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Internal ID UUID643fe90d5a57a696849658
Scientific name Prismatomeris tetrandra
Authority K.Schum.
First published in Nat. Pflanzenfam. 4(4): 138 (1891)

Description Top

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Synonyms Top

Scientific name Authority First published in
Coffea tetrandra Roxb. Fl. Ind. 2: 193 (1824)
Prismatomeris tetrandra var. multiflora (Ridl.) Y.Z.Ruan Acta Phytotax. Sin. 26: 447 1988

Common names Top

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Language Common/alternative name
Chinese 南山花
Chinese 拉拉藤
Chinese 黄根
Chinese 四蕊三角瓣花
Chinese 多花三角瓣花
Chinese 海南三角瓣花

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Prismatomeris tetrandra subsp. malayana (Ridl.) J.T.Johanss. Opera Bot. 94: 29 (1987)
Prismatomeris tetrandra subsp. tetrandra Unknown

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-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Malaya
      • Philippines

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000283198
Tropicos 50058414
KEW urn:lsid:ipni.org:names:761152-1
The Plant List kew-165482
Open Tree Of Life 474175
NCBI Taxonomy 110690
IPNI 761152-1
iNaturalist 426489
GBIF 2909739
EOL 1106120

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
Iridoid Derivatives as Anticancer Agents: An Updated Review from 1970–2022 Ndongwe T, Witika BA, Mncwangi NP, Poka MS, Skosana PP, Demana PH, Summers B, Siwe-Noundou X Cancers (Basel) 26-Jan-2023
PMCID:PMC9913650
doi:10.3390/cancers15030770
PMID:36765728
Synthesis and Biological Evaluations of Betulinic Acid Derivatives With Inhibitory Activity on Hyaluronidase and Anti-Inflammatory Effects Against Hyaluronic Acid Fragment Induced Inflammation Luo Z, He H, Tang T, Zhou J, Li H, Seeram NP, Li D, Zhang K, Ma H, Wu P Front Chem 04-May-2022
PMCID:PMC9115581
doi:10.3389/fchem.2022.892554
PMID:35601554
Ethnomedicinal Plants in Herbal Remedies Used for Treatment of Skin Diseases by Traditional Healers in Songkhla Province, Thailand Saising J, Maneenoon K, Sakulkeo O, Limsuwan S, Götz F, Voravuthikunchai SP Plants (Basel) 25-Mar-2022
PMCID:PMC9003147
doi:10.3390/plants11070880
PMID:35406860
Chemistry, Biosynthesis, Physicochemical and Biological Properties of Rubiadin: A Promising Natural Anthraquinone for New Drug Discovery and Development Watroly MN, Sekar M, Fuloria S, Gan SH, Jeyabalan S, Wu YS, Subramaniyan V, Sathasivam KV, Ravi S, Mat Rani NN, Lum PT, Vaijanathappa J, Meenakshi DU, Mani S, Fuloria NK Drug Des Devel Ther 03-Nov-2021
PMCID:PMC8576757
doi:10.2147/DDDT.S338548
PMID:34764636
Plant Functional Niches in Forests Across Four Climatic Zones: Exploring the Periodic Table of Niches Based on Plant Functional Traits Yu R, Huang J, Xu Y, Ding Y, Zang R Front Plant Sci 17-Jun-2020
PMCID:PMC7311788
doi:10.3389/fpls.2020.00841
PMID:32625227
Data Analysis in Chemistry and Bio-Medical Sciences Todeschini R, Pazos A, Arrasate S, González-Díaz H Int J Mol Sci 14-Dec-2016
PMCID:PMC5187905
doi:10.3390/ijms17122105
PMID:27983646
Hyaluronidase Inhibitory Activity of Pentacylic Triterpenoids from Prismatomeris tetrandra (Roxb.) K. Schum: Isolation, Synthesis and QSAR Study Abdullah NH, Thomas NF, Sivasothy Y, Lee VS, Liew SY, Noorbatcha IA, Awang K Int J Mol Sci 14-Feb-2016
PMCID:PMC4783877
doi:10.3390/ijms17020143
PMID:26907251
Secondary Metabolites from Rubiaceae Species Martins D, Nunez CV Molecules 22-Jul-2015
PMCID:PMC6331836
doi:10.3390/molecules200713422
PMID:26205062
Prismatomerin, a new iridoid from Prismatomeris tetrandra. Structure elucidation, determination of absolute configuration, and cytotoxicity. Krohn K, Gehle D, Dey SK, Nahar N, Mosihuzzaman M, Sultana N, Sohrab MH, Stephens PJ, Pan JJ, Sasse F J Nat Prod 01-Aug-2007
doi:10.1021/NP070202+
PMID:17665951
Anthraquinones from the Roots of Prismatomeris tetrandra. Zi‐Ming Feng, Jian‐Shuang Jiang, Ying‐Hong Wang, Pei‐Cheng Zhang Wiley 03-Mar-2006
doi:10.1002/CHIN.200612237
Anthraquinones from the roots of Prismatomeris tetrandra. Feng ZM, Jiang JS, Wang YH, Zhang PC Chem Pharm Bull (Tokyo) 01-Oct-2005
doi:10.1248/CPB.53.1330
PMID:16204995

