NO20042618L - Anvendelse av anti-histaminika for akutt reduksjon av hevet intrakranielt trykk - Google Patents

Anvendelse av anti-histaminika for akutt reduksjon av hevet intrakranielt trykk

Info

Publication number: NO20042618L
Authority: NO; Norway
Prior art keywords: intracranial pressure; brain injury; traumatic; antihistamines; elevated intracranial
Prior art date: 2001-11-23

Application number

NO20042618A

Other languages

English (en)

Other versions

NO333656B1 (no

Inventor

Manuel Jesus Alcazar-Vaca

Jose Manuel Bartolome-Nebreda

Pedro Martinez-Jimenez

Francisco Javi Fernandez-Gadea

Frans Eduard Janssens

Joseph Elisabeth Leenaerts

Frank Tegtmeier

Koenraad Arthur Van Rossem

Jozef Leo Henri Van Reempts

Original Assignee

Janssen Pharmaceutica Nv

Priority date (The priority date 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 date listed.)

2001-11-23

Filing date

2004-06-22

Publication date

2004-06-22

2004-06-22 Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv

2004-06-22 Publication of NO20042618L publication Critical patent/NO20042618L/no

2013-08-05 Publication of NO333656B1 publication Critical patent/NO333656B1/no

Links

239000000739 antihistaminic agent Substances 0.000 title abstract 3
201000009941 intracranial hypertension Diseases 0.000 title abstract 2
230000001154 acute effect Effects 0.000 title 1
229940125715 antihistaminic agent Drugs 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
229960003790 alimemazine Drugs 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
GJSURZIOUXUGAL-UHFFFAOYSA-N Clonidine Chemical compound ClC1=CC=CC(Cl)=C1NC1=NCCN1 GJSURZIOUXUGAL-UHFFFAOYSA-N 0.000 abstract 1
229940122236 Histamine receptor antagonist Drugs 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
208000030886 Traumatic Brain injury Diseases 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
208000029028 brain injury Diseases 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
229960000725 brompheniramine Drugs 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
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
229960000428 carbinoxamine 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
229950010123 carebastine Drugs 0.000 abstract 1
229960001803 cetirizine Drugs 0.000 abstract 1
229960004831 chlorcyclizine Drugs 0.000 abstract 1
229960003291 chlorphenamine Drugs 0.000 abstract 1
SOYKEARSMXGVTM-UHFFFAOYSA-N chlorphenamine Chemical compound C=1C=CC=NC=1C(CCN(C)C)C1=CC=C(Cl)C=C1 SOYKEARSMXGVTM-UHFFFAOYSA-N 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
DERZBLKQOCDDDZ-JLHYYAGUSA-N cinnarizine Chemical compound C1CN(C(C=2C=CC=CC=2)C=2C=CC=CC=2)CCN1C\C=C\C1=CC=CC=C1 DERZBLKQOCDDDZ-JLHYYAGUSA-N 0.000 abstract 1
229960000876 cinnarizine Drugs 0.000 abstract 1
229960002881 clemastine Drugs 0.000 abstract 1
YNNUSGIPVFPVBX-NHCUHLMSSA-N clemastine Chemical compound CN1CCC[C@@H]1CCO[C@@](C)(C=1C=CC(Cl)=CC=1)C1=CC=CC=C1 YNNUSGIPVFPVBX-NHCUHLMSSA-N 0.000 abstract 1
CJXAEXPPLWQRFR-UHFFFAOYSA-N clemizole Chemical compound C1=CC(Cl)=CC=C1CN1C2=CC=CC=C2N=C1CN1CCCC1 CJXAEXPPLWQRFR-UHFFFAOYSA-N 0.000 abstract 1
229950002020 clemizole Drugs 0.000 abstract 1
ZSQANMZWGKYDER-JXMROGBWSA-N clocinizine Chemical compound C1=CC(Cl)=CC=C1C(C=1C=CC=CC=1)N1CCN(C\C=C\C=2C=CC=CC=2)CC1 ZSQANMZWGKYDER-JXMROGBWSA-N 0.000 abstract 1
229960003826 clocinizine Drugs 0.000 abstract 1
229960002896 clonidine Drugs 0.000 abstract 1
229960003564 cyclizine Drugs 0.000 abstract 1
UVKZSORBKUEBAZ-UHFFFAOYSA-N cyclizine Chemical compound C1CN(C)CCN1C(C=1C=CC=CC=1)C1=CC=CC=C1 UVKZSORBKUEBAZ-UHFFFAOYSA-N 0.000 abstract 1
229960001140 cyproheptadine Drugs 0.000 abstract 1
JJCFRYNCJDLXIK-UHFFFAOYSA-N cyproheptadine Chemical compound C1CN(C)CCC1=C1C2=CC=CC=C2C=CC2=CC=CC=C21 JJCFRYNCJDLXIK-UHFFFAOYSA-N 0.000 abstract 1
229960001271 desloratadine Drugs 0.000 abstract 1
229960001882 dexchlorpheniramine 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
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
229960002686 niaprazine Drugs 0.000 abstract 1
229960004872 nizatidine Drugs 0.000 abstract 1
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
229960002698 oxatomide 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
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
229960001190 pheniramine Drugs 0.000 abstract 1
229950010674 picumast Drugs 0.000 abstract 1
230000002265 prevention Effects 0.000 abstract 1
229960003910 promethazine Drugs 0.000 abstract 1
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
229950005829 temelastine Drugs 0.000 abstract 1
229960000351 terfenadine Drugs 0.000 abstract 1
229950011533 tiotidine Drugs 0.000 abstract 1
230000009529 traumatic brain injury Effects 0.000 abstract 1
230000000472 traumatic effect 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

