CY1109108T1 - Η χρηση ανταγωνιστων υποδοχεα ισταμινης για την ελαττωση της ενδοκρανιακης πιεσης - Google Patents
Η χρηση ανταγωνιστων υποδοχεα ισταμινης για την ελαττωση της ενδοκρανιακης πιεσηςInfo
- Publication number
- CY1109108T1 CY1109108T1 CY20091100559T CY091100559T CY1109108T1 CY 1109108 T1 CY1109108 T1 CY 1109108T1 CY 20091100559 T CY20091100559 T CY 20091100559T CY 091100559 T CY091100559 T CY 091100559T CY 1109108 T1 CY1109108 T1 CY 1109108T1
- Authority
- CY
- Cyprus
- Prior art keywords
- cinnarine
- injury
- intracranial pressure
- histamin
- competitive
- Prior art date
Links
- 230000002860 competitive effect Effects 0.000 title 1
- ZZHLYYDVIOPZBE-UHFFFAOYSA-N Trimeprazine Chemical compound C1=CC=C2N(CC(CN(C)C)C)C3=CC=CC=C3SC2=C1 ZZHLYYDVIOPZBE-UHFFFAOYSA-N 0.000 abstract 4
- 208000014674 injury Diseases 0.000 abstract 3
- 208000027418 Wounds and injury Diseases 0.000 abstract 2
- 229960003790 alimemazine Drugs 0.000 abstract 2
- 239000000739 antihistaminic agent Substances 0.000 abstract 2
- 230000006378 damage Effects 0.000 abstract 2
- QTQPVLDZQVPLGV-UHFFFAOYSA-N oxomemazine Chemical compound C1=CC=C2N(CC(CN(C)C)C)C3=CC=CC=C3S(=O)(=O)C2=C1 QTQPVLDZQVPLGV-UHFFFAOYSA-N 0.000 abstract 2
- WFNAKBGANONZEQ-UHFFFAOYSA-N 1-[(4-chlorophenyl)-phenylmethyl]-4-methylpiperazine Chemical compound C1CN(C)CCN1C(C=1C=CC(Cl)=CC=1)C1=CC=CC=C1 WFNAKBGANONZEQ-UHFFFAOYSA-N 0.000 abstract 1
- SFOVDSLXFUGAIV-UHFFFAOYSA-N 1-[(4-fluorophenyl)methyl]-n-piperidin-4-ylbenzimidazol-2-amine Chemical compound C1=CC(F)=CC=C1CN1C2=CC=CC=C2N=C1NC1CCNCC1 SFOVDSLXFUGAIV-UHFFFAOYSA-N 0.000 abstract 1
- YDDXVAXDYKBWDX-UHFFFAOYSA-N 1-cyano-3-[2-[[2-(diaminomethylideneamino)-4-thiazolyl]methylthio]ethyl]-2-methylguanidine Chemical compound N#CNC(=NC)NCCSCC1=CSC(N=C(N)N)=N1 YDDXVAXDYKBWDX-UHFFFAOYSA-N 0.000 abstract 1
- BAWMMJAUVBLLEE-UHFFFAOYSA-N 2-[2-[4-[bis(4-fluorophenyl)methyl]piperazin-1-yl]ethoxy]acetic acid Chemical compound C1CN(CCOCC(=O)O)CCN1C(C=1C=CC(F)=CC=1)C1=CC=C(F)C=C1 BAWMMJAUVBLLEE-UHFFFAOYSA-N 0.000 abstract 1
- VNIOQSAWKLOGLY-UHFFFAOYSA-N 3-[(5-methylfuran-2-yl)methyl]-n-piperidin-4-ylimidazo[4,5-b]pyridin-2-amine Chemical compound O1C(C)=CC=C1CN1C2=NC=CC=C2N=C1NC1CCNCC1 VNIOQSAWKLOGLY-UHFFFAOYSA-N 0.000 abstract 1
- USCSJAIWXWYTEH-UHFFFAOYSA-N 7-[3-[4-[(4-chlorophenyl)methyl]piperazin-1-yl]propoxy]-3,4-dimethylchromen-2-one Chemical compound C1=CC=2C(C)=C(C)C(=O)OC=2C=C1OCCCN(CC1)CCN1CC1=CC=C(Cl)C=C1 USCSJAIWXWYTEH-UHFFFAOYSA-N 0.000 abstract 1
- MBUVEWMHONZEQD-UHFFFAOYSA-N Azeptin Chemical compound C1CN(C)CCCC1N1C(=O)C2=CC=CC=C2C(CC=2C=CC(Cl)=CC=2)=N1 MBUVEWMHONZEQD-UHFFFAOYSA-N 0.000 abstract 1
