CN102388044A - 用于治疗疾病的组胺受体的杂环抑制剂 - Google Patents
用于治疗疾病的组胺受体的杂环抑制剂 Download PDFInfo
- Publication number
- CN102388044A CN102388044A CN2009801427590A CN200980142759A CN102388044A CN 102388044 A CN102388044 A CN 102388044A CN 2009801427590 A CN2009801427590 A CN 2009801427590A CN 200980142759 A CN200980142759 A CN 200980142759A CN 102388044 A CN102388044 A CN 102388044A
- Authority
- CN
- China
- Prior art keywords
- group
- hydrogen
- forming
- halogen
- compound
- 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.)
- Pending
Links
- 0 **C1=Nc2c(*)c(*)c(*)c(*)c2*2*1=***2 Chemical compound **C1=Nc2c(*)c(*)c(*)c(*)c2*2*1=***2 0.000 description 64
- LCZWNRSELOSSFW-AATRIKPKSA-N CN(C)/C=C/c(c([N+]([O-])=O)c1)ccc1Cl Chemical compound CN(C)/C=C/c(c([N+]([O-])=O)c1)ccc1Cl LCZWNRSELOSSFW-AATRIKPKSA-N 0.000 description 2
- ZLCIALUBLCAXPL-UHFFFAOYSA-N Nc1ccc(C(F)(F)F)cc1C#N Chemical compound Nc1ccc(C(F)(F)F)cc1C#N ZLCIALUBLCAXPL-UHFFFAOYSA-N 0.000 description 2
- FSGAJDOLPUZINO-ARJAWSKDSA-N C/C=C\C(c(c(NC1=O)c2)ccc2Cl)=C1N=C Chemical compound C/C=C\C(c(c(NC1=O)c2)ccc2Cl)=C1N=C FSGAJDOLPUZINO-ARJAWSKDSA-N 0.000 description 1
- TWMUVXNHKNIMLP-UHFFFAOYSA-N C=Cc1c(c2cc(C(F)(F)F)ccc2nc2N3CCNCC3)[n]2nc1C(F)(F)F Chemical compound C=Cc1c(c2cc(C(F)(F)F)ccc2nc2N3CCNCC3)[n]2nc1C(F)(F)F TWMUVXNHKNIMLP-UHFFFAOYSA-N 0.000 description 1
- NWHXNECRIRBREL-UHFFFAOYSA-N CC(NC(C(Nc(cc1)c2cc1Cl)=O)=C2O)=O Chemical compound CC(NC(C(Nc(cc1)c2cc1Cl)=O)=C2O)=O NWHXNECRIRBREL-UHFFFAOYSA-N 0.000 description 1
- VPRKSGGDPPUFRZ-UHFFFAOYSA-N CC(c(cc(cc1)Cl)c1NC1=O)=C1[N+]([O-])=O Chemical compound CC(c(cc(cc1)Cl)c1NC1=O)=C1[N+]([O-])=O VPRKSGGDPPUFRZ-UHFFFAOYSA-N 0.000 description 1
- SWOITNLLAAPQKN-GPUBVSRWSA-N CC/C(/C)=N\N(C(C)=Nc1ccc(C)cc11)C1=N Chemical compound CC/C(/C)=N\N(C(C)=Nc1ccc(C)cc11)C1=N SWOITNLLAAPQKN-GPUBVSRWSA-N 0.000 description 1
- KKEWFIGMKJZQCD-UHFFFAOYSA-N CC1N=C(C(N2CCNCC2)=Nc(cc2F)c3cc2F)N3N=C1C Chemical compound CC1N=C(C(N2CCNCC2)=Nc(cc2F)c3cc2F)N3N=C1C KKEWFIGMKJZQCD-UHFFFAOYSA-N 0.000 description 1
- VCGDMLSYJWYDQU-UHFFFAOYSA-N CCC(C(C)CC=C1)C=C2N1c(cc(C)cc1)c1N=C2N1CC(C)(C)NCC1 Chemical compound CCC(C(C)CC=C1)C=C2N1c(cc(C)cc1)c1N=C2N1CC(C)(C)NCC1 VCGDMLSYJWYDQU-UHFFFAOYSA-N 0.000 description 1
- GKUHMZAVXJTWJD-UHFFFAOYSA-N CCC1N=CN(c(cc(c(C(F)(F)F)c2)Cl)c2N=C2N3CCN(C)CC3)C2=C1 Chemical compound CCC1N=CN(c(cc(c(C(F)(F)F)c2)Cl)c2N=C2N3CCN(C)CC3)C2=C1 GKUHMZAVXJTWJD-UHFFFAOYSA-N 0.000 description 1
- FTFFLDGXCGQVQP-UHFFFAOYSA-N CCC1c(c(cc(C)cc2)c2nc2C)c2N=CC1C Chemical compound CCC1c(c(cc(C)cc2)c2nc2C)c2N=CC1C FTFFLDGXCGQVQP-UHFFFAOYSA-N 0.000 description 1
- FDCAQGUVOUYLHS-UHFFFAOYSA-N CCCC#Cc1cc(C)ccc1N Chemical compound CCCC#Cc1cc(C)ccc1N FDCAQGUVOUYLHS-UHFFFAOYSA-N 0.000 description 1
