Luo J, Sun Y, Li Q, Kong L (2022) Research progress of meliaceous limonoids from 2011 to 2021. Nat Prod Rep 39:1325–1365. https://doi.org/10.1039/D2NP00015F

Article  CAS  PubMed  Google Scholar 

Riyadi SA, Naini AA, Supratman U (2023) Sesquiterpenoids from meliaceae family and their biological activities. Molecules 28:4874. https://doi.org/10.3390/molecules28124874

Article  CAS  PubMed  PubMed Central  Google Scholar 

Nugroho AE, Wong CP, Hirasawa Y, Kaneda T, Tougan T, Horii T, Morita H (2023) Antimalarial ceramicines Q-T from Chisocheton ceramicus. J Nat Med 77:596–603. https://doi.org/10.1007/s11418-023-01706-w

Article  CAS  PubMed  PubMed Central  Google Scholar 

Tringali C (2000) Bioactive compounds from natural sources: isolation characterization and biological properties. Taylor & Francis, Abingdon

Book  Google Scholar 

Naini AA, Mayanti T, Maharani R, Fajriah S, Kabayama K, Shimoyama A, Manabe Y, Supratman U (2023) Dysoticans F-H: three unprecedented dimeric cadinanes from Dysoxylum parasiticum (Osbeck) Kosterm. stem bark. RSC Adv 13:9370–9376. https://doi.org/10.1039/D3RA01085F

Article  CAS  PubMed  PubMed Central  Google Scholar 

Naini AA, Mayanti T, Harneti D, Maharani R, Farabi K, Herlina T, Supratman U, Chakthong S (2023) Sesquiterpenoids and sesquiterpenoid dimers from the stem bark of Dysoxylum parasiticum (osbeck) kosterm. Phytochemistry 205:113477. https://doi.org/10.1016/j.phytochem.2022.113477

Article  CAS  PubMed  Google Scholar 

Nagakura Y, Yamanaka R, Hirasawa Y, Hosoya T, Rahman A, Kusumawati I, Morita H (2010) Gaudichaudysolin A, a new limonoid from the bark of Dysoxylum gaudichaudianum. Heterocycles 80:1471–1477. https://doi.org/10.3987/COM-09-S(S)106

Article  CAS  Google Scholar 

Chen JL, Kernan MR, Jolad SD, Stoddart CA, Bogan M, Cooper R (2007) Dysoxylins A−D, Tetranortriterpenoids with Potent Anti-RSV Activity from Dysoxylum gaudichaudianum. J Nat Prod 70:312–315. https://doi.org/10.1021/np060398y

Article  CAS  PubMed  Google Scholar 

Luo XD, Wu SH, Wu DG, Ma YB, Qi SH (2002) Novel antifeeding limonoids from Dysoxylum hainanense. Tetrahedron 58:7797–7804. https://doi.org/10.1016/S0040-4020(02)00944-4

Article  CAS  Google Scholar 

Han ML, Zhao JX, Liu HC, Ni G, Ding J, Yang SP, Yue JM (2015) Limonoids and Triterpenoids from Dysoxylum mollissimum var. glaberrimum. J Nat Prod 78:754–761. https://doi.org/10.1021/np500967k

Article  CAS  PubMed  Google Scholar 

Lakshmi V, Pandey K, Agarwal SK (2009) Bioactivity of the compounds in genus Dysoxylum. Acta Ecol Sin 29:30–44. https://doi.org/10.1016/j.chnaes.2009.04.005

Article  Google Scholar 

Suwardi AB, Navia ZI, Harmawan T, Seprianto S, Syamsuardi S, Mukhtar E (2022) Diversity of wild edible fruit plant species and their threatened status in the Aceh Province, Indonesia. Biodiversitas 23:1310–1318. https://doi.org/10.13057/biodiv/d230315

Article  Google Scholar 

Nishizawa M, Inoue A, Sastrapradja S, Hayashi Y (1983) (+)-8-Hydroxycalamenene: a fish-poison principle of Dysoxylum acutangulum and D. Alliaceum Phytochem 22:2083–2085. https://doi.org/10.1016/0031-9422(83)80052-1

Article  CAS  Google Scholar 

Nishizawa M, Yamada H, Sastrapradja S, Hayashi Y (1985) Structure and synthesis of bicalamenene. Tetrahedron Lett 26:1535–1536. https://doi.org/10.1016/S0040-4039(00)98545-9

Article  CAS  Google Scholar 

Lin BD, Yuan T, Zhang CR, Dong L, Zhang B, Wu Y, Yue JM (2009) Structurally diverse limonoids from the fruits of Swietenia mahagoni. J Nat Prod 72:2084–2090. https://doi.org/10.1021/np900522h

Article  CAS  PubMed  Google Scholar 

Zhang JC, Liao Q, Shen L, Wu J (2020) Twenty-five limonoids from the Hainan mangrove Xylocarpus granatum. Bioorganic Chem 100:103903. https://doi.org/10.1016/j.bioorg.2020.103903

Article  CAS  Google Scholar 

Pudhom K, Sommit D, Nuclear P, Ngamrojanavanich N, Petsom A (2010) Moluccensins H− J, 30-Ketophragmalin Limonoids from Xylocarpus moluccensis. J Nat Prod 73:263–266. https://doi.org/10.1021/np900583h

Article  CAS  PubMed  Google Scholar 

Hofer M, Greger H, Mereiter K (2009) 6α-Acetoxygedunin. Acta Crystallographica Sect E: Struct Rep Online 65:1942–1943

Article  Google Scholar 

Kipassa NT, Iwagawa T, Okamura H, Doe M, Morimoto Y, Nakatani M (2008) Limonoids from the stem bark of Cedrela odorata. Phytochemistry 69:1782–1787. https://doi.org/10.1016/j.phytochem.2007.12.015

Article  CAS  PubMed  Google Scholar 

Deng Z, Liu S, Cui S, Zhou L, Yao Q (2012) Cytotoxic activity of five limonoids from Meliae cortex and their structure-activity relationship. Chin J Nat Med 10:238–240. https://doi.org/10.3724/SP.J.1009.2012.00238

Article  CAS  Google Scholar 

Grimblat N, Zanardi MM, Sarotti AM (2015) Beyond DP4+ An improved probability for the stereochemical assignment of isomeric compounds using quantum chemical calculations of NMR shifts. J Org Chem 80:12526–12534. https://doi.org/10.1021/acs.joc.5b02396

Article  CAS  PubMed  Google Scholar