl, -NR 7 R 8 , -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is lower alkyl
• R 7 andR 8 are independently alkyl, and linked together forming a 6-membered monocyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be carboxy.
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , and R 6 ⁇ are independently selected from the group consisting of hydrogen and carboxy;
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, -(O(CH 2 ) ) ⁇ .
• R 7 and R 8 are independently alkyl, and linked together forming a 6-membered monocyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be carboxy.
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , and R 6 ⁇ are independently selected from the group consisting of hydrogen and carboxy;
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 are independently selected from the group consisting of hydrogen, halogen, heteroaryl, lower alkoxy, -(O(CH 2 ) ) ⁇ -3 -O-lower alkyl, heteroaryl lower alkoxy, and heterocyclic lower alkoxy, all of which can be optionally substituted by one or more selected from the group consisting of hydroxy, hydroxyalkyl, -NR 7 R 8 , -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is lower alkyl
• R 7 and R 8 are independently alkyl, and linked together forming a 6-membered monocyclic or benzofused ring
• one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heteroaryl; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be carboxy.
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , and R 6 ⁇ are independently selected from the group consisting of hydrogen and carboxy;
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, fluorine, chlorine, methoxy, ethoxy, propoxy, 3-(l-mo ⁇ holino) propoxy, 2-(l- mo ⁇ holino) ethoxy, CH 3 O(CH 2 ) 2 O(CH 2 ) 2 -,
• R 4 ⁇ , R 5 ⁇ or R ⁇ must be selected from the group consisting of thiophen-s- yl, thiophen-3-yl, benzo[b]thiophen-2-yl, benzo[b]thiophen-3-yl, indol-2-yl, indol-3-yl, pyrrol- 2-yl, pyrrol-3-yl, l-methyl-indol-2-yl, l-methyl-indol-3-yl, N-Boc-indol-2-yl, N-Boc-indol-3- yl, N-Boc-pyrrol-2'yl, and N-Boc-pyrrol-3-yl; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be carboxy.
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , and R 6 ⁇ are independently selected from the group consisting of hydrogen and carboxy;
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, methoxy, 3-(l-mo ⁇ holino) propoxy, 2-(l-mo ⁇ holino) ethoxy, andCH3 ⁇ (CH 2 ) 2 O(CH 2 ) 2 ; wherein one of R 4 ⁇ , R 5 ° or R 6 ⁇ must be selected from the group consisting of thiophen-s- yl, benzo[b]thiophen-2-yl, indol-2-yl, l-methyl-indol-2-yl, N-Boc-indol-2-yl, N-Boc-pyrrol- 2'yl, and N-Boc-pyrrol-3-yl; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be carboxy.
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein: R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , and R 6 ⁇ are independently selected from the group consisting of hydrogen and carboxy; R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ .
• R 7 andR 8 are independently alkyl, and linked together forming a 6-membered monocyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be carboxy.
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , and R 6 ⁇ are independently selected from the group consisting of hydrogen and carboxy;
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, -(O(CH 2 ) 2 ) 1-3 -O-lower alkyl, heteroaryl lower alkoxy, and heterocyclic lower alkoxy, all of which can be optionally substituted by one or more selected from the group consisting of hydroxy, hydroxyalkyl, - NR 7 R 8 , -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is lower alkyl; R 7 and R 8 are independently alkyl, and linked together forming a 6-membered monocyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked tetrahydrofurn-2-yl or dihydrofuran-2-yl; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be carboxy.
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of -C(O)NH 2 , -C(O)NHR 2 , -C(O)N(R 2 ) 2 , -C(O)NR 7 R 8 , -C(O)NHC(O)NHR 2 , - C(O)NHC(O)N(R 2 ) 2 , -C(O)NHC(O)
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 2 C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, alditol, carbohydrate, polyol alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ .
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl,
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of -C(O)NH 2 , -C(O)NHR 2 , -C(O)N(R 2 ) 2 , -C(O)NR 7 R 8 , -C(O)NHC(O)NHR 2 , - C(O)NHC(O)N(R 2 ) 2 , -C(O)NHC(O)
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, alkyl, lower alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, haloalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, -C(O)R 2 , R 2 C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, polyol alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, polyoxyalkylene,
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of -C(O)NH 2 , -C(O)NHR 2 , -C(O)N(R 2 ) 2 , -C(O)NR 7 R 8 , -C(O)NHC(O)NHR 2 , - C(O)NHC(O)N(R 2 ) 2 , -C(O)NHC(O)
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ° and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, alkyl, lower alkyl, cycloalkyl, cycloalkylalkyl, haloalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, heterocyclicamino lower alkyl,
• R 1 is. independently selected from the group consisting of hydrogen, lower alkyl, cycloalkyl, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, lower alkyl, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, -C(O)NR 7 R 8 , and - C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, cycloalkyl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, lower alkyl, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 8-membered monocyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ;
• R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of -C(O)NH 2 , -C(O)NHR 2 , -C(O)N(R 2 ) 2 , -C(O)NR 7 R 8 , -C(O)NHC(O)R 2 , and - C(O)NHSO 2 R 2 ; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, lower alkyl, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, lower alkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ - 3 -O-lower alkyl, polyoxyalkylene, heteroaryl lower alkoxy, heterocyclicalkoxy, heterocyclic lower alkoxy, -N(R 2 )C(O)R 2 , - C(O)NH 2 , and -C(O)NHR 2 , all of which can be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino
• R 1 is independently selected from the group consisting of hydrogen, and lower alkyl which may be optionally substituted by one or more selected from the group consisting of halo, lower alkyl, -NR 7 R 8 , alkoxy, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, heteroaryl, and heterocyclic, wherein all may be substituted by one or more selected from the group consisting of halo, lower alkyl, -NR 7 R 8 , alkoxy, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently alkyl, and linked together forming a 5- to 7-membered monocyclic ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ° must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of -C(O)NH 2 , -C(O)NHR 2 , -C(O)NHC(O)R 2 , and -C(O)NHSO 2 R 2 ; wherein all R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, lower alkyl, heterocyclic, amino, aminoalkyl, and - NR 7 R 8 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ - 3 -O-lower alkyl, heteroaryl lower alkoxy, heterocyclic lower alkoxy, -N(R )C(O)R , -C(O)NH 2 , and - C(O)NHR 2 , all of which can be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxy
• R 1 is hydrogen
• R 2 is lower alkyl; R 7 and R 8 are independently alkyl, and linked together forming a 6-membered monocyclic ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of-C(O)NH 2 , -C(O)NHR 2 , -C(O)NHC(O)R 2 , and -C(O)NHSO 2 R 2 ; wherein all R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of heterocyclic, amino, aminoalkyl, and -NR 7 R 8 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein: R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 " are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicthio lower alkyl
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of thiol, -SC(R 1 ) 2 C(O)OH, -SC(R 1 ) 2 C(O)OR 2 , -SCH 2 C(O)OH, SCF 2 C(O)OH, -SO 2 NH 2 , -SO 2 NHR 2 , -SO 2 N(R 2 ) 2 , SO 2 NR 7 R 8 ,
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein: R ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicthio lower alkyl
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ; R 7 and R 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, -C(O)R 2 , R 2 C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, polyol alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ .
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, cycloalkyl, arylarylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, -C(O)NR 7 R 8 , and -C(O)N(R 2 ;h;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, cycloalkyl, aryl, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl,
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R , R 3 , or R 4 ⁇ must be selected from the group consisting of -SC ⁇ ' ⁇ C ⁇ OH, -SC(R') 2 C(O)OR 2 , -SCH 2 C(O)OH,
• R 1 , R 2 , R 7 and R substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl,
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, heterocyclicamino lower alkyl,
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, cycloalkyl, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, lower alkyl, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, -C(O)NR 7 R 8 , and - C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, cycloalkyl, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, lower alkyl, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ; R 7 and R 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 8-membered monocyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the provis
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein: R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 " are independently selected from the group consisting of hydrogen, halogen, lower alkyl, alkenyl, alkynyl, carbocycle, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, hydroxyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, polyoxyalkylene, heteroaryl lower alkoxy, heterocyclicalkoxy, heterocyclic lower alkoxy, -N(R 2 )C(O)R 2 , -SCH 2 C(O)OH - SO 2 NH 2 , -SO 2 NHR 2 , -SO 2 N(R 2 ) 2
• R 1 is independently selected from the group consisting of hydrogen and lower alkyl, which may be optionally substituted by one or more selected from the group consisting of halo, lower alkyl, -NR 7 R 8 , alkoxy, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl and lower alkyl, which may be substituted by one or more selected from the group consisting of halo, lower alkyl, - NR 7 R 8 , alkoxy, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 and R 8 are independently alkyl, and linked together forming a 5- to 7-membered monocyclic ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of -SC(R') 2 C(O)OR 2 , -SCH 2 C(O)OH, -SO 2 NH 2 , -SO 2 NHR 2 , -SO 2 N(R 2 ) 2 , SO 2 NR 7 R 8 , and -SO 2 NHC(O)R 2 ; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, -NR
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 " are independently selected from the group consisting of hydrogen, halogen, alkenyl, alkynyl, carbocycle, heteroaryl, heterocyclic, hydroxyl, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, heteroaryl lower alkoxy, heterocyclic lower alkoxy, -N(R 2 )C(O)R 2 , -SO 2 NH 2 , -SO 2 NHR 2 , SO 2 NHC(O)R 2 , -SR 2 , SO 2 NHC(O)NHR 2 , -SO 2 NHC(O)N(R 2 ) 2 , -SO 2 NHC(O)NR 7 R
