WO2011133637A2 - Compounds and methods for kinase modulation, and indications therefor - Google Patents
Compounds and methods for kinase modulation, and indications therefor Download PDFInfo
- Publication number
- WO2011133637A2 WO2011133637A2 PCT/US2011/033192 US2011033192W WO2011133637A2 WO 2011133637 A2 WO2011133637 A2 WO 2011133637A2 US 2011033192 W US2011033192 W US 2011033192W WO 2011133637 A2 WO2011133637 A2 WO 2011133637A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- fluoro
- formula
- lower alkyl
- compounds
- optionally substituted
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 0 *c1c(*)ncc(Nc2ccc(C(c3c[n]c4ncnc(*)c34)=O)c(F)n2)c1 Chemical compound *c1c(*)ncc(Nc2ccc(C(c3c[n]c4ncnc(*)c34)=O)c(F)n2)c1 0.000 description 5
- QLKMPKAWWDMXFO-UHFFFAOYSA-N C(C1)C1Nc1c(cc[nH]2)c2ncn1 Chemical compound C(C1)C1Nc1c(cc[nH]2)c2ncn1 QLKMPKAWWDMXFO-UHFFFAOYSA-N 0.000 description 1
- RCDLCRXBHXOKSE-UHFFFAOYSA-O CS(c1ncc(Cc(c2cc(Cl)cnc22)c[n]2S(c2ccccc2)(=O)=O)cn1)[OH2+] Chemical compound CS(c1ncc(Cc(c2cc(Cl)cnc22)c[n]2S(c2ccccc2)(=O)=O)cn1)[OH2+] RCDLCRXBHXOKSE-UHFFFAOYSA-O 0.000 description 1
- KNJHCNJDLOENAA-UHFFFAOYSA-N CSc1ncc(C(c(c2cc(Cl)cnc22)c[n]2S(c2ccccc2)(=O)=O)O)cn1 Chemical compound CSc1ncc(C(c(c2cc(Cl)cnc22)c[n]2S(c2ccccc2)(=O)=O)O)cn1 KNJHCNJDLOENAA-UHFFFAOYSA-N 0.000 description 1
- NXYJGRDGHPDSRT-CYBMUJFWSA-N C[C@H](COC)Nc1ncnc2c1c(C(c1ccc(Nc3cnc(C4CC4)cc3)nc1F)=O)c[nH]2 Chemical compound C[C@H](COC)Nc1ncnc2c1c(C(c1ccc(Nc3cnc(C4CC4)cc3)nc1F)=O)c[nH]2 NXYJGRDGHPDSRT-CYBMUJFWSA-N 0.000 description 1
- IQMVRNITTPEXDF-UHFFFAOYSA-N Cc1c(c(I)c[n]2S(c3ccccc3)(=O)=O)c2ncn1 Chemical compound Cc1c(c(I)c[n]2S(c3ccccc3)(=O)=O)c2ncn1 IQMVRNITTPEXDF-UHFFFAOYSA-N 0.000 description 1
- WNHFADHFYQHYFL-UHFFFAOYSA-N Cc1cnc2[nH]cc(C(c(ccc(Nc3cnc(C4CC4)cc3)n3)c3F)=O)c2c1 Chemical compound Cc1cnc2[nH]cc(C(c(ccc(Nc3cnc(C4CC4)cc3)n3)c3F)=O)c2c1 WNHFADHFYQHYFL-UHFFFAOYSA-N 0.000 description 1
- LZTOGEVTAZHIFX-UHFFFAOYSA-N Clc(cc12)cnc1[nH]cc2I Chemical compound Clc(cc12)cnc1[nH]cc2I LZTOGEVTAZHIFX-UHFFFAOYSA-N 0.000 description 1
- BPTCCCTWWAUJRK-UHFFFAOYSA-N Clc1c(cc[nH]2)c2ncn1 Chemical compound Clc1c(cc[nH]2)c2ncn1 BPTCCCTWWAUJRK-UHFFFAOYSA-N 0.000 description 1
- MFZQJIKENSPRSJ-UHFFFAOYSA-N Clc1cnc2[nH]ccc2c1 Chemical compound Clc1cnc2[nH]ccc2c1 MFZQJIKENSPRSJ-UHFFFAOYSA-N 0.000 description 1
- GERXHPDEXFUVFK-UHFFFAOYSA-N FC(CC1)(CCC1Nc1ccc(Cc(c2c3)c[nH]c2ncc3Cl)c(F)n1)F Chemical compound FC(CC1)(CCC1Nc1ccc(Cc(c2c3)c[nH]c2ncc3Cl)c(F)n1)F GERXHPDEXFUVFK-UHFFFAOYSA-N 0.000 description 1
- VZXZRNATZJUUQW-UHFFFAOYSA-N O=S(c1ccccc1)([n](cc(c1c2)I)c1ncc2Cl)=O Chemical compound O=S(c1ccccc1)([n](cc(c1c2)I)c1ncc2Cl)=O VZXZRNATZJUUQW-UHFFFAOYSA-N 0.000 description 1
- MVXVYAKCVDQRLW-UHFFFAOYSA-N c1c[nH]c2c1cccn2 Chemical compound c1c[nH]c2c1cccn2 MVXVYAKCVDQRLW-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/02—Muscle relaxants, e.g. for tetanus or cramps
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Definitions
- compounds are provided, as well as various salts thereof, formulations thereof, conjugates thereof, derivatives thereof, forms thereof and uses thereof.
- the compounds are active on one or more protein kinases, including Fms, Kit, Flt3, TrkA, TrkB and/or TrkC, including any mutations thereof.
- compounds are active on Fms kinase.
- compounds are active on Fms and Kit kinase.
- compounds are selectively active on Fms kinase relative to Kit kinase.
- compounds are active on Fms kinase and Flt3 kinase.
- compounds are active on Fms kinase and one or more of TrkA, TrkB and TrkC kinase.
- Also contemplated in accordance with the present invention are methods for the use of the compounds in treating diseases and conditions associated with regulation of the activity of one or more of Fms, Kit, Flt3, TrkA, TrkB and TrkC, including any mutations thereof.
- the use of compounds for therapeutic methods involving modulation of protein kinases are provided.
- the compounds are used for therapeutic methods involving the treatment of a variety of indications, including, but not limited to, rheumatoid arthiritis, osteoarthritis, osteoporosis, peri- prosthetic osteolysis, systemic sclerosis, demyelinating disorders, multiple sclerosis, Charcot Marie Tooth syndrome, amyotrophic lateral sclerosis, Alzheimer's disease, Parkinson's disease, global ischemia, ulcerative colitis, Crohn's disease, immune thrombocytopenic purpura, atherosclerosis, systemic lupus erythematosis, myelopreparation for autologous transplantation, transplant rejection, glomerulonephritis, interstitial nephritis, Lupus nephritis, tubular necrosis, diabetic nephropathy, renal hypertrophy, type I diabetes, acute pain, inflammatory pain, neuropathic pain, acute myeloid leukemia, melanoma, multiple mye
- Li is -C(H 2 )- or -C(O)-;
- R 2 is selected from the group consisting of hydrogen, cycloalkyl, lower alkyl optionally substituted with one or more R 8 , -N(R 9a )(R 9b ), and -O-R 9 ;
- R 1 is fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- each R 4 is independently selected from the group consisting of fluoro, -OH, lower alkyl optionally substitituted with one or more fluoro, and lower alkoxy optionally substituted with one or more fluoro;
- each R 5 is independently selected from the group consisting of fluoro, chloro, -O-R 10 , -S-R 11 , -S(0 2 )-R 12 , and lower alkyl optionally substitituted with one or more R 13 ;
- each R 6 is independently selected from the group consisting of fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, and lower alkoxy optionally substituted with one or more fluoro; or two R 6 bound to adjacent carbon atoms of the heteroaryl ring, taken together, form a fused cycloalkyl ring;
- R 7 is cycloalkyl, lower alkoxy or lower alkyl optionally substituted with one or more fluoro;
- R 8 is fluoro or lower alkoxy optionally substitituted with one or more fluoro
- R 9a is H and R 9b is selected from the group consisting of (i) H, lower alkyl, lower alkyl substituted with one or more fluoro, lower alkyl substituted with lower alkoxy or lower alkyl substituted with hydroxyl and (ii) cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, arylalkyl, heteroarylalkyl, each of which is optionally substituted with one to three members selected from lower alkyl, haloalkyl, lower alkoxy or fluoro; or
- R 9a and R 9b together with the nitrogen to which they are attached form a 5- or 6-membered ring having from 0 to 1 additional heteroatom selected from O, N or S, each of which is optionally substituted with one to three members selected from lower alkyl, haloalkyl, lower alkoxy or fluoro;
- R 9 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy;
- each R 10 , R 11 and R 12 are independently lower alkyl optionally substituted with one or more
- each R 13 is independently selected from the group consisting of fluoro, -OH, and lower alkoxy optionally substituted with one or more fluoro.
- R 3 is fluoro.
- the salt is a pharmaceutically acceptable salt.
- the invention provides compounds of Formula I or any of the subformulas as described herein, or a pharmaceutically acceptable salt, a solvate, a tautomer or a stereoisomer thereof.
- compounds of Formula I or any of the subformulas as described herein, or a pharmaceutically acceptable salt or a solvate thereof there are provided compounds of Formula I or any of the subformulas as described herein, or a pharmaceutically acceptable salt or a solvate thereof.
- the solvate is a hydrate.
- R 2 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- Cyi is cycloalkyl optionally substituted with one or more R 4 , phenyl optionally substituted with one or more R 5 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 6 and optionally substituted on an available nitrogen atom with R 7 , wherein cycloalkyl is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl, and heteroaryl is pyridinyl or pyrazolyl.
- Cyi is cycloalkyl optionally substituted with one or more R 4 , phenyl optionally substituted with one or more R 5 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 6 and optionally substituted on an available nitrogen atom with R 7 , wherein cycloalkyl is cyclohexyl, or cycloheptyl, and heteroaryl is pyridin-3-yl or pyrazol-4-yl.
- Li is -C(H 2 )-. In some embodiments of compounds of Formula I, further to any of the above embodiments of Formula I, Li is -C(O)-.
- Xi is N and all the other variables are as defined herein.
- Li is CH 2 , Yi is CH and R 3 is F.
- Li is CH 2 , Yi is N and R 3 is F.
- Xi is - R 1 ) ⁇ R 1 and all the other variables are as defined herein.
- Li is CH 2 , Yi is CH and R 3 is F.
- Li is -CH 2 - , Yi is N and R 3 is F.
- Cyi is cycloalkyl optionally substituted with one or more R 4 .
- Cyi is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopentyl, each of which is optionally substituted with from 1 to 3 R 4 . All the other variables are as defined herein.
- Cyi is phenyl optionally substituted with one or more R 5 and all the other variables are as defined herein.
- Cyi is 5 or 6-membered heteroaryl optionally substituted on an available carbon atom with one or more R 6 and optionally substituted on an available nitrogen atom with R 7 .
- Cyi is 3-pyridyl, 2-pyrrolyl, 3- pyrrolyl or 4-pyrazolyl, optionally substituted on an available carbon atom with from 1 to 3 R 6 and optionally substituted on an available nitrogen atom with R 7 .
- each R 6 is independently selected from the group consisting of fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with from one to three fluoro, and lower alkoxy optionally substituted with one to three fluoro; or two R 6 bound to adjacent carbon atoms of the heteroaryl ring form a fused cycloalkyl ring. All the other variables are as defined herein.
- R 9a is H and R 9b is selected from H, lower alkyl, lower alkyl substituted with hydroxy, lower alkyl substituted with lower alkoxy, lower alkyl substituted with 1 to 3 fluoro groups, cycloalkyl optionally substituted with lower alkyl or one to three fluoro, cycloalkylalkyl optionally substituted with lower alkyl or one to three fluoro substituents, heterocycloalkyl optionally substituted with lower alkyl, heterocycloalkylalkyl, arylalkyl optionally substituted with from 1 to 3 members selected from lower alkyl, fluoro or haloalkyl and
- R 9a is H and R 9b is selected from (i) H, methyl, ethyl, t-butyl, propyl, isopropyl, 2-butyl, n-butyl, 2-hydroxy-2-methylpropyl, 2-methoxy ethyl, 3-methoxypropyl, 2,2,2- trifluoroethyl, or 4-methoxybutyl and (ii) cyclopropyl, cyclobutyl, cyclopentyl, cylohexyl, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexymethyl, benzyl, 1 -methylbenzyl, 4,4-difluorocyclohexyl, 2-tetrahydrofuranylmethyl, 4-piperadinyl, 3-pyr
- -N(R 9a )(R 9b ) is 1 -piperadinyl, 4- morpholinyl, 1 -piperazinyl or 1 -pyrrolidinyl, each of which is optionally substituted with one to three members selected from lower alkyl, haloalkyl, lower alkoxy or fluoro. All the other variables are as defined herein.
- L 2 is -C(H 2 )- or -C(O)-;
- Cy 2 is cycloalkyl optionally substituted with one or more R , phenyl optionally substituted with one or more R 17 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 18 and optionally substituted on an available nitrogen atom with R 19 ;
- R 14 is selected from the group consisting of cycloalkyl, lower alkyl optionally substituted with one or more R 20 , -N(R 9a )(R 9b ), and -O-R 21 ;
- each R 16 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- each R is independently selected from the group consisting of fluoro, chloro, -O-R , -S-R , -S(0 2 )-R 24 , and lower alkyl optionally substitituted with one or more R 25 ;
- each R 18 is independently selected from the group consisting of fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, and lower alkoxy optionally substituted with one or more fluoro; or two R 18 bound to adjacent carbon atoms of the heteroaryl ring, taken together, form a fused cycloalkyl ring;
- R 19 is cycloalkyl, lower alkoxy, or lower alkyl optionally substituted with one or more fluoro;
- R 20 is fluoro or lower alkoxy optionally substitituted with one or more fluoro;
- R 21 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy;
- each R 22 , R 2"3 and 24 are independently lower alkyl optionally substituted with one or more
- each R 25 is independently selected from the group consisting of fluoro, -OH, and lower alkoxy optionally substituted with one or more fluoro.
- R 14 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 14 is selected from the group consisting of C3.6 cycloalkyl, C 1 .3 alkyl, C 1 .3 alkoxy, and Ci_3 alkoxy substituted with C 1 .3 alkoxy.
- R 14 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- Cy 2 is cycloalkyl optionally substituted with one or more R 16 , phenyl optionally substituted with one or more R 17 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 18 and optionally substituted on an available nitrogen atom with R 19 , wherein cycloalkyl is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl, and heteroaryl is pyridinyl or pyrazolyl.
- Cy 2 is cycloalkyl optionally substituted with one or more R 16 , phenyl optionally substituted with one or more R , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 18 and optionally substituted on an available nitrogen atom with R 19 , wherein cycloalkyl is cyclohexyl, or cycloheptyl, and heteroaryl is pyridin-3-yl or pyrazol-4-yl.
- L 2 is -C(H 2 )-. In some embodiments of compounds of Formula la, further to any of the above embodiments of Formula la, L 2 is -C(O)-.
- Cy 3 is cycloalkyl optionally substituted with one or more R 27 , phenyl optionally substituted with one or more R 28 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 29 and optionally substituted on an available nitrogen atom with R 30 ;
- R 26 is selected from the group consisting of cycloalkyl, lower alkyl optionally substituted with one or more R 31 , and -O-R 32 ;
- each R 27 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- each R is independently selected from the group consisting of fluoro, chloro, -O-R , -S-R , -S(0 2 )-R 35 , and lower alkyl optionally substitituted with one or more R 36 ;
- each R 29 is independently selected from the group consisting of fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, and lower alkoxy optionally substituted with one or more fluoro; or two R 29 bound to adjacent carbon atoms of the heteroaryl ring, taken together, form a fused cycloalkyl ring;
- R 30 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro;
- R 31 is fluoro or lower alkoxy optionally substitituted with one or more fluoro; R is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy;
- each R , ⁇ and R" are independently lower alkyl optionally substituted with one or more
- each R 36 is independently selected from the group consisting of fluoro, -OH, and lower alkoxy optionally substituted with one or more fluoro.
- R 26 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 26 is selected from the group consisting of C3.6 cycloalkyl, C 1 .3 alkyl, C 1 .3 alkoxy, and Ci_3 alkoxy substituted with C 1 .3 alkoxy.
- R 26 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- Cy 3 is cycloalkyl optionally substituted with one or more R 27 , phenyl optionally substituted with one or more R 28 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 29 and optionally substituted on an available nitrogen atom with R 30 , wherein cycloalkyl is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl, and heteroaryl is pyridinyl or pyrazolyl.
- Cy 3 is cycloalkyl optionally substituted with one or more R 27 , phenyl optionally substituted with one or more R 28 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 29 and optionally substituted on an available nitrogen atom with R 30 , wherein cycloalkyl is cyclohexyl, or cycloheptyl, and heteroaryl is pyridin-3-yl or pyrazol-4-yl.
- Cy 4 is cycloalkyl optionally substituted with one or more R 38 , phenyl optionally substituted with one or more R 39 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 40 and optionally substituted on an available nitrogen atom with R 41 ;
- R is selected from the group consisting of cycloalkyl, lower alkyl optionally substituted with one or more R 42 , and -O-R 43 ;
- each R 38 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- each R 39 is independently selected from the group consisting of fluoro, chloro, -O-R 44 , -S-R 45 , -S(0 2 )-R 46 , and lower alkyl optionally substitituted with one or more R 47 ;
- each R 40 is independently selected from the group consisting of fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, and lower alkoxy optionally substituted with one or more fluoro; or two R 40 bound to adjacent carbon atoms of the heteroaryl ring, taken together, form a fused cycloalkyl ring;
- R 41 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro;
- R 42 is fluoro or lower alkoxy optionally substitituted with one or more fluoro;
- R 43 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy;
- each R 44 , R 45 and R 46 are independently lower alkyl optionally substituted with one or more
- each R 47 is independently selected from the group consisting of fluoro, -OH, and lower alkoxy optionally substituted with one or more fluoro.
