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Chisocheton macrophyllus

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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 UUID644010e91705d202687202
Scientific name Chisocheton macrophyllus
Authority King
First published in J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 64: 22 (1895)

Description Top

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Synonyms Top

Scientific name Authority First published in
Chisocheton kingii Harms Nat. Pflanzenfam. 3(4): 295 (1896)
Chisocheton nicobarianus Debnath & Sreek. J. Econ. Taxon. Bot. 16: 553 (1992)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Chisocheton macrophyllus subsp. fulvescens Mabb. Bull. Brit. Mus. (Nat. Hist.), Bot. 6: 346 (1979)

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indo-China
      • Nicobar Nicobar
      • Thailand
    • Malesia
      • Borneo
      • Malaya
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000602911
Tropicos 100311032
KEW urn:lsid:ipni.org:names:577897-1
The Plant List kew-2718957
Open Tree Of Life 385552
NCBI Taxonomy 155629
IUCN Red List 149621312
IPNI 577897-1
iNaturalist 428138
GBIF 7271507
Wikipedia Chisocheton_macrophyllus

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
Emerging paradigms of viral diseases and paramount role of natural resources as antiviral agents Sagaya Jansi R, Khusro A, Agastian P, Alfarhan A, Al-Dhabi NA, Arasu MV, Rajagopal R, Barcelo D, Al-Tamimi A Sci Total Environ 07-Nov-2020
PMCID:PMC7833357
doi:10.1016/j.scitotenv.2020.143539
PMID:33234268
The Translation Inhibitor Rocaglamide Targets a Biomolecular Cavity between eIF4A and Polypurine RNA Iwasaki S, Iwasaki W, Takahashi M, Sakamoto A, Watanabe C, Shichino Y, Floor SN, Fujiwara K, Mito M, Dodo K, Sodeoka M, Imataka H, Honma T, Fukuzawa K, Ito T, Ingolia NT Mol Cell 27-Dec-2018
PMCID:PMC6386617
doi:10.1016/j.molcel.2018.11.026
PMID:30595437
Phytochemical Studies on Meliaceous Plants. VIII. Structures and Inhibitory Effects on Epstein-Barr Virus Activation of Triterpenoids from Leaves of Chisocheton macrophyllus King. Akira INADA, Midori SOMEKAWA, Hiroko MURATA, Tsutomu NAKANISHI, Harukuni TOKUDA, Hoyoku NISHINO, Akio IWASHIMA, Dedy DARNAEDI, Jin MURATA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.41.617

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
(5R,8R,9R,10R,13R,14R,17S)-17-[(5R)-5-hydroxy-6-methylhepta-1,6-dien-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 162962166 Click to see CC(=C)C(CCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(=O)C4(C)C)C)C)C)O 440.70 unknown https://doi.org/10.1248/CPB.41.617
17-(5-Hydroxy-6-methylhepta-1,6-dien-2-yl)-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 73082657 Click to see CC(=C)C(CCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(=O)C4(C)C)C)C)C)O 440.70 unknown https://doi.org/10.1248/CPB.41.617
2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-4,5,6,6a,7,8,8a,11,12,13,14,14a-dodecahydro-3H-picene-4a-carboxylic acid 14345396 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C(=O)O)C 454.70 unknown https://doi.org/10.1248/CPB.41.617
3-Oxolup-20(29)-en-28-oic acid 289985 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown https://doi.org/10.1248/CPB.41.617
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown https://doi.org/10.1248/CPB.41.617
Moronic acid 489941 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C(=O)O)C 454.70 unknown https://doi.org/10.1248/CPB.41.617
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.41.617
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.41.617

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