• R 1 is hydrogen; R 2 is lower;
• R 7 and R 8 are independently alkyl, and linked together forming a 6-membered monocyclic ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of -SC(R 1 ) 2 C(O)OR 2 , -SO 2 NH 2 , - SO 2 NR 7 R 8 , and -SO 2 NHC(O)R 2 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 2 C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, alditol, carbohydrate, polyol alkyl, alkoxy, lower alkoxy, -(O(CH 2 )2) ⁇ - 3 -O-lower alkyl, polyoxyalkylene, cycloalkyloxy, cycloalkylalkoxy, haloalkoxy, aryloxy, arylalkoxy, heteroaryloxy, heteroarylalkoxy, heteroaryl lower alkoxy, heterocyclicoxy, heterocyclicalkoxy, heterocyclic lower alkoxy, - OC(R') 2 C(O)OH, -OC(R') 2 C(O)OR 2 , -OC(R') 2 C(O)NH 2 , -OC(R 1 ) 2
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, ary
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of amino, -NHR 2 , N(R 2 ) 2 , NR 7 R 8 , -NHC(R') 2 C(O)OH, -NHC(R 1 ) 2 C(O)OR 2 , - NHC(O)R 2 , -N(R 2 )C(O)R 2 , -NHC(O)OR 2 ,
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein: '
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, heteroaryl lower alkoxy, heterocyclic lower alkoxy, , all of which can be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently alkyl, and linked together forming a 6-membered monocyclic ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of amino, -N(C(O)NHR 2 ) 2 , NR 2 SO 2 R 2 and -NR 2 SO 2 R 2 ; wherein all R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , al
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 " are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicalkyl lower thioalkyl, lower alkyl S(O)-lower alkyl, lower
• R 2 C(O)alkyl, aminoalkyl, cycloalkylaminoalkyl, arylamino lower alkyl, heteroarylamino lower alkyl, heterocyclicamino lower alkyl, hydroxyl, hydroxyalkyl, alditol, carbohydrate, polyol alkyl, alkoxy, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ - 3 -O-lower alkyl, polyoxyalkylene, cycloalkyloxy, cycloalkylalkoxy, haloalkoxy, aryloxy, arylalkoxy, heteroaryloxy, heteroarylalkoxy, heteroaryl lower alkoxy, heterocyclicoxy, heterocyclicalkoxy, heterocyclic lower alkoxy, - OC(R') 2 C(O)OH, -OC R ⁇ C ⁇ OR 2 , -OC(R') 2 C(O)NH 2 , -0C(R') 2 C(0)N
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl,
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl,
• R 7 8 heterocyclic, amino, aminoalkyl, -NR R , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from the group consisting of -OC(R') 2 C(O)OH, -
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein: R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, -(O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, heteroaryl lower alkoxy, heterocyclic lower alkoxy, -OC(R 1 ) 2 C(O)OH, - OC(R 1 ) 2 C(O)N(R 2 ) 2 , -OC(R') 2 C(O)NR 7 R 8 , all of which can be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyal
• R 1 is hydrogen or lower alkyl optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl,
• R 2 is lower alkyl optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, - C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 and R 8 are independently alkyl, and linked together forming a 6-membered monocyclic ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; with the proviso that at least one of R 2 ⁇ , R 3 ⁇ , or R 4 ⁇ must be selected from - OC(R') 2 C(O)OH; wherein all R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, al
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein: R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicthio lower alkyl
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl,
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl,
• R 7 8 heterocyclic, amino, aminoalkyl, -NR R , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; and or
• R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and ⁇ C(O)N(R 2 ) 2 .
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, (O(CH 2 ) 2 ) ⁇ .
• R 7 andR 8 are independently selected from the group consisting of alkyl, linked together forming a 6-membered monocyclic ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; and/or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together, or R 3 ⁇ and R 4 " taken together or
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein: R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, nitro, alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, cycloalkylalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroaryl lower alkyl, heterocyclic, heterocyclic lower alkyl, alkylthioalkyl, cycloalkylthioalkyl, arylthio lower alkyl, aralkyl lower thioalkyl, heteroarylthio lower alkyl, heteroaralkyl lower thioalkyl, heterocyclicthio lower alkyl, heterocyclicthio lower alkyl
• R 1 is independently selected from the group consisting of hydrogen, lower alkyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl,
• R 2 is independently selected from the group consisting of alkyl, lower alkyl, alkenyl, alkynyl, carbocycle, cycloalkyl, aryl, heteroaryl, heterocyclic, arylalkyl, heteroarylalkyl, and heterocyclicalkyl, wherein all may be substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl,
• R 7 andR 8 are independently selected from the group consisting of alkyl, alkenyl and aryl and linked together forming a 4- to 12-membered monocyclic, bicylic, tricyclic or benzofused ring; wherein one of R 4 ⁇ , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; and/or
• R 1 , R 2 , R 7 and R 8 substituents can be optionally substituted with one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) ) 2 2-
• the invention is represented by Formula I or its pharmaceutically acceptable salt or ester, wherein:
• R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ are independently selected from the group consisting of hydrogen, halogen, heteroaryl, heterocyclic, lower alkoxy, (O(CH 2 ) 2 ) ⁇ -3 -O-lower alkyl, heteroaryl lower alkoxy, heterocyclic lower alkoxy, all of which can be optionally substituted by one or more selected from the group consisting of halo, alkyl, lower alkyl, alkenyl, cycloalkyl, acyl, hydroxy, hydroxyalkyl, heterocyclic, amino, aminoalkyl, -NR 7 R 8 , alkoxy, oxo, cyano, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)NR 7 R 8 , and -C(O)N(R 2 ) 2 ;
• R 2 is independently alkyl or lower alkyl
• R 7 andR 8 are independently selected from the group consisting of alkyl, linked together forming a 6-membered monocyclic ring; wherein one of R 4 , R 5 ⁇ or R 6 ⁇ must be a carbon-carbon linked heterocyclic or heteroaryl, and only one of R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ or R 6 ⁇ can be -OCH 3 ; and/or
• R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together or R 3 ⁇ and R 4 ⁇ taken together or R 4 ⁇ and R 5 ⁇ taken together form a 5 -membered ring containing one nitrogen, which may optionally be substituted with one or more selected from the group consisting of alkyl, lower alkyl, cycloalkyl, hydroxyalkyl, aminoalkyl, carboxyalkyl, alkoxycarbonyl; provided that R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ , R 6 ⁇ , R 2 ⁇ , R 3 ⁇ , R 4 ⁇ , R 5 ⁇ and R 6 ⁇ cannot be -OC(R 1 ) 2 COOH.
