IL132661A - Agonists specific for peripheral cannabinoid receptors - Google Patents
Agonists specific for peripheral cannabinoid receptorsInfo
- Publication number
- IL132661A IL132661A IL132661A IL13266199A IL132661A IL 132661 A IL132661 A IL 132661A IL 132661 A IL132661 A IL 132661A IL 13266199 A IL13266199 A IL 13266199A IL 132661 A IL132661 A IL 132661A
- Authority
- IL
- Israel
- Prior art keywords
- designates
- hydrogen
- peripheral
- activity
- ch2oh
- Prior art date
Links
- 230000002093 peripheral effect Effects 0.000 title claims abstract description 33
- 102000018208 Cannabinoid Receptor Human genes 0.000 title abstract description 11
- 108050007331 Cannabinoid receptor Proteins 0.000 title abstract description 11
- 239000000556 agonist Substances 0.000 title description 18
- 150000001875 compounds Chemical class 0.000 claims abstract description 23
- 230000036407 pain Effects 0.000 claims abstract description 22
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 13
- 206010061218 Inflammation Diseases 0.000 claims abstract description 9
- 230000004054 inflammatory process Effects 0.000 claims abstract description 9
- 208000018522 Gastrointestinal disease Diseases 0.000 claims abstract description 8
- 206010020772 Hypertension Diseases 0.000 claims abstract description 8
- 238000000034 method Methods 0.000 claims abstract description 7
- 239000004480 active ingredient Substances 0.000 claims abstract description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 31
- 239000001257 hydrogen Substances 0.000 claims description 31
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 26
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- -1 1, 1 -dimethyl heptyl Chemical group 0.000 claims description 7
- 239000003814 drug Substances 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims description 7
- 208000027753 pain disease Diseases 0.000 claims description 7
- 208000027520 Somatoform disease Diseases 0.000 claims description 5
- 150000002431 hydrogen Chemical class 0.000 claims description 5
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 4
- 125000001033 ether group Chemical group 0.000 claims 6
- 230000000694 effects Effects 0.000 abstract description 36
- 241000699670 Mus sp. Species 0.000 abstract description 20
- 230000001404 mediated effect Effects 0.000 abstract description 16
- 208000002193 Pain Diseases 0.000 abstract description 15
- 210000003169 central nervous system Anatomy 0.000 abstract description 14
- 230000036772 blood pressure Effects 0.000 abstract description 12
- CYQFCXCEBYINGO-UHFFFAOYSA-N THC Natural products C1=C(C)CCC2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3C21 CYQFCXCEBYINGO-UHFFFAOYSA-N 0.000 abstract description 11
- 230000003110 anti-inflammatory effect Effects 0.000 abstract description 11
- CYQFCXCEBYINGO-IAGOWNOFSA-N delta1-THC Chemical compound C1=C(C)CC[C@H]2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3[C@@H]21 CYQFCXCEBYINGO-IAGOWNOFSA-N 0.000 abstract description 11
- 229960004242 dronabinol Drugs 0.000 abstract description 9
- 230000000202 analgesic effect Effects 0.000 abstract description 8
- 230000008991 intestinal motility Effects 0.000 abstract description 5
- 238000009227 behaviour therapy Methods 0.000 abstract description 4
- 208000023275 Autoimmune disease Diseases 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- CFMRIVODIXTERW-BHIFYINESA-N [(1r,2r,5r)-2-[2,6-dimethoxy-4-(2-methyloctan-2-yl)phenyl]-6,6-dimethyl-4-bicyclo[3.1.1]hept-3-enyl]methanol Chemical compound COC1=CC(C(C)(C)CCCCCC)=CC(OC)=C1[C@H]1[C@H](C2(C)C)C[C@H]2C(CO)=C1 CFMRIVODIXTERW-BHIFYINESA-N 0.000 description 61
- 102100036214 Cannabinoid receptor 2 Human genes 0.000 description 32
- 229930003827 cannabinoid Natural products 0.000 description 17
- 239000003557 cannabinoid Substances 0.000 description 17
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 16
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 16
- 108010073376 CB2 Cannabinoid Receptor Proteins 0.000 description 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 14
- 239000005557 antagonist Substances 0.000 description 14
