JP4668527B2 - 湿疹治療用フラボノイド誘導体 - Google Patents
湿疹治療用フラボノイド誘導体 Download PDFInfo
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- JP4668527B2 JP4668527B2 JP2003304920A JP2003304920A JP4668527B2 JP 4668527 B2 JP4668527 B2 JP 4668527B2 JP 2003304920 A JP2003304920 A JP 2003304920A JP 2003304920 A JP2003304920 A JP 2003304920A JP 4668527 B2 JP4668527 B2 JP 4668527B2
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- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- RQFLGKYCYMMRMC-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O RQFLGKYCYMMRMC-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229960001679 octinoxate Drugs 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000000242 pagocytic effect Effects 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 125000001312 palmitoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 229940100460 peg-100 stearate Drugs 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 125000001805 pentosyl group Chemical group 0.000 description 1
- 238000005325 percolation Methods 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 230000003711 photoprotective effect Effects 0.000 description 1
- 239000011772 phylloquinone Substances 0.000 description 1
- MBWXNTAXLNYFJB-LKUDQCMESA-N phylloquinone Chemical compound C1=CC=C2C(=O)C(C/C=C(C)/CCCC(C)CCCC(C)CCCC(C)C)=C(C)C(=O)C2=C1 MBWXNTAXLNYFJB-LKUDQCMESA-N 0.000 description 1
- 239000000467 phytic acid Substances 0.000 description 1
- 235000002949 phytic acid Nutrition 0.000 description 1
- 229940068041 phytic acid Drugs 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229940048845 polyglyceryl-3 diisostearate Drugs 0.000 description 1
- 229940100518 polyglyceryl-4 isostearate Drugs 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229960005205 prednisolone Drugs 0.000 description 1
- 229960004618 prednisone Drugs 0.000 description 1
- XOFYZVNMUHMLCC-ZPOLXVRWSA-N prednisone Chemical compound O=C1C=C[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 XOFYZVNMUHMLCC-ZPOLXVRWSA-N 0.000 description 1
- 230000035935 pregnancy Effects 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- HVBPXNVEYTXFAO-UHFFFAOYSA-N propan-2-yl hexadecanoate propan-2-yl tetradecanoate Chemical compound C(CCCCCCCCCCCCCCC)(=O)OC(C)C.C(C)(C)OC(CCCCCCCCCCCCCCC)=O.C(CCCCCCCCCCCCC)(=O)OC(C)C.C(C)(C)OC(CCCCCCCCCCCCC)=O HVBPXNVEYTXFAO-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- YNZOICUNEVJUEJ-UHFFFAOYSA-N propane-1,2,3-triol Chemical compound OCC(O)CO.OCC(O)CO.OCC(O)CO YNZOICUNEVJUEJ-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000002633 protecting effect Effects 0.000 description 1
- 239000011252 protective cream Substances 0.000 description 1
