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Xylocarpus rumphii

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ffb9df2ea2572753032
Scientific name Xylocarpus rumphii
Authority (Kostel.) Mabb.
First published in Malaysian Forester 45: 450 (1982)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Xylocarpus forstenii Miq. Ann. Mus. Bot. Lugduno-Batavi 4: 62 (1868)
Aglaia zollingeri C.DC. Bull. Herb. Boissier 2: 579 (1894)
Carapa rumphii Kostel. Allg. Med.-Pharm. Fl. 5: 1988 (1836)

Common names Top

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Language Common/alternative name
Indonesian nyiri laut

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
      • Solomon Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000428213
Tropicos 50144952
INPN 673693
KEW urn:lsid:ipni.org:names:911650-1
The Plant List kew-2467179
Open Tree Of Life 3942294
NCBI Taxonomy 1962071
IPNI 911650-1
iNaturalist 425826
GBIF 3850981
EOL 3102196
Wikipedia Xylocarpus_rumphii

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Chromosome-scale genomes of commercially important mahoganies, Swietenia macrophylla and Khaya senegalensis Sahu SK, Liu M, Wang G, Chen Y, Li R, Fang D, Sahu DN, Mu W, Wei J, Liu J, Zhao Y, Zhang S, Lisby M, Liu X, Xu X, Li L, Wang S, Liu H, He C Sci Data 25-Nov-2023
PMCID:PMC10676371
doi:10.1038/s41597-023-02707-w
PMID:38007506
Fascinating Furanosteroids and Their Pharmacological Profile Dembitsky VM Molecules 26-Jul-2023
PMCID:PMC10419491
doi:10.3390/molecules28155669
PMID:37570639
Interspecific variation and phylogenetic relationship between mangrove and non-mangrove species of a same family (Meliaceae)—insights from comparative analysis of complete chloroplast genome Tan F, Li W, Feng H, Huang Y, Banerjee AK PeerJ 26-Jun-2023
PMCID:PMC10309054
doi:10.7717/peerj.15527
PMID:37397021
Chloroplast genome skimming of a potential agroforestry species Melia dubia. Cav and its comparative phylogenetic analysis with major Meliaceae members Samji A, Eashwarlal K, Shanmugavel S, Kumar S, Warrier RR 3 Biotech 31-Dec-2022
PMCID:PMC9805483
doi:10.1007/s13205-022-03447-1
PMID:36597460
The complete chloroplast genome of Sonneratia griffithii Kurz (Lythraceae) Sangsrakru D, Sonthirod C, Nawae W, Yundaeng C, Promchoo W, Pootakham W, Tangphatsornruang S Mitochondrial DNA B Resour 03-Oct-2022
PMCID:PMC9553166
doi:10.1080/23802359.2022.2119818
PMID:36237205
Bioprospecting of underutilized mangrove fruits used by coastal communities in the Odisha coast, India: a review Rout P Food Sci Biotechnol 09-Dec-2021
PMCID:PMC8817954
doi:10.1007/s10068-021-01013-8
PMID:35186345
Comparative Analyses of Chloroplast Genomes From 14 Zanthoxylum Species: Identification of Variable DNA Markers and Phylogenetic Relationships Within the Genus Zhao K, Li L, Quan H, Yang J, Zhang Z, Liao Z, Lan X Front Plant Sci 13-Jan-2021
PMCID:PMC7838127
doi:10.3389/fpls.2020.605793
PMID:33519856
Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes Lautié E, Russo O, Ducrot P, Boutin JA Front Pharmacol 07-Apr-2020
PMCID:PMC7154113
doi:10.3389/fphar.2020.00397
PMID:32317969
Residual Dipolar Couplings in Structure Determination of Natural Products Li GW, Liu H, Qiu F, Wang XJ, Lei XX Nat Prod Bioprospect 25-Jun-2018
PMCID:PMC6102172
doi:10.1007/s13659-018-0174-x
PMID:29943349
Bioprospecting of Marine Macrophytes Using MS-Based Lipidomics as a New Approach Maciel E, Leal MC, Lillebø AI, Domingues P, Domingues MR, Calado R Mar Drugs 08-Mar-2016
PMCID:PMC4820303
doi:10.3390/md14030049
PMID:27005634
Weakly anti-inflammatory limonoids from the seeds of Xylocarpus rumphii. Sarigaputi C, Sommit D, Teerawatananond T, Pudhom K J Nat Prod 26-Sep-2014
doi:10.1021/NP5003687
PMID:25140384
Molecular understanding of lung cancers-A review Singh CR, Kathiresan K Asian Pac J Trop Biomed 01-May-2014
PMCID:PMC4025309
doi:10.12980/APJTB.4.2014C597
PMID:25183110
Xylorumphiins A-D, mexicanolide limonoids from the seed kernels of Xylocarpus rumphii. Sarigaputi C, Nuanyai T, Teerawatananond T, Pengpreecha S, Muangsin N, Pudhom K J Nat Prod 27-Aug-2010
doi:10.1021/NP100423W
PMID:20677782
Xyloccensin E Sarigaputi C, Teerawatananond T, Pengpreecha S, Muangsin N, Pudhom K Acta Crystallogr Sect E Struct Rep Online 15-May-2010
PMCID:PMC2979606
doi:10.1107/S1600536810016582
PMID:21579436