- 102000005962 receptors Human genes 0.000 description 14
- 108020003175 receptors Proteins 0.000 description 14
- REOYOKXLUFHOBV-UHFFFAOYSA-N 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-n-piperidin-1-ylpyrazole-3-carboxamide;hydron;chloride Chemical compound Cl.CC=1C(C(=O)NN2CCCCC2)=NN(C=2C(=CC(Cl)=CC=2)Cl)C=1C1=CC=C(Cl)C=C1 REOYOKXLUFHOBV-UHFFFAOYSA-N 0.000 description 13
- 102000009135 CB2 Cannabinoid Receptor Human genes 0.000 description 13
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 description 12
- SUGVYNSRNKFXQM-XRHWURSXSA-N SR 144528 Chemical compound C1=CC(C)=CC=C1CN1C(C=2C=C(C)C(Cl)=CC=2)=CC(C(=O)N[C@@H]2C([C@@H]3CC[C@@]2(C)C3)(C)C)=N1 SUGVYNSRNKFXQM-XRHWURSXSA-N 0.000 description 12
- 241000700159 Rattus Species 0.000 description 11
- 238000007912 intraperitoneal administration Methods 0.000 description 11
- RCRCTBLIHCHWDZ-UHFFFAOYSA-N 2-Arachidonoyl Glycerol Chemical compound CCCCCC=CCC=CCC=CCC=CCCCC(=O)OC(CO)CO RCRCTBLIHCHWDZ-UHFFFAOYSA-N 0.000 description 10
- LGEQQWMQCRIYKG-UHFFFAOYSA-N arachidonic acid ethanolamide Natural products CCCCCC=CCC=CCC=CCC=CCCCC(=O)NCCO LGEQQWMQCRIYKG-UHFFFAOYSA-N 0.000 description 10
- LGEQQWMQCRIYKG-DOFZRALJSA-N anandamide Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)NCCO LGEQQWMQCRIYKG-DOFZRALJSA-N 0.000 description 9
- 229940065144 cannabinoids Drugs 0.000 description 9
- 238000002347 injection Methods 0.000 description 9
- 239000007924 injection Substances 0.000 description 9
- 229940114079 arachidonic acid Drugs 0.000 description 8
- 235000021342 arachidonic acid Nutrition 0.000 description 8
- 238000003556 assay Methods 0.000 description 8
- CGIGDMFJXJATDK-UHFFFAOYSA-N indomethacin Chemical compound CC1=C(CC(O)=O)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 CGIGDMFJXJATDK-UHFFFAOYSA-N 0.000 description 8
- 230000000506 psychotropic effect Effects 0.000 description 8
- 208000001953 Hypotension Diseases 0.000 description 7
- 238000011282 treatment Methods 0.000 description 7
- 206010014025 Ear swelling Diseases 0.000 description 5
- 241000452413 Sabra Species 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 230000001077 hypotensive effect Effects 0.000 description 5
- 230000005764 inhibitory process Effects 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 210000001519 tissue Anatomy 0.000 description 5
- 229940124802 CB1 antagonist Drugs 0.000 description 4
- 229940079593 drug Drugs 0.000 description 4
- 230000036543 hypotension Effects 0.000 description 4
- 229960000905 indomethacin Drugs 0.000 description 4
- 230000000968 intestinal effect Effects 0.000 description 4
- 210000000578 peripheral nerve Anatomy 0.000 description 4
- 238000002560 therapeutic procedure Methods 0.000 description 4
- 208000009132 Catalepsy Diseases 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- 206010047853 Waxy flexibility Diseases 0.000 description 3
- 230000036592 analgesia Effects 0.000 description 3
- 230000003502 anti-nociceptive effect Effects 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 230000013872 defecation Effects 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 230000002550 fecal effect Effects 0.000 description 3
- 230000002496 gastric effect Effects 0.000 description 3
- 210000000548 hind-foot Anatomy 0.000 description 3
- 208000021822 hypotensive Diseases 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 230000000144 pharmacologic effect Effects 0.000 description 3
- 229940044551 receptor antagonist Drugs 0.000 description 3
- 239000002464 receptor antagonist Substances 0.000 description 3
- JZCPYUJPEARBJL-UHFFFAOYSA-N rimonabant Chemical compound CC=1C(C(=O)NN2CCCCC2)=NN(C=2C(=CC(Cl)=CC=2)Cl)C=1C1=CC=C(Cl)C=C1 JZCPYUJPEARBJL-UHFFFAOYSA-N 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 230000024883 vasodilation Effects 0.000 description 3
- KWVPFECTOKLOBL-KTKRTIGZSA-N 2-[(z)-octadec-9-enoxy]ethanol Chemical compound CCCCCCCC\C=C/CCCCCCCCOCCO KWVPFECTOKLOBL-KTKRTIGZSA-N 0.000 description 2
- 102000009132 CB1 Cannabinoid Receptor Human genes 0.000 description 2
- 108010073366 CB1 Cannabinoid Receptor Proteins 0.000 description 2