- 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
- 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
- A61K31/505—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
- 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
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
- 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
- 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
- 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
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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NO20042618A 2001-11-23 2004-06-22 Benzimidazo[2,1-b][3]benzazepin-forbindelse og anvendelse derav NO333656B1 (no)

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EP01204574		2001-11-23
PCT/EP2002/013180 WO2003044023A1 (en)	2001-11-23	2002-11-22	The use of anti-histaminics for acute reduction of elevated intracranial pressure

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NO20042618L true NO20042618L (no)	2004-06-22
NO333656B1 NO333656B1 (no)	2013-08-05

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US (1)	US7732437B2 (no)
EP (2)	EP1832287B1 (no)
JP (2)	JP4505226B2 (no)
KR (1)	KR100967601B1 (no)
CN (2)	CN100379744C (no)
AT (2)	ATE370149T1 (no)
AU (1)	AU2002356715B2 (no)
CA (2)	CA2690483C (no)
CY (2)	CY1107472T1 (no)
DE (2)	DE60221891T2 (no)
DK (2)	DK1451196T3 (no)
ES (2)	ES2290364T3 (no)
HR (1)	HRP20040427B1 (no)
HU (1)	HU229118B1 (no)
IL (4)	IL162109A0 (no)
MX (1)	MXPA04004867A (no)
NO (1)	NO333656B1 (no)
NZ (2)	NZ532718A (no)
PL (1)	PL209953B1 (no)
PT (2)	PT1451196E (no)
RU (1)	RU2311418C2 (no)
SI (2)	SI1451196T1 (no)
UA (1)	UA76803C2 (no)
WO (1)	WO2003044023A1 (no)
ZA (1)	ZA200403923B (no)

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CA2690483C (en)	2001-11-23	2012-07-24	Janssen Pharmaceutica N.V.	The use of anti-histaminics for acute reduction of elevated intracranial pressure
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
CN103987932A (zh) *	2011-12-20	2014-08-13	丰田自动车株式会社	电加热式催化剂的故障检测装置
US9717726B2 (en) *	2013-03-14	2017-08-01	Maregade Rx, LLC	Product and method for treating diarrhea
EP3558296B1 (en)	2016-12-23	2023-06-28	Maregade RX, LLC	Low dose product and method for treating diarrhea
US10947253B2 (en)	2019-08-05	2021-03-16	Ankh Life Sciences Limited	Fused polycyclic dimers
US12129265B2 (en)	2020-07-21	2024-10-29	Ankh Life Sciences Limited	Therapeutic agents and uses thereof