- ZKLPARSLTMPFCP-UHFFFAOYSA-N Cetirizine Chemical compound C1CN(CCOCC(=O)O)CCN1C(C=1C=CC(Cl)=CC=1)C1=CC=CC=C1 ZKLPARSLTMPFCP-UHFFFAOYSA-N 0.000 abstract 1
- 229940122236 Histamine receptor antagonist Drugs 0.000 abstract 1
- 206010022773 Intracranial pressure increased Diseases 0.000 abstract 1
- PWWVAXIEGOYWEE-UHFFFAOYSA-N Isophenergan Chemical compound C1=CC=C2N(CC(C)N(C)C)C3=CC=CC=C3SC2=C1 PWWVAXIEGOYWEE-UHFFFAOYSA-N 0.000 abstract 1
- ZCVMWBYGMWKGHF-UHFFFAOYSA-N Ketotifene Chemical compound C1CN(C)CCC1=C1C2=CC=CC=C2CC(=O)C2=C1C=CS2 ZCVMWBYGMWKGHF-UHFFFAOYSA-N 0.000 abstract 1
- OCJYIGYOJCODJL-UHFFFAOYSA-N Meclizine Chemical compound CC1=CC=CC(CN2CCN(CC2)C(C=2C=CC=CC=2)C=2C=CC(Cl)=CC=2)=C1 OCJYIGYOJCODJL-UHFFFAOYSA-N 0.000 abstract 1
- HOKDBMAJZXIPGC-UHFFFAOYSA-N Mequitazine Chemical compound C12=CC=CC=C2SC2=CC=CC=C2N1CC1C(CC2)CCN2C1 HOKDBMAJZXIPGC-UHFFFAOYSA-N 0.000 abstract 1
- UEQUQVLFIPOEMF-UHFFFAOYSA-N Mianserin Chemical compound C1C2=CC=CC=C2N2CCN(C)CC2C2=CC=CC=C21 UEQUQVLFIPOEMF-UHFFFAOYSA-N 0.000 abstract 1
- PVLJETXTTWAYEW-UHFFFAOYSA-N Mizolastine Chemical compound N=1C=CC(=O)NC=1N(C)C(CC1)CCN1C1=NC2=CC=CC=C2N1CC1=CC=C(F)C=C1 PVLJETXTTWAYEW-UHFFFAOYSA-N 0.000 abstract 1
- IJHNSHDBIRRJRN-UHFFFAOYSA-N N,N-dimethyl-3-phenyl-3-(2-pyridinyl)-1-propanamine Chemical compound C=1C=CC=NC=1C(CCN(C)C)C1=CC=CC=C1 IJHNSHDBIRRJRN-UHFFFAOYSA-N 0.000 abstract 1
- KUBONGDXTUOOLM-UHFFFAOYSA-N N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]-1,3-benzothiazol-2-amine Chemical compound N=1C2=CC=CC=C2SC=1NCCCOC(C=1)=CC=CC=1CN1CCCCC1 KUBONGDXTUOOLM-UHFFFAOYSA-N 0.000 abstract 1
- JAUOIFJMECXRGI-UHFFFAOYSA-N Neoclaritin Chemical compound C=1C(Cl)=CC=C2C=1CCC1=CC=CN=C1C2=C1CCNCC1 JAUOIFJMECXRGI-UHFFFAOYSA-N 0.000 abstract 1
- OGEAASSLWZDQBM-UHFFFAOYSA-N Temelastine Chemical compound C1=NC(C)=CC=C1CC(C(N1)=O)=CN=C1NCCCCC1=NC=C(Br)C=C1C OGEAASSLWZDQBM-UHFFFAOYSA-N 0.000 abstract 1
- GUGOEEXESWIERI-UHFFFAOYSA-N Terfenadine Chemical compound C1=CC(C(C)(C)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 GUGOEEXESWIERI-UHFFFAOYSA-N 0.000 abstract 1
- UFLGIAIHIAPJJC-UHFFFAOYSA-N Tripelennamine Chemical compound C=1C=CC=NC=1N(CCN(C)C)CC1=CC=CC=C1 UFLGIAIHIAPJJC-UHFFFAOYSA-N 0.000 abstract 1
- 229960003792 acrivastine Drugs 0.000 abstract 1
- PWACSDKDOHSSQD-IUTFFREVSA-N acrivastine Chemical compound C1=CC(C)=CC=C1C(\C=1N=C(\C=C\C(O)=O)C=CC=1)=C/CN1CCCC1 PWACSDKDOHSSQD-IUTFFREVSA-N 0.000 abstract 1
- 229960002469 antazoline Drugs 0.000 abstract 1
- REYFJDPCWQRWAA-UHFFFAOYSA-N antazoline Chemical compound N=1CCNC=1CN(C=1C=CC=CC=1)CC1=CC=CC=C1 REYFJDPCWQRWAA-UHFFFAOYSA-N 0.000 abstract 1
- GXDALQBWZGODGZ-UHFFFAOYSA-N astemizole Chemical compound C1=CC(OC)=CC=C1CCN1CCC(NC=2N(C3=CC=CC=C3N=2)CC=2C=CC(F)=CC=2)CC1 GXDALQBWZGODGZ-UHFFFAOYSA-N 0.000 abstract 1
