MD3032F1 - Copper (II) naphthalidyosemicarbazides containing sulfanylamides - Google Patents
Copper (II) naphthalidyosemicarbazides containing sulfanylamides Download PDFInfo
- Publication number
- MD3032F1 MD3032F1 MDA20050322A MD20050322A MD3032F1 MD 3032 F1 MD3032 F1 MD 3032F1 MD A20050322 A MDA20050322 A MD A20050322A MD 20050322 A MD20050322 A MD 20050322A MD 3032 F1 MD3032 F1 MD 3032F1
- Authority
- MD
- Moldova
- Prior art keywords
- copper
- compounds
- invention consists
- exhibits
- naphthalidyosemicarbazides
- Prior art date
Links
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 title abstract 2
- RSPCKAHMRANGJZ-UHFFFAOYSA-N thiohydroxylamine Chemical class SN RSPCKAHMRANGJZ-UHFFFAOYSA-N 0.000 title 1
- 230000000845 anti-microbial effect Effects 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000003814 drug Substances 0.000 abstract 2
- 239000005749 Copper compound Substances 0.000 abstract 1
- 230000000844 anti-bacterial effect Effects 0.000 abstract 1
- 230000003385 bacteriostatic effect Effects 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 150000001880 copper compounds Chemical class 0.000 abstract 1
- 231100000053 low toxicity Toxicity 0.000 abstract 1
- 244000005700 microbiome Species 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical class NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- 229910052723 transition metal Inorganic materials 0.000 abstract 1
- 150000003624 transition metals Chemical class 0.000 abstract 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A40/00—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
- Y02A40/10—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in agriculture
- Y02A40/20—Fertilizers of biological origin, e.g. guano or fertilizers made from animal corpses
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Inventia se refera la chimie si medicina, si anume la un sir de compusi interni de cupru biologic activi din clasa tiosemicarbazidatilor metalelor de tranzitie care pot gasi aplicare in practica medicala si medicina veterinara in calitate de preparate antimicrobiene. Esenta inventiei consta in obtinerea naftalidentiosemicarbazidatilor de cupru(II) care contin sulfanilamide cu formula: I - XIunde R = H (I - V), C6H5 (VI - IX);Compusii I-IX manifesta activitate antimicrobiana.Rezultatul inventiei consta in sinteza compusilor I-IX, care au toxicitate joasa, manifesta activitate antimicrobiana fata de majoritatea microorganismelor, iar in cazul tulpinilor gram-pozitive ale culturilor testate manifesta activitate bacteriostatica si bactericida de 16...160 ori mai inalta. The invention relates to chemistry and medicine, namely to a number of biologically active internal copper compounds in the thiosemicarbazidate class of transition metals that can find application in medical practice and veterinary medicine as antimicrobial preparations. The essence of the invention consists in obtaining the naphthalidentesemicarbazidates of copper (II) containing sulphanilamides of the formula: I - XIunde R = H (I - V), C6H5 (VI - IX); Compounds I-IX show antimicrobial activity. The result of the invention consists in the synthesis of compounds. I-IX, which have low toxicity, exhibits antimicrobial activity against most microorganisms, and in the case of the gram-positive strains of the cultures tested, it exhibits bacteriostatic and bactericidal activity of 16 ... 160 times higher.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MDA20050322A MD3032G2 (en) | 2005-10-31 | 2005-10-31 | Sulfanilamide-containing naphthalidenethiosemicarbazidates of copper(II) |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MDA20050322A MD3032G2 (en) | 2005-10-31 | 2005-10-31 | Sulfanilamide-containing naphthalidenethiosemicarbazidates of copper(II) |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MD3032F1 true MD3032F1 (en) | 2006-04-30 |
| MD3032G2 MD3032G2 (en) | 2006-11-30 |
Family
ID=36202596
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MDA20050322A MD3032G2 (en) | 2005-10-31 | 2005-10-31 | Sulfanilamide-containing naphthalidenethiosemicarbazidates of copper(II) |
Country Status (1)
| Country | Link |
|---|---|
| MD (1) | MD3032G2 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MD4133C1 (en) * | 2010-07-19 | 2012-05-31 | Государственный Университет Молд0 | [(2-Carbamotioylhydrazone)propionato(2-)]-(4-aminobenzenesulfonamide)copper, manifesting antimicrobial activity against bacteria of the genus Bacillus cereus |
| MD4179C1 (en) * | 2011-05-23 | 2013-02-28 | Государственный Университет Молд0 | Coordinative compounds of copper(II), containing 4-phenylthiosemicarbazone 2-formylpyridine and sulfonylamides, exhibiting antimicrobial activity against bacteria of Bacillus cereus species |
| MD4252C1 (en) * | 2012-05-31 | 2014-05-31 | Государственный Университет Молд0 | Catena-(µ-nitrato)[µ-(2-hydroxybenzylidene)-4-prop-2-en-1-ylthiocarbazone-S]silver with antimicrobial activity against bacteria Salmonella abony |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MD4112C1 (en) * | 2010-05-17 | 2011-12-31 | Государственный Университет Молд0 | Coordinative compounds of copper with 4-(dimethylphenyl)-thiosemicarbazones of 2-formylpyridine |
| MD4127C1 (en) * | 2010-10-06 | 2012-04-30 | Государственный Университет Молд0 | Use of di(m-S)-bis{chloro-[1-(pyridine-2-yl)ethanone-4-methylthiosemicarbazonato(1-)]copper} as substance with antimicrobial activity against Staphylococcus aureus |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MD2942C2 (en) * | 2004-04-27 | 2006-06-30 | Государственный Медицинский И Фармацевтический Университет "Nicolae Testemitanu" Республики Молдова | Di(µ-O)-bis(3,5-dibromosalicylidene thiosemicarbazonatocopper) |
-
2005
- 2005-10-31 MD MDA20050322A patent/MD3032G2/en not_active IP Right Cessation
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MD4133C1 (en) * | 2010-07-19 | 2012-05-31 | Государственный Университет Молд0 | [(2-Carbamotioylhydrazone)propionato(2-)]-(4-aminobenzenesulfonamide)copper, manifesting antimicrobial activity against bacteria of the genus Bacillus cereus |
| MD4179C1 (en) * | 2011-05-23 | 2013-02-28 | Государственный Университет Молд0 | Coordinative compounds of copper(II), containing 4-phenylthiosemicarbazone 2-formylpyridine and sulfonylamides, exhibiting antimicrobial activity against bacteria of Bacillus cereus species |
| MD4252C1 (en) * | 2012-05-31 | 2014-05-31 | Государственный Университет Молд0 | Catena-(µ-nitrato)[µ-(2-hydroxybenzylidene)-4-prop-2-en-1-ylthiocarbazone-S]silver with antimicrobial activity against bacteria Salmonella abony |
Also Published As
| Publication number | Publication date |
|---|---|
| MD3032G2 (en) | 2006-11-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG4A | Patent for invention issued | ||
| KA4A | Patent for invention lapsed due to non-payment of fees (with right of restoration) | ||
| MM4A | Patent for invention definitely lapsed due to non-payment of fees |