BG64365B1 - Използване на 1-хидрокси-2-пиридони за лечение на себореен дерматит - Google Patents

Използване на 1-хидрокси-2-пиридони за лечение на себореен дерматит Download PDF

Info

Publication number: BG64365B1
Authority: BG; Bulgaria
Prior art keywords: hydroxy; pyridone; formula; alkyl; use according
Prior art date: 1996-09-27

Application number

BG103260A

Other languages

Bulgarian (bg)

English (en)

Other versions

BG103260A (en

Inventor

Manfred Bohn

Karl Kraemer

Astrid Markus

Original Assignee

Hoechst Aktiengesellschaft

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.)

1996-09-27

Filing date

1999-03-17

Publication date

2004-12-30

1999-03-17 Application filed by Hoechst Aktiengesellschaft filed Critical Hoechst Aktiengesellschaft

2000-01-31 Publication of BG103260A publication Critical patent/BG103260A/xx

2004-12-30 Publication of BG64365B1 publication Critical patent/BG64365B1/bg

Links

206010039793 Seborrhoeic dermatitis Diseases 0.000 title claims abstract description 11
208000008742 seborrheic dermatitis Diseases 0.000 title claims abstract description 11
150000001875 compounds Chemical class 0.000 claims abstract description 17
238000002360 preparation method Methods 0.000 claims abstract description 6
239000000203 mixture Chemical group 0.000 claims description 23
125000000217 alkyl group Chemical group 0.000 claims description 17
-1 chloro, bromo, methoxy Chemical group 0.000 claims description 17
239000002453 shampoo Substances 0.000 claims description 14
125000004432 carbon atom Chemical group C* 0.000 claims description 11
239000004094 surface-active agent Substances 0.000 claims description 9
SNUSZUYTMHKCPM-UHFFFAOYSA-N 1-hydroxypyridin-2-one Chemical compound ON1C=CC=CC1=O SNUSZUYTMHKCPM-UHFFFAOYSA-N 0.000 claims description 8
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SCKYRAXSEDYPSA-UHFFFAOYSA-N ciclopirox Chemical compound ON1C(=O)C=C(C)C=C1C1CCCCC1 SCKYRAXSEDYPSA-UHFFFAOYSA-N 0.000 claims description 5
229910052760 oxygen Inorganic materials 0.000 claims description 5
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
125000003118 aryl group Chemical group 0.000 claims description 4
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125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
150000001767 cationic compounds Chemical class 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
229960000541 cetyl alcohol Drugs 0.000 description 1
WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
229920001436 collagen Polymers 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
SPCNPOWOBZQWJK-UHFFFAOYSA-N dimethoxy-(2-propan-2-ylsulfanylethylsulfanyl)-sulfanylidene-$l^{5}-phosphane Chemical compound COP(=S)(OC)SCCSC(C)C SPCNPOWOBZQWJK-UHFFFAOYSA-N 0.000 description 1
SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 1
LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical class C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
125000003438 dodecyl group Chemical group [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])* 0.000 description 1
JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
229940079593 drug Drugs 0.000 description 1
239000003814 drug Substances 0.000 description 1
239000000975 dye Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
210000000744 eyelid Anatomy 0.000 description 1
239000003925 fat Substances 0.000 description 1
150000002193 fatty amides Chemical class 0.000 description 1
239000006260 foam Substances 0.000 description 1
238000005187 foaming Methods 0.000 description 1
210000001061 forehead Anatomy 0.000 description 1
230000035876 healing Effects 0.000 description 1
BICAGYDGRXJYGD-UHFFFAOYSA-N hydrobromide;hydrochloride Chemical compound Cl.Br BICAGYDGRXJYGD-UHFFFAOYSA-N 0.000 description 1
MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
238000000338 in vitro Methods 0.000 description 1
125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 1
229910001411 inorganic cation Inorganic materials 0.000 description 1
IYRMNDOLPONSCJ-UHFFFAOYSA-N isoquinolin-2-ium;chloride Chemical compound Cl.C1=NC=CC2=CC=CC=C21 IYRMNDOLPONSCJ-UHFFFAOYSA-N 0.000 description 1
159000000003 magnesium salts Chemical class 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
