메뉴 건너뛰기




Volumn 13, Issue 5, 2011, Pages 530-536

Pyrano[4,3-b]quinolines library generation via iodocyclization and palladium-catalyzed coupling reactions

Author keywords

cross coupling; Iodocyclization; Plasmodium falciparum; pyranoquinoline; rutaceae

Indexed keywords

ALDEHYDE; PALLADIUM; PYRAN DERIVATIVE; QUINOLINE DERIVATIVE;

EID: 80052761508     PISSN: 21568952     EISSN: None     Source Type: Journal    
DOI: 10.1021/co200100z     Document Type: Article
Times cited : (35)

References (48)
  • 1
    • 0037287085 scopus 로고    scopus 로고
    • A new green approach to the Friedlander synthesis of quinolines
    • Arcadi, A.; Chiarini, M.; Giuseppe, S. D.; Marinelli, F. A New Green Approach to the Friedlander Synthesis of Quinolines Synlett 2003, 203-206 (Pubitemid 36249937)
    • (2003) Synlett , Issue.2 , pp. 203-206
    • Arcadi, A.1    Chiarini, M.2    Di Giuseppe, S.3    Marinelli, F.4
  • 2
    • 33745316331 scopus 로고    scopus 로고
    • Clean Procedure for Synthesis of Chromeno[4,3- b ]benzo[ f ]quinolin-6-one Derivatives: Reaction of N -Arylidenenaphthalen-2-amine with 4-Hydroxycoumarin in Aqueous Media
    • Wangab, X. S.; Zhanga, M. M.; Zenga, Z. S.; Shiab, D. Q.; Tuab, S. J. Clean Procedure for Synthesis of Chromeno[4,3- b ]benzo[ f ]quinolin-6-one Derivatives: Reaction of N -Arylidenenaphthalen-2-amine with 4-Hydroxycoumarin in Aqueous Media Synth. Commun. 2006, 36, 2047-2057
    • (2006) Synth. Commun. , vol.36 , pp. 2047-2057
    • Wangab, X.S.1    Zhanga, M.M.2    Zenga, Z.S.3    Shiab, D.Q.4    Tuab, S.J.5
  • 3
    • 77956752566 scopus 로고
    • Brossi, A. Academic Press: London, Vol.
    • Grundon, M. F. In The Alkaloids; Brossi, A., Ed.; Academic Press: London, 1988; Vol. 32, pp 341-439.
    • (1988) The Alkaloids , vol.32 , pp. 341-439
    • Grundon, M.F.1
  • 4
    • 0003393801 scopus 로고
    • Coffey, S. Elsevier Publishing Co. New York, Vol.
    • Sainsbury, M. In Rodd's Chemistry of Carbon Compounds; Coffey, S., Ed.; Elsevier Publishing Co.: New York, 1978; Vol. IVG, pp 171-225.
    • (1978) Rodd's Chemistry of Carbon Compounds , pp. 171-225
    • Sainsbury, M.1
  • 5
    • 0000863597 scopus 로고
    • Alcalofdes Dihydrofuroquinoleiques de Quelques Rutaceae: Isolement, Structure, Proprietes Biologiques
    • Rideau, M.; Yerchere, C.; Hibon, P. Alcalofdes Dihydrofuroquinoleiques de Quelques Rutaceae: Isolement, Structure, Proprietes Biologiques Phytochemistry 1979, 18, 155-159
    • (1979) Phytochemistry , vol.18 , pp. 155-159
    • Rideau, M.1    Yerchere, C.2    Hibon, P.3
  • 8
    • 58149380196 scopus 로고    scopus 로고
    • Recent Advances in the Development of Multi-kinase Inhibitors
    • Krug, M.; Hilgeroth, A. Recent Advances in the Development of Multi-kinase Inhibitors Mini-Rev. Med. Chem. 2008, 8, 1312-1327
    • (2008) Mini-Rev. Med. Chem. , vol.8 , pp. 1312-1327
    • Krug, M.1    Hilgeroth, A.2
  • 9
    • 52749097817 scopus 로고    scopus 로고
    • Progress on Kinesin Spindle Protein Inhibitors as Anti-cancer Agents
    • Zhang, Y.; Xu, W. Progress on Kinesin Spindle Protein Inhibitors as Anti-cancer Agents Anticancer Agents Med. Chem. 2008, 8, 698-704
    • (2008) Anticancer Agents Med. Chem. , vol.8 , pp. 698-704