- 230000001012 protector Effects 0.000 description 1
- 108060006633 protein kinase Proteins 0.000 description 1
- 230000001823 pruritic effect Effects 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 229960003581 pyridoxal Drugs 0.000 description 1
- 235000008164 pyridoxal Nutrition 0.000 description 1
- 239000011674 pyridoxal Substances 0.000 description 1
- 235000008151 pyridoxamine Nutrition 0.000 description 1
- 239000011699 pyridoxamine Substances 0.000 description 1
- 235000008160 pyridoxine Nutrition 0.000 description 1
- 239000011677 pyridoxine Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000000241 respiratory effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 235000020944 retinol Nutrition 0.000 description 1
- 239000011607 retinol Substances 0.000 description 1
- 229960003471 retinol Drugs 0.000 description 1
- 229960000342 retinol acetate Drugs 0.000 description 1
- 235000019173 retinyl acetate Nutrition 0.000 description 1
- 239000011770 retinyl acetate Substances 0.000 description 1
- QGNJRVVDBSJHIZ-QHLGVNSISA-N retinyl acetate Chemical compound CC(=O)OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C QGNJRVVDBSJHIZ-QHLGVNSISA-N 0.000 description 1
- 201000004700 rosacea Diseases 0.000 description 1
- JUVIOZPCNVVQFO-HBGVWJBISA-N rotenone Chemical compound O([C@H](CC1=C2O3)C(C)=C)C1=CC=C2C(=O)[C@@H]1[C@H]3COC2=C1C=C(OC)C(OC)=C2 JUVIOZPCNVVQFO-HBGVWJBISA-N 0.000 description 1
- 125000000953 rutinose group Chemical group 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 210000001732 sebaceous gland Anatomy 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 230000037075 skin appearance Effects 0.000 description 1
- 210000004927 skin cell Anatomy 0.000 description 1
- 206010040882 skin lesion Diseases 0.000 description 1
- 231100000444 skin lesion Toxicity 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 235000019983 sodium metaphosphate Nutrition 0.000 description 1
- 235000010956 sodium stearoyl-2-lactylate Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- KNYAZNABVSEZDS-UHFFFAOYSA-M sodium;2-octadecanoyloxypropanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC(=O)OC(C)C([O-])=O KNYAZNABVSEZDS-UHFFFAOYSA-M 0.000 description 1
- PESXGULMKCKJCC-UHFFFAOYSA-M sodium;4-methoxycarbonylphenolate Chemical compound [Na+].COC(=O)C1=CC=C([O-])C=C1 PESXGULMKCKJCC-UHFFFAOYSA-M 0.000 description 1
- 210000001082 somatic cell Anatomy 0.000 description 1
