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| Concentration | Treated Time | Description | References | |
| MSSA ATCC 25923 | 3.9 µg/mL | 18 hours | To evaluate the antibacterial activity of Kurarinone against MSSA ATCC 25923, results showed significant antibacterial activity | J Adv Res. 2024 Mar;57:197-212 |
| MSSA ATCC 29213 | 7.8 µg/mL | 18 hours | To evaluate the antibacterial activity of Kurarinone against MSSA ATCC 29213, results showed significant antibacterial activity | J Adv Res. 2024 Mar;57:197-212 |
| MRSA (USA300) | 7.8 µg/mL | 18 hours | To evaluate the antibacterial activity of Kurarinone against MRSA, results showed significant antibacterial activity | J Adv Res. 2024 Mar;57:197-212 |
| HaCaT cells | 50 μM | 6 hours | To evaluate the effect of Kurarinone on HO-1 expression, results showed that Kurarinone induced HO-1 expression. | Antioxidants (Basel). 2020 Sep 9;9(9):842 |
| RAW264.7 cells | 50 μM | 6 hours | To evaluate the effect of Kurarinone on HO-1 expression, results showed that Kurarinone induced HO-1 expression. | Antioxidants (Basel). 2020 Sep 9;9(9):842 |
| PC3 cells | 50 μM | 6 hours | To evaluate the effect of Kurarinone on HO-1 mRNA expression, results showed that Kurarinone significantly increased HO-1 mRNA expression. | Antioxidants (Basel). 2020 Sep 9;9(9):842 |
| BEAS-2B cells | 5, 10, 15, 20 mg/mL | 12, 24, 48 hours | To evaluate the toxicity of Kurarinone on BEAS-2B cells. Results showed that Kurarinone had low toxicity on BEAS-2B cells. | Front Pharmacol. 2018 Mar 23;9:252 |
| NCI-H1975 cells | 5, 10, 15, 20 mg/mL | 12, 24, 48 hours | To evaluate the inhibitory effect of Kurarinone on the proliferation of NCI-H1975 cells. Results showed that Kurarinone had significant cytotoxicity against NCI-H1975 cells. | Front Pharmacol. 2018 Mar 23;9:252 |
| A549 cells | 5, 10, 15, 20 mg/mL | 12, 24, 48 hours | To evaluate the inhibitory effect of Kurarinone on the proliferation of A549 cells. Results showed that Kurarinone inhibited the proliferation of A549 cells in a time- and dose-dependent manner. | Front Pharmacol. 2018 Mar 23;9:252 |
| CDLN cells | 20 μg/ml | 72 hours | To investigate the effect of KU on Th17 cell differentiation and Rac1 expression in CDLN cells. Results showed that KU significantly inhibited Th17 cell differentiation and Rac1 expression. | J Adv Res. 2025 Mar;69:381-398 |
| Peripheral blood mononuclear cells (PBMCs) | 10 and 20 μg/ml | 72 hours | To evaluate the effect of KU on inflammatory cytokine production in PBMCs. Results showed that KU significantly inhibited Th17 cell differentiation and Rac1 expression, and reduced inflammatory cytokine production. | J Adv Res. 2025 Mar;69:381-398 |
| B16F10 cells | 5 and 10 μM | 48 hours | Enhanced intracellular tyrosinase activity and stimulated melanin production | Front Pharmacol. 2024 Jul 10;15:1422310 |
| Administration | Dosage | Frequency | Description | References | ||
| Zebra fish | Zebra fish larvae | 20 μM | 48 hours | Stimulated melanogenesis by 36.9% | Front Pharmacol. 2024 Jul 10;15:1422310 | |
| C57BL/6J mice | Experimental autoimmune uveitis (EAU) model | Intraperitoneal injection | 10, 20, 40 mg/kg | Once daily for 14 days | To evaluate the therapeutic effect of KU on EAU model mice. Results showed that KU significantly alleviated EAU symptoms, reduced retinal inflammatory cell infiltration, and regulated Th17/Treg balance. | J Adv Res. 2025 Mar;69:381-398 |
| ICR mice | MRSA skin wound infection model | Topical administration | 7.8 mg/kg | Once daily for 14 days | To evaluate the therapeutic effect of Kurarinone on MRSA skin wound infection, results showed significant promotion of wound healing and reduction of bacterial load | J Adv Res. 2024 Mar;57:197-212 |
| BALB/c mice | Bleomycin-induced pulmonary fibrosis model | Oral | 5 mg/kg and 10 mg/kg | Five times a week from day 7 to day 27 after bleomycin administration | Kurarinone improved mechanical lung function, reduced collagen accumulation in lung tissues, and suppressed phosphorylation of Smad2/3 and AKT in bleomycin-induced pulmonary fibrosis mice. | Int J Mol Sci. 2021 Aug 4;22(16):8388 |
| C57BL/6 mice | TNBS-induced colitis model | Intraperitoneal injection | 125 mg/kg/day | Once daily for 7 days | KAR significantly alleviates TNBS-induced colitis symptoms, including reduced weight loss, lower disease activity index, improved colonic tissue damage, decreased inflammatory cell infiltration, protection of goblet cells and tight junction structures, and restoration of gut microbiota balance. Mechanistically, KAR suppresses Th17 cell response and promotes IL-10 production via Blimp-1 | Front Immunol. 2025 May 1;16:1587479 |
| BALB/c nude mice | A549 xenograft model | Intraperitoneal injection | 20 and 40 mg/kg/day | Once daily for 27 days | To evaluate the inhibitory effect of Kurarinone on the growth of A549 xenograft tumors in vivo. Results showed that Kurarinone significantly inhibited tumor growth without apparent toxicity. | Front Pharmacol. 2018 Mar 23;9:252 |
| Mice | MPTP-induced PD model | 5, 10, and 20 mg/kg | Kurarinone dose-dependently alleviated MPTP-induced behavioral deficits and dopaminergic neurotoxicity, including the losses of neurotransmitters and tyrosine hydroxylase (TH)-positive cells. Furthermore, kurarinone attenuated MPTP-mediated neuroinflammation by suppressing the activation of microglia involved in the nuclear factor kappa B signaling pathway. | Proc Natl Acad Sci U S A. 2022 Mar 1;119(9):e2118818119 | ||
| DBA/1 mice | Collagen-induced arthritis (CIA) model | Oral | 100 mg/kg/day | Once daily for 21 days | Reduced arthritis symptoms, decreased inflammatory cytokine levels, inhibited Th1 and Th17 cell responses, and reduced oxidative stress | Int J Mol Sci. 2021 Apr 13;22(8):4002 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.28mL 0.46mL 0.23mL |
11.40mL 2.28mL 1.14mL |
22.80mL 4.56mL 2.28mL |
|
| CAS号 | 34981-26-5 |
| 分子式 | C26H30O6 |
| 分子量 | 438.51 |
| SMILES Code | O=C1C[C@@H](C2=CC=C(O)C=C2O)OC3=C1C(OC)=CC(O)=C3C[C@H](C(C)=C)CC=C(C)C |
| 别名 | 苦参酮 |
| 运输 | 蓝冰 |
| InChI Key | LTTQKYMNTNISSZ-MWTRTKDXSA-N |
| Pubchem ID | 11982640 |
| 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: 50 mg/mL(114.02 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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