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Volumn 16, Issue 4, 2007, Pages 179-187

Synthesis and evaluation of 1-benzhydryl-sulfonyl-piperazine derivatives as inhibitors of MDA-MB-231 human breast cancer cell proliferation

Author keywords

1 benzhydryl piperazine derivatives; Cell proliferation; MDA MB 231; Sulfonyl chlorides

Indexed keywords

1 BENZHYDRYL 4 (3,5 DIMETHYL ISOXAZOLE 4 SULFONYL)PIPERAZINE; 1 BENZHYDRYL 4 (4 CHLORO BENZENESULFONYL)PIPERAZINE; 1 BENZHYDRYL 4 (4 TERT BUTYL BENZENESULFONYL)PIPERAZINE; 1 BENZHYDRYL 4 (TOLUENE 4 SULFONYL)PIPERAZINE; 1 BENZHYDRYL 4 METHANESULFONYL PIPERAZINE; PIPERAZINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 40549101901     PISSN: 10542523     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00044-007-9022-y     Document Type: Article
Times cited : (56)

References (30)
  • 1
    • 17744400080 scopus 로고    scopus 로고
    • Synthesis of 2-substituted piperazines via direct α-lithation
    • M Berkheij 2005 Synthesis of 2-substituted piperazines via direct α-lithation Tetrahedron Lett 15 2369 2371 10.1016/j.tetlet.2005.02.085 1:CAS:528:DC%2BD2MXit1yltbo%3D Berkheij M, et al. (2005) Synthesis of 2-substituted piperazines via direct α-lithation. Tetrahedron Lett 15:2369–2371
    • (2005) Tetrahedron Lett , vol.15 , pp. 2369-2371
    • Berkheij, M1
  • 2
    • 0031929859 scopus 로고    scopus 로고
    • Piperazine derivatives of butyric acid as differentiating agents in human leukemic Cells
    • R Gillet P Jeannesson H Sefraoui ML Arnould-GueArin S Kirkiacharian JC Jardillier F Pieri 1998 Piperazine derivatives of butyric acid as differentiating agents in human leukemic Cells Cancer Chemother Pharmaco 41 252 255 10.1007/s002800050737 1:CAS:528:DyaK1cXls1WjsQ%3D%3D Gillet R, Jeannesson P,Sefraoui H, Arnould-GueArin ML, Kirkiacharian S, Jardillier JC, Pieri F (1998) Piperazine derivatives of butyric acid as differentiating agents in human leukemic Cells. Cancer Chemother Pharmaco 41:252–255
    • (1998) Cancer Chemother Pharmaco , vol.41 , pp. 252-255
    • Gillet, R1    Jeannesson, P2    Sefraoui, H3    Arnould-GueArin, ML4    Kirkiacharian, S5    Jardillier, JC6    Pieri, F7
  • 3
    • 0033981477 scopus 로고    scopus 로고
    • Tumor apoptosis induced by epoxide-containing piperazines: a new class of anti-cancer agents
    • FE Gabriel J Gu LM Slater K Hara JW Jacobs 2000 Tumor apoptosis induced by epoxide-containing piperazines: a new class of anti-cancer agents Cancer Chemother Pharmacol 45 183 191 10.1007/s002800050028 Gabriel FE, Gu J, Slater LM, Hara K, Jacobs JW (2000) Tumor apoptosis induced by epoxide-containing piperazines: a new class of anti-cancer agents. Cancer Chemother Pharmacol 45:183–191
    • (2000) Cancer Chemother Pharmacol , vol.45 , pp. 183-191
    • Gabriel, FE1    Gu, J2    Slater, LM3    Hara, K4    Jacobs, JW5
  • 4
    • 0033575465 scopus 로고    scopus 로고
    • Novel applications of ethylgyyoxalate with the Ugi MCR
    • C Hulme 1999 Novel applications of ethylgyyoxalate with the Ugi MCR Tetrahedron Lett 40 5295 10.1016/S0040-4039(99)00960-0 1:CAS:528:DyaK1MXksVyntr0%3D Hulme C, et al. (1999) Novel applications of ethylgyyoxalate with the Ugi MCR. Tetrahedron Lett 40:5295
    • (1999) Tetrahedron Lett , vol.40 , pp. 5295
    • Hulme, C1
  • 5
    • 1842787547 scopus 로고    scopus 로고