• the invention is a pharmaceutical composition coprising any of the above 80 embodiments or any of the specific Examples below together with one or more pharmaceutically acceptable carriers.
• An 82 nd embodiment includes embodiments 1-80 above or any of the Examples as a means to treat or prophylactically treat an inflammatory disorder including arthritis, rheumatoid arthritis, asthma, diabetic retinopathy, diabetic nephropathy, diabetic vasculopathy, multiple sclerosis, allergic rhinitis, chronic obstructive pulmonary disease, systemic lupus erthematosus, atherosclerosis, and restinosis.
• a further embodiment includes the intermediates used to make the final compounds of the invention. Said intermediates are useful as starting materials for making the compounds of the invention as well as having pharmaceutical activity alone.
• Another embodiment of the invention includes the process for making both the intermediates as well as the final compounds.
• a wavy line used as a bond denotes a bond which can be either the E- or Z- geometric isomer.
• alkyl or “alk”, alone or in combination, unless otherwise specified, refers to a saturated straight or branched primary, secondary, or tertiary hydrocarbon from 1 to 10 carbon atoms, including, but not limited to methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t- butyl, and sec-butyl,.
• lower alkyl alone or in combination refers to an alkyl having from 1 to 4 carbon atoms.
• the alkyl group may be optionally substituted with any moiety that does not otherwise interfere with the reaction or that provides an improvement in the process, including but not limited to but limited to halo, haloalkyl, hydroxyl, carboxyl, acyl, aryl, acyloxy, amino, amido, carboxyl derivatives, alkylamino, dialkylamino, arylamino, alkoxy, aryloxy, nitro, cyano, sulfonic acid, thiol, imine, sulfonyl, sulfanyl, sulfinyl, sulfamonyl, ester, carboxylic acid, amide, phosphonyl, phosphinyl, phosphoryl, phosphine, thioester, thioether, acid halide, anhydride, oxime, hydrozine, carbamate, phosphonic acid, phosphonate, either unprotected, or protected as necessary, as known to those
• alkenyl means a non-cyclic alkyl of 2 to 10 carbon atoms having one or more unsaturated carbon-carbon bonds.
• the alkenyl group may be optionally substituted with any moiety that does not otherwise interfere with the reaction or that provides an improvement in the process, including but not limited to but limited to halo, haloalkyl, hydroxyl, carboxyl, acyl, aryl, acyloxy, amino, amido, carboxyl derivatives, alkylamino, dialkylamino, arylamino, alkoxy, aryloxy, nitro, cyano, sulfonic acid, thiol, imine, sulfonyl, sulfanyl, sulfinyl, sulfamonyl, ester, carboxylic acid, amide, phosphonyl, phosphinyl, phosphoryl, phosphine
• alkynyl alone or in combination, means a non-cyclic alkyl of 2 to 10 carbon atoms having one or more triple carbon-carbon bonds, including but not limited to ethynyl and propynyl.
• the alkynyl group may be optionally substituted with any moiety that does not otherwise interfere with the reaction or that provides an improvement in the process, including but not limited to but limited to halo, haloalkyl, hydroxyl, carboxyl, acyl, aryl, acyloxy, amino, amido, carboxyl derivatives, alkylamino, dialkylamino, arylamino, alkoxy, aryloxy, nitro, cyano, sulfonic acid, thiol, imine, sulfonyl, sulfanyl, sulfinyl, sulfamonyl, ester, carboxylic acid, amide, phosphonyl, phosphinyl, phosphoryl, phospho
• alkoxycarbonyl and “carboalkoxy” are used interchangeably. Used alone or in combination, the terms mean refer to the radical -C(O)OR, wherein R is alkyl as defined herein.
