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The Chemistry of the Meliaceae and Ptaeroxylaceae of Southern and Eastern Africa and Madagascar

https://doi.org/10.2174/1385272003375941

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inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.11.057openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.phytochem.2008.12.004openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.phytochem.2009.07.016openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.phytochem.2011.01.010openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.phytochem.2011.08.005openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.phytochem.2011.12.016openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.phytol.2010.11.002openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.phytol.2012.05.005openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.sajb.2016.03.010openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.steroids.2006.04.010openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.tet.2005.06.099openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.tet.2006.05.030openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.tet.2007.04.078openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.tet.2007.05.107openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.tet.2011.02.049openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.tetlet.2003.10.216openalex-snapshot

Xyloccensin L, a novel limonoid from Xylocarpus granatum

inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.08.066openalex-snapshot

Swiemahogins A and B, two novel limonoids from Swietenia mahogani

inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.04.145openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.05.110openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.theochem.2007.04.031openalex-snapshot

Theoretical prediction of the stereochemistry of the OH groups in Turraesterodione

inferred← citeshttps://doi.org/10.1016/j.ympev.2010.06.023openalex-snapshot

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inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03557openalex-snapshot

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inferred← citeshttps://doi.org/10.1021/cr0782832openalex-snapshot

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inferred← citeshttps://doi.org/10.1021/cr9004023openalex-snapshot

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inferred← citeshttps://doi.org/10.1021/jo301182fopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/np0200562openalex-snapshot

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inferred← citeshttps://doi.org/10.1021/np050545copenalex-snapshot

Polyhydroxylated Phragmalins from the Fruit of a Chinese Mangrove, Xylocarpus granatum

inferred← citeshttps://doi.org/10.1021/np060632kopenalex-snapshot

Limonoids from the Seeds of the Marine Mangrove Xylocarpus granatum

inferred← citeshttps://doi.org/10.1021/np070146copenalex-snapshot

Limonoids from the Leaves and Stems of Toona ciliata

inferred← citeshttps://doi.org/10.1021/np070229topenalex-snapshot

Tetranortriterpenoids from Cipadessa baccifera

inferred← citeshttps://doi.org/10.1021/np070476xopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/np070487qopenalex-snapshot

Antiproliferative Limonoids of a Malleastrum sp. from the Madagascar Rainforest,

inferred← citeshttps://doi.org/10.1021/np1000158openalex-snapshot

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inferred← citeshttps://doi.org/10.1021/np100307fopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/np100423wopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/np100428uopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/np100566vopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/np200013gopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/np200579bopenalex-snapshot

Cytotoxic and Anti-inflammatory Triterpenoids from Toona ciliata

inferred← citeshttps://doi.org/10.1021/np2006296openalex-snapshot

Tirucallane-Type Triterpenoids from Dysoxylum lenticellatum

inferred← citeshttps://doi.org/10.1021/np300053fopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/np400408sopenalex-snapshot

Trichinenlides A–T, Mexicanolide-Type Limonoids from Trichilia sinensis

inferred← citeshttps://doi.org/10.1021/np800811bopenalex-snapshot

Terpenoids from Toona ciliata

inferred← citeshttps://doi.org/10.1021/np9003504openalex-snapshot

Moluccensins A−G, Phragmalins with a Conjugated C-30 Carbonyl Group from a Krishna Mangrove, Xylocarpus moluccensis

inferred← citeshttps://doi.org/10.1021/np900485topenalex-snapshot

Tetranortriterpenoids from Chisocheton paniculatus

inferred← citeshttps://doi.org/10.1021/np900583hopenalex-snapshot

Moluccensins H−J, 30-Ketophragmalin Limonoids from Xylocarpus moluccensis

inferred← citeshttps://doi.org/10.1021/np900625wopenalex-snapshot

Granatumins A−G, Limonoids from the Seeds of a Krishna Mangrove, Xylocarpus granatum

inferred← citeshttps://doi.org/10.1021/np900734copenalex-snapshot

Chuktabularins E−T, 16-Norphragmalin Limonoids from Chukrasia tabularis var. velutina

inferred← citeshttps://doi.org/10.1021/np900823copenalex-snapshot

Limonoids and Tirucallane Derivatives from the Seeds of a Krishna Mangrove, Xylocarpus moluccensis

inferred← citeshttps://doi.org/10.1021/ol049444gopenalex-snapshot

Xyloccensins O and P, Unique 8,9,30-Phragmalin Ortho Esters from Xylocarpus granatum

inferred← citeshttps://doi.org/10.1021/ol061466aopenalex-snapshot

Turrapubesins A and B, First Examples of Halogenated and Maleimide-Bearing Limonoids in Nature from Turraea pubescens

inferred← citeshttps://doi.org/10.1021/ol062101topenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/ol800885hopenalex-snapshot