    • Optically active antifungal azoles: synthesis and antifungal activity of (2R,3S)-2-(2,4-difluorophenyl)-3-(5-{2-[4-aryl-piperazin-1-yl]-ethyl}-tetrazol-2-yl/1-yl)-1-[1,2,4]-triazol-1-yl-butan-2-ol
    • RS Upadhayaya N Sinha S Jain N Kishore R Chandra SK Arora 2004 Optically active antifungal azoles: synthesis and antifungal activity of (2R,3S)-2-(2,4-difluorophenyl)-3-(5-{2-[4-aryl-piperazin-1-yl]-ethyl}-tetrazol-2-yl/1-yl)-1-[1,2,4]-triazol-1-yl-butan-2-ol Bioorg Med Chem 12 2225 15080922 10.1016/j.bmc.2004.02.014 1:CAS:528:DC%2BD2cXjtVKqu74%3D Upadhayaya RS, Sinha N, Jain S, Kishore N, Chandra R, Arora SK (2004) Optically active antifungal azoles: synthesis and antifungal activity of (2R,3S)-2-(2,4-difluorophenyl)-3-(5-{2-[4-aryl-piperazin-1-yl]-ethyl}-tetrazol-2-yl/1-yl)-1-[1,2,4]-triazol-1-yl-butan-2-ol. Bioorg Med Chem 12:2225
    • (2004) Bioorg Med Chem , vol.12 , pp. 2225
    • Upadhayaya, RS1    Sinha, N2    Jain, S3    Kishore, N4    Chandra, R5    Arora, SK6
  • 6
    • 32044472790 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of N-alkyl and N-aryl piperazine derivatives
    • P Choudhary R Kumar K Verma 2006 Synthesis and antimicrobial activity of N-alkyl and N-aryl piperazine derivatives Bioorg Med Chem 14 1819 1826 10.1016/j.bmc.2005.10.032 1:CAS:528:DC%2BD28XhtlKlsr4%3D Choudhary P, Kumar R, Verma K (2006) Synthesis and antimicrobial activity of N-alkyl and N-aryl piperazine derivatives. Bioorg Med Chem 14:1819–1826
    • (2006) Bioorg Med Chem , vol.14 , pp. 1819-1826
    • Choudhary, P1    Kumar, R2    Verma, K3
  • 7
    • 0027969994 scopus 로고
    • The design of a potent and orally bioavailable HIV protease inhibotor
    • JP Vacca 1994 The design of a potent and orally bioavailable HIV protease inhibotor J Med Chem 37 3443 7932573 10.1021/jm00047a001 Vacca JP, et al. (1994) The design of a potent and orally bioavailable HIV protease inhibotor. J Med Chem 37:3443
    • (1994) J Med Chem , vol.37 , pp. 3443
    • Vacca, JP1
  • 8
    • 0028147531 scopus 로고
    • Highly diastereoselective reaction of a chiral, non-racemic amide enolate with (S)-glycidyl tosylate. Synthesis of the orally active HIV-1 protease inhibitor L-735,524
    • D Askin 1994 Highly diastereoselective reaction of a chiral, non-racemic amide enolate with (S)-glycidyl tosylate. Synthesis of the orally active HIV-1 protease inhibitor L-735,524 Tetrahedron Lett 35 673 10.1016/S0040-4039(00)75787-X 1:CAS:528:DyaK2cXmsFKhtLc%3D Askin D, et al. (1994) Highly diastereoselective reaction of a chiral, non-racemic amide enolate with (S)-glycidyl tosylate. Synthesis of the orally active HIV-1 protease inhibitor L-735,524. Tetrahedron Lett 35:673
    • (1994) Tetrahedron Lett , vol.35 , pp. 673
    • Askin, D1
  • 9
    • 0029118635 scopus 로고
    • Asymmetric hydrogenation of tetrahydropyrazines: Synthesis of (S)-piperazine-2-tert-butylcarboxamide, an intermediate in the preparation of the HIV protease inhibitor indinavir
    • K Rossen 1995 Asymmetric hydrogenation of tetrahydropyrazines: Synthesis of (S)-piperazine-2-tert-butylcarboxamide, an intermediate in the preparation of the HIV protease inhibitor indinavir Tetrahedron Lett 36 6419 10.1016/0040-4039(95)01345-I 1:CAS:528:DyaK2MXnvFCls74%3D Rossen K, et al. (1995) Asymmetric hydrogenation of tetrahydropyrazines: Synthesis of (S)-piperazine-2-tert-butylcarboxamide, an intermediate in the preparation of the HIV protease inhibitor indinavir. Tetrahedron Lett 36:6419
