DD297807A5 - Hydroxyalkancarbonsaeure-derivate, deren herstellung und verwendung - Google Patents

Hydroxyalkancarbonsaeure-derivate, deren herstellung und verwendung Download PDF

Info

Publication number: DD297807A5
Authority: DD; German Democratic Republic
Prior art keywords: general formula; group; carbon atoms; acid; acid derivatives
Prior art date: 1989-02-17

Application number

DD90337871A

Other languages

German (de)

English (en)

Inventor

Christopher G Earnschaw

Gerald Kirsch

Petra Rach

Ruth Thieroff-Ekerdt

Michael Toepert

Original Assignee

��@��k��

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.)

1989-02-17

Filing date

1990-02-15

Publication date

1992-01-23

1990-02-15 Application filed by ��@��k�� filed Critical ��@��k��

1992-01-23 Publication of DD297807A5 publication Critical patent/DD297807A5/de

Links

239000002253 acid Substances 0.000 title claims description 26
238000002360 preparation method Methods 0.000 title claims description 12
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 16
125000000217 alkyl group Chemical group 0.000 claims abstract description 8
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 7
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 7
125000002252 acyl group Chemical group 0.000 claims abstract description 6
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 6
125000002947 alkylene group Chemical group 0.000 claims abstract description 5
125000004430 oxygen atom Chemical group O* 0.000 claims abstract description 5
229910052757 nitrogen Inorganic materials 0.000 claims abstract description 4
125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 4
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238000000034 method Methods 0.000 claims description 11
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239000012166 beeswax Substances 0.000 description 1
229960000686 benzalkonium chloride Drugs 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000008280 blood Substances 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
230000017531 blood circulation Effects 0.000 description 1
210000000988 bone and bone Anatomy 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
239000000872 buffer Substances 0.000 description 1
125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical group C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
229940119217 chamomile extract Drugs 0.000 description 1
235000020221 chamomile extract Nutrition 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
GPTXWRGISTZRIO-UHFFFAOYSA-N chlorquinaldol Chemical compound ClC1=CC(Cl)=C(O)C2=NC(C)=CC=C21 GPTXWRGISTZRIO-UHFFFAOYSA-N 0.000 description 1
MYSWGUAQZAJSOK-UHFFFAOYSA-N ciprofloxacin Chemical compound C12=CC(N3CCNCC3)=C(F)C=C2C(=O)C(C(=O)O)=CN1C1CC1 MYSWGUAQZAJSOK-UHFFFAOYSA-N 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
229920001436 collagen Polymers 0.000 description 1
201000004196 common wart Diseases 0.000 description 1
229940117173 croton oil Drugs 0.000 description 1
125000006254 cycloalkyl carbonyl group Chemical group 0.000 description 1
125000006638 cyclopentyl carbonyl group Chemical group 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
BEPAFCGSDWSTEL-UHFFFAOYSA-N dimethyl malonate Chemical compound COC(=O)CC(=O)OC BEPAFCGSDWSTEL-UHFFFAOYSA-N 0.000 description 1
230000003292 diminished effect Effects 0.000 description 1
SMVRDGHCVNAOIN-UHFFFAOYSA-L disodium;1-dodecoxydodecane;sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC SMVRDGHCVNAOIN-UHFFFAOYSA-L 0.000 description 1
PRAKJMSDJKAYCZ-UHFFFAOYSA-N dodecahydrosqualene Natural products CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 1
210000005069 ears Anatomy 0.000 description 1
208000033286 epidermolytic ichthyosis Diseases 0.000 description 1
210000000981 epithelium Anatomy 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
238000009472 formulation Methods 0.000 description 1
125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
239000003862 glucocorticoid Substances 0.000 description 1
125000000350 glycoloyl group Chemical group O=C([*])C([H])([H])O[H] 0.000 description 1
125000003630 glycyl group Chemical group [H]N([H])C([H])([H])C(*)=O 0.000 description 1
210000003780 hair follicle Anatomy 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002366 halogen compounds Chemical class 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
150000002367 halogens Chemical group 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000012676 herbal extract Substances 0.000 description 1
125000003104 hexanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
206010020718 hyperplasia Diseases 0.000 description 1
208000003532 hypothyroidism Diseases 0.000 description 1
230000002989 hypothyroidism Effects 0.000 description 1
206010021198 ichthyosis Diseases 0.000 description 1
