Natural Products from Callerya speciosa

Natural Products Isolated from Callerya speciosa

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.
  • Compounds should be stored according to the product specifications after receipt.
Natural products isolated from Callerya speciosa
Natural products isolated from Callerya speciosa

Natural Products from Callerya speciosa

13 natural product s associated with Callerya speciosa

Natural products and bioactive compounds from Callerya speciosa
Catalog No. Product Name CAS Number COA
BCN8346 6- Methoxydihydrosanguinarine
6- Methoxydihydrosanguinarine chemical structure
151890-26-5 COA
BCN2200 DL-alpha-Tocopherol
DL-alpha-Tocopherol chemical structure
59-02-9 COA
BCN1061 Formononetin
Formononetin chemical structure
485-72-3 COA
BCN5794 Gomisin A
Gomisin A chemical structure
58546-54-6 COA
BCN2775 Hypaphorine
Hypaphorine chemical structure
487-58-1 COA
BCN6332 Licochalcone A
Licochalcone A chemical structure
58749-22-7 COA
BCN5946 Liquiritigenin
Liquiritigenin chemical structure
578-86-9 COA
BCN1236 Maackiain
Maackiain chemical structure
19908-48-6 COA
BCN2324 Nardosinone
Nardosinone chemical structure
23720-80-1 COA
BCN4219 Psoralen
Psoralen chemical structure
66-97-7 COA
BCN1274 Shionone
Shionone chemical structure
10376-48-4 COA
BCN4376 Stigmasterol
Stigmasterol chemical structure
83-48-7 COA
BCN1019 Tectorigenin
Tectorigenin chemical structure
548-77-6 COA

References

Cell shape can be uncoupled from formononetin induction in a novel cell line from Callerya speciosa.[Pubmed: 29354881]


It is the first time that formononetin produced by cell culture and its accumulation was shown to be triggered by specific stress signalling linked jasmonate pathway. Callerya speciosa, an endangered traditional Chinese medicine plant, is intensively used in traditional folk medicine. To develop sustainable alternatives for the overexploitation of natural resources, a suspension cell line was created from C. speciosa. Ingredients of C. speciosa, for instance the isoflavone formononetin, are formed during a peculiar swelling response of the root, which is considered as a quality trait for commercial application. A cell strain with elongated cells was obtained by using synthetic cytokinin 6-benzylaminopurine (6-BA) and synthetic auxin picloram. Both, picloram and 6-BA, promote cell division, whereas picloram was shown to be crucial for the maintenance of axial cell expansion. We addressed the question, whether the loss of axiality observed in the maturating root is necessary and sufficient for the accumulation of formononetin. While we were able to mimic a loss of axiality for cell expansion, either by specific combinations of 6-BA and picloram, or by treatment with the anti-microtubular compound oryzalin, formononetin was not detectable. However, formononetin could be induced by the stress hormone methyl jasmonate (MeJA), as well as by the bacterial elicitor flagellin peptide (flg22), but not by a necrosis inducing protein. Combined the fact that none of these treatments induced the loss of axiality, we conclude that formononetin accumulates in response to basal defence and unrelated with cell swelling.


Transcriptome Analysis of Storage Roots and Fibrous Roots of the Traditional Medicinal Herb Callerya speciosa (Champ.) ScHot.[Pubmed: 27486800]


Callerya speciosa (Champ.) ScHot is a woody perennial plant in Fabaceae, the roots of which are used medicinally. The storage roots of C. speciosa are derived from fibrous roots, but not all fibrous roots can develop into storage roots. To detect key genes involved in storage roots formation, we performed Illumina sequencing of the C. speciosa storage roots and fibrous roots. De novo assembly resulted in 161,926 unigenes, which were subsequently annotated by BLAST, GO and KEGG analyses. After expression profiling, 4538 differentially expressed genes were identified. The KEGG pathway enrichment analysis revealed changes in the biosynthesis of cytokinin, phenylpropanoid, starch, sucrose, flavone and other secondary metabolites. Transcription factor-related differentially expressed genes (DEGs) were also identified, including such gene families as GRAS, COL, MIKC, ERF, LBD, and NAC. The DEGs related to light signaling, starch, sugar, photohormones and cell wall-loosening might be involved in the formation of storage roots. This study provides the first transcriptome profiling of C. speciosa roots, data that will facilitate future research of root development and metabolites with medicinal value as well as the breeding of C. speciosa.