GB1040733A - Mycobacteriostatic compositions - Google Patents
Mycobacteriostatic compositionsInfo
- Publication number
- GB1040733A GB1040733A GB1661264A GB1661264A GB1040733A GB 1040733 A GB1040733 A GB 1040733A GB 1661264 A GB1661264 A GB 1661264A GB 1661264 A GB1661264 A GB 1661264A GB 1040733 A GB1040733 A GB 1040733A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aliphatic
- group
- compositions
- oil
- carbon atoms
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
-
- 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
- A61K31/13—Amines
- A61K31/155—Amidines (), e.g. guanidine (H2N—C(=NH)—NH2), isourea (N=C(OH)—NH2), isothiourea (—N=C(SH)—NH2)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
-
- 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
- A61K8/43—Guanidines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/005—Antimicrobial preparations
-
- 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)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- Dermatology (AREA)
- Birds (AREA)
- Cosmetics (AREA)
Abstract
Soaps, liquid soaps and shampoos based on synthetic detergents contain a mycobacteriostat consisting of a compound having linked to a nitrogen atom of a biguanide either a halogen-containing aliphatic oxyphenyl group, the aliphatic oxy group of which has at least 2 carbon atoms, or an aliphatic oxyphenyl group in which the aliphatic substituent is a hydro-carbon substituent containing from 5 to 9 carbon atoms, or a salt of such a compound. Specified biguanides are those of the formula <FORM:1040733/C4-C5/1> where R is the aliphatic group which may be alkyl, alkenyl, cycloalkyl, or aralkyl. The phenyl nucleus may be further substituted, e.g. with a halogen atom, nitro, amino, aryl, or aliphatic group. A hydrogen atom in the biguanide residue may also be replaced by, for instance, an aliphatic or aromatic group. The salts may either be acid addition or quaternary ammonium salts. The synthetic detergent materials in shampoos may be ionic, e.g. alkali metal salt of a sulphonated olive or castor oil, non-ionic, e.g. an ester or ether of a polyethylene glycol, or a mixture of both types.ALSO:Mycobacteriostatic compositions comprise a base that is pharmaceutically acceptable for external human use and as active ingredient less than 1% by wt. of the composition of a compound having linked to a nitrogen atom of a bignamide either a halogen-containing aliphatic oxyphenyl group, the aliphatic oxy group of which has at least 2 carbon atoms, or an aliphatic oxyphenyl group in which the aliphatic substituent is a hydrocarbon substituent containing from 5 to 9 carbon atoms, or a salt of such a compound. Specified bignamides are those of the formula <FORM:1040733/A5-A6/1> where R is the aliphatic group, which may be alkyl, alkenyl, cycloalkyl, or aralkyl. The phenyl nucleus may be further substituted e.g. it may contain a halogen atom, a nitro, amino, aryl, or aliphatic group (e.g. one of those specified above with reference to R). A hydrogen atom in the bignamide residue may also be replaced by, for instance, an aliphatic or aromatic group. The salts may either be acid addition or quaternary ammonium salts. The compositions may be in the form of ointments i.e. anhydrous solutions or dispersions of the active ingredient in a suitable base e.g. animal, vegetable, or mineral grease such as lard or petroleum jelly, oil e.g. olive, arachis, cottonseed or sesame oil, or wax e.g. beeswax. The base may be an aqueous emulsion in which case the compositions contain either water-in-oil emulsifying agents such as lanolin or wool alcohols or oil-in-water emulsifying agents such as Emulsifying Wax B.P. Ear drops, medicated cosmetic and toilet preparations e.g. hand or body lotions, lipsticks, talcum powders, soaps, liquid soaps and shampoos based on synthetic detergents, may be other forms of the mycobacteriostatic compositions.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1661264A GB1040733A (en) | 1964-04-22 | 1964-04-22 | Mycobacteriostatic compositions |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1661264A GB1040733A (en) | 1964-04-22 | 1964-04-22 | Mycobacteriostatic compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1040733A true GB1040733A (en) | 1966-09-01 |
Family
ID=10080476
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1661264A Expired GB1040733A (en) | 1964-04-22 | 1964-04-22 | Mycobacteriostatic compositions |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1040733A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2379284A1 (en) * | 1977-02-08 | 1978-09-01 | Roussel Uclaf | NEW CHLORHEXIDINE-BASED MEDICINAL PRODUCT AND METHOD OF PREPARATION |
-
1964
- 1964-04-22 GB GB1661264A patent/GB1040733A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2379284A1 (en) * | 1977-02-08 | 1978-09-01 | Roussel Uclaf | NEW CHLORHEXIDINE-BASED MEDICINAL PRODUCT AND METHOD OF PREPARATION |
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