CH495750A - Produit capillaire - Google Patents
Produit capillaireInfo
- Publication number
- CH495750A CH495750A CH119365A CH119365A CH495750A CH 495750 A CH495750 A CH 495750A CH 119365 A CH119365 A CH 119365A CH 119365 A CH119365 A CH 119365A CH 495750 A CH495750 A CH 495750A
- Authority
- CH
- Switzerland
- Prior art keywords
- product according
- active compound
- cysteine
- hydrochloride
- methyl
- Prior art date
Links
- 206010039792 Seborrhoea Diseases 0.000 title abstract description 5
- 208000008742 seborrheic dermatitis Diseases 0.000 title abstract description 5
- 239000002304 perfume Substances 0.000 claims abstract description 7
- 239000000975 dye Substances 0.000 claims abstract description 5
- 150000003839 salts Chemical class 0.000 claims abstract description 4
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 3
- 230000000149 penetrating effect Effects 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims description 27
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- FBPINGSGHKXIQA-BYPYZUCNSA-N (2r)-2-amino-3-(2-carboxyethylsulfanyl)propanoic acid Chemical compound OC(=O)[C@@H](N)CSCCC(O)=O FBPINGSGHKXIQA-BYPYZUCNSA-N 0.000 claims description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 5
- FBPINGSGHKXIQA-UHFFFAOYSA-N S-carboxyethyl-L-cysteine Natural products OC(=O)C(N)CSCCC(O)=O FBPINGSGHKXIQA-UHFFFAOYSA-N 0.000 claims description 5
- GBFLZEXEOZUWRN-VKHMYHEASA-N S-carboxymethyl-L-cysteine Chemical compound OC(=O)[C@@H](N)CSCC(O)=O GBFLZEXEOZUWRN-VKHMYHEASA-N 0.000 claims description 5
- 239000002537 cosmetic Substances 0.000 claims description 4
- XUJNEKJLAYXESH-UHFFFAOYSA-L cysteinate(2-) Chemical compound [S-]CC(N)C([O-])=O XUJNEKJLAYXESH-UHFFFAOYSA-L 0.000 claims description 4
- -1 methoxy carbonyl methyl Chemical group 0.000 claims description 3
- 239000000725 suspension Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 239000006071 cream Substances 0.000 claims description 2
- 229960001305 cysteine hydrochloride Drugs 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 150000007524 organic acids Chemical class 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims 2
- QIJRTFXNRTXDIP-UHFFFAOYSA-N (1-carboxy-2-sulfanylethyl)azanium;chloride;hydrate Chemical compound O.Cl.SCC(N)C(O)=O QIJRTFXNRTXDIP-UHFFFAOYSA-N 0.000 claims 1
- DLMYFMLKORXJPO-FQEVSTJZSA-N (2R)-2-amino-3-[(triphenylmethyl)thio]propanoic acid Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(SC[C@H](N)C(O)=O)C1=CC=CC=C1 DLMYFMLKORXJPO-FQEVSTJZSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 238000004090 dissolution Methods 0.000 claims 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims 1
- 210000001732 sebaceous gland Anatomy 0.000 abstract description 2
- 241000700159 Rattus Species 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 235000019441 ethanol Nutrition 0.000 description 5
- 229960002433 cysteine Drugs 0.000 description 3
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 3
- 235000018417 cysteine Nutrition 0.000 description 3
- 230000000694 effects Effects 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 229960001913 mecysteine Drugs 0.000 description 2
- WHOHXJZQBJXAKL-UHFFFAOYSA-N methyl 2-amino-3-sulfanylpropanoate;hydrochloride Chemical compound Cl.COC(=O)C(N)CS WHOHXJZQBJXAKL-UHFFFAOYSA-N 0.000 description 2
- MCYHPZGUONZRGO-VKHMYHEASA-N methyl L-cysteinate Chemical compound COC(=O)[C@@H](N)CS MCYHPZGUONZRGO-VKHMYHEASA-N 0.000 description 2
- 210000004761 scalp Anatomy 0.000 description 2