238000000338 in vitro Methods 0.000 description 1
238000001727 in vivo Methods 0.000 description 1
230000001939 inductive effect Effects 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
230000004054 inflammatory process Effects 0.000 description 1
208000018381 inherited ichthyosis Diseases 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
229940119170 jojoba wax Drugs 0.000 description 1
230000001530 keratinolytic effect Effects 0.000 description 1
239000003410 keratolytic agent Substances 0.000 description 1
235000019388 lanolin Nutrition 0.000 description 1
229940039717 lanolin Drugs 0.000 description 1
125000000400 lauroyl 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])[H] 0.000 description 1
201000011486 lichen planus Diseases 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
230000002906 microbiologic effect Effects 0.000 description 1
230000003020 moisturizing effect Effects 0.000 description 1
210000004877 mucosa Anatomy 0.000 description 1
229940043348 myristyl alcohol Drugs 0.000 description 1
CLAHYJVFDMDAFN-UHFFFAOYSA-N n,n-dibutyl-11-hydroxyundecanamide Chemical compound CCCCN(CCCC)C(=O)CCCCCCCCCCO CLAHYJVFDMDAFN-UHFFFAOYSA-N 0.000 description 1
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
125000002801 octanoyl group Chemical group C(CCCCCCC)(=O)* 0.000 description 1
HVFSJXUIRWUHRG-UHFFFAOYSA-N oic acid Natural products C1CC2C3CC=C4CC(OC5C(C(O)C(O)C(CO)O5)O)CC(O)C4(C)C3CCC2(C)C1C(C)C(O)CC(C)=C(C)C(=O)OC1OC(COC(C)=O)C(O)C(O)C1OC(C(C1O)O)OC(COC(C)=O)C1OC1OC(CO)C(O)C(O)C1O HVFSJXUIRWUHRG-UHFFFAOYSA-N 0.000 description 1
230000036961 partial effect Effects 0.000 description 1
239000000312 peanut oil Substances 0.000 description 1
230000035515 penetration Effects 0.000 description 1
229940066842 petrolatum Drugs 0.000 description 1
235000019271 petrolatum Nutrition 0.000 description 1
125000004193 piperazinyl group Chemical group 0.000 description 1
125000003386 piperidinyl group Chemical group 0.000 description 1
206010035116 pityriasis rubra pilaris Diseases 0.000 description 1
230000003169 placental effect Effects 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
230000035755 proliferation Effects 0.000 description 1
229940055019 propionibacterium acne Drugs 0.000 description 1
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000010992 reflux Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
230000007017 scission Effects 0.000 description 1
210000001732 sebaceous gland Anatomy 0.000 description 1
210000002374 sebum Anatomy 0.000 description 1
239000012679 serum free medium Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
235000015424 sodium Nutrition 0.000 description 1
229940031439 squalene Drugs 0.000 description 1
TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 description 1
239000002600 sunflower oil Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
238000004114 suspension culture Methods 0.000 description 1
208000011580 syndromic disease Diseases 0.000 description 1
230000009885 systemic effect Effects 0.000 description 1
229940037128 systemic glucocorticoids Drugs 0.000 description 1
231100000211 teratogenicity Toxicity 0.000 description 1
238000002560 therapeutic procedure Methods 0.000 description 1
201000003875 tinea corporis Diseases 0.000 description 1
201000004647 tinea pedis Diseases 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
230000004584 weight gain Effects 0.000 description 1
235000019786 weight gain Nutrition 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
- 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
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C235/06—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Veterinary Medicine (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Chemical Kinetics & Catalysis (AREA)
Pharmacology & Pharmacy (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
Public Health (AREA)
Communicable Diseases (AREA)
Oncology (AREA)
Pain & Pain Management (AREA)
Rheumatology (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
Dermatology (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Cosmetics (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Polysaccharides And Polysaccharide Derivatives (AREA)

DD90337871A 1989-02-17 1990-02-15 Hydroxyalkancarbonsaeure-derivate, deren herstellung und verwendung DD297807A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE3905325A DE3905325A1 (de)	1989-02-17	1989-02-17	Hydroxyalkancarbonsaeure-derivate, deren herstellung und verwendung

Publications (1)

Publication Number	Publication Date
DD297807A5 true DD297807A5 (de)	1992-01-23

Family

ID=6374606

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD90337871A DD297807A5 (de)	1989-02-17	1990-02-15	Hydroxyalkancarbonsaeure-derivate, deren herstellung und verwendung

