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                同义名:
                    
                        
                            
                                NSC 94726; 3-hydroxy Urolithin
                            
                        
                    
                
                
                
                    
                     
                    
                     
                
            
Urolithin B是一种天然产物,具有抗增殖和抗氧化活性,能够穿越血脑屏障,并可能具有抗阿尔茨海默病的神经保护作用。它能在 47 μM 和 4.7 μM 的浓度下分别抑制人胎盘微粒体和 MCF-7 乳腺癌细胞中的芳香化酶活性。
 
                                 
                                
                            

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| 产品名称 | Aromatase ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Exemestane | +++ Aromatase (rat), IC50: 40 nM Aromatase (human), IC50: 30 nM | 97% | |||||||||||||||||
| Letrozole | 99% | ||||||||||||||||||
| Anastrozole | +++ Aromatase, IC50: 15 nM | 97% | |||||||||||||||||
| Obacunone | + Aromatase, IC50: 28.4 μM | Nrf2 | 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。 | |||||||||||||||||||
| 靶点 | 
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| 描述 | Urolithin B (30-100 μM; 24 h) exhibits anti-inflammatory properties in LPS-stimulated BV2 microglia by modulating pro- and anti-inflammatory molecules. It suppresses NF-κB and AP-1 signaling while upregulating AMPK and downregulating the Akt, JNK, and ERK signaling pathways in LPS-stimulated BV2 cells[1]. Urolithin B (15 μM; 24 h) promotes the growth and differentiation of C2C12 muscle ducts through increased protein synthesis and suppression of the ubiquitin-proteasome pathway[2]. | 
| 体内研究 | Urolithin B (50 mg/kg; ip; once daily for 4 days) suppresses microglial activation in the brains of LPS-injected mice under neuroinflammatory conditions[1]. Urolithin B (10 μg/day; mini-osmotic pump delivery, 28 days) triggers muscle hypertrophy and diminishes muscle atrophy following sciatic nerve transection in mice[2]. | 
| 体外研究 | Urolithin B (30-100 μM; 24 h) exhibits anti-inflammatory properties in LPS-stimulated BV2 microglia by modulating pro- and anti-inflammatory molecules. It suppresses NF-κB and AP-1 signaling while upregulating AMPK and downregulating the Akt, JNK, and ERK signaling pathways in LPS-stimulated BV2 cells[1]. Urolithin B (15 μM; 24 h) promotes the growth and differentiation of C2C12 muscle ducts through increased protein synthesis and suppression of the ubiquitin-proteasome pathway[2]. | 
| Concentration | Treated Time | Description | References | |
| Recombinant human MAO-B enzyme | 100 µM | 1 hour | To evaluate the inhibitory effect of Urolithin B on MAO-B enzyme, results showed low inhibition (<10–20%). | Metabolites. 2020 Jun 19;10(6):258 | 
| Recombinant human MAO-A enzyme | 0.4 and 2 µM | 1 hour | To evaluate the inhibitory effect of Urolithin B on MAO-A enzyme, results showed an IC50 value of 0.88 µM, displaying a mixed mode of inhibition. | Metabolites. 2020 Jun 19;10(6):258 | 
| RAW264.7 cells | 0, 20, 40, 60, 80, 100, 120, 140 µM | 2 and 5 days | To assess the effect of UB on cell viability. Results showed that UB concentrations below 100 μM did not affect cell viability. | J Cell Mol Med. 2022 Aug;26(16):4428-4439 | 
| BV2 cells | 10 µM, 20 µM, 40 µM | 2 hours pretreatment followed by 24 hours co-treatment withours LPS | To evaluate the effect of UB on LPS-induced inflammatory response in BV2 cells. UB significantly suppressed LPS-induced pro-inflammatory factors (TNF-α, IL-1β, IL-6) and M1 polarization marker iNOS expression, and partially restored the protein level of M2 polarization marker CD206. | CNS Neurosci Ther. 2025 Apr;31(4):e70379 | 
| C2C12 myotubes | 15 µM | 24 hours | Urolithin B enhances the growth and differentiation of C2C12 myotubes by increasing protein synthesis and repressing the ubiquitin–proteasome pathway. | J Cachexia Sarcopenia Muscle. 2017 Aug;8(4):583-597 | 
| Neuro-2a cells | 20, 40, 60 μg/mL | 24 hours | To evaluate the protective effect of UB on H2O2-induced oxidative injury and apoptosis in neuro-2a cells. Results showed that UB significantly reversed H2O2-induced decrease in cell viability and increase in LDH release, reduced ROS production and apoptosis. | Front Pharmacol. 2021 Nov 15;12:768097 | 
| Mouse podocytes | 100 µM | 24 hours or 48 hours | Evaluate the effect of high concentration Urolithin B on podocyte viability, results showed 100 µM UB significantly decreased podocyte viability | Cells. 2022 Aug 9;11(16):2471 | 
| Mouse podocytes | 10 µM | 24 hours or 48 hours | Evaluate the effect of Urolithin B on podocyte viability, results showed 10 µM UB significantly decreased podocyte viability | Cells. 2022 Aug 9;11(16):2471 | 
| RAW264.7 cells | 1, 5, 25 µM | 30 minutes to 3 days | Inhibited osteoclast-related gene and protein expression, down-regulated ERK/NF-κB signaling pathway | Cell Prolif. 2022 Oct;55(10):e13291 | 
| K562 cells | 25 µMol/mL | 48 hours | To evaluate the inhibitory effect of Urolithin B on the proliferation of K562 cells, results showed that Urolithin B significantly inhibited the proliferation of K562 cells | Int J Mol Sci. 2021 May 22;22(11):5465 | 