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HU223465B1 (hu) *	1992-12-04	2004-07-28	Janssen Pharmaceutica N.V.	Allergia elleni triazolo(pirrolo, tieno vagy furán)-azepin-származékok, eljárás előállításukra és az ezeket tartalmazó gyógyszerkészítmények
TW429256B (en)	1995-12-27	2001-04-11	Janssen Pharmaceutica Nv	1-(1,2-disubstituted piperidinyl)-4-(benzimidazolyl- and imidazopyridinyl)-piperidine derivatives
TW382017B (en) *	1995-12-27	2000-02-11	Janssen Pharmaceutica Nv	1-(1,2-disubstituted piperidinyl)-4-(fused imidazole)-piperidine derivatives
TW527186B (en)	1996-03-19	2003-04-11	Janssen Pharmaceutica Nv	Fused imidazole derivatives as multidrug resistance modulators
US6544979B1 (en) *	1997-09-18	2003-04-08	Janssen Pharmaceuticals, N.V.	Fused imidazole derivatives for improving oral bioavailability of pharmaceutical agents
US7476662B2 (en) *	2001-06-12	2009-01-13	Janssen Pharmaceutica N.V.	Substituted tetracyclic imidazole derivatives, processes for their preparation, pharmaceutical compositions comprising them and their use as a medicine
CA2690483C (en)	2001-11-23	2012-07-24	Janssen Pharmaceutica N.V.	The use of anti-histaminics for acute reduction of elevated intracranial pressure

2002
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- 2002-11-22 PT PT02803410T patent/PT1451196E/pt unknown
- 2002-11-22 DE DE60221891T patent/DE60221891T2/de not_active Expired - Lifetime
- 2002-11-22 KR KR1020047005513A patent/KR100967601B1/ko not_active Expired - Fee Related
- 2002-11-22 DK DK07107669T patent/DK1832287T3/da active
- 2002-11-22 AT AT02803410T patent/ATE370149T1/de active
- 2002-11-22 CN CNB2006100841411A patent/CN100478031C/zh not_active Expired - Fee Related
- 2002-11-22 EP EP07107669A patent/EP1832287B1/en not_active Expired - Lifetime
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- 2002-11-22 AT AT07107669T patent/ATE423599T1/de active
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- 2002-11-22 HU HU0402357A patent/HU229118B1/hu not_active IP Right Cessation
- 2002-11-22 WO PCT/EP2002/013180 patent/WO2003044023A1/en not_active Ceased
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2004
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2007
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2008
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Publication number	Publication date
PT1451196E (pt)	2007-10-25
CN100379744C (zh)	2008-04-09
MXPA04004867A (es)	2004-07-30
DK1832287T3 (da)	2009-06-08
PL209953B1 (pl)	2011-11-30
IL162109A0 (en)	2005-11-20
US7732437B2 (en)	2010-06-08
ZA200403923B (en)	2005-10-26
IL194992A0 (en)	2009-08-03
JP4991770B2 (ja)	2012-08-01
AU2002356715B2 (en)	2008-05-15
US20050070525A1 (en)	2005-03-31
PT1832287E (pt)	2009-05-05
NZ532718A (en)	2007-01-26
IL188457A (en)	2010-11-30
KR20050044328A (ko)	2005-05-12
RU2311418C2 (ru)	2007-11-27
HK1073309A1 (en)	2005-09-30
WO2003044023A1 (en)	2003-05-30
HRP20040427A2 (en)	2005-06-30
HU229118B1 (en)	2013-08-28
CA2467097A1 (en)	2003-05-30
DE60221891D1 (de)	2007-09-27
NO333656B1 (no)	2013-08-05
HRP20040427B1 (hr)	2012-09-30
JP2005509680A (ja)	2005-04-14
EP1832287A3 (en)	2007-12-26
ES2290364T3 (es)	2008-02-16
ATE370149T1 (de)	2007-09-15
AU2002356715A1 (en)	2003-06-10
EP1832287B1 (en)	2009-02-25
KR100967601B1 (ko)	2010-07-05
JP2009102417A (ja)	2009-05-14
DE60221891T2 (de)	2008-05-08
HUP0402357A3 (en)	2009-10-28
NZ550723A (en)	2008-06-30
DK1451196T3 (da)	2007-11-12
HUP0402357A2 (hu)	2005-02-28
SI1832287T1 (sl)	2009-06-30
CN1589273A (zh)	2005-03-02
HK1101672A1 (zh)	2007-10-26
CY1107472T1 (el)	2012-12-19
RU2004118838A (ru)	2005-04-10
ES2321987T3 (es)	2009-06-15
CN1895673A (zh)	2007-01-17
IL162109A (en)	2010-04-29
IL188457A0 (en)	2008-03-20
CY1109108T1 (el)	2014-07-02
JP4505226B2 (ja)	2010-07-21
UA76803C2 (uk)	2006-09-15
CA2690483A1 (en)	2003-05-30
IL194992A (en)	2010-12-30
ATE423599T1 (de)	2009-03-15
EP1832287A2 (en)	2007-09-12
EP1451196A1 (en)	2004-09-01
EP1451196B1 (en)	2007-08-15
CA2467097C (en)	2011-02-01
SI1451196T1 (sl)	2007-12-31
DE60231351D1 (de)	2009-04-09
CA2690483C (en)	2012-07-24
PL369864A1 (en)	2005-05-02
CN100478031C (zh)	2009-04-15