    • Zhang, Y.1    Xu, W.2
  • 10
    • 34347378261 scopus 로고    scopus 로고
    • Erlotinib: Success of a molecularly targeted agent for the treatment of advanced pancreatic cancer
    • DOI 10.2217/14796694.3.3.247
    • Welch, S. A. Moore, Erlotinib, M. Success of a Molecularly Targeted Agent for the Treatment of Advanced Pancreatic Cancer J. Future Oncol 2007, 3, 247-254 (Pubitemid 47018635)
    • (2007) Future Oncology , vol.3 , Issue.3 , pp. 247-254
    • Welch, S.A.1    Moore, M.J.2
  • 11
    • 33644793664 scopus 로고    scopus 로고
    • Gefitinib: Current and Future Status in Cancer Therapy
    • Herbst, R. S.; Kies, M. S. Gefitinib: Current and Future Status in Cancer Therapy Clin. Adv. Hematol. Oncol. 2003, 1, 466-472
    • (2003) Clin. Adv. Hematol. Oncol. , vol.1 , pp. 466-472
    • Herbst, R.S.1    Kies, M.S.2
  • 12
    • 36949021034 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of potent antitumor active quinoline and naphthyridine derivatives
    • DOI 10.2174/187152007784111313
    • Srivastava, S. K.; Jha, A.; Agarwal, S. K.; Mukherjee, R.; Burman, A. C. Synthesis and Structure-Activity Relationships of Potent Antitumor Active Quinoline and Naphthyridine Derivatives Anticancer Agents Med. Chem. 2007, 7, 685-709 (Pubitemid 350237773)
    • (2007) Anti-Cancer Agents in Medicinal Chemistry , vol.7 , Issue.6 , pp. 685-709
    • Srivastava, S.K.1    Jha, A.2    Agarwal, S.K.3    Mukherjee, R.4    Burman, A.C.5
  • 14
    • 76649107653 scopus 로고    scopus 로고
    • Antiproliferative Activity of novel Benzo[ b ][1,6]naphthyridines in Human Solid Tumor Cell Lines
    • Rudys, S.; Ríos-Luci, C.; Pérez-Roth, E.; Cikotiene, I.; Padrón, J. M. Antiproliferative Activity of novel Benzo[ b ][1,6]naphthyridines in Human Solid Tumor Cell Lines Bioorg. Med. Chem. Lett. 2010, 20, 1504-1506
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 1504-1506
    • Rudys, S.1    Ríos-Luci, C.2    Pérez-Roth, E.3    Cikotiene, I.4    Padrón, J.M.5
  • 16
    • 20144369074 scopus 로고    scopus 로고
    • Synthesis, structure-activity relationship, and receptor pharmacology of a new series of quinoline derivatives acting as selective, noncompetitive mGlu1 antagonists
    • DOI 10.1021/jm049499o
    • Mabire, D.; Coupa, S.; Adelinet, C.; Poncelet, A.; Simonnet, Y.; Venet, M.; Wouters, R.; Lesage, A. S. J.; Beijsterveldt, L. V.; Bischoff, F. Synthesis, Structure-Activity Relationship, and Receptor Pharmacology of a New Series of Quinoline Derivatives Acting as Selective, Noncompetitive m Glu1 Antagonists J. Med. Chem. 2005, 48, 2134-2153 (Pubitemid 40396342)
    • (2005) Journal of Medicinal Chemistry , vol.48 , Issue.6 , pp. 2134-2153
    • Mabire, D.1    Coupa, S.2    Adelinet, C.3    Poncelet, A.4    Simonnet, Y.5    Venet, M.6    Wouters, R.7    Lesage, A.S.J.8    Van Beijsterveldt, L.9    Bischoff, F.10
  • 17
    • 0036915726 scopus 로고    scopus 로고
    • Quinoline, quinazoline and acridone alkaloids
    • DOI 10.1039/b104971m
    • Michael, J. P. Quinoline, Quinazoline and Acridone Alkaloids Nat. Prod. Rep. 2002, 19, 742-760 (Pubitemid 36029228)
    • (2002) Natural Product Reports , vol.19 , Issue.6 , pp. 742-760
    • Michael, J.P.1