- 229960000383 azatadine Drugs 0.000 abstract 1
- SEBMTIQKRHYNIT-UHFFFAOYSA-N azatadine Chemical compound C1CN(C)CCC1=C1C2=NC=CC=C2CCC2=CC=CC=C21 SEBMTIQKRHYNIT-UHFFFAOYSA-N 0.000 abstract 1
- 229960004574 azelastine Drugs 0.000 abstract 1
- 229960000725 brompheniramine Drugs 0.000 abstract 1
- ZDIGNSYAACHWNL-UHFFFAOYSA-N brompheniramine Chemical compound C=1C=CC=NC=1C(CCN(C)C)C1=CC=C(Br)C=C1 ZDIGNSYAACHWNL-UHFFFAOYSA-N 0.000 abstract 1
- 229960001705 buclizine Drugs 0.000 abstract 1
- MOYGZHXDRJNJEP-UHFFFAOYSA-N buclizine Chemical compound C1=CC(C(C)(C)C)=CC=C1CN1CCN(C(C=2C=CC=CC=2)C=2C=CC(Cl)=CC=2)CC1 MOYGZHXDRJNJEP-UHFFFAOYSA-N 0.000 abstract 1
- 229960000428 carbinoxamine Drugs 0.000 abstract 1
- OJFSXZCBGQGRNV-UHFFFAOYSA-N carbinoxamine Chemical compound C=1C=CC=NC=1C(OCCN(C)C)C1=CC=C(Cl)C=C1 OJFSXZCBGQGRNV-UHFFFAOYSA-N 0.000 abstract 1
- 229950010123 carebastine Drugs 0.000 abstract 1
- XGHOVGYJHWQGCC-UHFFFAOYSA-N carebastine Chemical compound C1=CC(C(C)(C(O)=O)C)=CC=C1C(=O)CCCN1CCC(OC(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 XGHOVGYJHWQGCC-UHFFFAOYSA-N 0.000 abstract 1
- 229960001803 cetirizine Drugs 0.000 abstract 1
- 229960004831 chlorcyclizine Drugs 0.000 abstract 1
- 229960001380 cimetidine Drugs 0.000 abstract 1
- CCGSUNCLSOWKJO-UHFFFAOYSA-N cimetidine Chemical compound N#CNC(=N/C)\NCCSCC1=NC=N[C]1C CCGSUNCLSOWKJO-UHFFFAOYSA-N 0.000 abstract 1
- 229960001271 desloratadine Drugs 0.000 abstract 1
- SOYKEARSMXGVTM-HNNXBMFYSA-N dexchlorpheniramine Chemical compound C1([C@H](CCN(C)C)C=2N=CC=CC=2)=CC=C(Cl)C=C1 SOYKEARSMXGVTM-HNNXBMFYSA-N 0.000 abstract 1
- 229960001882 dexchlorpheniramine Drugs 0.000 abstract 1
- 229960004993 dimenhydrinate Drugs 0.000 abstract 1
- MZDOIJOUFRQXHC-UHFFFAOYSA-N dimenhydrinate Chemical compound O=C1N(C)C(=O)N(C)C2=NC(Cl)=N[C]21.C=1C=CC=CC=1C(OCCN(C)C)C1=CC=CC=C1 MZDOIJOUFRQXHC-UHFFFAOYSA-N 0.000 abstract 1
- 229960001992 dimetindene Drugs 0.000 abstract 1
- MVMQESMQSYOVGV-UHFFFAOYSA-N dimetindene Chemical compound CN(C)CCC=1CC2=CC=CC=C2C=1C(C)C1=CC=CC=N1 MVMQESMQSYOVGV-UHFFFAOYSA-N 0.000 abstract 1
- 229960001640 dimetotiazine Drugs 0.000 abstract 1
- VWNWVCJGUMZDIU-UHFFFAOYSA-N dimetotiazine Chemical compound C1=C(S(=O)(=O)N(C)C)C=C2N(CC(C)N(C)C)C3=CC=CC=C3SC2=C1 VWNWVCJGUMZDIU-UHFFFAOYSA-N 0.000 abstract 1
- 229960000520 diphenhydramine Drugs 0.000 abstract 1
- ZZVUWRFHKOJYTH-UHFFFAOYSA-N diphenhydramine Chemical compound C=1C=CC=CC=1C(OCCN(C)C)C1=CC=CC=C1 ZZVUWRFHKOJYTH-UHFFFAOYSA-N 0.000 abstract 1
- OWQUZNMMYNAXSL-UHFFFAOYSA-N diphenylpyraline Chemical compound C1CN(C)CCC1OC(C=1C=CC=CC=1)C1=CC=CC=C1 OWQUZNMMYNAXSL-UHFFFAOYSA-N 0.000 abstract 1
- 229960000879 diphenylpyraline Drugs 0.000 abstract 1