- R 37 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy. In one embodiment, R 37 is selected from the group consisting of C 3 _ 6 cycloalkyl, Ci_ 3 alkyl, Ci_ 3 alkoxy, and Ci_3 alkoxy substituted with Ci_ 3 alkoxy. In one embodiment, R 37 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- Cy 4 is cycloalkyl optionally substituted with one or more R 38 , phenyl optionally substituted with one or more R 39 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 40 and optionally substituted on an available nitrogen atom with R 41 , wherein cycloalkyl is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl, and heteroaryl is pyridinyl or pyrazolyl.
- Cy 4 is cycloalkyl optionally substituted with one or more R 38 , phenyl optionally substituted with one or more R 39 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 40 and optionally substituted on an available nitrogen atom with R 41 , wherein cycloalkyl is cyclohexyl, or cycloheptyl, and heteroaryl is pyridin-3-yl or pyrazol-4-yl.
- Cy 5 is cycloalkyl optionally substituted with one or more R 49 , phenyl optionally substituted with one or more R 50 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 51 and optionally substituted on an available nitrogen atom with R 52 ;
- R 48 is selected from the group consisting of cycloalkyl, lower alkyl optionally substituted with one or more R 53 , and -O-R 54 ;
- each R 49 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- each R 50 is independently selected from the group consisting of fluoro, chloro, -O-R 55 , -S-R 56 , -S(0 2 )-R 57 , and lower alkyl optionally substitituted with one or more R 58 ;
- each R 51 is independently selected from the group consisting of fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, and lower alkoxy optionally substituted with one or more fluoro; or two R 51 bound to adjacent carbon atoms of the heteroaryl ring, taken together, form a fused cycloalkyl ring;
- R 52 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro;
- R 53 is fluoro or lower alkoxy optionally substitituted with one or more fluoro;
- R 54 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy;
- each R 55 , R 56 and R 57 are independently lower alkyl optionally substituted with one or more
- each R 58 is independently selected from the group consisting of fluoro, -OH, and lower alkoxy optionally substituted with one or more fluoro.
- R 48 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 48 is selected from the group consisting of C3.6 cycloalkyl, C 1 .3 alkyl, C 1 .3 alkoxy, and Ci_3 alkoxy substituted with C 1 .3 alkoxy.
- R 48 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- Cy 5 is cycloalkyl optionally substituted with one or more R 49 , phenyl optionally substituted with one or more R 50 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 51 and optionally substituted on an available nitrogen atom with R 52 , wherein cycloalkyl is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl, and heteroaryl is pyridinyl or pyrazolyl.
- Cy 5 is cycloalkyl optionally substituted with one or more R 49 , phenyl optionally substituted with one or more R 50 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 51 and optionally substituted on an available nitrogen atom with R 52 , wherein cycloalkyl is cyclohexyl, or cycloheptyl, and heteroaryl is pyridin-3-yl or pyrazol-4-yl.
- Cy 6 is cycloalkyl optionally substituted with one or more R 60 , phenyl optionally substituted with one or more R 61 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 62 and optionally substituted on an available nitrogen atom with R 63 ;
- R 59 is selected from the group consisting of cycloalkyl, lower alkyl optionally substituted with one or more R 64 , and -O-R 65 ;
- each R 60 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- each R 61 is independently selected from the group consisting of fluoro, chloro, -O-R 66 , -S-R 67 , -S(0 2 )-R 68 , and lower alkyl optionally substitituted with one or more R 69 ;
- each R 62 is independently selected from the group consisting of fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, and lower alkoxy optionally substituted with one or more fluoro; or two R 62 bound to adjacent carbon atoms of the heteroaryl ring, taken together, form a fused cycloalkyl ring;
- R 63 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro; R is fluoro or lower alkoxy optionally substitituted with one or more fluoro;
- R 65 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy;
- each R 66 , R 67 and R 68 are independently lower alkyl optionally substituted with one or more
- each R 69 is independently selected from the group consisting of fluoro, -OH, and lower alkoxy optionally substituted with one or more fluoro.
- R 59 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 59 is selected from the group consisting of C3.6 cycloalkyl, C 1 .3 alkyl, C 1 .3 alkoxy, and Ci_3 alkoxy substituted with C 1 .3 alkoxy.
- R 59 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- ye is cycloalkyl optionally substituted with one or more R 60 , phenyl optionally substituted with one or more R 61 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 62 and optionally substituted on an available nitrogen atom with R 63 , wherein cycloalkyl is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl, and heteroaryl is pyridinyl or pyrazolyl.
- Cy 6 is cycloalkyl optionally substituted with one or more R 60 , phenyl optionally substituted with one or more R 61 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 62 and optionally substituted on an available nitrogen atom with R 63 , wherein cycloalkyl is cyclohexyl, or cycloheptyl, and heteroaryl is pyridin-3-yl or pyrazol-4-yl.
- L 3 is -C(H 2 )- or -C(O)-;
- Cy 7 is cycloalkyl optionally substituted with one or more R , phenyl optionally substituted with one or more R 73 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 74 and optionally substituted on an available nitrogen atom with R 75 ;
- R 70 is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro; each R 72 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- each R 73 is independently selected from the group consisting of fluoro, chloro, -O-R 76 , -S-R 77 , -S(0 2 )-R 78 , and lower alkyl optionally substitituted with one or more R 79 ;
- each R 74 is independently selected from the group consisting of fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, and lower alkoxy optionally substituted with one or more fluoro; or two R 74 bound to adjacent carbon atoms of the heteroaryl ring, taken together, form a fused cycloalkyl ring;
- R 75 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro;
- each R 76 , R 77 and R 78 are independently lower alkyl optionally substituted with one or more
- each R 79 is independently selected from the group consisting of fluoro, -OH, and lower alkoxy optionally substituted with one or more fluoro.
- R 70 is hydrogen, chloro or lower alkyl. In one embodiment, R 70 is hydrogen, chloro or Ci_ 3 alkyl. In one embodiment, R 70 is hydrogen, chloro or methyl.
- Cy 7 is cycloalkyl optionally substituted with one or more R 72 , phenyl optionally substituted with one or more R 73 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 74 and optionally substituted on an available nitrogen atom with R 75 , wherein cycloalkyl is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl, and heteroaryl is pyridinyl or pyrazolyl.
- Cy 7 is cycloalkyl optionally substituted with one or more R 72 , phenyl optionally substituted with one or more R 73 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 74 and optionally substituted on an available nitrogen atom with R 75 , wherein cycloalkyl is cyclohexyl, or cycloheptyl, and heteroaryl is pyridin-3-yl or pyrazol-4-yl.
- L 3 is -C(H 2 )-. In some embodiments of compounds of Formula If, further to any of the above embodiments of Formula If, L 3 is -C(O)-.
- Cyg is cycloalkyl optionally substituted with one or more R 81 , phenyl optionally substituted with one or more R 82 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 83 and optionally substituted on an available nitrogen atom with R 84 ;
- R 80 is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro; each R 81 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- each R 82 is independently selected from the group consisting of fluoro, chloro, -O-R 85 , -S-R 86 , -S(0 2 )-R 87 , and lower alkyl optionally substitituted with one or more R 88 ;
- each R 83 is independently selected from the group consisting of fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, and lower alkoxy optionally substituted with one or more fluoro; or two R 83 bound to adjacent carbon atoms of the heteroaryl ring, taken together, form a fused cycloalkyl ring;
- R 84 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro;
- each R 85 , R 86 and R 87 are independently lower alkyl optionally substituted with one or more
- each R 88 is independently selected from the group consisting of fluoro, -OH, and lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen, chloro or lower alkyl.
- R 80 is hydrogen, chloro or Ci_ 3 alkyl.
- R 80 is hydrogen, chloro or methyl.
- Cy 8 is cycloalkyl optionally substituted with one or more R 81 , phenyl optionally substituted with one or more R 82 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 83 and optionally substituted on an available nitrogen atom with R 84 , wherein cycloalkyl is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl, and heteroaryl is pyridinyl or pyrazolyl.
- Cyg is cycloalkyl optionally substituted with one or more R 81 , phenyl optionally substituted with one or more R 82 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 83 and optionally substituted on an available nitrogen atom with R 84 , wherein cycloalkyl is cyclohexyl, or cycloheptyl, and heteroaryl is pyridin-3-yl or pyrazol-4-yl.
- Cy 9 is cycloalkyl optionally substituted with one or more R 90 , phenyl optionally substituted with one or more R 91 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 92 and optionally substituted on an available nitrogen atom with R 93 ;
- R 89 is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro; each R 90 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- each R 91 is independently selected from the group consisting of fluoro, chloro, -O-R 94 , -S-R 95 , -S(0 2 )-R 96 , and lower alkyl optionally substitituted with one or more R 97 ;
- each R 92 is independently selected from the group consisting of fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, and lower alkoxy optionally substituted with one or more fluoro; or two R bound to adjacent carbon atoms of the heteroaryl ring, taken together, form a fused cycloalkyl ring;
- R 93 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro;
- each R 94 , R 95 and R 96 are independently lower alkyl optionally substituted with one or more
- each R 97 is independently selected from the group consisting of fluoro, -OH, and lower alkoxy optionally substituted with one or more fluoro.
- R 89 is hydrogen, chloro or lower alkyl. In one embodiment, R 89 is hydrogen, chloro or C 1 .3 alkyl. In one embodiment, R 89 is hydrogen, chloro or methyl.
- Cyg is cycloalkyl optionally substituted with one or more R 90 , phenyl optionally substituted with one or more R 91 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 92 and optionally substituted on an available nitrogen atom with R 93 , wherein cycloalkyl is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl, and heteroaryl is pyridinyl or pyrazolyl.
- Cy 9 is cycloalkyl optionally substituted with one or more R 90 , phenyl optionally substituted with one or more R 91 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 92 and optionally substituted on an available nitrogen atom with R 93 , wherein cycloalkyl is cyclohexyl, or cycloheptyl, and heteroaryl is pyridin-3-yl or pyrazol-4-yl.
- Cyio is cycloalkyl optionally substituted with one or more R 99 , phenyl optionally substituted with one or more R 100 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 101 and optionally substituted on an available nitrogen atom with
- R is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro; each R 99 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- each R 100 is independently selected from the group consisting of fluoro, chloro, -O-R 103 , -S-R 104 , -S(0 2 )-R 105 , and lower alkyl optionally substitituted with one or more R 106 ;
- each R 101 is independently selected from the group consisting of fluoro, chloro, bromo,
- cycloalkyl lower alkyl optionally substituted with one or more fluoro, and lower alkoxy optionally substituted with one or more fluoro; or two R 101 bound to adjacent carbon atoms of the heteroaryl ring, taken together, form a fused cycloalkyl ring;
- R 102 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro;
- each R 102 , R 104 and R 105 are independently lower alkyl optionally substituted with one or more fluoro;
- each R 106 is independently selected from the group consisting of fluoro, -OH, and lower alkoxy optionally substituted with one or more fluoro.
- R 98 is hydrogen, chloro or lower alkyl. In one embodiment, R 98 is hydrogen, chloro or Ci_ 3 alkyl. In one embodiment, R 98 is hydrogen, chloro or methyl.
- Cyio is cycloalkyl optionally substituted with one or more R 99 , phenyl optionally substituted with one or more R 100 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 101 and optionally substituted on an available nitrogen atom with R 102 , wherein cycloalkyl is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl, and heteroaryl is pyridinyl or pyrazolyl.
- Cyio is cycloalkyl optionally substituted with one or more R 99 , phenyl optionally substituted with one or more R 100 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 101 and optionally substituted on an available nitrogen atom with R 102 , wherein cycloalkyl is cyclohexyl, or cycloheptyl, and heteroaryl is pyridin-3-yl or pyrazol- 4-yl.
- Cyn is cycloalkyl optionally substituted with one or more R 108 , phenyl optionally substituted with one or more R 109 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 110 and optionally substituted on an available nitrogen atom with
- R is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro; each R 108 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- each R 109 is independently selected from the group consisting of fluoro, chloro, -O-R 112 , -S-R 113 , -S(0 2 )-R 114 , and lower alkyl optionally substitituted with one or more R 115 ;
- each R 110 is independently selected from the group consisting of fluoro, chloro, bromo,
- cycloalkyl lower alkyl optionally substituted with one or more fluoro, and lower alkoxy optionally substituted with one or more fluoro; or two R 110 bound to adjacent carbon atoms of the heteroaryl ring, taken together, form a fused cycloalkyl ring;
- R 111 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro;
- each R 112 , R 113 and R 114 are independently lower alkyl optionally substituted with one or more fluoro;
- each R 115 is independently selected from the group consisting of fluoro, -OH, and lower alkoxy optionally substituted with one or more fluoro.
- R 107 is hydrogen, chloro or lower alkyl.
- R 107 is hydrogen, chloro or Ci_ 3 alkyl. In one embodiment, R 107 is hydrogen, chloro or methyl.
- Cyn is cycloalkyl optionally substituted with one or more R 108 , phenyl optionally substituted with one or more R 109 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 110 and optionally substituted on an available nitrogen atom with R 111 , wherein cycloalkyl is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl, and heteroaryl is pyridinyl or pyrazolyl.
- Cyn is cycloalkyl optionally substituted with one or more R 108 , phenyl optionally substituted with one or more R 109 , or 5 or 6 membered heteroaryl optionally substituted on an available carbon atom with one or more R 110 and optionally substituted on an available nitrogen atom with R 111 , wherein cycloalkyl is cyclohexyl, or cycloheptyl, and heteroaryl is pyridin-3-yl or pyrazol- 4-yl.
- L 4 is -C(H 2 )- or -C(O)-;
- Cy i2 is cycloalkyl optionally substituted with one or more R 119 ;
- R 117 is selected from the group consisting of hydrogen, cycloalkyl, lower alkyl optionally substituted with one or more R 120 , and -O-R 121 ;
- R 116 is fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- each R 119 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- R 120 is fluoro or lower alkoxy optionally substitituted with one or more fluoro
- R 121 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- Cyi 2 is cyclopentyl optionally substituted with 1 or 2 R 119 , cyclohexyl optionally substituted with 1 or 2 R 119 , or cycloheptyl optionally substituted with 1 or 2 R 119 .
- Cyi 2 is cyclopentyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; cyclohexyl optionally substituted with 1 or 2 fluoro, or lor 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; or cycloheptyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy.
- Cy i2 is cyclopentyl, cyclopentyl substituted with 1 or 2 fluoro, cyclopentyl substituted with 1 or 2 lower alkyl, cyclopentyl substituted with 1 or 2 -OH, or cyclopentyl substituted with 1 or 2 lower alkoxy.
- Cy i2 is cyclohexyl, cyclohexyl substituted with 1 or 2 fluoro, cyclohexyl substituted with 1 or 2 lower alkyl, cyclohexyl substituted with 1 or 2 -OH, or cyclohexyl substituted with 1 or 2 lower alkoxy.
- Cyi 2 is cycloheptyl, cycloheptyl substituted with 1 or 2 fluoro, cycloheptyl substituted with 1 or 2 lower alkyl, cycloheptyl substituted with 1 or 2 -OH, or cycloheptyl substituted with 1 or 2 lower alkoxy.
- L 5 is -C(H 2 )- or -C(O)-;
- Cy i3 is cycloalkyl optionally substituted with one or more R 124 ;
- R 122 is selected from the group consisting of cycloalkyl, lower alkyl optionally substituted with one or more R 125 , and -O-R 126 ;
- each R 124 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- R 125 is fluoro or lower alkoxy optionally substitituted with one or more fluoro
- R 126 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R 122 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 122 is selected from the group consisting of C3.6 cycloalkyl, C 1 .3 alkyl, C 1 .3 alkoxy, and C 1 .3 alkoxy substituted with C 1 .3 alkoxy.
- R 122 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- Cy i3 is cyclopentyl optionally substituted with 1 or 2 R 124 , cyclohexyl
- Cy i3 is cyclopentyl optionally substituted with 1 or 2 fluoro, or l or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; cyclohexyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; or cycloheptyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy.
- Cy i3 is cyclopentyl, cyclopentyl substituted with 1 or 2 fluoro, cyclopentyl substituted with 1 or 2 lower alkyl, cyclopentyl substituted with 1 or 2 -OH, or cyclopentyl substituted with 1 or 2 lower alkoxy.
- Cyo is cyclohexyl, cyclohexyl substituted with 1 or 2 fluoro, cyclohexyl substituted with 1 or 2 lower alkyl, cyclohexyl substituted with 1 or 2 -OH, or cyclohexyl substituted with 1 or 2 lower alkoxy.
- Cyo is cycloheptyl, cycloheptyl substituted with 1 or 2 fluoro, cycloheptyl substituted with 1 or 2 lower alkyl, cycloheptyl substituted with 1 or 2 -OH, or cycloheptyl substituted with 1 or 2 lower alkoxy.
- L 5 is -C(H 2 )-. In some embodiments of compounds of Formula Im, further to any of the above embodiments of Formula Im, L 5 is -C(O)-.
- Cy i4 is cycloalkyl optionally substituted with one or more R 128 ;
- R 127 is selected from the group consisting of cycloalkyl, lower alkyl optionally substituted with one or more R 129 , and -O-R 130 ; each R is independently selected from the group consisting of fluoro, -OH, lower alkyl optionally substitituted with one or more fluoro, and lower alkoxy optionally substituted with one or more fluoro;
- R 129 is fluoro or lower alkoxy optionally substitituted with one or more fluoro
- R 130 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R 127 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 127 is selected from the group consisting of C3.6 cycloalkyl, C 1 .3 alkyl, C 1 .3 alkoxy, and C 1 .3 alkoxy substituted with C 1 .3 alkoxy.
- R 127 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- Cyi 4 is cyclopentyl optionally substituted with 1 or 2 R 128 , cyclohexyl optionally
- Cy i4 is cyclopentyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; cyclohexyl optionally substituted with 1 or 2 fluoro, or l or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; or cycloheptyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy.
- Cy i4 is cyclopentyl, cyclopentyl substituted with 1 or 2 fluoro, cyclopentyl substituted with 1 or 2 lower alkyl, cyclopentyl substituted with 1 or 2 -OH, or cyclopentyl substituted with 1 or 2 lower alkoxy.
