메뉴 건너뛰기




Volumn 70, Issue 3, 2005, Pages 131-136

Synthesis of biologically active steroid derivatives by the utility of Lawesson's reagent

Author keywords

Bioactivity; Lawesson's reagent; Organophosphorus; Steroids

Indexed keywords

2,4 BIS(4 METHOXYPHENYL) 1,3,2,4 DITHIAPHOSPHETANE 2,4 DISULFIDE; 3,20 DIOXIMINOPROGESTERONE; 3BETA HYDROXY 2' CYANOACETYL 3' (4 METHOXYPHENYL) 3' THIOXO 1',2',3' DIAZA PHOSPHOLO[4',5':16,17] 5ALPHA ANDROSTANE; 3BETA HYDROXY 5ALPHA ANDROSTAN 17 ACETYLHYDRAZONE; 3BETA HYDROXY 5ALPHA ANDROSTAN 17 CYANOACETYLHYDRAZONE; 3BETA HYDROXY 5ALPHA ANDROSTAN 17 OXIME; 3BETA MERCAPTO 5ALPHA ANDROSTAN 17 THIOACETYLHYDRAZONE; 3BETA MERCAPTO 5ALPHA ANDROSTAN 17 THIOXIME; 5' METHYL 3' (4 METHOXYPHENYL) 3' THIOXOSPIRO(2',1',3' OXAZAPHOSPHOL 4',17 ANDROS 4 ENE) 3 OXIME; AMPICILLIN; ANDROSTANE DERIVATIVE; DISULFIDE; NYSTATIN; PROGESTERONE DERIVATIVE; STEROID; UNCLASSIFIED DRUG;

EID: 14844314862     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2004.11.001     Document Type: Article
Times cited : (42)