- HCFDWZZGGLSKEP-UHFFFAOYSA-N doxylamine Chemical compound C=1C=CC=NC=1C(C)(OCCN(C)C)C1=CC=CC=C1 HCFDWZZGGLSKEP-UHFFFAOYSA-N 0.000 abstract 1
- 229960005178 doxylamine Drugs 0.000 abstract 1
- 229960001971 ebastine Drugs 0.000 abstract 1
- MJJALKDDGIKVBE-UHFFFAOYSA-N ebastine Chemical compound C1=CC(C(C)(C)C)=CC=C1C(=O)CCCN1CCC(OC(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 MJJALKDDGIKVBE-UHFFFAOYSA-N 0.000 abstract 1
- 229950003420 efletirizine Drugs 0.000 abstract 1
- 229960003449 epinastine Drugs 0.000 abstract 1
- WHWZLSFABNNENI-UHFFFAOYSA-N epinastine Chemical compound C1C2=CC=CC=C2C2CN=C(N)N2C2=CC=CC=C21 WHWZLSFABNNENI-UHFFFAOYSA-N 0.000 abstract 1
- XUFQPHANEAPEMJ-UHFFFAOYSA-N famotidine Chemical compound NC(N)=NC1=NC(CSCCC(N)=NS(N)(=O)=O)=CS1 XUFQPHANEAPEMJ-UHFFFAOYSA-N 0.000 abstract 1
- 229960001596 famotidine Drugs 0.000 abstract 1
- 229960003592 fexofenadine Drugs 0.000 abstract 1
- RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical compound C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 abstract 1
- 229960000930 hydroxyzine Drugs 0.000 abstract 1
- ZQDWXGKKHFNSQK-UHFFFAOYSA-N hydroxyzine Chemical compound C1CN(CCOCCO)CCN1C(C=1C=CC(Cl)=CC=1)C1=CC=CC=C1 ZQDWXGKKHFNSQK-UHFFFAOYSA-N 0.000 abstract 1
- 238000007917 intracranial administration Methods 0.000 abstract 1
- 208000028867 ischemia Diseases 0.000 abstract 1
- 229960004958 ketotifen Drugs 0.000 abstract 1
- 229960001120 levocabastine Drugs 0.000 abstract 1
- ZCGOMHNNNFPNMX-KYTRFIICSA-N levocabastine Chemical compound C1([C@@]2(C(O)=O)CCN(C[C@H]2C)[C@@H]2CC[C@@](CC2)(C#N)C=2C=CC(F)=CC=2)=CC=CC=C1 ZCGOMHNNNFPNMX-KYTRFIICSA-N 0.000 abstract 1
- 229960003088 loratadine Drugs 0.000 abstract 1
- JCCNYMKQOSZNPW-UHFFFAOYSA-N loratadine Chemical compound C1CN(C(=O)OCC)CCC1=C1C2=NC=CC=C2CCC2=CC(Cl)=CC=C21 JCCNYMKQOSZNPW-UHFFFAOYSA-N 0.000 abstract 1
- 229960001474 meclozine Drugs 0.000 abstract 1
- 229960000582 mepyramine Drugs 0.000 abstract 1
- YECBIJXISLIIDS-UHFFFAOYSA-N mepyramine Chemical compound C1=CC(OC)=CC=C1CN(CCN(C)C)C1=CC=CC=N1 YECBIJXISLIIDS-UHFFFAOYSA-N 0.000 abstract 1
- 229960005042 mequitazine Drugs 0.000 abstract 1
- HTMIBDQKFHUPSX-UHFFFAOYSA-N methdilazine Chemical compound C1N(C)CCC1CN1C2=CC=CC=C2SC2=CC=CC=C21 HTMIBDQKFHUPSX-UHFFFAOYSA-N 0.000 abstract 1
- 229960004056 methdilazine Drugs 0.000 abstract 1
- 229960003955 mianserin Drugs 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229960001144 mizolastine Drugs 0.000 abstract 1
- RSKQGBFMNPDPLR-UHFFFAOYSA-N niaprazine Chemical compound C=1C=CN=CC=1C(=O)NC(C)CCN(CC1)CCN1C1=CC=C(F)C=C1 RSKQGBFMNPDPLR-UHFFFAOYSA-N 0.000 abstract 1
