Cytotoxic activity and phytochemical composition of Stereospermum binhchauensis V.S. Dang leaves

References

• Asthana J, Yadav AK, Pant A, Pandey S, Gupta MM, Pandey R. 2015. Specioside ameliorates oxidative stress and promotes longevity in Caenorhabditis elegans. Comp Biochem Physiol Part C. 169:25–34.
   PubMed Web of Science ®Google Scholar
• Callmander MW, Phillipson PB, Schatz GE. 2012. Two new species Stereospermum (Bignoniaceae) from Madagascar. Novon. 22(2):141–147.
   Web of Science ®Google Scholar
• Dang VS. 2015. A new species of Stereospermum (Bignoniaceae) from Southern Vietnam. Acta Phytotax Geobot. 66:91–94.
   Web of Science ®Google Scholar
• Erlinda AJ, John AR, Consolation YR. 1997. Bioactive furanocoumarin derivatives from Ficus pumila (Morraceace). Philippine J Sci. :143–151.
   Google Scholar
• Ghogomu-Tih R, Bodo B, Nyasse B, Sondengam BL. 1985. Isolation and identification of (−)-olivil and (+)-cycloolivil from Stereospermum kunthianum. Planta Med. 51(5):464.
   PubMed Web of Science ®Google Scholar
• Ghogomu-Tih R, Nyasse B, Tsamo E, Sondengam BL. 1986. Chemical constituents of the stem heart wood of Stereospermum kunthianum. Planta Med. 52(4):342.
   Google Scholar
• Haque MR, Rahman KM, Iskander MN, Hasan CM, Rashid MA. 2006. Stereochenols A and B, two quinones from Stereospermum chelonoides. Phytochemistry. 67(24):2663–2665.
   PubMed Web of Science ®Google Scholar
• Kanchanapoom T, Noiarsa P, Otsuka H, Ruchirawat S. 2006. Lignan, phenolic and iridoid glycosides from Stereospermum cylindricum. Phytochemistry. 67(5):516–520.
   PubMed Web of Science ®Google Scholar
• Kingsley RB, Mishra M, Brindha P, Subramoniam A. 2013. Anti-diabetic activity of active fractions of Stereospermum tetragonum DC and isolation of active principles. J Young Pharm. 5:7–12.
   PubMedGoogle Scholar
• Kumar US, Aparna P, Rao RJ, Rao TP, Rao JM. 2003. 1-methylanthraquinones and their biogenetic precursors from Stereospermum personatum. Phytochemistry. 63(8):925–929.
   PubMed Web of Science ®Google Scholar
• Kumar US, Tiwari AK, Reddy SV, Aparna P, Rao RJ, Ali AZ, Rao JM. 2005. Free radical scavenging and xanthine oxidase inhibitory constituents from Stereospermu personatum. J Nat Prod. 68(11):1615–1621.
   PubMed Web of Science ®Google Scholar
• Kurkin VA. 2015. Saffloroside, A new flavonoid from flowers of Carthamus tinctorius L. J Pharm Phytochemistry. 4(1):29–31.
   Google Scholar
• Lee S, Choi MJ, Choi JM, Lee S, Kim HY, Cho EJ. 2012. Flavonoids from Taraxacum coreanum protect from radical-induced oxidative damage. J Med Plants Res. 6(40):5377–5384.
   Google Scholar
• Lenta BN, Weniger B, Antheaume C, Noungoue DT, Ngouela S, Assob JCN, Vonthron-Sénécheau C, Fokou PA, Devkota KP, Tsamo E, et al. 2007. Anthraquinones from the stem bark of Stereospermum zenkeri with antimicrobial activity. Phytochemistry. 68(11):1595–1599.
   PubMed Web of Science ®Google Scholar
• Malikov VM, Yuldashev MP. 2002. Phenolic compounds of plants of the Scutellaria L. genus. Chem Nat Comp. 38(4):358–406.