Country Status (13)

Country	Link
US (1)	US5089175A (fr)
EP (2)	EP0612719A1 (fr)
JP (1)	JPH03505216A (fr)
AT (1)	ATE113030T1 (fr)
AU (1)	AU626095B2 (fr)
CA (1)	CA2010261A1 (fr)
DD (1)	DD297807A5 (fr)
DE (2)	DE3905325A1 (fr)
GR (1)	GR900100035A (fr)
HU (1)	HU214317B (fr)
IE (1)	IE68670B1 (fr)
PT (1)	PT93155A (fr)
WO (1)	WO1990009373A1 (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5231087A (en) *	1988-03-16	1993-07-27	Cellegy Pharmaceuticals, Inc.	Treatment of skin diseases and tumors with esters and amides of monocarboxylic acids
CA1315803C (fr) *	1988-04-22	1993-04-06	Joseph P. Ciaudelli	N-alkoxyalkylamides d'hydroxyacides et compositions pour le traitement de la peau en contenant
ATE168557T1 (de) *	1989-03-13	1998-08-15	Cellegy Pharma Inc	Topische zubereitungen enthaltend aliphatische amine zur behandlung von hautkrankheiten
AU639373B2 (en) *	1990-10-22	1993-07-22	Unilever Plc	Cosmetic composition
GB9100816D0 (en) *	1991-01-15	1991-02-27	Unilever Plc	Cosmetic composition
DE4214895A1 (de) *	1992-05-07	1993-11-11	Schering Ag	Verfahren zur Herstellung von Hydroxyalkancarbonsäureamiden
DE19531084A1 (de)	1995-08-24	1997-02-27	Hoechst Schering Agrevo Gmbh	2,4-Diamino-1,3,5-triazine, Verfahren zu deren Herstellung und deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren
RU2203886C1 (ru) *	2001-12-11	2003-05-10	ОАО "Научно-исследовательский институт эластомерных материалов и изделий"	Аллиламиды перфторполиэфиркарбоновых кислот в качестве модификаторов резиновых смесей на основе фторкаучуков
DE102006053500A1 (de)	2006-11-14	2008-05-15	Evonik Goldschmidt Gmbh	Antimikrobielle Zusammensetzungen
US8729108B2 (en) *	2008-06-17	2014-05-20	Christopher J Dannaker	Waterborne topical compositions for the delivery of active ingredients such as azelaic acid
JP6247340B2 (ja) *	2016-06-08	2017-12-13	高級アルコール工業株式会社	アミドアルコールを含む化粧用基剤および化粧品

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2372797A (en) *	1940-01-26	1945-04-03	Nat Oil Prod Co	Condensation products
US2936325A (en) *	1957-12-27	1960-05-10	Pure Oil Co	Substituted amides as selective solvents for aromatic hydrocarbons

1989
- 1989-02-17 DE DE3905325A patent/DE3905325A1/de not_active Withdrawn
1990
- 1990-01-19 GR GR900100035A patent/GR900100035A/el unknown
- 1990-01-29 AT AT90902143T patent/ATE113030T1/de not_active IP Right Cessation
- 1990-01-29 EP EP94250072A patent/EP0612719A1/fr not_active Withdrawn
- 1990-01-29 JP JP2502524A patent/JPH03505216A/ja active Pending
- 1990-01-29 EP EP90902143A patent/EP0413006B1/fr not_active Expired - Lifetime
- 1990-01-29 WO PCT/DE1990/000057 patent/WO1990009373A1/fr not_active Ceased
- 1990-01-29 DE DE59007487T patent/DE59007487D1/de not_active Expired - Fee Related
- 1990-01-29 HU HU901484A patent/HU214317B/hu not_active IP Right Cessation
- 1990-02-15 PT PT93155A patent/PT93155A/pt not_active Application Discontinuation
- 1990-02-15 DD DD90337871A patent/DD297807A5/de not_active IP Right Cessation
- 1990-02-16 US US07/480,497 patent/US5089175A/en not_active Expired - Fee Related
- 1990-02-16 IE IE57290A patent/IE68670B1/en not_active IP Right Cessation
- 1990-02-16 CA CA002010261A patent/CA2010261A1/fr not_active Abandoned
- 1990-02-16 AU AU49876/90A patent/AU626095B2/en not_active Ceased

