货号:A732149
同义名:
广藿香醇
/ Patchoulol; Patchouli camphor
Patchouli alcohol是一种天然存在的倍半萜醇,主要存在于广藿香油中,具有抗菌、抗真菌和抗病毒作用。


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| 描述 | Patchouli alcohol (PA) is a natural tricyclic sesquiterpene extracted from Pogostemon cablin (Blanco) Benth, and exhibits anti-Helicobacter pylori and anti-inflammatory properties. Treatment with PA for 2 weeks exhibited highly efficient protective effect against H. pylori-induced gastritis and related damages[3]. PA ameliorated DSS-induced (dextran sulfate sodium) mice acute colitis by suppressing inflammation, maintaining the integrity of intestinal epithelial barrier, inhibiting cell death signaling, and suppressing tryptophan catabolism[4]. Treatment of patchouli alcohol reduced lipid accumulation in 3T3-L1 adipocytes in a dose-dependent manner without toxicity. Oral gavage of patchouli alcohol led to a significant reduction of body weight and fat accumulation in the mice fed with HFD (high-fat diet)[5]. PA significantly inhibited different IAV (anti-influenza virus) strains multiplication in vitro, and may block IAV infection through inactivating virus particles directly and interfering with some early stages after virus adsorption[6]. |
| Concentration | Treated Time | Description | References | |
| Human brain microvascular endothelial cells (HBMECs) | 2.5, 5, 10, 20 µM | 12 hours | To evaluate the protective effect of patchouli alcohol on OGD-exposed HBMECs. Results showed that patchouli alcohol significantly reduced the permeability of HBMECs and increased the expression of tight junction and adherens junction proteins. | Front Cell Dev Biol. 2021 Jul 22;9:693533 |
| Primary neurons | 5, 10, 20 µM | 24 hours | PTA ameliorated o-Aβ25-35-induced reduction of synapse-related proteins VAMP2 and PSD95 in primary neurons by enhancing ERβ/BDNF/TrkB/CREB pathways | Acta Pharmacol Sin. 2022 Sep;43(9):2226-2241 |
| H9C2 cells | 10 and 20 µM | 24 hours | To evaluate the alleviating effect of PatA on high glucose (HG) + palmitic acid (PA)-induced fibrotic and inflammatory responses, results showed that PatA mitigated these responses by inhibiting the JAK2/STAT3 signaling pathway. | Pharmaceuticals (Basel). 2024 May 14;17(5):631 |
| Primary microglia | 5, 10, 20 µM | 4 hours | PTA enhanced phagocytosis of o-FAM-Aβ42 in primary microglia by enhancing ERβ/TLR4 signaling | Acta Pharmacol Sin. 2022 Sep;43(9):2226-2241 |
| BV2 cells | 5, 10, 20 µM | 4 hours | PTA enhanced phagocytosis of o-FAM-Aβ42 in BV2 cells by enhancing ERβ/TLR4 signaling | Acta Pharmacol Sin. 2022 Sep;43(9):2226-2241 |
| Bone marrow-derived macrophages (BMMs) | 1-10 µM | 5 days | To evaluate the effect of patchouli alcohol on osteoclast differentiation, results showed that PA dose-dependently inhibited RANKL-induced osteoclast formation. | Front Pharmacol. 2021 Jun 8;12:684976 |
| Rat cardiomyocyte H9C2 | 1, 10, 100 µM | 8 hours | To evaluate the effect of PA on the viability of H9C2 cells subjected to simulated ischemia/reperfusion (SI/R) treatment. PA treatment significantly increased the viability of SI/R-treated H9C2 cells in a dose-dependent manner. | Pharm Biol. 2022 Dec;60(1):949-957 |
| Administration | Dosage | Frequency | Description | References | ||
| C57BL/6J mice | Ovariectomized (OVX) osteoporosis model | Intraperitoneal injection | 10 mg/kg | Every 2 days for 6 weeks | To evaluate the therapeutic effect of patchouli alcohol on osteoporosis, results showed that PA significantly reduced bone loss and osteoclast numbers. | Front Pharmacol. 2021 Jun 8;12:684976 |
| Sprague-Dawley rats | Spinal cord injury model | Intraperitoneal injection | 10 mg/kg/day | Once daily for 56 days | To evaluate the protective effect of patchouli alcohol on the integrity of the blood-spinal cord barrier after spinal cord injury. Results showed that patchouli alcohol significantly improved neurological deficits and reduced the disruption of the blood-spinal cord barrier. | Front Cell Dev Biol. 2021 Jul 22;9:693533 |
