甘草查尔酮ACAS号58749-22-7
甘草查尔酮ACAS号58749-22-7

甘草查尔酮A

¥240.00 ~¥3,490.00
5mg / 10mg / 1mg / 50mg / 100mg
5mg
北京
索莱宝
2026-04-21
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产品详情
中文名称:甘草查尔酮A中文别名:甘草查尔酮A
英文名称:Licochalcone ACAS:58749-22-7
产品分类:小分子化合物纯度:HPLC≥98%
产品编号品牌纯度规格库存价格
IL0110索莱宝HPLC≥98%5mg有现货540.00 元
IL0110索莱宝HPLC≥98%10mg有现货840.00 元
IL0110索莱宝HPLC≥98%1mg有现货240.00 元
IL0110索莱宝HPLC≥98%50mg有现货2,090.00 元
IL0110索莱宝HPLC≥98%100mg有现货3,490.00 元
标准名称:甘草查而酮英文名称:Licochalcone a
CAS:58749-22-7分子式:C21H22O4
分子量:338.396986484528颜色与性状:Yellow powder
密度:沸点:532.6°C at 760 mmHg
熔点:100°水溶性:
CAS58749-22-7
中文名称甘草查尔酮A
英文名称Licochalcone A
别名Licochalcone-A
分子式C21H22O4
分子量338.4
规格10mg ; 5mg ; 1mg ; 50mg ; 100mg
溶解性Soluble in DMSO
纯度HPLC≥98%
级别Cell Culture
外观(性状)Solid
储存条件Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
运输条件冷藏运输
ECEINECS 635-678-2
MDLMFCD01417903
SMILESO=C(C1=CC=C(O)C=C1)/C=C/C2=CC(C(C)(C)C=C)=C(O)C=C2OC
InChIKeyKAZSKMJFUPEHHW-DHZHZOJOSA-N
InChIInChI=1S/C21H22O4/c1-5-21(2,3)17-12-15(20(25-4)13-19(17)24)8-11-18(23)14-6-9-16(22)10-7-14/h5-13,22,24H,1H2,2-4H3/b11-8+
PubChem CID5318998
通路Others
背景说明是一种黄酮类化合物,具有抗癌、抗菌和抗病毒活性。
IC50Licochalcone A,an oxygenated chalcone isolated from the roots of Chinese licorice plant,inhibited the growth of both Leishmaniamajor and Leishmania donovani promastigotes and amastigotes. [2]The vegetative cell growth of Bacillus subtilis was inhibited in a licochalcone A concentration-dependentmanner and was completely prevented by 3micrograms of licochalcone A/ml. Licochalcone A showed a high level of resistance to heating at 80 to 121 degrees C for 15min. Licochalcone A didnot inhibit the germination of heat-treated spores of B. subtilis induced by L-alanine. Licochalcone A showed effects against all gram-positive bacteria tested and especially was effective against all Bacillus spp.[3]
In VitroIntraperitoneal administration of licochalcone A at doses of 2.5 and 5 mg/kg of body weight per day completely prevented lesion development in BALB/c mice infected with Leishmania major. Treatment of hamsters infected with L. donovani with intraperitoneal administration of licochalcone A at a dose of 20 mg/kg of body weight per day for 6 consecutive days resulted in a > 96% reduction of parasite load in the liver and the spleen compared with values for untreated control animals. The [3H]thymidine uptake by the parasites isolated from the treated hamsters was only about 1% of that observed in parasites isolated from the controls. Oral administration of licochalcone A at concentrations of 5 to 150 mg/kg of body weight per day for 6 consecutive days resulted in > 65 and 85% reductions of L. donovani parasite loads in the liver and the spleen,respectively,compared with those of untreated control hamsters.[1]
数据来源文献[1]. Chen M, Christensen SB, Theander TG, Kharazmi A. Antileishmanial activity of licochalcone A in mice infected with Leishmania major and in hamsters infected with Leishmania donovani. Antimicrob Agents Chemother. 1994 Jun;38(6):1339-44.
[2]. Chen M, Christensen SB, Blom J, Lemmich E, Nadelmann L, Fich K, Theander TG, Kharazmi A. Licochalcone A, a novel antiparasitic agent with potent activity against human pathogenic protozoan species of Leishmania. Antimicrob Agents Chemother. 1993 Dec;37(12):2550-6.
[3]. Tsukiyama R, Katsura H, Tokuriki N, Kobayashi M. Antibacterial activity of licochalcone A against spore-forming bacteria. Antimicrob Agents Chemother. 2002 May;46(5):1226-30.
单位
1mM-5mg14.7754mL
1mM-1mg2.9551mL
1mM-10mg29.5508mL
5mM-1mg0.591mL
5mM-5mg2.9551mL
5mM-10mg5.9102mL
10mM-1mg0.2955mL
10mM-5mg1.4775mL
10mM-10mg2.9551mL
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