- 102100033868 Cannabinoid receptor 1 Human genes 0.000 description 2
- XXGMIHXASFDFSM-UHFFFAOYSA-N Delta9-tetrahydrocannabinol Natural products CCCCCc1cc2OC(C)(C)C3CCC(=CC3c2c(O)c1O)C XXGMIHXASFDFSM-UHFFFAOYSA-N 0.000 description 2
- 241000699666 Mus <mouse, genus> Species 0.000 description 2
- 150000001200 N-acyl ethanolamides Chemical class 0.000 description 2
- 208000005141 Otitis Diseases 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 230000036760 body temperature Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 239000002621 endocannabinoid Substances 0.000 description 2
- 210000003038 endothelium Anatomy 0.000 description 2
- 239000002158 endotoxin Substances 0.000 description 2
- 210000002683 foot Anatomy 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 238000001727 in vivo Methods 0.000 description 2
- 210000002540 macrophage Anatomy 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 210000000056 organ Anatomy 0.000 description 2
- HXYVTAGFYLMHSO-UHFFFAOYSA-N palmitoyl ethanolamide Chemical compound CCCCCCCCCCCCCCCC(=O)NCCO HXYVTAGFYLMHSO-UHFFFAOYSA-N 0.000 description 2
- WEXRUCMBJFQVBZ-UHFFFAOYSA-N pentobarbital Chemical compound CCCC(C)C1(CC)C(=O)NC(=O)NC1=O WEXRUCMBJFQVBZ-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 230000000384 rearing effect Effects 0.000 description 2
- 238000012552 review Methods 0.000 description 2
- 229960003015 rimonabant Drugs 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 208000030507 AIDS Diseases 0.000 description 1
- 229940122578 Acetylcholine receptor agonist Drugs 0.000 description 1
- 206010002091 Anaesthesia Diseases 0.000 description 1
- 101150041968 CDC13 gene Proteins 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000008697 Cannabis sativa Nutrition 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- CYQFCXCEBYINGO-DLBZAZTESA-N Dronabinol Natural products C1=C(C)CC[C@H]2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3[C@H]21 CYQFCXCEBYINGO-DLBZAZTESA-N 0.000 description 1
- 240000001307 Myosotis scorpioides Species 0.000 description 1
- 238000003639 Student–Newman–Keuls (SNK) method Methods 0.000 description 1
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 1
- 206010047700 Vomiting Diseases 0.000 description 1
- 230000037005 anaesthesia Effects 0.000 description 1
- 238000000540 analysis of variance Methods 0.000 description 1
- 210000000709 aorta Anatomy 0.000 description 1
- 230000036528 appetite Effects 0.000 description 1
- 235000019789 appetite Nutrition 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 210000003719 b-lymphocyte Anatomy 0.000 description 1
- 230000003542 behavioural effect Effects 0.000 description 1
- 125000001743 benzylic group Chemical group 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 239000003556 cannabinoid 2 receptor agonist Substances 0.000 description 1
- 230000002149 cannabinoid effect Effects 0.000 description 1
- AIXAANGOTKPUOY-UHFFFAOYSA-N carbachol Chemical compound [Cl-].C[N+](C)(C)CCOC(N)=O AIXAANGOTKPUOY-UHFFFAOYSA-N 0.000 description 1
- 229960004484 carbachol Drugs 0.000 description 1
- 230000005792 cardiovascular activity Effects 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000001684 chronic effect Effects 0.000 description 1
- 230000006957 competitive inhibition Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000006806 disease prevention Effects 0.000 description 1
- 238000001647 drug administration Methods 0.000 description 1
- 210000005069 ears Anatomy 0.000 description 1
- 230000002526 effect on cardiovascular system Effects 0.000 description 1
- 210000001105 femoral artery Anatomy 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 230000005176 gastrointestinal motility Effects 0.000 description 1
- 230000002008 hemorrhagic effect Effects 0.000 description 1
- 230000002631 hypothermal effect Effects 0.000 description 1
- 230000036737 immune function Effects 0.000 description 1
- 238000005462 in vivo assay Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 210000004731 jugular vein Anatomy 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 238000000670 ligand binding assay Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000037023 motor activity Effects 0.000 description 1