HRDXJKGNWSUIBT-UHFFFAOYSA-N methoxybenzene Chemical group [CH2]OC1=CC=CC=C1 HRDXJKGNWSUIBT-UHFFFAOYSA-N 0.000 description 1
CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
229940100573 methylpropanediol Drugs 0.000 description 1
230000003020 moisturizing effect Effects 0.000 description 1
210000004877 mucosa Anatomy 0.000 description 1
YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 description 1
WYZDCUGWXKHESN-UHFFFAOYSA-N n-benzyl-n-methyl-1-phenylmethanamine Chemical compound C=1C=CC=CC=1CN(C)CC1=CC=CC=C1 WYZDCUGWXKHESN-UHFFFAOYSA-N 0.000 description 1
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
239000000025 natural resin Substances 0.000 description 1
210000001331 nose Anatomy 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 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
150000007524 organic acids Chemical group 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
201000000508 pityriasis versicolor Diseases 0.000 description 1
229920001983 poloxamer Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
235000007686 potassium Nutrition 0.000 description 1
239000000047 product Substances 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
230000002294 pubertal effect Effects 0.000 description 1
GGOZGYRTNQBSSA-UHFFFAOYSA-N pyridine-2,3-diol Chemical class OC1=CC=CN=C1O GGOZGYRTNQBSSA-UHFFFAOYSA-N 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
229940071089 sarcosinate Drugs 0.000 description 1
206010040872 skin infection Diseases 0.000 description 1
235000015424 sodium Nutrition 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000001587 sorbitan monostearate Substances 0.000 description 1
235000011076 sorbitan monostearate Nutrition 0.000 description 1
229940035048 sorbitan monostearate Drugs 0.000 description 1
239000007921 spray Substances 0.000 description 1
125000004079 stearyl 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])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
AGGIJOLULBJGTQ-UHFFFAOYSA-N sulfoacetic acid Chemical compound OC(=O)CS(O)(=O)=O AGGIJOLULBJGTQ-UHFFFAOYSA-N 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
229910021653 sulphate ion Inorganic materials 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
229940073455 tetraethylammonium hydroxide Drugs 0.000 description 1
LRGJRHZIDJQFCL-UHFFFAOYSA-M tetraethylazanium;hydroxide Chemical compound [OH-].CC[N+](CC)(CC)CC LRGJRHZIDJQFCL-UHFFFAOYSA-M 0.000 description 1
125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
238000002560 therapeutic procedure Methods 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
238000011200 topical administration Methods 0.000 description 1
125000005208 trialkylammonium group Chemical group 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical compound OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
241001148471 unidentified anaerobic bacterium Species 0.000 description 1
229940099259 vaseline Drugs 0.000 description 1
239000003643 water by type Substances 0.000 description 1
230000003442 weekly effect Effects 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 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
- A61K31/33—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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/006—Antidandruff preparations
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4412—Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4926—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having six membered rings
- 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
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
- 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
- A61P17/08—Antiseborrheics
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Veterinary Medicine (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Pharmacology & Pharmacy (AREA)
General Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Dermatology (AREA)
Epidemiology (AREA)
Bioinformatics & Cheminformatics (AREA)
Engineering & Computer Science (AREA)
Communicable Diseases (AREA)
Oncology (AREA)
Birds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Cosmetics (AREA)
Pyridine Compounds (AREA)

