These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 29535790)

  • 1. A Comparative QSAR Analysis, Molecular Docking and PLIF Studies of Some N-arylphenyl-2, 2-Dichloroacetamide Analogues as Anticancer Agents.
    Fereidoonnezhad M; Faghih Z; Mojaddami A; Rezaei Z; Sakhteman A
    Iran J Pharm Res; 2017; 16(3):981-998. PubMed ID: 29535790
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A comparative QSAR analysis and molecular docking studies of phenyl piperidine derivatives as potent dual NK
    Zare S; Fereidoonnezhad M; Afshar D; Ramezani Z
    Comput Biol Chem; 2017 Apr; 67():22-37. PubMed ID: 28043073
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Quinazoline analogues as cytotoxic agents; QSAR, docking, and
    Emami L; Sabet R; Khabnadideh S; Faghih Z; Thayori P
    Res Pharm Sci; 2021 Oct; 16(5):528-546. PubMed ID: 34522200
    [TBL] [Abstract][Full Text] [Related]  

  • 4. QSAR study of antimicrobial 3-hydroxypyridine-4-one and 3-hydroxypyran-4-one derivatives using different chemometric tools.
    Sabet R; Fassihi A
    Int J Mol Sci; 2008 Dec; 9(12):2407-2423. PubMed ID: 19330084
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Comparison of MLR, PLS and GA-MLR in QSAR analysis.
    Saxena AK; Prathipati P
    SAR QSAR Environ Res; 2003; 14(5-6):433-45. PubMed ID: 14758986
    [TBL] [Abstract][Full Text] [Related]  

  • 6. QSAR study of Phenoxypyrimidine Derivatives as Potent Inhibitors of p38 Kinase using different chemometric tools.
    Edraki N; Hemmateenejad B; Miri R; Khoshneviszade M
    Chem Biol Drug Des; 2007 Dec; 70(6):530-9. PubMed ID: 18034684
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Application of GA-MLR for QSAR Modeling of the Arylthioindole Class of Tubulin Polymerization Inhibitors as Anticancer Agents.
    Ahmadi S; Habibpour E
    Anticancer Agents Med Chem; 2017; 17(4):552-565. PubMed ID: 27528182
    [TBL] [Abstract][Full Text] [Related]  

  • 8. QSAR based docking studies of marine algal anticancer compounds as inhibitors of protein kinase B (PKBβ).
    Davis GD; Vasanthi AH
    Eur J Pharm Sci; 2015 Aug; 76():110-8. PubMed ID: 25936945
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dichloroacetate and Pyruvate Metabolism: Pyruvate Dehydrogenase Kinases as Targets Worth Investigating for Effective Therapy of Toxoplasmosis.
    Ferrarini MG; Nisimura LM; Girard RMBM; Alencar MB; Fragoso MSI; Araújo-Silva CA; Veiga AA; Abud APR; Nardelli SC; Vommaro RC; Silber AM; France-Sagot M; Ávila AR
    mSphere; 2021 Jan; 6(1):. PubMed ID: 33408226
    [TBL] [Abstract][Full Text] [Related]  

  • 10. QSAR study of PETT derivatives as potent HIV-1 reverse transcriptase inhibitors.
    Sabet R; Fassihi A; Moeinifard B
    J Mol Graph Model; 2009 Sep; 28(2):146-55. PubMed ID: 19570701
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A simple and robust model to predict the inhibitory activity of α-glucosidase inhibitors through combined QSAR modeling and molecular docking techniques.
    Izadpanah E; Riahi S; Abbasi-Radmoghaddam Z; Gharaghani S; Mohammadi-Khanaposhtanai M
    Mol Divers; 2021 Aug; 25(3):1811-1825. PubMed ID: 33565001
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A QSAR analysis of 2-phenoxy-N-substituted acetamide analogues as hypoxia-inducible factor-1(HIF-1) inhibitors: a rational approach to anticancer drug design.
    Noolvi MN; Patel HM; Kamboj S
    Med Chem; 2012 Jul; 8(4):599-614. PubMed ID: 22530909
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exploring QSAR for substituted 2-sulfonyl-phenyl-indol derivatives as potent and selective COX-2 inhibitors using different chemometrics tools.
    Khoshneviszadeh M; Edraki N; Miri R; Hemmateenejad B
    Chem Biol Drug Des; 2008 Dec; 72(6):564-74. PubMed ID: 19090923
    [TBL] [Abstract][Full Text] [Related]  

  • 14.
    Vaghefinezhad N; Farsani SF; Gharaghani S
    Curr Drug Discov Technol; 2021; 18(1):139-157. PubMed ID: 31721705
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Application of Genetic Algorithms for Pixel Selection in MIA-QSAR Studies on Anti-HIV HEPT Analogues for New Design Derivatives.
    Doroudi Z; Niazi A
    Iran J Pharm Res; 2019; 18(3):1239-1252. PubMed ID: 32641935
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of potent aldose reductase inhibitors as antidiabetic (Anti-hyperglycemic) agents using QSAR based virtual Screening, molecular Docking, MD simulation and MMGBSA approaches.
    Bakal RL; Jawarkar RD; Manwar JV; Jaiswal MS; Ghosh A; Gandhi A; Zaki MEA; Al-Hussain S; Samad A; Masand VH; Mukerjee N; Nasir Abbas Bukhari S; Sharma P; Lewaa I
    Saudi Pharm J; 2022 Jun; 30(6):693-710. PubMed ID: 35812153
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A study on quantitative structure-activity relationship and molecular docking of metalloproteinase inhibitors based on L-tyrosine scaffold.
    Abbasi M; Ramezani F; Elyasi M; Sadeghi-Aliabadi H; Amanlou M
    Daru; 2015 Apr; 23(1):29. PubMed ID: 25925871
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Application of different chemometric tools in QSAR study of azolo-adamantanes against influenza A virus.
    Karbakhsh R; Sabet R
    Res Pharm Sci; 2011 Jan; 6(1):23-33. PubMed ID: 22049275
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 3-Hydroxypyrimidine-2, 4-dione Derivatives as HIV Reverse Transcriptase-Associated RNase H Inhibitors: QSAR Analysis and Molecular Docking Studies.
    Mostoufi A; Chamkouri N; Kordrostami S; Alghasibabaahmadi E; Mojaddami A
    Iran J Pharm Res; 2020; 19(1):84-97. PubMed ID: 32922472
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Development of a less toxic dichloroacetate analogue by docking and descriptor analysis.
    Subramanian K; Ramaian AS
    Bioinformation; 2010 Jul; 5(2):73-6. PubMed ID: 21346867
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.