Chuktabrins A and B, Two Novel Limonoids from the Twigs and Leaves of Chukrasia tabularis

inferred← citeshttps://doi.org/10.1021/ol802678sopenalex-snapshot

Two Limonoids, Khayalenoids A and B with an Unprecedented 8-Oxa-tricyclo[4.3.2.02,7]undecane Motif, from Khaya senegalensis

inferred← citeshttps://doi.org/10.1021/ol900589hopenalex-snapshot

Chukvelutins A−C, 16-Norphragmalin Limonoids with Unprecedented Skeletons from Chukrasia tabularis var. velutina

inferred← citeshttps://doi.org/10.1021/ol902565sopenalex-snapshot

Structure Determination of Grandifotane A from Khaya grandifoliola by NMR, X-ray Diffraction, and ECD Calculation

inferred← citeshttps://doi.org/10.1039/c0cc04698aopenalex-snapshot

A concise total synthesis of (±)-cipadonoid B from synthetic azedaralide

inferred← citeshttps://doi.org/10.1039/c1ob06150jopenalex-snapshot

Protolimonoids and norlimonoids from the stem bark of Toona ciliata var. pubescens

inferred← citeshttps://doi.org/10.1039/c1ob06666hopenalex-snapshot

Kv1.2 potassium channel inhibitors from Chukrasia tabularis

inferred← citeshttps://doi.org/10.1039/c5ob02300aopenalex-snapshot

Trichiconlides A and B: two novel limonoids from the fruits of Trichilia connaroides

inferred← citeshttps://doi.org/10.1039/c7ra01785eopenalex-snapshot

Phragmalin-type limonoids from the roots of Trichilia sinensis

inferred← citeshttps://doi.org/10.1039/c8ob02325eopenalex-snapshot

Rearranged ergostane-type natural products: chemistry, biology, and medicinal aspects

inferred← citeshttps://doi.org/10.1055/s-0029-1186038openalex-snapshot

Turrealabdane, Turreanone and an Antisalmonellal Agent fromTurraeanthus africanus

inferred← citeshttps://doi.org/10.1071/ch09301openalex-snapshot

A Synthetic and Computational Investigation into the Direct Synthesis of α-Hydroxymethylated Enones from β-Keto Phosphonates

inferred← citeshttps://doi.org/10.1080/02773813.2022.2048668openalex-snapshot

Analysis of sugar components related to heartwood formation in young Swietenia mahagoni (L.) Jacq trees

inferred← citeshttps://doi.org/10.1080/10286020.2017.1392513openalex-snapshot

Ergostane steroids from the ethanol extract of Dysoxylum mollissimum

inferred← citeshttps://doi.org/10.1080/10286020.2018.1488831openalex-snapshot

Two new compounds from the roots of Swietenia macrophylla

inferred← citeshttps://doi.org/10.1080/10286020801966690openalex-snapshot

The absolute stereochemistry of protoxylogranatin A – a new protolimonoid from the seeds of Chinese mangrove Xylocarpus granatum

inferred← citeshttps://doi.org/10.1080/14786419.2011.625499openalex-snapshot

Limonoids from the leaves ofSwietenia macrophylla

inferred← citeshttps://doi.org/10.1080/14786419.2023.2233045openalex-snapshot

Swietenolide isolated from Swietenia macrophylla King in Hook seeds shows in vitro anti-colorectal cancer activity through inhibition of mouse double minute 2 (MDM2) homolog

inferred← citeshttps://doi.org/10.1093/aob/mcr076openalex-snapshot

Phylogeny, evolutionary trends and classification of the Spathelia–Ptaeroxylon clade: morphological and molecular insights

inferred← citeshttps://doi.org/10.1107/s1600536810028527openalex-snapshot

Xyloccensin L

inferred← citeshttps://doi.org/10.1111/jfbc.13668openalex-snapshot

Limonoids isolated from fruits of Swietenia macrophylla king enhance glucose consumption in insulin‐resistant HepG2 cells via activating PPARγ

inferred← citeshttps://doi.org/10.1111/jphp.13005openalex-snapshot

Phytochemistry and pharmacology of the genus Entandrophragma over the 50 years from 1967 to 2018: a ‘golden’ overview

inferred← citeshttps://doi.org/10.1155/2013/803835openalex-snapshot

Effect of Aqueous Stem Bark Extract ofKhaya senegalensison Some Biochemical, Haematological, and Histopathological Parameters of Rats

inferred← citeshttps://doi.org/10.1177/1934578x0600100603openalex-snapshot

A Pregnane Derivative and an Anti-plasmodial Labdane Diterpenoid from the Stem Bark of Turraenthus Africanus

inferred← citeshttps://doi.org/10.1177/1934578x1000501003openalex-snapshot

Terpenoids from Turraeanthus species

inferred← citeshttps://doi.org/10.1248/cpb.54.1582openalex-snapshot

Xylogranatins A-D, New Mexicanolides from the Fruit of a Chinese Mangrove Xylocarpus granatum