- Cyi 4 is cyclohexyl, cyclohexyl substituted with 1 or 2 fluoro, cyclohexyl substituted with 1 or 2 lower alkyl, cyclohexyl substituted with 1 or 2 -OH, or cyclohexyl substituted with 1 or 2 lower alkoxy.
- Cyi 4 is cycloheptyl, cycloheptyl substituted with 1 or 2 fluoro, cycloheptyl substituted with 1 or 2 lower alkyl, cycloheptyl substituted with 1 or 2 -OH, or cycloheptyl substituted with 1 or 2 lower alkoxy.
- compounds of Formula I having the structure according to the following Formula Io are provided:
- Cy i5 is cycloalkyl optionally substituted with one or more R 132 ;
- R 131 is selected from the group consisting of cycloalkyl, lower alkyl optionally substituted with one or more R 133 , and -O-R 134 ;
- each R 132 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- R 133 is fluoro or lower alkoxy optionally substitituted with one or more fluoro
- R 134 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R 131 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 131 is selected from the group consisting of C3.6 cycloalkyl, C 1 .3 alkyl, C 1 .3 alkoxy, and C 1 .3 alkoxy substituted with C 1 .3 alkoxy.
- R 131 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- Cyi 5 is cyclopentyl optionally substituted with 1 or 2 R 132 , cyclohexyl optionally
- Cy i5 is cyclopentyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; cyclohexyl optionally substituted with 1 or 2 fluoro, or l or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; or cycloheptyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy.
- Cy i5 is cyclopentyl, cyclopentyl substituted with 1 or 2 fluoro, cyclopentyl substituted with 1 or 2 lower alkyl, cyclopentyl substituted with 1 or 2 -OH, or cyclopentyl substituted with 1 or 2 lower alkoxy.
- Cy i5 is cyclohexyl, cyclohexyl substituted with 1 or 2 fluoro, cyclohexyl substituted with 1 or 2 lower alkyl, cyclohexyl substituted with 1 or 2 -OH, or cyclohexyl substituted with 1 or 2 lower alkoxy.
- Cyi 5 is cycloheptyl, cycloheptyl substituted with 1 or 2 fluoro, cycloheptyl substituted with 1 or 2 lower alkyl, cycloheptyl substituted with 1 or 2 -OH, or cycloheptyl substituted with 1 or 2 lower alkoxy.
- Cy i6 is cycloalkyl optionally substituted with one or more R 136 ;
- R 135 is selected from the group consisting of cycloalkyl, lower alkyl optionally substituted with one or more R 137 , and -O-R 138 ;
- each R 136 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- R 137 is fluoro or lower alkoxy optionally substitituted with one or more fluoro
- R 138 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R 135 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 135 is selected from the group consisting of C3.6 cycloalkyl, C 1 .3 alkyl, C 1 .3 alkoxy, and Ci_ 3 alkoxy substituted with Ci_ 3 alkoxy.
- R 135 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- Cy i6 is cyclopentyl optionally substituted with 1 or 2 R 136 , cyclohexyl optionally substituted with 1 or 2 R 136 , or cycloheptyl optionally substituted with 1 or 2 R 136 .
- Cy i6 is cyclopentyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; cyclohexyl optionally substituted with 1 or 2 fluoro, or lor 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; or cycloheptyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy.
- Cyi 6 is cyclopentyl, cyclopentyl substituted with 1 or 2 fluoro, cyclopentyl substituted with 1 or 2 lower alkyl, cyclopentyl substituted with 1 or 2 -OH, or cyclopentyl substituted with 1 or 2 lower alkoxy.
- Cyi 6 is cyclohexyl, cyclohexyl substituted with 1 or 2 fluoro, cyclohexyl substituted with 1 or 2 lower alkyl, cyclohexyl substituted with 1 or 2 -OH, or cyclohexyl substituted with 1 or 2 lower alkoxy.
- Cy i6 is cycloheptyl, cycloheptyl substituted with 1 or 2 fluoro, cycloheptyl substituted with 1 or 2 lower alkyl, cycloheptyl substituted with 1 or 2 -OH, or cycloheptyl substituted with 1 or 2 lower alkoxy.
- Cy i6 is cycloalkyl optionally substituted with one or more R 140 ;
- R 139 is selected from the group consisting of cycloalkyl, lower alkyl optionally substituted with one or more R 141 , and -O-R 142 ; each R is independently selected from the group consisting of fluoro, -OH, lower alkyl optionally substitituted with one or more fluoro, and lower alkoxy optionally substituted with one or more fluoro;
- R 141 is fluoro or lower alkoxy optionally substitituted with one or more fluoro
- R 142 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R 139 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 139 is selected from the group consisting of C3.6 cycloalkyl, C 1 .3 alkyl, C 1 .3 alkoxy, and C 1 .3 alkoxy substituted with C 1 .3 alkoxy.
- R 139 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- Cyn is cyclopentyl optionally substituted with 1 or 2 R 140 , cyclohexyl optionally substituted with 1 or 2 R 140 , or cycloheptyl optionally substituted with 1 or 2 R 140 .
- Cyn is cyclopentyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; cyclohexyl optionally substituted with 1 or 2 fluoro, or l or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; or cycloheptyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy.
- Cyn is cyclopentyl, cyclopentyl substituted with 1 or 2 fluoro, cyclopentyl substituted with 1 or 2 lower alkyl, cyclopentyl substituted with 1 or 2 -OH, or cyclopentyl substituted with 1 or 2 lower alkoxy.
- Cyn is cyclohexyl, cyclohexyl substituted with 1 or 2 fluoro, cyclohexyl substituted with 1 or 2 lower alkyl, cyclohexyl substituted with 1 or 2 -OH, or cyclohexyl substituted with 1 or 2 lower alkoxy.
- Cyn is cycloheptyl, cycloheptyl substituted with 1 or 2 fluoro, cycloheptyl substituted with 1 or 2 lower alkyl, cycloheptyl substituted with 1 or 2 -OH, or cycloheptyl substituted with 1 or 2 lower alkoxy.
- compounds of Formula I having the structure according to the following Formula Ir are provide
- L 6 is -C(H 2 )- or -C(0)-;
- Cyig is cycloalkyl optionally substituted with one or more R 145 ;
- R 143 is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- each R 145 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- R 143 is hydrogen, chloro or lower alkyl. In one embodiment, R 143 is hydrogen, chloro or Ci_ 3 alkyl. In one embodiment, R 143 is hydrogen, chloro or methyl.
- Cy i8 is cyclopentyl optionally substituted with 1 or 2 R 145 , cyclohexyl optionally substituted with 1 or 2 R 145 , or cycloheptyl optionally substituted with 1 or 2 R 145 .
- Cyig is cyclopentyl optionally substituted with 1 or 2 fluoro, or lor 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; cyclohexyl optionally substituted with 1 or 2 fluoro, or lor 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; or cycloheptyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy.
- Cyig is cyclopentyl, cyclopentyl substituted with 1 or 2 fluoro, cyclopentyl substituted with 1 or 2 lower alkyl, cyclopentyl substituted with 1 or 2 -OH, or cyclopentyl substituted with 1 or 2 lower alkoxy.
- Cyi 8 is cyclohexyl, cyclohexyl substituted with 1 or 2 fluoro, cyclohexyl substituted with 1 or 2 lower alkyl, cyclohexyl substituted with 1 or 2 -OH, or cyclohexyl substituted with 1 or 2 lower alkoxy.
- Cyig is cycloheptyl, cycloheptyl substituted with 1 or 2 fluoro, cycloheptyl substituted with 1 or 2 lower alkyl, cycloheptyl substituted with 1 or 2 -OH, or cycloheptyl substituted with 1 or 2 lower alkoxy.
- L 6 is -C(H 2 )-. In some embodiments of compounds of Formula Ir, further to any of the above embodiments of Formula Ir, L 6 is -C(O)-.
- Cy i9 is cycloalkyl optionally substituted with one or more R 147 ;
- R 146 is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- each R 147 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- R 146 is hydrogen, chloro or lower alkyl. In one embodiment, R 146 is hydrogen, chloro or C 1 .3 alkyl. In one embodiment, R 146 is hydrogen, chloro or methyl. [0122] In some embodiments of compounds of Formula Is, further to any of the above embodiments of Formula Is, Cy i9 is cyclopentyl optionally substituted with 1 or 2 R 147 , cyclohexyl optionally substituted with 1 or 2 R 147 , or cycloheptyl optionally substituted with 1 or 2 R 147 .
- Cy i9 is cyclopentyl optionally substituted with 1 or 2 fluoro, or lor 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; cyclohexyl optionally substituted with 1 or 2 fluoro, or lor 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; or cycloheptyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy.
- Cyig is cyclopentyl, cyclopentyl substituted with 1 or 2 fluoro, cyclopentyl substituted with 1 or 2 lower alkyl, cyclopentyl substituted with 1 or 2 -OH, or cyclopentyl substituted with 1 or 2 lower alkoxy.
- Cyig is cyclohexyl, cyclohexyl substituted with 1 or 2 fluoro, cyclohexyl substituted with 1 or 2 lower alkyl, cyclohexyl substituted with 1 or 2 -OH, or cyclohexyl substituted with 1 or 2 lower alkoxy.
- Cy i9 is cycloheptyl, cycloheptyl substituted with 1 or 2 fluoro, cycloheptyl substituted with 1 or 2 lower alkyl, cycloheptyl substituted with 1 or 2 -OH, or cycloheptyl substituted with 1 or 2 lower alkoxy.
- Cy 2 o is cycloalkyl optionally substituted with one or more R 149 ;
- R 148 is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro; and each R is independently selected from the group consisting of fluoro, -OH, lower alkyl optionally substitituted with one or more fluoro, and lower alkoxy optionally substituted with one or more fluoro.
- R 148 is hydrogen, chloro or lower alkyl. In one embodiment, R 148 is hydrogen, chloro or Ci_ 3 alkyl. In one embodiment, R 148 is hydrogen, chloro or methyl.
- Cy 2 o is cyclopentyl optionally substituted with 1 or 2 R 149 , cyclohexyl optionally substituted with 1 or 2 R 149 , or cycloheptyl optionally substituted with 1 or 2 R 149 .
- Cy 2 o is cyclopentyl optionally substituted with 1 or 2 fluoro, or lor 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; cyclohexyl optionally substituted with 1 or 2 fluoro, or lor 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; or cycloheptyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy.
- Cy 2 o is cyclopentyl, cyclopentyl substituted with 1 or 2 fluoro, cyclopentyl substituted with 1 or 2 lower alkyl, cyclopentyl substituted with 1 or 2 -OH, or cyclopentyl substituted with 1 or 2 lower alkoxy.
- Cy 2 o is cyclohexyl, cyclohexyl substituted with 1 or 2 fluoro, cyclohexyl substituted with 1 or 2 lower alkyl, cyclohexyl substituted with 1 or 2 -OH, or cyclohexyl substituted with 1 or 2 lower alkoxy.
- Cy 2 o is cycloheptyl, cycloheptyl substituted with 1 or 2 fluoro, cycloheptyl substituted with 1 or 2 lower alkyl, cycloheptyl substituted with 1 or 2 -OH, or cycloheptyl substituted with 1 or 2 lower alkoxy.
- Cy 2 i is cycloalkyl optionally substituted with one or more R 151 ;
- R 150 is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- each R 151 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- R 150 is hydrogen, chloro or lower alkyl. In one embodiment, R 150 is hydrogen, chloro or C 1 .3 alkyl. In one embodiment, R 150 is hydrogen, chloro or methyl.
- Cy 2 i is cyclopentyl optionally substituted with 1 or 2 R 151 , cyclohexyl optionally substituted with 1 or 2 R 151 , or cycloheptyl optionally substituted with 1 or 2 R 151 .
- Cy 2 i is cyclopentyl optionally substituted with 1 or 2 fluoro, or l or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; cyclohexyl optionally substituted with 1 or 2 fluoro, or l or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; or cycloheptyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy.
- Cy 2 i is cyclopentyl, cyclopentyl substituted with 1 or 2 fluoro, cyclopentyl substituted with 1 or 2 lower alkyl, cyclopentyl substituted with 1 or 2 -OH, or cyclopentyl substituted with 1 or 2 lower alkoxy.
- Cy 2 i is cyclohexyl, cyclohexyl substituted with 1 or 2 fluoro, cyclohexyl substituted with 1 or 2 lower alkyl, cyclohexyl substituted with 1 or 2 -OH, or cyclohexyl substituted with 1 or 2 lower alkoxy.
- Cy 2 i is cycloheptyl, cycloheptyl substituted with 1 or 2 fluoro, cycloheptyl substituted with 1 or 2 lower alkyl, cycloheptyl substituted with 1 or 2 -OH, or cycloheptyl substituted with 1 or 2 lower alkoxy.
- Cy 22 is cycloalkyl optionally substituted with one or more R 153 ;
- R 152 is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- each R 153 is independently selected from the group consisting of fluoro, -OH, lower alkyl
- R 152 is hydrogen, chloro or lower alkyl. In one embodiment, R 152 is hydrogen, chloro or C 1 .3 alkyl. In one embodiment, R 152 is hydrogen, chloro or methyl.
- Cy 22 is cyclopentyl optionally substituted with 1 or 2 R 153 , cyclohexyl optionally substituted with 1 or 2 R 153 , or cycloheptyl optionally substituted with 1 or 2 R 153 .
- Cy 22 is cyclopentyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; cyclohexyl optionally substituted with 1 or 2 fluoro, or l or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy; or cycloheptyl optionally substituted with 1 or 2 fluoro, or 1 or 2 lower alkyl, or 1 or 2 -OH, or 1 or 2 lower alkoxy.
- Cy 22 is cyclopentyl, cyclopentyl substituted with 1 or 2 fluoro, cyclopentyl substituted with 1 or 2 lower alkyl, cyclopentyl substituted with 1 or 2 -OH, or cyclopentyl substituted with 1 or 2 lower alkoxy.
- Cy 22 is cyclohexyl, cyclohexyl substituted with 1 or 2 fluoro, cyclohexyl substituted with 1 or 2 lower alkyl, cyclohexyl substituted with 1 or 2 -OH, or cyclohexyl substituted with 1 or 2 lower alkoxy.
- Cy 2 2 is cycloheptyl, cycloheptyl substituted with 1 or 2 fluoro, cycloheptyl substituted with 1 or 2 lower alkyl, cycloheptyl substituted with 1 or 2 -OH, or cycloheptyl substituted with 1 or 2 lower alkoxy.
- L 7 is -C(H 2 )- or -C(O)-;
- R 155 is selected from the group consisting of hydrogen, cycloalkyl, lower alkyl optionally substituted with one or more R 158 , and -O-R 159 ;
- R 154 is fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- R 157 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro;
- R 158 is fluoro or lower alkoxy optionally substitituted with one or more fluoro
- R 159 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R 155 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 155 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- R 157 is cycloalkyl or lower alkyl.
- R 157 is C 3 _6 cycloalkyl or lower alkyl.
- R 157 is cyclopropyl or lower alkyl.
- R 157 is lower alkyl.
- R 157 is Q_ 3 alkyl.
- R 157 is ethyl
- L 7 is -C(H 2 )-. In some embodiments of compounds of Formula Iw, further to any of the above embodiments of Formula Iw, L 7 is -C(O)-.
- L 8 is -C(H 2 )- or -C(0)-;
- R 160 is selected from the group consisting of hydrogen, cycloalkyl, lower alkyl optionally
- R 162 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro;
- R 163 is fluoro or lower alkoxy optionally substitituted with one or more fluoro
- R 164 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R 160 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 160 is selected from the group consisting of C3.6 cycloalkyl, C 1 .3 alkyl, C 1 .3 alkoxy, and C 1 .3 alkoxy substituted with C 1 .3 alkoxy.
- R 160 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- R 162 is cycloalkyl or lower alkyl.
- R 162 is C 3 . 6 cycloalkyl or lower alkyl.
- R 162 is cyclopropyl or lower alkyl.
- R 162 is lower alkyl
- R 162 is C 1 .3 alkyl.
- R 162 is ethyl
- R 165 is selected from the group consisting of hydrogen, cycloalkyl, lower alkyl optionally
- R 166 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro;
- R 167 is fluoro or lower alkoxy optionally substitituted with one or more fluoro
- R 168 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R 165 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 165 is selected from the group consisting of C3.6 cycloalkyl, C 1 .3 alkyl, C 1 .3 alkoxy, and Ci_ 3 alkoxy substituted with Ci_ 3 alkoxy.
- R 165 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- R 166 is cycloalkyl or lower alkyl.
- R 166 is C3.6 cycloalkyl or lower alkyl.
- R 166 is cyclopropyl or lower alkyl.
- R 166 is lower alkyl.
- R 166 is Ci_ 3 alkyl.
- R 166 is ethyl
- R 169 is selected from the group consisting of hydrogen, cycloalkyl, lower alkyl optionally
- R 170 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro;
- R 171 is fluoro or lower alkoxy optionally substitituted with one or more fluoro
- R 172 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R 169 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy. In one embodiment, R 169 is selected from the group consisting of C3.6 cycloalkyl, C1.3 alkyl, C1.3 alkoxy, and C1.3 alkoxy substituted with C1.3 alkoxy. In one embodiment, R 169 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- R 170 is cycloalkyl or lower alkyl.
- R 170 is C3.6 cycloalkyl or lower alkyl.
- R 170 is cyclopropyl or lower alkyl.
- R 170 is lower alkyl.
- R 170 is Ci_ 3 alkyl.
- R 170 is ethyl
- R 173 is selected from the group consisting of hydrogen, cycloalkyl, lower alkyl optionally
- R 174 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro;
- R 175 is fluoro or lower alkoxy optionally substitituted with one or more fluoro
- R 176 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R 173 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 173 is selected from the group consisting of C3.6 cycloalkyl, C 1 .3 alkyl, C 1 .3 alkoxy, and Ci_ 3 alkoxy substituted with Ci_ 3 alkoxy.
