References
- Celoy RM , VanEtten HD . 2014. (+)-Pisatin biosynthesis: from (-) enantiomeric intermediates via an achiral 7,2′-dihydroxy-4′,5′-methylenedioxyisoflav-3-ene. Phytochemistry. 98:120–127.10.1016/j.phytochem.2013.10.017
- Chamberlain DF . 1970. Melilotus L. In: Davis PH , editor. Flora of Turkey and The East Aegean Islands. Edinburgh: University of Edinburgh; p. 448–452.
- EMEA . 2008. Committee on herbal medicinal products (HMPC) Melilotus officinalis (L) Lam, herba. London (UK).
- Ghareeb MA , Saad AM , Abdou AM , Refahy LAG , Ahmed WS . 2016. A new kaempferol glycoside with antioxidant activity from Chenopodium ambrosioides growing in Egypt. Orient J Chem. 32:3053–3061.10.13005/ojc
- Hamid A , Raina AK . 2014. Ethnobotanical uses of plants in and around Kanji wildlife sanctuary, North West Himalaya. Int J Sci Res. 3:538–545.
- Hyun SK , Jung HA , Min BS , Jung JH , Choi JS . 2010. Isolation of phenolics, nucleosides, saccharides and an alkaloid from the root of Aralia cordata . Nat Prod Sci. 16:20–25.
- Kang SS , Lim CH , Lee SY . 1987. Soyasapogenols B and E from Melilotus officinalis . Arch Pharm Res. 10:9–13.10.1007/BF02855614
- Kim HJ , Kim BG , Ahn JH . 2013. Regioselective synthesis of flavonoid bisglycosides using Escherichia coli harboring two glycosyltransferases. Appl Microbiol Biotechnol. 97:5275–5282.10.1007/s00253-013-4844-7
- Kite GC , Stoneham CA , Veitch NC . 2007. Flavonol tetraglycosides and other constituents from leaves of Styphnolobium japonicum (Leguminosae) and related taxa. Phytochemistry. 68:1407–1416.10.1016/j.phytochem.2007.03.004
- Kuang Y , Li B , Fan J , Qiao X , Ye M . 2018. Antitussive and expectorant activities of licorice and its major compounds. Bioorg Med Chem. 26:278–284.10.1016/j.bmc.2017.11.046
- Kumar V , Yadav N , Kartha KPR . 2014. In(III) triflate-catalyzed detritylation and glycosylation by solvent-free ball milling. Carbohydr Res. 397:18–26.10.1016/j.carres.2014.08.002
- Luan GX , Wang HL , Lv HH , Hu N , Suo YR , Wang XY . 2016. Separation and purification of five flavone glucosides and one lignan from Caragana korshinskii Kom. by the combination of HSCCC and semi-preparative RPLC. Chromatographia. 79:823–831.10.1007/s10337-016-3090-4
- Miliauskas G , Venskutonis PR , van Beek TA . 2004. Screening of radical scavenging activity of some medicinal and aromatic plant extracts. Food Chem. 85:231–237.10.1016/j.foodchem.2003.05.007
- Pastorino G , Marchetti C , Borghesi B , Cornara L , Ribulla S , Burlando B . 2017. Biological activities of the legume crops Melilotus officinalis and Lespedeza capitata for skin care and pharmaceutical applications. Ind Crops Prod. 96:158–164.10.1016/j.indcrop.2016.11.047
- Qing-Hu W , Na-ren-chao-ke-tu H , Na-yin-tai D , Xiu-lan W , Wu-Li-Ji A . 2014. The structural elucidation and antimicrobial activities of two isoflavane glycosides from Astragalus membranaceus (Fisch) Bge. var. mongholicus (Bge) Hsiao. J Mol Struct. 1076:535–538.
- Song N , Xu W , Guan H , Liu X , Wang Y , Nie X . 2007. Several flavonoids from Capsella bursa-pastoris (L.) Medic. Asian J Tradit Med. 2:218–222.
- Trouillas P , Calliste CA , Allais DP , Simon A , Marfak A , Delage C , Duroux JL . 2003. Antioxidant, anti-inflammatory and antiproliferative properties of sixteen water plant extracts used in the Limousin countryside as herbal teas. Food Chem. 80:399–407.10.1016/S0308-8146(02)00282-0
- Udayama M , Kınjo J , Yoshıda N , Nohara T . 1998. A new oleanene glucuronide having a branched-chain sugar from Melilotus officinalis . Chem Pharm Bull (Tokyo). 46:526–527.10.1248/cpb.46.526
- Won D , Shin BK , Kang S , Hur HG , Kim M , Han J . 2008. Absolute configurations of isoflavan-4-ol stereoisomers. Bioorg Med Chem Lett. 18:1952–1957.10.1016/j.bmcl.2008.01.116
- Zheng C , Wang L , Han T , Xin H , Jiang Y , Pan L , Jia X , Qin L . 2016. Pruinosanones A-C, anti-inflammatory isoflavone derivatives from Caragana pruinosa . Sci Rep. 6:578.10.1038/srep31743