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Publication	Publication Date	Title
IL194992A0 (en)	2009-08-03	The use of anti-histaminics for acute reduction of elevated intracranial pressure
EP1034778A3 (de)	2001-08-16	Verwendung von Octocrylen zur Solubilisierung von 2,4-Bis- [4-(2-Ethyl-hexyloxy)-2-hydroxy]-phenyl -6-(4-methoxyphenyl)-1,3,5-triazin in kosmetischen oder dermatologischen Lichtschutzmitteln
RU2004133764A (ru)	2005-07-20	Производные бензимидазола в качестве н3-гистаминовых антагонистов
RU2007104096A (ru)	2008-08-10	Способ лечения аллергии или вызываемых аллергией поражений дыхательных путей и фармацевтическая композиция
CA2330469A1 (fr)	2001-07-13	Compositions cosmetiques contenant un amidon amphotere et un agent conditionneur cationique et leurs utilisations
ES2636253T3 (es)	2017-10-05	Preparación cosmética estable
CA2415345A1 (en)	2002-01-31	Linkage of agents using microparticles
ES2110858T3 (es)	1998-02-16	Composicion siliconada que contiene un agente activo sensible al agua.
ATE494381T1 (de)	2011-01-15	Verbesserte expressionselemente
AR014828A1 (es)	2001-03-28	Una composicion cosmetica capilar y un metodo de modelado capilar
CN112469819A (zh)	2021-03-09	包括神经干细胞培养肉汤作为活性成分的用于抗衰老或减少皱纹的化妆品组合物和其制备方法
DE60001232D1 (de)	2003-02-20	Hautreinigungsmittel
WO2002079239A3 (en)	2003-10-02	Chimeric filovirus glycoprotein
WO2003009819A3 (en)	2003-06-19	Temperature insensitive one-phase microemulsions
BRPI0416716A (pt)	2007-01-16	composições de siloxano cìclico para a liberação de ingredientes ativos
ES2366041T3 (es)	2011-10-14	Preparación cosmética que contiene 1,2-alcanodiol(es) y triazina(s).
ATE457384T1 (de)	2010-02-15	Von weichmachender lotion durchdrungenes tissuepapier
DE602005020815D1 (de)	2010-06-02	Verändertes vp-1capsidprotein von parvovirus b19
Quinones-Torrelo et al.	2001	Retention pharmacokinetic and pharmacodynamic parameter relationships of antihistamine drugs using biopartitioning micellar chromatography
ES2430194T3 (es)	2013-11-19	Uso de derivados de triazina asimétricamente sustituidos para alcanzar o aumentar la solubilidad de derivados de triazina simétricamente sustituidos en componentes de aceite
DE60216242D1 (de)	2007-01-04	Lösung von Wirkstoffen in HFA-Treibgasen mittels Emulsionen
JPH10316524A (ja)	1998-12-02	洗浄用化粧品組成物及びその使用
BRPI0501401A (pt)	2006-04-11	composições de esmalte de unhas, processo cosmético para maquilagem ou cuidado não terapêutico das unhas e uso de um polìmero hidrossolúvel ou hidrodispersìvel
Banita	2025	Navigating roots and routes: the topos of return in contemporary Nigerian and Nigerian diaspora literature
Korte et al.	2004	S 2-42: Expression of CAP1 and CAP2 in developing and adult mouse tissues