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Macranthoidin A

CAS No.:140360-29-8

Macranthoidin A
Catalogue No.: BP0908
Formula: C59H96O27
Mol Weight: 1237.39
Botanical Source: Lonicerae flos
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Macranthoidin A

CAS No.:140360-29-8

Macranthoidin A
Catalogue No.: BP0908
Formula: C59H96O27
Mol Weight: 1237.39
Botanical Source: Lonicerae flos
Contacts
+86-28-82633860  +86-18080483897
 
Email: sales@biopurify.com biopurify@gmail.com
Over 15 years of industry experience in phytochemicals from R&D(reference substances) to Industrialization, please feel free to contact us!

Synonym name: Giganteaside J; Giganteoside J
Catalogue No.: BP0908
Cas No.: 140360-29-8
Formula: C59H96O27
Mol Weight: 1237.39
Botanical Source: Dipsacus asper, Aralia elata, Cephalaria gigantea and Lonicera macranthoides

Purity: 95%~99%
Analysis Method: HPLC-DAD or/and HPLC-ELSD
Identification Method: Mass, NMR
Packing: Brown vial or HDPE plastic bottle
Can be supplied from milligrams to grams.

For Reference Standard and R&D, Not for Human Use Directly.
Inquire for bulk scale.

 

 

Description:

Macranthoidin A, found in the herbs of Lonicera japonica Thunb., has anti-inflammation activity.

 

References:

Journal of Chromatography B Volume 877, Issue 3, 15 January 2009, Pages 159–165    

Liquid chromatography–mass spectrometry analysis of macranthoidin B, macranthoidin A, dipsacoside B, and macranthoside B in rat plasma for the pharmacokinetic investigation   

METHODS AND RESULTS:

A liquid chromatography-electrospray ionization–mass spectrometry method has been developed and validated for identification and quantification of four major bioactive saponins in rat plasma after oral administration of extraction of saponins from Flos Lonicerae, i.e., macranthoidin B, Macranthoidin A, dipsacoside B, and macranthoside B. Plasma samples were extracted with solid-phase extraction, separated on a Shim-pack CLC-ODS column and detected by MS in negative selective ion monitoring mode. Calibration curves offered linear ranges of two orders of magnitude with r2 > 0.999. The method showed the low limit quantification of 7.72, 6.06, 7.16, and 1.43 ng/mL for macranthoidin B, Macranthoidin A, dipsacoside B, and macranthoside B, respectively. The inter- and intra-CV precision (R.S.D.) were all within 10% and accuracy (% bias) ranged from −10 to 10%. The overall recovery was more than 70%. 

CONCLUSIONS:

This developed method was subsequently successfully applied to pharmacokinetic profiles of the four saponins in rats. After oral administration of extraction of saponins in rats, the concentration–time course was found to be the double peaks of curve. 

 

HPLC of Macranthoidin A

  

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