- R 173 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- R 174 is cycloalkyl or lower alkyl.
- R 174 is C3.6 cycloalkyl or lower alkyl.
- R 174 is cyclopropyl or lower alkyl.
- R 174 is lower alkyl. [0191] In some embodiments of compounds of Formula Iaa, further to any of the above embodiments of Formula Iaa, R 174 is Ci_ 3 alkyl.
- R 174 is ethyl
- R 177 is selected from the group consisting of hydrogen, cycloalkyl, lower alkyl optionally
- R 178 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro;
- R 179 is fluoro or lower alkoxy optionally substitituted with one or more fluoro
- R 180 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R 177 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 177 is selected from the group consisting of C3.6 cycloalkyl, C 1 .3 alkyl, C 1 .3 alkoxy, and Ci_ 3 alkoxy substituted with Ci_ 3 alkoxy.
- R 177 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- R 178 is cycloalkyl or lower alkyl.
- R 178 is C3.6 cycloalkyl or lower alkyl.
- R 178 is cyclopropyl or lower alkyl.
- R 178 is lower alkyl.
- R 178 is Ci_ 3 alkyl.
- R 178 is ethyl
- L 9 is -C(H 2 )- or -C(O)-;
- R 181 is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- R 183 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro.
- R 181 is hydrogen, chloro or lower alkyl. In one embodiment, R 181 is hydrogen, chloro or C 1 .3 alkyl. In one embodiment, R 181 is hydrogen, chloro or methyl.
- R 183 is cycloalkyl or lower alkyl.
- R 183 is C3.6 cycloalkyl or lower alkyl.
- R 183 is cyclopropyl or lower alkyl.
- R 183 is lower alkyl.
- R 183 is Ci_ 3 alkyl.
- R 183 is ethyl
- L 9 is -C(H 2 )-. In some embodiments of compounds of Formula Icc, further to any of the above embodiments of Formula Icc, L 9 is -C(O)-.
- R 182 is fluoro.
- R 184 is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- R 185 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro.
- R 184 is hydrogen, chloro or lower alkyl. In one embodiment, R 184 is hydrogen, chloro or Ci_ 3 alkyl. In one embodiment, R 184 is hydrogen, chloro or methyl.
- R 185 is cycloalkyl or lower alkyl.
- R 185 is C 3 . 6 cycloalkyl or lower alkyl.
- R 185 is cyclopropyl or lower alkyl. [0216] In some embodiments of compounds of Formula Idd, further to any of the above embodiments of Formula Idd, R 185 is lower alkyl.
- R 185 is Ci_ 3 alkyl.
- R 185 is ethyl
- R 186 is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- R 187 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro.
- R 186 is hydrogen, chloro or lower alkyl. In one embodiment, R 186 is hydrogen, chloro or C 1 .3 alkyl. In one embodiment, R 186 is hydrogen, chloro or methyl.
- R 187 is cycloalkyl or lower alkyl.
- R 187 is C 3 . 6 cycloalkyl or lower alkyl.
- R 187 is cyclopropyl or lower alkyl.
- R 187 is lower alkyl.
- R 187 is C 1 .3 alkyl.
- R 187 is ethyl.
- R 188 is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- R 189 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro.
- R 188 is hydrogen, chloro or lower alkyl. In one embodiment, R 188 is hydrogen, chloro or Ci_ 3 alkyl. In one embodiment, R 188 is hydrogen, chloro or methyl.
- R 189 is cycloalkyl or lower alkyl.
- R 189 is C 3 . 6 cycloalkyl or lower alkyl.
- R 189 is cyclopropyl or lower alkyl.
- R 189 is lower alkyl.
- R 189 is C 1 .3 alkyl.
- R 189 is ethyl.
- R 190 is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- R 191 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro.
- R 190 is hydrogen, chloro or lower alkyl. In one embodiment, R 190 is hydrogen, chloro or Ci_ 3 alkyl. In one embodiment, R 190 is hydrogen, chloro or methyl.
- R 191 is cycloalkyl or lower alkyl.
- R 191 is C 3 . 6 cycloalkyl or lower alkyl.
- R 191 is cyclopropyl or lower alkyl.
- R 191 is lower alkyl.
- R 191 is C 1 .3 alkyl.
- R 191 is ethyl
- Lio is -C(H 2 )- or -C(O)-;
- R 193 is selected from the group consisting of hydrogen, cycloalkyl, lower alkyl optionally substituted with one or more R 197 , and -O-R 198 ;
- R 192 is fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- R 195 is hydrogen and R 196 is hydrogen, fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro; or
- R 196 is hydrogen and R 195 is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro; R 197 is fluoro or lower alkoxy optionally substitituted with one or more fluoro; and
- R 198 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R 193 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 196 is hydrogen and R 195 is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 196 is hydrogen and R 195 is lower alkyl optionally substituted with one or more fluoro.
- R 196 is hydrogen and R 195 is lower alkyl.
- R 196 is hydrogen and R 195 is C 1 .3 alkyl. In some embodiments of compounds of Formula Ihh, further to any of the above embodiments of Formula Ihh, R 196 is hydrogen and R 195 is methyl.
- R 195 is hydrogen and R 196 is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 195 is hydrogen and R 196 is fluoro, chloro, bromo.
- R 195 is hydrogen and R 196 is cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 195 is hydrogen and R 196 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro.
- R 195 is hydrogen and R 196 is cycloalkyl or Ci_ 3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 195 is hydrogen and R 196 is cyclopropyl or Ci_3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 195 is hydrogen and R 196 is cyclopropyl, trifluoromethyl, methyl or ethyl.
- R 195 is hydrogen and R 196 is cycloalkyl.
- R 195 is hydrogen and R 196 is cyclopropyl.
- R 195 is hydrogen and R 196 is lower alkyl optionally substituted with one or more fluoro.
- R is hydrogen and R is Ci_ 3 alkyl optionally substituted with 1 , 2, or 3 fluoro.
- R 195 is hydrogen and R 196 is trifluoromethyl, methyl or ethyl.
- R 195 is hydrogen and R 196 is trifluoromethyl.
- R 195 is hydrogen and R 196 is methyl. In some embodiments of compounds of Formula Ihh, further to any of the above embodiments of Formula Ihh, R 195 is hydrogen and R 196 is ethyl.
- R 195 is hydrogen and R 196 is lower alkoxy optionally substituted with one or more fluoro.
- R 195 is hydrogen and R 196 is lower alkoxy.
- R 195 is hydrogen and R 196 is C 1 .3 alkoxy.
- R 195 is hydrogen and R 196 is methoxy or ethoxy.
- R 195 is hydrogen and R 196 is methoxy. In some embodiments of compounds of Formula Ihh, further to any of the above embodiments of Formula Ihh, R 195 is hydrogen and R 196 is ethoxy.
- L 10 is -C(H 2 )-. In some embodiments of compounds of Formula Ihh, further to any of the above embodiments of Formula Ihh, L 10 is -C(O)-.
- L u is -C(H 2 )- or -C(0)-;
- R 199 is selected from the group consisting of hydrogen, cycloalkyl, lower alkyl optionally
- R 201 is hydrogen and R 202 is hydrogen, fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro; or
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro; R 203 is fluoro or lower alkoxy optionally substitituted with one or more fluoro; and
- R 204 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R 199 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 199 is selected from the group consisting of C3.6 cycloalkyl, C 1 .3 alkyl, C 1 .3 alkoxy, and Ci_ 3 alkoxy substituted with Ci_ 3 alkoxy.
- R 199 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 202 is hydrogen and R 201 is lower alkyl optionally substituted with one or more fluoro.
- compounds of Formula Iii further to any of the above
- R is hydrogen and R is lower alkyl.
- R 202 is hydrogen and R 201 is C 1 .3 alkyl.
- R 202 is hydrogen and R 201 is methyl.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is fluoro, chloro, bromo.
- R is hydrogen and R is fluoro, chloro, bromo.
- R 201 is hydrogen and R 202 is cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 201 is hydrogen and R 202 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro.
- R 201 is hydrogen and R 202 is cycloalkyl or Ci_ 3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R is hydrogen and R is cyclopropyl or Ci_3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 201 is hydrogen and R 202 is cyclopropyl, trifluoromethyl, methyl or ethyl.
- R is hydrogen and R is cycloalkyl.
- R 201 is hydrogen and R 202 is cyclopropyl.
- R 201 is hydrogen and R 202 is lower alkyl optionally substituted with one or more fluoro.
- R 201 is hydrogen and R 202 is Ci_ 3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 201 is hydrogen and R 202 is trifluoromethyl, methyl or ethyl.
- R 201 is hydrogen and R 202 is trifluoromethyl. In some embodiments of compounds of Formula Iii, further to any of the above embodiments of Formula Iii, R 201 is hydrogen and R 202 is methyl. In some embodiments of compounds of Formula Iii, further to any of the above embodiments of Formula Iii,
- R 201 is hydrogen and R 202 is ethyl.
- R is hydrogen and R is lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is lower alkoxy.
- R 201 is hydrogen and R 202 is C1.3 alkoxy.
- R 202 is C1.3 alkoxy.
- R is hydrogen and R is methoxy or ethoxy.
- R is hydrogen and R is methoxy or ethoxy.
- R is hydrogen and R is methoxy.
- R is hydrogen and R is ethoxy.
- L u is -C(H 2 )-.
- Lu is -C(O)-.
- R 205 is selected from the group consisting of hydrogen, cycloalkyl, lower alkyl optionally
- R is hydrogen and R is hydrogen, fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro; or
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro; R 208 is fluoro or lower alkoxy optionally substitituted with one or more fluoro; and
- R 209 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R 205 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 205 is selected from the group consisting of C3.6 cycloalkyl, C 1 .3 alkyl, C 1 .3 alkoxy, and C 1 .3 alkoxy substituted with C 1 .3 alkoxy.
- R 205 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 20V is hydrogen and R206 is lower alkyl optionally substituted with one or more fluoro.
- R 20V is hydrogen and R206 is lower alkyl.
- R 207 is hydrogen and R 206 is Ci_3 alkyl.
- R 20V is hydrogen and R206 is methyl.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is fluoro, chloro, bromo.
- R 206 is hydrogen and R20V is cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 206 is hydrogen and R20V is cycloalkyl or lower alkyl optionally substituted with one or more fluoro.
- R 206 is hydrogen and R20V is cycloalkyl or Ci_ 3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- compounds of Formula Ijj are hydrogen and R20V is cycloalkyl or Ci_ 3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R is hydrogen and R is cyclopropyl or Ci_3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 206 is hydrogen and R20V is cyclopropyl, trifluoromethyl, methyl or ethyl.
- R 206 is hydrogen and R20V is cycloalkyl. In some embodiments of compounds of Formula Ijj, further to any of the above embodiments of Formula Ijj, R 206 is hydrogen and R 207 is cyclopropyl.
- R 206 is hydrogen and R20V is lower alkyl optionally substituted with one or more fluoro. In some embodiments of compounds of Formula Ijj, further to any of the above embodiments of Formula Ijj, R 206 is hydrogen and R20V is C 1 .3 alkyl optionally substituted with 1, 2, or 3 fluoro. In some embodiments of compounds of Formula Ijj, further to any of the above embodiments of Formula Ijj, R 206 is hydrogen and R20V is trifluoromethyl, methyl or ethyl. In some embodiments of compounds of Formula Ijj, further to any of the above embodiments of Formula Ijj,
- R 206 is hydrogen and R 20V is trifluoromethyl. In some embodiments of compounds of Formula Ijj, further to any of the above embodiments of Formula Ijj, R 206 is hydrogen and R 20V is methyl. In some embodiments of compounds of Formula Ijj, further to any of the above embodiments of Formula Ijj,
- R 206 is hydrogen and R 20V is ethyl.
- R 206 is hydrogen and R 20V is lower alkoxy optionally substituted with one or more fluoro.
- R 20V is lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is lower alkoxy.
- R 206 is hydrogen and R 207 is C 1 .3 alkoxy.
- R 207 is C 1 .3 alkoxy.
- R is hydrogen and R is methoxy or ethoxy.
- R is hydrogen and R is methoxy or ethoxy.
- R is hydrogen and R is methoxy.
- R is hydrogen and R is ethoxy.
- R 210 is selected from the group consisting of hydrogen, cycloalkyl, lower alkyl optionally
- R 211 is hydrogen and R 212 is hydrogen, fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro; or
- R 212 is hydrogen and R 211 is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro; R 213 is fluoro or lower alkoxy optionally substitituted with one or more fluoro; and
- R 214 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 210 is selected from the group consisting of C3.6 cycloalkyl, C1.3 alkyl, C1.3 alkoxy, and Ci_ 3 alkoxy substituted with Ci_ 3 alkoxy.
- R 210 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- R 212 is hydrogen and R 211 is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 212 is hydrogen and R 211 is lower alkyl optionally substituted with one or more fluoro.
- R 212 is hydrogen and R 211 is lower alkyl.
- R 212 is hydrogen and R 211 is C1.3 alkyl. In some embodiments of compounds of Formula Ikk, further to any of the above embodiments of Formula Ikk, R 212 is hydrogen and R 211 is methyl.
- R 211 is hydrogen and R 212 is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 211 is hydrogen and R 212 is fluoro, chloro, bromo.
- R 211 is hydrogen and R 212 is cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 211 is hydrogen and R 212 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro.
- R 211 is hydrogen and R 212 is cycloalkyl or C1.3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 211 is hydrogen and R 212 is cyclopropyl or Ci_3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 211 is hydrogen and R 212 is cyclopropyl, trifluoromethyl, methyl or ethyl.
- R 211 is hydrogen and R 212 is cycloalkyl.
- R 211 is hydrogen and R 212 is cyclopropyl.
- R 211 is hydrogen and R 212 is lower alkyl optionally substituted with one or more fluoro.
- R 211 is hydrogen and R 212 is C1.3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 211 is hydrogen and R 212 is trifluoromethyl, methyl or ethyl.
- R 211 is hydrogen and R 212 is trifluoromethyl.
- R 211 is hydrogen and R 212 is methyl. In some embodiments of compounds of Formula Ikk, further to any of the above embodiments of Formula Ikk, R 211 is hydrogen and R 212 is ethyl.
- R 211 is hydrogen and R 212 is lower alkoxy optionally substituted with one or more fluoro. In some embodiments of compounds of Formula Ikk, further to any of the above embodiments of Formula Ikk, R 211 is hydrogen and R 212 is lower alkoxy. In some embodiments of compounds of Formula Ikk, further to any of the above embodiments of Formula Ikk, R 211 is hydrogen and R 212 is Ci_ 3 alkoxy. In some embodiments of compounds of Formula Ikk, further to any of the above embodiments of Formula Ikk, R 211 is hydrogen and R 212 is methoxy or ethoxy.
- R 211 is hydrogen and R 212 is methoxy. In some embodiments of compounds of Formula Ikk, further to any of the above embodiments of Formula Ikk, R 211 is hydrogen and R 212 is ethoxy.
- R 215 is selected from the group consisting of hydrogen, cycloalkyl, lower alkyl optionally
- R is hydrogen and R is hydrogen, fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro; or
- R 217 is hydrogen and R 216 is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro; R 218 is fluoro or lower alkoxy optionally substitituted with one or more fluoro; and
- R 219 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R 215 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 215 is selected from the group consisting of C3.6 cycloalkyl, C1.3 alkyl, C1.3 alkoxy, and C1.3 alkoxy substituted with C1.3 alkoxy.
- R 215 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- R 217 is hydrogen and R 216 is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 217 is hydrogen and R 216 is lower alkyl optionally substituted with one or more fluoro.
- R 217 is hydrogen and R 216 is lower alkyl.
- R 217 is hydrogen and R 216 is Ci_ 3 alkyl. In some embodiments of compounds of Formula Imm, further to any of the above embodiments of Formula Imm, R 217 is hydrogen and R 216 is methyl.
- R 216 is hydrogen and R 217 is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 216 is hydrogen and R 217 is fluoro, chloro, bromo.
- R 216 is hydrogen and R 217 is cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 216 is hydrogen and R 217 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro.
- R 216 is hydrogen and R 217 is cycloalkyl or Ci_ 3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 216 is hydrogen and R 217 is cyclopropyl or Ci_3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 216 is hydrogen and R 217 is cyclopropyl, trifluoromethyl, methyl or ethyl.
- R 216 is hydrogen and R 217 is cycloalkyl. In some embodiments of compounds of Formula Imm, further to any of the above embodiments of Formula Imm, R 216 is hydrogen and R 217 is cyclopropyl.
- R 216 is hydrogen and R 217 is lower alkyl optionally substituted with one or more fluoro. In some embodiments of compounds of Formula Imm, further to any of the above embodiments of Formula Imm, R 216 is hydrogen and R 217 is C1.3 alkyl optionally substituted with 1, 2, or 3 fluoro. In some embodiments of compounds of Formula Imm, further to any of the above embodiments of Formula Imm, R 216 is hydrogen and R 217 is trifluoromethyl, methyl or ethyl.
- R 216 is hydrogen and R 217 is trifluoromethyl. In some embodiments of compounds of Formula Imm, further to any of the above embodiments of Formula Imm, R 216 is hydrogen and R 217 is methyl. In some embodiments of compounds of Formula Imm, further to any of the above embodiments of Formula Imm, R 216 is hydrogen and R 217 is ethyl.
- R 216 is hydrogen and R 217 is lower alkoxy optionally substituted with one or more fluoro. In some embodiments of compounds of Formula Imm, further to any of the above embodiments of Formula Imm, R 216 is hydrogen and R 217 is lower alkoxy. In some embodiments of compounds of Formula Imm, further to any of the above embodiments of Formula Imm, R 216 is hydrogen and R 217 is C1.3 alkoxy. In some embodiments of compounds of Formula Imm, further to any of the above embodiments of Formula Imm, R 216 is hydrogen and R 217 is methoxy or ethoxy.
- R 216 is hydrogen and R 217 is methoxy. In some embodiments of compounds of Formula Imm, further to any of the above embodiments of Formula Imm, R 216 is hydrogen and R 217 is ethoxy.
