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枣属

枣属

Cat. No. Product Name CAS No. Purity Chemical Structure
TN1812 Jujuboside B1
酸枣仁皂苷 B1
68144-21-8 98%
TargetMol Chemical Structure Jujuboside B1
Jujubosides have hypnotic effect on normal rats, may be influenced by circadian rhythm and the serotonergic system may involve in the hypnotic effect of jujubosi...
TN2928 Pygenic acid A
脓毒酸A
52213-27-1 98%
TargetMol Chemical Structure Pygenic acid A
3-Epicorosolic acid has a potent inhibitory effect on Epstein-Barr virus early antigen (EBV-EA) induction, it has potential anti-inflammatory activities as well ...
TN1813 Jujuboside D
酸枣仁皂苷D
194851-84-8 98%
TargetMol Chemical Structure Jujuboside D
Jujuboside D shows lipoxygenase-inhibiting activity.
TN3613 Ceanothic acid acetate
化合物 TN3613
119533-63-0 98%
TargetMol Chemical Structure Ceanothic acid acetate
Ceanothic acid acetate 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3613,CAS号为 119533-63-0。
TN1477 Ceanothic acid
美洲茶酸
21302-79-4 98%
TargetMol Chemical Structure Ceanothic acid
Ceanothic acid derivatives show cytotoxic effect against OVCAR-3 and HeLa cancer cell lines.
TN5941 2,3-O-Isopropylidenyl euscaphic acid
蔷薇酸丙酮化物
220880-90-0 98%
TargetMol Chemical Structure 2,3-O-Isopropylidenyl euscaphic acid
2,3-O-Isopropylidenyl euscaphic acid shows good hepatoprotective effect,the EC50 value of 88.36±3.25 uM in Hep G2 cells.
TN1442 Betulinic acid methyl ester
桦木酸甲酯
2259-06-5 98%
TargetMol Chemical Structure Betulinic acid methyl ester
Betulinic acid methyl ester showed antiplasmodial activity against chloroquine-resistant Plasmodium falciparum parasites in vitro.It also inhibited B16 2F2 cell ...
TN4402 Labd-13-ene-8,15-diol
化合物 TN4402
10267-31-9 98%
TargetMol Chemical Structure Labd-13-ene-8,15-diol
13(E)-Labd-13-ene-8alpha,15-diol shows antiviral and anticancer activity, it shows strong anti-HRV2 and HRV3 activity with a 50% inhibitory concentration (IC50) ...
TN1379 Alphitolic acid
化合物Alphitolic acid
19533-92-7 98%
TargetMol Chemical Structure Alphitolic acid
Alphitolic acid is a potent Hh/GLI signaling inhibitor, it shows an important relationship between Hh/GLI signaling inhibition, the decrease of BCL2, and cytotox...
T5S2228 6‴-Feruloylspinosin
6-阿魏酰斯皮诺素
77690-92-7 99.65%
TargetMol Chemical Structure 6‴-Feruloylspinosin
6‴-Feruloylspinosin (6'''-Feruloylspinosin) 是一种类黄酮,分离自 Ziziphus jujuba 种子中。在大鼠海马神经元中,它能透过血脑屏障,增强 GABAAα1、GABAAα5、GABABR1 的 mRNA 表达。
T5782 Bevirimat
贝韦立马
174022-42-5 99.58%
TargetMol Chemical Structure Bevirimat
Bevirimat (PA-457) 是一种 HIV-1 成熟抑制剂,可在病毒体成熟过程中阻断 Gag 衣壳 (CA) 前体 CA-SPI 裂解为成熟的 CA 蛋白。
TL0002 Liquiritin apioside
甘草素二糖苷
74639-14-8 99.03%
TargetMol Chemical Structure Liquiritin apioside
Liquiritin apioside 是一种从甘草中获得的黄酮,具有镇咳活性。
T2S0765 Epibetulinic acid
表白桦脂酸
38736-77-5 99.02%
TargetMol Chemical Structure Epibetulinic acid
Epibetulinic acid 对细菌内毒素刺激的小鼠巨噬细胞 (RAW 264.7) 中 NO 和前列腺素 E(2) 的产生具有有效的抑制作用,IC50分别为 0.7 和 0.6 μM,具有抗炎活性。
TN1134 Euscaphic acid
野鸦椿酸
53155-25-2 98.93%
TargetMol Chemical Structure Euscaphic acid
Euscaphic acid 是来源于枣的一种三萜,是DNA 聚合酶抑制剂,可诱导细胞凋亡。它抑制小牛 DNA 聚合酶 α 和大鼠 DNA 聚合酶 β 的IC50值分别为 61 和 108 μM。
T3781 Jujuboside B
酸枣仁皂苷B
55466-05-2 98.89%
TargetMol Chemical Structure Jujuboside B
Jujuboside B 是一种提取自Zizyphus jujuba 中的活性成分,对血小板聚集具有抑制作用。
T3782 Jujuboside A
酸枣仁皂苷 A
55466-04-1 98.49%
TargetMol Chemical Structure Jujuboside A
Jujuboside A 是从中药酸枣仁中提取的一种糖苷,可用于失眠和焦虑的相关研究。
T6S2227 Spinosin
斯皮诺素
72063-39-9 98.16%
TargetMol Chemical Structure Spinosin
Spinosin (Flavoayamenin) 是一种具有神经保护作用的 C-糖苷类黄酮,从 Zizyphus jujube 种子分离得到,能够激活 Nrf2/HO-1 通路,并抑制 Aβ1-42的产生和聚合。
T6674 L-Ascorbic acid sodium salt
维生素C钠
134-03-2
TargetMol Chemical Structure L-Ascorbic acid sodium salt
L-Ascorbic acid sodium salt (Vitamin C sodium salt) 是一种电子供体,是一种内源性抗氧化剂。它还是一种胶原沉积促进剂和弹性生成抑制剂。它选择性抑制 Cav3.2 通道(Cav3.2 channels),IC50为 6.5 μM。
Jujuboside B1
TN1812
Jujubosides have hypnotic effect on normal rats, may be influenced by circadian rhythm and the serotonergic system may involve in the hypnotic effect of jujubosi...