- OWZFULPEVHKEKS-UHFFFAOYSA-N CCOC(C(Cl)=O)=O Chemical compound CCOC(C(Cl)=O)=O OWZFULPEVHKEKS-UHFFFAOYSA-N 0.000 description 1
- YMRRYMMIAFZAGC-UHFFFAOYSA-N CCOC(C1=C(C)C(C)C(C)=NCC1CCc1cc(Cl)ccc1[N+]([O-])=O)=O Chemical compound CCOC(C1=C(C)C(C)C(C)=NCC1CCc1cc(Cl)ccc1[N+]([O-])=O)=O YMRRYMMIAFZAGC-UHFFFAOYSA-N 0.000 description 1
- WCYWWQVINNRZRQ-UHFFFAOYSA-N CN(CC1)CCN1C1=Nc(ccc(OC(F)(F)F)c2)c2N2C1=[N]=C2 Chemical compound CN(CC1)CCN1C1=Nc(ccc(OC(F)(F)F)c2)c2N2C1=[N]=C2 WCYWWQVINNRZRQ-UHFFFAOYSA-N 0.000 description 1
- XZZUEHPJFDGUCZ-UHFFFAOYSA-N CN(CC1)CCN1c(c([o]cc1)c1c1c2)nc1ccc2Cl Chemical compound CN(CC1)CCN1c(c([o]cc1)c1c1c2)nc1ccc2Cl XZZUEHPJFDGUCZ-UHFFFAOYSA-N 0.000 description 1
- SUDLHJZERVBPLV-UHFFFAOYSA-N CNc(c1cc(Cl)ccc1nc1)c1[N+]([O-])=O Chemical compound CNc(c1cc(Cl)ccc1nc1)c1[N+]([O-])=O SUDLHJZERVBPLV-UHFFFAOYSA-N 0.000 description 1
- XQXZKKSAYLUUKE-UHFFFAOYSA-N CNc1c(cc(cc2)Cl)c2ncc1N Chemical compound CNc1c(cc(cc2)Cl)c2ncc1N XQXZKKSAYLUUKE-UHFFFAOYSA-N 0.000 description 1
- CQJSIRUAMPCLBQ-UHFFFAOYSA-N COC(Nc(cc(c(Cl)c1)Cl)c1C#N)=O Chemical compound COC(Nc(cc(c(Cl)c1)Cl)c1C#N)=O CQJSIRUAMPCLBQ-UHFFFAOYSA-N 0.000 description 1
- PEBCCJMBOTZXJF-UHFFFAOYSA-N COC(Nc1ccc(C(F)(F)F)cc1C#N)=O Chemical compound COC(Nc1ccc(C(F)(F)F)cc1C#N)=O PEBCCJMBOTZXJF-UHFFFAOYSA-N 0.000 description 1
- LHZYKEIFFNOIMI-UHFFFAOYSA-N COc1cc(OC)c(CNc(c(cc(cc2)Cl)c2nc2)c2N)cc1 Chemical compound COc1cc(OC)c(CNc(c(cc(cc2)Cl)c2nc2)c2N)cc1 LHZYKEIFFNOIMI-UHFFFAOYSA-N 0.000 description 1
- AQURFXLIZXOCLU-UHFFFAOYSA-N COc1ccc(CNN)cc1 Chemical compound COc1ccc(CNN)cc1 AQURFXLIZXOCLU-UHFFFAOYSA-N 0.000 description 1
- XCUVBHUIUUBVEW-UHFFFAOYSA-N Cc(nc1-c(cc(C(F)(F)F)cc2)c2N2)n[n]1C2=O Chemical compound Cc(nc1-c(cc(C(F)(F)F)cc2)c2N2)n[n]1C2=O XCUVBHUIUUBVEW-UHFFFAOYSA-N 0.000 description 1
- AYWUBZPWLQDASZ-UHFFFAOYSA-N Cc(nc1-c(cc(c(Cl)c2)Cl)c2N2)n[n]1C2=O Chemical compound Cc(nc1-c(cc(c(Cl)c2)Cl)c2N2)n[n]1C2=O AYWUBZPWLQDASZ-UHFFFAOYSA-N 0.000 description 1
- KUWCBLVNOUIWLR-UHFFFAOYSA-N Cc(nc12)n[n]1c(cc(cc1)Cl)c1nc2N1CCNCC1 Chemical compound Cc(nc12)n[n]1c(cc(cc1)Cl)c1nc2N1CCNCC1 KUWCBLVNOUIWLR-UHFFFAOYSA-N 0.000 description 1
- YBWFEYSYILVRJM-UHFFFAOYSA-N Cc1n[n]2c(N3CCN(C)CC3)nc3ccc(C)cc3c2n1 Chemical compound Cc1n[n]2c(N3CCN(C)CC3)nc3ccc(C)cc3c2n1 YBWFEYSYILVRJM-UHFFFAOYSA-N 0.000 description 1
- HORSFVGJZPEWOF-UHFFFAOYSA-N Clc(cc1)cc([n]2c3nnc2)c1nc3C1=CCNCC1 Chemical compound Clc(cc1)cc([n]2c3nnc2)c1nc3C1=CCNCC1 HORSFVGJZPEWOF-UHFFFAOYSA-N 0.000 description 1
- NHWQMJMIYICNBP-UHFFFAOYSA-N N#Cc1ccccc1Cl Chemical compound N#Cc1ccccc1Cl NHWQMJMIYICNBP-UHFFFAOYSA-N 0.000 description 1