References (27)
  • 1
    • 0028970008 scopus 로고
    • New steroidal antiinflammatory antedrugs: Steroidal[16α, 17α-d]-3′-carbethoxisoxazo lines
    • T. Kwon, A.S. Heiman, E.T. Oriaku, K. Yoon, and H.J. Lee New steroidal antiinflammatory antedrugs: Steroidal[16α, 17α-d]-3′- carbethoxisoxazo lines J Med Chem 38 6 1995 1048 1051
    • (1995) J Med Chem , vol.38 , Issue.6 , pp. 1048-1051
    • Kwon, T.1    Heiman, A.S.2    Oriaku, E.T.3    Yoon, K.4    Lee, H.J.5
  • 2
    • 0035246591 scopus 로고    scopus 로고
    • Synthesis and neuromuscular blocking activity of 16β- piperidinosteroidal derivatives
    • D.P. Jindal, P. Piplani, H. Fajrak, C. Prior, and I.G. Marshall Synthesis and neuromuscular blocking activity of 16β-piperidinosteroidal derivatives Eur J Med Chem 36 2001 195 202
    • (2001) Eur J Med Chem , vol.36 , pp. 195-202
    • Jindal, D.P.1    Piplani, P.2    Fajrak, H.3    Prior, C.4    Marshall, I.G.5
  • 3
    • 0037153203 scopus 로고    scopus 로고
    • Synthesis of halogen-substituted pyridyl and pyrimidyl derivatives of [3,2-c]pyrazole corticosteroids: Strategies for the development of glucocrticoid receptor mediated imaging agents
    • R.M. Hoyte, J. Zhong, R. Lerum, A. Oluyemi, P. Persaud, and C. O'Connor Synthesis of halogen-substituted pyridyl and pyrimidyl derivatives of [3,2-c]pyrazole corticosteroids: Strategies for the development of glucocrticoid receptor mediated imaging agents J Med Chem 45 24 2002 5397 5405
    • (2002) J Med Chem , vol.45 , Issue.24 , pp. 5397-5405
    • Hoyte, R.M.1    Zhong, J.2    Lerum, R.3    Oluyemi, A.4    Persaud, P.5    O'Connor, C.6
  • 4
    • 0142200470 scopus 로고    scopus 로고
    • Organophosphorus compounds VII: Transformation of steroidal ketones with Lawesson's reagent into thioxo and heterofused steroids. Results of antimicrobial and antifungal activity
    • N.R. Mohamed, G.A. Elmegeed, and M. Younis Organophosphorus compounds VII: Transformation of steroidal ketones with Lawesson's reagent into thioxo and heterofused steroids. Results of antimicrobial and antifungal activity Phosphorus Sulfur Silicon 178 2003 2003 2017
    • (2003) Phosphorus Sulfur Silicon , vol.178 , pp. 2003-2017
    • Mohamed, N.R.1    Elmegeed, G.A.2    Younis, M.3
  • 5
    • 0033203050 scopus 로고    scopus 로고
    • Sultamo-steroids analogues: Part VII, synthesis of epi-androsterone derivatives with potential activity
    • S.H. Doss, N.A. Louca, G.A. Elmegeed, and R.M. Mohareb Sultamo-steroids analogues: Part VII, synthesis of epi-androsterone derivatives with potential activity Arch Pharm Res 22 5 1999 496 501
    • (1999) Arch Pharm Res , vol.22 , Issue.5 , pp. 496-501
    • Doss, S.H.1    Louca, N.A.2    Elmegeed, G.A.3    Mohareb, R.M.4
  • 6
    • 2642566906 scopus 로고    scopus 로고
    • Synthesis and antimicrobial evaluation of some novel cholestane heterocyclic derivatives
    • G.A. Elmegeed, W.W. Wardakhan, N.A. Louca, and M. Younis Synthesis and antimicrobial evaluation of some novel cholestane heterocyclic derivatives Archiv der Pharmazie 337 3 2004 140 147
    • (2004) Archiv der Pharmazie , vol.337 , Issue.3 , pp. 140-147
    • Elmegeed, G.A.1    Wardakhan, W.W.2    Louca, N.A.3    Younis, M.4
  • 7
    • 14844325246 scopus 로고    scopus 로고
    • Synthesis of novel pyrazolo, pyrimidino and pyrido androstane derivatives of pharmacological interest
    • G.A. Elmegeed Synthesis of novel pyrazolo, pyrimidino and pyrido androstane derivatives of pharmacological interest Egypt J Chem. 47 6 2004 575 585
    • (2004) Egypt J Chem. , vol.47 , Issue.6 , pp. 575-585
    • Elmegeed, G.A.1
  • 8
    • 49249152717 scopus 로고
    • Studies on organophosphorus compounds XVIII. Synthesis of 3H-1,2-dithiole-3-thiones and 4H-1,3,2-oxaza-phosphorine derivatives from the dimer of p-methoxyphenylthiono phosphine sulfide and derivatives of 3-oxocarboxylic acids
    • B.S. Pederson, and S.O. Lawesson Studies on organophosphorus compounds XVIII. Synthesis of 3H-1,2-dithiole-3-thiones and 4H-1,3,2-oxaza-phosphorine derivatives from the dimer of p-methoxyphenylthiono phosphine sulfide and derivatives of 3-oxocarboxylic acids Tetrahedrone 35 1979 2433 2437
    • (1979) Tetrahedrone , vol.35 , pp. 2433-2437
    • Pederson, B.S.1    Lawesson, S.O.2
  • 9
    • 0025773616 scopus 로고
    • Synthesis, stereochemical analysis and neuromuscular blocking activity of oximino ether derivatives of progesterone
    • N. Khouri, A. Usubillaga, A. Cedillo Vaz, and J.N. Delgado Synthesis, stereochemical analysis and neuromuscular blocking activity of oximino ether derivatives of progesterone J Pharm Sci 80 7 1991 661 664
    • (1991) J Pharm Sci , vol.80 , Issue.7 , pp. 661-664
    • Khouri, N.1    Usubillaga, A.2    Cedillo Vaz, A.3    Delgado, J.N.4
  • 11
    • 0033074830 scopus 로고    scopus 로고
    • NMR vs. molecular modeling Part II- steroid chemical shift calculations
    • W.B. Smith NMR vs. molecular modeling Part II- steroid chemical shift calculations Magn Reson Chem 37 2 1999 103 106
    • (1999) Magn Reson Chem , vol.37 , Issue.2 , pp. 103-106
    • Smith, W.B.1
  • 12
    • 84942705127 scopus 로고
    • Joint Commission on Biochemical Nomenclature (JCBN). Nomenclature of steroids
    • IUPAC Joint Commission on Biochemical Nomenclature (JCBN). Nomenclature of steroids Pure Appl Chem 61 1989 1783 1822