- 229950004959 sorbitan oleate Drugs 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- ARCJQKUWGAZPFX-UHFFFAOYSA-N stilbene oxide Chemical compound O1C(C=2C=CC=CC=2)C1C1=CC=CC=C1 ARCJQKUWGAZPFX-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-M succinate(1-) Chemical compound OC(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-M 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 125000005555 sulfoximide group Chemical group 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 210000000106 sweat gland Anatomy 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 235000019157 thiamine Nutrition 0.000 description 1
- 229960003495 thiamine Drugs 0.000 description 1
- 239000011721 thiamine Substances 0.000 description 1
- DPJRMOMPQZCRJU-UHFFFAOYSA-M thiamine hydrochloride Chemical compound Cl.[Cl-].CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N DPJRMOMPQZCRJU-UHFFFAOYSA-M 0.000 description 1
- 229960002663 thioctic acid Drugs 0.000 description 1
- 235000019303 thiodipropionic acid Nutrition 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 229940094937 thioredoxin Drugs 0.000 description 1
- 108060008226 thioredoxin Proteins 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 210000004906 toe nail Anatomy 0.000 description 1
- QURCVMIEKCOAJU-UHFFFAOYSA-N trans-isoferulic acid Natural products COC1=CC=C(C=CC(O)=O)C=C1O QURCVMIEKCOAJU-UHFFFAOYSA-N 0.000 description 1
- ZCIHMQAPACOQHT-ZGMPDRQDSA-N trans-isorenieratene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/c1c(C)ccc(C)c1C)C=CC=C(/C)C=Cc2c(C)ccc(C)c2C ZCIHMQAPACOQHT-ZGMPDRQDSA-N 0.000 description 1
- LOIYMIARKYCTBW-OWOJBTEDSA-N trans-urocanic acid Chemical compound OC(=O)\C=C\C1=CNC=N1 LOIYMIARKYCTBW-OWOJBTEDSA-N 0.000 description 1
- LOIYMIARKYCTBW-UHFFFAOYSA-N trans-urocanic acid Natural products OC(=O)C=CC1=CNC=N1 LOIYMIARKYCTBW-UHFFFAOYSA-N 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- 229960005294 triamcinolone Drugs 0.000 description 1
- GFNANZIMVAIWHM-OBYCQNJPSA-N triamcinolone Chemical compound O=C1C=C[C@]2(C)[C@@]3(F)[C@@H](O)C[C@](C)([C@@]([C@H](O)C4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 GFNANZIMVAIWHM-OBYCQNJPSA-N 0.000 description 1
- 229960002117 triamcinolone acetonide Drugs 0.000 description 1
- YNDXUCZADRHECN-JNQJZLCISA-N triamcinolone acetonide Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H]3OC(C)(C)O[C@@]3(C(=O)CO)[C@@]1(C)C[C@@H]2O YNDXUCZADRHECN-JNQJZLCISA-N 0.000 description 1
- MHNHYTDAOYJUEZ-UHFFFAOYSA-N triphenylphosphane Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 MHNHYTDAOYJUEZ-UHFFFAOYSA-N 0.000 description 1
- 229960003232 troxerutin Drugs 0.000 description 1