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
> Benzenoids / Anthracenes / Anthraquinones
1-Hydroxy-2-methylanthraquinone 160817 Click to see CC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 238.24 unknown https://doi.org/10.1248/CPB.53.1330
1-Hydroxy-2,3-dimethoxy-7-methyl-9,10-anthraquinone 11637974 Click to see CC1=CC2=C(C=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)OC)OC 298.29 unknown https://doi.org/10.1248/CPB.53.1330
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3-Dihydroxy-2-methoxyanthracene-9,10-dione 146101 Click to see COC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 270.24 unknown https://doi.org/10.1248/CPB.53.1330
1,5,6-Trimethoxy-2-methyl-3-hydroxy-9,10-anthraquinone 11515404 Click to see CC1=C(C=C2C(=C1OC)C(=O)C3=C(C2=O)C(=C(C=C3)OC)OC)O 328.30 unknown https://doi.org/10.1248/CPB.53.1330
2-Hydroxy-3-(hydroxymethyl)anthraquinone 44445519 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C(=C3)CO)O 254.24 unknown https://doi.org/10.1248/CPB.53.1330
9,10-Anthracenedione, 1,3-dihydroxy-5,6-dimethoxy-2-methyl- 11652569 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=C(C2=O)C(=C(C=C3)OC)OC)O 314.29 unknown https://doi.org/10.1248/CPB.53.1330
Rubiadin 124062 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown https://doi.org/10.1002/CHIN.200612237
https://doi.org/10.1248/CPB.53.1330
Rubiadin 1-methyl ether 96191 Click to see CC1=C(C=C2C(=C1OC)C(=O)C3=CC=CC=C3C2=O)O 268.26 unknown https://doi.org/10.1248/CPB.53.1330
https://doi.org/10.1002/CHIN.200612237
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Gaertneroside 44559436 Click to see COC(=O)C1=COC(C2C1C=CC23C=C(C(=O)O3)C(C4=CC=C(C=C4)O)O)OC5C(C(C(C(O5)CO)O)O)O 548.50 unknown https://doi.org/10.1021/NP070202+
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
3-o-Acetylprismatomerin 23625550 Click to see CC(=O)OC1=CC=C(C=C1)C=C2C3C4(C=CC5C4C(O3)OC=C5C(=O)OC)OC2=O 410.40 unknown https://doi.org/10.1021/NP070202+
methyl (1S,4S,8R,10S,11Z,14S)-11-[(4-hydroxyphenyl)methylidene]-12-oxo-7,9,13-trioxatetracyclo[6.5.1.01,10.04,14]tetradeca-2,5-diene-5-carboxylate 129846269 Click to see COC(=O)C1=COC2C3C1C=CC34C(O2)C(=CC5=CC=C(C=C5)O)C(=O)O4 368.30 unknown https://doi.org/10.1021/NP070202+
Prismatomerin 23625548 Click to see COC(=O)C1=COC2C3C1C=CC34C(O2)C(=CC5=CC=C(C=C5)O)C(=O)O4 368.30 unknown https://doi.org/10.1021/NP070202+

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