BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 23410044)

  • 1. Combinatorial synthesis of pyrazoloquinoline and pyrazoloacridine derivatives with high regioselectivity.
    Chen DS; Zhou YJ; Li YL; Yao CS; Wang XS
    Comb Chem High Throughput Screen; 2013 Jun; 16(7):550-61. PubMed ID: 23410044
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Combinatorial synthesis of pyrrolo[3,2-f]quinoline and pyrrolo[3,2-a]acridine derivatives via a three-component reaction under catalyst-free conditions.
    Zhou YJ; Chen DS; Li YL; Liu Y; Wang XS
    ACS Comb Sci; 2013 Sep; 15(9):498-502. PubMed ID: 23914831
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An efficient one-pot, three-component synthesis of indeno[1,2-b]quinoline-9,11(6H,10H)-dione, acridine-1,8(2H,5H)-dione and quinoline-3-carbonitrile derivatives from enaminones.
    Tu SJ; Jiang B; Jia RH; Zhang JY; Zhang Y; Yao CS; Shi F
    Org Biomol Chem; 2006 Oct; 4(19):3664-8. PubMed ID: 16990942
    [TBL] [Abstract][Full Text] [Related]  

  • 4. One-pot combinatorial synthesis of 4-aryl-1H-thiopyrano[3,4-b]pyridine-5-one derivatives.
    Yao CS; Wang CH; Jiang B; Tu SJ
    J Comb Chem; 2010 Jul; 12(4):472-5. PubMed ID: 20443618
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Efficient one-pot synthesis of novel spirooxindole derivatives via three-component reaction in aqueous medium.
    Chen H; Shi D
    J Comb Chem; 2010 Jul; 12(4):571-6. PubMed ID: 20515044
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Development of a new cascade reaction for convergent synthesis of pyrazolo[1,5-a]quinoline derivatives under transition-metal-free conditions.
    Kato JY; Aoyama H; Yokomatsu T
    Org Biomol Chem; 2013 Feb; 11(7):1171-8. PubMed ID: 23306805
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Synthesis and structure-activity relationship studies in translocator protein ligands based on a pyrazolo[3,4-b]quinoline scaffold.
    Cappelli A; Bini G; Valenti S; Giuliani G; Paolino M; Anzini M; Vomero S; Giorgi G; Giordani A; Stasi LP; Makovec F; Ghelardini C; Di Cesare Mannelli L; Concas A; Porcu P; Biggio G
    J Med Chem; 2011 Oct; 54(20):7165-75. PubMed ID: 21916402
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Combinatorial synthesis of fused tetracyclic heterocycles containing [1,6]naphthyridine derivatives under catalyst free conditions.
    Li C; Mu XY; Li YL; Liu Y; Wang XS
    ACS Comb Sci; 2013 May; 15(5):267-72. PubMed ID: 23581605
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Structural comparisons of isomeric series of 7-aryl-benzo[h]pyrazolo[3,4-b]quinolines and 11-aryl-benzo[f]pyrazolo[3,4-b]quinolines.
    Portilla J; Quiroga J; Nogueras M; de la Torre JM; Cobo J; Low JN; Glidewell C
    Acta Crystallogr B; 2008 Feb; 64(Pt 1):72-83. PubMed ID: 18204214
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A diversity-oriented synthesis of pyrazolo[4,3-f]quinoline derivatives with potential bioactivities via microwave-assisted multi-component reactions.
    Shi F; Zhang S; Wu SS; Gao Y; Tu SJ
    Mol Divers; 2011 May; 15(2):497-505. PubMed ID: 20814822
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Design, synthesis and evaluation of acridine and fused-quinoline derivatives as potential anti-tuberculosis agents.
    Muscia GC; Buldain GY; Asís SE
    Eur J Med Chem; 2014 Feb; 73():243-9. PubMed ID: 24412719
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Facile syntheses of novel benzo-1,3-dioxolo-, benzothiazolo-, pyrido-, and quinolino-fused 5H-benzo[d]-pyrazolo[5,1-b][1,3]-oxazines and 1H-pyrazoles.
    Avila B; Solano DM; Haddadin MJ; Kurth MJ
    Org Lett; 2011 Mar; 13(5):1060-3. PubMed ID: 21294577
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A facile and regioselective one-pot synthesis of novel pyrazolo[1[Formula: see text],5[Formula: see text]:1,2]pyrrolo[3,4-b]quinoline-2,3-dicarboxylate hybrids via intramolecular Wittig reaction.
    Largani TH; Imanzadeh G; Pesyan NN; Şahin E; Shamkhali AN; Notash B
    Mol Divers; 2018 Feb; 22(1):37-46. PubMed ID: 29058230
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Magnetite Nanoparticles-Supported APTES as a Powerful and Recoverable Nanocatalyst for the Preparation of 2-Amino-5,10-dihydro- 5,10-dioxo-4H-benzo[g]chromenes and Tetrahydrobenzo[g]quinoline-5,10- diones.
    Ghasemzadeh MA; Elyasi Z; Azimi-Nasrabad M; Mirhosseini-Eshkevari B
    Comb Chem High Throughput Screen; 2017; 20(1):64-76. PubMed ID: 28017132
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Synthesis, antimicrobial activity and molecular docking studies of spiroquinoline-indoline-dione and spiropyrazolo-indoline-dione derivatives.
    Gul M; Turk Celikoglu E; Idil O; Tas G; Pelit E
    Sci Rep; 2023 Jan; 13(1):1676. PubMed ID: 36717728
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Interferon inducing activities of derivatives of 1,3-dimethyl-4-(3-dimethylaminopropylamino)-1H-pyrazolo(3,4-b)quinoline and related compounds.
    Crenshaw RR; Luke GM; Siminoff P
    J Med Chem; 1976 Feb; 19(2):262-75. PubMed ID: 1249806
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 8-tert-Butyl-7-(4-chlorophenyl)-10-phenyl-5,6-dihydro-10H-benzo[h]pyrazolo[3,4-b]quinoline.
    Portilla J; Quiroga J; Cobo J; Low JN; Glidewell C
    Acta Crystallogr C; 2007 Oct; 63(Pt 10):o582-4. PubMed ID: 17917227
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A domino synthetic strategy leading to two-carbon-tethered fused acridine/indole pairs and fused acridine derivatives.
    Jiang B; Wang X; Li MY; Wu Q; Ye Q; Xu HW; Tu SJ
    Org Biomol Chem; 2012 Nov; 10(42):8533-8. PubMed ID: 23011183
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Structure-activity relationships of imidazo[4,5-f]quinoline partial structures and analogs. Discovery of pyrazolo[3,4-f]quinoline derivatives as potent immunostimulants.
    Moyer MP; Weber FH; Gross JL
    J Med Chem; 1992 Nov; 35(24):4595-601. PubMed ID: 1469690
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Synthesis of indolylquinolines, indolylacridines, and indolylcyclopenta[b]quinolines from the Baylis-Hillman adducts: an in situ [1,3]-sigmatropic rearrangement of an indole nucleus to access indolylacridines and indolylcyclopenta[b]quinolines.
    Ramesh C; Lei PM; Janreddy D; Kavala V; Kuo CW; Yao CF
    J Org Chem; 2012 Oct; 77(19):8451-64. PubMed ID: 22967265
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.