209416-34-2Relevant academic research and scientific papers
Synthesis and antimicrobial activity of some condensed [4-(2,4,6- trimethylphenyl)-1(2H)-oxo-phthalazin-2-yl]acetic acid hydrazide
El-Hashash, Maher A.,El-Kady, Ahmed Y.,Taha, Mamdouh A.,El-Shamy, Ibrahim E.
, p. 616 - 626 (2012/05/05)
Some new 1,2,4-triazolo-, 1,3,4-oxadiazolo-, 1,3,4-thiadiazol-, and pyrazolo-2,4,6-trimethylphenyl-1(2H)-oxo-phthalazine derivatives were synthesized and identified by IR, 1H NMR, 13C NMR, MS and elemental analysis. The new compounds were synthesized with the objective of studying their antimicrobial activity.
Synthesis and antimicrobial ealuation of some annelated phthalazine deriaties and acyclo C-nucleosides from 1-chloro-4-(2,4,6-trimethylphenyl) phthalazine precursor
El-Hashash, Maher Abdel Aziz,Soliman, Ahmed Youssef,El-Shamy, Ibrahim Essam
, p. 347 - 366 (2012/06/30)
A highly efficient and ersatile synthetic approach to the synthesis of annelated phthalazine deriaties iz. 1,2,4-triazolo[3,4-a]phthalazine 11a,b, 14, 18, 19a,b, 29-31, 33, 1,2,4-triazino[3,4-a]phthalazine 25a,b-28, 1,3,5-triazino[4,3-a]phthalazine 22, tetrazolo[5,1-a] phthalazine 23, imidazophthalazine 9a,b,15, and pyrimidinophthlazine 6, 10, 16, 17, 20 is presented. Moreoer, acyclo C -nucleoside and double headed acyclo C-nucleoside of 1,2,4-triazolo[3,4-a]phthalazine 12, 13 were obtained ia heterocyclization reaction of 1-chloro-4-(2,4,6-trimethylphenyl)phthalazine (4) with gluconic acid hydrazide and galactaric acid bis hydrazide, respectiely. The new compounds were synthesized with the objectie of studying their antimicrobial actiity. TUeBITAK.
Isoquinolinamine and phthalazinamine derivatives: corticotropin-releasing factor receptor CRF1 specific ligands
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Page column 15, (2010/01/30)
Disclosed are compounds that are highly selective partial agonists or antagonists at human CRF1receptors that are useful in the diagnosis and treatment of treating stress related disorders such as post traumatic stress disorder (PTSD) as well as depression, headache and anxiety. The compounds have the formula or the pharmaceutically acceptable salts thereof wherein Ar, R1, R2, R3, R4and W are various organic and inorganic substituents.
Isoquinolinamine and phthalazinamine derivatives: corticotropin-releasing factor receptor CRF1 specific ligands
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, (2008/06/13)
Disclosed are compounds that are highly selective partial agonists or antagonists at human CRF1 receptors that are useful in the diagnosis and treatment of treating stress related disorders such as post traumatic stress disorder (PTSD) as well as depression, headache and anxiety. The compounds have the formula or the pharmaceutically acceptable salts thereof wherein Ar, R1, R2, R3, R4 and W are various organic and inorganic substituents.