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- SGXXNSQHWDMGGP-IZZDOVSWSA-N nizatidine Chemical compound [O-][N+](=O)\C=C(/NC)NCCSCC1=CSC(CN(C)C)=N1 SGXXNSQHWDMGGP-IZZDOVSWSA-N 0.000 abstract 1
- 229950009470 noberastine Drugs 0.000 abstract 1
- BAINIUMDFURPJM-UHFFFAOYSA-N oxatomide Chemical compound O=C1NC2=CC=CC=C2N1CCCN(CC1)CCN1C(C=1C=CC=CC=1)C1=CC=CC=C1 BAINIUMDFURPJM-UHFFFAOYSA-N 0.000 abstract 1
- 229960002698 oxatomide Drugs 0.000 abstract 1
- 229960003045 oxomemazine Drugs 0.000 abstract 1
- CHOBRHHOYQKCOU-UHFFFAOYSA-N phenbenzamine Chemical compound C=1C=CC=CC=1N(CCN(C)C)CC1=CC=CC=C1 CHOBRHHOYQKCOU-UHFFFAOYSA-N 0.000 abstract 1
- 229950003863 phenbenzamine Drugs 0.000 abstract 1
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- 229950010674 picumast Drugs 0.000 abstract 1
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- 229960000620 ranitidine Drugs 0.000 abstract 1
- VMXUWOKSQNHOCA-LCYFTJDESA-N ranitidine Chemical compound [O-][N+](=O)/C=C(/NC)NCCSCC1=CC=C(CN(C)C)O1 VMXUWOKSQNHOCA-LCYFTJDESA-N 0.000 abstract 1
- JUQLTPCYUFPYKE-UHFFFAOYSA-N ritanserin Chemical compound CC=1N=C2SC=CN2C(=O)C=1CCN(CC1)CCC1=C(C=1C=CC(F)=CC=1)C1=CC=C(F)C=C1 JUQLTPCYUFPYKE-UHFFFAOYSA-N 0.000 abstract 1
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- 229950011533 tiotidine Drugs 0.000 abstract 1
- 230000000472 traumatic effect Effects 0.000 abstract 1
- 230000008736 traumatic injury Effects 0.000 abstract 1
- 229960003223 tripelennamine Drugs 0.000 abstract 1
- 229960001128 triprolidine Drugs 0.000 abstract 1
- CBEQULMOCCWAQT-WOJGMQOQSA-N triprolidine Chemical compound C1=CC(C)=CC=C1C(\C=1N=CC=CC=1)=C/CN1CCCC1 CBEQULMOCCWAQT-WOJGMQOQSA-N 0.000 abstract 1
Classifications
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- 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
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- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
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- A61P9/12—Antihypertensives
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- C—CHEMISTRY; METALLURGY
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- 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
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- 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
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Abstract
