Venuloxanthone, a new pyranoxanthone from the stem bark of Calophyllum venulosum
A new pyranoxanthone, venuloxanthone (1), was isolated from the stem bark of Calophyllum venulosum, together with three other xanthones, tovopyrifolin C (2), ananixanthone (3) and caloxanthone I (4), along with two common triterpenes, friedelin (5) and lupeol (6). The structures of these compounds w...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Taylor and Francis Ltd.
2015
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| Subjects: | |
| Online Access: | View Fulltext in Publisher View in Scopus |
| LEADER | 02722nam a2200709Ia 4500 | ||
|---|---|---|---|
| 001 | 10.1080-10286020.2015.1047353 | ||
| 008 | 220112s2015 CNT 000 0 und d | ||
| 020 | |a 10286020 (ISSN) | ||
| 245 | 1 | 0 | |a Venuloxanthone, a new pyranoxanthone from the stem bark of Calophyllum venulosum |
| 260 | 0 | |b Taylor and Francis Ltd. |c 2015 | |
| 856 | |z View Fulltext in Publisher |u https://doi.org/10.1080/10286020.2015.1047353 | ||
| 856 | |z View in Scopus |u https://www.scopus.com/inward/record.uri?eid=2-s2.0-84947032886&doi=10.1080%2f10286020.2015.1047353&partnerID=40&md5=b74d0c840fd4e85c5c8f307f5ca31623 | ||
| 520 | 3 | |a A new pyranoxanthone, venuloxanthone (1), was isolated from the stem bark of Calophyllum venulosum, together with three other xanthones, tovopyrifolin C (2), ananixanthone (3) and caloxanthone I (4), along with two common triterpenes, friedelin (5) and lupeol (6). The structures of these compounds were identified using several spectroscopic analyses which are NMR, GCMS and FTIR experiments. © 2015 Taylor and Francis. | |
| 650 | 0 | 4 | |a ananixanthone |
| 650 | 0 | 4 | |a Article |
| 650 | 0 | 4 | |a bark |
| 650 | 0 | 4 | |a Calophyllum |
| 650 | 0 | 4 | |a Calophyllum venulosum |
| 650 | 0 | 4 | |a Calophyllum venulosum extract |
| 650 | 0 | 4 | |a caloxanthone I |
| 650 | 0 | 4 | |a carbon nuclear magnetic resonance |
| 650 | 0 | 4 | |a carbonyl derivative |
| 650 | 0 | 4 | |a chemical structure |
| 650 | 0 | 4 | |a chemistry |
| 650 | 0 | 4 | |a Clusiaceae |
| 650 | 0 | 4 | |a crystal structure |
| 650 | 0 | 4 | |a drug formulation |
| 650 | 0 | 4 | |a drug isolation |
| 650 | 0 | 4 | |a drug structure |
| 650 | 0 | 4 | |a Fourier transform infrared photoacoustic spectroscopy |
| 650 | 0 | 4 | |a friedelin |
| 650 | 0 | 4 | |a heteronuclear multiple bond correlation |
| 650 | 0 | 4 | |a hydroxyl group |
| 650 | 0 | 4 | |a isolation and purification |
| 650 | 0 | 4 | |a lupeol |
| 650 | 0 | 4 | |a melting point |
| 650 | 0 | 4 | |a Molecular Structure |
| 650 | 0 | 4 | |a molecular weight |
| 650 | 0 | 4 | |a nuclear magnetic resonance |
| 650 | 0 | 4 | |a Nuclear Magnetic Resonance, Biomolecular |
| 650 | 0 | 4 | |a Plant Bark |
| 650 | 0 | 4 | |a plant extract |
| 650 | 0 | 4 | |a powder |
| 650 | 0 | 4 | |a proton nuclear magnetic resonance |
| 650 | 0 | 4 | |a pyran derivative |
| 650 | 0 | 4 | |a pyranoxanthone |
| 650 | 0 | 4 | |a Pyrans |
| 650 | 0 | 4 | |a radiation absorption |
| 650 | 0 | 4 | |a tovopyrifolin C |
| 650 | 0 | 4 | |a triterpene |
| 650 | 0 | 4 | |a Triterpenes |
| 650 | 0 | 4 | |a unclassified drug |
| 650 | 0 | 4 | |a venuloxanthone |
| 650 | 0 | 4 | |a xanthone derivative |
| 650 | 0 | 4 | |a Xanthones |
| 700 | 1 | 0 | |a Awang, K. |e author |
| 700 | 1 | 0 | |a Bin Daud, S. |e author |
| 700 | 1 | 0 | |a Bin Ismail, A.A.F. |e author |
| 700 | 1 | 0 | |a Ee, G.C.L. |e author |
| 700 | 1 | 0 | |a Hashim, N.M. |e author |
| 700 | 1 | 0 | |a Teh, S.S. |e author |
| 773 | |t Journal of Asian Natural Products Research | ||