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Microtropis triflora

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 UUID6440593bdf955061602319
Scientific name Microtropis triflora
Authority Merr. & Freeman
First published in Proc. Amer. Acad. Arts 73: 288 (1940)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Microtropis triflora var. sichuanensis C.Y.Cheng & T.C.Kao Acta Phytotax. Sin. 26: 314 (1988)
Microtropis fokienensis var. longipedunculata W.C.Cheng Contr. Biol. Lab. Sci. Soc. China 9: 199 1934

Common names Top

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Language Common/alternative name
Chinese 三花假卫矛

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001275845
Tropicos 50283488
KEW urn:lsid:ipni.org:names:162230-1
The Plant List tro-50283488
Open Tree Of Life 1045126
NCBI Taxonomy 1089421
IPNI 162230-1
iNaturalist 736442
GBIF 7265485
EOL 2888857

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
The Complete Chloroplast Genome of Catha edulis: A Comparative Analysis of Genome Features with Related Species Gu C, Tembrock LR, Zheng S, Wu Z Int J Mol Sci 09-Feb-2018
PMCID:PMC5855747
doi:10.3390/ijms19020525
PMID:29425128
A New Friedelane Type Triterpene from Euonymus hederaceus Sun CR, Hu HJ, Xu RS, Yang JH, Wan HT Molecules 17-Jul-2009
PMCID:PMC6255324
doi:10.3390/molecules14072650
PMID:19633630
Novel Triterpenoids from <i>Microtropis triflora</i> with Antitumor Activities Kui‐Wu Wang, Hong Zhang, Yuan‐Jiang Pan Wiley 20-Feb-2007
doi:10.1002/HLCA.200790031

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
(4aS,6aS,6aR,6bS,8aS,9R,12aS,14aS,14bS)-2,2,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid 44593504 Click to see 456.70 unknown https://doi.org/10.1002/HLCA.200790031
2,2,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid 75055060 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C)C 456.70 unknown https://doi.org/10.1002/HLCA.200790031
29-Hydroxyfriedelan-3-one 14108943 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)C 442.70 unknown https://doi.org/10.1002/HLCA.200790031
D:A-Friedooleanan-3-one, 29-hydroxy-, (20alpha)- 588284 Click to see 442.70 unknown https://doi.org/10.1002/HLCA.200790031
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1002/HLCA.200790031
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1002/HLCA.200790031
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(2R,4aS,6aS,6aR,6bS,11S,12aS,14aS,14bR)-11-hydroxy-2,4a,6a,6a,9,14a-hexamethyl-1,2,4,5,6,6b,7,8,11,12,12a,13,14,14b-tetradecahydropicene-3,10-dione 16115339 Click to see CC1CC2C(CCC3(C2(CCC4(C3CCC5=C(C(=O)C(CC54)O)C)C)C)C)(CC1=O)C 426.60 unknown https://doi.org/10.1002/HLCA.200790031
11-Hydroxy-2,4a,6a,6a,9,14a-hexamethyl-1,2,4,5,6,6b,7,8,11,12,12a,13,14,14b-tetradecahydropicene-3,10-dione 163073443 Click to see CC1CC2C(CCC3(C2(CCC4(C3CCC5=C(C(=O)C(CC54)O)C)C)C)C)(CC1=O)C 426.60 unknown https://doi.org/10.1002/HLCA.200790031
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1R,4S,5R,8R,9S,11R,13S,14S,17R,18S,20S,21R,24R)-9,20,21-trihydroxy-5,8,11,14,17,24-hexamethyl-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracosane-10,23-dione 162995009 Click to see 488.70 unknown https://doi.org/10.1002/HLCA.200790031
(1R,4S,5R,8R,9S,11R,13S,14S,17R,18S,21S,24R)-9,21-dihydroxy-5,8,11,14,17,24-hexamethyl-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracosane-10,23-dione 162871560 Click to see 472.70 unknown https://doi.org/10.1002/HLCA.200790031
9,20,21-Trihydroxy-5,8,11,14,17,24-hexamethyl-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracosane-10,23-dione 162995008 Click to see CC1CC2C(CCC3(C2(CCC4(C3CCC56C4CC(C(C5C)(OC6=O)O)O)C)C)C)(C(C1=O)O)C 488.70 unknown https://doi.org/10.1002/HLCA.200790031
9,21-Dihydroxy-5,8,11,14,17,24-hexamethyl-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracosane-10,23-dione 162871559 Click to see CC1CC2C(CCC3(C2(CCC4(C3CCC56C4CCC(C5C)(OC6=O)O)C)C)C)(C(C1=O)O)C 472.70 unknown https://doi.org/10.1002/HLCA.200790031
> Organoheterocyclic compounds / Naphthopyrans
(1R,4S,5R,8R,9S,11R,13S,14S,17R,18S,20S,23R,24S)-9,20,24-trihydroxy-5,8,11,14,17,23-hexamethyl-21-oxahexacyclo[18.2.2.01,18.04,17.05,14.08,13]tetracosane-10,22-dione 102273879 Click to see CC1CC2C(CCC3(C2(CCC4(C3CCC56C4CC(C(C5C)O)(OC6=O)O)C)C)C)(C(C1=O)O)C 488.70 unknown https://doi.org/10.1002/HLCA.200790031
9,20,24-Trihydroxy-5,8,11,14,17,23-hexamethyl-21-oxahexacyclo[18.2.2.01,18.04,17.05,14.08,13]tetracosane-10,22-dione 163036181 Click to see 488.70 unknown https://doi.org/10.1002/HLCA.200790031

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