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6-Geranylchrysin

中文名称
——
中文别名
——
英文名称
6-Geranylchrysin
英文别名
6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-2-phenylchromen-4-one
6-Geranylchrysin化学式
CAS
——
化学式
C25H26O4
mdl
——
分子量
390.479
InChiKey
ZGOCQRKXVIGZMZ-SFQUDFHCSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    6.8
  • 重原子数:
    29
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    66.8
  • 氢给体数:
    2
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    香叶基溴白杨素四乙基碘化铵 作用下, 以 甲醇 为溶剂, 以20.91%的产率得到6-Geranylchrysin
    参考文献:
    名称:
    C-Isoprenylation of Flavonoids Enhances Binding Affinity toward P-Glycoprotein and Modulation of Cancer Cell Chemoresistance
    摘要:
    Previous studies have shown that flavones bind to P-glycoprotein (Pgp) with higher affinity than isoflavones, flavanones, and glycosylated derivatives. In the present work, a series of C- or O-substituted hydrophobic derivatives of chrysin were synthesized to further investigate structural requirements of the A ring toward Pgp modulation. Increasing hydrophobicity at either position 6, 8, or 7 increased the affinity of in vitro binding to a purified cytosolic domain of Pgp, but only benzyl and 3,3-dimethylallyl C-substitution produced a high maximal quenching of the protein intrinsic fluorescence. Inhibition of membrane Pgp within leukemic cells, characterized by intracellular drug accumulation, was specifically produced by isoprenylated derivatives, with 8-(3,3-dimethylallyl)chrysin being even more efficient than the commonly used cyclosporin A.
    DOI:
    10.1021/jm991128y
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文献信息

  • CHALLENGE TEST FOR DIAGNOSING SUBTYPE OF AUTISM SPECTRUM DISEASE
    申请人:Stalicla S.A.
    公开号:EP3479845A1
    公开(公告)日:2019-05-08
    The present invention is directed to a method of identifying autism spectrum disorder (ASD) subtype 1 patients, wherein the method comprises: administering an Nrf2-activator to an ASD patient previously diagnosed with ASD or a subject displaying clinical signs of ASD, and identifying the ASD patient as an ASD subtype 1 patient if the patient shows a negative response after administration of the Nrf2-activator. Likewise, the present invention is directed to an Nrf2-activator for use in identifying autism spectrum disorder (ASD) subtype 1 patients, wherein the Nrf2-activator is administered to a subject, wherein the subject is a patient previously diagnosed with ASD or a subject displaying clinical signs of ASD and wherein an ASD subtype 1 patient is identified by a negative response.
    本发明涉及一种鉴别自闭症谱系障碍(ASD)亚型1患者的方法,其中该方法包括:向先前诊断为ASD的ASD患者或显示ASD临床症状的受试者施用Nrf2-激活剂,如果患者在施用Nrf2-激活剂后显示阴性反应,则将该ASD患者鉴别为ASD亚型1患者。同样,本发明涉及一种用于鉴定自闭症谱系障碍(ASD)亚型1患者的Nrf2-激活剂,其中将Nrf2-激活剂施用给受试者,受试者是先前诊断为ASD的患者或显示ASD临床症状的受试者,并且通过阴性反应鉴定ASD亚型1患者。
  • Prenylflavonoids and prenyl/alkyl-phloroacetophenones: Synthesis and antitumour biological evaluation☆
    作者:P. Basabe、M. de Román、I.S. Marcos、D. Diez、A. Blanco、O. Bodero、F. Mollinedo、B.G. Sierra、J.G. Urones
    DOI:10.1016/j.ejmech.2010.06.025
    日期:2010.9
    Several prenylflavonoids have been synthesised and tested against human tumour cell lines. The prenyl unit has been geranyl or a labdane diterpene. These labdane-flavonoids have been synthesised for the first time. The antitumour activity increase with the prenylation at C-8 position. Twenty-three C and O-prenylated acylphloroglucinols have been synthesised as well. In this case the C-alkylation products have resulted, in general, more active. (C) 2010 Elsevier Masson SAS. All rights reserved.
  • CHALLENGE TEST FOR DIAGNOSING A SUBTYPE OF AUTISM SPECTRUM DISEASE
    申请人:Stalicla S.A.
    公开号:EP3706806A1
    公开(公告)日:2020-09-16
  • METABOLIC PROFILING FOR THE DIAGNOSIS OF A SUBSET OF IDIOPATHIC AUTISM SPECTRUM DISORDER PATIENTS, ASD PHENOTYPE 1
    申请人:Stalicla S.A.
    公开号:EP3877540A1
    公开(公告)日:2021-09-15
  • METHOD OF IDENTIFYING ASD PHENOTYPE 1 PATIENTS
    申请人:Stalicla S.A.
    公开号:US20190134229A1
    公开(公告)日:2019-05-09
    The present invention is directed to a method of identifying autism spectrum disorder (ASD) phenotype 1 patients, wherein the method comprises: administering an Nrf2-activator to an ASD patient previously diagnosed with idiopathic ASD or a subject displaying clinical signs of ASD, and identifying the ASD patient as an ASD phenotype 1 patient if the patient shows a negative response after administration of the Nrf2-activator. Likewise, the present invention is directed to a method for classifying autism spectrum disorder (ASD) phenotype 1 patients, the method comprising: administering an Nrf2-activator to a subject, and observing if the subject shows a negative response after administration of the Nrf2-activator, in which the subject is a patient previously diagnosed with idiopathic ASD or a subject displaying clinical signs of ASD and in which the negative response supports classification of the subject as an ASD phenotype 1 patient.
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