Aba-Toumnou L, Wango SP, Kosh-Komba E, Namkosséréna S, Bolevane-Ouatinam SF, Lakouèténé DP-B, Semballa S, Yongo O-D, Syssa-Magale J-L, Dogo S, et al. 2012. Utilisation des plantes indigènes à effet insecticide pour la protection des denrées stockées contre des insectes ravageurs à Boukoko (Centrafrique). Int J Biol. 6 (3): 1040–1050.
Corrado T., 2001. Bioactive compounds from natural sources: isolation, characterization and biological properties. Nakatani M, editor. London; p. 529–550. Chap. 13.
De Carvalho A, Ndi CP, Tsopmo A, Tane P, Ayafor J, Connolly JD, Teem JL., 2002. A novel natural product compound enhances cAMP-regulated chloride conductance of cells expressing CFTR [Δ] F508. Mol Med. 8 (2): 75–87.
Deharo E, Ginsburg H., 2011. Analysis of additivity and synergism in the antiplasmodial effect of purified compounds from plant extracts. Malar J. 10 (S1): S5. http://www.malariajournal.com/content/10/S1/S5.
Fusetani N, Yasumuro K, Matsunaga S, Hirota H., 1989. Haliclamines A et B, cytotoxic macrocyclic alkaloids from sponge of the genus haliclona. Tetrahedron Lett. 30 (49): 6891–6894.
Hwang IH, Oh J, Kochanowska-Karamyan A, Doerksen RJ, Na M, Hamann MT., 2013. A novel natural phenyl alkene with cytotoxic activity. Tetrahedron Lett. 54 (29): 3872–3876.
Kowa TK, Tchokouaha LRY, Cieckiewicz E, Philips TJ, Dotse E, Wabo HK, Tchinda AT, Tane P, Frédérich M., 2019. Antileishmanial and cytotoxic activities of a new limonoid and a new phenyl alkene from the stem bark of Trichilia gilgiana (Meliaceae). Nat Prod Res. 19: 1–7.
Kowa TK, Zofou D, Mbouangouere R, Feussi TM, Wabo HK, Tan N-H, Titanji VPK, Tane P., 2016. Antiplasmodial activity and cytotoxicity of isolated compound from the stem bark of Anthocleista liebrechtsiana. Rec Nat Prod. 10 (3): 287–293.
Krief S, Martin MT, Grellier P, Kasenene J, Sevenet T., 2004. Novel antimalarial compounds isolated in survey of self-medicative behavior of wild chimpanzees in Uganda. Antimicrob Agents Chemother. 48 (8): 3196–3199.
Louppe D., 2008. Bois d’oeuvre 1. France: Prota; p. 785.
Mc Farland K, Mulholland DA, Fraser LA., 2004. Limonoids from Turraea floribunda (Meliaceae). Phytochemistry. 65 (14): 2031–2037.
Mohamad K, Hirasawa Y, Litaudon M, Awang K, Hadi AHA, Takeya K, Ekasari W, Widyawaruyanti A, Zaini NC, Morita H., 2009. Ceramicines B-D, new antiplasmodial limonoids from Chisocheton ceramicus. Bioorg Med Chem. 17 (2): 727–730.
Rahelivao MP, Lübken T, Gruner M, Kataeva O, Ralambondrahety R, Andriamanantoanina H, Checinski MP, Bauer I, Knölker H., 2017. Isolation and structure elucidation of natural products of three soft corals and a sponge from the coast of Madagascar. Org Biomol Chem. 15 (12): 2593–2608.
Tacham WN, Fonge AB, Fonkou T., 2015. Traditional Medicine and ethnobotanical use of wild plants by the Mundani people of Wabane, South West Region, Cameroon. J Ethnobiol Trad Med Photon. 125: 1060–1080.
Tsamo TA, Melong R, Mkounga P, Nkengfack AE., 2018. Rubescins I and J, further limonoid derivatives from the stem bark of Trichilia rubescens (Meliaceae). Nat Prod Res.
Tsamo AT, Pagna JIM, Nangmo PK, Mkounga P, Laatsch H, Nkengfack AEZ., 2019. Rubescins F-H, new vilasinin-type limonoids from the leaves of Trichilia rubescens (Meliaceae)). Z Naturforsch C J Biosci. 74 (7–8): 175–182.