   Web of Science ®Google Scholar
• Ngo TN, Phan NM, Bui TD, Dang VS, Tran CL, Mai DT, Nguyen TP. 2017. Cytotoxic cycloartane triterpenoids from the leaves of Markhamia stipulata var. canaense. Phytochem Lett. 22:251–254.
   Web of Science ®Google Scholar
• Ngo TN, Vo CT, Pham NKT, Phan NM, Bui TD, Ngo QL, Dang VS, Tran CL, Mai DT, Nguyen TP. 2018. Markhacanasin C, cycloartane triterpenoid from the leaves of Markhamia stipulata var. canaense V.S. Dang. Nat Prod Res. 1–6.
   PubMed Web of Science ®Google Scholar
• Ngo TN, Nguyen NDP, Nguyen NTL, Pham NKT, Phan NM, Bui TD, Dang VS, Tran CL, Mai DT, Nguyen TP. 2019. Markhasphingolipid A, new phytosphingolipid from the leaves of Markhamia stipulata var. canaense V.S. Dang. Nat Prod Res. 1–6.
   Web of Science ®Google Scholar
• Nguyen TP, Le TVH, Mai DT, Dung LT, Phan NM, Bui D. 2015. Two new oleanane-type triterpene saponins from the leaves of Schefflera sessiliflora De P.V. Phytochem Lett. 11:102–105.
   Web of Science ®Google Scholar
• Nguyen TP, Le TD, Phan NM, Bui TD, Mai DT. 2016. Triterpene saponins with α-glucosidase inhibition and cytotoxic activity from the leaves of Schefflera sessiliflora. J Asian Nat Prod Res. 18(6):542–549.
   PubMed Web of Science ®Google Scholar
• Nguyen TP, Tran TTV, Mai DT, Le TD, Phan NM, Bui TD. 2015. New C20-gibberellin diterpene from the leaves of Schefflera sessiliflora De P. V. Nat Prod Res. 29(15):1432–1436.
   PubMed Web of Science ®Google Scholar
• Onegi B, Kraft C, Kohler I, Freund M, Jenett-Siems K, Siems K, Beyer G, Melzig MF, Bienzle U, Eich E. 2002. Antiplasmodial activity of naphthoquinones and one anthraquinone from Stereospermum kunthianum. Phytochemistry. 60(1):39–44.
   PubMed Web of Science ®Google Scholar
• Pendse R, Rao AVR, Venkataraman K. 1973. 5,7-dihydroxychromone from Arachis hypogoea shells. Phytochemistry. 22:2033–2034.
   Web of Science ®Google Scholar
• Ragab EA, Hosny M, Kadry HA, Ammar HA. 2010. Flavanone glycosides from Gleditsia caspia. J Nat Prod. 3:35–46.
   Web of Science ®Google Scholar
• Ramsay KST, Wafo P, Ali Z, Khan A, Oluyemisi OO, Marasini BP, Khan IA, Bonaventure NT, Choudhary MI. Atta-Ur-Rahman. 2012. Chemical constituents of Stereospermum acuminatissimum and their urease and α-chymotrypsin inhibitions. Fitoterapia. 83:204–208.
   PubMed Web of Science ®Google Scholar
• Rao KV, McBride TJ, Oleson JJ. 1968. Recognition and evaluation of lapachol as an antitumor agent. Cancer Res. 28:1952–1954.
   Web of Science ®Google Scholar
• Venkata C, Prakash S, Prakash I. 2012. Isolation and structural characterization of lupane triterpenes from Polypodium vulgare. Res J Pharm Sci. 1(1):23–27.
   Google Scholar
• Wahab Sab BA, Jacob J, Manjunath GG, Singh VK, Mundkinajeedu D, Shankarappa S. 2015. Cycloolivil, a lignan from the roots of Stereospermum suaveolens. Pharmacognosy Res. 7(1):45–48.
   PubMed Web of Science ®Google Scholar
• Zuhal G, Hilal O, Ayse K, Cavit K, Lomur D. 2009. Secondary metabolites from Nepeta heliotropifolia. Turk J Chem. 33:667–675.
   Web of Science ®Google Scholar