CAS: 569-83-5; Xanthohumol(Random Configuration)

该化合物是一个富兰类化合物,显示各种生物活动,其特点是具有复杂结构,包括多种羟基组和混合氧组,有助于其潜在的抗氧化特性.这种化合物的存在表明,它可能参与迈克尔的附加反应,增强它的再活动.由于它能够改变各种生物化学途径,因此经常研究这种化合物的潜在治疗作用,包括反氟化和抗癌活动.此外,其溶性性和稳定性可能受到功能组的存在的影响,使其在药用化学和天然产品研究中都受到关注.

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    上下游产品

    isoxanthohumol 1-{2,4-bis(methoxymethoxy)-6-[(3-methylbut-2-en-1-yl)oxy]phenyl}ethanone 1-[6-hydroxy-2,4-bis(methoxymethoxy)-3-(3-methylbut-2-en-1-yl)phenyl]ethanone 3,5-dihydroxyphenolisoxanthohumol α,β-dihydroxanthohumol 5-methoxy-8-(3-methyl-but-2-enyl)-7-(4-nitro-benzoyloxy)-2-[4-(4-nitro-benzoyloxy)-phenyl]-chroman-4-one Tetrahydroxanthohumol

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      专利信息


      专利号:US-7435861-B2
      优先权日:2005-04-29
      标 题 :Methods for synthesis of carotenoids, including analogs, derivatives, and synthetic and biological intermediates
      发明人:LOCKWOOD SAMUEL F; TANG PENG CHO; NADOLSKI GEOFF; JACKSON HENRY L; FANG ZHIQIANG; DU YISHU; YANG MIN; GEISS WILLIAM; WILLIAMS RICHARD; BURDICK DAVID
      权利人:CARDAX PHARMACEUTICALS INC
      摘要:A method for synthesizing intermediates for use in the synthesis of carotenoid synthetic intermediates, carotenoid analogs, and/or carotenoid derivatives. The carotenoid analog, derivative, or intermediate may be administered to a subject for the inhibition and/or amelioration of any disease that involves production of reactive oxygen species, reactive nitrogen species, radicals and/or non-radicals. In some embodiments, the invention may include methods for synthesizing chemical compounds including an analog or derivative of a carotenoid. Carotenoid analogs or derivatives may include acyclic end groups. In some embodiments, a carotenoid analog or derivative may include at least one substituent. The substituent may enhance the solubility of the carotenoid analog or derivative such that the carotenoid analog or derivative at least partially dissolves in water.

      专利号:US-2008221377-A1
      优先权日:2006-06-16
      标题 :Methods for synthesis of carotenoids, including analogs, derivatives, and synthetic and biological intermediates
      发明人:LOCKWOOD SAMUEL F; TANG PENG CHO; NADOLSKI GEOFF; JACKSON HENRY L; FANG ZHIQIANG; DU YISHU; YANG MIN; GEISS WILLIAM; WILLIAMS RICHARD; BURDICK DAVID; BRAUN CRISTI L
      权利人:LOCKWOOD SAMUEL F; TANG PENG CHO; NADOLSKI GEOFF; JACKSON HENRY L; FANG ZHIQIANG; DU YISHU; YANG MIN; GEISS WILLIAM; WILLIAMS RICHARD; BURDICK DAVID; BRAUN CRISTI L
      摘要:A method for synthesizing intermediates for use in the synthesis of carotenoid synthetic intermediates, carotenoid analogs, and/or carotenoid derivatives. The carotenoid analog, derivative, or intermediate may be administered to a subject for the inhibition and/or amelioration of any disease that involves production of reactive oxygen species, reactive nitrogen species, radicals and/or non-radicals. In some embodiments, the invention may include methods for synthesizing chemical compounds including an analog or derivative of a carotenoid. Carotenoid analogs or derivatives may include acyclic end groups. In some embodiments, a carotenoid analog or derivative may include at least one substituent. The substituent may enhance the solubility of the carotenoid analog or derivative such that the carotenoid analog or derivative at least partially dissolves in water.

      专利号:US-2009099061-A1
      优先权日:2006-01-27
      标 题:Synthesis of carotenoid analogs or derivatives with improved antioxidant characteristics
      发明人:FOSS BENTE J; NADOLSKI GEOFFRY T; LOCKWOOD SAMUEL F
      权利人:FOSS BENTE J; NADOLSKI GEOFFRY T; LOCKWOOD SAMUEL F
      摘要:A method is described for synthesizing and administering carotenoid compounds with improved antioxidant characteristics. In some embodiments, extension or improvement of conjugation may be employed in structural modification of carotenoids. In other embodiments, reduction of ring/chain steric hindrance may improve the lambda max, and hence, the overall antioxidant capability, of particular compounds. In other embodiments, introduction and/or increase in synthetic handles for conjugation may improve the stoichiometric ratios of conjugating moieties to the polyene backbone. The methods may be used to improve natural and/or synthetic compounds for medicinal application in the treatment of disease.