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(1R,6R,7R,10R,11S,12S,14R,15R,16S,18R)-6-(furan-3-yl)-16-hydroxy-12-(2-methoxy-2-oxoethyl)-7,11,13,13-tetramethyl-18-(2-methylpropanoyloxy)-4-oxo-5,17-dioxapentacyclo[13.2.1.01,10.02,7.011,16]octadec-2-en-14-yl] (2S)-2-methylbutanoate 46919683 Click to see 656.80 unknown https://doi.org/10.1021/NP100423W
[(1R,6R,7R,10R,11S,12S,14S,15S,16R,18R)-6-(furan-3-yl)-15,16-dihydroxy-12-(2-methoxy-2-oxoethyl)-7,11,13,13-tetramethyl-18-[(2S)-2-methylbutanoyl]oxy-4-oxo-5,17-dioxapentacyclo[13.2.1.01,10.02,7.011,16]octadec-2-en-14-yl] (2S)-2-methylbutanoate 118716049 Click to see 686.80 unknown https://doi.org/10.1021/NP5003687
[(1S,2R,6R,7R,10R,11S,12S,14S,15S,16R,18R)-6-(furan-3-yl)-15,16-dihydroxy-12-(2-methoxy-2-oxoethyl)-7,11,13,13-tetramethyl-14-(2-methylpropanoyloxy)-4-oxo-5,17-dioxapentacyclo[13.2.1.01,10.02,7.011,16]octadecan-18-yl] (2S)-2-methylbutanoate 118716046 Click to see 674.80 unknown https://doi.org/10.1021/NP5003687
[(1S,2R,6R,7R,10R,11S,12S,14S,15S,16R,18R)-6-(furan-3-yl)-15,16-dihydroxy-12-(2-methoxy-2-oxoethyl)-7,11,13,13-tetramethyl-18-(2-methylpropanoyloxy)-4-oxo-5,17-dioxapentacyclo[13.2.1.01,10.02,7.011,16]octadecan-14-yl] (2S)-2-methylbutanoate 46919682 Click to see 674.80 unknown https://doi.org/10.1021/NP100423W
[(1S,2R,6R,7R,10R,11S,12S,14S,15S,16R,18R)-6-(furan-3-yl)-15,16-dihydroxy-12-(2-methoxy-2-oxoethyl)-7,11,13,13-tetramethyl-18-(2-methylpropanoyloxy)-4-oxo-5,17-dioxapentacyclo[13.2.1.01,10.02,7.011,16]octadecan-14-yl] 2-methylpropanoate 46919589 Click to see CC(C)C(=O)OC1C(C(C2(C3CCC4(C(C35C(C1(C2(O5)O)O)OC(=O)C(C)C)CC(=O)OC4C6=COC=C6)C)C)CC(=O)OC)(C)C 660.70 unknown https://doi.org/10.1021/NP100423W
[6-(Furan-3-yl)-15,16-dihydroxy-12-(2-methoxy-2-oxoethyl)-7,11,13,13-tetramethyl-18-(2-methylpropanoyloxy)-4-oxo-5,17-dioxapentacyclo[13.2.1.01,10.02,7.011,16]octadecan-14-yl] 2-methylbutanoate 75254606 Click to see CCC(C)C(=O)OC1C(C(C2(C3CCC4(C(C35C(C1(C2(O5)O)O)OC(=O)C(C)C)CC(=O)OC4C6=COC=C6)C)C)CC(=O)OC)(C)C 674.80 unknown https://doi.org/10.1021/NP100423W
[6-(Furan-3-yl)-15,16-dihydroxy-12-(2-methoxy-2-oxoethyl)-7,11,13,13-tetramethyl-18-(2-methylpropanoyloxy)-4-oxo-5,17-dioxapentacyclo[13.2.1.01,10.02,7.011,16]octadecan-14-yl] 2-methylpropanoate 73226664 Click to see 660.70 unknown https://doi.org/10.1021/NP100423W