    • (1995) Tetrahedron Lett , vol.36 , pp. 6419
    • Rossen, K1
  • 10
    • 85121062279 scopus 로고    scopus 로고
    • EGYT (1975) Pyridine derivatives having antidepressant activity. US-3865828
  • 11
    • 0033397898 scopus 로고    scopus 로고
    • MST-16, a Novel Bis- dioxopiperazine Anticancer Agent, Ameliorates Doxorubicin-induced Acute Toxicity While Maintaining Antitumor Efficacy
    • M Yoshida Y Maehara K Sugimachi 1999 MST-16, a Novel Bis-dioxopiperazine Anticancer Agent, Ameliorates Doxorubicin-induced Acute Toxicity While Maintaining Antitumor Efficacy Clinical Cancer Research 5 4295 4300 10632373 1:CAS:528:DC%2BD3cXlsV2msQ%3D%3D Yoshida M, Maehara Y,Sugimachi K (1999) MST-16, a Novel Bis-dioxopiperazine Anticancer Agent, Ameliorates Doxorubicin-induced Acute Toxicity While Maintaining Antitumor Efficacy. Clinical Cancer Research 5:4295–4300
    • (1999) Clinical Cancer Research , vol.5 , pp. 4295-4300
    • Yoshida, M1    Maehara, Y2    Sugimachi, K3
  • 12
    • 2942601916 scopus 로고    scopus 로고
    • Synthesis and functional activity of (2-aryl-1-piperizinyl)-N-(3- methylphenyl) acetamides: selective dopamine D4 receptor agonists
    • A Mark 2004 Synthesis and functional activity of (2-aryl-1-piperizinyl)-N-(3-methylphenyl) acetamides: selective dopamine D 4 receptor agonists Bioorg Med Chem 12 3471 3483 10.1016/j.bmc.2004.04.035 1:CAS:528:DC%2BD2cXks12ktLY%3D Mark A, et al. (2004) Synthesis and functional activity of (2-aryl-1-piperizinyl)-N-(3-methylphenyl) acetamides: selective dopamine D 4 receptor agonists. Bioorg Med Chem 12:3471–3483
    • (2004) Bioorg Med Chem , vol.12 , pp. 3471-3483
    • Mark, A1
  • 13
    • 0030961684 scopus 로고    scopus 로고
    • Substituted [(4-Phenylpiperazinyl)- methyl]benzamides: Selective Dopamine D4 Agonists
    • SA Glase HC Akunne LM Georgic TG Heffner RG Mackenzie PJ Manley TA Pugsley LD Wise 1997 Substituted [(4-Phenylpiperazinyl)-methyl]benzamides: Selective Dopamine D 4 Agonists J Med Chem 40 1771 9191952 10.1021/jm970021c 1:CAS:528:DyaK2sXjtFyhurs%3D Glase SA, Akunne HC, Georgic LM, Heffner TG, Mackenzie RG, Manley PJ, Pugsley TA, Wise LD (1997) Substituted [(4-Phenylpiperazinyl)-methyl]benzamides: Selective Dopamine D 4 Agonists. J Med Chem 40:1771
    • (1997) J Med Chem , vol.40 , pp. 1771
    • Glase, SA1    Akunne, HC2    Georgic, LM3    Heffner, TG4    Mackenzie, RG5    Manley, PJ6    Pugsley, TA7    Wise, LD8
  • 14
    • 0034719396 scopus 로고    scopus 로고
    • A Structure-Affinity Relationship Study on Derivatives of N-[2-[4-(4- Chlorophenyl) piperazin-1-yl]ethyl]-3-methoxybenzamide, a High-Affinity and Selective D4 Receptor Ligand
    • R Perrone F Berardi NA Colabufo M Leopoldo V Tortorella 2000 A Structure-Affinity Relationship Study on Derivatives of N-[2-[4-(4-Chlorophenyl) piperazin-1-yl]ethyl]-3-methoxybenzamide, a High-Affinity and Selective D4 Receptor Ligand J Med Chem 43 270 10649982 10.1021/jm991138z 1:CAS:528:DyaK1MXotFGgtb0%3D Perrone R, Berardi F, Colabufo NA, Leopoldo M, Tortorella V (2000) A Structure-Affinity Relationship Study on Derivatives of N-[2-[4-(4-Chlorophenyl) piperazin-1-yl]ethyl]-3-methoxybenzamide, a High-Affinity and Selective D4 Receptor Ligand. J Med Chem 43:270
    • (2000) J Med Chem , vol.43 , pp. 270
