货号:A106244
同义名:
Loganoside; NSC 606403
Loganin是一种天然的 iridoid 糖苷,具有抗氧化、保肝和神经保护作用,并且是一种 COX-1 抑制剂,IC50 值为 3.55 µM,抑制 TNF-α 的形成,并减少一氧化氮的产生。


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| 产品名称 | COX ↓ ↑ | COX-1 ↓ ↑ | COX-2 ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Piroxicam | ✔ | 98% | |||||||||||||||||
| Salicylic acid | ✔ | 98% | |||||||||||||||||
| Phenacetin | ✔ | 98% | |||||||||||||||||
| Etodolac | ✔ | 99% | |||||||||||||||||
| Flunixin meglumine | ✔ | 98% | |||||||||||||||||
| Ibuprofen L-lysine | ✔ | 98% | |||||||||||||||||
| Nabumetone | ✔ | 98% | |||||||||||||||||
| Acemetacin | ✔ | 98% | |||||||||||||||||
| Diflunisal | ✔ | 98% | |||||||||||||||||
| Pranoprofen | ✔ | 98% | |||||||||||||||||
| Ampiroxicam | ✔ | 98% | |||||||||||||||||
| Meloxicam | ✔ | 98% | |||||||||||||||||
| Sulindac | ✔ | 98% | |||||||||||||||||
| Ketoprofen | ✔ | 98% | |||||||||||||||||
| Mefenamic Acid | ✔ | 95% | |||||||||||||||||
| Bromfenac sodium | ✔ | 98% | |||||||||||||||||
| Oxaprozin | ✔ | 99% | |||||||||||||||||
| Aspirin | ✔ | 99% | |||||||||||||||||
| Nepafenac | ✔ | 98% | |||||||||||||||||
| Zaltoprofen | ✔ | 99% | |||||||||||||||||
| Salicin | ✔ | 98% | |||||||||||||||||
| Suprofen | ✔ | 99%+ | |||||||||||||||||
| Xanthohumol | ✔ | 99% | |||||||||||||||||
| Parecoxib | ✔ | 98% | |||||||||||||||||
| Tolfenamic Acid |
+++
COX-2, IC50: 0.2 μM |
98% | |||||||||||||||||
| Etoricoxib | ✔ | 99% | |||||||||||||||||
| Niflumic Acid | ✔ | 98% | |||||||||||||||||
| Valdecoxib |
++++
COX-2, IC50: 5 nM |
99+% | |||||||||||||||||
| Ibuprofen |
+
COX-1, IC50: 13 μM |
+
COX-2, IC50: 370 μM |
98% | ||||||||||||||||
| Indomethacin |
++
COX1, IC50: 0.28 μM |
+
COX-2, IC50: 14 μM |
97% | ||||||||||||||||
| Lornoxicam |
++++
COX-1, IC50: 5 nM |
++++
COX-2, IC50: 8 nM |
98% | ||||||||||||||||
| Meclofenamic acid sodium |
++++
COX-1, IC50: 40 nM |
+++
COX-2, IC50: 50 nM |
99% | ||||||||||||||||
| Asaraldehyde | ✔ | 98% | |||||||||||||||||
| Naproxen |
+
COX-1, IC50: 8.7 μM |
+
COX-2, IC50: 5.2 μM |
98% | ||||||||||||||||
| Diclofenac Sodium Salt |
+++
COX-1, IC50: 60 nM |
+++
COX-2, IC50: 200 nM |
98% | ||||||||||||||||
| NS-398 |
++
COX-2, IC50: 3.8 μM |
95% | |||||||||||||||||
| Amfenac Sodium Hydrate |
++
COX-1, IC50: 250 nM |
+++
COX-2, IC50: 150 nM |
98%+ | ||||||||||||||||
| Nimesulide |
+
COX-2, IC50: 26 μM |
98% | |||||||||||||||||
| Lumiracoxib |
++
COX-1, Ki: 3 μM |
+++
COX-2, Ki: 60 nM |
98% | ||||||||||||||||
| Rutaecarpine | ✔ | 95% | |||||||||||||||||
| Celecoxib |
++++
COX-2, IC50: 40 nM |
98% | |||||||||||||||||
| Carprofen |
++++
canine COX2, IC50: 30 nM |
98% | |||||||||||||||||
| Ketorolac |
++
COX-1 (human), IC50: 1.23 μM |
++
COX-2 (human), IC50: 3.50 μM |
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 |
|
| 描述 | Loganin, a major iridoid glycoside obtained from Corni fructus, has been shown to have anti-inflammatory and anti-shock effects. |
| Concentration | Treated Time | Description | References | |
| Transgenic cell line S10 | 200 μM | 14 days | To investigate the effect of continuous loganin supply on TIA accumulation, results showed that continuous loganin supply significantly increased TIA content but had no significant effect on TDC activity. | Plant Physiol. 1998 Feb 1;116(2):853-7 |
| Transgenic cell line S10 | 500 μM | 3 days or 3 days | To study the effect of loganin on TIA content, results showed that exogenous loganin significantly increased TIA content while depleting tryptamine content. | Plant Physiol. 1998 Feb 1;116(2):853-7 |
| BEnd.3 cells | 6.25 µM | 24 hours | Evaluate the cytotoxicity of LA-1 and loganin on BEnd.3 cells, results showed LA-1 did not exhibit significant cytotoxicity under the given conditions | Antioxidants (Basel). 2024 Nov 1;13(11):1339 |
| Rat Schwann cell line RSC96 | 0.1, 1, 10, 25, 50 μM | 48 hours | Loganin pretreatment attenuated high glucose-induced RSC96 cell viability loss, ROS generation, NF-κB nuclear translocation, P2X7 purinergic receptor and TXNIP expression, NLRP3 inflammasome activation, IL-1β and IL-18 maturation, and gasdermin D cleavage. | Cells. 2020 Aug 23;9(9):1948 |