      专利号:US-2007036742-A1
      优先权日:2005-08-09
      标题 :Methods and compositions for modulating hair growth or regrowth
      发明人:ROUFS JAMES B; DUVEL LANE A; FAST DAVID J; GLYNN KELLY M
      权利人:ACCESS BUSINESS GROUP INT LLC
      摘要:The present invention relates to compositions and methods for modulating hair growth or regrowth. The compositions of the present invention comprise extracts of one or more of the following: Boswellia serrata, Undaria pinnatifida, green tea (e.g., Camellia sinensis ), shiso, Pureraria mirifica, luteolin (e.g. Perilla ocymoides leaf extract), astilbin, vitamin E, amentoflavone, tetrahydropiperine, licochalcone, astaxanthin, red clover, Brassica juncea, unfermented green rooibos, enzyme CoQ10, salvia, ximenynic acid, hops oleoresin, apple, soy, saw palmetto, or ellagic extract, or any derivative thereof. In particular, the compositions and methods of the present invention can be used to stimulate or increase hair growth and/or prevent or slow the loss of hair by having one or more of the following functions: (a) inhibiting synthesis of DHT; (b) inhibiting proteasomal activity; (c) inhibiting IL-1 activity; (d) increasing vascularization; (e) increasing expression of vascular endothelial growth factor; (f) increasing expression of keratinocyte growth factor; (g) inhibiting inflammation; or (h) acting as an antibacterial.

      专利号:US-2008031986-A1
      优先权日:2005-12-09
      标题:Protein kinase modulation by hops and acacia products
      发明人:TRIPP MATTHEW L; BABISH JOHN G; BLAND JEFFREY S; HALL AMY J; KONDA VEERA; PACIORETTY LINDA M; DESAI ANU
      权利人:METAPROTEOMICS LLC
      摘要:Botanical compounds to modulate kinase activity are disclosed. The compounds and methods disclosed also inhibit expression of COX-2, inhibit synthesis of prostaglandins selectively in target cells, and inhibit inflammatory response selectively. The compositions contain at least one fraction isolated or derived from hops or Acacia.

      专利号:US-2007015735-A1
      优先权日:2005-03-23
      标 题 :Water-dispersible carotenoids, including analogs and derivatives
      发明人:LOCKWOOD SAMUEL F; NADOLSKI GEOFF
      权利人:LOCKWOOD SAMUEL F; NADOLSKI GEOFF
      摘要:A method used for synthesizing intermediates for use in the synthesis of carotenoid synthetic intermediates, carotenoid analogs, and/or carotenoid derivatives. The analog, derivative, or intermediate may be administered such that a subject's risk of experiencing diseases associated with reactive oxygen species, reactive nitrogen species, radicals and/or non-radicals may be thereby reduced. The analog or analog combination may be administered to a subject for the inhibition and/or amelioration of any disease that involves production of reactive oxygen species, reactive nitrogen species, radicals and/or non-radicals. In some embodiments, the invention may include methods for synthesizing chemical compounds including an analog or derivative of a carotenoid. The carotenoid analog or derivative may be synthetic. In some embodiments, a carotenoid analog or derivative may include at least one substituent. The substituent may enhance the solubility of the carotenoid analog or derivative such that the carotenoid analog or derivative at least partially dissolves in water.

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      ✅ COA系统入驻 | 共享模式

      合成参考文献


      参考文献:10.1016/s0278-6915(99)00019-8
      摘要:Miranda CL, Stevens JF, Helmrich A, Henderson MC, Rodriguez RJ, Yang YH, Deinzer ML, Barnes DW, Buhler DR. Antiproliferative and cytotoxic effects of prenylated flavonoids from hops (Humulus lupulus) in human cancer cell lines. Food Chem Toxicol. 1999 Apr;37(4):271–85. doi: 10.1016/s0278-6915(99)00019-8.
      参考文献:10.1038/oby.2008.66
      摘要:Yang JY, Della-Fera MA, Rayalam S, Baile CA. Enhanced effects of xanthohumol plus honokiol on apoptosis in 3T3-L1 adipocytes. Obesity (Silver Spring). 2008 Jun;16(6):1232–8. doi: 10.1038/oby.2008.66.
      参考文献:10.1016/j.intimp.2010.02.002
      摘要:Cho YC, You SK, Kim HJ, Cho CW, Lee IS, Kang BY. Xanthohumol inhibits IL-12 production and reduces chronic allergic contact dermatitis. Int Immunopharmacol. 2010 May;10(5):556–61. doi: 10.1016/j.intimp.2010.02.002.
      参考文献:10.1016/j.ejmech.2010.01.060
      摘要:Vogel S, Barbic M, Jürgenliemk G, Heilmann J. Synthesis, cytotoxicity, anti-oxidative and anti-inflammatory activity of chalcones and influence of A-ring modifications on the pharmacological effect. European Journal of Medicinal Chemistry. 2010 Jun;45(6):2206–13. doi: 10.1016/j.ejmech.2010.01.060.
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