- 208000001072 type 2 diabetes mellitus Diseases 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 238000002137 ultrasound extraction Methods 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 229940116269 uric acid Drugs 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- NCYCYZXNIZJOKI-UHFFFAOYSA-N vitamin A aldehyde Natural products O=CC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C NCYCYZXNIZJOKI-UHFFFAOYSA-N 0.000 description 1
- 235000019156 vitamin B Nutrition 0.000 description 1
- 239000011720 vitamin B Substances 0.000 description 1
- 235000019166 vitamin D Nutrition 0.000 description 1
- 239000011710 vitamin D Substances 0.000 description 1
- 150000003710 vitamin D derivatives Chemical class 0.000 description 1
- 235000001892 vitamin D2 Nutrition 0.000 description 1
- 239000011653 vitamin D2 Substances 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 229940011671 vitamin b6 Drugs 0.000 description 1
- 229940046008 vitamin d Drugs 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- VHBFFQKBGNRLFZ-UHFFFAOYSA-N vitamin p Natural products O1C2=CC=CC=C2C(=O)C=C1C1=CC=CC=C1 VHBFFQKBGNRLFZ-UHFFFAOYSA-N 0.000 description 1
- 239000003357 wound healing promoting agent Substances 0.000 description 1
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
- C07H17/04—Heterocyclic radicals containing only oxygen as ring hetero atoms
- C07H17/06—Benzopyran radicals
- C07H17/065—Benzo[b]pyrans
- C07H17/07—Benzo[b]pyran-4-ones
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring 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
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
- A61K31/573—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7048—Compounds having saccharide radicals and heterocyclic rings having oxygen as a ring hetero atom, e.g. leucoglucosan, hesperidin, erythromycin, nystatin, digitoxin or digoxin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- A61P17/04—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
- A61P17/00—Drugs for dermatological disorders
- A61P17/10—Anti-acne agents
-
- 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
- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dermatology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Genetics & Genomics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Cosmetics (AREA)
- Saccharide Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pyrane Compounds (AREA)
Description
Z1〜Z4およびZ6〜Z10は、それぞれ、互いに独立に、H、OH、CH3COO、アルコキシ、ヒドロキシアルコキシ、モノ−またはオリゴグリコシド基であり、アルコキシ基およびヒドロキシアルコキシ基は分岐でも非分岐でもよく、1〜18個の炭素原子を含み得るものであって、基:
Z5は、モノ−またはオリゴグリコシド基であり、その場合下記基:
また、置換基Z1〜Z10中で言及したグリコシド基のOH基中の1個または複数の水素原子は、それぞれ、互いに独立に、アセチル基または1〜8個の炭素原子を有するアルキル基で置換されていてもよく、いずれの場合も、互いに独立に、硫酸塩またはリン酸塩を置換基Z1〜Z10中で言及した基中の1個または複数の水酸基に結合してもよい)