Η εφεύρεση αφορά στη χρήση ενός ανταγωνιστή υποδοχέα HI- και/ή Η2-ισταμίνης για την μείωση της ενδοκρανιακής πίεσης (ICP), ιδιαίτερα για την πρόληψη και αντιμετώπιση της αυξημένης ενδοκρανιακής πίεσης και/ή της δευτερογενούς ισχαιμίας, που ιδιαίτερα προκαλείται από κρανιακό τραυματισμό, που ειδικότερα προκαλείται από τραυματικό (TBI) και μη-τραυματικό κρανιακό τραυματισμό. Συγκεκριμένα, ο ανταγωνιστής ισταμίνης επιλέγεται από την ομάδα των acrivastine, alimemazine, antazoline, astemizole, azatadine, azelastine, brompheniramine, buclizine, carbinoxamine, carebastine, cetirizine, chlorcyclizine, chlorpheniramine, cinnarizine, clemastine, clemizole, clocinizine, clonidine, cyclizine, cyproheptadine, descarboethoxyloratidine, dexchlorpheniramine, dimenhydrinate, dimethindene, dimethothiazine, diphenhydramine, diphenylpyraline, doxylamine, ebastine, efletirizine, epinastine, fexofenadine, hydroxyzine, ketotifen, levocabastine, loratidine, meclizine, mequitazine, methdilazine, mianserin, mizolastine, niaprazine, noberastine, norastemizole, oxatomide, oxomemazine, phenbenzamine, pheniramine, picumast, promethazine, pyrilamine, temelastine, terfenadine, trimeprazine, tripelennamine, triprolidine, ranitidine, cimetidine, famotidine, nizatidine, tiotidine, zolantidine, ritanserine, και παράγωγα αυτών και μίγματα οποιωνδήποτε δύο ή περισσοτέρων από τα προηγούμενα.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP01204574 | 2001-11-23 | ||
| EP07107669A EP1832287B1 (en) | 2001-11-23 | 2002-11-22 | The use of histamine receptor antagonists for the reduction of intracranial pressure |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CY1109108T1 true CY1109108T1 (el) | 2014-07-02 |
Family
ID=8181317
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CY20071101471T CY1107472T1 (el) | 2001-11-23 | 2007-11-14 | Η χρηση παραγωγων υποκατεστημενης τετρακυκλικης ιμιδαζολης ως αντιισταμινικων |
| CY20091100559T CY1109108T1 (el) | 2001-11-23 | 2009-05-25 | Η χρηση ανταγωνιστων υποδοχεα ισταμινης για την ελαττωση της ενδοκρανιακης πιεσης |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CY20071101471T CY1107472T1 (el) | 2001-11-23 | 2007-11-14 | Η χρηση παραγωγων υποκατεστημενης τετρακυκλικης ιμιδαζολης ως αντιισταμινικων |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US7732437B2 (el) |
| EP (2) | EP1451196B1 (el) |
| JP (2) | JP4505226B2 (el) |
| KR (1) | KR100967601B1 (el) |
| CN (2) | CN100478031C (el) |
| AT (2) | ATE423599T1 (el) |
| AU (1) | AU2002356715B2 (el) |
| CA (2) | CA2467097C (el) |
| CY (2) | CY1107472T1 (el) |
| DE (2) | DE60231351D1 (el) |
| DK (2) | DK1832287T3 (el) |
| ES (2) | ES2290364T3 (el) |
| HK (2) | HK1073309A1 (el) |
| HR (1) | HRP20040427B1 (el) |
| HU (1) | HU229118B1 (el) |
| IL (4) | IL162109A0 (el) |
| MX (1) | MXPA04004867A (el) |
| NO (1) | NO333656B1 (el) |
| NZ (2) | NZ532718A (el) |
| PL (1) | PL209953B1 (el) |
| PT (2) | PT1832287E (el) |
| RU (1) | RU2311418C2 (el) |
| SI (2) | SI1451196T1 (el) |
| UA (1) | UA76803C2 (el) |
| WO (1) | WO2003044023A1 (el) |