  • 18
    • 0142216387 scopus 로고    scopus 로고
    • Quinoline, quinazoline and acridone alkaloids
    • DOI 10.1039/b208140g
    • Michael, J. P. Quinoline, Quinazoline and Acridone Alkaloids Nat. Prod. Rep. 2003, 20, 476-493 (Pubitemid 37298577)
    • (2003) Natural Product Reports , vol.20 , Issue.5 , pp. 476-493
    • Michael, J.P.1
  • 19
    • 34547327918 scopus 로고    scopus 로고
    • Silver versus gold catalysis in tandem reactions of carbonyl functions onto alkynes: A versatile access to furoquinoline and pyranoquinoline cores
    • DOI 10.1002/chem.200700202
    • Godet, T.; Vaxelaire, C.; Michel, C.; Milet, A.; Belmont, P. Silver versus Gold-Catalysis in Tandem Reactions of Carbonyl Functions onto Alkynes: A Versatile Access to Furoquinoline and Pyranoquinoline cores Chem.-Eur. J. 2007, 13, 5632-5641 (Pubitemid 47151848)
    • (2007) Chemistry - A European Journal , vol.13 , Issue.19 , pp. 5632-5641
    • Godet, T.1    Vaxelaire, C.2    Michel, C.3    Milet, A.4    Belmont, P.5
  • 20
    • 33845327840 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of new 4H-pyrano[2,3-b]quinoline derivatives that block acetylcholinesterase and cell calcium signals, and cause neuroprotection against calcium overload and free radicals
    • DOI 10.1016/j.ejmech.2006.06.016, PII S0223523406002984
    • Marco-Contelles, J.; León, R.; López, M. G.; García, A. G.; Villarroya, M. Synthesis and Biological Evaluation of New 4 H -Pyrano[2, 3-b ]quinoline Derivatives that Block Acetylcholinesterase and Cell Calcium Signals, and cause Neuroprotection against Calcium overload and Free Radicals Eur. J. Med. Chem. 2006, 41, 1464-1469 (Pubitemid 44880506)
    • (2006) European Journal of Medicinal Chemistry , vol.41 , Issue.12 , pp. 1464-1469
    • Marco-Contelles, J.1    Leon, R.2    Lopez, M.G.3    Garcia, A.G.4    Villarroya, M.5
  • 21
    • 0035848581 scopus 로고    scopus 로고
    • Angular methoxy-substituted furo- and pyranoquinolinones as blockers of the voltage-gated potassium channel Kv1.3
    • DOI 10.1021/jm001007u
    • Butenschon, I.; Moller, K.; Hansel, W. Angular Methoxy-Substituted Furo- and Pyranoquinolinones as Blockers of the Voltage-Gated Potassium Channel Kv1.3 J. Med. Chem. 2001, 44, 1249-1256 (Pubitemid 32861759)
    • (2001) Journal of Medicinal Chemistry , vol.44 , Issue.8 , pp. 1249-1256
    • Butenschon, I.1    Moller, K.2    Hansel, W.3
  • 22
    • 33748967759 scopus 로고    scopus 로고
    • Synthesis of novel pyrano[2,3-b]quinolines from simple acetanilides via intramolecular 1,3-dipolar cycloaddition
    • DOI 10.1016/j.tetlet.2006.08.086, PII S0040403906017047
    • Kalita, K. P.; Baruah, B.; Bhuyan, P. J. Synthesis of Novel Pyrano[2,3- b ]quinolines from Simple Acetanilides via Intramolecular 1,3-dipolar Cycloaddition Tetrahedron Lett. 2006, 47, 7779-7782 (Pubitemid 44441483)
    • (2006) Tetrahedron Letters , vol.47 , Issue.44 , pp. 7779-7782
    • Kalita, P.K.1    Baruah, B.2    Bhuyan, P.J.3
  • 24
    • 33746806249 scopus 로고    scopus 로고
    • The reaction of o-alkynylarene and heteroarene carboxaldehyde derivatives with iodonium ions and nucleophiles: A versatile and regioselective synthesis of 1H-isochromene, naphthalene, indole, benzofuran, and benzothiophene compounds