で表わされる化合物を記述している。これらの化合物は化粧品および医薬品の処方で使用するに適している。特に、PCT/EP 02/01200は、これらの化合物が、紫外線フィルター、および酸化ストレスからの保護および皮膚老化を防ぐための活性成分として使用するのに適していることを記載している。これらの化合物が抗アレルギー性、抗炎症性、炎症抑止効果、および抗刺激性を示し、したがって、特に皮膚について、アレルギー、炎症および刺激の治療や予防処置のために使用できると記載されている。
Z1〜Z4およびZ6〜Z10は、それぞれ、互いに独立に、H、OH、CH3COO、アルコキシ、ヒドロキシアルコキシ、モノ−またはオリゴグリコシド基であり、アルコキシ基およびヒドロキシアルコキシ基は分岐でも非分岐でもよく、1〜18個の炭素原子を含み得るものであって、基:
Z5は、モノ−またはオリゴグリコシド基であり、その場合下記基:
a)上記式Iの少なくとも1つの化合物、
b)皮膚許容性の賦形剤、
c)場合によっては、1種または複数の、スキンケアおよび/または炎症抑止効果を有するさらなる活性成分
を含む局所適用のための処方である。
・急性症状を大きく軽減できること、
・急性症状の発生頻度を低減することができること
・一般に、皮膚像の改善に寄与すること
が見出された。
R4は、モノまたはジグルコシド基であり、少なくとも1つの基は次式から選択される:
Z5、n、m、kおよびMは、請求項1で定義される通りであるが、置換基Z5中に存在するX、X1、X2およびX3は、それぞれ、互いに独立に、OH、1〜8個の炭素原子を有するアルコキシ基またはモノグリコシド基であり、
置換基Z1〜Z10で言及したグリコシド基のOH基中の1個または複数の水素原子は、それぞれ、互いに独立に、1〜8個の炭素原子を有するアルキル基で置換されていてもよく、いずれの場合も互いに独立に硫酸塩またはリン酸塩が、置換基Z1〜Z10で言及した基中の1個または複数の水酸基に結合してもよい。
R4は、モノ−またはジグルコシド基であり、少なくとも1つの基は以下から選択される:
また、グリコシド基のOH基中の1個または複数の水素原子は、それぞれ、互いに独立に、1〜8個の炭素原子を有するアルキル基で置換されていてもよく、いずれの場合も、互いに独立に、硫酸塩またはリン酸塩を式IAの化合物の1個または複数の水酸基に結合してもよい。
・ヒドロキシエクトイン(hydroxyectoin)
[(S,S)−1,4,5,6−テトラヒドロ−5−ヒドロキシ−2−メチル−4−ピリミジンカルボン酸]
・例えば、アラントインなどの傷治療剤として有用である活性成分
・例えば、エチル3−[N−n−ブチルN−アセチル]アミノプロピオネート[CAS 52304−36−6]などの虫忌避剤
・スキンケア用ソルビトール[例えばKarion(登録商標)F液体またはKarion(登録商標)FP液体]
・ビオチン
・例えば、ヒドロキシプロリンまたはヒドロキシプロリンの誘導体を含む混合物、例えば、レシチン、ヒドロキシプロリンジパルミテート、シトステロール、リノール酸、トコフェロール、アスコビル酸ナトリウム、マンニトール、フェノキシエタノール、メチルパラベン、エチルパラベン、プロピルパラベン、ブチルパラベン、水を含む混合物[例えば、RonaCare(商標)ASC III(登録商標)]、または例えば、レシチン、ヒドロキシル化レシチン、L−ヒドロキシプロリン、ジソディウムルチニル二硫酸塩、フェノキシエタノール、マンニトール、マグネシウムアスコルビン酸リン酸塩、メチルパラベン、エチルパラベン、プロピルパラベン、ブチルパラベン、シトステロール、トコフェロール、アスコビン酸ナトリウム、水を含む混合物[例えば、RonaCare(商標)VTA]
・ビサボロール(bisabolol)。
原料 INCI名
Abil WE 09 ポリグリセリル4−イソステアレート、
セチルジメチコーン
コポリオール、ヘキシルラウレート
Antaron V−220 PVP/エイコセンコポリマー
Arlacel 80 ソルビタンオレエート
Arlacel 165V グリセリルステアレート、PEG−100ステ
アレート
アボカド油 ペルセアグラティッシマ
(Persea Gratissima)
蜜ロウ 蜜ロウ
Biobase(商標)EP グリセリルステアレート、
セテアリルアルコール、
ステアロイル乳酸ナトリウム、レシチン
Carbopol ETD 2050 カーボマー(Carbomer)
Cetiol V オレイン酸デシル
セチルアルコール セチルアルコール
セチルイソノナエート セチルイソノナエート
Cutina HR 水素化ヒマシ油
Dimeticon ジメチコーン
Eusolex(登録商標)232 フェニルベンジルイミダゾールスルホン酸
Eusolex(登録商標)2292 オクチルメトキシシンナメート、BHT
Eusolex(登録商標)6300 4−メチルベンジリデンカンファー
Eusolex 8300 4−メチルベンジリデン
Eusolex(登録商標)9020 ブチルメトキシジベンゾイルメタン
Eusolex(登録商標)HMS ホモサレート(Homosalate)
Eusolex T−Aqua アクア(水)、二酸化チタン、アルミナ、
ナトリウムメタリン酸塩、
フェノキシエタノール、
メチルパラベンナトリウム
Eutanol G オクチルドデカノール
GermabenII プロピレングリコール、ジアゾリジニル尿素、
メチルパラベン、プロピルパラベン
原料 INCI名
Germaben II−E プロピレングリコール、ジアゾリジニル尿素、
メチルパラベン、プロピルパラベン
グリセリン グリセリン
グリセリン(87%) グリセリン
グリセリン(87%特別精製品) グリセリン
グリセリン、無水 グリセリン
Hetester PHA プロピレングリコールイソセテス−3
アセテート
ヘキシルラウレート ヘキシルラウレート
Imwitor 960 Kフレーク グリセリルステアレート SE
Isolan PDI ジイソステアロイルポリグリセリル3−
ジイソステアレート
イソプロピルミリステート イソプロピルミリステート
イソプロピルパルミテート イソプロピルパルミテート
ホホバ油 Buxus Chinensis(ホホバ油)
Karion F液体 ソルビトール
Keltrol RD キサンタンガム
