Catalogue Number
BN-O0992
Analysis Method
HPLC,NMR,MS
Specification
98%(HPLC)
Storage
-20℃
Molecular Weight
242.27
Appearance
Powder
Botanical Source
This product is isolated and purified from the herbs of Bletilla striata
Structure Type
Phenols
Category
Standards;Natural Pytochemical;API
SMILES
COC1=CC(=CC2=C1C3=C(CC2)C=C(C=C3)O)O
Synonyms
coelin/9,10-dihydro-4-methoxyphenanthrene-2,7-diol/4-methoxy-9,10-dihydrophenanthrene-2,7-diol/2,7-dihydroxy-4-methoxy-9,10-dihydrophenanthrene
IUPAC Name
4-methoxy-9,10-dihydrophenanthrene-2,7-diol
Density
Solubility
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Flash Point
Boiling Point
Melting Point
InChl
InChI=1S/C15H14O3/c1-18-14-8-12(17)7-10-3-2-9-6-11(16)4-5-13(9)15(10)14/h4-8,16-17H,2-3H2,1H3
InChl Key
OPPGAHUCKDKQJR-UHFFFAOYSA-N
WGK Germany
RID/ADR
HS Code Reference
2933990000
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
provides coniferyl ferulate(CAS#:82344-82-9) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate
No Technical Documents Available For This Product.
32074105
Bletilla striata is an endangered traditional Chinese medicinal plant with multiple uses and a slow regeneration rate of its germplasm resources. To evaluate the callus growth kinetics and accumulation of secondary metabolites (SMs), a callus suspension culture was proven to be a valuable approach for acquiring high yields of medicinal compounds. An effective callus suspension culture for obtaining B. striata callus growth and its SMs was achieved with the in vitro induction of calluses from B. striata seeds. The callus growth kinetics and accumulation of SMs were analyzed using a mathematical model. The resulting callus growth kinetic model revealed that the growth curves of B. striata suspension-cultured calluses were sigmoidal, indicating changes in the growth of the suspension-cultured calluses. Improved Murashige and Skoog callus growth medium was the most favorable medium for B. striata callus formation, with the highest callus growth occurring during the stationary phase of the cultivation period. Callus growth acceleration started after 7 days and thereafter gradually decreased until day 24 of the cultivation period and reached its highest at day 36 period in both the dry weight and fresh weight analyses. The coelonin concentration peaked during the exponential growth stage and decreased afterward during the stationary stage of the callus suspension culture. The maximum content of coelonin (approximately 0.3323 mg/g callus dry weight) was observed on the 18th day of the cultivation cycle, while dactylorhin A and militarine reached the highest concentrations at day 24, and p-hydroxybenzyl alcohol at day 39. This investigation also laid a foundation for a multimathematical model to better describe the accumulation variation of SMs. The production of SMs showed great specificity during callus growth and development. This research provided a well-organized way to increase the accumulation and production of SMs during the scaled-up biosynthesis of calluses in B. striata callus suspension cultures.
Callus growth kinetics and accumulation of secondary metabolites of Bletilla striata Rchb.f. using a callus suspension culture
Yinchi Pan, Writing - original draft,#1,2 Lin Li, Project administration, Supervision,#1 Shiji Xiao, Data curation, Formal analysis,3 Zhongjie Chen, Writing - original draft,1 Surendra Sarsaiya, Writing - review & editing,4 Shebo Zhang, Investigation,1 Yanni ShangGuan, Data curation,1 Houbo Liu, Methodology,1 and Delin Xu, Conceptualization, Funding acquisition, Project administration, Supervision, Writing - original draft, Writing - review & editing1,*
2020;
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