    • DOI 10.1002/chem.200501505
    • Barluenga, J.; Vazquez-Villa, H.; Merino, I.; Ballesteros, A.; Gonzalez, J. M. The Reaction of o -Alkynylarene and Heteroarene Carboxaldehyde Derivatives with Iodonium Ions and Nucleophiles: A Versatile and Regioselective Synthesis of 1 H -Isochromene, Naphthalene, Indole, Benzofuran, and Benzothiophene Compounds Chem.-Eur. J. 2006, 12, 5790-5805 (Pubitemid 44179188)
    • (2006) Chemistry - A European Journal , vol.12 , Issue.22 , pp. 5790-5805
    • Barluenga, J.1    Vazquez-Villa, H.2    Merino, I.3    Ballesteros, A.4    Gonzalez, J.M.5
  • 25
    • 33646259513 scopus 로고    scopus 로고
    • Syntheses of Isochromenes and Naphthalenes by Electrophilic Cyclization of Acetylenic Arenecarboxaldehydes
    • Yue, D.; Ca, N. D.; Larock, R. C. Syntheses of Isochromenes and Naphthalenes by Electrophilic Cyclization of Acetylenic Arenecarboxaldehydes J. Org. Chem. 2006, 71, 3381-3388
    • (2006) J. Org. Chem. , vol.71 , pp. 3381-3388
    • Yue, D.1    Ca, N.D.2    Larock, R.C.3
  • 26
    • 2542606253 scopus 로고    scopus 로고
    • Efficient syntheses of heterocycles and carbocycles by electrophilic cyclization of acetylenic aldehydes and ketones
    • DOI 10.1021/ol049690s
    • Yue, D.; Ca, N. D.; Larock, R. C. Efficient Syntheses of Heterocycles and Carbocycles by Electrophilic Cyclization of Acetylenic Aldehydes and Ketones Org. Lett. 2004, 6, 1581-1584 (Pubitemid 38698456)
    • (2004) Organic Letters , vol.6 , Issue.10 , pp. 1581-1584
    • Yue, D.1    Della Ca, N.2    Larock, R.C.3
  • 27
    • 77949291633 scopus 로고    scopus 로고
    • Iodine/Palladium Approaches to the Synthesis of Polyheterocyclic Compounds
    • Mehta, S.; Larock, R. C. Iodine/Palladium Approaches to the Synthesis of Polyheterocyclic Compounds J. Org. Chem. 2010, 75, 1652-1658
    • (2010) J. Org. Chem. , vol.75 , pp. 1652-1658
    • Mehta, S.1    Larock, R.C.2
  • 28
    • 57549084501 scopus 로고    scopus 로고
    • Parallel Synthesis of a Multi-Substituted Benzo[ b ]furan Library
    • Cho, C. H.; Neuenswander, B.; Lushington, G. H.; Larock, R. C. Parallel Synthesis of a Multi-Substituted Benzo[ b ]furan Library J. Comb. Chem. 2008, 10, 941-947
    • (2008) J. Comb. Chem. , vol.10 , pp. 941-947
    • Cho, C.H.1    Neuenswander, B.2    Lushington, G.H.3    Larock, R.C.4
  • 29
    • 70449427458 scopus 로고    scopus 로고
    • Solution-Phase Synthesis of a Diverse Isocoumarin Library
    • Roy, S.; Roy, S.; Neuenswander, B.; Hill, D.; Larock, R. C. Solution-Phase Synthesis of a Diverse Isocoumarin Library J. Comb. Chem. 2009, 11, 1128-1135
    • (2009) J. Comb. Chem. , vol.11 , pp. 1128-1135
    • Roy, S.1    Roy, S.2    Neuenswander, B.3    Hill, D.4    Larock, R.C.5
  • 30
    • 70449369054 scopus 로고    scopus 로고
    • Palladium and Copper-Catalyzed Solution Phase Synthesis of a Diverse Library of Isoquinolines
    • Roy, S.; Roy, S.; Neuenswander, B.; Hill, D.; Larock, R. C. Palladium and Copper-Catalyzed Solution Phase Synthesis of a Diverse Library of Isoquinolines J. Comb. Chem. 2009, 11, 1061-1065
    • (2009) J. Comb. Chem. , vol.11 , pp. 1061-1065
    • Roy, S.1    Roy, S.2    Neuenswander, B.3    Hill, D.4    Larock, R.C.5