硫酸マグネシウム 硫酸マグネシウム
硫酸マグネシウム7水塩 硫酸マグネシウム
メチル4−ヒドロキシベンゾエート メチルパラベン
Miglyol 812 カプリリック/カプリックトリグリセリド
Miglyol 812N カプリリック/カプリックトリグリセリド
Miglyol 812、中性油 カプリリック/カプリックトリグリセリド
Mirasil CM5 シクロメチコーン
Mirasil DM 350 ジメチコーン
Montanov 68 セテアリルアルコール、セテアリルグルコシド
塩化ナトリウム 塩化ナトリウム
水酸化ナトリウム溶液、10% 水酸化ナトリウム
原料 INCI名
Oxynex(登録商標)K PEG−8、トコフェロール、アスコルビン酸
パルミテート、
アスコルビン酸、クエン酸
Panthenol−D パンテノール
Paracera M マイクロワックス
パラフィン油、液体 鉱油
芳香油TND−2417 香料
Pemulen TR−1 アクリレート/C10〜30アルキル
アクリレート
架橋ポリマー
Pemulen(登録商標)TR−2 クリレート/C10〜30アルキルアクリレート
架橋ポリマー
Performa(登録商標)V 825 合成ロウ
ポリグリセリル2−ジポリヒドロキシ ポリグリセリル2−ジポリヒドロキシ
ステアレート ステアレート
Prisorine 2021 イソプロピル/イソステアレート
1,2−プロパンジオール プロピレングリコール
プロピル4−ヒドロキシベンゾエート プロピルパラベン
Rhodicare S キサンタンガム
RonaCare(商標)ASC III 水、レシチン、ジパルミトイルヒドロキシ
プロリン、
フェノキシエタノール、
トール油ステロール、
リノール酸、トコフェロール、アスコビル酸
ナトリウム、マンニトール
メチルパラベン、エチルパラベン、
プロピルパラベン、ブチルパラベン
RonaCare(商標)Bisabolol ビサボロール(Bisabolol)
RonaCare(商標)Ectoin エクトイン
RonaCare(商標)LPO ラウリルp−クレゾールケトオキシム
RonaCare(商標)トコフェロール トコフェロールアセテート
アセテート
Sepigel 305 ポリアクリルアミド、C13〜14
イソパラフィン、Laureth−7
原料 INCI名
SFE 839 シクロペンタンシロキサン、
ジメチコーン/ビニルジメチ
コーン架橋ポリマー
シアバター シアバター
Steareth−2 Steareth−2
Steareth−10 Steareth−10
ステアリン酸 ステアリン酸
DL−α−トコフェロールアセテート トコフェロールアセテート
トリエタノールアミン トリエタノールアミン
トリエタノールアミン(特別精製品) トリエタノールアミン
水、脱塩 アクア(水)
ステアリン酸亜鉛 ステアリン酸亜鉛
硫酸化されたチリロシド、ナトリウム塩の調製
水200mlおよび32%水酸化ナトリウム溶液19.4g(155.2mmol)を、撹拌しながらチリロシド29.7g(50mmol)に添加する。ピリジンスルホン19.9g(125mmol)を続いて加え、32%水酸化ナトリウム溶液の追加によってpHをpH8に調節する。反応バッチを12時間N2下で撹拌し、次いでろ過し、ろ液を減圧(T=60℃;p=100mbar)下、50gまで濃縮する。濃縮したろ液にメタノール250mlを1時間かけて滴下し、沈殿した固体(硫酸ナトリウム)をろ過して除去する。乾燥により硫酸化されたチリロシド(ナトリウム塩)を得る。
実施例1
皮膚適用用ローション(W/O)
重量%
A.ポリグリセリル 2−ジポリヒドロキシステアレート 5.0
蜜ロウ 0.5
ステアリン酸亜鉛 0.5
ヘキシルラウレート 9.0
セチルイソノナノエート 6.0
シアバター 0.5
DL−α−トコフェロールアセテート 1.0
チリロシド 0.5
B.グリセリン 5.0
硫酸マグネシウム・7水塩 1.0
保存剤 q.s
(=必要量)
水、脱塩 合計100
調製
相Aを75℃に、相Bを80℃に加熱する。相Bを相Aに撹拌しながらゆっくり添加する。均質にした後に、混合物を撹拌しながら冷却する。香料は40℃の温度で添加する。
使用する保存剤は下記の通りである:
プロピル4−ヒドロキシベンゾエート 0.05%
メチル4−ヒドロキシベンゾエート 0.15%
実施例2
皮膚適用用ローション(W/O)
重量%
A.ポリグリセリル 2−ジポリヒドロキシステアレート 5.0
蜜ロウ 0.5
ステアリン酸亜鉛 0.5
ヘキシルラウレート 9.0
セチルイソノナノエート 6.0
シアバター 0.5
DL−α−トコフェロールアセテート 1.0
B.硫酸化したチロリシド、ナトリウム塩(実施例A) 1.0
グリセリン 5.0
硫酸マグネシウム・7水塩 1.0
保存剤 q.s
水、脱塩 合計100
調製
相Aを75℃に、相Bを80℃に加熱する。相Bを相Aに撹拌しながらゆっくり添加する。均質にした後に、混合物を撹拌しながら冷却する。香料は40℃の温度で添加する。
使用する保存剤は下記の通りである:
プロピル4−ヒドロキシベンゾエート 0.05%
メチル4−ヒドロキシベンゾエート 0.15%
実施例3
皮膚適用用ローション(W/O)
重量%
A.4,6,3’,4’−テトラヒドロシキベンジル 1.0
−3−クマラノン
ポリグリセリル 2−ジポリヒドロキシステアレート 5.0
蜜ロウ 0.5
ステアリン酸亜鉛 0.5
ヘキシルラウレート 9.0
セチルイソノナノエート 6.0
シアバター 0.5
DL−α−トコフェロールアセテート 1.0
チリロシド 1.0
B.グリセリン 5.0
硫酸マグネシウム・7水塩 1.0
保存剤 q.s
水、脱塩 合計100
調製
相Aを75℃に、相Bを80℃に加熱する。相Bを相Aに撹拌しながらゆっくり添加する。均質にした後に、混合物を撹拌しながら冷却する。香料は40℃の温度で添加する。
使用する保存剤は下記の通りである:
プロピル4−ヒドロキシベンゾエート 0.05%
メチル4−ヒドロキシベンゾエート 0.15%
実施例4
エクトインを含むクリーム(O/W)を以下の成分から調製する:
