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Loganin/马钱子苷 {[allProObj[0].p_purity_real_show]}

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。

Loganin/马钱子苷 化学结构 CAS号:18524-94-2
Loganin/马钱子苷 化学结构
CAS号:18524-94-2
Loganin/马钱子苷 3D分子结构
CAS号:18524-94-2
Loganin/马钱子苷 化学结构 CAS号:18524-94-2
Loganin/马钱子苷 3D分子结构 CAS号:18524-94-2
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Loganin/马钱子苷 纯度/质量文件 产品仅供科研

货号:A106244 标准纯度: {[allProObj[0].p_purity_real_show]}
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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。

Loganin/马钱子苷 生物活性

靶点
  • AChE

    AChE, IC50:3.95 μM

描述 Loganin, a major iridoid glycoside obtained from Corni fructus, has been shown to have anti-inflammatory and anti-shock effects.

Loganin/马钱子苷 细胞实验

Cell Line
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

Loganin/马钱子苷 动物实验

Species
Animal Model
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

Loganin/马钱子苷 参考文献

[1]Yao L, Peng SX, et al. Unexpected Neuroprotective Effects of Loganin on 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine-Induced Neurotoxicity and Cell Death in Zebrafish. J Cell Biochem. 2017 Mar;118(3):615-628.

[2]Kim MJ, et al. Loganin protects against pancreatitis by inhibiting NF-κB activation. Eur J Pharmacol. 2015 Oct 15;765:541-50.

Loganin/马钱子苷 实验方案

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

Loganin/马钱子苷 技术信息

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

请根据您的动物给药指南选择适当的溶解方案。
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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