Pygenic acid A
TN2928
3-Epicorosolic acid has a potent inhibitory effect on Epstein-Barr virus early antigen (EBV-EA) induction, it has potential anti-inflammatory activities as well ...
Jujuboside D
TN1813
Jujuboside D shows lipoxygenase-inhibiting activity.
Ceanothic acid acetate
TN3613
Ceanothic acid acetate 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3613,CAS号为 119533-63-0。
Ceanothic acid
TN1477
Ceanothic acid derivatives show cytotoxic effect against OVCAR-3 and HeLa cancer cell lines.
2,3-O-Isopropylidenyl euscaphic acid
TN5941
2,3-O-Isopropylidenyl euscaphic acid shows good hepatoprotective effect,the EC50 value of 88.36±3.25 uM in Hep G2 cells.
Betulinic acid methyl ester
TN1442
Betulinic acid methyl ester showed antiplasmodial activity against chloroquine-resistant Plasmodium falciparum parasites in vitro.It also inhibited B16 2F2 cell ...
Labd-13-ene-8,15-diol
TN4402
13(E)-Labd-13-ene-8alpha,15-diol shows antiviral and anticancer activity, it shows strong anti-HRV2 and HRV3 activity with a 50% inhibitory concentration (IC50) ...
Alphitolic acid
TN1379
Alphitolic acid is a potent Hh/GLI signaling inhibitor, it shows an important relationship between Hh/GLI signaling inhibition, the decrease of BCL2, and cytotox...
6‴-Feruloylspinosin
T5S2228
6‴-Feruloylspinosin (6'''-Feruloylspinosin) 是一种类黄酮,分离自 Ziziphus jujuba 种子中。在大鼠海马神经元中,它能透过血脑屏障,增强 GABAAα1、GABAAα5、GABABR1 的 mRNA 表达。
Bevirimat
T5782
Bevirimat (PA-457) 是一种 HIV-1 成熟抑制剂,可在病毒体成熟过程中阻断 Gag 衣壳 (CA) 前体 CA-SPI 裂解为成熟的 CA 蛋白。
Liquiritin apioside
TL0002
Liquiritin apioside 是一种从甘草中获得的黄酮,具有镇咳活性。
Epibetulinic acid
T2S0765
Epibetulinic acid 对细菌内毒素刺激的小鼠巨噬细胞 (RAW 264.7) 中 NO 和前列腺素 E(2) 的产生具有有效的抑制作用,IC50分别为 0.7 和 0.6 μM,具有抗炎活性。
Euscaphic acid
TN1134
Euscaphic acid 是来源于枣的一种三萜,是DNA 聚合酶抑制剂,可诱导细胞凋亡。它抑制小牛 DNA 聚合酶 α 和大鼠 DNA 聚合酶 β 的IC50值分别为 61 和 108 μM。
Jujuboside B
T3781
Jujuboside B 是一种提取自Zizyphus jujuba 中的活性成分,对血小板聚集具有抑制作用。
Jujuboside A
T3782
Jujuboside A 是从中药酸枣仁中提取的一种糖苷,可用于失眠和焦虑的相关研究。
Spinosin
T6S2227
Spinosin (Flavoayamenin) 是一种具有神经保护作用的 C-糖苷类黄酮,从 Zizyphus jujube 种子分离得到,能够激活 Nrf2/HO-1 通路,并抑制 Aβ1-42的产生和聚合。
L-Ascorbic acid sodium salt
T6674
L-Ascorbic acid sodium salt (Vitamin C sodium salt) 是一种电子供体,是一种内源性抗氧化剂。它还是一种胶原沉积促进剂和弹性生成抑制剂。它选择性抑制 Cav3.2 通道(Cav3.2 channels),IC50为 6.5 μM。
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