1139-83-9
- Product Name：Urolithin B
- Molecular Formula：C13H8 O3
- Purity：99%
- Molecular Weight：212.205
Product Details
Melting Point:247 °C
Purity:99%
Manufacturer Supply Best Quality Urolithin B 1139-83-9 with Efficient Transportation
- Molecular Formula:C13H8 O3
- Molecular Weight:212.205
- Vapor Pressure:4.34E-08mmHg at 25°C
- Melting Point:247 °C
- Boiling Point:432.6°C at 760 mmHg
- PKA:9.03±0.20(Predicted)
- Flash Point:196.6°C
- PSA：50.44000
- Density:1.395g/cm3
- LogP:2.65180
3-HYDROXY-6H-DIBENZO[B,D]PYRAN-6-ONE(Cas 1139-83-9) Usage
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Biochem/physiol Actions |
Urolithin B is a natural product with antiproliferative and antioxidant activity. Urolithin B is formed by metabolism from polyphenols found in some nuts and fruits, particularly pomegranates. Urolithin B has been shown to cross the blood brain barrier, and may have neuroprotective effects against Alzheimer′s Disease. |
| Uses | Urolithin B (UB) is a natural product derived from ellagitannins, a class of antioxidant polyphenols, and a metabolite of gut microbiota. It has many biological activities, including: Anti-inflammatory, Cardioprotective, Metabolic and Skeletal muscle. |
| Manufacturer | Xi'an Lyna Bio-Tech Co., Ltd. is a leading plant extracts and biomedical health raw materials manufacturer, located in Chang'an District, Xi'an, Shaanxi Province, China. It is a modern high-tech company dedicated to the biomedical health industry, born under the background of the attention to health for all. |
InChI:InChI=1/C13H8O3/c14-8-5-6-10-9-3-1-2-4-11(9)13(15)16-12(10)7-8/h1-7,14H
1139-83-9 Relevant articles
Design, synthesis, and biological evaluation of novel 6h-benzo[c]chromen-6-one derivatives as potential phosphodiesterase ii inhibitors
Tang, Long,Jiang, Jianchun,Song, Guoqiang,Wang, Yajing,Zhuang, Ziheng,Tan, Ying,Xia, Yan,Huang, Xianfeng,Feng, Xiaoqing
, (2021/05/29)
Urolithins (hydroxylated 6H-benzo[c]chro...
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-...
Urolithin compound, preparation method, pharmaceutical composition and application
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Paragraph 0066-0075, (2021/09/04)
The invention belongs to the field of me...
1139-83-9 Process route
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- 6217-54-5
docosahexaenoic acid
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- 89-84-9
2',4'-dihydroxy-4-acetophenone
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- 1139-83-9
urolithin B
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- 480-66-0,67471-34-5
2,4,6-trihydroxyacetophenone
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- 1143-70-0
urolithin B
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- 118-93-4,104809-67-8
o-hydroxyacetophenone
| Conditions | Yield |
|---|---|
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|
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- 10417-94-4
all cis-5,8,11,14,17-eicosapentaenoic acid
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- 1139-83-9
urolithin B
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- 1143-70-0
urolithin B
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- 65-85-0,8013-63-6
benzoic acid
| Conditions | Yield |
|---|---|
|
In methanol; at 25 ℃; for 168h; Product distribution / selectivity;
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|
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iron(II) sulfate; In methanol; at 25 ℃; for 168h; Product distribution / selectivity;
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1139-83-9 Upstream products
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3722-44-9
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recorcinol
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1139-83-9 Downstream products
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35224-33-0
3-acetoxy-benzo[c]chromen-6-one
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1143-62-0
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76244-81-0
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76244-78-5
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