Urolithin

Base Information

  • PRODUCT:Urolithin
  • CAS.:1143-70-0
  • MF:C13H8O4
  • Molecular Weight:228.204
  • Purity:99%

Product Details

CAS: 1143-70-0

MF: C13H8O4

Buy High Quality Top Purity Urolithin 1143-70-0 Efficient Delivery

  • Molecular Formula:C13H8O4
  • Molecular Weight:228.204
  • Vapor Pressure:9.24E-12mmHg at 25°C 
  • Melting Point:340-345 °C 
  • Refractive Index:1.717 
  • Boiling Point:527.9 °C at 760 mmHg 
  • PKA:9.07±0.20(Predicted) 
  • Flash Point:214.2 °C 
  • PSA:70.67000 
  • Density:1.516 g/cm3 
  • LogP:2.35740 

3,8-dihydroxy-6H-dibenzo(b,d)pyran-6-one(Cas 1143-70-0) Usage

Description

Urolithin A is a metabolite of ellagic acid. It is produced by the body after you ingest compounds found in particularly high concentration in pomegranates (particularly the bitter components such as the skin and seeds) and can help recycle defective mitochondria. Since it is a metabolite that results from the transformation of the tannins in pomegranate by gut bacteria, it can be classified as a postbiotic.It has been demonstrated to stimulate mitophagy and improve muscle health in old animals and in preclinical models of aging.

Uses

Urolithin A is a major metabolite of ellagitannin and exhibits anti-inflammatory and antioxidant properties.

Definition

ChEBI: Urolithin A is a member of coumarins. It has a role as a geroprotector.

Preparation

2-bromo-5-methoxybenzoic acid is coupled with resorcinol to yield the intermediate “methoxy” product (Intermediate A), which is then isolated via filtration and dried for use in step 2. The solvent methanol is utilized in this step.the intermediate product, "Intermediate A", is treated with the Lewis acid, AlCl3, in order to obtain a crude urolithin A. The ether cleavage of Intermediate A is accomplished by activation of the methyl ether through the addition of the Lewis acid, AlCl3, in toluene. The activated species is then hydrolyzed by the addition of water. Following hydrolysis, the crude product is filtered and dried.crude urolithin A is dissolved in dimethyl sulfoxide (DMSO) for a polish filtration and subsequently precipitated from this DMSO solution by the addition of water. The filter cake is rinsed by water, followed by methanol. The raw urolithin A is then triturated with acetic acid (HOAc) to further purify the product and then collected by filtration. Following filtration, the purified product is rinsed with HOAc followed by tert-butyl-methyl ether (TBME), then dried to yield the final product, urolithin A.Synthesis of Urolithin A

benefits

As you age, ATP production begins to put strain on your mitochondria, and eventually, energy output falls. But when exposed to urolithin A, these failing mitochondria are broken down and eliminated (very similar to taking out the trash!) to make room for new, properly functioning mitochondria to grow.Ellagitannins and punicalagins are two natural polyphenols found in pomegranates. They have been shown to have anti-inflammatory and anticancer effects, but once metabolized by gut bacteria, they also produce urolithin A in the digestive tract. So supplementation with pomegranate extract, along with specific bacterial species (probiotics) that can help the pomegranate compounds to produce urolithin A, can be an effective approach to maintaining healthy mitochondria.

Biochem/physiol Actions

Urolithin A is a natural product with antiproliferative and antioxidant activity. Urolithin A is formed by metabolism from polyphenols found in some nuts and fruits, particularly pomegranates. Urolithin A has been shown to cross the blood brain barrier, and may have neuroprotective effects against Alzheimer′s Disease.

Side effects

The urolithin A supplementation was generally well-tolerated, although there were a few side effects recorded: increased lipids, triglycerides, LDL cholesterol, and chest pains.(But there was very little difference between the placebo group — where similar adverse effects were recorded — and the intervention group.) Most of these were mild and only one person withdrew from the trial due to side effects.

Metabolism

lt appears that the majority of ingested ellagitannins and EA are metabolized by thegut microbiota into a variety of urolithins. Urolithins are dibenzopyran-6-one derivatives that are produced from EA through the loss of one of the two lactonespresent in EA and then by successive removal of hydroxyl groups.Urolithin D isproduced first,followed sequentially by urolithin C, urolithin A, and urolithin B.Urolithins appear in the circulatory system almost exclusively as glucuronide,sulfateand methylated forms as a result of phase Il metabolism after absorption in the colonand passage through the liver.

Clinical claims and research

Some of the earliest research on urolithin A was performed on C. elegans worms, which experienced a 45 percent longer life span than worms not given the compound. Rodents given urolithin A experienced markedly improved muscular function and clearance of damaged mitochondria. Compared to a control group, these rodents showed a 57 to 65 percent increase in exercise capacity, 42 percent increase in running endurance, and a 9 percent increase in grip strength—all markers that correlate with longevity.In addition, researchers have exposed colon cancer stem cells to a mixture containing urolithin A and found it to be effective at inhibiting the number and size of colon cancer stem cells and also in inhibiting the activity of aldehyde dehydrogenase, a marker of resistance to chemotherapy. Urolithin A can also cross the blood-brain barrier to protect against neurotoxicity and amyloid plaque accumulation.