- 210000002464 muscle smooth vascular Anatomy 0.000 description 1
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 description 1
- 238000001543 one-way ANOVA Methods 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- 229960001412 pentobarbital Drugs 0.000 description 1
- 210000001428 peripheral nervous system Anatomy 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229950010765 pivalate Drugs 0.000 description 1
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
- 239000013612 plasmid Substances 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 238000000159 protein binding assay Methods 0.000 description 1
- 238000001525 receptor binding assay Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 210000001044 sensory neuron Anatomy 0.000 description 1
- 238000012453 sprague-dawley rat model Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000007619 statistical method Methods 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 238000007492 two-way ANOVA Methods 0.000 description 1
- 229940124549 vasodilator Drugs 0.000 description 1
- 239000003071 vasodilator agent Substances 0.000 description 1
- 230000008673 vomiting Effects 0.000 description 1
Classifications
-
- 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
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
-
- 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
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/216—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acids having aromatic rings, e.g. benactizyne, clofibrate
-
- 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
- A61K31/075—Ethers or acetals
- A61K31/085—Ethers or acetals having an ether linkage to aromatic ring nuclear carbon
- A61K31/09—Ethers or acetals having an ether linkage to aromatic ring nuclear carbon having two or more such linkages
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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
- A61P35/00—Antineoplastic agents
-
- 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
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
Priority Applications (16)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IL132661A IL132661A (en) | 1999-10-31 | 1999-10-31 | Agonists specific for peripheral cannabinoid receptors |
| EP00974023A EP1244440B1 (en) | 1999-10-31 | 2000-10-30 | Agonists specific for the peripheral cannabinoid receptor |
| CA002385928A CA2385928A1 (en) | 1999-10-31 | 2000-10-30 | Agonists specific for the peripheral cannabinoid receptor |
| HU0203681A HUP0203681A3 (en) | 1999-10-31 | 2000-10-30 | Pharmaceutical compositions containing agonists specific for the peripheral cannabinoid receptor and their use |
| PCT/US2000/029903 WO2001032169A1 (en) | 1999-10-31 | 2000-10-30 | Agonists specific for the peripheral cannabinoid receptor |
| NZ518054A NZ518054A (en) | 1999-10-31 | 2000-10-30 | Agonists specific for the peripheral cannabinoid receptor |
| JP2001534374A JP4231906B2 (ja) | 1999-10-31 | 2000-10-30 | 末梢カンナビノイド受容体に特異的なアゴニスト |
| US09/698,071 US6864291B1 (en) | 1999-10-31 | 2000-10-30 | Agonists specific for the peripheral cannabinoid receptor |
| KR1020027005566A KR100770695B1 (ko) | 1999-10-31 | 2000-10-30 | 말초 카나비노이드 수용체 특이적 아고니스트 |
| DE60017287T DE60017287T2 (de) | 1999-10-31 | 2000-10-30 | Spezifische Agonisten für periphere Cannabinoid-Rezeptoren |
| AT00974023T ATE286389T1 (de) | 1999-10-31 | 2000-10-30 | Spezifische anonisten für peripherische cannabinoid-rezeptoren |
| AU12458/01A AU778149B2 (en) | 1999-10-31 | 2000-10-30 | Agonists specific for the peripheral cannabinoid receptor |
| ZA200202181A ZA200202181B (en) | 1999-10-31 | 2002-03-18 | Agonists specific for the peripheral cannabinoid receptor. |
| IL148796A IL148796A (en) | 1999-10-31 | 2002-03-20 | Use of cannabinoid-specific agonist-specific agonists for the preparation of drugs against autoimmune diseases and cancers |
| US10/133,153 US6903137B2 (en) | 1999-10-31 | 2002-04-26 | Agonists specific for the peripheral cannabinoid receptor |
