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Planchonella duclitan

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fe7d0068a0909731177
Scientific name Planchonella duclitan
Authority (Blanco) Bakh.f.
First published in Blumea 12: 62 (1963)

Description Top

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Synonyms Top

Scientific name Authority First published in
Planchonella celebica Dubard Ann. Mus. Colon. Marseille , sér. 2, 10: 61 (1912)
Planchonella nitida Dubard Ann. Mus. Colon. Marseille , sér. 2, 10: 62 (1912)
Planchonella sundaica Dubard Ann. Mus. Colon. Marseille , sér. 2, 10: 62 (1912)
Pouteria duclitan (Blanco) Baehni Candollea 9: 283 (1942)
Pouteria nitida (Blume) S.P.Teo Sarawak Mus. J. 51: 217. 1998 (1997 publ. 1998)
Sideroxylon balitbitan Blanco Fl. Filip. : 130 (1837)
Sideroxylon celebicum Pierre ex Burck Ann. Jard. Bot. Buitenzorg 5: 8 (1885)
Sideroxylon duclitan Blanco Fl. Filip. : 129 (1837)
Sideroxylon nitidum Blume Bijdr. Fl. Ned. Ind. : 675 (1826)
Sideroxylon ramiflorum Merr. Publ. Bur. Sci. Gov. Lab. 17: 43 (1904)
Sideroxylon sundaicum Burck Ann. Jard. Bot. Buitenzorg 5: 9 (1885)
Beccariella balitbitan (Blanco) Pierre Notes Bot. Sapot. : 30 (1890)
Beccariella celebica Pierre Notes Bot. Sapot. : 30 (1890)
Beccariella duclitan (Blanco) Pierre Notes Bot. Sapot. : 30 (1890)
Xantolis nitida (Blume) Baehni Boissiera 11: 23 (1965)
Chrysophyllum rhodoneurum Hassk. Flora 38: 579 (1855)
Chrysophyllum sundaicum Miq. Fl. Ned. Ind., Eerste Bijv. : 578 (1861)

Common names Top

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Language Common/alternative name
Chinese 蘭嶼山欖

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
    • Malesia
      • Borneo
      • Christmas Island
      • Jawa
      • Lesser Sunda Islands
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000274110
Tropicos 50307118
KEW urn:lsid:ipni.org:names:788610-1
The Plant List kew-156829
Open Tree Of Life 61704
NCBI Taxonomy 1199023
IUCN Red List 138231531
IPNI 788610-1
GBIF 5334160
EOL 1152158
Wikipedia Planchonella_duclitan

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
Rotundic acid induces Cas3-MCF-7 cell apoptosis through the p53 pathway Nan ML, Wang X, Li HJ, Yu DH, Sun WY, Xu HM, He YF, Zhao QC Oncol Lett 24-Oct-2018
PMCID:PMC6313092
doi:10.3892/ol.2018.9616
PMID:30655810
Triterpene Acids from the Leaves of<i>Planchonella Duclitan</i>(Blanco) Bakhuizan Tzong-Huei Lee, Shin-Hun Juang, Feng-Lin Hsu, Cheng-Yi Wu Wiley 01-May-2015
doi:10.1002/JCCS.200500184
Synthesis, Characterization and Cytotoxicity of New Rotundic Acid Derivatives He YF, Nan ML, Sun JM, Meng ZJ, Yue FG, Zhao QC, Yang XH, Wang H Molecules 31-Jan-2012
PMCID:PMC6268532
doi:10.3390/molecules17021278
PMID:22293846

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
(1R,2R,5R,6R,7S,8R,10S,11R,14S,15S,16R,17R,20S)-7,8,16-trihydroxy-6-(hydroxymethyl)-2,6,10,16,17-pentamethylhexacyclo[12.8.1.01,14.02,11.05,10.015,20]tricos-12-ene-20-carboxylic acid 162852299 Click to see CC1CCC2(CCC34CC3(C2C1(C)O)C=CC5C4(CCC6C5(CC(C(C6(C)CO)O)O)C)C)C(=O)O 502.70 unknown https://doi.org/10.1002/JCCS.200500184
(1S,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-10,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 15917996 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1002/JCCS.200500184
1,10-Dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 12315074 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1002/JCCS.200500184
11-hydroxy-10-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 72730089 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1C)C)C(=O)O 618.80 unknown https://doi.org/10.1002/JCCS.200500184
23-Hydroxytormenticacid 14055735 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)O 504.70 unknown https://doi.org/10.1002/JCCS.200500184
3beta-[[(E)-3-(4-Hydroxyphenyl)propenoyl]oxy]-2alpha-hydroxyurs-12-ene-28-oic acid 14335960 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1C)C)C(=O)O 618.80 unknown https://doi.org/10.1002/JCCS.200500184
7,8,16-Trihydroxy-6-(hydroxymethyl)-2,6,10,16,17-pentamethylhexacyclo[12.8.1.01,14.02,11.05,10.015,20]tricos-12-ene-20-carboxylic acid 162852298 Click to see CC1CCC2(CCC34CC3(C2C1(C)O)C=CC5C4(CCC6C5(CC(C(C6(C)CO)O)O)C)C)C(=O)O 502.70 unknown https://doi.org/10.1002/JCCS.200500184
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1002/JCCS.200500184
CID 3838010 3838010 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown https://doi.org/10.1002/JCCS.200500184
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1002/JCCS.200500184
Myrianthic acid 182497 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)O 504.70 unknown https://doi.org/10.1002/JCCS.200500184
Pomolic acid 382831 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown https://doi.org/10.1002/JCCS.200500184
Rotundic acid 12315075 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1002/JCCS.200500184
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1002/JCCS.200500184

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