| ZA (1) | ZA200403923B (el) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MXPA04004867A (es) | 2001-11-23 | 2004-07-30 | Janssen Pharmaceutica Nv | El uso de antihistaminicos para la reduccion aguda de presion intracraneal elevada. |
| TWI290140B (en) * | 2003-08-25 | 2007-11-21 | Schering Corp | 2-Substituted benzimidazole derivatives as selective melanin concentrating hormone receptor antagonists for thr treatment of obesity and related disorders |
| EP2796683A4 (en) * | 2011-12-20 | 2015-05-20 | Toyota Motor Co Ltd | ERROR DETECTION DEVICE FOR AN ELECTRICALLY HEATABLE CATALYST |
| US9717726B2 (en) | 2013-03-14 | 2017-08-01 | Maregade Rx, LLC | Product and method for treating diarrhea |
| ES2953520T3 (es) | 2016-12-23 | 2023-11-14 | Maregade Rx Llc | Producto a baja dosis y método para el tratamiento de la diarrea |
| US10947253B2 (en) | 2019-08-05 | 2021-03-16 | Ankh Life Sciences Limited | Fused polycyclic dimers |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ258553A (en) * | 1992-12-04 | 1996-06-25 | Janssen Pharmaceutica Nv | Azepine derivatives; compounds, process for preparation and pharmaceutical compositions containing such compounds |
| TW382017B (en) * | 1995-12-27 | 2000-02-11 | Janssen Pharmaceutica Nv | 1-(1,2-disubstituted piperidinyl)-4-(fused imidazole)-piperidine derivatives |
| TW429256B (en) | 1995-12-27 | 2001-04-11 | Janssen Pharmaceutica Nv | 1-(1,2-disubstituted piperidinyl)-4-(benzimidazolyl- and imidazopyridinyl)-piperidine derivatives |
| TW527186B (en) * | 1996-03-19 | 2003-04-11 | Janssen Pharmaceutica Nv | Fused imidazole derivatives as multidrug resistance modulators |
| WO1999013871A2 (en) * | 1997-09-18 | 1999-03-25 | Janssen Pharmaceutica N.V. | Fused imidazole derivatives for improving oral bioavailability of pharmaceutical agents |
| WO2002100862A2 (en) * | 2001-06-12 | 2002-12-19 | Janssen Pharmaceutica N.V. | Novel substituted tetracyclic imidazole derivatives, processes for their preparation, pharmaceutical compositions comprising them and their use as a medicine |
| MXPA04004867A (es) | 2001-11-23 | 2004-07-30 | Janssen Pharmaceutica Nv | El uso de antihistaminicos para la reduccion aguda de presion intracraneal elevada. |
-
2002
- 2002-11-22 MX MXPA04004867A patent/MXPA04004867A/es active IP Right Grant
- 2002-11-22 RU RU2004118838/04A patent/RU2311418C2/ru not_active IP Right Cessation
- 2002-11-22 EP EP02803410A patent/EP1451196B1/en not_active Expired - Lifetime
- 2002-11-22 PT PT07107669T patent/PT1832287E/pt unknown
- 2002-11-22 EP EP07107669A patent/EP1832287B1/en not_active Expired - Lifetime
- 2002-11-22 CN CNB2006100841411A patent/CN100478031C/zh not_active Expired - Fee Related
- 2002-11-22 HU HU0402357A patent/HU229118B1/hu not_active IP Right Cessation