- R 220 is selected from the group consisting of hydrogen, cycloalkyl, lower alkyl optionally
- R 221 is hydrogen and R 222 is hydrogen, fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro; or
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro; R 223 is fluoro or lower alkoxy optionally substitituted with one or more fluoro; and
- R 224 is lower alkyl, lower alkyl substituted with one or more fluoro, or lower alkyl substituted with lower alkoxy.
- R 220 is selected from the group consisting of cycloalkyl, lower alkyl, lower alkoxy, and lower alkoxy substituted with lower alkoxy.
- R 220 is selected from the group consisting of C3.6 cycloalkyl, C1.3 alkyl, C1.3 alkoxy, and C1.3 alkoxy substituted with C1.3 alkoxy.
- R 220 is selected from the group consisting of methyl, cyclopropyl, methoxy, ethoxy, and 2-methoxy-ethoxy.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 222 is hydrogen and R 221 is lower alkyl optionally substituted with one or more fluoro.
- R 222 is hydrogen and R 221 is lower alkyl.
- R 222 is hydrogen and R 221 is Ci_ 3 alkyl. In some embodiments of compounds of Formula Inn, further to any
- R is hydrogen and R is methyl.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is fluoro, chloro, bromo.
- R is hydrogen and R is fluoro, chloro, bromo.
- R 221 is hydrogen and R 222 is cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 221 is hydrogen and R 222 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro.
- R 221 is hydrogen and R 222 is cycloalkyl or C1.3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- compounds of Formula Inn are hydrogen and R 222 is cycloalkyl or C1.3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R is hydrogen and R is cyclopropyl or Ci_3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 221 is hydrogen and R 222 is cyclopropyl, trifluoromethyl, methyl or ethyl.
- R 221 is hydrogen and R 222 is cycloalkyl. In some embodiments of compounds of Formula Inn, further to any of the above embodiments of Formula Inn, R 221 is hydrogen and R 222 is cyclopropyl.
- R 221 is hydrogen and R 222 is lower alkyl optionally substituted with one or more fluoro.
- R 221 is hydrogen and R 222 is Ci_ 3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 221 is hydrogen and R 222 is trifluoromethyl, methyl or ethyl.
- R is hydrogen and R is trifluoromethyl.
- R 221 is hydrogen and R 222 is methyl.
- R 222 is methyl.
- R 221 is hydrogen and R 222 is ethyl.
- R 221 is hydrogen and R 222 is lower alkoxy optionally substituted with one or more fluoro.
- R 222 is lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is lower alkoxy. In some embodiments of compounds of Formula Inn, further to any of the above embodiments of Formula Inn, R is hydrogen and R 222 is Ci_ 3 alkoxy. In some embodiments of compounds of Formula Inn, further to any
- R is hydrogen and R is methoxy or ethoxy.
- R is hydrogen and R is methoxy or ethoxy.
- R is hydrogen and R is methoxy.
- R is hydrogen and R is ethoxy.
- R 225 is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- R 22V is hydrogen and R 228 is hydrogen, fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro; or
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 225 is hydrogen, chloro or lower alkyl.
- R 225 is hydrogen, chloro or Ci_ 3 alkyl. In one embodiment, R 225 is hydrogen, chloro or methyl.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 228 is hydrogen and R 22V is lower alkyl optionally substituted with one or more fluoro.
- compounds of Formula loo further to any of the above
- R is hydrogen and R is lower alkyl.
- R 228 is hydrogen and R is Ci_ 3 alkyl.
- R is hydrogen and R is lower alkyl.
- R is hydrogen and R is methyl.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is fluoro, chloro, bromo.
- R is hydrogen and R is fluoro, chloro, bromo.
- R 22V is hydrogen and R 228 is cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 22V is hydrogen and R 228 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro.
- R 22V is hydrogen and R 228 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro.
- R is hydrogen and R is cycloalkyl or C1.3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R is hydrogen and R is cycloalkyl or C1.3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R is hydrogen and R is cyclopropyl or Ci_3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R is hydrogen and R is cyclopropyl, trifluoromethyl, methyl or ethyl.
- R is hydrogen and R is cycloalkyl.
- R 227 is hydrogen and R 228 is cyclopropyl.
- R 22V is hydrogen and R 228 is lower alkyl optionally substituted with one or more fluoro.
- R 22V is hydrogen and R 228 is C1.3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 22V is hydrogen and R 228 is C1.3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R is hydrogen and R is trifluoromethyl, methyl or ethyl.
- R is hydrogen and R is trifluoromethyl, methyl or ethyl.
- R is hydrogen and R is trifluoromethyl.
- R is hydrogen and R is methyl.
- R is hydrogen and R is methyl.
- R 22V is hydrogen and R 228 is ethyl.
- R is hydrogen and R is lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is lower alkoxy.
- R 227 is hydrogen and R 228 is C 1 .3 alkoxy.
- R 228 is C 1 .3 alkoxy.
- R is hydrogen and R is methoxy or ethoxy.
- R is hydrogen and R is methoxy or ethoxy.
- R is hydrogen and R is methoxy.
- R is hydrogen and R is ethoxy.
- L i2 is -C(H 2 )-.
- L 12 is -C(O)-.
- R 229 is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- R is hydrogen and R is hydrogen, fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro; or
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro. [0307] In some embodiments of compounds of Formula Ipp, R is hydrogen, chloro or lower alkyl.
- R 229 is hydrogen, chloro or Ci_ 3 alkyl. In one embodiment, R 229 is hydrogen, chloro or methyl.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 231 is hydrogen and R 230 is lower alkyl optionally substituted with one or more fluoro.
- R 231 is hydrogen and R 230 is lower alkyl.
- R 231 is hydrogen and R 230 is C1.3 alkyl.
- R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is methyl.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is fluoro, chloro, bromo.
- R is hydrogen and R is fluoro, chloro, bromo.
- R 230 is hydrogen and R 231 is cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 230 is hydrogen and R 231 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro.
- R 230 is hydrogen and R 231 is cycloalkyl or C1.3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R is hydrogen and R is cyclopropyl or Ci_3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 230 is hydrogen and R 231 is cyclopropyl, trifluoromethyl, methyl or ethyl.
- R 230 is hydrogen and R 231 is cycloalkyl. In some embodiments of compounds of Formula Ipp, further to any of the above embodiments of Formula Ipp, R 230 is hydrogen and R 231 is cyclopropyl. [0312] In some embodiments of compounds of Formula Ipp, further to any of the above
- R 230 is hydrogen and R 231 is lower alkyl optionally substituted with one or more fluoro.
- R 230 is hydrogen and R 231 is Ci_ 3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 230 is hydrogen and R 231 is trifluoromethyl, methyl or ethyl.
- R is hydrogen and R is trifluoromethyl.
- R 230 is hydrogen and R 231 is methyl.
- R 231 is methyl.
- R 230 is hydrogen and R 231 is ethyl.
- R 230 is hydrogen and R 231 is lower alkoxy optionally substituted with one or more fluoro.
- R 230 is hydrogen and R 231 is lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is lower alkoxy.
- R 230 is hydrogen and R 231 is Ci_ 3 alkoxy.
- R 231 is Ci_ 3 alkoxy.
- R is hydrogen and R is methoxy or ethoxy.
- R is hydrogen and R is methoxy or ethoxy.
- R is hydrogen and R is methoxy.
- R is hydrogen and R is ethoxy.
- R 232 is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- R 233 is hydrogen and R 234 is hydrogen, fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro; or R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 232 is hydrogen, chloro or lower alkyl.
- R 232 is hydrogen, chloro or Ci_ 3 alkyl. In one embodiment, R 232 is hydrogen, chloro or methyl.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 234 is hydrogen and R 233 is lower alkyl optionally substituted with one or more fluoro.
- R 234 is hydrogen and R 233 is lower alkyl.
- R 233 is C1.3 alkyl.
- R is hydrogen and R is methyl.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is fluoro, chloro, bromo.
- R is hydrogen and R is fluoro, chloro, bromo.
- R 233 is hydrogen and R 234 is cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 233 is hydrogen and R 234 is cycloalkyl or lower alkyl optionally substituted with one or more fluoro.
- R 233 is hydrogen and R 234 is cycloalkyl or C1.3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R is hydrogen and R is cyclopropyl or Ci_3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 233 is hydrogen and R 234 is cyclopropyl, trifluoromethyl, methyl or ethyl.
- R 233 is hydrogen and R 234 is cycloalkyl. In some embodiments of compounds of Formula Iqq, further to any of the above embodiments of Formula Iqq, R 233 is hydrogen and R 234 is cyclopropyl.
- R 233 is hydrogen and R 234 is lower alkyl optionally substituted with one or more fluoro.
- R 233 is hydrogen and R 234 is C1.3 alkyl optionally substituted with 1, 2, or 3 fluoro.
- R 233 is hydrogen and R 234 is trifluoromethyl, methyl or ethyl.
- R is hydrogen and R is trifluoromethyl.
- R 233 is hydrogen and R 234 is methyl.
- R 234 is methyl.
- R 233 is hydrogen and R 234 is ethyl.
- R 233 is hydrogen and R 234 is lower alkoxy optionally substituted with one or more fluoro.
- R 234 is lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is lower alkoxy.
- R 233 is hydrogen and R 234 is Ci_ 3 alkoxy.
- R 234 is Ci_ 3 alkoxy.
- R is hydrogen and R is methoxy or ethoxy.
- R is hydrogen and R is methoxy or ethoxy.
- R is hydrogen and R is methoxy.
- R is hydrogen and R is ethoxy.
- R is hydrogen, fluoro, chloro, or lower alkyl optionally substitituted with one or more fluoro;
- R 236 is hydrogen and R 237 is hydrogen, fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro; or
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 235 is hydrogen, chloro or lower alkyl.
- R 235 is hydrogen, chloro or C1.3 alkyl. In one embodiment, R 235 is hydrogen, chloro or methyl.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R 23V is hydrogen and R 236 is lower alkyl optionally substituted with one or more fluoro.
- compounds of Formula Irr further to any of the above
- R is hydrogen and R is lower alkyl.
- R 237 is hydrogen and R 236 is d.3 alkyl.
- R 23V is hydrogen and R 236 is methyl.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
- R is hydrogen and R is fluoro, chloro, bromo, cycloalkyl, lower alkyl optionally substituted with one or more fluoro, or lower alkoxy optionally substituted with one or more fluoro.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Oncology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Transplantation (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Vascular Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Priority Applications (26)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES11772612.5T ES2641643T3 (es) | 2010-04-21 | 2011-04-20 | Compuestos y métodos para la modulación de quinasas, e indicaciones de los mismos |
| NZ603087A NZ603087A (en) | 2010-04-21 | 2011-04-20 | Compounds and methods for kinase modulation, and indications therefor |
| HRP20171660TT HRP20171660T1 (hr) | 2010-04-21 | 2011-04-20 | Spojevi i postupci za modulaciju kinaze, te indikacije za njih |
| CN201180030925.5A CN102947305B (zh) | 2010-04-21 | 2011-04-20 | 用于激酶调节的化合物和方法及其适应症 |
| EA201290973A EA028105B1 (ru) | 2010-04-21 | 2011-04-20 | Соединения и способы модулирования киназ и показания по их применению |
| AU2011242778A AU2011242778B2 (en) | 2010-04-21 | 2011-04-20 | Compounds and methods for kinase modulation, and indications therefor |
| PH1/2012/502103A PH12012502103A1 (en) | 2010-04-21 | 2011-04-20 | Compounds and methods for kinase modulation, and indications therefor |
| GEAP201112896A GEP20156251B (en) | 2010-04-21 | 2011-04-20 | Compounds and methods for kinase modulation, and indications therefor |
| EP11772612.5A EP2560972B1 (en) | 2010-04-21 | 2011-04-20 | Compounds and methods for kinase modulation, and indications therefor |
| MX2012012197A MX336056B (es) | 2010-04-21 | 2011-04-20 | Compuestos y metodos para la modulacion de quinasa e indicaciones de la misma. |
| LTEP11772612.5T LT2560972T (lt) | 2010-04-21 | 2011-04-20 | Kinazės moduliavimui skirti junginiai ir būdai bei jų indikacijos |
| SI201131348T SI2560972T1 (sl) | 2010-04-21 | 2011-04-20 | Spojine in postopki za kinazno modulacijo in indikacije za to |
| DK11772612.5T DK2560972T3 (da) | 2010-04-21 | 2011-04-20 | Forbindelser og fremgangsmåder til kinasemodulering og indikationer hertil |
| SM20170458T SMT201700458T1 (it) | 2010-04-21 | 2011-04-20 | Composti e metodi per modulazione di chinasi, e loro indicazioni |
| KR1020127030470A KR101799126B1 (ko) | 2010-04-21 | 2011-04-20 | 키나아제 조절을 위한 화합물 및 방법, 및 그에 대한 적응증 |
| SG2012076584A SG184874A1 (en) | 2010-04-21 | 2011-04-20 | Compounds and methods for kinase modulation, and indications therefor |
| RS20171089A RS56588B1 (sr) | 2010-04-21 | 2011-04-20 | Jedinjenja i postupci za modulaciju kinaze i njenih indikacija |
| JP2013506264A JP5808793B2 (ja) | 2010-04-21 | 2011-04-20 | キナーゼ調節のための化合物および方法、ならびにそれらの適応症 |
| CA2796998A CA2796998C (en) | 2010-04-21 | 2011-04-20 | Compounds and methods for kinase modulation, and indications therefor |
| UAA201212061A UA109128C2 (ru) | 2010-04-21 | 2011-04-20 | Соединения и способ модулирования киназ и показания к их применению |
| BR112012026927A BR112012026927A2 (pt) | 2010-04-21 | 2011-04-20 | composto e métodos para modulação de cinase, e indicações para os mesmos. |
| PL11772612T PL2560972T3 (pl) | 2010-04-21 | 2011-04-20 | Związki i sposoby do modulacji kinazy i ich wskazania |
| MA35365A MA34229B1 (fr) | 2010-04-21 | 2011-04-20 | Compositions et méthodes de modulation des kinases et leurs indications |
| IL222498A IL222498A (en) | 2010-04-21 | 2012-10-17 | Compounds and methods for kinase modulation and indications therefor |
| ZA2012/07898A ZA201207898B (en) | 2010-04-21 | 2012-10-19 | Compounds and methods for kinase modulation,and indications therefor |
| CY20171101332T CY1120554T1 (el) | 2010-04-21 | 2017-12-19 | Ενωσεις και μεθοδοι για διαμορφωση κινασων και ενδειξεις αυτων |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US32662610P | 2010-04-21 | 2010-04-21 | |
| US61/326,626 | 2010-04-21 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2011133637A2 true WO2011133637A2 (en) | 2011-10-27 |
| WO2011133637A3 WO2011133637A3 (en) | 2012-02-09 |
Family
ID=44816304
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2011/033192 Ceased WO2011133637A2 (en) | 2010-04-21 | 2011-04-20 | Compounds and methods for kinase modulation, and indications therefor |
Country Status (39)
Cited By (59)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012137089A1 (en) | 2011-04-05 | 2012-10-11 | Pfizer Limited | Pyrrolo [2, 3 -d] pyrimidine derivatives as inhibitors of tropomyosin- related kinases |
| WO2014053968A1 (en) | 2012-10-04 | 2014-04-10 | Pfizer Limited | Pyrrolo[3,2-c]pyridine tropomyosin-related kinase inhibitors |
