JP2005501050A5 - - Google Patents

Info

Publication number

JP2005501050A5

JP2005501050A5 JP2003516496A JP2003516496A JP2005501050A5 JP 2005501050 A5 JP2005501050 A5 JP 2005501050A5 JP 2003516496 A JP2003516496 A JP 2003516496A JP 2003516496 A JP2003516496 A JP 2003516496A JP 2005501050 A5 JP2005501050 A5 JP 2005501050A5

Authority

JP

Japan

Prior art keywords

photosensitizer

ala ester

ala

ester

wound

Prior art date

2002-07-25

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

• Espacenet
• Global Dossier
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• 150000002148 esters Chemical group 0.000 claims 30
• 206010052428 Wound Diseases 0.000 claims 23
• 208000027418 Wounds and injury Diseases 0.000 claims 23
• 239000003504 photosensitizing agent Substances 0.000 claims 20
• -1 1-methylpentyl Chemical group 0.000 claims 15
• 208000025865 Ulcer Diseases 0.000 claims 9
• 231100000397 ulcer Toxicity 0.000 claims 9
• 238000000034 method Methods 0.000 claims 8
• ZGXJTSGNIOSYLO-UHFFFAOYSA-N 88755TAZ87 Chemical class NCC(=O)CCC(O)=O ZGXJTSGNIOSYLO-UHFFFAOYSA-N 0.000 claims 7
• 229960002749 aminolevulinic acid Drugs 0.000 claims 7
• 125000000217 alkyl group Chemical group 0.000 claims 5
• 239000003814 drug Substances 0.000 claims 5
• 238000004519 manufacturing process Methods 0.000 claims 5
• 150000003839 salts Chemical class 0.000 claims 5
• 239000002738 chelating agent Substances 0.000 claims 4
• 230000035515 penetration Effects 0.000 claims 4
• 238000011282 treatment Methods 0.000 claims 4
• 241000894006 Bacteria Species 0.000 claims 2
• KSFOVUSSGSKXFI-GAQDCDSVSA-N CC1=C/2NC(\C=C3/N=C(/C=C4\N\C(=C/C5=N/C(=C\2)/C(C=C)=C5C)C(C=C)=C4C)C(C)=C3CCC(O)=O)=C1CCC(O)=O Chemical compound CC1=C/2NC(\C=C3/N=C(/C=C4\N\C(=C/C5=N/C(=C\2)/C(C=C)=C5C)C(C=C)=C4C)C(C)=C3CCC(O)=O)=C1CCC(O)=O KSFOVUSSGSKXFI-GAQDCDSVSA-N 0.000 claims 2
• HUVXQFBFIFIDDU-UHFFFAOYSA-N aluminum phthalocyanine Chemical compound [Al+3].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 HUVXQFBFIFIDDU-UHFFFAOYSA-N 0.000 claims 2
• 150000001875 compounds Chemical class 0.000 claims 2
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
• 244000000010 microbial pathogen Species 0.000 claims 2
• OYINILBBZAQBEV-UWJYYQICSA-N (17s,18s)-18-(2-carboxyethyl)-20-(carboxymethyl)-12-ethenyl-7-ethyl-3,8,13,17-tetramethyl-17,18,22,23-tetrahydroporphyrin-2-carboxylic acid Chemical compound N1C2=C(C)C(C=C)=C1C=C(N1)C(C)=C(CC)C1=CC(C(C)=C1C(O)=O)=NC1=C(CC(O)=O)C([C@@H](CCC(O)=O)[C@@H]1C)=NC1=C2 OYINILBBZAQBEV-UWJYYQICSA-N 0.000 claims 1
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
• 125000006218 1-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 claims 1
• 125000004847 2-fluorobenzyl group Chemical group [H]C1=C([H])C(F)=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
• 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 1
• 125000006179 2-methyl benzyl group Chemical group [H]C1=C([H])C(=C(C([H])=C1[H])C([H])([H])*)C([H])([H])[H] 0.000 claims 1
• 125000005916 2-methylpentyl group Chemical group 0.000 claims 1
• 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims 1
• 125000006284 3-fluorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(F)=C1[H])C([H])([H])* 0.000 claims 1
• 125000006180 3-methyl benzyl group Chemical group [H]C1=C([H])C(=C([H])C(=C1[H])C([H])([H])[H])C([H])([H])* 0.000 claims 1
• 125000004217 4-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C([H])([H])* 0.000 claims 1
• UJKPHYRXOLRVJJ-MLSVHJFASA-N CC(O)C1=C(C)/C2=C/C3=N/C(=C\C4=C(CCC(O)=O)C(C)=C(N4)/C=C4\N=C(\C=C\1/N\2)C(C)=C4C(C)O)/C(CCC(O)=O)=C3C Chemical group CC(O)C1=C(C)/C2=C/C3=N/C(=C\C4=C(CCC(O)=O)C(C)=C(N4)/C=C4\N=C(\C=C\1/N\2)C(C)=C4C(C)O)/C(CCC(O)=O)=C3C UJKPHYRXOLRVJJ-MLSVHJFASA-N 0.000 claims 1
• 208000003790 Foot Ulcer Diseases 0.000 claims 1
• 206010040943 Skin Ulcer Diseases 0.000 claims 1
• 208000007107 Stomach Ulcer Diseases 0.000 claims 1
• 208000000558 Varicose Ulcer Diseases 0.000 claims 1
• 229940043215 aminolevulinate Drugs 0.000 claims 1
• 125000003118 aryl group Chemical group 0.000 claims 1
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
• 230000003115 biocidal effect Effects 0.000 claims 1
• SURLGNKAQXKNSP-DBLYXWCISA-N chlorin Chemical compound C\1=C/2\N/C(=C\C3=N/C(=C\C=4NC(/C=C\5/C=CC/1=N/5)=CC=4)/C=C3)/CC\2 SURLGNKAQXKNSP-DBLYXWCISA-N 0.000 claims 1
• 125000006165 cyclic alkyl group Chemical group 0.000 claims 1
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
• 239000000645 desinfectant Substances 0.000 claims 1
• 201000005917 gastric ulcer Diseases 0.000 claims 1
• 230000035876 healing Effects 0.000 claims 1
• 229960003569 hematoporphyrin Drugs 0.000 claims 1
• 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
• 238000001727 in vivo Methods 0.000 claims 1
• 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 claims 1
• 125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 claims 1
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
• 229940109328 photofrin Drugs 0.000 claims 1
• 208000017983 photosensitivity disease Diseases 0.000 claims 1
• 231100000434 photosensitization Toxicity 0.000 claims 1
• IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical class N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 claims 1
• 229950003776 protoporphyrin Drugs 0.000 claims 1
• 230000001105 regulatory effect Effects 0.000 claims 1
• 125000000547 substituted alkyl group Chemical group 0.000 claims 1
• LYPFDBRUNKHDGX-UHFFFAOYSA-N temoporfin Chemical compound OC1=CC=CC(C=2C3=CC=C(N3)C(C=3C=C(O)C=CC=3)=C3C=CC(=N3)C(C=3C=C(O)C=CC=3)=C3C=CC(N3)=C(C=3C=C(O)C=CC=3)C=3CCC=2N=3)=C1 LYPFDBRUNKHDGX-UHFFFAOYSA-N 0.000 claims 1
• 230000029663 wound healing Effects 0.000 claims 1