- AEXBIMAIMSXSQT-UHFFFAOYSA-N NN(C(Nc1c2cc(C(F)(F)F)cc1)O)C2=N Chemical compound NN(C(Nc1c2cc(C(F)(F)F)cc1)O)C2=N AEXBIMAIMSXSQT-UHFFFAOYSA-N 0.000 description 1
- KRTLKMRDOJTSCS-UHFFFAOYSA-N NNc(c1c2)nc(N3CCNCC3)nc1ccc2Cl Chemical compound NNc(c1c2)nc(N3CCNCC3)nc1ccc2Cl KRTLKMRDOJTSCS-UHFFFAOYSA-N 0.000 description 1
- OERKZOSLSXFLMY-UHFFFAOYSA-N Nc(c(C#N)c1)cc(Cl)c1Cl Chemical compound Nc(c(C#N)c1)cc(Cl)c1Cl OERKZOSLSXFLMY-UHFFFAOYSA-N 0.000 description 1
- PIOKGAUSPFWRMD-UHFFFAOYSA-N Nc(c(N)c1)ccc1OC(F)(F)F Chemical compound Nc(c(N)c1)ccc1OC(F)(F)F PIOKGAUSPFWRMD-UHFFFAOYSA-N 0.000 description 1
- PIVBKAASVHERMS-UHFFFAOYSA-N O=C(C(Nc1c2)=O)Nc1ccc2OC(F)(F)F Chemical compound O=C(C(Nc1c2)=O)Nc1ccc2OC(F)(F)F PIVBKAASVHERMS-UHFFFAOYSA-N 0.000 description 1
- VZDVNLKIWIQTJA-UHFFFAOYSA-N O=C1[n]2nc(C(F)(F)F)nc2-c2cc(C(F)(F)F)ccc2N1 Chemical compound O=C1[n]2nc(C(F)(F)F)nc2-c2cc(C(F)(F)F)ccc2N1 VZDVNLKIWIQTJA-UHFFFAOYSA-N 0.000 description 1
- ZDFBKZUDCQQKAC-UHFFFAOYSA-N [O-][N+](c(cc1)ccc1Br)=O Chemical compound [O-][N+](c(cc1)ccc1Br)=O ZDFBKZUDCQQKAC-UHFFFAOYSA-N 0.000 description 1
- LSMIOKSCDLKEJW-UHFFFAOYSA-N [O-][N+](c(cnc(c1c2)ccc2Cl)c1Cl)=O Chemical compound [O-][N+](c(cnc(c1c2)ccc2Cl)c1Cl)=O LSMIOKSCDLKEJW-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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
-
- 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
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/12—Antidiarrhoeals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/02—Nasal agents, e.g. decongestants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- 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
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/04—Antipruritics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- 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
-
- 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
- A61P21/04—Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/16—Otologicals
-
- 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
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- 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
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/14—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
-
- 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
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Ophthalmology & Optometry (AREA)
- Neurology (AREA)
- Endocrinology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Neurosurgery (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Transplantation (AREA)
- Otolaryngology (AREA)
- Urology & Nephrology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9582608P | 2008-09-10 | 2008-09-10 | |