| C57BL/6 male mice | Myocardial ischemia-reperfusion (MI/R) model | Intraperitoneal injection | 10, 20, 40 mg/kg | Once daily for 30 days | To evaluate the protective effect of PA on cardiac function in MI/R mice. PA treatment improved hemodynamic parameter changes and myocardial enzyme levels, increased left ventricular ejection fraction and left ventricular fractional shortening, reduced left ventricular end-systolic diameter, and inhibited CK-MB, cTnI, and cTnT levels. Additionally, PA attenuated myocardial tissue damage and apoptosis. | Pharm Biol. 2022 Dec;60(1):949-957 |
| C57BL/6J mice | DSS-induced ulcerative colitis model | Oral gavage | 20 mg/kg and 40 mg/kg | Once daily for 14 days | To evaluate the anti-inflammatory effects of PA on DSS-induced ulcerative colitis, results showed PA significantly alleviated inflammatory response and intestinal barrier damage | Sci Rep. 2024 Jul 20;14(1):16745 |
| APP/PS1 transgenic mice | Alzheimer’s disease model | Oral gavage | 20, 40 mg/kg/day | Once daily for 90 days | PTA reduced amyloid plaque deposition by promoting microglial phagocytosis and improved synaptic integrity through enhancing BDNF/TrkB/CREB signaling, while ameliorating oxidative stress by increasing Catalase levels | Acta Pharmacol Sin. 2022 Sep;43(9):2226-2241 |
| TgCRND8 transgenic mice | Alzheimer's disease model | Intragastric administration | 25 and 50 mg/kg | Once daily for 4 consecutive months | Patchouli alcohol significantly improved activities of daily living (ADL), ameliorated the anxiety-related behavioral deficits and cognitive impairments in TgCRND8 mice. PA modulated the amyloid precursor protein (APP) processing. PA also markedly reduced the levels of beta-amyloid (Aβ) 40 and Aβ42, suppressed Aβ plaque burdens, inhibited tau protein hyperphosphorylation at several sites and relieved neuroinflammation in the brains of TgCRND8 mice. | J Neuroinflammation. 2023 Jan 30;20(1):19 |
| C57BL/6 mice | Streptozotocin (STZ)-induced type 1 diabetes model | Oral | 5 and 15 mg/kg | Once daily for 16 weeks | To evaluate the protective effect of PatA on diabetes-induced cardiac injury and dysfunction, results showed that PatA protected the heart by regulating myocardial fibrosis rather than reducing hyperglycemia. | Pharmaceuticals (Basel). 2024 May 14;17(5):631 |
| Sprague-Dawley rats | Chronic restraint stress-induced IBS-D model | Gavage administration | 5, 10, 20 mg/kg | Once daily for 2 weeks | To evaluate the effects of patchouli alcohol on visceral sensitivity, diarrhea symptoms, and intestinal transit in IBS-D rats. Results showed that PA significantly reduced visceral sensitivity, diarrhea symptoms, and intestinal transit rate, and decreased the proportion of excitatory neurons and acetylcholine (Ach)- and substance P (SP)-positive neurons in the distal colon. | Front Pharmacol. 2022 Nov 14;13:943119 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
4.50mL 0.90mL 0.45mL |
22.49mL 4.50mL 2.25mL |
44.97mL 8.99mL 4.50mL |
|
| CAS号 | 5986-55-0 |
| 分子式 | C15H26O |
| 分子量 | 222.37 |
| SMILES Code | O[C@@]1(C2(C)C)CC[C@H](C)[C@]3([H])C[C@@]2([H])CC[C@]13C |
| MDL No. | MFCD00209526 |
| 别名 | 广藿香醇 ;Patchoulol; Patchouli camphor; (-)-Patchouli Alcohol |
| 运输 | 蓝冰 |
| InChI Key | GGHMUJBZYLPWFD-CUZKYEQNSA-N |
| Pubchem ID | 10955174 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place,Inert atmosphere,2-8°C |
| 溶解方案 |
DMSO: 105 mg/mL(472.19 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 无水乙醇: 20 mg/mL(89.94 mM),配合低频超声助溶,注意:无水乙醇开封后,易挥发,也会吸收空气中的水分,导致溶解能力下降,请避免使用开封较久的乙醇 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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