الصفحة الرئيسية>>Signaling Pathways>> Others>> Toxicology>>3-Methoxycatechol

3-Methoxycatechol (Synonyms: 1,2-Dihydroxy-3-methoxybenzene, 3-Methoxypyrocatechol, NSC 66525, Pyrogallol 1-monomethyl ether)

رقم الكتالوجGC49874

A lignan-derived phenol

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3-Methoxycatechol التركيب الكيميائي

Cas No.: 934-00-9

الحجم السعر المخزون الكميّة
5g
22٫00
متوفر
25g
65٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.

Description of 3-Methoxycatechol

3-Methoxycatechol is a lignan-derived phenol.1 It is an agonist of G protein-coupled receptor 35 (GPR35) with an EC50 value of 147 µM in a dynamic mass redistribution (DMR) assay using HT-29 cells.2 Dietary administration of 3-methoxycatechol (2%) alone, or in a model of multiorgan carcinogenesis induced by nitrosamines, promotes esophageal carcinogenesis in rats.3 3-Methoxycatechol has been used as a precursor in the enzymatic synthesis of the phenols pyrogallol and purpurogallin and in the electro-organic synthesis of coumestan derivatives.1,4

1.Zhang, S., Xiaofeng, W., and Xiao, Y.Conversion of lignin-derived 3-methoxycatechol to the natural product purpurogallin using bacterial P450 GcoAB and laccase CueOAppl. Microbiol. Biotechnol.106(2)593-603(2022) 2.Deng, H., and Fang, Y.The three tatecholics benserazide, catechol and pyrogallol are GPR35 agonistsPharmaceuticals (Basel)6(4)500-509(2013) 3.Hirose, M., Tnaka, H., Takahashi, S., et al.Effects of sodium nitrite and catechol, 3-methoxycatechol, or butylated hydroxyanisole in combination in a rat multiorgan carcinogenesis modelCancer Res.53(1)32-37(1993) 4.Golabi, S.M., and Nematollahi, D.Electrochemical study of catechol and some 3-substituted catechols in the prescence of 4-hydroxy coumarin: Application to the electro-organic synthesis of new coumestan derivativesJ. Electroanal. Chem.420(1-2)127-134(1997)

Chemical Properties of 3-Methoxycatechol

Cas No. 934-00-9 SDF
المرادفات 1,2-Dihydroxy-3-methoxybenzene, 3-Methoxypyrocatechol, NSC 66525, Pyrogallol 1-monomethyl ether
Canonical SMILES OC1=CC=CC(OC)=C1O
Formula C7H8O3 M.Wt 140.1
الذوبان DMF: 3 mg/ml,DMSO: 2 mg/ml,Ethanol: 2 mg/ml,PBS (pH 7.2): 2 mg/ml Storage -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of 3-Methoxycatechol

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1 mg 5 mg 10 mg
1 mM 7.1378 mL 35.6888 mL 71.3776 mL
5 mM 1.4276 mL 7.1378 mL 14.2755 mL
10 mM 0.7138 mL 3.5689 mL 7.1378 mL
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In vivo Formulation Calculator (Clear solution) of 3-Methoxycatechol

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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.
3. All of the above co-solvents are available for purchase on the GlpBio website.

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Review for 3-Methoxycatechol

Average Rating: 5 ★★★★★ (Based on Reviews and 36 reference(s) in Google Scholar.)

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