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Isoliquiritigenin

  • CAS:961-29-5
  • MF:C15H12O4
  • Purity:99%
  • Molecular Weight:256.258
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Product Details

  • CAS: 961-29-5
  • MF: C15H12O4
  • Appearance: powder
  • Quality Factory Supply 99% Pure Isoliquiritigenin 961-29-5 with Efficient Delivery

    • Molecular Formula:C15H12O4
    • Molecular Weight:256.258
    • Appearance/Colour:powder 
    • Melting Point:206-210 °C 
    • Boiling Point:504.015 °C at 760 mmHg 
    • PKA:7.50±0.35(Predicted) 
    • Flash Point:272.711 °C 
    • PSA:77.76000 
    • Density:1.384 g/cm3 
    • LogP:2.69950 

    Isoliquiritigenin(Cas 961-29-5) Usage

    Biochem/physiol Actions

    Isoliquiritigenin is a soluble guanylyl cyclase activator and possesses antitumor activity. It also possesses antioxidant, antiplatelet and estrogenic properties.

    Anticancer Research

    It is extracted from Dipteryx odorata seeds, found to be active in induction of quininereductase, and thus prevents chemical carcinogenesis. In a dose- and time-dependentmanner, it significantly inhibits the proliferation of prostate cancer cells,and this isoliquiritigenin-induced cell cycle arrest and antiproliferative effects maybe manifested by growth arrest- and DNA damage-inducible gene 153 (GADD153).It induces apoptosis in prostate cancer cells through mitochondrial apoptosispathway in which mitochondrial membrane potential is disrupted, cytochrome-cand Smac/Diablo are released, and caspase-9 is activated. It is reported to enhancethe expression of universal inhibitor of cyclin-dependent kinases, p21CIP1/WAF1, in adose- and time-dependent manner in A549 human lung cancer cells (Kanazawaet al. 2003; Ii et al. 2004; Balunas and Kinghorn 2005; Jung et al. 2006).

    General Description

    Isoliquiritigenin is an aromatic ketone and belongs to the chalcone group of compound. It is derived from licorice and is a component in medicine and food.

    InChI:InChI=1/C15H12O4/c16-11-4-1-10(2-5-11)3-8-14(18)13-7-6-12(17)9-15(13)19/h1-9,16-17,19H/b8-3+

    961-29-5 Relevant articles

    Discovery of isoliquiritigenin analogues that reverse acute hepatitis by inhibiting macrophage polarization

    Yang, Junjie,Hu, Fanjie,Guo, Chengjun,Liang, Yuqing,Song, Haiying,Cheng, Kui

    , (2021/06/15)

    Screening a natural product library of 8...

    Synthesis and biological evaluation of isoliquiritigenin derivatives as a neuroprotective agent against glutamate mediated neurotoxicity in HT22 cells

    Selvaraj, Baskar,Kim, Dae Won,Huh, Gyuwon,Lee, Heesu,Kang, Kyungsu,Lee, Jae Wook

    , (2020/03/05)

    Glutamate-induced neurotoxicity is chara...

    Isoliquiritigenin Derivatives Inhibit RANKL-Induced Osteoclastogenesis by Regulating p38 and NF-κB Activation in RAW 264.7 Cells

    Choi, Jung-Won,Hwang, Ki-Chul,Jeong, Seongtae,Kim, Kundo,Kim, Sang Woo,Lee, Jiyun,Lee, Seahyoung,Lee, Yunmi,Lim, Soyeon,Oh, Sena

    , (2020/09/17)

    Bone diseases may not be imminently life...

    Synthesis and evaluation of butein derivatives for in vitro and in vivo inflammatory response suppression in lymphedema

    Kang, Hee,Ku, Jin-Mo,Lee, Jung-hun,Lee, Sukchan,Park, Kye Won,Roh, Kangsan,Song, Youngju

    , (2020/05/01)

    Herein, we demonstrate that butein (1) c...

    961-29-5 Process route

    Neolicurosid

    Neolicurosid

    β-D-glucose
    492-61-5

    β-D-glucose

    isoliquirtigenin
    961-29-5,13745-20-5

    isoliquirtigenin

    liquiritigenin
    578-86-9,41680-09-5

    liquiritigenin

    3-C-(hydroxymethyl)-β-D-erythrofuranose
    20230-73-3,30738-01-3,30912-14-2,41546-43-4,41546-44-5,41546-45-6,41546-46-7,41546-47-8,41546-48-9,41546-49-0,41546-50-3,63865-04-3,36465-64-2

    3-C-(hydroxymethyl)-β-D-erythrofuranose

    Conditions
    Conditions Yield
    With hydrogenchloride; In methanol; water; at 70 ℃; for 2h;
    isoliquiritigenin-4'-O-β-D-apiosylglucoside

    isoliquiritigenin-4'-O-β-D-apiosylglucoside

    β-D-glucose
    492-61-5

    β-D-glucose

    isoliquirtigenin
    961-29-5,13745-20-5

    isoliquirtigenin

    liquiritigenin
    578-86-9,41680-09-5

    liquiritigenin

    3-C-(hydroxymethyl)-β-D-erythrofuranose
    20230-73-3,30738-01-3,30912-14-2,41546-43-4,41546-44-5,41546-45-6,41546-46-7,41546-47-8,41546-48-9,41546-49-0,41546-50-3,63865-04-3,36465-64-2

    3-C-(hydroxymethyl)-β-D-erythrofuranose

    Conditions
    Conditions Yield
    With hydrogenchloride; In methanol; water; at 70 ℃; for 2h;

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