- 2002-11-22 JP JP2003545660A patent/JP4505226B2/ja not_active Expired - Lifetime
- 2002-11-22 AT AT07107669T patent/ATE423599T1/de active
- 2002-11-22 AU AU2002356715A patent/AU2002356715B2/en not_active Ceased
- 2002-11-22 KR KR1020047005513A patent/KR100967601B1/ko not_active IP Right Cessation
- 2002-11-22 ES ES02803410T patent/ES2290364T3/es not_active Expired - Lifetime
- 2002-11-22 PL PL369864A patent/PL209953B1/pl unknown
- 2002-11-22 SI SI200230617T patent/SI1451196T1/sl unknown
- 2002-11-22 DE DE60231351T patent/DE60231351D1/de not_active Expired - Lifetime
- 2002-11-22 DE DE60221891T patent/DE60221891T2/de not_active Expired - Lifetime
- 2002-11-22 PT PT02803410T patent/PT1451196E/pt unknown
- 2002-11-22 NZ NZ532718A patent/NZ532718A/en not_active IP Right Cessation
- 2002-11-22 WO PCT/EP2002/013180 patent/WO2003044023A1/en active Application Filing
- 2002-11-22 US US10/494,006 patent/US7732437B2/en active Active
- 2002-11-22 CN CNB028230140A patent/CN100379744C/zh not_active Expired - Fee Related
- 2002-11-22 NZ NZ550723A patent/NZ550723A/en not_active IP Right Cessation
- 2002-11-22 IL IL16210902A patent/IL162109A0/xx unknown
- 2002-11-22 DK DK07107669T patent/DK1832287T3/da active
- 2002-11-22 CA CA2467097A patent/CA2467097C/en not_active Expired - Fee Related
- 2002-11-22 ES ES07107669T patent/ES2321987T3/es not_active Expired - Lifetime
- 2002-11-22 SI SI200230813T patent/SI1832287T1/sl unknown
- 2002-11-22 DK DK02803410T patent/DK1451196T3/da active
- 2002-11-22 CA CA2690483A patent/CA2690483C/en not_active Expired - Fee Related
- 2002-11-22 UA UA20040604966A patent/UA76803C2/uk unknown
- 2002-11-22 AT AT02803410T patent/ATE370149T1/de active
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2004
- 2004-05-13 HR HRP20040427AA patent/HRP20040427B1/xx not_active IP Right Cessation
- 2004-05-20 ZA ZA2004/03923A patent/ZA200403923B/en unknown
- 2004-05-20 IL IL162109A patent/IL162109A/en not_active IP Right Cessation
- 2004-06-22 NO NO20042618A patent/NO333656B1/no not_active IP Right Cessation
-
2005
- 2005-07-15 HK HK05106036A patent/HK1073309A1/xx not_active IP Right Cessation
- 2005-07-15 HK HK07106604.8A patent/HK1101672A1/xx not_active IP Right Cessation
-
2007
- 2007-11-14 CY CY20071101471T patent/CY1107472T1/el unknown
- 2007-12-27 IL IL188457A patent/IL188457A/en not_active IP Right Cessation
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2008
- 2008-10-30 IL IL194992A patent/IL194992A/en not_active IP Right Cessation
-
2009
- 2009-02-04 JP JP2009023575A patent/JP4991770B2/ja not_active Expired - Lifetime
- 2009-05-25 CY CY20091100559T patent/CY1109108T1/el unknown
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