  • 32
    • 69249186664 scopus 로고    scopus 로고
    • Benzotriazole: An Excellent Ligand for the Copper-Catalyzed N -Arylation of Indoles
    • Verma, A. K.; Singh, J.; Choudhary, R.; Larock, R. C. Benzotriazole: An Excellent Ligand for the Copper-Catalyzed N -Arylation of Indoles Tetrahedron 2009, 65, 8434-8439
    • (2009) Tetrahedron , vol.65 , pp. 8434-8439
    • Verma, A.K.1    Singh, J.2    Choudhary, R.3    Larock, R.C.4
  • 33
    • 27744512710 scopus 로고    scopus 로고
    • Highly Efficient One Pot Synthesis of 1-Substituted 1,2,3,4- Tetrahydropyrazino[1,2- A ]indoles
    • Tiwari, R. K.; Singh, J.; Verma, A. K.; Singh, D.; Chandra, R. Highly Efficient One Pot Synthesis of 1-Substituted 1,2,3,4-Tetrahydropyrazino[1,2- a ]indoles Tetrahedron 2005, 61, 9513-9518
    • (2005) Tetrahedron , vol.61 , pp. 9513-9518
    • Tiwari, R.K.1    Singh, J.2    Verma, A.K.3    Singh, D.4    Chandra, R.5
  • 34
    • 34248547200 scopus 로고    scopus 로고
    • Benzotriazole: an excellent ligand for Cu-catalyzed N-arylation of imidazoles with aryl and heteroaryl halides
    • DOI 10.1016/j.tetlet.2007.04.061, PII S0040403907007277
    • Verma, A. K.; Singh, J.; Sankar, V. K.; Choudhary, R.; Chandra, R. Benzotriazole: An Excellent Ligand for Cu-Catalyzed N -Arylation of Imidazoles with Aryl and Heteroaryl Halides Tetrahedron Lett. 2007, 48, 4207-4210 (Pubitemid 46754383)
    • (2007) Tetrahedron Letters , vol.48 , Issue.24 , pp. 4207-4210
    • Verma, A.K.1    Singh, J.2    Sankar, V.K.3    Chaudhary, R.4    Chandra, R.5
  • 35
    • 34047121177 scopus 로고    scopus 로고
    • Synthesis, characterization and in vitro biological studies of novel cyano derivatives of N-alkyl and N-aryl piperazine
    • DOI 10.1016/j.ejmech.2006.10.009, PII S0223523406003813
    • Chaudhary, P.; Nimesh, S.; Yadav, V.; Verma, A. K.; Kumar, R. Synthesis, Characterization and in-vitro Biological Studies of Novel Cyano Derivatives of N -Alkyl and N -Aryl Piperazine Eur. J. Med. Chem. 2007, 42, 471-476 (Pubitemid 46517784)
    • (2007) European Journal of Medicinal Chemistry , vol.42 , Issue.4 , pp. 471-476
    • Chaudhary, P.1    Nimesh, S.2    Yadav, V.3    Verma, A.Kr.4    Kumar, R.5
  • 37
    • 0037940265 scopus 로고    scopus 로고
    • Novel Synthesis of 1,2,3,4-Tetrahydropyrazino[1,2- A ]indoles
    • Katritzky, A. R.; Verma, A. K.; He, H. Y.; Chandra, R. Novel Synthesis of 1,2,3,4-Tetrahydropyrazino[1,2- a ]indoles J. Org. Chem. 2003, 68, 4938-4940
    • (2003) J. Org. Chem. , vol.68 , pp. 4938-4940
    • Katritzky, A.R.1    Verma, A.K.2    He, H.Y.3    Chandra, R.4
  • 39
    • 70349512252 scopus 로고    scopus 로고
    • Imino Diels-Alder Reactions: Efficient Synthesis of Pyrano and Furanoquinolines Catalyzed by Antimony (III) Sulfate
    • Goudar, M., A.; Jayadevappa, H.; Sudhakara, A.; Mahadevan, K., M. Imino Diels-Alder Reactions: Efficient Synthesis of Pyrano and Furanoquinolines Catalyzed by Antimony (III) Sulfate Lett. Org.Chem. 2008, 5, 628-632
    • (2008) Lett. Org.Chem. , vol.5 , pp. 628-632
    • Goudar . M, A.1    Jayadevappa, H.2    Sudhakara, A.3    Mahadevan . K, M.4
  • 40
    • 77953196172 scopus 로고    scopus 로고