• thio alone or in combination, means the radical -S-.
• thiol alone or in combination, means the radical -SH.
• hydroxy alone or in combination means the radical -OH.
• sulfonyl alone or in combination means the radical -S(O) 2 -.
• carbocycle alone or in combination, means any stable 3- to 7-membered monocyclic or bicyclic or 7- to 14-membered bicyclic or tricyclic or an up to 26-membered polycyclic carbon ring, any of which may be saturated, partially unsaturated, or aromatic. Examples of such carbocyles include, but are not limited to, cyclopropyl, cyclopentyl, cyclohexyl, phenyl, biphenyl, naphthyl, indanyl, adamantyl, or tetrahydronaphthyl (tetralin).
• cycloalkyl alone or in combination, means a saturated or partially unsaturated cyclic alkyl, having from 1 to 10 carbon atoms, including but not limited to mono- or bi-cyclic ring systems such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexenyl, and cyclohexyl.
• aryl alone or in combination, means a carbocyclic aromatic system containing one, two or three rings wherein such rings may be attached together in a pendent manner or may be fused.
• the "aryl” group can be optionally substituted with one or more of the moieties selected from the group consisting of alkyl, alkenyl, alkynyl, heteroaryl, heterocyclic, carbocycle, alkoxy, oxo, aryloxy, arylalkoxy, cycloalkyl, tetrazolyl, heteroaryloxy; heteroarylalkoxy, carbohydrate, amino acid, amino acid esters, amino acid amides, alditol, halogen, haloalkylthi, haloalkoxy, haloalkyl, hydroxyl, carboxyl, acyl, acyloxy, amino, aminoalkyl, aminoacyl, amido, alkylamino, dialkylamino, arylamino, nitro,
• heterocyclic refers to a nonaromatic cyclic group that may be partially (containing at least one double bond) or fully saturated and wherein the ring contains at least one heteroatom selected from oxygen, sulfur, nitrogen, or phosphorus.
• heteroaryl or “heteroaromatic”, alone or in combination, refer to an aromatic ring containing at least one heteroatom selected from sulfur, oxygen, nitrogen or phosphorus.
• the heteroaryl or heterocyclic ring may optionally be substituted by one or more substituent listed as optional substituents for aryl.
• heteroaryl or heterocyclic ring may combine to form a 5- to 7-membered carbocyclic, aryl, heteroaryl or heterocyclic ring, which in turn may be substituted as above.
• heterocylics and heteroaromatics are pyrrolidinyl, tetrahydrofuryl, tetrahydrofuranyl, pyranyl, purinyl, tetrahydropyranyl, piperazinyl, piperidinyl, mo ⁇ holino, thiomo ⁇ holino, tetrahydropyranyl, imidazolyl, pyrolinyl, pyrazolinyl, indolinyl, dioxolanyl, or 1,4-dioxanyl.
• Suitable protecting groups can include trimethylsilyl, dimethylhexylsilyl, t-butyldimethylsilyl, and t-butyldiphenylsilyl, trityl or substituted trityl, alkyl groups, acyl groups such as acetyl and propionyl, methanesulfonyl, and p-toluenesulfonyl.
• thienyl alone or in combination, refers to a five member cyclic group wherein the ring contains one sulfur atom and two double bonds.
• benzothienyl refers to a five member cyclic group wherein the ring contains one sulfur atom and two double bonds fused to a phenyl ring.
• aryloxy alone or in combination, refers to an aryl group bound to the molecule through an oxygen atom.
• heteroaryloxy refers to a heteroaryl group bound to the molecule through an oxygen atom.
• aralkoxy refers to an aryl group attached to an alkyl group which is attached to the molecule through an oxygen atom.
• heterocyclearalkoxy refers to a heterocyclic group attached to an aryl group attached to an alkyl-O- group.
• the heterocyclic, aryl and alkyl groups can be optionally substituted as described above.
• halo and halogen, alone or in combination, refer to chloro, bromo, iodo and fluoro.
• alkoxy or "alkylthio”, alone or in combination, refers to an alkyl group as defined above bonded through an oxygen linkage (-O-) or a sulfur linkage (-S-), respectively.
• lower alkoxy or “lower alkylthio”, alone or in combination, refers to a lower alkyl group as defined above bonded through an oxygen linkage (-O-) or a sulfur linkage (-S-), respectively.
• acyl refers to a group of the formula C(O)R', wherein R' is an alkyl, aryl, alkaryl or aralkyl group, or substituted alkyl, aryl, aralkyl or alkaryl, wherein these groups are as defined above.
• acetyl alone or in combination, refers to the radical -C(O)CH 3 .
• amino alone or in combination, denotes the radical -NH 2 or -NH-.
• nitro alone or in combination, denotes the radical -NO 2 .
• substituted means that one or more hydrogen on the designated atom or substituent is replaced with a selection from the indicated group, provided that the designated atom's normal valency is not exceeded, and the that the substitution results in a stable compound.
• oxo keto
• alditol refers to a carbohydrate in which the aldehyde or ketone group has been reduced to an alcohol moiety.