| Jurkat cells | 25 µMol/mL | 48 hours | To evaluate the inhibitory effect of Urolithin B on the proliferation of Jurkat cells, results showed that Urolithin B significantly inhibited the proliferation of Jurkat cells | Int J Mol Sci. 2021 May 22;22(11):5465 | 
| Bone marrow macrophages (BMMs) | 1, 5, 25 µM | 5 days | Inhibited RANKL-induced osteoclast differentiation, reduced osteoclast number and area | Cell Prolif. 2022 Oct;55(10):e13291 | 
| RAW264.7 cells | 0, 10, 50, 100 µM | 5 days | To measure the effect of UB on RANKL-induced intracellular ROS production. Results showed that UB reduced intracellular ROS production in a dose-dependent manner. | J Cell Mol Med. 2022 Aug;26(16):4428-4439 | 
| RAW264.7 cells | 0, 10, 30, 50, 100 µM | 5 days | To evaluate the effect of UB on RANKL-induced osteoclast differentiation. Results showed that UB inhibited TRAP-positive multinucleated osteoclast formation in a dose-dependent manner. | J Cell Mol Med. 2022 Aug;26(16):4428-4439 | 
| Human aortic endothelial cells (HAECs) | 15 µM | 5 minutes and 24 hours | To evaluate the effect of Urolithin B on NO release and eNOS activation. Results showed that Urolithin B at 15 μM did not significantly modify NO metabolite production in HAECs after both 5 min and 24 h of incubation. | Molecules. 2016 Aug 2;21(8):1009 | 
| Administration | Dosage | Frequency | Description | References | ||
| C57BL/6 J mice | Chronic unpredictable stress (CUS) and lipopolysaccharide (LPS)-induced depression models | Intraperitoneal injection | 10 mg/kg | Once daily for 7 days | To evaluate the effect of UB on depression-like behaviors, neuroinflammation, and microglial activation. UB significantly improved CUS- and LPS-induced depression-like behaviors, suppressed microglial activation and neuroinflammation, and restored the expression of SIRT1 and FOXO1 in the hippocampus. | CNS Neurosci Ther. 2025 Apr;31(4):e70379 | 
| Mice | Sciatic nerve denervation model | Continuous delivery via mini-osmotic pumps | 10 μg/day | Continuous delivery for 28 days | Urolithin B induces muscle hypertrophy in mice and reduces muscle atrophy after sciatic nerve section. | J Cachexia Sarcopenia Muscle. 2017 Aug;8(4):583-597 | 
| C57BL/6 mice | Ovariectomy (OVX)-induced osteoporosis model | Intraperitoneal injection | 10, 50 mg/kg | Every two days for 8 weeks | Alleviated bone loss in OVX mice, reduced the number of NFATc1, MMP9 and TRAP-positive osteoclasts in bone tissues, and decreased serum CTX-1 content | Cell Prolif. 2022 Oct;55(10):e13291 | 
| Wistar rats | Normal-diet fed rats | Intraperitoneal (IP) injection | 2.5 mg/kg | Four times a week for four weeks | To evaluate the effects of Urolithin B on liver and kidney functions and gut microbiota composition in normal-diet fed rats. Results showed that Urolithin B improved liver and kidney functions without affecting body weight. Additionally, Urolithin B induced the growth of Akkermansia and influenced the composition of other gut microbiota. | Nutrients. 2021 Oct 29;13(11):3885 | 
| Human | Postpartum women | Oral | 30 g of walnuts | Once daily for three days | To evaluate the association of urolithin metabotypes with the restoration of gut microbiota and anthropometric profiles postpartum. Results showed that metabotype-A mothers had a higher proportion of weight loss (≥2 kg) (75%) compared to metabotype-B (54%). The microbiota of metabotype-A mothers changed over the year, unlike metabotype-B, which barely changed. | Nutrients. 2019 Sep 3;11(9):2079 | 
| Human | Healthy individuals | Oral | 33 g/day | Once daily for three days | To evaluate the impact of short-term walnut consumption on gut microbiota modulation in healthy individuals, showing that the gut microbiota of UM-B individuals was more sensitive to the walnut intervention. | Nutrients. 2019 Oct 16;11(10):2483 | 
| C57BL/6 mice | D-galactose-induced aging model | Intragastric gavage | 50, 100, 150 mg/kg/day | Once daily for 8 weeks | To evaluate the protective effect of UB on cognitive deficits and brain injury in D-galactose-induced aging mice. Results showed that UB significantly ameliorated deficits in learning and memory by inhibiting oxidative stress and neuronal apoptosis, and promoting neuronal survival. | Front Pharmacol. 2021 Nov 15;12:768097 | 
| Dose | Rat: 20 mg/kg - 80 mg/kg[2] (o.g.) Mice: 10 mg/kg[3] (p.o.) | 
| Administration | o.g., p.o. | 
| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 4.71mL 0.94mL 0.47mL | 23.56mL 4.71mL 2.36mL | 47.13mL 9.43mL 4.71mL | |
| CAS号 | 1139-83-9 | 
| 分子式 | C13H8O3 | 
| 分子量 | 212.2 | 
| SMILES Code | O=C1C2=CC=CC=C2C3=CC=C(O)C=C3O1 | 
| MDL No. | MFCD00034338 | 
| 别名 | NSC 94726; 3-hydroxy Urolithin | 
| 运输 | 蓝冰 | 
| InChI Key | WXUQMTRHPNOXBV-UHFFFAOYSA-N | 
| Pubchem ID | 5380406 | 
| 存储条件 | In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Inert atmosphere, 2-8°C | 
| 溶解方案 | DMSO: 250 mg/mL(1178.13 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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