ABSTRACT
An online SPE-HPLC method for simultaneous determination of cordycepin (3'-deoxyadenosine) and 2'-deoxyadenosine in Cordyceps genus (C. sinensis,C. militaris,Hirsutella sinensis and C. sobolifera) was developed. The samples were enriched on a ZORBAX SB-AQ (4.6 mm×12.5 mm,5 μm) column with isocratic elution by 9% methanol solution. The separation of analytes was performed on a ZORBAX SB-AQ (4.6 mm×150 mm,5 μm) column with gradient elution by 0.1% formic acid solution and methanol (91∶9). The flow rate was 1.0 mL•min⁻¹. Column temperature was 40 ℃ and detection wavelength was 260 nm. This method has been applied for analysis of different Cordyceps genus. The 2'-deoxyadenosine was detected in C. sinensis,Hirsutella sinensis and C. sobolifera. The cordycepin was detected in C. militaris. In summary,the cordycepin chromatographic peak from C. sinensis in some past reports may be the 2'-deoxyadenosine chromatographic peak or the mixture peak of 2'-deoxyadenosine and cordycepin in which 2'-deoxyadenosine content was higher than cordycepin. The developed method is suitable for analysis of cordycepin and 2'-deoxyadenosine in Cordyceps genus.
ABSTRACT
Objective: To study the chemical constituents from flowers of Carthamus tinctorius. Methods: The chemical constituents were isolated and purified by multiple chromatographic methods. Their structures were identified on the basis of spectral data and physicochemical properties. Results: Ten compounds were identified as l-phenylalanine (1), thymine (2), inosine (3), guanosine hydrate (4), thymidine (5), 2'-O-methyluridine (6), banegasine (7), adenosine (8), 2'-deoxyadenosine (9), and 5'-deoxy-5'- methylamino-adenosine (10). Conclusion: Compound 3, 5, 6, 9, and 10 are isolated from this plant for the first time.