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甘草黃酮B_91433-17-9_產(chǎn)品詳情
91433-17-9
  • names:

    Licoflavone B

  • CAS號(hào):

    91433-17-9

    MDL Number:
  • MF(分子式): C25H26O4 MW(分子量): 390.47
  • EINECS: Reaxys Number:
  • Pubchem ID:11349817 Brand:BIOFOUNT
甘草黃酮B
甘草黃酮B(91433-17-9,Licoflavone B)是一種從黃草甘草中分離出來(lái)的類黃酮,甘草黃酮B可以抑制血吸蟲的活性。
貨品編碼 規(guī)格 純度 價(jià)格 (¥) 現(xiàn)價(jià)(¥) 特價(jià)(¥) 庫(kù)存描述 數(shù)量 總計(jì) (¥)
YZM000828-5mg 5mg >95% ¥ 3402.00 ¥ 3402.00 Backorder
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0.00
YZM000828-1mg 1mg >95% ¥ 1092.00 ¥ 1092.00 Backorder
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中文別名 甘草黃酮B(91433-17-9,Licoflavone B)
英文別名 Licoflavone B(91433-17-9);Prenyllicoflavone A
CAS號(hào) 91433-17-9
Inchi InChI=1S/C25H26O4/c1-15(2)5-7-17-11-19(9-10-21(17)26)24-14-23(28)20-12-18(8-6-16(3)4)22(27)13-25(20)29-24/h5-6,9-14,26-27H,7-8H2,1-4H3
InchiKey GLDVIKFETPAZNV-UHFFFAOYSA-N
分子式 Formula C25H26O4
分子量 Molecular Weight 390.47
溶解度Solubility
性狀 Solid
儲(chǔ)藏條件 Storage conditions 存放在陰涼干燥處,短期(數(shù)天至數(shù)周)在0-4℃,長(zhǎng)期(數(shù)月至數(shù)年)在-20℃。

甘草黃酮B(91433-17-9,Licoflavone B)實(shí)驗(yàn)注意事項(xiàng):
1.實(shí)驗(yàn)前需戴好防護(hù)眼鏡,穿戴防護(hù)服和口罩,佩戴手套,避免與皮膚接觸。
2.實(shí)驗(yàn)過(guò)程中如遇到有毒或者刺激性物質(zhì)及有害物質(zhì)產(chǎn)生,必要時(shí)實(shí)驗(yàn)操作需要手套箱內(nèi)完成以免對(duì)實(shí)驗(yàn)人員造成傷害
3.實(shí)驗(yàn)后產(chǎn)生的廢棄物需分類存儲(chǔ),并交于專業(yè)生物廢氣物處理公司處理,以免造成環(huán)境污染

Licoflavone B(91433-17-9) Experimental considerations:
1. Wear protective glasses, protective clothing and masks, gloves, and avoid contact with the skin during the experiment.
2. The waste generated after the experiment needs to be stored separately, and handed over to a professional biological waste gas treatment company to avoid environmental pollution.

Tag:甘草黃酮B(91433-17-9,Licoflavone B),甘草黃酮B試劑,甘草黃酮B抑制劑,甘草黃酮B的純度,甘草黃酮B的作用,甘草黃酮B的合成,甘草黃酮B的廠家,甘草黃酮B的價(jià)格,甘草黃酮B的外觀,甘草黃酮B的溶解度,甘草黃酮B的含量,甘草黃酮B的MSDS
產(chǎn)品說(shuō)明 甘草黃酮B(91433-17-9,Licoflavone B)是一種從黃草甘草中分離出來(lái)的類黃酮,甘草黃酮B可以抑制血吸蟲的活性。
IntroductionLicoflavone B (91433-17-9, 甘草黃酮B) is a flavonoid isolated from yellow licorice root. Licorice flavone B can inhibit the activity of schistosomes.
Application1
Application2
Application3
Pharmacological Activities and Phytochemical Constituents(Liquorice,2017)
Synthesis of 6,7-Dibromoflavone and Its Regioselective Diversification via Suzuki–Miyaura Reactions(Synthesis,2017)
Traditional Uses, Bioactive Chemical Constituents, and Pharmacological and Toxicological Activities of Glycyrrhiza glabra L. (Fabaceae) PMID 32106571; Biomolecules 2020 Feb; 10(3): (Review Article)
Chemical studies of Chinese licorice-roots. I. Elucidation of five new flavonoid constituents from the roots of Glycyrrhiza glabra L. collected in Xinjiang PMID 8069956; Chemical & pharmaceutical bull
Schistosomicidal activity and docking of Schistosoma mansoni ATPDase 1 with licoflavone B isolated from Glycyrrhiza inflata (Fabaceae) PMID 26454044; Experimental parasitology 2015 Dec; 159(?):207-14

Schistosomicidal activity and docking of Schistosoma mansoni ATPDase 1 with licoflavone B isolated from Glycyrrhiza inflata (Fabaceae)
Abstract:
Schistosomiasis is one of the world's major public health problems, and its treatment is widely dependent on praziquantel (PZQ), the only available drug. Schistosoma mansoni ATP diphosphohydrolases are ecto-enzymes localized on the external tegumental surface of S. mansoni and considered an important target for action of new drugs. In this work, the in vitro schistosomicidal activity of the crude extract of Glycyrrhiza inflata roots (GI) and its isolated compounds echinatin, licoflavone A and licoflavone B were evaluated against S. mansoni adult worms. Results showed that GI (200 μg/mL) was active against adult schistosomes, causing 100% mortality after 24 h of incubation. Chromatographic fractionation of GI led to isolation of echinatin, licoflavone A and licoflavone B. Licoflavone B (25-100 μM) caused 100% mortality, tegumental alterations, and reduction of oviposition and motor activity of all adult worms, without affecting mammalian Vero cells. Confocal laser scanning microscopy showed tegumental morphological alterations and changes on the numbers of tubercles of S. mansoni worms in a dose-dependent manner after incubation with licoflavone B. Licoflavone B also showed high S. mansoni ATPase (IC50 of 23.78 μM) and ADPase (IC50 of 31.50 μM) inhibitory activities. Docking studies predicted different interactions between licoflavone B and S. mansoni ATPDase 1, corroborating with the in vitro inhibitory activity. This report demonstrated the first evidence for the schistosomicidal activity of licoflavone B and suggests that its mechanism of action involve the inhibition of S. mansoni ATP diphosphohydrolases.

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