BG103260A 1996-09-27 1999-03-17 Използване на 1-хидрокси-2-пиридони за лечение на себореен дерматит BG64365B1 (bg)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19639818A DE19639818A1 (de)	1996-09-27	1996-09-27	Verwendung von 1-Hydroxy-2-pyridonen zur Behandlung der Seborrhoischen Dermatitis

Publications (2)

Publication Number	Publication Date
BG103260A BG103260A (en)	2000-01-31
BG64365B1 true BG64365B1 (bg)	2004-12-30

Family

ID=7807118

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BG103260A BG64365B1 (bg)	1996-09-27	1999-03-17	Използване на 1-хидрокси-2-пиридони за лечение на себореен дерматит

Country Status (31)

Country	Link
EP (1)	EP0928183B1 (sr)
JP (2)	JP2001500884A (sr)
KR (1)	KR100494207B1 (sr)
CN (1)	CN1104231C (sr)
AR (1)	AR008860A1 (sr)
AT (1)	ATE209891T1 (sr)
AU (1)	AU716208B2 (sr)
BG (1)	BG64365B1 (sr)
BR (1)	BR9711575A (sr)
CA (1)	CA2267165C (sr)
CY (1)	CY2362B1 (sr)
CZ (1)	CZ291485B6 (sr)
DE (2)	DE19639818A1 (sr)
DK (1)	DK0928183T3 (sr)
ES (1)	ES2167721T3 (sr)
HU (1)	HU226955B1 (sr)
ID (1)	ID21874A (sr)
IL (1)	IL129141A0 (sr)
MA (1)	MA24333A1 (sr)
MY (1)	MY125674A (sr)
NO (1)	NO312492B1 (sr)
NZ (1)	NZ334850A (sr)
OA (1)	OA11028A (sr)
PL (1)	PL188033B1 (sr)
PT (1)	PT928183E (sr)
RS (1)	RS49801B (sr)
TR (1)	TR199900662T2 (sr)
TW (1)	TW519491B (sr)
UA (1)	UA57754C2 (sr)
WO (1)	WO1998013009A2 (sr)
ZA (1)	ZA978640B (sr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19639816A1 (de)	1996-09-27	1998-04-02	Hoechst Ag	Antimykotische Mittel mit hoher Wirkstofffreisetzung
US20040039030A1 (en)	1996-09-27	2004-02-26	Hoechst Akeengesellschaft	Use of 1-hydroxy-2-pyridones for the treatment of seborrheic dermatitis
US20050095215A1 (en) *	2003-11-03	2005-05-05	Popp Karl F.	Antimicrobial shampoo compositions
PL2197440T3 (pl)	2007-08-31	2013-05-31	Janssen Pharmaceutica Nv	Kombinacje imazalilu i hydroksypirydonów
US20100305161A1 (en)	2007-11-30	2010-12-02	Jan Peter Hendrik Bosselaers	Combinations of fungicidal azoles and pyrion compounds
CA2711762C (en)	2008-02-06	2016-11-01	Jan Pieter Hendrik Bosselaers	Combinations of phenylpyrroles and pyrion compounds
WO2012001028A1 (en)	2010-07-01	2012-01-05	Janssen Pharmaceutica Nv	Antimicrobial combinations of pyrion compounds with polyethyleneimines
PL2646035T3 (pl) *	2010-12-02	2016-08-31	Univ Kansas	Proleki 6-cykloheksylo-1-hydroksy-4-metylopirydyn-2(1h)-onu i ich pochodne
JP5528629B2 (ja) *	2011-07-19	2014-06-25	リジェンティス株式会社	酵母菌から抽出されたポリリン酸，ポリリン酸の塩又はポリリン酸の溶媒和物を含むポリリン酸組成物及びその製造方法。
FR2983858B1 (fr) *	2011-12-08	2014-01-03	Fabre Pierre Dermo Cosmetique	Nouveaux composes inhibiteurs de la lipogenese
CN104744359B (zh) *	2015-03-06	2017-10-10	上药康丽（常州）药业有限公司	一种环吡酮的精制方法

Citations (1)

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DE2234009A1 (de) *	1972-07-11	1974-01-24	Hoechst Ag	Kosmetische zubereitungen

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NL8601762A (nl) *	1986-07-07	1988-02-01	Bouke Jan Lange	Werkwijze voor de reiniging en conditionering en eventuele medicinale behandeling van het haar en de hoofdhuid, een voor dit doel bruikbare tweefasen shampoo, alsmede een verpakking daarvoor.
AU5096393A (en) *	1992-09-08	1994-03-29	Procter & Gamble Company, The	Mild, substantially colorless shampoo composition
DE4333893A1 (de) *	1993-10-05	1995-04-06	Hoechst Ag	Kosmetische Zubereitungen
FR2722689B1 (fr) *	1994-07-20	1996-10-04	Fabre Pierre Dermo Cosmetique	Nouveau produit de combinaison comprenant un agent antifongique et du crotamiton comme potentialisateur de l'activite de l'agent antifongique, et compositions dermatologiques et/ou cosmetiques le comprenant