• the alditols of the present invention can also be optionally substituted or deoxygenated at one or more positions.
• substituents include hydrogen, halo, haloalkyl, carboxyl, acyl, acyloxy, amino, amido, carboxyl derivatives, alkylamino, dialkylamino, arylamino, alkoxy, aryloxy, nitro, cyano, sulfonic acid, thiol, imine, sulfonyl, sulfanyl, sulfinyl, sulfamonyl, ester, carboxylic acid, amide, amino acid, amino acid esters and amides, phosphonyl, phosphinyl, phosphoryl, thioester, thioether, oxime, hydrazine, carbamate, phosphonic acid, and phosphonate,.
• substituents include amine and halo, particularly fluorine.
• the substituent or alditol can be either unprotected, or protected as necessary, as known to those skilled in the art, for example, as taught in Greene, et al, Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1999, hereby inco ⁇ orated by reference.
• the alditol may have 3, 4, 5, 6 or 7 carbons.
• Examples of useful alditols are those derived from reduction of monosaccharides, including specifically those derived from the reduction of pyranose and furanose sugars.
• carbohydrate refers to a compound of carbon, hydrogen and oxygen that contains an aldehyde or ketone group in combination with at least two hydroxyl groups.
• the carbohydrates of the present invention can also be optionally substituted or deoxygenated at one or more positions. Carbohydrates thus include substituted and unsubstituted monosaccharides, disaccharides, oligosaccharides, and polysaccharides.
• the saccharide can be an aldose or ketose, and may comprise 3, 4, 5, 6, or 7 carbons.
• the carbohydrates are monosaccharides.
• the carbohydrates are pyranose and furanose sugars.
• the term "patient” refers to warm-blooded animals or mammals, and in particular humans, who are in need of the therapy described herein.
• the term "host”, as used herein, refers to a unicellular or multicellular organism, including cell lines and animals, and preferably a human.
• Compounds of the present invention are prepared either by reacting a heteroaryl- or heterocyclic-substituted aryl or heteroaryl ketone with a suitably substituted aryl aldehyde or by reacting a suitably substituted aryl ketone with a heteroaryl- or heterocyclic-substituted aryl or heteroaryl aldehyde.
• This reaction which is a condensation reaction, is suitably carried out under base- or acid-catalyzed conditions.
• the reaction may be suitably carried out in water or protic organic solvents such as lower alcohols (e.g. methanol, ethanol, tert-butanol), lower carboxylic acid (e.g.
• the base may be selected from sodium, lithium, potassium, barium, calcium, magnesium, aluminum, ammonium, or quartemary ammonium hydroxides, lower alkoxides
• the aldol condensation reaction can also be carried out in an aprotic solvent such as tetrahydrofuran (THF) with an organic base.
• THF tetrahydrofuran
• LDA lithium diisopropylamide
• Acid catalysts may be selected from hydrogen chloride, hydrogen bromide, hydrogen iodide, sulfuric acid, sulfonic acids (such as paratoluenesulfonic or methansulfonic acid), lower carboxylic acid (such as formic, acetic, or propionic acid), lower halogenated carboxylic acid
• the reaction may be carried out at temperatures in the range of -80 °C to +150 °C, preferrably in the range of 0 °C to +100 °C, and more preferably at room temperature.
• the time of reaction may be from 30 minutes to approximately 24 hours.
• R, R', R", R'", and R" can be any substitution including H;
• R, R', R", R'", and R"" can be suitabaly functionalized
• R, R', R", R'", and R" can represent multiple substitutions
• Dashed double bond can be at any location of a ring; 6.
• Y, Y', Y", and Y'" independently represent N(H), O, or S,
• X and X' independently represent Cl, Br, or I;
• HetAr represents suitably substituted heterocyclic aryl; 10.
• Cy represents cyclohexyl.
• Ex-IB [Bis(ethoxycarbonyl)methyldenedioxy]benzene obtained from Ex-IA (3.9 g, 14.7 mmol) was dissolved in THF (100 mL) and cooled with ice-water. Lithium aluminum hydride (1 M solution in THF, 44 mL) was added dropwise, and the mixture was stirred overnight. The reaction was carefully quenched with saturated sodium sulfate until there was no further bubbling. The mixture was stirred overnight, then filtered, and the filtrate was dried over magnesium sulfate.
• Ex-ID A solution of 5-bromo-3,4-dimethoxybenzaldehyde (10.23 g, 41.7 mmol) in 359 mL of ethylene glycol dimethyl ether was purged with nitrogen gas for 30 min. The solution was treated with tetrakis(triphenylphosphine)palladium(0) (5.0 g, 4.3 mmol), thiophene-2-boronic acid (8.01 g, 62.6 mmol), and a solution of 2 N sodium carbonate 72 mL, 3.45 mmol). The reaction was refluxed for 16 h.
• the reaction mixture was concentrated, diluted with an aqueous solution of saturated sodium bicarbonate (75 mL), and extracted with dichloromethane (2 x 100 mL). The organic layer was dried over sodium sulfate and concentrated to a brown solid.
