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Nicotinic Acetylcholine Receptors Study

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  1. Cytisine derivatives containing a triple bond

    U. N. Zainutdinov, A. G. Makhsumov, P. Il'khamdzhanov +3

    МақолаSynthesis and Biological EvaluationChemistry of Heterocyclic Compounds19710 иқтибос
    ABI

  2. Synthesis of tritium labeled Boc‐[Nle<sup>11</sup>] ‐substance P<sub>5</sub>‐11

    Naoki Sasaki, R. Michelot, J.L. Morgat +2

    МақолаChemical Synthesis and AnalysisInternational journal of peptide & protein research19860 иқтибос
    ABI

  3. Arenobufagin and gamabufotalin from the venom of the Central Asian green toadBufo viridis. Introduction, structural?functional features

    М. С. Ташмухамедов, Sh. Ya. Mirzaakhmedov, Б. Т. Ибрагимов +4

    МақолаVenomous Animal Envenomation and StudiesChemistry of Natural Compounds19950 иқтибос
    ABI

  4. Structural-functional characteristics of toxins from spiders of the araneidae family

    B. U. Atakuziev, L. Ya. Yukel'son

    МақолаNicotinic Acetylcholine Receptors StudyChemistry of Natural Compounds19960 иқтибос
    ABI

  5. Presynaptic and postsynaptic neurotoxins. Investigation of the structures of the immune recognition sections

    Behzod Z. Dolimbek, M. Zouhair Atassi, Ш. И. Салихов

    МақолаVenomous Animal Envenomation and StudiesChemistry of Natural Compounds19980 иқтибос
    ABI

  6. Local Anesthetics Inhibit Muscarinic Receptor-mediated Activation of Extracellular Signal-regulated Kinases in Rat Pheochromocytoma PC12 Cells 

    Zhiming Tan, Shuji Dohi, Kenji Ohguchi +2

    МақолаCancer, Stress, Anesthesia, and Immune ResponseAnesthesiology19990 иқтибос
    ABI

  7. X-ray Diffraction Analysis of the Structure of 3-Nicotinehydroxamic Acid and Pyrazinecarbohydroxamic Acid Monohydrate

    N. K. Makhmudova, Z. Ch. Kadyrova, E. A. Del'yaridi +1

    МақолаNicotinic Acetylcholine Receptors StudyRussian Journal of Organic Chemistry20010 иқтибос
    ABI

  8. Nicotinic Acid Release from a Transdermal Therapeutic System

    N. A. Azimova, M. M. Miralimov

    МақолаAdvancements in Transdermal Drug DeliveryPharmaceutical Chemistry Journal20010 иқтибос
    ABI

  9. Modified coumarins. 22. Synthesis of N-coumarinyloxyacetyl derivatives of cytisine

    I. P. Dubovik, M. M. Garazd, Валентина И. Виноградова +1

    МақолаSynthesis of Organic CompoundsChemistry of Natural Compounds20060 иқтибос
    ABI

  10. Modified coumarins. 20. Furocoumarin derivatives of cytisine

    M. V. Veselovskaya, M. M. Garazd, Валентина И. Виноградова +1

    МақолаNicotinic Acetylcholine Receptors StudyChemistry of Natural Compounds20060 иқтибос
    ABI

  11. Structure of methylene-bis-cytisine

    K. K. Turgunov, Б. Ташходжаев, T. F. Ibragimov +1

    МақолаNicotinic Acetylcholine Receptors StudyChemistry of Natural Compounds20060 иқтибос
    ABI

  12. Reaction of cytisine with formalin

    Ш. Б. Рахимов, Alexander S. Shashkov, Валентина И. Виноградова

    МақолаChemical Synthesis and AnalysisChemistry of Natural Compounds20060 иқтибос
    ABI

  13. Modified coumarins. 25. N-acyl cytisine derivatives containing a coumarin fragment

    I. V. Nagorichna, A. S. Ogorodniichuk, M. M. Garazd +2

    МақолаNicotinic Acetylcholine Receptors StudyChemistry of Natural Compounds20070 иқтибос
    ABI

  14. Mechanistic details of BK channel inhibition by the intermediate conductance, Ca<sup>2+</sup>-activated K channel

    Jill L. Thompson, Ted Begenisich

    МақолаIon channel regulation and functionChannels20090 иқтибос
    ABI

  15. 1,2,4-Thiadiazol derivatives of cytisine alkaloid: solvate formation and phase transitions

    U.S. Makhmudov, L. Yu. Izotova, B. Tashkhodjaev +2

    МақолаSynthesis and Reactivity of HeterocyclesJournal of Inclusion Phenomena and Macrocyclic Chemistry20110 иқтибос
    ABI

  16. Codeine

    Shakhnoza S. Azimova, Marat S. Yunusov

    БобNicotinic Acetylcholine Receptors Study20120 иқтибос
    ABI

  17. Cytisine

    Shakhnoza S. Azimova, Marat S. Yunusov

    БобNicotinic Acetylcholine Receptors Study20120 иқтибос
    ABI

  18. 6β-(2′-Methyl-2′-vinylacetoxy]-furanoeremophil-1(10)-en-9-one (6β-[2′-Methyl-2′-vinylacetoxy]-euryopsin-9-one)

    Shakhnoza S. Azimova, Ashraf I. Saidkhodzhaev

    БобNeuroscience and Neuropharmacology Research20120 иқтибос
    ABI

  19. (±)-Nitramine

    Shakhnoza S. Azimova, Marat S. Yunusov

    БобChemical synthesis and alkaloids20120 иқтибос
    ABI

  20. (−)-Nicotine

    Shakhnoza S. Azimova, Marat S. Yunusov

    БобNicotinic Acetylcholine Receptors Study20120 иқтибос
    ABI

  21. 3β-Angeloyloxy-6β-hydroxy-furanoeremophil-1(10)-ene (6β-Hydroxy-3β-angeloyloxy-euryopsin)

    Shakhnoza S. Azimova, Ashraf I. Saidkhodzhaev

    БобNatural product bioactivities and synthesis20120 иқтибос
    ABI

  22. 3β-Tigloyloxy-6β-hydroxy-furanoeremophil-1(10)-ene (6β-Hydroxy-3β-tiglinoyloxy-euryopsin)

    Shakhnoza S. Azimova, Ashraf I. Saidkhodzhaev

    БобNeuroscience and Neuropharmacology Research20120 иқтибос
    ABI

  23. 6β-Isobutyroyloxy-1,10α-epoxy-furanoeremophil-9-one (6β-Isobutyryloxy-9-oxo-1,10-epoxy-euryopsin)

    Shakhnoza S. Azimova, Ashraf I. Saidkhodzhaev

    БобChemical Synthesis and Analysis20120 иқтибос
    ABI

  24. 3β-Angeloyloxy-furanoeremophil-1(10)-ene (3β-Angeloyloxy-euryopsine)

    Shakhnoza S. Azimova, Ashraf I. Saidkhodzhaev

    БобNatural product bioactivities and synthesis20120 иқтибос
    ABI

  25. 3β-(3′-Methylvaleroyloxy)-furanoeremophil-1(10)-ene (3β-(3-Methyl-pentanoyloxy-euryopsine)

    Shakhnoza S. Azimova, Ashraf I. Saidkhodzhaev

    БобNatural product bioactivities and synthesis20120 иқтибос
    ABI