    • Perrone, R1    Berardi, F2    Colabufo, NA3    Leopoldo, M4    Tortorella, V5
  • 15
    • 1942438497 scopus 로고    scopus 로고
    • Design, synthesis, and structure-activity relationships of pyrazolo[3,4-d]pyrimidines: a novel class of potent enterovirus inhibitors
    • JH Chern 2004 Design, synthesis, and structure-activity relationships of pyrazolo[3,4-d]pyrimidines: a novel class of potent enterovirus inhibitors Bioorg Med Chem Lett 14 2519 2525 15109643 10.1016/j.bmcl.2004.02.092 1:CAS:528:DC%2BD2cXjsVKht70%3D Chern JH, et al. (2004) Design, synthesis, and structure-activity relationships of pyrazolo[3,4-d]pyrimidines: a novel class of potent enterovirus inhibitors. Bioorg Med Chem Lett 14:2519–2525
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 2519-2525
    • Chern, JH1
  • 16
    • 85121067027 scopus 로고    scopus 로고
    • Kimura M, et al. (2003a) Synthesis of novel diphenyl piperazine derivatives and their activities as inhibitors of dopamine uptake in the central nervous system. Bio Med Chem 11:1621–1630
  • 17
    • 85121080485 scopus 로고    scopus 로고
    • Kimura M, et al. (2003b) Novel diphenylalkyl piperazine derivatives with high affinities for the dopamine Transporter. Bio Med Chem 11:3953–3963
  • 18
    • 2442625358 scopus 로고    scopus 로고
    • Efficient asymmetric syntheses, determination of absolute configurations and biological activities of 1-[4,4-bis(4-fluorophenyl)butyl]-4-[2-hydroxy-3- (phenylamino)propyl]-piperazine as a novel potent dopamine uptake inhibotor in the central nervous system
    • M Kimura 2004 Efficient asymmetric syntheses, determination of absolute configurations and biological activities of 1-[4,4-bis(4-fluorophenyl)butyl]-4-[2-hydroxy-3-(phenylamino)propyl]-piperazine as a novel potent dopamine uptake inhibotor in the central nervous system Bioorg Med Chem 12 3069 3078 15142566 10.1016/j.bmc.2004.02.041 1:CAS:528:DC%2BD2cXktVKqtLo%3D Kimura M, et al. (2004) Efficient asymmetric syntheses, determination of absolute configurations and biological activities of 1-[4,4-bis(4-fluorophenyl)butyl]-4-[2-hydroxy-3-(phenylamino)propyl]-piperazine as a novel potent dopamine uptake inhibotor in the central nervous system. Bioorg Med Chem 12:3069–3078
    • (2004) Bioorg Med Chem , vol.12 , pp. 3069-3078
    • Kimura, M1
  • 19
    • 1842817632 scopus 로고    scopus 로고
    • Chloroalkyl piperazine and nitrogen mustard porphyrins: Synthesis and anticancer activity
    • CC Guo RB Tong KL Li 2004 Chloroalkyl piperazine and nitrogen mustard porphyrins: Synthesis and anticancer activity Bioorg Med Chem 12 2469 2475 15080942 10.1016/j.bmc.2004.01.045 1:CAS:528:DC%2BD2cXjtVOjs74%3D Guo CC, Tong RB, Li KL (2004) Chloroalkyl piperazine and nitrogen mustard porphyrins: Synthesis and anticancer activity. Bioorg Med Chem 12:2469–2475
    • (2004) Bioorg Med Chem , vol.12 , pp. 2469-2475
    • Guo, CC1    Tong, RB2    Li, KL3
  • 20
    • 3142730590 scopus 로고    scopus 로고
    • Antioxidative activities of novel diphenylalkyl piperazine derivatives with high affinities for the dopamine transporter
    • M Kimara T Masuda K Yamada 2004 Antioxidative activities of novel diphenylalkyl piperazine derivatives with high affinities for the dopamine transporter Bioorg Med Chem Lett 14 4287 4290 10.1016/j.bmcl.2004.05.091 1:CAS:528:DC%2BD2cXlvVWjtrc%3D Kimara M, Masuda T, Yamada K (2004) Antioxidative activities of novel diphenylalkyl piperazine derivatives with high affinities for the dopamine transporter. Bioorg Med Chem Lett 14:4287–4290
