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K.M. Shakhidoyatov

14 та иш

Institute of the Chemistry of Plant Substances, Academy of Sciences of Uzbekistan, 77, Mirzo Ulugbek Str., 100170 Tashkent, Uzbekistan

  1. Discovery of diethyl 2,5-diaminothiophene-3,4-dicarboxylate derivatives as potent anticancer and antimicrobial agents and screening of anti-diabetic activity: Synthesis and in vitro biological evaluation. Part 1

    Khurshed Bozorov, Hairong Ma, Jiangyu Zhao +7

    МақолаSynthesis and biological activityEuropean Journal of Medicinal Chemistry201411 иқтибос
    ABI

  2. 2-Methyl-4-oxo-6,7,8,9-tetrahydrothieno[2′,3′:4,5]pyrimidino[1,2-<i>a</i>]pyridine-3-carboxylic acid

    Burkhon Elmuradov, Khurshed Bozorov, R. Ya. Okmanov +2

    МақолаCrystal structures of chemical compoundsActa Crystallographica Section E Structure Reports Online20116 иқтибос
    ABI

  3. Peptide fragmentation as an approach in modeling of an active peptide and designing a competitive inhibitory peptide for HMG-CoA reductase

    Valeriy V. Pak, Minseon Koo, Dae Young Kwon +2

    МақолаComputational Drug Discovery MethodsBioorganic & Medicinal Chemistry20105 иқтибос
    ABI

  4. 2,3-Trimethylene-7,8-dihydropyrrolo[1,2-<i>a</i>]thieno[2,3-<i>d</i>]pyrimidin-4(6<i>H</i>)-one

    Khurshed Bozorov, Burkhon Elmuradov, K.M. Shakhidoyatov +2

    МақолаSynthesis and biological activityActa Crystallographica Section E Structure Reports Online20134 иқтибос
    ABI

  5. Tricyclic Quinazoline Alkaloids Conjugated to Ferrocene: Synthesis, Structure, and Redox Behavior of Ferrocenylmethylene‐Substituted 7<i>H</i>‐Deoxyvasicinones

    Burkhon Elmuradov, K.M. Shakhidoyatov, Gerald Dräger +1

    МақолаFerrocene Chemistry and ApplicationsEuropean Journal of Organic Chemistry20154 иқтибос
    ABI

  6. 9-Furfurylidene-2,3-dimethyl-6,7,8,9-tetrahydro-4<i>H</i>-thieno[2′,3′:4,5]pyrimidino[1,2-<i>a</i>]pyridin-4-one

    Khurshed Bozorov, Burkhon Elmuradov, R. Ya. Okmanov +2

    МақолаSynthesis and biological activityActa Crystallographica Section E Structure Reports Online20103 иқтибос
    ABI

  7. (<i>E</i>)-3-[4-(Dimethylamino)benzylidene]-2,3-dihydro-1<i>H</i>,9<i>H</i>-pyrrolo[2,1-<i>b</i>]quinazolin-9-one

    Burkhon Elmuradov, R. Ya. Okmanov, А. Ш. Абдуразаков +2

    МақолаQuinazolinone synthesis and applicationsActa Crystallographica Section E Structure Reports Online20102 иқтибос
    ABI

  8. 2,3-Dihydropyrrolo[2,1-<i>b</i>]quinazoline-9(1<i>H</i>)-thione

    A. Nasrullayev, Burkhon Elmuradov, K. K. Turgunov +2

    МақолаQuinazolinone synthesis and applicationsActa Crystallographica Section E Structure Reports Online20122 иқтибос
    ABI

  9. Poly[di-μ-chlorido-μ-(1,2,3,9-tetrahydropyrrolo[2,1-<i>b</i>]quinazolin-9-one-κ<sup>2</sup><i>N</i>:<i>O</i>)-mercury(II)]

    K. K. Turgunov, Yutian Wang, Ulli Englert +1

    МақолаQuinazolinone synthesis and applicationsActa Crystallographica Section E Structure Reports Online20111 иқтибос
    ABI

  10. 3,5,6-Trimethylthieno[2,3-<i>d</i>]pyrimidin-4(3<i>H</i>)-one

    K. Khatamov, Fozil Saitqulov, Jamshid Ashurov +1

    МақолаSynthesis and biological activityActa Crystallographica Section E Structure Reports Online20121 иқтибос
    ABI

  11. 3-Methyl-2-(3,3,3-trichloro-2-hydroxypropyl)quinazolin-4(3<i>H</i>)-one

    Fotima Rabbimovna Utayeva, R. Ya. Okmanov, N. I. Mukarramov +2

    МақолаQuinazolinone synthesis and applicationsActa Crystallographica Section E Structure Reports Online20131 иқтибос
    ABI

  12. 11-(2-Oxopyrrolidin-1-ylmethyl)-1,2,3,4,5,6,11,11a-octahydropyrido[2,1-<i>b</i>]quinazolin-6-one dihydrate

    Z. U. Samarov, R. Ya. Okmanov, K. K. Turgunov +2

    МақолаQuinazolinone synthesis and applicationsActa Crystallographica Section E Structure Reports Online20100 иқтибос
    ABI

  13. (4-Nitrophenyl)(1,2,3,9-tetrahydropyrrolo[2,1-<i>b</i>]quinazolin-3-yl)methanol monohydrate

    Burkhon Elmuradov, C.E. Makhmadiyarova, K. K. Turgunov +2

    МақолаQuinazolinone synthesis and applicationsActa Crystallographica Section E Structure Reports Online20110 иқтибос
    ABI

  14. N-Monobenzoylation (acetylation, arylsulfonation), N-, C- di- and N-, C-, O- tribenzoylation of 5H(chloro, nitro)-2-methyl(ethyl)benzimidazoles

    K.M. Shakhidoyatov, Tozagul Dzhumatanova, Ubaydullo Yakubov +2

    МақолаSynthesis and biological activityAmerican Chemical Science Journal20150 иқтибос
    ABI