Also Published As

Publication number	Publication date
PT93155A (pt)	1990-08-31
IE68670B1 (en)	1996-07-10
AU626095B2 (en)	1992-07-23
IE900572L (en)	1990-08-17
HU214317B (hu)	1998-03-02
HU901484D0 (en)	1991-03-28
ATE113030T1 (de)	1994-11-15
GR900100035A (el)	1991-06-28
EP0413006B1 (fr)	1994-10-19
EP0612719A1 (fr)	1994-08-31
HUT57179A (en)	1991-11-28
CA2010261A1 (fr)	1990-08-17
DE3905325A1 (de)	1990-09-06
WO1990009373A1 (fr)	1990-08-23
DE59007487D1 (de)	1994-12-01
AU4987690A (en)	1990-08-23
JPH03505216A (ja)	1991-11-14
EP0413006A1 (fr)	1991-02-20
US5089175A (en)	1992-02-18

Legal Events

Date	Code	Title	Description
1995-05-11	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
DE69426629T2 (de)	2001-08-02	Therapeutische verbindung - fettsäurekonjugate
DE69205725T2 (de)	1996-05-30	Iminoderivate, Verfahren zu ihrer Herstellung und ihre Verwendung in der Human- und Tiermedizin und in der Kosmetik.
DE69103636T2 (de)	1995-02-09	Biaromatische verbindungen und ihre anwendung in menschen- und tierheilkunde und in der kosmetik.
JP2683390B2 (ja)	1997-11-26	局所適用のための医薬又は化粧品組成物
EP0176033A2 (fr)	1986-04-02	Dérivés de l'acide isoxazolecarboxylique, leur préparation et utilisation
DE3872937T2 (de)	1993-01-21	Benzoylaminophenoxybuttersaeure-derivate.
DD143902A5 (de)	1980-09-17	Verfahren zur herstellung von aminderivaten von glyzerin und propandiolen
EP0188749A2 (fr)	1986-07-30	Dérivés d'acide fumarique, leur procédé de préparation et compositions pharmaceutiques les contenant
DE69631688T2 (de)	2005-01-20	Indanverbindungen mit relaxierender Wirkung auf die glatten Muskeln und/oder mit Mastzellen stabilisierender und/oder entzündungshemmender Wirkung
DE3141586C2 (fr)	1991-02-21
DE3851262T2 (de)	1995-02-02	Benzoylaminophenoxybuttersäure-Derivate.
DD297807A5 (de)	1992-01-23	Hydroxyalkancarbonsaeure-derivate, deren herstellung und verwendung
DE3728917A1 (de)	1989-03-09	Neue lipide mit unsymmetrisch substituierter disulfidbruecke
DE2102172A1 (de)	1972-07-27	Neue Mitel zur Behandlung und Pflege der Haut
DE60013947T2 (de)	2005-10-06	(Poly)thia-alkin-Verbindungen und ihre Derivate, diese enthaltende Zusammensetzungen und ihre Anwendung
CH619211A5 (en)	1980-09-15	Process for the preparation of 11-cis-13-desmethyl vitamin A acid and all-trans-13-desmethyl vitamin A acid and their derivatives
DE69017295T2 (de)	1995-08-31	Bi-aromatische Ester, Verfahren zu ihrer Herstellung und ihre Verwendung in der menschlichen oder tierischen Heilkunde und in der Kosmetik.
DE68902772T2 (de)	1993-01-21	Sulfurierte eicosanoide und deren verwendung in arzneimitteln und kosmetika.
CH542201A (de)	1973-09-30	Verfahren zur Herstellung von Indolinderivaten
DE4032187A1 (de)	1992-04-16	N-retinoyl-l-aminomercapto-verbindungen
EP0009777A1 (fr)	1980-04-16	N-(carboxy)phényl amides de l'acide rétinoique et 7,8-déhydro-rétinoique, procédé de préparation et compositions pharmaceutiques les contenant
EP0017705B1 (fr)	1982-07-21	Dérivés de phénylalanyl-tryptophane, médicaments les contenant, leur préparation et leur utilisation
DE3882816T2 (de)	1993-12-09	Zimtsäureamid-Derivate.
EP0571062A1 (fr)	1993-11-24	Dérivés de l'acide hydroxyalkanecarboxylique, leur préparation et utilisation
DE3874603T2 (de)	1993-02-18	Zimtsaeureamid-derivate.