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Natural Products from Camellia sinensis

Natural Products Isolated from Camellia sinensis

BioCrick provides high-purity natural products and bioactive compounds isolated and purified from natural sources for scientific research.

  • Natural product compounds selected from diverse chemical and biological sources.
  • Broad structural diversity and coverage of biological activities.
  • Product activity information can be supported by published literature, patents and research reports.
  • Natural products can be selected according to source, target, activity and disease research interests.
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Natural products isolated from Camellia sinensis
Natural products isolated from Camellia sinensis

Natural Products from Camellia sinensis

21 natural product s associated with Camellia sinensis

Natural products and bioactive compounds from Camellia sinensis
Catalog No. Product Name CAS Number COA
BCN5330 (-)-Catechin gallate(CG)
(-)-Catechin gallate(CG) chemical structure
130405-40-2 COA
BCN6327 (-)-Epicatechin gallate
(-)-Epicatechin gallate chemical structure
1257-08-5 COA
BCN6326 (-)-Epigallocatechin gallate
(-)-Epigallocatechin gallate chemical structure
989-51-5 COA
BCN4519 (-)-Epigallocatechin(EGC)
(-)-Epigallocatechin(EGC) chemical structure
970-74-1 COA
BCN1336 (-)-Epigallocatechin-3-(3''-O-methyl) gallate
(-)-Epigallocatechin-3-(3''-O-methyl) gallate chemical structure
83104-87-4 COA
BCN6328 (-)-Gallocatechin gallate
(-)-Gallocatechin gallate chemical structure
4233-96-9 COA
BCN8136 Alpha-Terpineol
Alpha-Terpineol chemical structure
10482-56-1 COA
BCN5807 Caffeine
Caffeine chemical structure
58-08-2 COA
BCN3871 Camelliaside A
Camelliaside A chemical structure
135095-52-2 COA
BCN3872 Camelliaside B
Camelliaside B chemical structure
131573-90-5 COA
BCN5416 Cyasterone
Cyasterone chemical structure
17086-76-9 COA
BCN5597 Epicatechin
Epicatechin chemical structure
490-46-0 COA
BCN1668 Gallic acid
Gallic acid chemical structure
149-91-7 COA
BCN6151 Lutein
Lutein chemical structure
127-40-2 COA
BCN7159 Oleic acid
Oleic acid chemical structure
112-80-1 COA
BCN5419 Theaflavin
Theaflavin chemical structure
4670-05-7 COA
BCN5920 Theaflavin 3,3'-di-O-gallate
Theaflavin 3,3'-di-O-gallate chemical structure
30462-35-2 COA
BCN5421 Theaflavin-3'-gallate
Theaflavin-3'-gallate chemical structure
28543-07-9 COA
BCN2316 Theaflavin-3-gallate
Theaflavin-3-gallate chemical structure
30462-34-1 COA
BCN1227 Theobromine
Theobromine chemical structure
83-67-0 COA
BCN1258 Theophylline
Theophylline chemical structure
58-55-9 COA

References

Gene co-expression network analysis reveals coordinated regulation of three characteristic secondary biosynthetic pathways in tea plant (Camellia sinensis).[Pubmed: 30111282]


The leaves of tea plants (Camellia sinensis) are used to produce tea, which is one of the most popular beverages consumed worldwide. The nutritional value and health benefits of tea are mainly related to three abundant characteristic metabolites; catechins, theanine and caffeine. Weighted gene co-expression network analysis (WGCNA) is a powerful system for investigating correlations between genes, identifying modules among highly correlated genes, and relating modules to phenotypic traits based on gene expression profiling. Currently, relatively little is known about the regulatory mechanisms and correlations between these three secondary metabolic pathways at the omics level in tea.


Epigallocatechin-3-gallate prevents disruption of connective tissue in periodontium and salivary glands of rats during systemic inflammation.[Pubmed: 30099426]


Introduction: The connective tissue remodeling is essential for periodontal and salivary glands (SG) pathology. Recently there has been demonstrated the number of pharmacological effects of green tea (Camellia sinensis) such as antioxidant, anti-inflammatory, anti-aging, antibacterial, antiviral and DNA-protective effects, associated with the presence of epigallocatechin-3-gallate (EGCG) as an inducer of the Keap1 / Nrf2 / antioxidant response element signaling pathway. However, the EGCG effects on the components of soft connective tissues of periodontium and SG are still unclear. The aim: To investigate the effect of EGCG on markers of disruption of periodontal and submandibular SG connective tissues in rats during the conditions of experimental systemic inflammation (SI).


Genome-wide identification and characterization of ALTERNATIVE OXIDASE genes and their response under abiotic stresses in Camellia sinensis (L.) O. Kuntze.[Pubmed: 30097722]


Four typical ALTERNATIVE OXIDASE genes have been identified in tea plants, and their sequence features and gene expression profiles have provided useful information for further studies on function and regulation. Alternative oxidase (AOX) is a terminal oxidase located in the respiratory electron transport chain. AOX catalyzes the oxidation of quinol and the reduction of oxygen into water. In this study, a genome-wide search and subsequent DNA cloning were performed to identify and characterize AOX genes in tea plant (Camellia sinensis (L.) O. Kuntze cv. Longjing43). Our results showed that tea plant possesses four AOX genes, i.e., CsAOX1a, CsAOX1d, CsAOX2a and CsAOX2b. Gene structure and protein sequence analyses revealed that all CsAOXs share a four-exon/three-intron structure with highly conserved regions and amino acid residues, which are necessary for AOX secondary structures, catalytic activities and post-translational regulations. All CsAOX were shown to localize in mitochondria using the green fluorescent protein (GFP)-targeting assay. Both CsAOX1a and CsAOX1d were induced by cold, salt and drought stresses, and with different expression patterns in young and mature leaves. Reactive oxygen species (ROS) accumulated strongly after 72 and 96 h cold treatments in both young and mature leaves, while the polyphenol and total catechin decreased significantly only in mature leaves. In comparison to AtAOX1a in Arabidopsis thaliana, CsAOX1a lost almost all of the stress-responsive cis-acting regulatory elements in its promoter region (1500 bp upstream), but possesses a flavonoid biosynthesis-related MBSII cis-acting regulatory element. These results suggest a link between CsAOX1a function and the metabolism of some secondary metabolites in tea plant. Our studies provide a basis for the further elucidation of the biological function and regulation of the AOX pathway in tea plants.


Comparison of the Metabolic Behaviors of Six Systemic Insecticides in a Newly Established Cell Suspension Culture Derived from Tea ( Camellia sinensis L.) Leaves.[Pubmed: 30074784]


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