InChI:InChI=1/C13H8O4/c14-7-1-3-9-10-4-2-8(15)6-12(10)17-13(16)11(9)5-7/h1-6,14-15H

1143-70-0 Relevant articles

Urolithins, intestinal microbial metabolites of pomegranate ~ellagitannins, exhibit potent antioxidant activity in a cell-based assay

Dobroslawa, Bialonska,Kasimsetty, Sashi G.,Khan, Shabana I.,Daneel, Ferreira

, p. 10181 - 10186 (2009)

Many health benefits of pomegranate prod...

Urolithin C, a gut metabolite of ellagic acid, induces apoptosis in PC12 cells through a mitochondria-mediated pathway

Yin, Peipei,Zhang, Jianwei,Yan, Linlin,Yang, Lingguang,Sun, Liwei,Shi, Lingling,Ma, Chao,Liu, Yujun

, p. 17254 - 17263 (2017)

Urolithins (Uros), metabolites of ellagi...

Urolithin as a Converging Scaffold Linking Ellagic acid and Coumarin Analogues: Design of Potent Protein Kinase CK2 Inhibitors

Cozza, Giorgio,Gianoncelli, Alessandra,Bonvini, Paolo,Zorzi, Elisa,Pasquale, Riccardo,Rosolen, Angelo,Pinna, Lorenzo A.,Meggio, Flavio,Zagotto, Giuseppe,Moro, Stefano

, p. 2273 - 2286 (2011)

Casein kinase2 (CK2) is a ubiquitous, es...

Gut Microbiota conversion of dietary ellagic acid into bioactive phytoceutical urolithin a inhibits heme peroxidases

Saha, Piu,Yeoh, Beng San,Singh, Rajbir,Chandrasekar, Bhargavi,Vemula, Praveen Kumar,Haribabu, Bodduluri,Vijay-Kumar, Matam,Jala, Venkatakrishna R.

, (2016)

Numerous studies signify that diets rich...

Urolithin and reduced urolithin derivatives as potent inhibitors of tyrosinase and melanogenesis: Importance of the 4-substituted resorcinol moiety

Lee, Sanggwon,Choi, Heejeong,Park, Yujin,Jung, Hee Jin,Ullah, Sultan,Choi, Inkyu,Kang, Dongwan,Park, Chaeun,Ryu, Il Young,Jeong, Yeongmu,Hwang, Yeji,Hong, Sojeong,Chun, Pusoon,Moon, Hyung Ryong

, (2021/05/29)

We previously reported (E)-β-phenyl-α,β-...

Synthesis, Characterization, Molecular Docking, and Biological Activities of Some Natural and Synthetic Urolithin Analogs

Noshadi, Bahareh,Ercetin, Tugba,Luise, Chiara,Yuksel, Mine Yarim,Sippl, Wolfgang,Sahin, Mustafa Fethi,Gazi, Mustafa,Gulcan, Hayrettin Ozan

, (2020/07/24)

Urolithins (that is, hydroxy substituted...

Urolithins as immune response enhancers

-

Page/Page column 30-31, (2020/11/23)

Disclosed are compounds for use in raisi...

Synthetic method of urolithin A

-

, (2020/12/08)

The invention discloses a synthetic meth...

1143-70-0 Process route

docosahexaenoic acid
6217-54-5

docosahexaenoic acid

2',4'-dihydroxy-4-acetophenone
89-84-9

2',4'-dihydroxy-4-acetophenone

urolithin B
1139-83-9

urolithin B

2,4,6-trihydroxyacetophenone
480-66-0,67471-34-5

2,4,6-trihydroxyacetophenone

urolithin B
1143-70-0

urolithin B

o-hydroxyacetophenone
118-93-4,104809-67-8

o-hydroxyacetophenone

Conditions
Conditions Yield
all cis-5,8,11,14,17-eicosapentaenoic acid
10417-94-4

all cis-5,8,11,14,17-eicosapentaenoic acid

urolithin B
1139-83-9

urolithin B

urolithin B
1143-70-0

urolithin B

benzoic acid
65-85-0,8013-63-6

benzoic acid

Conditions
Conditions Yield
In methanol; at 25 ℃; for 168h; Product distribution / selectivity;
iron(II) sulfate; In methanol; at 25 ℃; for 168h; Product distribution / selectivity;

1143-70-0 Upstream products

  • 58380-11-3
    58380-11-3

    2-bromo-5-hydroxybenzoic acid

  • 108-46-3
    108-46-3

    recorcinol

  • 133730-29-7
    133730-29-7

    N,N-Diethyl-2',4,4'-trimethoxy-2-biphenylcarboxamide

  • 10034-85-2
    10034-85-2

    hydrogen iodide

1143-70-0 Downstream products

  • 713520-51-5
    713520-51-5

    3,8-di(t-butyldimethylsilyloxy)-6-phenoxydibenzo[b,d]pyran

  • 713520-69-5
    713520-69-5

    3,8-di(t-butyldimethylsilyloxy)-6-[4-[2-(1-pyrrolidino)ethoxy]-phenyl]dibenzo[b,d]pyran

  • 713520-58-2
    713520-58-2

    3,8-di(t-butyldimethylsilyloxy)-6-[4-[2-(1-piperidino)ethoxy]-phenyl]dibenzo[b,d]pyran

  • 165393-06-6
    165393-06-6

    urolithin C

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