MedKoo Cat#: 414157 | Name: Euparin

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Euparin exhibits a moderate antioxidant activity, it also exhibits antifungal activity against Trichophyton mentagrophytes. Euparin has antiviral activity, it exerts its effect during the early events of the replication cycle, from the virus adsorption to cells up to the first twenty minutes after infection.

Chemical Structure

Euparin
Euparin
CAS#532-48-9

Theoretical Analysis

MedKoo Cat#: 414157

Name: Euparin

CAS#: 532-48-9

Chemical Formula: C13H12O3

Exact Mass: 216.0786

Molecular Weight: 216.24

Elemental Analysis: C, 72.21; H, 5.59; O, 22.20

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
Euparin
IUPAC/Chemical Name
1-(6-Hydroxy-2-(1-methylethenyl)-5-benzofuranyl)ethanone
InChi Key
OPUFDNZTKHPZHM-UHFFFAOYSA-N
InChi Code
InChI=1S/C13H12O3/c1-7(2)12-5-9-4-10(8(3)14)11(15)6-13(9)16-12/h4-6,15H,1H2,2-3H3
SMILES Code
CC(C1=C(O)C=C(OC(C(C)=C)=C2)C2=C1)=O
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 216.24 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Han XM, Huang F, Jiao ML, Liu HR, Zhao ZH, Zhan HQ, Guo SY. Antidepressant Activity of Euparin: Involvement of Monoaminergic Neurotransmitters and SAT1/NMDAR2B/BDNF Signal Pathway. Biol Pharm Bull. 2020 Oct 1;43(10):1490-1500. doi: 10.1248/bpb.b20-00093. Epub 2020 Aug 13. PMID: 32788507. 2: Ezzatzadeh E, Hossaini Z. Green synthesis and antioxidant activity of novel series of benzofurans from euparin extracted of Petasites hybridus. Nat Prod Res. 2019 Jun;33(11):1617-1623. doi: 10.1080/14786419.2018.1428598. Epub 2018 Jan 28. PMID: 29376428. 3: Visintini Jaime MF, Campos RH, Martino VS, Cavallaro LV, Muschietti LV. Antipoliovirus Activity of the Organic Extract of Eupatorium buniifolium: Isolation of Euparin as an Active Compound. Evid Based Complement Alternat Med. 2013;2013:402364. doi: 10.1155/2013/402364. Epub 2013 Jul 17. PMID: 23956770; PMCID: PMC3730360. 4: Mohammadi M, Yousefi M, Habibi Z, Dastan D. Chemical composition and antioxidant activity of the essential oil of aerial parts of Petasites albus from Iran: a good natural source of euparin. Nat Prod Res. 2012;26(4):291-7. doi: 10.1080/14786410903374819. Epub 2011 Jul 11. PMID: 21416453. 5: Ezzatzadeh E, Hossaini Z. Four-component green synthesis of benzochromene derivatives using nano-KF/clinoptilolite as basic catalyst: study of antioxidant activity. Mol Divers. 2020 Feb;24(1):81-91. doi: 10.1007/s11030-019-09935-6. Epub 2019 Mar 4. PMID: 30830596. 6: Ezzatzadeh E, Hossaini Z. A novel one-pot three-component synthesis of benzofuran derivatives via Strecker reaction: Study of antioxidant activity. Nat Prod Res. 2020 Apr;34(7):923-929. doi: 10.1080/14786419.2018.1542389. Epub 2018 Dec 26. PMID: 30587038. 7: Xie XL, Xu XJ, Li RM, Wan JZ, Xie CY, Yang DP, Chen X. Isolation and simultaneous determination of two benzofurans in Radix Eupatorii Chinensis. Nat Prod Res. 2010 Nov;24(19):1854-60. doi: 10.1080/14786419.2010.482935. PMID: 21104532. 8: Ezzat MI, Ezzat SM, El Deeb KS, El Fishawy AM. In vitro evaluation of cytotoxic activity of the ethanol extract and isolated compounds from the corms of Liatris spicata (L.) willd on HepG2. Nat Prod Res. 2017 Jun;31(11):1325-1328. doi: 10.1080/14786419.2016.1239091. Epub 2016 Oct 6. PMID: 27712097. 9: Radulović NS, Đorđević MR. Chemical composition of the tuber essential oil from Helianthus tuberosus L. (Asteraceae). Chem Biodivers. 2014 Mar;11(3):427-37. doi: 10.1002/cbdv.201300323. PMID: 24634072. 10: Toyoda K, Yaoita Y, Kikuchi M. Three new dimeric benzofuran derivatives from the roots of Ligularia stenocephala MATSUM. et KOIDZ. Chem Pharm Bull (Tokyo). 2005 Dec;53(12):1555-8. doi: 10.1248/cpb.53.1555. PMID: 16327188.