Urgamal M, Oyuntsetseg B, Nyambayar D, Dulamsuren C, Sanchir C, Jamsran T (2014) Conspectus of the vascular plants of Mongolia. Admon Press, Ulaanbaatar
Ligaa U, Davaasuren B, Ninjil N (2005) Medicinal Plants of Mongolia Used in Western and Eastern Medicine. JCK Printing, Ulaanbaatar
Tserenbaljid G (2002) The colour atlas of antropophilus plants of Mongolia. Admon Press, Ulaanbaatar
Abdullah S (2013) Anticancer drug capable of clearing blood and diminishing inflammation. CN102886014B
Boldbaatar D, El Seedi HR, Findakly M, Jabri S, Javzan B, Choidash B, Göransson U, Hellman B (2014) Antigenotoxic and antioxidant effects of the Mongolian medicinal plant Leptopyrum fumarioides (L): an in vitro study. J Ethnopharmacol 155:599–606. https://doi.org/10.1016/j.jep.2014.06.005
Nikolaev S, Zandanov A, Sambueva Z, IaG R, Fedorov A (2012) Effect of Leptopyrum fumarioides (Ranunculaceae) extract on choleresis in white rats with toxic hepatitis. Clin Exp Gastroenterol 40:21–24
Doncheva T, Solongo A, Kostova N, OdGerelt Y, Selenge D, Philipov S (2015) Leptopyrine, new alkaloid from Leptopyrum fumarioides L. (Ranunculaceae). Nat Prod Res 29:853–856
Article PubMed CAS Google Scholar
Solongo A, Doncheva T, Delgerbat B, Selenge D (2022) Review of phytochemical and some biological activity of Leptopyrum fumarioides (L.) Reichenb. Proc Univ Appl Chem Biotechnol 12:231–237
Solongo A, Doncheva T, Kostova N, Yadamsuren GO, Philipov S, Ivanovska N (2020) Alkaloids from the aerial parts of Leptopyrum fumarioides express immunomodulatory activity. J Asian Nat Prod Res 22:886–894
Article PubMed CAS Google Scholar
Van MJ, Kaspers GJL, Cloos J (2011) Cell sensitivity assays: the MTT assay. In: Cree IA (ed) Cancer cell culture: methods and protocols. Humana Press, Totowa, pp 237–245
Eberhardt J, Santos-Martins D, Tillack AF, Forli S (2021) AutoDock Vina 1.2. 0: New docking methods, expanded force field, and python bindings. J Chem Inf Model 61:3891–3898. https://doi.org/10.1021/acs.Jcim.1c00203
Article PubMed PubMed Central CAS Google Scholar
Orlando BJ, Malkowski MG (2016) Crystal structure of rofecoxib bound to human cyclooxygenase-2. Acta Cryst F 72:772–776. https://doi.org/10.1107/S2053230X16014230
Mehallah H, Djebli N, Khanh PN, Ha NX, Ha VT, Huong TT, Cuong NM (2024) In silico and in vivo study of anti-inflammatory activity of Morinda longissima (Rubiaceae) extract and phytochemicals for treatment of inflammation-mediated diseases. J Ethnopharmacol 328:118051. https://doi.org/10.1016/j.jep.2024.118051
Article PubMed CAS Google Scholar
Lee SS, Lai YC, Chen CK, Tseng LH, Wang CY (2007) Characterization of isoquinoline alkaloids from Neolitsea sericea var. aurata by HPLC-SPE-NMR. J Nat Prod 70:637–642. https://doi.org/10.1021/np060636p
Article PubMed CAS Google Scholar
Wang R, Liu Y, Shi G, Zhou J, Li J, Li L, Yuan J, Li X, Yu D (2020) Bioactive bisbenzylisoquinoline alkaloids from the roots of Stephania tetrandra. Bioorg Chem 98:103697. https://doi.org/10.1016/j.bioorg.2020.103697
Article PubMed CAS Google Scholar
Dembitsky VM, Gloriozova TA, Poroikov VV (2015) Naturally occurring plant isoquinoline N-oxide alkaloids: Their pharmacological and SAR activities. Phytomedicine 22:183–202. https://doi.org/10.1016/j.phymed.2014.11.002
Article PubMed CAS Google Scholar
Zhou Q, Fu YH, Li XB, Chen GY, Wu SY, Song XP, Liu YP, Han CR (2015) Bioactive benzylisoquinoline alkaloids from Artabotrys hexapetalus. Phytochem Lett 11:296–300. https://doi.org/10.1016/j.phytol.2015.01.017
Suau R, Segura RG, Silva MV, Valpuesta M, Dominguez D, Castedo L (1995) Structural and conformational analysis of naturally occurring cularine N-oxide alkaloids. Heterocycles 41:2575–2586
Costa EV, Soares LN, Chaar JS, Silva VR, Santos LS, Koolen HH, Silva FM, Tavares JF, Zengin G, Soares MB (2021) Benzylated dihydroflavones and isoquinoline-derived alkaloids from the bark of Diclinanona calycina (Annonaceae) and their cytotoxicities. Molecules 26:3714. https://doi.org/10.3390/molecules26123714
Article PubMed PubMed Central CAS Google Scholar
Lee SS, Doskotch RW (1999) Four dimeric aporphine-containing alkaloids from Thalictrum fauriei. J Nat Prod 62:803–810. https://doi.org/10.1021/np980311b
Article PubMed CAS Google Scholar
Zheng XK, Li DD, Yan H, Li M, He JL, Feng WS (2013) Two new alkaloids from Corydalis humosa. J Asian Nat Prod Res 15:1158–1162
Article PubMed CAS Google Scholar
Doskotch RW, Phillipson J, Ray A, Beal JL (1971) Alkaloids of thalictrum. XII. Synthesis of the thalictrum alkaloids, adiantifoline, and thalicmidine. J Org Chem 36:2409–2413. https://doi.org/10.1021/jo00816a006
Article PubMed CAS Google Scholar
Parameswaran N, Patial S (2010) Tumor necrosis factor-α signaling in macrophages. Crit Rev Eukaryot Gene Expr. https://doi.org/10.1615/CritRevEukarGeneExpr.v20.i2.10
Article PubMed PubMed Central Google Scholar
Yang CM, Yang CC, Hsiao LD, Yu CY, Tseng HC, Hsu CK, Situmorang JH (2021) Upregulation of COX-2 and PGE2 induced by TNF-α mediated through TNFR1/MitoROS/PKCα/P38 MAPK, JNK1/2/FoxO1 cascade in human cardiac fibroblasts. J Inflamm Res. https://doi.org/10.2147/jIR.S313665
Article PubMed PubMed Central Google Scholar
Karthein R, Dietz R, Nastainczyk W, Ruf HH (1988) Higher oxidation states of prostaglandin H synthase: EPR study of a transient tyrosyl radical in the enzyme during the peroxidase reaction. Eur J Biochem 171:313–320. https://doi.org/10.1111/j.1432-1033.1988.tb13792.x
Article PubMed CAS Google Scholar
Dadashpour S, Tuylu Kucukkilinc T, Unsal Tan O, Ozadali K, Irannejad H, Emami S (2015) Design, synthesis and in vitro study of 5, 6-diaryl-1, 2, 4-triazine-3-ylthioacetate derivatives as COX-2 and β-amyloid aggregation inhibitors. Arch Pharm 348:179–187. https://doi.org/10.1002/ardp.201400400
Comments (0)