• the crude material was purified by silica gel chromatography (1 :1 ethyl acetate/hexanes) to give 9.42 g (90%) of the desired 3,4-dimethoxy-5-(thien-2-yl)benzaldehyde product.
• Ex-2A 4-(Thien-2-yl)benzaldehyde was obtained in a similar manner as described in Ex-ID from 4-bromobenzaldehyde.
• Ex-3A A sample of 5-bromo-2,4-dimethoxybenzaldehyde (4.9 g, 20.0 mmol) was dissolved in ethylene glycol dimethyl ether (50 mL). Tetrakis(triphenylphosphine)palladium(0) (2.32 g, 2 mmol) was added, and the mixture was stirred at room temperature under nitrogen for 5 min. Benzo[b]thiophene-2-boronic acid (4.27 g, 24 mmol) and sodium carbonate solution (2 M, 20 mL) were added. The mixture was stirred at reflux under nitrogen for 24 hours. Upon cooling to room temperature, the mixture was poured into water and extracted with ethyl acetate.
• Ex-4A 4-Pyrimidin-5-yl-benzaldehyde was obtained pyrimidine-5-boronic acid and 4- bromobenzaldehyde in a similar manner as described in Ex-3A, 88.6% yield.
• the reaction was diluted with H 2 O (200 mL) and transferred to a separatory funnel containing EtOAc (200 mL) and H 2 O (200 mL). The layers were cut and the aqueous layer was extracted with EtOAc (100 L). The combined organic cuts were filtered through a pre-washed pad of solka floe (5 g). The pad of solka floe and spent catalyst were washed with fresh EtOAc (200 mL) and this wash combined with the batch. The resultant filtrate was concentrated to dryness. The crude product was dissolved in THF (38 mL) and crystallized upon heptane (152 mL) addition.
• Ex-14A A solution of l-(4-amino-phenyl)-3E-(3,4-dimethoxy-5-thiophen-2-yl-phenyl)- propenone ( ⁇ x-11, 472.2 mg, 1.3 mmol) and triethylamine (398.63 ⁇ L, 2.86 mmol) was stirred in 20 mL of anhydrous dichloromethane. The mixture was treated with mesyl chloride (100 ⁇ L, 1.3 mmol). The reaction mixture was stirred for 16 hours and heated gently for another 4 hours.
• Ex-17A 4'-Bromoacetophenone (3.98 g, 20 mmol) was dissolved in ethylene glycol dimethyl ether and then the solution was degassed with nitrogen for 15 minutes. Tetrakis(triphenylphosphine)palladium(0) (2.31 g, 2 mmol) was added, and the solution was further degassed for 10 minutes. Thiophene-2-boronic acid (3.07 g, 24 mmol) was added followed by the addition of sodium carbonate solution (2 M, 45 mL). The mixture was stirred at reflux under nitrogen overnight. Most of the solvent was removed, and water was added to the remainder.
• Ex-20B A solution of 4-fluoro-3-(thiophen-2-yl)-benzaldehyde (1.11 g, 5.38 mmol) from Ex- 20A and pyrrolidine (13.0 g, 183.0 mmol) in dimethylformamide (30 mL) was treated with solid K 2 CO 3 (1.7 g, 12.3 mmol), and the resulting mixture was stirred at reflux for 1 week. Upon cooling to room temperature, the reaction was poured into water (100 mL) and extracted with ethyl acetate (2 X 100 mL). The organic phase was dried over magnesium sulfate, and the solvent was removed under reduced pressure.
• Ex-29B 5-Bromo-2-hydroxy-4-methoxybenzaldehyde obtained from Ex-29A (1.5 g, 6.5 mmol) and thiophene-2-boronic acid (0.91 g, 7.1 mmol) were dissolved in tetrahydrofuran (15 mL). Nitrogen was bubbled into the solution for 10 min followed by the sequential addition of potassium fluoride (0.80 g, 14 mmol, spray-dried) and bis(tri-t-butylphosphine)palladium (0) (0.033 g, 0.065 mmol). The solution was immediately heated to 60 °C and aged for 1.5 h.
• Ex-29C To a solution of 2-hydroxy-4-methoxy-5-thiophen-2-yl-benzaldehyde from Ex-29B (0.10 g, 0.43 mmol) in NN-dimethylformamide (3 mL) was added potassium carbonate (0.18 g, 1.3 mmol) and the resulting yellow slurry was heated to 80°C. Once at 80 °C, l-bromo-2-(2- methoxyethoxy)ethane (0.24 g, 1.3 mmol) was added dropwise in three equal portions with stirring at 1 h intervals. After the last addition, the reaction was stirred for an additional 1 h at 80 °C and cooled to room temperature.
