货号:A614383
同义名:
6-Hydroxyquercetin; NSC 115916
Quercetagetin (6-Hydroxyquercetin) 是一种黄酮类化合物,作为一种中度强效且选择性的细胞可渗透 pim-1 激酶抑制剂,IC50 为 0.34 μM。它具有抗炎和抗肿瘤活性。


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| 产品名称 | Pim1 ↓ ↑ | Pim2 ↓ ↑ | Pim3 ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| SMI-4a |
++
Pim1, IC50: 17 nM |
99%+ | |||||||||||||||||
| SGI-1776 free base |
++
Pim1, IC50: 7 nM |
+
Pim2, IC50: 363 nM |
+
Pim3, IC50: 69 nM |
FLT3 | 99+% | ||||||||||||||
| AZD-1208 |
+++
Pim1, IC50: 0.4 nM |
+++
Pim2, IC50: 5 nM |
+++
Pim3, IC50: 1.9 nM |
98% | |||||||||||||||
| CX-6258 HCl |
+++
Pim1, IC50: 5 nM |
+
Pim2, IC50: 25 nM |
++
Pim3, IC50: 16 nM |
98% | |||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| Concentration | Treated Time | Description | References | |
| NIH3T3 cells | NIH3T3 cells | Inhibited H-Ras-induced cell transformation | J Mol Biol. 2013 Jan 23;425(2):411-23. | |
| OCI-Ly19 cells | OCI-Ly19 cells | Evaluate the effect of Quercetagetin on NHL cell proliferation, showing significant toxicity on OCI-Ly19 cells | Mol Cancer. 2015 Dec 8;14:205. | |
| SUDHL6 cells | SUDHL6 cells | Evaluate the effect of Quercetagetin on NHL cell proliferation, showing anti-proliferative effects on SUDHL6 cells | Mol Cancer. 2015 Dec 8;14:205. | |
| OCI-Ly10 cells | OCI-Ly10 cells | Evaluate the effect of Quercetagetin on NHL cell proliferation, showing anti-proliferative effects on OCI-Ly10 cells | Mol Cancer. 2015 Dec 8;14:205. | |
| OCI-Ly3 cells | OCI-Ly3 cells | Evaluate the effect of Quercetagetin on NHL cell proliferation, showing anti-proliferative effects on OCI-Ly3 cells | Mol Cancer. 2015 Dec 8;14:205. | |
| Ramos cells | Ramos cells | Evaluate the effect of Quercetagetin on NHL cell proliferation, showing anti-proliferative effects on Ramos cells | Mol Cancer. 2015 Dec 8;14:205. | |
| Raji cells | Raji cells | Evaluate the effect of Quercetagetin on NHL cell proliferation, showing anti-proliferative effects on Raji cells | Mol Cancer. 2015 Dec 8;14:205. | |
| JB6 P+ cells | JB6 P+ cells | Inhibited UVB-induced AP-1 and NF-κB transactivation | J Mol Biol. 2013 Jan 23;425(2):411-23. | |
| Huh7.5 cells | Huh7.5 cells | Evaluate the inhibitory effect of Quercetagetin on HCV genotype 2a infectious strain replication, showing dose-dependent inhibition | Nucleic Acids Res. 2014 Aug;42(14):9399-409. | |
| Huh7.5 cells | Huh7.5 cells | Western blot analysis showed Quercetagetin dose-dependently inhibited NS5B protein expression | Nucleic Acids Res. 2014 Aug;42(14):9399-409. | |
| Huh7.5 cells | Huh7.5 cells | Evaluate the inhibitory effect of Quercetagetin on HCV genotype 1b subgenomic replicon replication, showing dose-dependent inhibition | Nucleic Acids Res. 2014 Aug;42(14):9399-409. | |
| H9c2 cardiomyoblasts | H9c2 cardiomyoblasts | To investigate the inhibitory effects of Quercetagetin on LPS-induced MAPK phosphorylation and COX-2 expression in H9c2 cells. Results showed that Quercetagetin significantly inhibited LPS-induced phosphorylation of ERK1/2, p38, and JNK, and reduced COX-2 expression. | Cell Mol Biol Lett. 2017 Sep 4;22:19. | |
| bone marrow-derived monocytes (BMMs) | bone marrow-derived monocytes (BMMs) | To evaluate the inhibitory effect of Quercetagetin on LPS-induced osteoclast differentiation. Results showed that 2 µM Quercetagetin significantly inhibited LPS-driven osteoclast differentiation and function. | Arthritis Res Ther. 2025 Mar 8;27(1):54. | |
| Caco-2/TC7 cells | Caco-2/TC7 cells | To evaluate the inhibitory ability of Quercetagetin on human α-glucosidases (sucrase, maltase, and isomaltase). Results showed that quercetagetin was the strongest inhibitor of α-glucosidases among the tested flavonols, with inhibition constants approaching those of acarbose. | Foods. 2021 Aug 20;10(8):1939. | |
| Administration | Dosage | Frequency | Description | References | ||
| SKH-1 hairless mice | Two-stage skin carcinogenesis model | Topical application | 4 or 20 nmol | Significantly inhibited UVB-induced skin cancer development, reduced tumor incidence and volume | J Mol Biol. 2013 Jan 23;425(2):411-23. | |
| DBA/1 male mice | Collagen antibody-induced arthritis (CAIA) model | Intraperitoneal (IP) injection | 40 mg/kg | Once daily until day 13 | To validate the therapeutic effect of Quercetagetin in the CAIA model. Results showed that 40 mg/kg Quercetagetin significantly alleviated joint destruction and inflammation. | Arthritis Res Ther. 2025 Mar 8;27(1):54. |
| Rabbits | ZEN-induced liver injury model | Oral | 100 mg/kg | 28 days | To assess the alleviative effect of quercetagetin (QG) on zearalenone (ZEN)-induced liver injury in rabbits. Results showed that QG alleviated the ZEN-induced oxidative damage and liver injury caused by inflammatory reaction through the Keap1-Nrf2-ARE signal pathway. | Front Pharmacol. 2023 Oct 3;14:1271384 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
3.14mL 0.63mL 0.31mL |
15.71mL 3.14mL 1.57mL |
31.42mL 6.28mL 3.14mL |
|
| CAS号 | 90-18-6 |
| 分子式 | C15H10O8 |
| 分子量 | 318.24 |
| SMILES Code | O=C1C2=C(OC(C3=CC=C(C(O)=C3)O)=C1O)C=C(O)C(O)=C2O |
| MDL No. | MFCD00017428 |
| 别名 | 6-Hydroxyquercetin; NSC 115916 |
| 运输 | 蓝冰 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, sealed in dry, 2-8°C |
| 溶解方案 |
DMSO: 120 mg/mL(377.08 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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