1996
- 1996-09-27 DE DE19639818A patent/DE19639818A1/de not_active Withdrawn
1997
- 1997-09-16 AT AT97910294T patent/ATE209891T1/de active
- 1997-09-16 CA CA002267165A patent/CA2267165C/en not_active Expired - Lifetime
- 1997-09-16 NZ NZ334850A patent/NZ334850A/en not_active IP Right Cessation
- 1997-09-16 RS YUP-134/99A patent/RS49801B/sr unknown
- 1997-09-16 DE DE59705697T patent/DE59705697D1/de not_active Expired - Lifetime
- 1997-09-16 HU HU9903811A patent/HU226955B1/hu unknown
- 1997-09-16 KR KR10-1999-7002553A patent/KR100494207B1/ko not_active Expired - Lifetime
- 1997-09-16 UA UA99042351A patent/UA57754C2/uk unknown
- 1997-09-16 BR BR9711575A patent/BR9711575A/pt not_active Application Discontinuation
- 1997-09-16 CZ CZ19991075A patent/CZ291485B6/cs not_active IP Right Cessation
- 1997-09-16 JP JP10515223A patent/JP2001500884A/ja active Pending
- 1997-09-16 PT PT97910294T patent/PT928183E/pt unknown
- 1997-09-16 PL PL33260397A patent/PL188033B1/pl unknown
- 1997-09-16 ES ES97910294T patent/ES2167721T3/es not_active Expired - Lifetime
- 1997-09-16 TR TR1999/00662T patent/TR199900662T2/xx unknown
- 1997-09-16 WO PCT/EP1997/005070 patent/WO1998013009A2/de not_active Ceased
- 1997-09-16 ID IDW990129A patent/ID21874A/id unknown
- 1997-09-16 IL IL12914197A patent/IL129141A0/xx not_active IP Right Cessation
- 1997-09-16 EP EP97910294A patent/EP0928183B1/de not_active Expired - Lifetime
- 1997-09-16 AU AU47746/97A patent/AU716208B2/en not_active Expired
- 1997-09-16 DK DK97910294T patent/DK0928183T3/da active
- 1997-09-16 CN CN97198266A patent/CN1104231C/zh not_active Expired - Lifetime
- 1997-09-25 TW TW086113944A patent/TW519491B/zh not_active IP Right Cessation
- 1997-09-25 AR ARP970104432A patent/AR008860A1/es not_active Application Discontinuation
- 1997-09-26 MY MYPI97004501A patent/MY125674A/en unknown
- 1997-09-26 ZA ZA9708640A patent/ZA978640B/xx unknown
- 1997-09-29 MA MA24814A patent/MA24333A1/fr unknown
1999
- 1999-03-17 BG BG103260A patent/BG64365B1/bg unknown
- 1999-03-25 NO NO19991460A patent/NO312492B1/no not_active IP Right Cessation
- 1999-03-26 OA OA9900071A patent/OA11028A/fr unknown
2003
- 2003-05-26 CY CY0300044A patent/CY2362B1/xx unknown
2006
- 2006-03-22 JP JP2006078057A patent/JP2006176540A/ja not_active Abandoned

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2234009A1 (de) *	1972-07-11	1974-01-24	Hoechst Ag	Kosmetische zubereitungen

Also Published As

Publication number	Publication date
DE59705697D1 (de)	2002-01-17
ATE209891T1 (de)	2001-12-15
DK0928183T3 (da)	2002-04-02
NZ334850A (en)	2001-02-23
TR199900662T2 (xx)	1999-06-21
CY2362B1 (en)	2004-06-04
IL129141A0 (en)	2000-02-17
EP0928183B1 (de)	2001-12-05
CN1231595A (zh)	1999-10-13
HK1022267A1 (en)	2000-08-04
HU226955B1 (en)	2010-03-29
AU716208B2 (en)	2000-02-24
WO1998013009A3 (de)	1998-05-14
BG103260A (en)	2000-01-31
NO312492B1 (no)	2002-05-21
JP2001500884A (ja)	2001-01-23
KR100494207B1 (ko)	2005-06-13
ID21874A (id)	1999-08-05
RS49801B (sr)	2008-06-05
NO991460D0 (no)	1999-03-25
PL332603A1 (en)	1999-09-27
PL188033B1 (pl)	2004-11-30
CZ291485B6 (cs)	2003-03-12
AU4774697A (en)	1998-04-17
EP0928183A2 (de)	1999-07-14
PT928183E (pt)	2002-05-31
CN1104231C (zh)	2003-04-02
HUP9903811A3 (en)	2001-11-28
MA24333A1 (fr)	1998-04-01
JP2006176540A (ja)	2006-07-06
CA2267165A1 (en)	1998-04-02
NO991460L (no)	1999-03-25
CA2267165C (en)	2003-12-16
OA11028A (fr)	2003-03-06
YU13499A (sh)	2001-09-28
UA57754C2 (uk)	2003-07-15
CZ107599A3 (cs)	1999-06-16
WO1998013009A2 (de)	1998-04-02
HUP9903811A1 (hu)	2000-04-28
KR20000048613A (ko)	2000-07-25
MY125674A (en)	2006-08-30
AR008860A1 (es)	2000-02-23
TW519491B (en)	2003-02-01
BR9711575A (pt)	1999-08-24
DE19639818A1 (de)	1998-04-02
ZA978640B (en)	1998-03-27
ES2167721T3 (es)	2002-05-16

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