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Methoxatin disodium salt (Pyrroloquinolinequinone disodium salt) Sale

(Synonyms: 吡咯喹啉醌二钠盐; PQQ disodium salt; Methoxatin disodium salt) 目录号 : GC31766

A quinone with diverse biological activities

Methoxatin disodium salt (Pyrroloquinolinequinone disodium salt) Chemical Structure

Cas No.:122628-50-6

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5mg
¥630.00
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10mg
¥900.00
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25mg
¥1,800.00
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50mg
¥2,700.00
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100mg
¥4,050.00
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产品描述

Pyrroloquinoline quinone (PQQ) is a quinone and redox enzyme cofactor that has been found in a variety of bacteria and has diverse biological activities.1,2,3,4,5 It inhibits fibril formation by the amyloid proteins amyloid-β (1-42) (Aβ42) and mouse prion protein when used at a concentrations of 100 and 300 μM.1 PQQ stimulates cell proliferation, reduces glutamate-induced production of reactive oxygen species (ROS), necrosis, and caspase-3 activity, and increases activity of superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPX) in neural stem and progenitor cells.2 It inhibits LPS-induced production of nitric oxide (NO) and prostaglandin E2 (PGE2) and suppresses LPS-induced expression of the pro-inflammatory mediators iNOS, COX-2, TNF-α, IL-1β, IL-6, MCP-1, and MIP-1α in primary microglia.6 In vivo, PQQ (3 and 10 mg/kg) reduces Iba-1 expression, a marker of microglial activation, in the cerebral cortex and hippocampal dentate gyrus in mice. PQQ decreases the number of hepatic cells positive for α-smooth muscle actin (α-SMA) and reduces collagen deposition and hepatic hydroxyproline levels in a mouse model of liver fibrosis.4 It also decreases serum glucose and total cholesterol levels, increases brain SOD, CAT, and GPX activities, and decreases brain lipid hydroperoxide levels in mice with diabetes induced by streptozotocin .5

1.Kim, J., Kobayashi, M., Fukuda, M., et al.Pyrroloquinoline quinone inhibits the fibrillation of amyloid proteinsPrion4(1)26-31(2010) 2.Guan, S., Xu, J., Guo, Y., et al.Pyrroloquinoline quinone against glutamate-induced neurotoxicity in cultured neural stem and progenitor cellsInt. J. Dev. Neurosci.4237-45(2015) 3.Yang, C., Yu, L., Kong, L., et al.Pyrroloquinoline quinone (PQQ) inhibits lipopolysaccharide induced inflammation in part via downregulated NF-κB and p38/JNK activation in microglial and attenuates microglia activation in lipopolysaccharide treatment micePLoS One9(10)e109502(2014) 4.Jia, D., Duan, F., Peng, P., et al.Pyrroloquinoline-quinone suppresses liver fibrogenesis in micePLoS One10(3)e0121939(2015) 5.Kumar, N., and Kar, A.Pyrroloquinoline quinone ameliorates oxidative stress and lipid peroxidation in the brain of streptozotocin-induced diabetic miceCan. J. Physiol. Pharmacol.93(1)71-79(2015) 6.Yang, Y., Kuwano, T., Lagor, W.R., et al.Lipidomic analyses of female mice lacking hepatic lipase and endothelial lipase indicate selective modulation of plasma lipid speciesLipids49(6)505-515(2014)

Chemical Properties

Cas No. 122628-50-6 SDF
别名 吡咯喹啉醌二钠盐; PQQ disodium salt; Methoxatin disodium salt
Canonical SMILES O=C(C(N1)=CC(C2=O)=C1C3=C(N=C(C([O-])=O)C=C3C(O)=O)C2=O)[O-].[Na+].[Na+]
分子式 C14H4N2Na2O8 分子量 374.17
溶解度 Water : 6.16 mg/mL (16.46 mM) 储存条件 Store at -20°C
General tips 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。
Shipping Condition 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。

溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.6726 mL 13.3629 mL 26.7258 mL
5 mM 0.5345 mL 2.6726 mL 5.3452 mL
10 mM 0.2673 mL 1.3363 mL 2.6726 mL
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Research Update

Kinetic study of the antioxidant activity of pyrroloquinolinequinol (PQQH(2), a reduced form of pyrroloquinolinequinone) in micellar solution

Kinetic study of the aroxyl radical-scavenging action of pyrroloquinolinequinol [PQQH(2), a reduced form of pyrroloquinolinequinone (PQQ)] and water-soluble antioxidants (vitamin C, cysteine, glutathione, and uric acid) has been performed. The second-order rate constants (k(s)) for the reaction of aroxyl radical with PQQH(2) and water-soluble antioxidants were measured in Triton X-100 micellar solution (5.0 wt %) (pH 7.4), using stopped-flow and UV-visible spectrophotometers. The k(s) values decreased in the order PQQH(2) > vitamin C >> cysteine > uric acid > glutathione. The aroxyl radical-scavenging activity of PQQH(2) was 7.4 times higher than that of vitamin C, which is well-known as the most active water-soluble antioxidant. Furthermore, PQQNa(2) (disodium salt of PQQ) was easily reduced to PQQH(2) by reaction of PQQNa(2) with glutathione and cysteine in buffer solution (pH 7.4) under nitrogen atmosphere. The result suggests that PQQ exists as a reduced form throughout the cell and plays a role as antioxidant.

Kinetic study of the quenching reaction of singlet oxygen by Pyrroloquinolinequinol (PQQH(2), a reduced form of Pyrroloquinolinequinone) in micellar solution

A kinetic study of the quenching reaction of singlet oxygen ((1)O(2)) with pyrroloquinolinequinol (PQQH(2), a reduced form of pyrroloquinolinequinone (PQQ)), PQQNa(2) (disodium salt of PQQ), and seven kinds of natural antioxidants (vitamin C (Vit C), uric acid (UA), epicatechin (EC), epigallocatechin (EGC), α-tocopherol (α-Toc), ubiquinol-10 (UQ(10)H(2)), and β-carotene (β-Car)) has been performed. The second-order rate constants k(Q) (k(Q) = k(q) + k(r), physical quenching and chemical reaction) for the reaction of (1)O(2) with PQQH(2), PQQNa(2), and seven kinds of antioxidants were measured in 5.0 wt % Triton X-100 micellar solution (pH 7.4), using UV-visible spectrophotometry. The k(Q) values decreased in the order of β-Car > PQQH(2) > α-Toc > UA > UQ(10)H(2) > Vit C ? EGC > EC ? PQQNa(2). PQQH(2) is a water-soluble antioxidant. The singlet oxygen-quenching activity of PQQH(2) was found to be 6.3, 2.2, 6.1, and 22 times as large as the corresponding those of water-soluble antioxidants (Vit C, UA, EGC, and EC). Further, the activity of PQQH(2) was found to be 2.2 and 3.1 times as large as the corresponding activity of lipid-soluble antioxidants (α-Toc and UQ(10)H(2)). On the other hand, the activity of PQQH(2) is 6.4 times as small as that of β-Car. It was observed that the chemical reaction (k(r)) is almost negligible in the quenching reaction of (1)O(2) by PQQH(2). The result suggests that PQQH(2) may contribute to the protection of oxidative damage in biological systems, by quenching (1)O(2).