Urolithin A (Standard)
Based on 1 Customer Validation
Urolithin A (Standard) is the analytical standard of Urolithin A (HY-100599). This product is intended for research and analytical applications. Urolithin A, a gut-microbial metabolite of ellagic acid, exerts anti-inflammatory, antiproliferative, and antioxidant properties. Urolithin A induces autophagy and apoptosis, suppresses cell cycle progression, and inhibits DNA synthesis.
연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.
- CAS No.: 1143-70-0
- 화학식: C13H8O4
- 분자량:228.20
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Product Information
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Chemical Information
- 순도&문서
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Help & FAQs
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HY-100599
Urolithin AMitophagy Activator -
HY-N0523
Gallic acidBioactive Polyhydroxyphenolic Compound -
HY-14596
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HY-N1201
ApigeninCytochrome P450 Inhibitor -
HY-16561
ResveratrolPolyphenolic Phytoalexin -
HY-N0523R
Gallic acid (Standard)Bioactive Polyhydroxyphenolic Compound -
HY-14596R
Genistein (Standard) -
HY-B0166
L-Ascorbic acidAntioxidant -
HY-16561R
Resveratrol (Standard) -
HY-B1776
SpermidinePolyamine Compound -
HY-N0005
Curcuminp300 Histone Acetylatransferase Inhibitor -
HY-D0187
L-Glutathione reducedAntioxidant
Product Information
Information
신청
The compound is the grade of analytical standard, which is the reference standard supplied assay. It is commonly used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS.
Chemical Information
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CAS No. 1143-70-0
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Appearance Solid
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분자량 228.20
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화학식 C13H8O4
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Color White to yellow
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SMILES
O=C1C2=CC(O)=CC=C2C3=CC=C(O)C=C3O1
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Structure Classification
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Initial Source
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Please store the product under the recommended conditions in the Certificate of Analysis.
순도&문서
References
[1]. Gong Z, et al. Urolithin A attenuates memory impairment and neuroinflammation in APP/PS1 mice. [Content Brief]
[2]. Wang Y, et al. In vitro antiproliferative and antioxidant effects of urolithin A, the colonic metabolite of ellagic acid, on hepatocellular carcinomas HepG2 cells. Toxicol In Vitro. 2015 Aug;29(5):1107-15. [Content Brief]
[3]. Zhao W, et al. Metabolite of ellagitannins, urolithin A induces autophagy and inhibits metastasis in human sw620colorectal cancer cells. Mol Carcinog. 2018 Feb;57(2):193-200. [Content Brief]
[4]. Ishimoto H, et al. In vivo anti-inflammatory and antioxidant properties of ellagitannin metabolite urolithin A. Bioorg Med Chem Lett. 2011 Oct 1;21(19):5901-4. [Content Brief]
[5]. Qiu Z, et al. In vitro antioxidant and antiproliferative effects of ellagic acid and its colonic metabolite, urolithins, on human bladder cancer T24 cells. Food Chem Toxicol. 2013 Sep;59:428-37. [Content Brief]
[6]. González-Sarrías A, et al. Antiproliferative activity of the ellagic acid-derived gut microbiota isourolithin A and comparison with its urolithin A isomer: the role of cell metabolism.Eur J Nutr. 2017 Mar;56(2):831-841. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Urolithin A (Standard) Related Classifications
HY-100599R Related Classifications
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