    • (1989) Pure Appl Chem , vol.61 , pp. 1783-1822
    • Iupac1
  • 13
    • 0013177651 scopus 로고
    • Joint Commission on Biochemical Nomenclature (JCBN). Definitive rules for nomenclature of steroids
    • IUPAC Joint Commission on Biochemical Nomenclature (JCBN). Definitive rules for nomenclature of steroids J Am Chem Soc 82 1960 5577 5581
    • (1960) J Am Chem Soc , vol.82 , pp. 5577-5581
    • Iupac1
  • 14
    • 0024976769 scopus 로고
    • Joint Commission on Biochemical Nomenclature (JCBN). The nomenclature of steroids, Recommendations 1989
    • IUPAC Joint Commission on Biochemical Nomenclature (JCBN). The nomenclature of steroids, Recommendations 1989 Eur J Biochem 186 1989 429 458
    • (1989) Eur J Biochem , vol.186 , pp. 429-458
    • Iupac1
  • 16
    • 0015347342 scopus 로고
    • Standardized single-disc method for antibiotic susceptibility testing of anaerobic bacteria
    • T.D. Wilkins, L.V. Holdman, I.J. Abramson, and W.E. Moore Standardized single-disc method for antibiotic susceptibility testing of anaerobic bacteria Antimicrob Agents Chemother 1 1972 451 459
    • (1972) Antimicrob Agents Chemother , vol.1 , pp. 451-459
    • Wilkins, T.D.1    Holdman, L.V.2    Abramson, I.J.3    Moore, W.E.4
  • 18
    • 44349183414 scopus 로고
    • Tetrahedron report number 192: Thionation reactions of Lawesson's reagents
    • M.P. Cava, and M.I. Levinson Tetrahedron report number 192: Thionation reactions of Lawesson's reagents Tetrahedron 41 1985 5061 5087
    • (1985) Tetrahedron , vol.41 , pp. 5061-5087
    • Cava, M.P.1    Levinson, M.I.2
  • 19
    • 0001485155 scopus 로고
    • Studies on organophosphorus compounds 51: The reaction of oximes with 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiaphosphetane-2,4-disulphide (LR). Transformation of oximes to thioamides, thioketones and phosphorus containing heterocycles
    • R. Shabana, A.A. El-Barbary, A.B.A.G. Gatos, S.O. Lawesson, and C. Roemming Studies on organophosphorus compounds 51: The reaction of oximes with 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiaphosphetane-2,4-disulphide (LR). Transformation of oximes to thioamides, thioketones and phosphorus containing heterocycles Sulfur Lett 2 6 1984 223 239
    • (1984) Sulfur Lett , vol.2 , Issue.6 , pp. 223-239
    • Shabana, R.1    El-Barbary, A.A.2    Gatos, A.B.A.G.3    Lawesson, S.O.4    Roemming, C.5
  • 20
    • 0042453108 scopus 로고
    • Studies on organophosphorus compounds XXXVI. Simple new route to phosphorines from 2-hydroxy, 2-mercapto and 2-aminobenzoic acids and their derivatives
    • A.A. El-Barbary, and S.O. Lawesson Studies on organophosphorus compounds XXXVI. Simple new route to phosphorines from 2-hydroxy, 2-mercapto and 2-aminobenzoic acids and their derivatives Tetrahedron 37 15 1981 2647 2650
    • (1981) Tetrahedron , vol.37 , Issue.15 , pp. 2647-2650
    • El-Barbary, A.A.1    Lawesson, S.O.2
  • 23
    • 0000904591 scopus 로고
    • Studies on organophosphorus compounds XXXIV. Synthesis of 2,3-dihydro-1,3,4,2-thiadiazaphospholes and thiohydrazides
    • A.A. El-Barbary, S. Scheibye, S.O. Lawesson, and H. Fritz Studies on organophosphorus compounds XXXIV. Synthesis of 2,3-dihydro-1,3,4,2- thiadiazaphospholes and thiohydrazides Acta Chem Scand B34 1980 597 602
    • (1980) Acta Chem Scand , vol.34 , pp. 597-602
    • El-Barbary, A.A.1    Scheibye, S.2    Lawesson, S.O.3    Fritz, H.4
  • 24
    • 8544219691 scopus 로고
    • 2O two-phase system. A straight forward preparation of C(6)/C(7)-sulfenimine derivatives of penicillin and cephalosporin
    • 2O two-phase system. A straight forward preparation of C(6)/C(7)-sulfenimine derivatives of penicillin and cephalosporin Chem Lett 1984 1823
    • (1984) Chem Lett , pp. 1823
    • Toril, S.1    Tanaka, H.2    Hamano, S.3    Tada, N.4    Nokami, J.5    Sasaoka, M.6
  • 25
    • 0033853913 scopus 로고    scopus 로고
    • Antimicrobial and cancer cell growth inhibitory activities of 3β-acetoxy-17β-(l-prolyl) amino- 5α-androstane in vitro
    • R.K. Pettit, G.D. Cage, G.R. Pettit, and J.A. Liebman Antimicrobial and cancer cell growth inhibitory activities of 3β-acetoxy-17β-(l-prolyl) amino- 5α-androstane in vitro Int J Antimicrob Agent 15 4 2000 299 304
    • (2000) Int J Antimicrob Agent , vol.15 , Issue.4 , pp. 299-304
    • Pettit, R.K.1    Cage, G.D.2    Pettit, G.R.3    Liebman, J.A.4
  • 26
    • 0015987127 scopus 로고
    • Synthesis and antimicrobial properties of 17β-Amino-4-aza-5α- androstane and derivatives
    • W.E. Solomons, and N.J. Doorenbos Synthesis and antimicrobial properties of 17β-Amino-4-aza-5α-androstane and derivatives J. Pharm. Sci. 63 1 1974 19 23
    • (1974) J. Pharm. Sci. , vol.63 , Issue.1 , pp. 19-23
    • Solomons, W.E.1    Doorenbos, N.J.2
  • 27
    • 1842850530 scopus 로고    scopus 로고
    • A novel synthesis of phosphorus heterocycles. Reaction of α-hydazidoyl halides with phosphoranes and Lawesson's reagent
    • N.R. Mohamed, M.M. El-Saidi, H.M. Hassaneen, and A.W. Erian A novel synthesis of phosphorus heterocycles. Reaction of α-hydazidoyl halides with phosphoranes and Lawesson's reagent Phosphorus Sulfur Silicon 179 2004 521 528
    • (2004) Phosphorus Sulfur Silicon , vol.179 , pp. 521-528
    • Mohamed, N.R.1    El-Saidi, M.M.2    Hassaneen, H.M.3    Erian, A.W.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.