CAS: 511-28-4; Vitamin D4 (Impurity)

该化合物是一种在体内钙化和磷代谢作用的毒杀虫剂化合物,是一种不太为人所知的维生素D形式,与更普遍公认的D2(ergocalciferol)和D3(choolecalciferol)一道,维生素D4来自酵和真菌,通过对ERgosterol的紫外线辐照产生,其化学结构具有复杂的类固醇骨,这是维生素D化合物的特征.尽管它具有某种生物活动,但对人类的威力和效力远远低于D2和D3, 维生素D4在饮食补充或营养方面没有被广泛使用,其作用也不太为人所了解.然而,它在某些治疗环境中可能具有潜在用途.但与其他形式的维生素D一样,它对于保持骨质健康并可能影响免疫功能十分重要.需要进一步研究,以充分阐明其生物影响和潜在健康利益.

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65445-14-9 511-28-4 116559-84-3

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合成工艺路线路线简述

    📜(1R,3Ar,4S,7Ar)-4-Benzenesulfonyl-7A-Methyl-1-[(1R,4S)-1,4,5-Trimethyl-Hexyl]-octahydroindene置于sodium Amalgam体系中,化学反应生成 维生素d4
    参考文献:Kocienski,P.J. Et Al.,Journal Of The Chemical Society. Perkin Transactions I,1979,P. 1290-1293
    标题:Kocienski,P.J. Et Al.,Journal Of The Chemical Society. Perkin Transactions I,1979,P. 1290-1293

    海关参考信息

    专利信息


    专利号:US-5869472-A
    优先权日:1994-07-18
    标 题 :Synthesis of 1α-hydroxy vitamin D
    发明人:MORIARTY ROBERT M; GUO LIANG; PENMASTA RAJU A
    权利人:BONE CARE INT INC
    摘要:A method for 1α-hydroxylation of vitamin D compounds using the appropriate vitamin D as the starting material. The method requires no separatory procedures prior to the actual hydroxylation step.

    专利号:US-9212137-B2
    优先权日:2012-05-30
    标题:Crystallization of (20R,22R)-2-methylene-19-nor-22-methyl-1α,25-dihydroxyvitamin D3 and related precursors
    发明人:DELUCA HECTOR F; GRZYWACZ PAWEL; PLUM LORI A; FLORES AGNIESZKA; THODEN JAMES B; HOLDEN HAZEL M
    权利人:WISCONSIN ALUMNI RES FOUND
    摘要:Disclosed are methods of purifying the compound (20R,22R)-2-methylene-19-nor-22-methyl-1α,25-dihydroxyvitamin D 3 to obtain the compound in crystalline form. The methods typically include the steps of dissolving a product containing the compound in a solvent comprising hexane and 2-propanol, cooling the solvent and dissolved product below ambient temperature for a sufficient amount of time to form a precipitate of crystals, and recovering the crystals. Certain diol precursors formed during the synthesis of the compound and its diasteromers also may be obtained in crystalline form using ethyl acetate as a solvent.

    专利号:AU-7364094-A
    优先权日:1994-07-18
    标题 :Synthesis of 1alpha-hydroxy vitamin d

    专利号:CA-2195414-A1
    优先权日:1994-07-18
    标 题 :Synthesis of 1.alpha.-hydroxy vitamin d

    专利号:US-6281249-B1
    优先权日:1997-07-21
    标题:18-substituted-19-nor-vitamin D compounds
    发明人:DELUCA HECTOR F; CAI ZU Y
    权利人:WISCONSIN ALUMNI RES FOUND
    摘要:This invention provides a novel class of vitamin D compounds, namely, 13-ethyl and 13-vinyl-18,19-dinor-vitamin D derivatives, as well as a general method for their chemical synthesis. The compounds have the formula: n where Y 1 and Y 2 , which may be the same or different, are each selected from the group consisting of hydrogen and a hydroxy-protecting group, R 6 is selected from the group consisting of an ethyl or vinyl radical, and where the group R represents any of the typical side chains known for vitamin D type compounds. These 18-substituted compounds are characterized by minimal intestinal calcium transport activity and minimal bone calcium mobilization activity resulting in novel therapeutic agents for the treatment of secondary hyperparathyroidism. These compounds also exhibit pronounced activity in arresting the proliferation of undifferentiated cells and inducing their differentiation to the monocyte thus evidencing use as anti-cancer agents and for the treatment of diseases such as psoriasis.

    专利号:US-6359152-B2
    优先权日:1997-07-21
    标 题 :18-substituted-19-nor-vitamin D compounds
    发明人:DELUCA HECTOR F; CAI ZU Y
    权利人:WISCONSIN ALUMNI RES FOUND
    摘要:This invention provides a novel class of vitamin D compounds, namely, 13-ethyl and 13-vinyl-18,19-dinor-vitamin D derivatives, as well as a general method for their chemical synthesis. The compounds have the formula: n where Y 1 and Y 2 , which may be the same or different, are each selected from the group consisting of hydrogen and a hydroxy-protecting group, R 6 is selected from the group consisting of an ethyl or vinyl radical, and where the group R represents any of the typical side chains known for vitamin D type compounds. These 18-substituted compounds are characterized by minimal intestinal calcium transport activity and minimal bone calcium mobilization activity resulting in novel therapeutic agents for the treatment of secondary hyperparathyroidism. These compounds also exhibit pronounced activity in arresting the proliferation of undifferentiated cells and inducing their differentiation to the monocyte thus evidencing use as anti-cancer agents and for the treatment of diseases such as psoriasis.

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    ✅ COA系统入驻 | 共享模式

    主要参考文献

    [参考文献]: Katherine M Phillips, Et Al. Vitamin D4 In Mushrooms. Plos One. 2012;7(8):E40702.
    [参考文献]: Silver J, Et Al. Regulation By Vitamin D Metabolites Of Parathyroid Hormone Gene Transcription In Vivo In The Rat. J Clin Invest. 1986 Nov;78(5):1296-301.
    [参考文献]: Zittermann A, Et Al. Vitamin D And Cardiovascular Disease: An Update. Anticancer Res. 2019 Sep;39(9):4627-4635.
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