• the mixture was diluted with water (10 mL), acidified with a 1 ⁇ hydrochloric acid solution, and extracted with ethyl acetate (3 x 15 mL). The combined organic extracts were dried over sodium sulfate and evaporated to dryness. The crude oil was taken up in ethyl alcohol (3 mL) and warmed to 60 °C to obtain complete dissolution and allowed to cool to room temperature. The resulting precipitate was collected and dried in vacuo to yield 0.14 g (85%) of the title compound as a yellow solid, m.p. 145-146 °C.
• Ex-31A 2,4-Dimethoxy-5-pyrimidin-5-yl-benzaldehyde was prepared from 5-bromo-2,4- dimethoxybenzaldehyde and pyrimidine-5-boronic acid in a similar manner as described in Ex- 3A, 98% yield.
• ⁇ -NMR (CDC1 3 ) ⁇ 10.37 (s, IH), 9.15 (s, IH), 8.87 (s, 2H) 7.86(s, IH), 6.57 (s, IH), 4.03 (s, 3H), 3.96 (s, 3H).
• Ex-33A 5-(3,5-Dimethyl-isoxazol-4-yl)-2,4-dimethoxy-benzaldehyde was prepared from 5- bromo-2,4-dimethoxybenzaldehyde and 3,5-dimethyl-isoxazole-4-boronic acid in a similar manner as described in Ex-3A, 75% yield.
• ⁇ -NMR (CDC1 3 ) ⁇ 10.34 (s, IH), 7.63 (s, IH), 6.52 (s, IH), 4.00 (s, 3H), 3.90 (s, 3H), 2.12(s, 6H).
• Ex-34A A solution of 2-hydroxy-4-methoxy-benzaldehyde (5.0 g, 32.86 mmol) in dichloromethane (65 mL) was cooled to 0 °C and then pyridine (13.3 mL, 164.4 mmol) was added in 1 portion. Triflic anhydride (14.8 mL, 87.97 mmol) was then added over 2 h while maintaining an internal temperature below 5 °C. The resulting solution was allowed to warm to room temperature overnight and then was slowly poured into ice water (100 mL). After diluting further with 1 N HCl (100 mL) the solution was extracted with dichloromethane (2 X 100 mL).
• Ex-34B A solution of trifluoro-methanesulfonic acid 2-formyl-5-methoxy-phenyl ester (Ex- 34A, 1.6 g, 5.63 mmol) in 1,4-dioxane (15 mL) was stirred at room temperature under nitrogen for 5 min.
• tetrakis(triphenylphosphine)- palladium(O) (0.65 g, 0.56 mmol)
• a potassium phosphate 2.2 g, 10.36 mmol
• Ex-36A 2-(5-Formyl-2,4-dimethoxy-phenyl)-indole-l -carboxylic acid tert-butyl ester was prepared from 5-bromo-2,4-dimethoxybenzaldehyde and N-Boc-indole-2-boronic acid in a similar manner as described in Ex-3A. Yellow oil, 79% yield.
• Ex-39A 2,4-Dimethoxy-6-thiophen-2-yl-benzaldehyde was prepared in a similar manner as described in Ex-34A, 40% yield.
• ⁇ -NMR (CDC1 3 ) ⁇ 10.02 (s, 1 H), 7.40 (d, IH), 7.07 (m, 2H), 6.58 (d, IH), 6.50 (d, IH), 3.93 (s, 3H), 3.89 (s, 3H).
• the title compound was prepared by condensing 2,4-dimethoxy-6-thiophen-2-yl-benzaldehyde (Ex-39A) and 4-acetylbenzoic acid in a similar manner as described in Ex-3.
• Ex-41A 4-Methoxy-3-(thiophen-2-yl)-benzaldehyde was prepared from 3-bromo-4- methoxybenzaldehyde and thiophene-2-boronic acid in a similar manner as described in Ex- 3A. Orange oil, 96% yield.
• Ex-42A 3-(Thiophen-2-yl)-benzaldehyde was prepared from 3-bromobenzaldehyde and thiophene-2-boronic acid in a similar manner as described in Ex-3A. Orange oil, 93% yield.
• Ex-44A 3-Benzo[t>]thiophen-2-yl-2-hydroxy-4-methoxy-benzaldehyde was prepared through Suzuki coupling as described in Ex-3A using 3-bromo-2-hydroxy-4-methoxybenzaldehyde (obtained as a minor product from Ex-29A).
• Ex-44B 3-Benzo[t)]thiophen-2-yl-2-hydroxy-4-methoxy-benzaldehyde (Ex-44A, 57.4 mg, 0.202 mmol) was dissolved in acetone (5 mL) and potassium carbonate (31 mg, 0.22 mmol) was added. Methyl iodide (25 uL, 0.40 mmol) was added and the solution was heated to reflux for 3.5 h. After cooling, the crude reaction mix was concentrated on the rotavap. The resulting residue was taken up in 10 mL of a 1 :9 mix of saturated, aqueous NH 4 C1 to water and extracted with EtOAc (2x15 mL).
• Ex-45A 2-Methoxy-5-(thiophen-2-yl)-benzaldehyde was prepared from 5-bromo-2- methoxybenzaldehyde and thiophene-2-boronic acid in a similar manner as described in Ex- 3A.

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