    • Solvent-Controlled Selective Electrophilic Cyclization and Oxidative Esterification of o -Alkynyl Aldehydes
    • Verma, A. K.; Aggarwal, T.; Rustagi, V.; Larock, R. C. Solvent-Controlled Selective Electrophilic Cyclization and Oxidative Esterification of o -Alkynyl Aldehydes Chem Comm. 2010, 46, 4064-4066
    • (2010) Chem Comm. , vol.46 , pp. 4064-4066
    • Verma, A.K.1    Aggarwal, T.2    Rustagi, V.3    Larock, R.C.4
  • 41
    • 78449233407 scopus 로고    scopus 로고
    • Iodine-Mediated Solvent-Controlled Selective Electrophilic Cyclization and Oxidative Esterification of o -Alkynyl Aldehydes: An Easy Access to Pyranoquinolines, Pyranoquinolinones, and Isocumarins
    • Verma, A. K.; Rustagi, V.; Aggarwal, T.; Singh, A. P. Iodine-Mediated Solvent-Controlled Selective Electrophilic Cyclization and Oxidative Esterification of o -Alkynyl Aldehydes: An Easy Access to Pyranoquinolines, Pyranoquinolinones, and Isocumarins J. Org. Chem. 2010, 75, 7691-7703
    • (2010) J. Org. Chem. , vol.75 , pp. 7691-7703
    • Verma, A.K.1    Rustagi, V.2    Aggarwal, T.3    Singh, A.P.4
  • 42
    • 2042507954 scopus 로고
    • Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
    • Miyaura, N.; Suzuki, A. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds Chem. Rev. 1995, 95, 2457-2483
    • (1995) Chem. Rev. , vol.95 , pp. 2457-2483
    • Miyaura, N.1    Suzuki, A.2
  • 44
    • 84855742669 scopus 로고    scopus 로고
    • CCDC 808029 4 { 7 } contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from Cambridge Crystallographic Data Centre via
    • CCDC 808029 4 { 7 } contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/ request/cif.
  • 45
    • 0000702671 scopus 로고
    • Palladium-Catalyzed Vinylation of Organic Halides
    • Heck, R. F. Palladium-Catalyzed Vinylation of Organic Halides Org. React. 1982, 27, 345-390
    • (1982) Org. React. , vol.27 , pp. 345-390
    • Heck, R.F.1
  • 46
    • 0017311840 scopus 로고
    • Human Malaria Parasites in Continuous Culture
    • Trager, W.; Jensen, J. B. Human Malaria Parasites in Continuous Culture Science 1976, 193, 673-675
    • (1976) Science , vol.193 , pp. 673-675
    • Trager, W.1    Jensen, J.B.2
  • 47
    • 2142640849 scopus 로고    scopus 로고
    • Simple and Inexpensive Fluorescence-Based Technique for High-Throughput Antimalarial Drug Screening
    • DOI 10.1128/AAC.48.5.1803-1806.2004
    • Smilkstein, M.; Sriwilaijaroen, N.; Kelly, J. X.; Wilairat, P.; Riscoe, M. Simple and Inexpensive Fluorescence-Based Technique for High-Throughput Antimalarial Drug Screening Antimicrob. Agents Chemother. 2004, 48, 1803-1806 (Pubitemid 38544392)
    • (2004) Antimicrobial Agents and Chemotherapy , vol.48 , Issue.5 , pp. 1803-1806
    • Smilkstein, M.1    Sriwilaijaroen, N.2    Kelly, J.X.3    Wilairat, P.4    Riscoe, M.5
  • 48
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
    • Mosmann, T. Rapid Colorimetric Assay for Cellular Growth and Survival: Application to Proliferation and Cytotoxicity Assays J. Immunol. Methods 1983, 65, 55-63 (Pubitemid 14203433)
    • (1983) Journal of Immunological Methods , vol.65 , Issue.1-2 , pp. 55-63
    • Mosmann, T.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.