| WO2014053967A1 (en) | 2012-10-04 | 2014-04-10 | Pfizer Limited | Pyrrolo[2,3-d]pyrimidine tropomyosin-related kinase inhibitors |
| WO2014053965A1 (en) | 2012-10-04 | 2014-04-10 | Pfizer Limited | Tropomyosin-related kinase inhibitors |
| WO2015017533A1 (en) | 2013-07-30 | 2015-02-05 | Blueprint Medicines Corporation | Ntrk2 fusions |
| EP2709622A4 (en) * | 2011-05-17 | 2015-03-04 | Plexxikon Inc | CINEMA MODULATION AND INDICATIONS THEREFOR |
| WO2015092610A1 (en) | 2013-12-20 | 2015-06-25 | Pfizer Limited | N-acylpiperidine ether tropomyosin-related kinase inhibitors |
| US9150570B2 (en) | 2012-05-31 | 2015-10-06 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
| WO2015159175A1 (en) | 2014-04-15 | 2015-10-22 | Pfizer Inc. | Tropomyosin-related kinase inhibitors containing both a 1h-pyrazole and a pyrimidine moiety |
| US9169250B2 (en) | 2006-11-22 | 2015-10-27 | Plexxikon Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
| WO2015170218A1 (en) | 2014-05-07 | 2015-11-12 | Pfizer Inc. | Tropomyosin-related kinase inhibitors |
| WO2016009296A1 (en) | 2014-07-16 | 2016-01-21 | Pfizer Inc. | N-acylpiperidine ether tropomyosin-related kinase inhibitors |
| WO2016020784A1 (en) | 2014-08-05 | 2016-02-11 | Pfizer Inc. | N-acylpyrrolidine ether tropomyosin-related kinase inhibitors |
| US9358235B2 (en) | 2012-03-19 | 2016-06-07 | Plexxikon Inc. | Kinase modulation, and indications therefor |
| US9505765B2 (en) | 2012-07-26 | 2016-11-29 | Confluence Life Sciences Inc. | 4-alkoxy/aralkoxy-5-substituted-pyrrolopyrimidine compounds as TAK1 inhibitors in disease treatment |
| WO2016196671A1 (en) | 2015-06-01 | 2016-12-08 | Loxo Oncology, Inc. | Methods of diagnosing and treating cancer |
| WO2017011776A1 (en) | 2015-07-16 | 2017-01-19 | Array Biopharma, Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
| US9624213B2 (en) | 2011-02-07 | 2017-04-18 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| US9630968B1 (en) | 2015-12-23 | 2017-04-25 | Arqule, Inc. | Tetrahydropyranyl amino-pyrrolopyrimidinone and methods of use thereof |
| WO2017075107A1 (en) | 2015-10-26 | 2017-05-04 | Nanda Nisha | Point mutations in trk inhibitor-resistant cancer and methods relating to the same |
| US9663517B2 (en) | 2009-04-03 | 2017-05-30 | Plexxikon Inc. | Compositions and uses thereof |
| US9718822B2 (en) | 2010-05-20 | 2017-08-01 | Array Biopharma, Inc. | Macrocyclic compounds as Trk kinase inhibitors |
| US9782414B2 (en) | 2014-11-16 | 2017-10-10 | Array Biopharma, Inc. | Crystalline form of (S)-N-(5-((R)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-A]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide hydrogen sulfate |
| US9782415B2 (en) | 2009-07-09 | 2017-10-10 | Array Biopharma, Inc. | Substituted pyrazolo[1,5-a]pyrimidine compounds as Trk kinase inhibitors |
| WO2017176744A1 (en) | 2016-04-04 | 2017-10-12 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
| WO2017176751A1 (en) | 2016-04-04 | 2017-10-12 | Loxo Oncology, Inc. | Liquid formulations of (s)-n-(5-((r)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide |
| US9795611B2 (en) | 2008-09-22 | 2017-10-24 | Array Biopharma, Inc. | Method of treatment using substituted imidazo[1,2b]pyridazine compounds |
| WO2018071454A1 (en) | 2016-10-10 | 2018-04-19 | Andrews Steven W | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
| WO2018071447A1 (en) | 2016-10-10 | 2018-04-19 | Andrews Steven W | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
| US10005783B2 (en) | 2008-10-22 | 2018-06-26 | Array Biopharma Inc. | Method of treatment using substituted pyrazolo[1,5-a] pyrimidine compounds |
| WO2018136663A1 (en) | 2017-01-18 | 2018-07-26 | Array Biopharma, Inc. | Ret inhibitors |
| WO2018136661A1 (en) | 2017-01-18 | 2018-07-26 | Andrews Steven W | SUBSTITUTED PYRAZOLO[1,5-a]PYRAZINE COMPOUNDS AS RET KINASE INHIBITORS |
| US10045991B2 (en) | 2016-04-04 | 2018-08-14 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
| WO2018170381A1 (en) | 2017-03-16 | 2018-09-20 | Andrews Steven W | Macrocyclic compounds as ros1 kinase inhibitors |
| US10150783B2 (en) | 2015-01-23 | 2018-12-11 | Aclaris Therapeutics, Inc. | Heterocyclic ITK inhibitors for treating inflammation and cancer |
| WO2019075114A1 (en) | 2017-10-10 | 2019-04-18 | Mark Reynolds | FORMULATIONS COMPRISING 6- (2-HYDROXY-2-METHYLPROPOXY) -4- (6- (6 - ((6-METHOXYPYRIDIN-3-YL) METHYL) -3,6-DIAZABICYCLO [3.1.1] HEPTAN-3- YL) PYRIDIN-3-YL) PYRAZOLO [1,5-A] pYRIDINE-3-carbonitrile |
| WO2019075108A1 (en) | 2017-10-10 | 2019-04-18 | Metcalf Andrew T | CRYSTALLINE FORMS |
| WO2019084285A1 (en) | 2017-10-26 | 2019-05-02 | Qian Zhao | FORMULATIONS OF A MACROCYCLIC TRK KINASE INHIBITOR |
| WO2019143994A1 (en) | 2018-01-18 | 2019-07-25 | Array Biopharma Inc. | Substituted pyrazolyl[4,3-c]pyridinecompounds as ret kinase inhibitors |
| WO2019143977A1 (en) | 2018-01-18 | 2019-07-25 | Array Biopharma Inc. | Substituted pyrrolo[2,3-d]pyrimidines compounds as ret kinase inhibitors |
| WO2019191659A1 (en) | 2018-03-29 | 2019-10-03 | Loxo Oncology, Inc. | Treatment of trk-associated cancers |
| WO2020028258A1 (en) | 2018-07-31 | 2020-02-06 | Loxo Oncology, Inc. | Spray-dried dispersions and formulations of (s)-5-amino-3-(4-((5-fluoro-2-methoxybenzamido)methyl)phenyl)-1-(1,1,1-trifluoro propan-2-yl)-1h-pyrazole-4-carboxamide |
| WO2020055672A1 (en) | 2018-09-10 | 2020-03-19 | Array Biopharma Inc. | Fused heterocyclic compounds as ret kinase inhibitors |
| WO2020131674A1 (en) | 2018-12-19 | 2020-06-25 | Array Biopharma Inc. | 7-((3,5-dimethoxyphenyl)amino)quinoxaline derivatives as fgfr inhibitors for treating cancer |
| WO2020131627A1 (en) | 2018-12-19 | 2020-06-25 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as inhibitors of fgfr tyrosine kinases |
| US10981908B2 (en) | 2017-02-01 | 2021-04-20 | Phenex Pharmaceuticals Ag | Aryl hydrocarbon receptor (AHR) modulator compounds |
| US11020398B2 (en) | 2016-08-24 | 2021-06-01 | Arqule, Inc. | Amino-pyrrolopyrimidinone compounds and methods of use thereof |
| US11091486B2 (en) | 2016-10-26 | 2021-08-17 | Array Biopharma, Inc | Process for the preparation of pyrazolo[1,5-a]pyrimidines and salts thereof |
| US11192936B2 (en) | 2014-01-10 | 2021-12-07 | Bioverativ Therapeutics Inc. | Factor VIII chimeric proteins and uses thereof |
| US11214571B2 (en) | 2016-05-18 | 2022-01-04 | Array Biopharma Inc. | Process for the preparation of (S)-N-(5-((R)-2-(2,5-difluorophenyl)pyrrolidin-1-yl)-pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide and salts thereof |
| US11376241B2 (en) | 2017-02-01 | 2022-07-05 | Phenex Pharmaceuticals Ag | Aryl hydrocarbon receptor (AhR) modulator compounds |
| CN114920744A (zh) * | 2021-11-16 | 2022-08-19 | 中国药科大学 | 一种非共价btk激酶抑制剂及其生物用途 |
| US11524963B2 (en) | 2018-01-18 | 2022-12-13 | Array Biopharma Inc. | Substituted pyrazolo[3,4-d]pyrimidines as RET kinase inhibitors |
| US11897889B2 (en) | 2020-08-18 | 2024-02-13 | Incyte Corporation | Process and intermediates for preparing a JAK1 inhibitor |
| US11905292B2 (en) | 2020-08-18 | 2024-02-20 | Incyte Corporation | Process and intermediates for preparing a JAK inhibitor |
| US12030925B2 (en) | 2018-05-18 | 2024-07-09 | Bioverativ Therapeutics Inc. | Methods of treating hemophilia A |
| US12071439B2 (en) | 2021-07-12 | 2024-08-27 | Incyte Corporation | Process and intermediates for preparing a JAK inhibitor |
| US12161696B2 (en) | 2016-12-02 | 2024-12-10 | Bioverativ Therapeutics Inc. | Methods of treating hemophilic arthropathy using chimeric clotting factors |
| EP4480949A4 (en) * | 2022-03-25 | 2025-06-18 | Jumbo Drug Bank Co., Ltd. | Crystal form of 1h-pyrrolo[2,3-c]pyridine compound and preparation method therefor |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG183036A1 (en) | 2007-07-17 | 2012-08-30 | Plexxikon Inc | Compounds and methods for kinase modulation, and indications therefor |
| WO2009143018A2 (en) | 2008-05-19 | 2009-11-26 | Plexxikon, Inc. | Compounds and methods for kinase modulation, and indications therefor |
| MX2012005284A (es) | 2009-11-06 | 2012-06-28 | Plexxikon Inc | Compuestos y metodos para la modulacion de cinasas. e indicaciones para ello. |
| CN102740698A (zh) | 2009-11-18 | 2012-10-17 | 普莱希科公司 | 用于激酶调节的化合物和方法及其适应症 |
| BR112012015745A2 (pt) | 2009-12-23 | 2016-05-17 | Plexxikon Inc | compostos e métodos para a modulação de quinase, e indicações dos mesmos |
| TWI619713B (zh) | 2010-04-21 | 2018-04-01 | 普雷辛肯公司 | 用於激酶調節的化合物和方法及其適應症 |
| WO2014039714A2 (en) | 2012-09-06 | 2014-03-13 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| CA2895239C (en) | 2012-12-21 | 2020-10-27 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| US20140303121A1 (en) | 2013-03-15 | 2014-10-09 | Plexxikon Inc. | Heterocyclic compounds and uses thereof |
| WO2014145051A1 (en) | 2013-03-15 | 2014-09-18 | Jiazhong Zhang | Heterocyclic compounds and uses thereof |
| BR112015028845A2 (pt) | 2013-05-30 | 2017-07-25 | Plexxikon Inc | compostos para a modulação da quinase e indicações da mesma |
| US9771369B2 (en) | 2014-03-04 | 2017-09-26 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| WO2016044067A1 (en) | 2014-09-15 | 2016-03-24 | Plexxikon Inc. | Heterocyclic compounds and uses thereof |
| US20180263945A1 (en) * | 2014-12-19 | 2018-09-20 | Research Institute At Nationwide Children's Hospital | Pyruvate compounds for treatment of peripheral neuropathy |
| WO2016164641A1 (en) | 2015-04-08 | 2016-10-13 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| BR112017023540B1 (pt) | 2015-05-06 | 2023-04-04 | Plexxikon, Inc. | Processos de preparação de derivados de 1h-pirrolo[2,3-b]piridina que modulam quinases |
| HRP20201383T1 (hr) | 2015-05-06 | 2020-11-27 | Plexxikon Inc. | Kruti oblici spoja za moduliranje kinaza |
| US10316032B2 (en) | 2015-05-22 | 2019-06-11 | Plexxikon Inc. | Solid forms of a compound for modulating kinases |
| WO2017019804A2 (en) | 2015-07-28 | 2017-02-02 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| EP3353179B1 (en) | 2015-09-21 | 2022-02-09 | Plexxikon Inc. | Heterocyclic compounds and uses thereof |
| WO2017100201A1 (en) | 2015-12-07 | 2017-06-15 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| ES2904615T3 (es) | 2016-03-16 | 2022-04-05 | Plexxikon Inc | Compuestos y métodos para la modulación de quinasas e indicaciones al respecto |
| EP3454860B1 (en) * | 2016-05-11 | 2025-09-17 | Beta Pharma, Inc. | 2-anilinopyrimidine derivatives as therapeutic agents for treatment of brain cancers |
| TW201815766A (zh) | 2016-09-22 | 2018-05-01 | 美商普雷辛肯公司 | 用於ido及tdo調節之化合物及方法以及其適應症 |
| US20180153922A1 (en) | 2016-12-06 | 2018-06-07 | New York Society For The Ruptured And Crippled Maintaining The Hospital For Special Surgery | Inhibition of expansion and function of pathogenic age-associated b cells and use for the prevention and treatment of autoimmune disease |
| WO2018136202A2 (en) | 2016-12-23 | 2018-07-26 | Plexxikon Inc. | Compounds and methods for cdk8 modulation and indications therefor |
| CA3056777A1 (en) | 2017-03-20 | 2018-09-27 | Plexxikon Inc. | Crystalline forms of 4-(1-(1,1-di(pyridin-2-yl)ethyl)-6-(3,5-dimethylisoxazol-4-yl)-1h- pyrrolo[3,2-b]pyridin-3-yl)benzoic acid that inhibits bromodomain |
| WO2018226846A1 (en) | 2017-06-07 | 2018-12-13 | Plexxikon Inc. | Compounds and methods for kinase modulation |
| TWI805599B (zh) | 2017-07-25 | 2023-06-21 | 美商第一三共公司 | 激酶調節化合物之調配物 |
| US10717735B2 (en) | 2017-10-13 | 2020-07-21 | Plexxikon Inc. | Solid forms of a compound for modulating kinases |
| TWI803530B (zh) | 2017-10-27 | 2023-06-01 | 美商普雷辛肯公司 | 調節激酶之化合物之調配物 |
| WO2019157119A1 (en) * | 2018-02-07 | 2019-08-15 | University Of Cincinnati | System and method for detecting small blood-tissue barrier disruption |
| WO2019183145A1 (en) | 2018-03-20 | 2019-09-26 | Plexxikon Inc. | Compounds and methods for ido and tdo modulation, and indications therefor |
| KR102129114B1 (ko) * | 2018-07-26 | 2020-07-02 | 주식회사 온코파마텍 | TrkA 저해 활성을 갖는 화합물 및 이를 유효성분으로 함유하는 통증의 예방 또는 치료용 약학적 조성물 |
| CN110833557A (zh) * | 2018-08-15 | 2020-02-25 | 广西梧州制药(集团)股份有限公司 | 吡唑并嘧啶衍生物在治疗肾小管肾炎的用途 |
| CN110833552A (zh) * | 2018-08-15 | 2020-02-25 | 广西梧州制药(集团)股份有限公司 | 吡唑并嘧啶衍生物在治疗狼疮肾炎的用途 |
| US11969472B2 (en) | 2018-08-22 | 2024-04-30 | Cullgen (Shanghai), Inc. | Tropomyosin receptor kinase (TRK) degradation compounds and methods of use |
| EP3841098A4 (en) | 2018-08-22 | 2022-05-04 | Cullgen (Shanghai), Inc. | TROPOMYOSIN RECEPTOR KINASE (TRK) DEGRADATION COMPOUNDS AND METHOD OF USE |
| AU2020271836B2 (en) | 2019-04-09 | 2025-11-13 | Opna Bio SA | Condensed azines for EP300 or CBP modulation and indications therefor |
| CN110643672A (zh) * | 2019-10-15 | 2020-01-03 | 西安交通大学 | 高表达TrkB作为新型靶点在抑制胰腺癌转移方面的医药用途 |
| CN115697989B (zh) | 2020-02-26 | 2025-03-18 | 上海睿跃生物科技有限公司 | 原肌球蛋白受体激酶(trk)降解化合物和使用方法 |
| AU2021261383A1 (en) | 2020-04-23 | 2022-11-17 | Opna Bio SA | Compounds and methods for CD73 modulation and indications therefor |
| EP4143168A1 (en) | 2020-04-29 | 2023-03-08 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
| JP2023542473A (ja) | 2020-08-21 | 2023-10-10 | プレキシコン インコーポレーテッド | 併用薬抗がん治療 |
| KR20230058134A (ko) * | 2020-09-25 | 2023-05-02 | 점보 드러그 뱅크 컴퍼니 리미티드 | 1H-피롤로[2,3-c]피리딘계 화합물 및 이의 용도 |
| WO2025244944A1 (en) * | 2024-05-20 | 2025-11-27 | Opna Bio SA | Crystal forms of an agent |
Family Cites Families (75)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6316474B1 (en) | 1999-10-29 | 2001-11-13 | Merck & Co., Inc. | 2-benzyl and 2-heteroaryl benzimidazole NMDA/NR2B antagonists |
| SK17342002A3 (sk) | 2000-06-26 | 2004-06-08 | Pfizer Products Inc. | Derivát pyrolo[2,3-d]pyrimidínu ako činidlo potlačujúce imunitu |
| GB0107368D0 (en) * | 2001-03-23 | 2001-05-16 | Novartis Ag | Organic compounds |
| WO2002092087A1 (en) | 2001-05-11 | 2002-11-21 | Vertex Pharmaceuticals Incorporated | 2,5-disubstituted pyridine, pyrimidine, pyridazine and 1, 2, 4-triazine derivatives for use as p38 inhibitors |
| CN101001857B (zh) | 2002-01-22 | 2011-06-22 | 沃尼尔·朗伯有限责任公司 | 2-(吡啶-2-基氨基)-吡啶并[2,3-d]嘧啶-7-酮 |
| US20040171062A1 (en) | 2002-02-28 | 2004-09-02 | Plexxikon, Inc. | Methods for the design of molecular scaffolds and ligands |
| EP1558751A4 (en) | 2002-09-16 | 2007-08-22 | Plexxikon Inc | CRYSTALLINE STRUCTURE OF PROTEIN KINASE PIM-1 |
| GB0226370D0 (en) * | 2002-11-12 | 2002-12-18 | Novartis Ag | Organic compounds |
| US20050048573A1 (en) | 2003-02-03 | 2005-03-03 | Plexxikon, Inc. | PDE5A crystal structure and uses |
| SE0300456D0 (sv) | 2003-02-19 | 2003-02-19 | Astrazeneca Ab | Novel compounds |
| JP2007524374A (ja) | 2003-02-28 | 2007-08-30 | プレキシコン,インコーポレーテッド | Pyk2結晶構造および使用 |
| US20050079548A1 (en) | 2003-07-07 | 2005-04-14 | Plexxikon, Inc. | Ligand development using PDE4B crystal structures |
| DK1648889T3 (da) | 2003-07-11 | 2009-01-05 | Warner Lambert Co | Isethionatsalt af en selektiv CDK4-inhibitor |
| US7348338B2 (en) | 2003-07-17 | 2008-03-25 | Plexxikon, Inc. | PPAR active compounds |
| WO2005009958A1 (en) | 2003-07-17 | 2005-02-03 | Plexxikon, Inc. | Ppar active compounds |
| US20050164300A1 (en) | 2003-09-15 | 2005-07-28 | Plexxikon, Inc. | Molecular scaffolds for kinase ligand development |
| US7517970B2 (en) | 2003-12-19 | 2009-04-14 | Plexxikon, Inc. | Nucleic acids encoding kinase and phosphatase enzymes, expression vectors and cells containing same |
