MD4174C1 - Derivaţi tiosemicarbazonici ai acidului 4-formil-3-hidroxi-2-naftoic cu proprietăţi antibacteriene - Google Patents

Derivaţi tiosemicarbazonici ai acidului 4-formil-3-hidroxi-2-naftoic cu proprietăţi antibacteriene

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Publication number
MD4174C1
MD4174C1 MDA20110096A MD20110096A MD4174C1 MD 4174 C1 MD4174 C1 MD 4174C1 MD A20110096 A MDA20110096 A MD A20110096A MD 20110096 A MD20110096 A MD 20110096A MD 4174 C1 MD4174 C1 MD 4174C1
Authority
MD
Moldova
Prior art keywords
formyl
hydroxy
naphthoic acid
antibacterial properties
thiosemicarbazone derivatives
Prior art date
Application number
MDA20110096A
Other languages
English (en)
Russian (ru)
Other versions
MD4174B1 (ro
Inventor
Ana Lazarescu
Elena ZARICIUC
Daniela Cojocari
Constantin Turta
Veaceslav Gonciar
Polina Bouros
Original Assignee
Институт Химии Академии Наук Молдовы
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.)
Filing date
Publication date
Application filed by Институт Химии Академии Наук Молдовы filed Critical Институт Химии Академии Наук Молдовы
Priority to MDA20110096A priority Critical patent/MD4174C1/ro
Publication of MD4174B1 publication Critical patent/MD4174B1/ro
Publication of MD4174C1 publication Critical patent/MD4174C1/ro

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  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Invenţia se referă la compuşi organici din clasa tiosemicarbazonelor care posedă activitate antibacteriană. Compuşii pot fi utilizaţi în medicină, medicina veterinară şi agricultură.Esenţa invenţiei constă în sinteza derivaţilor noi ai acidului 4-formil-3-hidroxi-2-naftoic cu formula:unde R = H (1) şi C6H5 (2). Compuşii manifestă proprietăţi bacteriostatice şi bactericide faţă de microorganismele patogene S. aureus şi E.coli.
MDA20110096A 2011-10-25 2011-10-25 Derivaţi tiosemicarbazonici ai acidului 4-formil-3-hidroxi-2-naftoic cu proprietăţi antibacteriene MD4174C1 (ro)

Priority Applications (1)

Application Number Priority Date Filing Date Title
MDA20110096A MD4174C1 (ro) 2011-10-25 2011-10-25 Derivaţi tiosemicarbazonici ai acidului 4-formil-3-hidroxi-2-naftoic cu proprietăţi antibacteriene

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
MDA20110096A MD4174C1 (ro) 2011-10-25 2011-10-25 Derivaţi tiosemicarbazonici ai acidului 4-formil-3-hidroxi-2-naftoic cu proprietăţi antibacteriene

Publications (2)

Publication Number Publication Date
MD4174B1 MD4174B1 (ro) 2012-06-30
MD4174C1 true MD4174C1 (ro) 2013-01-31

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Application Number Title Priority Date Filing Date
MDA20110096A MD4174C1 (ro) 2011-10-25 2011-10-25 Derivaţi tiosemicarbazonici ai acidului 4-formil-3-hidroxi-2-naftoic cu proprietăţi antibacteriene

Country Status (1)

Country Link
MD (1) MD4174C1 (ro)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3457301A (en) * 1965-04-29 1969-07-22 Ugine Kuhlmann Disazomethine pigments
SU437306A3 (ru) * 1970-10-24 1974-07-25 Басф Аг (Фирма) Способ получения дисазометинового пигмента
US3839434A (en) * 1970-04-27 1974-10-01 Basf Ag Amidine substituted naphthalene carboxylic acid
MD678G2 (ro) * 1996-07-17 1997-09-30 Государственный Университет Молд0 DI-(mu-O)-di[N-(2-oxo-1-naftal)-N'-alfa-oxobenzalhidrazincupru] dihidrat care manifestă proprietăţi antimicrobiene selective
MD3371G2 (ro) * 2006-08-30 2008-02-29 Технический университет Молдовы Aparat de diagnosticare a transmisiei longitudinale
MD4127C1 (ro) * 2010-10-06 2012-04-30 Государственный Университет Молд0 Utilizare a di(µ-S)-bis{cloro-[1-(piridin-2-il)etanon-4-metiltiosemicarbazonato(1-)]cupru} în calitate de substanţă cu activitate antimicrobiană faţă de Staphylococcus aureus

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3457301A (en) * 1965-04-29 1969-07-22 Ugine Kuhlmann Disazomethine pigments
DE1569710A1 (de) * 1965-04-29 1970-07-09 Ugine Kuhlmann Disazomethin-Verbindungen,Verfahren zu ihrer Herstellung und ihre Verwendung
US3839434A (en) * 1970-04-27 1974-10-01 Basf Ag Amidine substituted naphthalene carboxylic acid
SU437306A3 (ru) * 1970-10-24 1974-07-25 Басф Аг (Фирма) Способ получения дисазометинового пигмента
MD678G2 (ro) * 1996-07-17 1997-09-30 Государственный Университет Молд0 DI-(mu-O)-di[N-(2-oxo-1-naftal)-N'-alfa-oxobenzalhidrazincupru] dihidrat care manifestă proprietăţi antimicrobiene selective
MD3371G2 (ro) * 2006-08-30 2008-02-29 Технический университет Молдовы Aparat de diagnosticare a transmisiei longitudinale
MD4127C1 (ro) * 2010-10-06 2012-04-30 Государственный Университет Молд0 Utilizare a di(µ-S)-bis{cloro-[1-(piridin-2-il)etanon-4-metiltiosemicarbazonato(1-)]cupru} în calitate de substanţă cu activitate antimicrobiană faţă de Staphylococcus aureus

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
D.X. West, J.J. Ingram, N.M. Kozub, G.A. Bain, A.E. Liberta, Trans. Met. Chem. 21 (1996), p. 213 *
J. Marthakutty, V. Suni, Maliyeckal R., et al. Polyhedron, 23 (2004), p. 3069 *
L. Latheef, E. Manoj, M.R.P. Kurup, Acta Crystallogr., Sect. C 62 (2006), p. 16 *
M. B. Ferrari, F. Bisceglie, C. Casoli, et al. J. Med. Chem. 48 (2005), p. 1671 *
M.A. Ali, A.H. Mirza, A.M.S. Hossain, M. Nazimuddin, Polyhedron 20 (2001), p. 1045 *
Yu.K. Bhoon, Polyhedron, 2 (1983) nr. 5, p. 365 *

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