| US61/095,826 | 2008-09-10 | ||
| US23174909P | 2009-08-06 | 2009-08-06 | |
| US61/231,749 | 2009-08-06 | ||
| PCT/US2009/056519 WO2010030785A2 (en) | 2008-09-10 | 2009-09-10 | Heterocyclic inhibitors of histamine receptors for the treatment of disease |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN102388044A true CN102388044A (zh) | 2012-03-21 |
Family
ID=42005738
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2009801427590A Pending CN102388044A (zh) | 2008-09-10 | 2009-09-10 | 用于治疗疾病的组胺受体的杂环抑制剂 |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US20100120741A1 (enExample) |
| EP (1) | EP2324029A4 (enExample) |
| JP (1) | JP2012502067A (enExample) |
| KR (1) | KR20110095857A (enExample) |
| CN (1) | CN102388044A (enExample) |
| AR (1) | AR073574A1 (enExample) |
| AU (1) | AU2009291719A1 (enExample) |
| CA (1) | CA2735369A1 (enExample) |
| CL (1) | CL2011000431A1 (enExample) |
| MX (1) | MX2011002264A (enExample) |
| RU (1) | RU2011113419A (enExample) |
| TW (1) | TW201024297A (enExample) |
| UY (1) | UY32111A (enExample) |
| WO (1) | WO2010030785A2 (enExample) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105531272A (zh) * | 2013-07-25 | 2016-04-27 | 雅盖隆大学 | 作为5-ht6拮抗剂的吡咯并喹啉衍生物、其制备方法和用途 |
| CN109705141A (zh) * | 2019-02-20 | 2019-05-03 | 苏州大学 | 一种恶唑并喹啉类化合物及其制备方法与应用 |
| WO2019200500A1 (zh) * | 2018-04-15 | 2019-10-24 | 苏州大学张家港工业技术研究院 | 1,2,4-三氮唑及其制备方法 |
| CN116332789A (zh) * | 2023-03-10 | 2023-06-27 | 上海康鹏科技股份有限公司 | 一种4-氨基-2-氟苯甲酰胺的制备方法 |
| CN116969943A (zh) * | 2022-04-28 | 2023-10-31 | 轩竹生物科技股份有限公司 | 三并环类二酰甘油激酶抑制剂及其用途 |
| WO2024027370A1 (zh) * | 2022-08-03 | 2024-02-08 | 上海和誉生物医药科技有限公司 | 一种含氮三稠环prmt5抑制剂,其制备方法和药学上的用途 |
| WO2024067433A1 (zh) * | 2022-09-26 | 2024-04-04 | 上海湃隆生物科技有限公司 | 新型prmt5抑制剂及其应用 |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102004031656A1 (de) * | 2004-06-30 | 2006-01-19 | Merck Patent Gmbh | Tetrahydrochinoline |
| PT2268618E (pt) | 2008-03-03 | 2015-10-12 | Novartis Ag | Compostos e composições moduladores da actividade tlr |
| TWI547522B (zh) | 2009-07-07 | 2016-09-01 | 愛爾康研究有限公司 | 環氧乙烷環氧丁烷嵌段共聚物組成物 |
| SG178552A1 (en) * | 2009-08-26 | 2012-03-29 | Cylene Pharmaceuticals Inc | Condensed quinolines as protein kinase modulators |
| JP2013053070A (ja) * | 2009-11-06 | 2013-03-21 | Takeda Chem Ind Ltd | ジヒドロピロロキノリン誘導体 |
| TW201200518A (en) | 2010-03-10 | 2012-01-01 | Kalypsys Inc | Heterocyclic inhibitors of histamine receptors for the treatment of disease |
| DE102010025786A1 (de) * | 2010-07-01 | 2012-01-05 | Merck Patent Gmbh | Pyrazolochinoline |
| TW201206936A (en) | 2010-07-19 | 2012-02-16 | Alcon Res Ltd | Methods and compositions for the treatment of allergy |
