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Antithyroid drags
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(a) Cooper, D. S. Antithyroid drags. N. Engl. J. Med. 2005, 352, 905-917.
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Thyroid Hormone Synthesis and Secretion. Thyroidmanager.org/Chapter2/2-frame.htm
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Rousset, B.A.1
Dunn, J.T.2
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3
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14C-labeled 1-methyl-2-mercaptoimidazole in vitro and in vivo
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and references therein
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14C-labeled 1-methyl-2-mercaptoimidazole in vitro and in vivo. Endocrinology 1989, 124, 30-39, and references therein.
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Endocrinology
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Taurog, A.1
Dorris, M.L.2
Guziec, F.S.3
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4
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0025238759
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The mechanism of action of synthetic antithyroid drugs: Iodine complexation during oxidation of iodine
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(b) Raby, C.; Lagorce, J. F.; Jambut-Absil, A. C.; Buxeraud, J.; Catanzano, G. The mechanism of action of synthetic antithyroid drugs: iodine complexation during oxidation of iodine. Endocrinology 1990, 126, 1683-1691.
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Raby, C.1
Lagorce, J.F.2
Jambut-Absil, A.C.3
Buxeraud, J.4
Catanzano, G.5
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5
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0028941087
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Irreversible inactivation of lactoperoxidase by mercaptomethylimidazole through generation of a thiyl radical: Its use as a probe to study the active site
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(c) Bandyopadhyay, U.; Bhattacharyya, D. K.; Chatterjee, R.; Banerjee, R. K. Irreversible inactivation of lactoperoxidase by mercaptomethylimidazole through generation of a thiyl radical: its use as a probe to study the active site. Biochem. J. 1995, 306, 751-757.
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Bandyopadhyay, U.1
Bhattacharyya, D.K.2
Chatterjee, R.3
Banerjee, R.K.4
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6
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2
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2. J. Am. Chem. Soc. 2002, 124, 4538-4539.
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Aragoni, M.C.1
Area, M.2
Demartin, F.3
Devillanova, F.A.4
Garau, A.5
Isaia, F.6
Lippolis, V.7
Verani, G.8
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7
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0002914467
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Structure and molecular interactions of antithyroid drags. Part 3. Methimazole: A diiodine sponge
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and references therein
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Laurence, C.; El Ghomari, M. J.; Le Questel, J.-Y.; Mokhlisse, R. Structure and molecular interactions of antithyroid drags. Part 3. Methimazole: a diiodine sponge. J. Chem. Soc., Perkin Trans. 2 1998, 1545-1551, and references therein.
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Laurence, C.1
El Ghomari, M.J.2
Le Questel, J.-Y.3
Mokhlisse, R.4
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8
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2S). J. Am. Chem. Soc. 1988, 110, 2586-2591.
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2S). J. Am. Chem. Soc. 1988, 110, 2586-2591.
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9
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46849097669
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Lippolis, V.; Isaia, F. Charge-Transfer (C.-T.) Adducts and Related Compounds. In Handbook of Chalcogen Chemistry; Devillanova, F. A., Ed.; RCS Publishing: Cambridge, U.K., 2007; pp 477-496.
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(a) Lippolis, V.; Isaia, F. Charge-Transfer (C.-T.) Adducts and Related Compounds. In Handbook of Chalcogen Chemistry; Devillanova, F. A., Ed.; RCS Publishing: Cambridge, U.K., 2007; pp 477-496.
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10
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0002553187
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Refinement of the crystal structure of iodine at 110 K
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(b) van Bolhuis, F.; Koster, P. B.; Migchelsen, T. Refinement of the crystal structure of iodine at 110 K. Acta Crystallogr. 1967, 23, 90-93.
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van Bolhuis, F.1
Koster, P.B.2
Migchelsen, T.3
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11
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0028932659
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The methylation, oxidation and crystallographic characterization of imidazole derivatives
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(c) Vampa, G.; Benvenuti, S.; Severi, F.; Malmusi, M.; Antolini, N. The methylation, oxidation and crystallographic characterization of imidazole derivatives. J. Heterocycl. Chem. 1995, 32, 227-234.
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Vampa, G.1
Benvenuti, S.2
Severi, F.3
Malmusi, M.4
Antolini, N.5
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13
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0017195606
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Effect of antithyroid agents 6-propyl-2-thiouracil and 1-methyl-2-mercaptoimidazole on human thyroid iodine peroxidase
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Nagasaka, A.; Hidaka, H. Effect of antithyroid agents 6-propyl-2-thiouracil and 1-methyl-2-mercaptoimidazole on human thyroid iodine peroxidase. J. Clin. Endocrinol. Metab. 1976, 43, 152-158.
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Nagasaka, A.1
Hidaka, H.2
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14
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46849113312
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2 with an equimolar amount of MMI.
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2 with an equimolar amount of MMI.
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15
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46849101846
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2.
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2.
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17
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24644511758
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Studies of polyhalide ions in aqueous and non-aqueous solution by electrospray mass spectrometry
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(c) McIndoe, J. S.; Tuck, D. G. Studies of polyhalide ions in aqueous and non-aqueous solution by electrospray mass spectrometry. Dalton Trans. 2003, 244-248.
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Dalton Trans
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McIndoe, J.S.1
Tuck, D.G.2
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18
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46849095516
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c(25°C) = 723. Daniele, G. Misura della costante di equilibrio del triioduro di potassio con un metodo spettrofotometrico. Gazz. Chim. Ital. 1960, 90, 1068-1075.
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c(25°C) = 723. Daniele, G. Misura della costante di equilibrio del triioduro di potassio con un metodo spettrofotometrico. Gazz. Chim. Ital. 1960, 90, 1068-1075.
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19
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46849093271
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The nature of the oxidation products was not investigated. According to Taurog (ref 2a) and Doerge U.S. Patent 5,371,102, year 1994, the formation of 1-methylimidazole and sulfate/sulfite anions is expected
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The nature of the oxidation products was not investigated. According to Taurog (ref 2a) and Doerge (U.S. Patent 5,371,102, year 1994), the formation of 1-methylimidazole and sulfate/sulfite anions is expected.
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20
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0023888136
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Doerge reported that LPO catalyzed S-oxygenation of thiocarbamides produces a reactive intermediate (MMI-sulfonic acid) that binds covalently to the active-site heme. We think that the formation of such intermediate might more easily be achieved from 1 than MMI. Doerge, D. Mechanism-based inhibition of lactoperoxidase by thiocarbamide goitrogens. Identification of turnover and inactivation pathways. Biochemistry 1988, 27, 3697-3700
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Doerge reported that LPO catalyzed S-oxygenation of thiocarbamides produces a reactive intermediate (MMI-sulfonic acid) that binds covalently to the active-site heme. We think that the formation of such intermediate might more easily be achieved from 1 than MMI. Doerge, D. Mechanism-based inhibition of lactoperoxidase by thiocarbamide goitrogens. Identification of turnover and inactivation pathways. Biochemistry 1988, 27, 3697-3700.
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21
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1542287649
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Biomimetic studies on anti-thyroid drags and thyroid hormone synthesis
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Roy, G.; Nethaji, M.; Mugesh, G. Biomimetic studies on anti-thyroid drags and thyroid hormone synthesis. J. Am. Chem. Soc. 2004, 126, 2712-2713.
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J. Am. Chem. Soc
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Roy, G.1
Nethaji, M.2
Mugesh, G.3
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22
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77049143386
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The determination of enzyme inhibitor constants
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Dixon, M. The determination of enzyme inhibitor constants. Biochem. J. 1953, 55, 170-171.
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Biochem. J
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Dixon, M.1
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