| SH-SY5Y cells | 10 μM | 24 hours | Loganin attenuates high glucose-induced SH-SY5Y cell pyroptosis by inhibiting ROS generation and NLRP3 inflammasome activation, improving cell viability. | Cells. 2021 Oct 8;10(10):2688 |
| Mouse bone marrow monocytes | 1, 5, 10 μM | 5 days | To investigate the effect of Loganin on the differentiation of mouse bone marrow monocytes. Results showed that Loganin treatment significantly decreased TRAP activity and the number of TRAP-positive multinucleated cells, indicating that Loganin inhibited osteoclast differentiation. | Int J Mol Sci. 2022 Nov 16;23(22):14128 |
| Mouse preosteoblast MC3T3-E1 cells | 1, 5, 10 μM | 3 days | To investigate the effect of Loganin on the differentiation of mouse preosteoblasts. Results showed that Loganin treatment increased ALP activity and the number of ALP-positive cells, indicating that Loganin promoted osteoblast differentiation. | Int J Mol Sci. 2022 Nov 16;23(22):14128 |
| Adipose-derived stem cells (ADSCs) | 2, 5, 10 μM | 8 days | Loganin reduced mRNA expression levels of Pparγ, Cebpa, Plin2, Fasn, and Srebp1 and decreased the number of oil Red O-positive cells. | Int J Mol Sci. 2023 Mar 1;24(5):4752 |
| 3T3-L1 mouse preadipocytes | 2, 5, 10 μM | 8 days | Loganin significantly decreased the mRNA expression levels of Pparg, Cebpa, Plin2, Fasn, and Srebp1 in a dose-dependent manner and reduced the number of oil Red O-positive cells. | Int J Mol Sci. 2023 Mar 1;24(5):4752 |
| Administration | Dosage | Frequency | Description | References | ||
| Sprague Dawley (SD) rats | STZ-NA-induced diabetic neuropathy model | Intraperitoneal injection | 5 mg/kg | Once daily for 4 weeks | Loganin improved pain behaviors (allodynia and hyperalgesia), insulin resistance index (HOMA-IR), and serum levels of superoxide dismutase (SOD), catalase, and glutathione in diabetic neuropathic pain rats. Loganin also reduced the expression of pain-associated channel protein CaV3.2 and calcitonin gene-related peptide (CGRP) in the superficial spinal dorsal horn of PDN rats. | Cells. 2021 Oct 8;10(10):2688 |
| DdY mice | Ovariectomy-induced osteoporosis model | Oral | 2, 10, 50 mg/kg/day | Once daily for 12 weeks | To investigate the effect of Loganin on ovariectomy-induced osteoporosis. Results showed that Loganin treatment prevented BMD loss, improved trabecular microstructure, and increased the serum OPG/RANKL ratio, indicating that Loganin has anti-osteoporotic effects. | Int J Mol Sci. 2022 Nov 16;23(22):14128 |
| Sprague-Dawley rats | Chronic constriction injury (CCI) model | Intraperitoneal injection | 5 mg/kg/day | Once daily for 7 days | Loganin alleviates CCI-induced neuropathic pain by modulating autophagic flux and reducing neuroinflammation and apoptosis | Int J Mol Sci. 2022 Dec 14;23(24):15873 |
| C57BL/6 mice | Cisplatin-induced acute kidney injury model | Oral | 1, 10, and 20 mg/kg | Administered 1 h before cisplatin injection and lasted for 72 hours | Loganin attenuates the severity of cisplatin-induced acute kidney injury by inhibiting ERK1/2 activation | Int J Mol Sci. 2021 Jan 31;22(3):1421 |
| Mice | OVX- and high-fat diet (HFD)-induced obesity models | Oral | 2 and 10 mg/kg/day | 12 weeks | Loganin prevented weight gain induced by OVX and HFD, reduced hepatic steatosis and adipocyte enlargement, and decreased plasma leptin and insulin levels. | Int J Mol Sci. 2023 Mar 1;24(5):4752 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.56mL 0.51mL 0.26mL |
12.81mL 2.56mL 1.28mL |
25.62mL 5.12mL 2.56mL |
|
| CAS号 | 18524-94-2 |
| 分子式 | C17H26O10 |
| 分子量 | 390.38 |
| SMILES Code | O=C(C1=CO[C@@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O2)[C@@]3([H])[C@]1([H])C[C@H](O)[C@@H]3C)OC |
| MDL No. | MFCD00075645 |
| 别名 | Loganoside; NSC 606403; 7-hydroxy-6-desoxy Verbenalin |
| 运输 | 蓝冰 |
| InChI Key | AMBQHHVBBHTQBF-UOUCRYGSSA-N |
| Pubchem ID | 87691 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, room temperature |
| 溶解方案 |
DMSO: 50 mg/mL(128.08 mM),配合低频超声,并水浴加热至45℃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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