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- 201000004384 Alopecia Diseases 0.000 description 1
- 101100382541 Escherichia coli (strain K12) casD gene Proteins 0.000 description 1
- 241000880493 Leptailurus serval Species 0.000 description 1
- 101100387131 Myxococcus xanthus (strain DK1622) devS gene Proteins 0.000 description 1
- ILVGMCVCQBJPSH-WDSKDSINSA-N Ser-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@@H](N)CO ILVGMCVCQBJPSH-WDSKDSINSA-N 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 101150049463 cas5 gene Proteins 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 208000024963 hair loss Diseases 0.000 description 1
- 230000003676 hair loss Effects 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- XMJHPCRAQCTCFT-UHFFFAOYSA-N methyl chloroformate Chemical compound COC(Cl)=O XMJHPCRAQCTCFT-UHFFFAOYSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
- A61K8/447—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof containing sulfur
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR961897A FR1472021A (fr) | 1964-01-29 | 1964-01-29 | Nouveau produit capillaire |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH495750A true CH495750A (fr) | 1970-09-15 |
Family
ID=8821950
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH119365A CH495750A (fr) | 1964-01-29 | 1965-01-28 | Produit capillaire |
Country Status (8)
| Country | Link |
|---|---|
| AT (1) | AT267754B (en, 2012) |
| BE (1) | BE658449A (en, 2012) |
| CH (1) | CH495750A (en, 2012) |
| DE (1) | DE1492071B2 (en, 2012) |
| FR (1) | FR1472021A (en, 2012) |
| GB (1) | GB1051870A (en, 2012) |
| IT (1) | IT943009B (en, 2012) |
| NL (1) | NL142587B (en, 2012) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999015136A1 (en) * | 1997-09-22 | 1999-04-01 | The Gillette Company | Reduction of hair growth |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU55371A1 (en, 2012) * | 1968-01-29 | 1969-08-21 | Oreal | |
| LU55935A1 (en, 2012) * | 1968-04-19 | 1969-11-14 | Oreal | |
| US3624143A (en) * | 1968-05-10 | 1971-11-30 | Merck & Co Inc | Compounds of the class {62 -aralkylthio-substituted-{60 -amino acids |
| BE733993A (en, 2012) * | 1968-06-14 | 1969-12-03 | ||
| LU58634A1 (en, 2012) * | 1969-05-12 | 1971-03-09 | Oreal | |
| BE755674A (fr) * | 1969-09-04 | 1971-03-03 | Oreal | Nouveaux composes derives de la pyridine et compositions cosmetiques les contenant |
-
0
- GB GB1051870D patent/GB1051870A/en active Active
-
1964
- 1964-01-29 FR FR961897A patent/FR1472021A/fr not_active Expired
-
1965
- 1965-01-18 IT IT263265A patent/IT943009B/it active
- 1965-01-18 BE BE658449D patent/BE658449A/xx unknown
- 1965-01-22 NL NL6500849A patent/NL142587B/xx not_active IP Right Cessation
- 1965-01-25 AT AT59365A patent/AT267754B/de active
- 1965-01-26 DE DE1965O0010624 patent/DE1492071B2/de active Granted
- 1965-01-28 CH CH119365A patent/CH495750A/fr not_active IP Right Cessation
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999015136A1 (en) * | 1997-09-22 | 1999-04-01 | The Gillette Company | Reduction of hair growth |
| US5939458A (en) * | 1997-09-22 | 1999-08-17 | Henry; James P. | Reduction of hair growth |
Also Published As
| Publication number | Publication date |
|---|---|
| GB1051870A (en, 2012) | |
| BE658449A (en, 2012) | 1965-07-19 |
| AT267754B (de) | 1969-01-10 |
| IT943009B (it) | 1973-04-02 |
| NL6500849A (en, 2012) | 1965-07-30 |
| DE1492071B2 (de) | 1973-11-08 |
| DE1492071A1 (de) | 1969-11-13 |
| NL142587B (nl) | 1974-07-15 |