重量%
A.パラフィン、液体(1) 8.0
イソプロピルミリステート(1) 4.0
Mirasil CM5(2) 3.0
ステアリン酸(1) 3.0
Arlacel 165V(3) 5.0
チリロシド 1.0
B.グリセリン(87%)(1) 3.0
Germaben II(4) 0.5
水、脱塩 合計100
C.RonaCare(商標)Ectoin(1) 1.0
調製
初めに相Aと相Bを別々に75℃に加熱する。次いで、相Aを相Bに撹拌しながらゆっくり添加し、均質混合物を形成するまで撹拌を継続する。均質になった後、乳濁液を撹拌しながら30℃に冷却する。引き続いて混合物を35℃に温め、相Cを添加して均一になるまで撹拌する。
材料の供給元は以下の通りである:
(1)Merck KGaA
(2)Rhodia
(3)Uniqema
(4)ISP
実施例5
W/O乳濁液としての局所用組成物
重量%
A.Isolan PDI(2) 3.0
パラフィン油、液体(1) 17.0
イソプロピルミリステート 5.0
蜜ロウ 0.2
Cutina HR(2) 0.3
チリロシド 1.0
B.水、脱塩 合計100
グリセリン(87%) 4.0
硫酸マグネシウム 1.0
Germaben II−E(3) 1.0
C.RonaCare(商標)LPO(1) 2.0
調製
相Aと相Bを別々に75℃に加熱する。相Bを相Aに撹拌しながらゆっくり添加する。引き続いて混合物をTurraxを用いて9000rpmで2分間均質化する。得られた混合物を30〜35℃に冷却し、撹拌しながらCを添加する。
材料の供給元は以下の通りである:
(1)Merck KGaA
(2)Goldschmidt AG
(3)ISP
神経皮膚炎の治療
以下に記載する実験で使用した基礎クリームはNivea(商標)クリーム(Beiersdorf AG(ハンブルク))(成分:水、液体パラフィン(Paraffinum Liquidum)、微結晶ロウ、グリセリン、ラノリンアルコール(Eucerit(登録商標)、パラフィン、硫酸マグネシウムデシルオレエート、オクチルドデカノール、ステアリン酸アルミニウム、パンテノール、クエン酸、ステアリン酸マグネシウム、香料)とした。
例1:
女性被験者(31)は、誕生以来慢性の神経皮膚炎を罹患しており、これをPrednisolon(商標)で治療している。急性段階で、チリロシド1%を添加含有する基礎クリームを、病気の皮膚領域に3日間毎日2度薄く塗った。急性症状は2日以内にすべて完全に消えた。また、5週以内には新たな症状は生じなかった。再発時にも同一の観察結果が得られ、その後活性が失われることなく持続した。
例2:
女性被験者(42)は神経皮膚炎に罹患している。チリロシドなしの基礎クリームと比較して、基礎クリーム(1%チリロシド添加)による治療は、皮膚像における著しい改善を示した。チリロシドを含む基礎クリームにより紅変は完全に消失した。
Claims (10)
- 式IA:
R4は、モノまたはジグルコシド基であり、その場合下記基:
の化合物の、湿疹の予防および/または治療のための製剤を製造するための使用。 - 前記製剤が、幼児性湿疹、神経皮膚炎、痒疹および乾燥性皮膚炎などのアトピー性湿疹の予防および/または治療に適した製剤であることを特徴とする請求項1または2に記載の使用。
- 式IA1の化合物が植物抽出物または精製植物抽出物の形態あるいは植物抽出物から調製された純物質の形態で使用され、該植物抽出物が5〜90重量%の式IA1の化合物を含むことを特徴とする、請求項1〜3のいずれかに記載の使用。
- 前記植物抽出物がシダ・グラジオヴィ(Sida glaziovii)植物からの抽出によって単離されたものであることを特徴とする、請求項4に記載の使用。
- 前記製剤中に0.001〜20重量%の量の式IAの1個または複数の化合物が存在することを特徴とする請求項1〜5のいずれかに記載の使用。
- 前記製剤が1種または複数の酸化防止剤および/またはスキンケアおよび/または炎症抑止作用を有する1種類または複数のさらなる活性成分を含むことを特徴とする請求項1〜6のいずれか1項に記載の使用。
- 前記式IAの化合物がチリロシドであることを特徴とする、請求項1から7のいずれかに記載の使用。
- 前記チリロシドが、植物抽出物または精製植物抽出物の形態あるいは植物抽出物から調製された純物質の形態であることを特徴とする請求項8に記載の使用。
- a)少なくとも1つの請求項1に記載の化合物、
b)皮膚許容性の賦形剤、
c)グルココルチコイドおよびタクロリムスから選択される炎症抑止効果を有する1または複数のさらなる活性成分、
を含む、湿疹の予防および/または治療における局所適用のための製剤。
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BRPI0722054A2 (pt) * | 2006-12-28 | 2014-04-01 | Limerick Biopharma Inc | Composição, kit, e métodos para diminuir um efeito colateral de tratamento com um inibidor da calcineurina, para aumentar um efeito terapêutico de um inibidor da calcineurina e para mudar a concentração de tacrolimus ou um análogo de tacrolimus em um compartimento fisiológico. |
DE102007013857A1 (de) | 2007-03-20 | 2008-09-25 | Maria Clementine Martin Klosterfrau Vertriebsgesellschaft Mbh | Neue Zusammensetzungen, insbesondere für die topische Behandlung von Hauterkrankungen |
EA016247B1 (ru) | 2007-04-19 | 2012-03-30 | Мэри Кэй Инк. | Топическая композиция для уменьшения темных кругов, отечности и отвисания кожи в области глаз человека и способ ее применения |
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FR2932680B1 (fr) * | 2008-06-19 | 2010-08-27 | Clarins Lab | Association de tiliroside et d'un peptide |
WO2009158031A2 (en) * | 2008-06-27 | 2009-12-30 | Limerick Biopharma, Inc. | Methods and compositions for therapeutic treatment |
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EP2353596A1 (en) * | 2010-02-02 | 2011-08-10 | SIGMA-TAU Industrie Farmaceutiche Riunite S.p.A. | Combination composition, comprising as active ingredients L-carnitine or propionyl L-carnitine, for the prevention or treatment of chronic venous insufficiency |
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JP6516246B2 (ja) * | 2014-10-02 | 2019-05-22 | オリザ油化株式会社 | フィラグリン及びインボルクリンの発現促進剤 |
CN108451900A (zh) * | 2018-05-08 | 2018-08-28 | 钟啟铭 | 一种治疗手足部皮肤角质细菌感染的药材及其加工方法 |
JP6635615B2 (ja) * | 2018-09-25 | 2020-01-29 | オリザ油化株式会社 | フィラグリン及びインボルクリンの発現促進剤 |
KR102272653B1 (ko) * | 2019-10-29 | 2021-07-05 | 순천대학교 산학협력단 | 항염증 활성을 나타내는 켐페롤-3-오-글루코실-6¨-오-펜타디오닉산 화합물 및 이를 유효성분으로 포함하는 항염증용 조성물 |
CN111035583A (zh) * | 2019-12-23 | 2020-04-21 | 广州市拉凯尔干细胞研究所 | 一种改善真表皮连接层的护肤品组合物 |
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-
2002
- 2002-09-02 DE DE10240923A patent/DE10240923A1/de not_active Withdrawn
-
2003
- 2003-07-16 DE DE60307749T patent/DE60307749T2/de not_active Expired - Lifetime
- 2003-07-16 EP EP03015616A patent/EP1393733B1/en not_active Expired - Lifetime
- 2003-07-16 AT AT03015616T patent/ATE336996T1/de not_active IP Right Cessation
- 2003-07-16 ES ES03015616T patent/ES2271433T3/es not_active Expired - Lifetime
- 2003-08-28 JP JP2003304920A patent/JP4668527B2/ja not_active Expired - Fee Related
- 2003-09-02 US US10/652,043 patent/US20040053860A1/en not_active Abandoned
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DE19544905A1 (de) * | 1995-12-01 | 1997-06-05 | Robugen Gmbh | Verfahren zur Herstellung von Pflanzenextrakten |
JP2000026263A (ja) * | 1998-05-15 | 2000-01-25 | Coletica | フラボノイド組成物及び化粧剤におけるその新規使用 |
WO2000028035A1 (en) * | 1998-11-10 | 2000-05-18 | Human Genome Sciences Inc. | CHEMOKINE β-7 |
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EP1393733A1 (en) | 2004-03-03 |
ES2271433T3 (es) | 2007-04-16 |
DE10240923A1 (de) | 2004-03-04 |
JP2004091489A (ja) | 2004-03-25 |
DE60307749D1 (de) | 2006-10-05 |
DE60307749T2 (de) | 2007-08-16 |
ATE336996T1 (de) | 2006-09-15 |
US20040053860A1 (en) | 2004-03-18 |
EP1393733B1 (en) | 2006-08-23 |
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