Sanguinarine
Cat.No:IS0030 Solarbio
CAS:2447-54-3
Storage:Powder:2-8℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year
Purity:HPLC≥98%
Appearance:Solid
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Apoptosis >
SanguinarineCAS:2447-54-3
Storage:Powder:2-8℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year
Purity:HPLC≥98%
Appearance:Solid
Qty:
Size:
CAS | 2447-54-3 |
Name | Sanguinarine |
Molecular Formula | C20H14NO4 |
Molecular Weight | 332.33 |
Solubility | Soluble in DMSO |
Purity | HPLC≥98% |
Appearance | Solid |
Storage | Powder:2-8℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year |
EC | EINECS 219-503-3 |
MDL | MFCD00064925 |
SMILES | C[N+]1=CC2=C3C(OCO3)=CC=C2C(C=CC4=C5)=C1C4=CC6=C5OCO6 |
InChIKey | INVGWHRKADIJHF-UHFFFAOYSA-N |
InChI | InChI=1S/C20H14NO4/c1-21-8-15-12(4-5-16-20(15)25-10-22-16)13-3-2-11-6-17-18(24-9-23-17)7-14(11)19(13)21/h2-8H,9-10H2,1H3/q+1 |
PubChem CID | 5154 |
Target Point | Others |
Passage | Others |
Background | Sanguinarine is an alkaloid that can stimulate cell apoptosis by activating the production of reactive oxygen species (ROS). Sanguinarine induced apoptosis and JNK and NF- κ B activation. |
Biological Activity | Sanguinarine 是一种来源于 Sanguinaria Canadensis 的生物碱,可通过激活活性氧 (ROS) 的产生来刺激细胞凋亡。Sanguinarine 诱导的细胞凋亡与 JNK 和 NF-κB 的活化有关。[1] |
In Vitro | Sanguinarine(SANG)诱导的细胞凋亡与JNK和NF-κB信号通路的激活有关。为了确定Sanguinarine对细胞活力的影响,用不同浓度的Sanguinarine刺激22B-cFluc细胞24小时,然后用CKK刺激细胞凋亡。进行-8测定。 Sanguinarine治疗以剂量依赖性方式降低22B细胞的增殖。同时,测量用不同剂量的血根碱处理的22B-cFluc细胞的胞质提取物,以使用Ac-DEVD-pNA检测细胞半胱天冬酶-3活性,所述Ac-DEVD-pNA是经验证的半胱天冬酶-3底物。 450 nm处的吸光度以剂量依赖性方式增加,表明Sanguinarine刺激的caspase-3活性增加[1]。 |
In Vivo | 为了评估Sanguinarine(SANG)在体内诱导的细胞凋亡,将22B-cFluc细胞皮下接种到裸鼠的一侧,并允许异种移植模型建立。用10mg/kg血根碱静脉内治疗小鼠。在处理后24,48和72小时,在用150mg/kg D-荧光素底物ip注射小鼠后进行生物发光成像。 Sanguinarine治疗早在初始治疗后48小时就会引起明显的发光信号增加。在整个实验过程中观察到持续的生物发光成像(BLI)强度增加。在处理后72小时,收集肿瘤并进行TUNEL染色以评估细胞凋亡。与对照肿瘤相比,Sanguinarine治疗组表现出明显更多的细胞凋亡,表明来自散发性凋亡细胞的绿色信号增加[1]。 |
Cell Experiment | 使用细胞计数试剂盒-8通过CCK-8测定法测定血根碱的细胞活力。简而言之,将22B-cFluc细胞接种在96孔板(5×103细胞/孔)中,并用不同浓度的血根碱(0.5μM,1μM,2μM,4μM)处理24小时。然后向每个孔中加入10mL CKK-8,持续4小时,用酶标仪测量450nm处的吸光度。确定光密度(OD)值以反映来自每个孔的活细胞群[1]。 |
Animal Experiment | 小鼠[1]通过将悬浮在PBS中的1×10 7个22B-cFluc细胞注射到裸鼠(n = 6)中来制备异种移植肿瘤模型。在肿瘤达到约100mm 3的体积后,将血根碱(10mg/kg)静脉内注射到小鼠中。注射24小时,48小时和72小时后,给小鼠单剂量150mg/kg D-荧光素,并使用Xenogen Lumina II系统进行生物发光成像。使用Living Image软件4.1表示感兴趣区域中的信号强度。对于抗肿瘤治疗研究,一组荷瘤小鼠(n = 6)在整个实验期间每隔一天静脉注射10mg/kg血根碱,而对照组小鼠(n = 6)仅接受DMSO 。计算肿瘤生长测量[1]。 |
Kinase Experiment | 使用胱天蛋白酶-3活性测定试剂盒测量胱天蛋白酶-3活性。简而言之,收集用不同浓度的血根碱(0.5μM,1μM,2μM,4μM)或对照DMSO处理的细胞,洗涤并在裂解缓冲液中在冰上裂解30分钟。然后通过以1,2000rpm离心10分钟收集上清液。向每个样品中加入Ac-DEVD-pNA(2mM)并在37℃下孵育1小时。最后使用分光光度计在405nm的波长下量化每个样品的光密度(OD)。 p-NA标准用于校准每个样品的caspase-3活性[1]。 |
Data Literature Source | [1]. Wang Y,Noninvasive bioluminescence imaging of the dynamics of sanguinarine induced apoptosis via activation of reactive oxygen species. Oncotarget. 2016 Apr 19;7(16):22355-67. |
Unit | Bottle |
Specification | 5mg 10mg |
是一种生物碱,可通过激活活性氧 (ROS) 的产生来刺激细胞凋亡。诱导的细胞凋亡与 JNK 和 NF-κB 的活化有关。
Remark:These protocols are for reference only. Solarbio does not independently validate these methods.
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