| US9540379B2 (en) | 2011-01-31 | 2017-01-10 | Boehringer Ingelheim International Gmbh | (1,2,4)triazolo[4,3-A]quinoxaline derivatives as inhibitors of phosphodiesterases |
| EP2699572B1 (en) * | 2011-04-21 | 2016-08-10 | Origenis GmbH | Heterocyclic compounds as kinase inhibitors |
| US8859550B2 (en) | 2011-09-12 | 2014-10-14 | Kalypsys, Inc. | Heterocyclic inhibitors of histamine receptors for the treatment of disease |
| PL2760865T3 (pl) * | 2011-09-30 | 2018-12-31 | C&C Research Laboratories | Nowe pochodne heterocykliczne i ich zastosowania |
| AU2012318694B2 (en) * | 2011-10-04 | 2016-12-22 | Janus Biotherapeutics, Inc. | Novel imidazole quinoline-based immune system modulators |
| US20140045856A1 (en) | 2012-07-31 | 2014-02-13 | Boehringer Ingelheim International Gmbh | 4-Methyl-2,3,5,9,9b-pentaaza-cyclopenta[a]naphthalenes |
| WO2014060113A1 (en) * | 2012-10-19 | 2014-04-24 | Origenis Gmbh | Novel kinase inhibitors |
| US9255105B2 (en) * | 2012-12-06 | 2016-02-09 | Enaltec Labs Private Limited | Process of preparing alcaftadine |
| CA2898018C (en) | 2013-02-01 | 2021-02-09 | Wellstat Therapeutics Corporation | Substituted quinolin-4-amine compounds and pharmaceutical compositions thereof having anti-inflammatory, antifungal, antiparasitic and anticancer activity |
| WO2014152029A2 (en) * | 2013-03-15 | 2014-09-25 | Epigenetix, Inc. | Oxazolo[5,4-c]quinolin-2-one compounds as bromodomain inhibitors |
| WO2016200717A1 (en) * | 2015-06-11 | 2016-12-15 | Merck Sharp & Dohme Corp. | Aminopyrazine compounds with a2a antagonist properties |
| WO2018139876A1 (ko) | 2017-01-26 | 2018-08-02 | 동화약품주식회사 | 신규한 [1, 2, 4] 트리아졸로 [4, 3-a]퀴녹살린 유도체, 이의 제조방법 및 이를 유효성분으로 함유하는 bet 단백질 관련 질환의 예방 또는 치료용 약학적 조성물 |
| WO2019177971A1 (en) * | 2018-03-12 | 2019-09-19 | Mavupharma, Inc. | Ectonucleotide pyrophosphatase-phosphodiesterase 1 (enpp-1) inhibitors and uses thereof |
| WO2019206242A1 (zh) * | 2018-04-27 | 2019-10-31 | 北京鼎材科技有限公司 | 有机电致发光材料及器件 |
| TW202021969A (zh) * | 2018-05-31 | 2020-06-16 | 南韓商C&C新藥研究所 | 雜環衍生物及其用途 |
| WO2021098734A1 (zh) * | 2019-11-19 | 2021-05-27 | 南京明德新药研发有限公司 | 作为atm抑制剂的有取代的喹啉吡咯酮类合物及其应用 |
| WO2021150613A1 (en) | 2020-01-20 | 2021-07-29 | Incyte Corporation | Spiro compounds as inhibitors of kras |
| WO2021231526A1 (en) | 2020-05-13 | 2021-11-18 | Incyte Corporation | Fused pyrimidine compounds as kras inhibitors |
| US11999752B2 (en) | 2020-08-28 | 2024-06-04 | Incyte Corporation | Vinyl imidazole compounds as inhibitors of KRAS |
| WO2022072783A1 (en) | 2020-10-02 | 2022-04-07 | Incyte Corporation | Bicyclic dione compounds as inhibitors of kras |
| WO2022204112A1 (en) | 2021-03-22 | 2022-09-29 | Incyte Corporation | Imidazole and triazole kras inhibitors |
| EP4067357A1 (en) * | 2021-03-30 | 2022-10-05 | JW Pharmaceutical Corporation | Novel crystalline form of 1-(8-bromopyrido[2,3-e][1,2,4]triazolo[4,3-a]pyrazin-4-yl)-n-methylazetidin-3-amine hydrogen sulfate monohydrate |
| AU2022306671A1 (en) | 2021-07-07 | 2024-01-25 | Incyte Corporation | Tricyclic compounds as inhibitors of kras |
| JP2024534187A (ja) | 2021-08-31 | 2024-09-18 | インサイト・コーポレイション | Krasの阻害剤としてのナフチリジン化合物 |
| US12030883B2 (en) | 2021-09-21 | 2024-07-09 | Incyte Corporation | Hetero-tricyclic compounds as inhibitors of KRAS |
| CA3234375A1 (en) | 2021-10-01 | 2023-04-06 | Incyte Corporation | Pyrazoloquinoline kras inhibitors |
| PE20242113A1 (es) | 2021-10-14 | 2024-10-28 | Incyte Corp | Compuestos de quinolina como inhibidores de kras |
| WO2024069235A2 (en) | 2022-09-30 | 2024-04-04 | Sixfold Bioscience Ltd. | Compositions containing oligonucleotides with theranostic applications |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4053600A (en) * | 1973-03-08 | 1977-10-11 | Sandoz, Inc. | Tricyclic 1,2,4-triazolo-quinazolines |
| US4495187A (en) * | 1982-10-18 | 1985-01-22 | Pfizer Inc. | Method of using [1,2,4]triazolo[4,3-a]quinoxaline-4-amine derivatives as antidepressant and antifatigue agents |
| IN160956B (enExample) * | 1982-10-18 | 1987-08-22 | Pfizer | |
| CA2310072A1 (en) * | 1997-11-11 | 1999-05-20 | Hiroyuki Ohno | Fused pyrazine compounds |
| AU2002361374A1 (en) * | 2001-12-21 | 2003-07-09 | JSW-Research Forschungslabor GmbH% | Pyrazolyl-substituted triazoloquinoxalines |
| EP2066645A2 (en) * | 2006-09-12 | 2009-06-10 | UCB Pharma S.A. | 2 amino-pyrimidine derivatives as h4 receptor antagonists, processes for preparing them and their use in pharmaceutical compositions |
| EP1972629A1 (en) * | 2007-03-23 | 2008-09-24 | Mutabilis SA | New imidazolo-heteroaryl derivatives with antibacterial properties |
| FR2921927B1 (fr) * | 2007-10-03 | 2012-10-12 | Univ De Montpellier 1 | Imidazo°1,2-a!quinoxalines et derives pour le traitement des cancers |
-
2009
- 2009-09-10 UY UY0001032111A patent/UY32111A/es not_active Application Discontinuation
- 2009-09-10 CN CN2009801427590A patent/CN102388044A/zh active Pending
- 2009-09-10 TW TW098130500A patent/TW201024297A/zh unknown
- 2009-09-10 CA CA2735369A patent/CA2735369A1/en not_active Abandoned
- 2009-09-10 KR KR1020117008096A patent/KR20110095857A/ko not_active Withdrawn
- 2009-09-10 WO PCT/US2009/056519 patent/WO2010030785A2/en not_active Ceased
- 2009-09-10 US US12/556,866 patent/US20100120741A1/en not_active Abandoned
- 2009-09-10 AU AU2009291719A patent/AU2009291719A1/en not_active Abandoned
- 2009-09-10 AR ARP090103487A patent/AR073574A1/es not_active Application Discontinuation
- 2009-09-10 RU RU2011113419/04A patent/RU2011113419A/ru not_active Application Discontinuation
- 2009-09-10 MX MX2011002264A patent/MX2011002264A/es not_active Application Discontinuation
- 2009-09-10 JP JP2011526310A patent/JP2012502067A/ja active Pending
- 2009-09-10 EP EP09813607A patent/EP2324029A4/en not_active Withdrawn
-
2011
- 2011-02-28 CL CL2011000431A patent/CL2011000431A1/es unknown
- 2011-11-21 US US13/301,131 patent/US20120065187A1/en not_active Abandoned
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105531272A (zh) * | 2013-07-25 | 2016-04-27 | 雅盖隆大学 | 作为5-ht6拮抗剂的吡咯并喹啉衍生物、其制备方法和用途 |
| CN105531272B (zh) * | 2013-07-25 | 2017-12-22 | 雅盖隆大学 | 作为5‑ht6拮抗剂的吡咯并喹啉衍生物、其制备方法和用途 |
| WO2019200500A1 (zh) * | 2018-04-15 | 2019-10-24 | 苏州大学张家港工业技术研究院 | 1,2,4-三氮唑及其制备方法 |
| US11072589B2 (en) | 2018-04-15 | 2021-07-27 | Soochow University | 1,2,4-triazole and preparation method therefor |
| CN109705141A (zh) * | 2019-02-20 | 2019-05-03 | 苏州大学 | 一种恶唑并喹啉类化合物及其制备方法与应用 |
| CN116969943A (zh) * | 2022-04-28 | 2023-10-31 | 轩竹生物科技股份有限公司 | 三并环类二酰甘油激酶抑制剂及其用途 |
| WO2024027370A1 (zh) * | 2022-08-03 | 2024-02-08 | 上海和誉生物医药科技有限公司 | 一种含氮三稠环prmt5抑制剂,其制备方法和药学上的用途 |
| WO2024067433A1 (zh) * | 2022-09-26 | 2024-04-04 | 上海湃隆生物科技有限公司 | 新型prmt5抑制剂及其应用 |
| US12173002B2 (en) | 2022-09-26 | 2024-12-24 | Shanghai Apeiron Therapeutics Company Limited | PRMT5 inhibitors and methods of use |
| CN116332789A (zh) * | 2023-03-10 | 2023-06-27 | 上海康鹏科技股份有限公司 | 一种4-氨基-2-氟苯甲酰胺的制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| UY32111A (es) | 2010-04-30 |
| CA2735369A1 (en) | 2010-03-18 |
| AU2009291719A1 (en) | 2010-03-18 |
| CL2011000431A1 (es) | 2012-01-20 |
| MX2011002264A (es) | 2011-05-23 |
| AR073574A1 (es) | 2010-11-17 |
| RU2011113419A (ru) | 2012-10-20 |
| US20120065187A1 (en) | 2012-03-15 |
| US20100120741A1 (en) | 2010-05-13 |
| EP2324029A4 (en) | 2011-09-14 |
| TW201024297A (en) | 2010-07-01 |
| JP2012502067A (ja) | 2012-01-26 |
| EP2324029A2 (en) | 2011-05-25 |
| WO2010030785A2 (en) | 2010-03-18 |
| KR20110095857A (ko) | 2011-08-25 |
| WO2010030785A3 (en) | 2010-07-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN102388044A (zh) | 用于治疗疾病的组胺受体的杂环抑制剂 | |
| CN102869666B (zh) | 用于疾病治疗的组胺受体的杂环抑制剂 | |
| US20110257137A1 (en) | Heterocyclic inhibitors of histamine receptors for the treatment of disease | |
| KR102815607B1 (ko) | 전사 활성화 단백질의 이미다조피페라진 억제제 | |
| CN102186479A (zh) | 用于治疗疾病的组胺受体的氨基嘧啶抑制剂 | |
| CN111433200A (zh) | 用于治疗疾病的新化合物及其药物组合物 | |
| HK1181038B (en) | Tetrazolo[1,5-a]pyrazine compounds as inhibitors of histamine receptors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20120321 |