| US20070066641A1 (en) | 2003-12-19 | 2007-03-22 | Prabha Ibrahim | Compounds and methods for development of RET modulators |
| US7504509B2 (en) | 2003-12-19 | 2009-03-17 | Plexxikon, Inc. | Compounds and methods for development of Ret modulators |
| ES2424642T3 (es) * | 2004-02-14 | 2013-10-07 | Irm Llc | Compuestos y composiciones como inhibidores de la proteína quinasa |
| JP4866723B2 (ja) * | 2004-02-26 | 2012-02-01 | 協和発酵キリン株式会社 | 好中球性炎症疾患の予防及び/または治療剤 |
| CA2565965A1 (en) | 2004-05-06 | 2006-07-27 | Plexxikon, Inc. | Pde4b inhibitors and uses therefor |
| WO2005116035A1 (en) | 2004-05-27 | 2005-12-08 | Pfizer Products Inc. | Pyrrolopyrimidine derivatives useful in cancer treatment |
| US20060058339A1 (en) | 2004-06-17 | 2006-03-16 | Ibrahim Prabha N | Compounds modulating c-kit activity and uses therefor |
| US7498342B2 (en) | 2004-06-17 | 2009-03-03 | Plexxikon, Inc. | Compounds modulating c-kit activity |
| CA2583428A1 (en) | 2004-09-03 | 2006-03-09 | Plexxikon, Inc. | Bicyclic heteroaryl pde4b inhibitors |
| CA2589896A1 (en) | 2004-11-30 | 2006-06-08 | Plexxikon, Inc. | Indole derivatives for use as ppar active compounds |
| AU2005311925A1 (en) | 2004-11-30 | 2006-06-08 | Plexxikon, Inc. | Indole derivatives for use as PPAR PPAR active compounds |
| US20060160135A1 (en) | 2004-12-08 | 2006-07-20 | Weiru Wang | SF-1 and LRH-1 modulator development |
| CN101223169A (zh) * | 2005-05-17 | 2008-07-16 | 普莱希科公司 | 吡咯并[2,3-b]吡啶衍生物蛋白激酶抑制剂 |
| WO2007013896A2 (en) | 2005-05-17 | 2007-02-01 | Plexxikon, Inc. | Pyrrol (2,3-b) pyridine derivatives protein kinase inhibitors |
| TWI473808B (zh) | 2005-06-22 | 2015-02-21 | Plexxikon Inc | 用於激酶調節的化合物及方法及其適應症 |
| CN101304992A (zh) | 2005-09-07 | 2008-11-12 | 普莱希科公司 | 用作ppar调节剂的1,3-二取代吲哚衍生物 |
| JP2009507846A (ja) | 2005-09-07 | 2009-02-26 | プレキシコン,インコーポレーテッド | Ppar活性化合物 |
| US20080234349A1 (en) | 2005-09-07 | 2008-09-25 | Jack Lin | PPAR active compounds |
| WO2008063888A2 (en) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
| US8093246B2 (en) | 2006-12-14 | 2012-01-10 | Lexicon Pharmaceuticals, Inc. | O-linked pyrimidin-4-amine-based compounds, compositions comprising them, and methods of their use to treat cancer |
| WO2008079909A1 (en) | 2006-12-21 | 2008-07-03 | Plexxikon, Inc. | Pyrrolo [2,3-b] pyridines as kinase modulators |
| JP2010514695A (ja) | 2006-12-21 | 2010-05-06 | プレキシコン,インコーポレーテッド | キナーゼ調節のための化合物および方法およびそのための適応症 |
| PE20121126A1 (es) | 2006-12-21 | 2012-08-24 | Plexxikon Inc | Compuestos pirrolo [2,3-b] piridinas como moduladores de quinasa |
| PE20090159A1 (es) | 2007-03-08 | 2009-02-21 | Plexxikon Inc | COMPUESTOS DERIVADOS DE ACIDO INDOL-PROPIONICO COMO MODULADORES PPARs |
| JP2010520303A (ja) | 2007-03-08 | 2010-06-10 | プレキシコン,インコーポレーテッド | Ppar活性化合物 |
| EP2148875A1 (en) * | 2007-05-04 | 2010-02-03 | Irm Llc | Compounds and compositions as c-kit and pdgfr kinase inhibitors |
| SG183036A1 (en) | 2007-07-17 | 2012-08-30 | Plexxikon Inc | Compounds and methods for kinase modulation, and indications therefor |
| JO3240B1 (ar) * | 2007-10-17 | 2018-03-08 | Janssen Pharmaceutica Nv | c-fms مثبطات كيناز |
| CL2009000400A1 (es) * | 2008-02-22 | 2010-09-10 | Irm Llc | Compuestos heterociclicos derivados de 3-fenil-1,6- naftiridin-2-ona; moduladores de la actividad cinasa; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como trastornos alergicos, trastornos autoinmunes, neoplasias, rechazo en trasplante de organos, entre otras. |
| WO2009115084A2 (de) | 2008-03-20 | 2009-09-24 | Schebo Biotech Ag | Neue pyrrolopyrimidin-derivate und deren verwendungen |
| US8865732B2 (en) | 2008-03-21 | 2014-10-21 | Novartis Ag | Heterocyclic compounds and uses thereof |
| PE20091846A1 (es) | 2008-05-19 | 2009-12-16 | Plexxikon Inc | DERIVADOS DE PIRROLO[2,3-d]-PIRIMIDINA COMO MODULADORES DE CINASAS |
| WO2009143018A2 (en) | 2008-05-19 | 2009-11-26 | Plexxikon, Inc. | Compounds and methods for kinase modulation, and indications therefor |
| WO2009152087A1 (en) | 2008-06-10 | 2009-12-17 | Plexxikon, Inc. | Bicyclic heteroaryl compounds and methods for kinase modulation, and indications therefor |
| CN104530052A (zh) | 2008-06-10 | 2015-04-22 | 普莱希科公司 | 用于激酶调节的5h-吡咯[2,3-b]吡嗪衍生物和其适应症 |
| BRPI0917459B1 (pt) | 2008-08-20 | 2017-09-12 | Zoetis Services Llc | N-methyl-1- [trans-4- [methyl (7h-pyrrol [2,3-d] pyridol [2,3-d] pyrimidine compounds, use of these in therapy and crystalline a form of n-methyl- pyrimidin-4-yl) amino] cyclohexyl} methanosulphonamide |
| TR201807039T4 (tr) | 2008-10-22 | 2018-06-21 | Array Biopharma Inc | Trk kinaz inhibitörleri olarak sübstitüe edilmiş pirazolo[1,5-]pirimidin bileşikleri. |
| KR101663339B1 (ko) | 2009-03-11 | 2016-10-06 | 플렉시콘 인코퍼레이티드 | Raf 키나제의 억제를 위한 피롤로[2,3-b]피리딘 유도체 |
| CN102421775A (zh) | 2009-03-11 | 2012-04-18 | 普莱希科公司 | 抑制Raf激酶的吡咯并[2,3-b]吡啶衍生物 |
| WO2010111527A1 (en) | 2009-03-26 | 2010-09-30 | Plexxikon, Inc. | Pyrazolo [ 3, 4 -b] pyridines as kinase inhibitors and their medical use |
| AU2010232670B2 (en) | 2009-04-03 | 2015-07-09 | F. Hoffmann-La Roche Ag | Propane- I-sulfonic acid {3- [5- (4 -chloro-phenyl) -1H-pyrrolo [2, 3-b] pyridine-3-carbonyl] -2, 4-difluoro-pheny l } -amide compositions and uses thereof |
| MX2011011735A (es) | 2009-05-04 | 2011-11-29 | Plexxikon Inc | Compuestos y metodos para la inhibicion de renina, e indicaciones para ello. |
| TW201041888A (en) | 2009-05-06 | 2010-12-01 | Plexxikon Inc | Compounds and methods for kinase modulation, and indications therefor |
| MX2012005284A (es) | 2009-11-06 | 2012-06-28 | Plexxikon Inc | Compuestos y metodos para la modulacion de cinasas. e indicaciones para ello. |
| CN102740698A (zh) | 2009-11-18 | 2012-10-17 | 普莱希科公司 | 用于激酶调节的化合物和方法及其适应症 |
| BR112012015745A2 (pt) | 2009-12-23 | 2016-05-17 | Plexxikon Inc | compostos e métodos para a modulação de quinase, e indicações dos mesmos |
| TWI619713B (zh) * | 2010-04-21 | 2018-04-01 | 普雷辛肯公司 | 用於激酶調節的化合物和方法及其適應症 |
| US8642606B2 (en) | 2010-09-29 | 2014-02-04 | Plexxikon Inc. | ZAP-70 active compounds |
| KR101911972B1 (ko) | 2011-02-07 | 2018-10-25 | 플렉시콘 인코퍼레이티드 | 키나제 조절을 위한 화합물 및 방법, 및 그에 대한 적응증 |
| SG194847A1 (en) | 2011-05-17 | 2013-12-30 | Plexxikon Inc | Kinase modulation and indications therefor |
| US9358235B2 (en) | 2012-03-19 | 2016-06-07 | Plexxikon Inc. | Kinase modulation, and indications therefor |
| US9150570B2 (en) | 2012-05-31 | 2015-10-06 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
| WO2014039714A2 (en) | 2012-09-06 | 2014-03-13 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| CA2895239C (en) | 2012-12-21 | 2020-10-27 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| WO2014145051A1 (en) | 2013-03-15 | 2014-09-18 | Jiazhong Zhang | Heterocyclic compounds and uses thereof |
| US20140303121A1 (en) | 2013-03-15 | 2014-10-09 | Plexxikon Inc. | Heterocyclic compounds and uses thereof |
| BR112015028845A2 (pt) | 2013-05-30 | 2017-07-25 | Plexxikon Inc | compostos para a modulação da quinase e indicações da mesma |
| US9771369B2 (en) | 2014-03-04 | 2017-09-26 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
-
2011
- 2011-04-19 TW TW104127657A patent/TWI619713B/zh not_active IP Right Cessation
- 2011-04-19 TW TW100113512A patent/TWI510487B/zh not_active IP Right Cessation
- 2011-04-20 HU HUE11772612A patent/HUE036461T2/hu unknown
- 2011-04-20 PH PH1/2012/502103A patent/PH12012502103A1/en unknown
- 2011-04-20 WO PCT/US2011/033192 patent/WO2011133637A2/en not_active Ceased
- 2011-04-20 ES ES11772612.5T patent/ES2641643T3/es active Active
- 2011-04-20 PE PE2012002054A patent/PE20130240A1/es active IP Right Grant
- 2011-04-20 CN CN201180030925.5A patent/CN102947305B/zh active Active
- 2011-04-20 MY MYPI2012004649A patent/MY160780A/en unknown
- 2011-04-20 SM SM20170458T patent/SMT201700458T1/it unknown
- 2011-04-20 JP JP2013506264A patent/JP5808793B2/ja active Active
- 2011-04-20 SG SG10201505606QA patent/SG10201505606QA/en unknown
- 2011-04-20 NZ NZ603087A patent/NZ603087A/en not_active IP Right Cessation
- 2011-04-20 BR BR112012026927A patent/BR112012026927A2/pt not_active IP Right Cessation
- 2011-04-20 SI SI201131348T patent/SI2560972T1/sl unknown
- 2011-04-20 US US13/090,969 patent/US8901118B2/en active Active
- 2011-04-20 MA MA35365A patent/MA34229B1/fr unknown
- 2011-04-20 MX MX2012012197A patent/MX336056B/es unknown
- 2011-04-20 EA EA201290973A patent/EA028105B1/ru not_active IP Right Cessation
- 2011-04-20 HR HRP20171660TT patent/HRP20171660T1/hr unknown
- 2011-04-20 AU AU2011242778A patent/AU2011242778B2/en active Active
- 2011-04-20 EP EP11772612.5A patent/EP2560972B1/en active Active
- 2011-04-20 GE GEAP201112896A patent/GEP20156251B/en unknown
- 2011-04-20 CA CA2796998A patent/CA2796998C/en active Active
- 2011-04-20 LT LTEP11772612.5T patent/LT2560972T/lt unknown
- 2011-04-20 PT PT117726125T patent/PT2560972T/pt unknown
- 2011-04-20 RS RS20171089A patent/RS56588B1/sr unknown
- 2011-04-20 UA UAA201212061A patent/UA109128C2/ru unknown
- 2011-04-20 AR ARP110101385A patent/AR080940A1/es not_active Application Discontinuation
- 2011-04-20 DK DK11772612.5T patent/DK2560972T3/da active
- 2011-04-20 NZ NZ703538A patent/NZ703538A/en not_active IP Right Cessation
- 2011-04-20 SG SG2012076584A patent/SG184874A1/en unknown
- 2011-04-20 PL PL11772612T patent/PL2560972T3/pl unknown
- 2011-04-20 KR KR1020127030470A patent/KR101799126B1/ko not_active Expired - Fee Related
- 2011-04-25 UY UY0001033346A patent/UY33346A/es not_active Application Discontinuation
-
2012
- 2012-10-10 EC ECSP12012245 patent/ECSP12012245A/es unknown
- 2012-10-17 IL IL222498A patent/IL222498A/en active IP Right Grant
- 2012-10-19 CR CR20120536A patent/CR20120536A/es unknown
- 2012-10-19 ZA ZA2012/07898A patent/ZA201207898B/en unknown
- 2012-10-19 CL CL2012002937A patent/CL2012002937A1/es unknown
- 2012-10-22 CO CO12187143A patent/CO6620045A2/es not_active Application Discontinuation
-
2014
- 2014-12-01 US US14/556,709 patent/US9682981B2/en active Active
-
2015
- 2015-09-09 JP JP2015177852A patent/JP2016028073A/ja active Pending
-
2017
- 2017-06-19 US US15/627,223 patent/US20170283423A1/en not_active Abandoned
- 2017-12-19 CY CY20171101332T patent/CY1120554T1/el unknown
-
2019
- 2019-09-03 AR ARP190102503A patent/AR115233A2/es unknown
Non-Patent Citations (2)
| Title |
|---|
| None |
| See also references of EP2560972A4 |
Cited By (126)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9169250B2 (en) | 2006-11-22 | 2015-10-27 | Plexxikon Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
| US10011604B2 (en) | 2008-09-22 | 2018-07-03 | Array Biopharma, Inc. | Method of treatment using substituted imidazo[1,2b]pyridazine compounds |
| US9796723B2 (en) | 2008-09-22 | 2017-10-24 | Array Biopharma, Inc. | Method of treatment using substituted imidazo[1,2b]pyridazine compounds |
| US10590139B2 (en) | 2008-09-22 | 2020-03-17 | Array Biopharma Inc. | Method of treatment using substituted imidazo[1,2b]pyridazine compounds |
| US9795611B2 (en) | 2008-09-22 | 2017-10-24 | Array Biopharma, Inc. | Method of treatment using substituted imidazo[1,2b]pyridazine compounds |
| US10774085B2 (en) | 2008-10-22 | 2020-09-15 | Array Biopharma Inc. | Method of treatment using substituted pyrazolo[1,5-A] pyrimidine compounds |
| US10047097B2 (en) | 2008-10-22 | 2018-08-14 | Array Biopharma Inc. | Method of treatment using substituted pyrazolo[1,5-a] pyrimidine compounds |
| US11267818B2 (en) | 2008-10-22 | 2022-03-08 | Array Biopharma Inc. | Method of treatment using substituted pyrazolo[1,5-a] pyrimidine compounds |
| US10005783B2 (en) | 2008-10-22 | 2018-06-26 | Array Biopharma Inc. | Method of treatment using substituted pyrazolo[1,5-a] pyrimidine compounds |
| US9663517B2 (en) | 2009-04-03 | 2017-05-30 | Plexxikon Inc. | Compositions and uses thereof |
| US9782415B2 (en) | 2009-07-09 | 2017-10-10 | Array Biopharma, Inc. | Substituted pyrazolo[1,5-a]pyrimidine compounds as Trk kinase inhibitors |
| US10251889B2 (en) | 2009-07-09 | 2019-04-09 | Array BioPharm Inc. | Substituted pyrazolo[1,5-a]pyrimidine compounds as Trk kinase inhibitors |
| US10758542B2 (en) | 2009-07-09 | 2020-09-01 | Array Biopharma Inc. | Substituted pyrazolo[l,5-a]pyrimidine compounds as Trk kinase inhibitors |
| US9796724B2 (en) | 2009-07-09 | 2017-10-24 | Array Biopharma, Inc. | Substituted pyrazolo[1,5-a]pyrimidine compounds as Trk kinase inhibitors |
| US9840519B2 (en) | 2010-05-20 | 2017-12-12 | Array Biopharma, Inc. | Macrocyclic compounds as TRK kinase inhibitors |
| US9750744B2 (en) | 2010-05-20 | 2017-09-05 | Array Biopharma, Inc. | Macrocyclic compounds as Trk kinase inhibitors |
| US9902741B2 (en) | 2010-05-20 | 2018-02-27 | Array Biopharma Inc. | Macrocyclic compounds as TRK kinase inhibitors |
| US9718822B2 (en) | 2010-05-20 | 2017-08-01 | Array Biopharma, Inc. | Macrocyclic compounds as Trk kinase inhibitors |
| US10647730B2 (en) | 2010-05-20 | 2020-05-12 | Array Biopharma Inc. | Macrocyclic compounds as TRK kinase inhibitors |
| US11337976B2 (en) | 2011-02-07 | 2022-05-24 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| US9624213B2 (en) | 2011-02-07 | 2017-04-18 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| US12076322B2 (en) | 2011-02-07 | 2024-09-03 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| WO2012137089A1 (en) | 2011-04-05 | 2012-10-11 | Pfizer Limited | Pyrrolo [2, 3 -d] pyrimidine derivatives as inhibitors of tropomyosin- related kinases |
| US9550768B2 (en) | 2011-05-17 | 2017-01-24 | Plexxikon Inc. | Kinase modulation and indications therefor |
| EP2709622A4 (en) * | 2011-05-17 | 2015-03-04 | Plexxikon Inc | CINEMA MODULATION AND INDICATIONS THEREFOR |
| US9730918B2 (en) | 2012-03-19 | 2017-08-15 | Plexxikon Inc. | Kinase modulation, and indications therefor |
| US10123998B2 (en) | 2012-03-19 | 2018-11-13 | Plexxikon Inc. | Kinase modulation, and indications therefor |
| US9358235B2 (en) | 2012-03-19 | 2016-06-07 | Plexxikon Inc. | Kinase modulation, and indications therefor |
| US9150570B2 (en) | 2012-05-31 | 2015-10-06 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
| US9695169B2 (en) | 2012-05-31 | 2017-07-04 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
| US9505765B2 (en) | 2012-07-26 | 2016-11-29 | Confluence Life Sciences Inc. | 4-alkoxy/aralkoxy-5-substituted-pyrrolopyrimidine compounds as TAK1 inhibitors in disease treatment |
| WO2014053968A1 (en) | 2012-10-04 | 2014-04-10 | Pfizer Limited | Pyrrolo[3,2-c]pyridine tropomyosin-related kinase inhibitors |
| WO2014053967A1 (en) | 2012-10-04 | 2014-04-10 | Pfizer Limited | Pyrrolo[2,3-d]pyrimidine tropomyosin-related kinase inhibitors |
| WO2014053965A1 (en) | 2012-10-04 | 2014-04-10 | Pfizer Limited | Tropomyosin-related kinase inhibitors |
| WO2015017533A1 (en) | 2013-07-30 | 2015-02-05 | Blueprint Medicines Corporation | Ntrk2 fusions |
| EP3628749A1 (en) | 2013-07-30 | 2020-04-01 | Blueprint Medicines Corporation | Ntrk2 fusions |
| US10407509B2 (en) | 2013-07-30 | 2019-09-10 | Blueprint Medicines Corporation | NTRK2 fusions |
| WO2015092610A1 (en) | 2013-12-20 | 2015-06-25 | Pfizer Limited | N-acylpiperidine ether tropomyosin-related kinase inhibitors |
| US11192936B2 (en) | 2014-01-10 | 2021-12-07 | Bioverativ Therapeutics Inc. | Factor VIII chimeric proteins and uses thereof |
| WO2015159175A1 (en) | 2014-04-15 | 2015-10-22 | Pfizer Inc. | Tropomyosin-related kinase inhibitors containing both a 1h-pyrazole and a pyrimidine moiety |