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 4287-4290
    • Kimara, M1    Masuda, T2    Yamada, K3
  • 21
    • 1942438497 scopus 로고    scopus 로고
    • Design, synthesis, and structure–activity relationships of pyrazolo[3,4-d]pyrimidines: a novel class of potent enterovirus inhibitors
    • JH Chern 2004 Design, synthesis, and structure–activity relationships of pyrazolo[3,4-d]pyrimidines: a novel class of potent enterovirus inhibitors Bioorg Med Chem Lett 14 10 2519 2525 15109643 10.1016/j.bmcl.2004.02.092 1:CAS:528:DC%2BD2cXjsVKht70%3D Chern JH, et al. (2004) Design, synthesis, and structure–activity relationships of pyrazolo[3,4-d]pyrimidines: a novel class of potent enterovirus inhibitors. Bioorg Med Chem Lett 14(10):2519–2525
    • (2004) Bioorg Med Chem Lett , vol.14 , Issue.10 , pp. 2519-2525
    • Chern, JH1
  • 22
    • 0035829429 scopus 로고    scopus 로고
    • Three-Dimensional Quantitative Structure-Activity Relationship (3D-QSAR) Models for a Novel Class of Piperazine-Based Stromelysin-1 (MMP-3) Inhibitors: Applying a “Divide and Conquer” Strategy
    • EA Amin WJ Welsh 2003 Three-Dimensional Quantitative Structure-Activity Relationship (3D-QSAR) Models for a Novel Class of Piperazine-Based Stromelysin-1 (MMP-3) Inhibitors: Applying a “Divide and Conquer” Strategy J Med Chem 44 3849 3855 10.1021/jm010236t 1:CAS:528:DC%2BD3MXnsV2ksL0%3D Amin EA, Welsh WJ (2003) Three-Dimensional Quantitative Structure-Activity Relationship (3D-QSAR) Models for a Novel Class of Piperazine-Based Stromelysin-1 (MMP-3) Inhibitors: Applying a “Divide and Conquer” Strategy. J Med Chem 44:3849–3855
    • (2003) J Med Chem , vol.44 , pp. 3849-3855
    • Amin, EA1    Welsh, WJ2
  • 23
    • 30344457007 scopus 로고    scopus 로고
    • Microwave-assisted synthesis of N-alkylated benzotriazole derivatives: Antimicrobial Studies
    • S Nanjunda Swamy 2006 Microwave-assisted synthesis of N-alkylated benzotriazole derivatives: Antimicrobial Studies Bioorg Med Chem Lett 16 999 1004 16298529 10.1016/j.bmcl.2005.10.084 1:CAS:528:DC%2BD28Xhs1Kntw%3D%3D Nanjunda Swamy S, et al. (2006) Microwave-assisted synthesis of N-alkylated benzotriazole derivatives: Antimicrobial Studies. Bioorg Med Chem Lett 16:999–1004
    • (2006) Bioorg Med Chem Lett , vol.16 , pp. 999-1004
    • Nanjunda Swamy, S1
  • 24
    • 33747194780 scopus 로고    scopus 로고
    • Synthesis and in vitro antimicrobial studies of medicinally important novel N-alkyl and N-sulfonyl derivatives of -[bis(4-fluorophenyl)-methyl]piperazine
    • JN Narendra Sharath Chandra CT Sadashiva CV Kavitha KS Rangappa 2006 Synthesis and in vitro antimicrobial studies of medicinally important novel N-alkyl and N-sulfonyl derivatives of-[bis(4-fluorophenyl)-methyl]piperazine Bioorg Med Chem 14 6621 6627 16784863 10.1016/j.bmc.2006.05.064 1:CAS:528:DC%2BD28XosVOiurw%3D Narendra Sharath Chandra JN, Sadashiva CT, Kavitha CV, Rangappa KS (2006) Synthesis and in vitro antimicrobial studies of medicinally important novel N-alkyl and N-sulfonyl derivatives of-[bis(4-fluorophenyl)-methyl]piperazine. Bioorg Med Chem 14:6621–6627
    • (2006) Bioorg Med Chem , vol.14 , pp. 6621-6627
