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Calophyllum membranaceum

Calophyllum membranaceum

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Natural products/compounds from  Calophyllum membranaceum

  1. Cat.No. Product Name CAS Number COA
  2. BCN6283 Amentoflavone1617-53-4 Instructions
  3. BCN3617 Ammijin495-30-7 Instructions
  4. BCN2378 Nodakenin495-31-8 Instructions
  5. BCN5604 Nodakenetin495-32-9 Instructions

References

C-glycosides from the stems of Calophyllum membranaceum.[Pubmed: 29210296]


Three new C-glycosides, calophymembransides D-F (1-3), were isolated from the stems of Calophyllum membranaceum Gardn. et Champ.. The structures were assigned on the basis of spectroscopic data. RXRα transcriptional inhibition and α-glucosidase inhibition assays indicated that all the isolates were inactive.


RXRα transcriptional inhibitors from the stems of Calophyllum membranaceum.[Pubmed: 26569353]


Bioassay-guided fractionation of the 60% ethanol extract of the stems of Calophyllum membranaceum using the RXRα transcription activation assay led to the isolation of two new chromanones, calopolyanic acid methyl ester (1) and isopinetoric acid methyl ester (2), two new xanthones, calophylixanthones A-B (3-4), and one new C-glycoside, calophymembranside C (5), along with 13 known compounds. Their structures were elucidated on the basis of extensive spectroscopic data. Compounds 5, 11 and 18 showed transcriptional inhibitory activity of RXRα with 50% inhibitory concentration (IC50) values of 29.95 ± 1.08, 31.06 ± 9.02, and 25.88 ± 1.62 μM, respectively.


2-Hydr-oxy-1-methoxyxanthen-9-one monohydrate.[Pubmed: 21578390]


In the title compound, C(14)H(10)O(4)·H(2)O, isolated from the roots of Calophyllum membranaceum, the xanthene ring system is almost planar (r.m.s. deviation = 0.008 Å). In the crystal structure, inter-molecular O-H⋯O and O-H⋯(O,O) hydrogen bonds connect the mol-ecules.


Selective cyclooxygenase-2 inhibitors from Calophyllum membranaceum.[Pubmed: 16252917]


Chemical investigation of the anti-inflammatory Chinese folk medicine Calophyllum membranaceum has resulted in the isolation and characterization of three new xanthones (1-3), one new biphenyl C-glycoside (4), and one new phenylethanoid glycoside (5) along with 17 known compounds. Their structures were characterized on the basis of spectroscopic and chemical methods. Two xanthones, 2,6-dihydroxy-1,7-dimethoxyxanthone (1) and 3,4-dihydroxyxanthone, were found to exhibit selective inhibitory activity against cyclooxygenase-2 (IC(50)=2.99 and 1.80 microM) in vitro.