| WO2015170218A1 (en) | 2014-05-07 | 2015-11-12 | Pfizer Inc. | Tropomyosin-related kinase inhibitors |
| WO2016009296A1 (en) | 2014-07-16 | 2016-01-21 | Pfizer Inc. | N-acylpiperidine ether tropomyosin-related kinase inhibitors |
| WO2016020784A1 (en) | 2014-08-05 | 2016-02-11 | Pfizer Inc. | N-acylpyrrolidine ether tropomyosin-related kinase inhibitors |
| US10813936B2 (en) | 2014-11-16 | 2020-10-27 | Array Biopharma, Inc. | Crystalline form of (S)-N-(5-((R)-2-(2,5-difluorophenyl)-pyrrolidin-1-YL)-pyrazolo[1,5-A]pyrimidin-3-YL)-3-hydroxypyrrolidine-1-carboxamide hydrogen sulfate |
| US9782414B2 (en) | 2014-11-16 | 2017-10-10 | Array Biopharma, Inc. | Crystalline form of (S)-N-(5-((R)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-A]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide hydrogen sulfate |
| US10799505B2 (en) | 2014-11-16 | 2020-10-13 | Array Biopharma, Inc. | Crystalline form of (S)-N-(5-((R)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-A]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide hydrogen sulfate |
| US10285993B2 (en) | 2014-11-16 | 2019-05-14 | Array Biopharma Inc. | Crystalline form of (S)-N-(5-((R)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide hydrogen sulfate |
| US10172861B2 (en) | 2014-11-16 | 2019-01-08 | Array Biopharma Inc. | Crystalline form of (S)-N-(5-((R)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-A]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide hydrogen sulfate |
| US10150783B2 (en) | 2015-01-23 | 2018-12-11 | Aclaris Therapeutics, Inc. | Heterocyclic ITK inhibitors for treating inflammation and cancer |
| WO2016196671A1 (en) | 2015-06-01 | 2016-12-08 | Loxo Oncology, Inc. | Methods of diagnosing and treating cancer |
| EP3722441A1 (en) | 2015-06-01 | 2020-10-14 | Loxo Oncology Inc. | Method of diagnosing a cancer for a treatment with a trk inhibitor |
| US10023570B2 (en) | 2015-07-16 | 2018-07-17 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
| US10138243B2 (en) | 2015-07-16 | 2018-11-27 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as RET kinase inhibitors |
| US10174027B2 (en) | 2015-07-16 | 2019-01-08 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as RET kinase inhibitors |
| US10174028B2 (en) | 2015-07-16 | 2019-01-08 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
| WO2017011776A1 (en) | 2015-07-16 | 2017-01-19 | Array Biopharma, Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
| US10907215B2 (en) | 2015-10-26 | 2021-02-02 | Loxo Oncology, Inc. | Point mutations in TRK inhibitor-resistant cancer and methods relating to the same |
| US10655186B2 (en) | 2015-10-26 | 2020-05-19 | Loxo Oncology, Inc. | Point mutations in TRK inhibitor-resistant cancer and methods relating to the same |
| WO2017075107A1 (en) | 2015-10-26 | 2017-05-04 | Nanda Nisha | Point mutations in trk inhibitor-resistant cancer and methods relating to the same |
| US10724102B2 (en) | 2015-10-26 | 2020-07-28 | Loxo Oncology, Inc. | Point mutations in TRK inhibitor-resistant cancer and methods relating to the same |
| US10378068B2 (en) | 2015-10-26 | 2019-08-13 | Loxo Oncology, Inc. | Point mutations in TRK inhibitor-resistant cancer and methods relating to the same |
| US10370727B2 (en) | 2015-10-26 | 2019-08-06 | Loxo Oncology, Inc. | Point mutations in TRK inhibitor-resistant cancer and methods relating to the same |
| US10245263B2 (en) | 2015-12-23 | 2019-04-02 | Arqule, Inc. | Tetrahydropyranyl amino-pyrrolopyrimidinone and methods of use thereof |
| US10933065B2 (en) | 2015-12-23 | 2021-03-02 | Arqule Inc. | Tetrahydropyranyl amino-pyrrolopyrimidinone and methods of use thereof |
| US11020400B2 (en) | 2015-12-23 | 2021-06-01 | Arqule, Inc. | Tetrahydropyranyl amino-pyrrolopyrimidinone and methods of use thereof |
| US9630968B1 (en) | 2015-12-23 | 2017-04-25 | Arqule, Inc. | Tetrahydropyranyl amino-pyrrolopyrimidinone and methods of use thereof |
| US10137127B2 (en) | 2016-04-04 | 2018-11-27 | Loxo Oncology, Inc. | Liquid formulations of (S)-N-(5-((R)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-A]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide |
| US10668072B2 (en) | 2016-04-04 | 2020-06-02 | Loxo Oncology, Inc. | Liquid formulations of (S)-N-(5-((R)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide |
| US11484535B2 (en) | 2016-04-04 | 2022-11-01 | Loxo Oncology, Inc. | Liquid formulations of (S)-N-(5-((R)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-a] pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide |
| WO2017176744A1 (en) | 2016-04-04 | 2017-10-12 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
| WO2017176751A1 (en) | 2016-04-04 | 2017-10-12 | Loxo Oncology, Inc. | Liquid formulations of (s)-n-(5-((r)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide |
| US10045991B2 (en) | 2016-04-04 | 2018-08-14 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
| US10588908B2 (en) | 2016-04-04 | 2020-03-17 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
| US11191766B2 (en) | 2016-04-04 | 2021-12-07 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
| US11214571B2 (en) | 2016-05-18 | 2022-01-04 | Array Biopharma Inc. | Process for the preparation of (S)-N-(5-((R)-2-(2,5-difluorophenyl)pyrrolidin-1-yl)-pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide and salts thereof |
| US11020398B2 (en) | 2016-08-24 | 2021-06-01 | Arqule, Inc. | Amino-pyrrolopyrimidinone compounds and methods of use thereof |
| US11998545B2 (en) | 2016-10-10 | 2024-06-04 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as RET kinase inhibitors |
| US10112942B2 (en) | 2016-10-10 | 2018-10-30 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
| US10172845B2 (en) | 2016-10-10 | 2019-01-08 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
| US10172851B2 (en) | 2016-10-10 | 2019-01-08 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
| US10137124B2 (en) | 2016-10-10 | 2018-11-27 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as RET kinase inhibitors |
| EP4144735A1 (en) | 2016-10-10 | 2023-03-08 | Array Biopharma, Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
| US10144734B2 (en) | 2016-10-10 | 2018-12-04 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
| WO2018071454A1 (en) | 2016-10-10 | 2018-04-19 | Andrews Steven W | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
| US10441581B2 (en) | 2016-10-10 | 2019-10-15 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
| US11648243B2 (en) | 2016-10-10 | 2023-05-16 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
| US10555944B2 (en) | 2016-10-10 | 2020-02-11 | Eli Lilly And Company | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
| US10953005B1 (en) | 2016-10-10 | 2021-03-23 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as RET kinase inhibitors |
| EP3753939A1 (en) | 2016-10-10 | 2020-12-23 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
| US10881652B2 (en) | 2016-10-10 | 2021-01-05 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
| WO2018071447A1 (en) | 2016-10-10 | 2018-04-19 | Andrews Steven W | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
| US11091486B2 (en) | 2016-10-26 | 2021-08-17 | Array Biopharma, Inc | Process for the preparation of pyrazolo[1,5-a]pyrimidines and salts thereof |
| US12161696B2 (en) | 2016-12-02 | 2024-12-10 | Bioverativ Therapeutics Inc. | Methods of treating hemophilic arthropathy using chimeric clotting factors |
| WO2018136663A1 (en) | 2017-01-18 | 2018-07-26 | Array Biopharma, Inc. | Ret inhibitors |
| US11168090B2 (en) | 2017-01-18 | 2021-11-09 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyrazines as RET kinase inhibitors |
| WO2018136661A1 (en) | 2017-01-18 | 2018-07-26 | Andrews Steven W | SUBSTITUTED PYRAZOLO[1,5-a]PYRAZINE COMPOUNDS AS RET KINASE INHIBITORS |
| US11851434B2 (en) | 2017-01-18 | 2023-12-26 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyrazine compounds as ret kinase inhibitors |
| US10981908B2 (en) | 2017-02-01 | 2021-04-20 | Phenex Pharmaceuticals Ag | Aryl hydrocarbon receptor (AHR) modulator compounds |
| US11376241B2 (en) | 2017-02-01 | 2022-07-05 | Phenex Pharmaceuticals Ag | Aryl hydrocarbon receptor (AhR) modulator compounds |
| US10688100B2 (en) | 2017-03-16 | 2020-06-23 | Array Biopharma Inc. | Macrocylic compounds as ROS1 kinase inhibitors |
| US10966985B2 (en) | 2017-03-16 | 2021-04-06 | Array Biopharma Inc. | Macrocyclic compounds as ROS1 kinase inhibitors |
| WO2018170381A1 (en) | 2017-03-16 | 2018-09-20 | Andrews Steven W | Macrocyclic compounds as ros1 kinase inhibitors |
| WO2019075114A1 (en) | 2017-10-10 | 2019-04-18 | Mark Reynolds | FORMULATIONS COMPRISING 6- (2-HYDROXY-2-METHYLPROPOXY) -4- (6- (6 - ((6-METHOXYPYRIDIN-3-YL) METHYL) -3,6-DIAZABICYCLO [3.1.1] HEPTAN-3- YL) PYRIDIN-3-YL) PYRAZOLO [1,5-A] pYRIDINE-3-carbonitrile |
| WO2019075108A1 (en) | 2017-10-10 | 2019-04-18 | Metcalf Andrew T | CRYSTALLINE FORMS |
| WO2019084285A1 (en) | 2017-10-26 | 2019-05-02 | Qian Zhao | FORMULATIONS OF A MACROCYCLIC TRK KINASE INHIBITOR |
| US11472802B2 (en) | 2018-01-18 | 2022-10-18 | Array Biopharma Inc. | Substituted pyrazolyl[4,3-c]pyridine compounds as RET kinase inhibitors |
| US11524963B2 (en) | 2018-01-18 | 2022-12-13 | Array Biopharma Inc. | Substituted pyrazolo[3,4-d]pyrimidines as RET kinase inhibitors |
| WO2019143977A1 (en) | 2018-01-18 | 2019-07-25 | Array Biopharma Inc. | Substituted pyrrolo[2,3-d]pyrimidines compounds as ret kinase inhibitors |
| US11603374B2 (en) | 2018-01-18 | 2023-03-14 | Array Biopharma Inc. | Substituted pyrrolo[2,3-d]pyrimidines compounds as ret kinase inhibitors |
| WO2019143994A1 (en) | 2018-01-18 | 2019-07-25 | Array Biopharma Inc. | Substituted pyrazolyl[4,3-c]pyridinecompounds as ret kinase inhibitors |
| WO2019191659A1 (en) | 2018-03-29 | 2019-10-03 | Loxo Oncology, Inc. | Treatment of trk-associated cancers |
| US12030925B2 (en) | 2018-05-18 | 2024-07-09 | Bioverativ Therapeutics Inc. | Methods of treating hemophilia A |
| WO2020028258A1 (en) | 2018-07-31 | 2020-02-06 | Loxo Oncology, Inc. | Spray-dried dispersions and formulations of (s)-5-amino-3-(4-((5-fluoro-2-methoxybenzamido)methyl)phenyl)-1-(1,1,1-trifluoro propan-2-yl)-1h-pyrazole-4-carboxamide |
| US11964988B2 (en) | 2018-09-10 | 2024-04-23 | Array Biopharma Inc. | Fused heterocyclic compounds as RET kinase inhibitors |
| WO2020055672A1 (en) | 2018-09-10 | 2020-03-19 | Array Biopharma Inc. | Fused heterocyclic compounds as ret kinase inhibitors |
| WO2020131674A1 (en) | 2018-12-19 | 2020-06-25 | Array Biopharma Inc. | 7-((3,5-dimethoxyphenyl)amino)quinoxaline derivatives as fgfr inhibitors for treating cancer |
| WO2020131627A1 (en) | 2018-12-19 | 2020-06-25 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as inhibitors of fgfr tyrosine kinases |
| US11897889B2 (en) | 2020-08-18 | 2024-02-13 | Incyte Corporation | Process and intermediates for preparing a JAK1 inhibitor |
| US11905292B2 (en) | 2020-08-18 | 2024-02-20 | Incyte Corporation | Process and intermediates for preparing a JAK inhibitor |
| US12428426B2 (en) | 2020-08-18 | 2025-09-30 | Incyte Corporation | Process and intermediates for preparing a JAK1 inhibitor |
| US12479851B2 (en) | 2020-08-18 | 2025-11-25 | Incyte Corporation | Process and intermediates for preparing a JAK inhibitor |
| US12071439B2 (en) | 2021-07-12 | 2024-08-27 | Incyte Corporation | Process and intermediates for preparing a JAK inhibitor |
| CN114920744B (zh) * | 2021-11-16 | 2024-05-07 | 中国药科大学 | 一种非共价btk激酶抑制剂及其生物用途 |
| CN114920744A (zh) * | 2021-11-16 | 2022-08-19 | 中国药科大学 | 一种非共价btk激酶抑制剂及其生物用途 |
| EP4480949A4 (en) * | 2022-03-25 | 2025-06-18 | Jumbo Drug Bank Co., Ltd. | Crystal form of 1h-pyrrolo[2,3-c]pyridine compound and preparation method therefor |
| AU2023238511B2 (en) * | 2022-03-25 | 2025-11-27 | Jumbo Drug Bank Co., Ltd. | Crystal form of 1h-pyrrolo[2,3-c]pyridine compound and preparation method therefor |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US8901118B2 (en) | Compounds and methods for kinase modulation, and indications therefor | |
| AU2010315126B2 (en) | Compounds and methods for kinase modulation, and indications therefor | |
| EP2501236B1 (en) | N-[2-fluoro-3-(4-amino-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-phenyl]-4-benzenesulfonamide derivatives as Raf protein kinase modulators for the treatment of cancer | |
| AU2014233437A1 (en) | Heterocyclic compounds and uses thereof | |
| EP2516438A2 (en) | Compounds and methods for kinase modulation, and indications therefor | |
| HK1182382B (en) | Compounds and methods for kinase modulation, and indications therefor | |
| HK1182382A (en) | Compounds and methods for kinase modulation, and indications therefor | |
| HK1176238B (en) | N-[2-fluoro-3-(4-amino-7h-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-phenyl]-4 benzenesulfonamid e derivatives as raf protein kinase modulators for the treatment of cancer | |
| HK1176238A (en) | N-[2-fluoro-3-(4-amino-7h-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-phenyl]-4 benzenesulfonamid e derivatives as raf protein kinase modulators for the treatment of cancer |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| WWE | Wipo information: entry into national phase |
Ref document number: 201180030925.5 Country of ref document: CN |
|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 11772612 Country of ref document: EP Kind code of ref document: A2 |
|
| ENP | Entry into the national phase |
Ref document number: 2796998 Country of ref document: CA Ref document number: 2013506264 Country of ref document: JP Kind code of ref document: A |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 2012002937 Country of ref document: CL Ref document number: 9005/CHENP/2012 Country of ref document: IN Ref document number: 002054-2012 Country of ref document: PE Ref document number: CR2012-000536 Country of ref document: CR Ref document number: 12012502103 Country of ref document: PH Ref document number: MX/A/2012/012197 Country of ref document: MX |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 1201005548 Country of ref document: TH |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 12187143 Country of ref document: CO |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 201290973 Country of ref document: EA |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 12896 Country of ref document: GE |
|
| REEP | Request for entry into the european phase |
Ref document number: 2011772612 Country of ref document: EP |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 2011772612 Country of ref document: EP |
|
| WWE | Wipo information: entry into national phase |
Ref document number: A201212061 Country of ref document: UA |
|
| ENP | Entry into the national phase |
Ref document number: 20127030470 Country of ref document: KR Kind code of ref document: A |
|
| ENP | Entry into the national phase |
Ref document number: 2011242778 Country of ref document: AU Date of ref document: 20110420 Kind code of ref document: A |
|
| REG | Reference to national code |
Ref country code: BR Ref legal event code: B01A Ref document number: 112012026927 Country of ref document: BR |
|
| ENP | Entry into the national phase |
Ref document number: 112012026927 Country of ref document: BR Kind code of ref document: A2 Effective date: 20121019 |