    • Narendra Sharath Chandra, JN1    Sadashiva, CT2    Kavitha, CV3    Rangappa, KS4
  • 25
    • 85121062832 scopus 로고    scopus 로고
    • Priya BS, Anil Kumar C, Nanjunda Swamy S, Basappa, Naveen S, Rangappa KS (2007) 2-(2-(2-Ethoxybenzoylamino)-4-chlorophenoxy)-N-(2-ethoxybenzoyl)benzamine inhibits EAT cell induced angiogenesis by down regulation of VEGF secretion. Bioorg Med Chem Lett 17:2775–2780
  • 26
    • 34247560277 scopus 로고    scopus 로고
    • Synthesis and Evaluation of Tricyclic Dipyrido Diazepinone Derivatives as Inhibitors of Secretory Phospholipase A2 with Anti-Inflammatory Activity
    • NR Thimmegowda 2007 Synthesis and Evaluation of Tricyclic Dipyrido Diazepinone Derivatives as Inhibitors of Secretory Phospholipase A2 with Anti-Inflammatory Activity Curr Top Med Chem 7 811 820 17456044 10.2174/156802607780487650 1:CAS:528:DC%2BD2sXlvVGqu70%3D Thimmegowda NR, et al. (2007) Synthesis and Evaluation of Tricyclic Dipyrido Diazepinone Derivatives as Inhibitors of Secretory Phospholipase A2 with Anti-Inflammatory Activity. Curr Top Med Chem 7:811–820
    • (2007) Curr Top Med Chem , vol.7 , pp. 811-820
    • Thimmegowda, NR1
  • 27
    • 34247585152 scopus 로고    scopus 로고
    • Chemistry and Structural Evaluation of Different Phospholipase A2 Inhibitors in Arachidonic Acid Pathway Mediated Inflammation and Snake Venom Toxicity
    • JN Narendra Sharath Chandra 2007 Chemistry and Structural Evaluation of Different Phospholipase A2 Inhibitors in Arachidonic Acid Pathway Mediated Inflammation and Snake Venom Toxicity Curr Top Med Chem 7 787 800 17456042 10.2174/156802607780487678 1:STN:280:DC%2BD2s3kslGnug%3D%3D Narendra Sharath Chandra JN, et al. (2007) Chemistry and Structural Evaluation of Different Phospholipase A2 Inhibitors in Arachidonic Acid Pathway Mediated Inflammation and Snake Venom Toxicity. Curr Top Med Chem 7:787–800
    • (2007) Curr Top Med Chem , vol.7 , pp. 787-800
    • Narendra Sharath Chandra, JN1
  • 28
    • 34248674920 scopus 로고    scopus 로고
    • N- substituted-2-butyl-5-chloro-3H-imidazole-4-carbaldehyde derivatives as anti-tumor agents against Ehrlich ascites tumor cells in vivo.
    • C Anil Kumar 2007 N-substituted-2-butyl-5-chloro-3H-imidazole-4-carbaldehyde derivatives as anti-tumor agents against Ehrlich ascites tumor cells in vivo. J Med Chem 3 269 276 10.2174/157340607780620699 Anil Kumar C, et al. (2007) N-substituted-2-butyl-5-chloro-3H-imidazole-4-carbaldehyde derivatives as anti-tumor agents against Ehrlich ascites tumor cells in vivo. J Med Chem 3:269–276
    • (2007) J Med Chem , vol.3 , pp. 269-276
    • Anil Kumar, C1
  • 29
    • 85121062058 scopus 로고    scopus 로고
    • Anil Kumar C, et al. (2007) Pro-apoptotic activity of imidazole derivatives mediated by up-regulation of Bax and activation of CAD in Ehrlich Ascites Tumor cells. Invest New Drugs (in press). doi: 10.1007/s10367-006-9033-4
  • 30
    • 16544393544 scopus 로고    scopus 로고
    • Chondroitin Sulfate in Palatal Wound Healing
    • XH Zou 2004 Chondroitin Sulfate in Palatal Wound Healing J Dent Res 83 11 880 885 15505240 1:CAS:528:DC%2BD2cXhtVenur3I 10.1177/154405910408301111 Zou XH, (2004) Chondroitin Sulfate in Palatal Wound Healing. J Dent Res 83(11):880–885
    • (2004) J Dent Res , vol.83 , Issue.11 , pp. 880-885
    • Zou, XH1


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