| US11/043,089 US7214716B2 (en) | 1999-10-31 | 2005-01-27 | Agonists specific for the peripheral cannabinoid receptor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IL132661A IL132661A (en) | 1999-10-31 | 1999-10-31 | Agonists specific for peripheral cannabinoid receptors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL132661A0 IL132661A0 (en) | 2001-03-19 |
| IL132661A true IL132661A (en) | 2008-11-26 |
Family
ID=11073405
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL132661A IL132661A (en) | 1999-10-31 | 1999-10-31 | Agonists specific for peripheral cannabinoid receptors |
| IL148796A IL148796A (en) | 1999-10-31 | 2002-03-20 | Use of cannabinoid-specific agonist-specific agonists for the preparation of drugs against autoimmune diseases and cancers |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL148796A IL148796A (en) | 1999-10-31 | 2002-03-20 | Use of cannabinoid-specific agonist-specific agonists for the preparation of drugs against autoimmune diseases and cancers |
Country Status (13)
Families Citing this family (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6342611B1 (en) * | 1997-10-10 | 2002-01-29 | Cytovia, Inc. | Fluorogenic or fluorescent reporter molecules and their applications for whole-cell fluorescence screening assays for capsases and other enzymes and the use thereof |
| ATE247097T1 (de) | 1998-05-04 | 2003-08-15 | Univ Connecticut | Analgetische und immunomodulierende cannabinoiden |
| US7897598B2 (en) * | 1998-06-09 | 2011-03-01 | Alexandros Makriyannis | Inhibitors of the anandamide transporter |
| US7589220B2 (en) * | 1998-06-09 | 2009-09-15 | University Of Connecticut | Inhibitors of the anandamide transporter |
| US7276613B1 (en) | 1998-11-24 | 2007-10-02 | University Of Connecticut | Retro-anandamides, high affinity and stability cannabinoid receptor ligands |
| US7161016B1 (en) | 1998-11-24 | 2007-01-09 | University Of Connecticut | Cannabimimetic lipid amides as useful medications |
| US7119108B1 (en) | 1999-10-18 | 2006-10-10 | University Of Connecticut | Pyrazole derivatives as cannabinoid receptor antagonists |
| MXPA02005103A (es) | 1999-10-18 | 2003-09-25 | Alexipharma Inc | Ligandos selectivos del receptor de canabinoide (cb2) perifericos. |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| IL55274A (en) | 1978-08-02 | 1982-08-31 | Yissum Res Dev Co | 4-(2,6-dihydroxy-4-(dimethylheptyl)phenyl)substituted 2-pinen-10-ol and pinane derivatives,their preparation and pharmaceutical compositions comprising them |
| US5434295A (en) * | 1994-02-07 | 1995-07-18 | Yissum Research Development Company | Neuroprotective pharmaceutical compositions of 4-phenylpinene derivatives and certain novel 4-phenylpinene compounds |
| FR2735774B1 (fr) | 1995-06-21 | 1997-09-12 | Sanofi Sa | Utilisation de composes agonistes du recepteur cb2 humain pour la preparation de medicaments immunomodulateurs, nouveaux composes agonistes du recepteur cb2 et les compositions pharmaceutiques les contenant |
| IL132661A (en) * | 1999-10-31 | 2008-11-26 | Raphael Mechoulam | Agonists specific for peripheral cannabinoid receptors |
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- 2000-10-30 WO PCT/US2000/029903 patent/WO2001032169A1/en active IP Right Grant
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| HUP0203681A3 (en) | 2003-05-28 |
| AU1245801A (en) | 2001-05-14 |
| US7214716B2 (en) | 2007-05-08 |
| EP1244440A4 (en) | 2003-05-14 |
| HUP0203681A2 (hu) | 2003-04-28 |
| WO2001032169A1 (en) | 2001-05-10 |
| JP4231906B2 (ja) | 2009-03-04 |
| AU778149B2 (en) | 2004-11-18 |
| US20050165118A1 (en) | 2005-07-28 |
| JP2004505006A (ja) | 2004-02-19 |
| US6903137B2 (en) | 2005-06-07 |
| EP1244440A1 (en) | 2002-10-02 |
| ZA200202181B (en) | 2003-05-28 |
| EP1244440B1 (en) | 2005-01-05 |
| US20020173528A1 (en) | 2002-11-21 |
| KR100770695B1 (ko) | 2007-10-29 |
| IL148796A (en) | 2008-11-26 |
| DE60017287D1 (de) | 2005-02-10 |
| IL132661A0 (en) | 2001-03-19 |
| US6864291B1 (en) | 2005-03-08 |
| CA2385928A1 (en) | 2001-05-10 |
| ATE286389T1 (de) | 2005-01-15 |
| DE60017287T2 (de) | 2005-12-08 |
| KR20030008208A (ko) | 2003-01-24 |
| NZ518054A (en) | 2003-10-31 |
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