[6-(Furan-3-yl)-16-hydroxy-12-(2-methoxy-2-oxoethyl)-7,11,13,13-tetramethyl-18-(2-methylpropanoyloxy)-4-oxo-5,17-dioxapentacyclo[13.2.1.01,10.02,7.011,16]octadec-2-en-14-yl] 2-methylbutanoate 75254607 Click to see 656.80 unknown https://doi.org/10.1021/NP100423W
Angolensic acid methyl ester 419676 Click to see CC1(C(C2(C3CCC4(C(OC(=O)CC4(C3=C)OC2CC1=O)C5=COC=C5)C)C)CC(=O)OC)C 470.60 unknown https://doi.org/10.1021/NP100423W
methyl 2-[(1R,2R,3R,7S,8S,11S,12R,13S,15S,17R)-7-(furan-3-yl)-3,17-dihydroxy-8,12,14,14-tetramethyl-5,18-dioxo-6,16-dioxapentacyclo[10.4.2.02,11.03,8.015,17]octadecan-13-yl]acetate 162892208 Click to see CC1(C(C2(C3CCC4(C(OC(=O)CC4(C3C5C(C1O5)(C2=O)O)O)C6=COC=C6)C)C)CC(=O)OC)C 502.60 unknown https://doi.org/10.1021/NP100423W
methyl 2-[(1R,2S,3R,7S,8S,11S,12R,13S,15R,17S)-7-(furan-3-yl)-3-hydroxy-8,12,14,14-tetramethyl-5,18-dioxo-6,16-dioxapentacyclo[10.4.2.02,11.03,8.015,17]octadecan-13-yl]acetate 163011017 Click to see 486.60 unknown https://doi.org/10.1021/NP100423W
methyl 2-[(1S,2R,6R,7R,10R,12S,14S,15S,16S,17S,18S,19R,20R)-18,19,20-triacetyloxy-6-(furan-3-yl)-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.114,17.01,10.02,7.010,15.014,19]docosan-16-yl]acetate 163185983 Click to see 686.70 unknown https://doi.org/10.1021/NP100423W
Methyl 2-[18,19,20-triacetyloxy-6-(furan-3-yl)-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.114,17.01,10.02,7.010,15.014,19]docosan-16-yl]acetate 73226708 Click to see 686.70 unknown https://doi.org/10.1021/NP100423W
Methyl 2-[7-(furan-3-yl)-3-hydroxy-8,12,14,14-tetramethyl-5,18-dioxo-6,16-dioxapentacyclo[10.4.2.02,11.03,8.015,17]octadecan-13-yl]acetate 163011016 Click to see 486.60 unknown https://doi.org/10.1021/NP100423W
Methyl 2-[7-(furan-3-yl)-3,17-dihydroxy-8,12,14,14-tetramethyl-5,18-dioxo-6,16-dioxapentacyclo[10.4.2.02,11.03,8.015,17]octadecan-13-yl]acetate 162892207 Click to see 502.60 unknown https://doi.org/10.1021/NP100423W
Methyl angolensate 21596327 Click to see CC1(C(C2(C3CCC4(C(OC(=O)CC4(C3=C)OC2CC1=O)C5=COC=C5)C)C)CC(=O)OC)C 470.60 unknown https://doi.org/10.1021/NP100423W

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