| FR1472021A (fr) | 1967-03-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2148651C (fr) | Utilisation de composes antifongiques et de composes antibacteriens halogenes pour diminuer la chute des cheveux | |
| CA1160572A (fr) | Solution stable a l'oxydation d'au moins un acide gras essentiel notamment de vitamine f et d'huile de jojoba et compositions cosmetiques les contenants | |
| CA1177606A (fr) | Utilisation de derives hydroxyles du benzaldehyde pour la coloration des fibres keratiniques procede et composition les mettant en oeuvre | |
| CA2109424C (fr) | Composition topique anti-radicaux libres a base de superoxyde-dismutase et d'un derive phosphonique | |
| BE1000188A3 (fr) | Composition cosmetique permettant de lutter contre l'aspect gras des cheveux, et son utilisation. | |
| CA1341273C (fr) | Systeme anti-oxydant a base d'un ester d'ascorbyle stabilise et compositions contenant un tel systeme anti-oxydant | |
| FR2604357A1 (fr) | Composition pharmaceutique et cosmetique anti-acneique | |
| FR2939654A1 (fr) | Procede de coloration capillaire mettant en oeuvre un derive de l'hematoxyline, de l'hemateine, de la braziline ou de la brazileine, un sel metallique, du peroxyde d'hydrogene et du (bi)carbonate | |
| LU81257A1 (fr) | Composition cosmetique pour le traitement des cheveux et de la peau,contenant un extrait de salsepareille | |
| EP1005851B1 (fr) | Composition cosmétique ou dermatologique comprenant au moins un alkynyl carbamate et au moins un polyol | |
| EP0077742A1 (fr) | Lanolate de cuivre et compositions topiques le contenant | |
| CA1174171A (fr) | Composition anhydre, stable a l'oxydation, d'anthraline ou de l'un de ses derives dans un alkyl- ester d'acide gras et son utilisation dans le traitement des maladies de la peau | |
| LU86521A1 (fr) | Procede de teinture des cheveux avec des colorants hydroxyquinoniques et des sels metalliques | |
| FR2748937A1 (fr) | Utilisation d'alpha-alklyglucosides et d'esters d'alpha-alkylglucosides en tant qu'agents emulsionnants anti-microbiens | |
| CA2251003C (fr) | Nouveaux composes derives de n-aryl 2-hydroxy alkylamides | |
| CH495750A (fr) | Produit capillaire | |
| CA1341264C (fr) | Association de derives de 1,8-hydroxy et/ou acyloxy anthracene ou anthrone et de derives de pyrimidine pour induire et stimuler la croissance des cheveux et diminuer leur chute | |
| CA1180283A (fr) | Utilisation de benzoquinones pour la coloration directe des fibres keratiniques | |
| LU84511A1 (fr) | Utilisation de 5-hydroxynaphtoquinones pour la teinture des fibres keratiniques humaines,procede de teinture les mettant en oeuvre et composition tinctoriale utilisee | |
| CA1186231A (fr) | Utilisation d'hydroxynaphtoquinones pour la teinture des fibres keratiniques humaines, procede de teinture les mettant en oeuvre et composition tinctoriale utilisee | |
| CA2006891C (fr) | Composition pour induire et stimuler la croissance des cheveux et/ou freiner leur chute, a base de derives de pyrimidine et de filtres solaires | |
| CA2289817C (fr) | 2-amino, 4-alkylamino pyrimidine 3-oxydes comme apaisants | |
| CA1341268C (fr) | Composition pour induire et stimuler la croissance des cheveux et/ou freiner leur chute | |
| FR3068213B1 (fr) | Melange antimicrobien contenant du 4-(3-ethoxy-4-hydroxyphenyl)butan-2-one et un compose arginate, et composition cosmetique le contenant | |
| CA1083482A (fr) | Lotion demaquillante pour les yeux |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |