1-(2'-hydroxyphenyl)-3-(4-hydroxyphenyl)propan-1-one | 24271-94-1

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 直链 1,3-二芳基丙烷
• 英文名称: 1-(2'-hydroxyphenyl)-3-(4-hydroxyphenyl)propan-1-one
• 英文别名: 1-(2-Hydroxyphenyl)-3-(4-hydroxyphenyl)propan-1-one
• CAS: 24271-94-1
• 化学式: C₁₅H₁₄O₃
• 分子量: 242.274
• InChiKey: XDTIWXQUWIKIMB-UHFFFAOYSA-N

物化性质

• 熔点：
  109-111 °C
• 沸点：
  443.3±30.0 °C(Predicted)
• 密度：
  1.242±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.13
• 拓扑面积：
  57.5
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-(2'-hydroxyphenyl)-3-(4-hydroxyphenyl)propan-1-one 在 palladium(II) trifluoroacetate 、 5-硝基-1,10-菲咯啉 、 氧气 作用下， 以 二甲基亚砜 为溶剂， 反应 48.0h， 以47%的产率得到4-羟基黄烷酮
  参考文献：
  名称：

  钯 (II) 催化氧化环化从 2'-羟基二氢查尔酮合成黄酮和黄烷酮

  摘要：

  公开了通过有效的 Pd( II ) 催化合成黄酮和黄烷酮的不同且通用的合成路线。根据氧化剂和添加剂，这些 Pd( II ) 催化剂分别以高度原子经济的方式通过涉及脱氢的区分氧化环化序列，方便地从 2'-羟基二氢查耳酮中提供各种黄酮和黄烷酮作为常见的中间体。

  DOI：

  10.1039/d1ra01672e
• 作为产物：
  描述：

  2',4-dihydroxychalcone 在 palladium on activated charcoal 、 乙醇 作用下， 生成 1-(2'-hydroxyphenyl)-3-(4-hydroxyphenyl)propan-1-one
  参考文献：
  名称：

  Carpenter; Hunter, Journal of Applied Chemistry, 1951, vol. 1, p. 217,223

  摘要：

  DOI：

文献信息

• Total Synthesis of 3′,3′′′-Binaringenin and Related Biflavonoids
  作者：Gustavo Seoane、Gabriel Sagrera

  DOI：10.1055/s-0030-1258140

  日期：2010.8

  The synthesis of natural 3′,3′′′-binaringenin and four related biflavonoids was performed in good overall yield (15-35%) starting from readily available phloroglucinol and 4-hydroxy- or 4-methoxybenzaldehyde. Preliminary results indicate that some of these compounds have an interesting activity against S. aureus. binaringenin - biapigenin - protecting groups - antibacterial activity

  从容易获得的间苯三酚和4-羟基-或4-甲氧基苯甲醛开始，以良好的总收率（15-35％）进行天然3'，3''-联萘宁和四种相关双黄酮的合成。初步结果表明，其中一些化合物对金黄色葡萄球菌具有有趣的活性。 Binaringenin-Biapigenin-保护基-抗菌活性
• Stereoselective reduction of flavanones by marine-derived fungi
  作者：Iara L. de Matos、Willian G. Birolli、Darlisson de A. Santos、Marcia Nitschke、André Luiz M. Porto

  DOI：10.1016/j.mcat.2021.111734

  日期：2021.8

  enantiomeric excesses (ee) of both cis- and trans-diastereoisomers (up to >99% ee). Ten strains were screened for reduction of flavanone 2a in liquid medium and in phosphate buffer solution. The most selective strains Cladosporium sp. CBMAI 1237 and Acremonium sp. CBMAI1676 were employed for reduction of flavanones 2a-g. The fungus Cladosporium sp. CBMAI 1237 presented yields of 72–87% with 0–64% ee cis and

  生物转化是一种具有巨大潜力的替代方法，可以改变天然和合成类黄酮的结构。因此，描述了使用海洋来源的真菌对合成卤化黄烷酮进行生物还原，旨在合成具有高对映体过量 ( ee ) 的顺式和反式非对映异构体 (高达 >99% ee ) 的黄烷-4-醇3a-g）。在液体培养基和磷酸盐缓冲溶液中筛选了 10 株减少黄烷酮2a 的菌株。最具选择性的菌株Cladosporium sp。CBMAI 1237 和枝顶孢属。CBMAI1676 用于还原黄烷酮2a-g. 真菌Cladosporium sp。CBMAI 1237呈现的72-87％的收率与0-64％ee值顺式和0-30％的EE的反式与非对映异构比（博士从52:48至64:36（）顺式：反式）。而枝顶孢属。CBMAI 1676导致31％的产率与77-99％ee值的的顺式和95-99％ee值的的反式-非对映体3A-G与博士从54:46至96：4（顺式：反式）。据我们所知，这是溴化
• Synthesis, anticancer, structural, and computational docking studies of 3-benzylchroman-4-one derivatives
  作者：Lalitha Simon、Abdul Ajees Abdul Salam、S. Madan Kumar、T. Shilpa、K.K. Srinivasan、K. Byrappa

  DOI：10.1016/j.bmcl.2017.10.026

  日期：2017.12

  exhibited moderate activity against HeLa cells (IC50 = 42.8 µM). The molecular structures of 3h and 3i were solved by single crystal X-ray crystallographic technique. Additionally, the molecular docking studies between the tumour suppressor protein p53 with the lead compound 3h, which exhibited better anticancer activity against HeLa cells was examined.

  合成了一系列的3-苄基苯并吡喃-4-酮，并通过MTT法筛选了其抗癌活性。针对两种癌细胞系BT549（人类乳腺癌），HeLa（人类宫颈癌）和一种非癌细胞系vero（正常肾脏上皮细胞）对化合物进行了评估。发现3b是对抗BT549细胞（IC 50  = 20.1 µM）最活跃的分子，而3h是对抗HeLa细胞（IC 50  = 20.45 µM）最活跃的分子。3b还显示出对HeLa细胞的中等活性（IC 50  = 42.8 µM）。3h和3i的分子结构通过单晶X射线晶体学技术解决。此外，检查了在肿瘤抑制蛋白p53与先导化合物3h之间的分子对接研究，该化合物对HeLa细胞表现出更好的抗癌活性。
• AROMA COMPOSITIONS OF ALKAMIDES WITH HESPERETIN AND/OR 4-HYDROXYDIHYDROCHALCONES AND SALTS THEREOF FOR ENHANCING SWEET SENSORY IMPRESSIONS
  申请人：Ley Jakob

  公开号：US20080242740A1

  公开（公告）日：2008-10-02

  The invention primarily relates to aroma compositions of (i) certain saliva-stimulating alkamides having a tingling, pungent and/or hot flavor (such as for example pellitorines, spilanthol) with (ii) hesperetin (5,7-dihydroxy-3-(3-hydroxy-4-methoxyphenyl)-chroman-4-one) or the enantiomers and/or salts thereof and/or (iii) 4-hydroxydihydrochalcones (3-(4-hydroxyphenyl)-1-phenylpropan-1-ones) and/or the salts thereof, the use thereof to enhance the sweet flavor of sweet-tasting substances or the sweet odor impression of aroma substances which give rise to a sweet odor impression, but in particular to enhance the sweet initial flavor or odor (initial sweetness). The invention thus relates to the use of said aroma compositions as general sweetness enhancers and enhancers of initial sweetness. The invention further relates to certain preparations which contain an effective amount of said aroma compositions of (i) alkamides (such as in particular pellitorines, spilanthol) with (ii) hesperetin or the enantiomers and/or salts thereof and/or (iii) 4-hydroxydihydrochalcones and/or the salts thereof and methods for enhancing the sweet flavor or initial sweetness of a sweet-tasting substance or the sweet odor impression or initial sweetness of an aroma substance which gives rise to a sweet odor impression. The invention also relates to the use of certain alkamides (i) to enhance the initial sweetness of a preparation comprising (ii) hesperetin or the enantiomers and/or salts thereof and/or (iii) 4-hydroxydihydrochalcones and/or the salts thereof and (b) sweet-tasting substances and/or (c) aroma substances which give rise to a sweet odor impression.

  该发明主要涉及具有刺激唾液分泌的辣味、刺激性和/或辛辣风味的某些唾液激发烷酰胺（例如佩利托林、斯皮兰托尔）与（ii）橙皮素（5,7-二羟基-3-(3-羟基-4-甲氧基苯基)-4-羟基-香豆素）或其对映体和/或盐以及（iii）4-羟基二氢黄烷酮（3-(4-羟基苯基)-1-苯基丙酮）和/或其盐的香气组合物，其用途是增强甜味物质的甜味或产生甜味印象的香料物质的甜味印象，尤其是增强甜味的初始风味或香气（初始甜味）。该发明因此涉及将所述香气组合物用作一般甜味增强剂和初始甜味增强剂。该发明还涉及含有有效量所述香气组合物的某些配方（i）烷酰胺（例如特别是佩利托林、斯皮兰托尔）与（ii）橙皮素或其对映体和/或盐以及（iii）4-羟基二氢黄烷酮和/或其盐的方法，用于增强甜味物质的甜味或初始甜味或产生甜味印象的香料物质的甜味印象或初始甜味。该发明还涉及使用某些烷酰胺（i）来增强含有（ii）橙皮素或其对映体和/或盐以及（iii）4-羟基二氢黄烷酮和/或其盐的配方的初始甜味以及（b）甜味物质和/或（c）产生甜味印象的香料物质的初始甜味。
• Regioselective and chemoselective biotransformation of 2′-hydroxychalcone derivatives by marine-derived fungi
  作者：Iara Lisboa de Matos、Marcia Nitschke、André Luiz Meleiro Porto

  DOI：10.1080/10242422.2021.1956909

  日期：2023.1.2

  biotransformation of the 2′-hydroxychalcone 1a. The main products obtained were from hydrogenation, hydroxylation, and cyclization reactions. Penicillium raistrickii CBMAI 931 catalyzed the chemoselective reduction of 1a to produce 2′-hydroxydihydrochalcone 2a (72%) in 7 days of incubation in phosphate buffer (pH 7). Aspergillus sydowii CBMAI 935 promoted the hydroxylation of 1a to yield 2′,4-dihydroxy-dihydrochalcone

  摘要 八种真菌菌株（Penicillium raistrickii CBMAI 931、Cladosporium sp. CBMAI 1237、Aspergillus sydowii CBMAI 935、Penicillium oxalicum CBMAI 1996、Penicillium citrinum CBMAI 1186、Mucor racemosus CBMAI 847、Westerdykella sp. CBMAI 1679 和 Asperdykella sp. CBMAI 1679 和Aspergillus biorottransformation9 BMAI） 2'-羟基查尔酮1a。获得的主要产物来自氢化、羟基化和环化反应。雷氏青霉CBMAI 931 催化1a化学选择性还原生成 2'-羟基二氢查尔酮2a (72%) 在磷酸盐缓冲液 (pH 7) 中孵育 7 天。Aspergillus