inferred← citeshttps://doi.org/10.1248/cpb.59.1003openalex-snapshot

Limonoids and Triterpenoids from the Seeds of Melia azedarach

inferred← citeshttps://doi.org/10.1360/ssc-2025-0149openalex-snapshot

Progress in the study of non-limonoid natural products of the Meliaceae family

inferred← citeshttps://doi.org/10.1371/journal.pntd.0001727openalex-snapshot

In-silico Investigation of Antitrypanosomal Phytochemicals from Nigerian Medicinal Plants

inferred← citeshttps://doi.org/10.1371/journal.pone.0160843openalex-snapshot

The Limonoids TS3 and Rubescin E Induce Apoptosis in Human Hepatoma Cell Lines and Interfere with NF-κB Signaling

inferred← citeshttps://doi.org/10.1584/jpestics.g10-52openalex-snapshot

Khayasin and 2'S-methylbutanoylproceranolide: Promising candidate insecticides for the control of the coconut leaf beetle, Brontispa longissima

inferred← citeshttps://doi.org/10.1590/s0102-695x2008000500011openalex-snapshot

Melia azedarach L. extracts and their activity on Musca domestica L. (Diptera: Muscidae)

inferred← citeshttps://doi.org/10.21475/ajcs.18.12.11.p1526openalex-snapshot

Assessment of allelopathic activity of Swietenia mahagoni (L.) seed extracts on different plant species

inferred← citeshttps://doi.org/10.2174/1874848101003010001openalex-snapshot

Protoxylogranatin B, a Key Biosynthetic Intermediate from Xylocarpus granatum: Suggesting an Oxidative Cleavage Biogenetic Pathway to Limonoid

inferred← citeshttps://doi.org/10.2989/20702620.2023.2180453openalex-snapshot

Heartwood formation and its relationship with basic density and green moisture content of young small-leaf mahogany trees

inferred← citeshttps://doi.org/10.32328/turkjforsci.1903483openalex-snapshot

Maun (Swietenia mahagoni) odununun bazı karakteristik özelliklerinin belirlenmesi

inferred← citeshttps://doi.org/10.32749/nucleodoconhecimento.com.br/engenharia-quimica/aplicacoes-dos-oleosopenalex-snapshot

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inferred← citeshttps://doi.org/10.3390/md20050303openalex-snapshot

Exploring the Mangrove Fruit: From the Phytochemicals to Functional Food Development and the Current Progress in the Middle East

inferred← citeshttps://doi.org/10.3390/molecules14114476openalex-snapshot

In Vitro Antioxidant and Xanthine Oxidase Inhibitory Activities of Methanolic Swietenia mahagoni Seed Extracts

inferred← citeshttps://doi.org/10.3390/molecules180910465openalex-snapshot

Biological Activities and Phytochemicals of Swietenia macrophylla King

inferred← citeshttps://doi.org/10.3390/molecules24071291openalex-snapshot

Polyacetylenes from the Roots of Swietenia macrophylla King

inferred← citeshttps://doi.org/10.3390/molecules25051222openalex-snapshot

Cytotoxic Activity of Inositol Angelates and Tirucallane-Type Alkaloids from Amoora Dasyclada

inferred← citeshttps://doi.org/10.3390/plants10091796openalex-snapshot

The Ethnobotany and Chemistry of South African Meliaceae: A Review

inferred← citeshttps://doi.org/10.3390/plants9020143openalex-snapshot

The Phytochemical Composition of Melia volkensii and Its Potential for Insect Pest Management

inferred← citeshttps://doi.org/10.35229/jaes.1273990openalex-snapshot

Maun, dut ve kızılağaç odunlarının toprakta gelişen çeşitli zararlı organizmalara karşı maruz kalması sonrasında meydana gelen renk özelliklerinin belirlenmesi

inferred← citeshttps://doi.org/10.3762/bjoc.10.15openalex-snapshot

Synthesis of the B-seco limonoid core scaffold

inferred← citeshttps://doi.org/10.3987/com-09-s(s)106openalex-snapshot

Gaudichaudysolin A, a New Limonoid from the Bark of Dysoxylum gaudichaudianum

inferred← citeshttps://doi.org/10.4103/0974-8490.69107openalex-snapshot

Brine shrimp lethality and acute oral toxicity studies on Swietenia mahagoni (Linn.) Jacq. seed methanolic extract

inferred← citeshttps://doi.org/10.4314/ijbcs.v13i1.41openalex-snapshot

Activités biologiques et utilisations de Elaeis guineensis (Jacq) et de Khaya senegalensis (Desr) en médecine traditionnelle humaine et vétérinaire

inferred← citeshttps://doi.org/10.5897/jhf2015.0394openalex-snapshot

Phenotypic traits of Carapa procera fruits from riparian forests of Burkina Faso, West Africa

inferred← citeshttps://doi.org/10.70675/45c1b32az1256z4fb9z8a23zeb853ee93128openalex-snapshot

Etude chimique de colorants naturels et matériaux résineux traditionnels au Bénin dans le domaine artisanal

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