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Eumachia forsteriana

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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 UUID644069ed8a8f2717617552
Scientific name Eumachia forsteriana
Authority (A.Gray) Barrabé, C.M.Taylor & Razafim.
First published in Candollea 72: 309 (2017)

Description Top

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Synonyms Top

Scientific name Authority First published in
Psychotria forsteriana A.Gray Proc. Amer. Acad. Arts 4: 44 (1860)
Psychotria forsteriana var. vitiensis A.Gray Proc. Amer. Acad. Arts 4: 44. 1858
Uragoga forsteriana Drake Fl. Polynésie Franç. : 98 (1893)

Common names Top

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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
  • Pacific
    • South-central Pacific
      • Society Islands
    • Southwestern Pacific
      • Fiji
      • Samoa
      • Tonga
      • Vanuatu

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001426913
Tropicos 100452879
KEW urn:lsid:ipni.org:names:77164469-1
NCBI Taxonomy 1277318
IUCN Red List 197645433
IPNI 77164469-1
GBIF 10991442
Open Tree Of Life 784053

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
Vincosamide Has a Function for Inhibiting Malignant Behaviors of Hepatocellular Carcinoma Cells Zhu MY, Gong ZS, Feng HP, Zhang QY, Liu K, Lin B, Zhang MN, Lin HF, Li MS World J Oncol 22-Oct-2022
PMCID:PMC9635790
doi:10.14740/wjon1514
PMID:36406198
Biological Activity of Naturally Derived Naphthyridines Chabowska G, Barg E, Wójcicka A Molecules 16-Jul-2021
PMCID:PMC8306249
doi:10.3390/molecules26144324
PMID:34299599
Recent Advances on the Total Syntheses of the Communesin Alkaloids and Perophoramidine Trost BM, Osipov M Chemistry 10-Sep-2015
PMCID:PMC4698125
doi:10.1002/chem.201501735
PMID:26353936
Studies on the Alkaloids of the Calycanthaceae and Their Syntheses Xu JB, Cheng KJ Molecules 15-Apr-2015
PMCID:PMC6272451
doi:10.3390/molecules20046715
PMID:25884552
Preliminary Study of the Alkaloids of<i>Psychotria forsteriana</i> A. Roth, B. Kuballa, P. Cabalion, R. Anton Georg Thieme Verlag KG 06-Mar-2007
doi:10.1055/S-2007-969491
Dimeric alkaloids fromPsychotria forsteriana Yacoub Adjibade, Bernard Weniger, Jean C. Quirion, Bernard Kuballa, Pierre Cabalion, Robert Anton Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83062-P
Action of calycanthine on nervous transmission in cockroach central nervous system. Adjibadé Y, Hue B, Pelhate M, Anton R Planta Med 01-Apr-1991
doi:10.1055/S-2006-960040
PMID:1653964
Cytotoxicity on human leukemic and rat hepatoma cell lines of alkaloid extracts of Psychotria forsteriana. Adjibadé Y, Kuballa B, Cabalion P, Jung ML, Beck JP, Anton R Planta Med 01-Dec-1989
doi:10.1055/S-2006-962098
PMID:2616674
Cytotoxic activity of polyindoline alkaloids of Psychotria forsteriana (Rubiaceae) (1). Roth A, Kuballa B, Bounthanh C, Cabalion P, Sévenet T, Beck JP, Anton R Planta Med 01-Dec-1986
doi:10.1055/S-2007-969251
PMID:3494261
Polyindolinic Alkaloids from Psychotria forsteriana. Potent Inhibitors of the Aggregation of Human Platelets. Beretz A, Roth-Georger A, Corre G, Kuballa B, Anton R, Cazenave JP Planta Med 01-Aug-1985
doi:10.1055/S-2007-969496
PMID:17340518

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
(-)-Chimonanthine 599086 Click to see CN1CCC2(C1NC3=CC=CC=C32)C45CCN(C4NC6=CC=CC=C56)C 346.50 unknown https://doi.org/10.1016/0031-9422(91)83062-P
(+)-Chimonanthine 442058 Click to see CN1CCC2(C1NC3=CC=CC=C32)C45CCN(C4NC6=CC=CC=C56)C 346.50 unknown https://doi.org/10.1016/0031-9422(91)83062-P
(3aS)-8b-[(3aS)-3-methyl-1,2,3a,4-tetrahydropyrrolo[2,3-b]indol-8b-yl]-3-methyl-1,2,3a,4-tetrahydropyrrolo[2,3-b]indole 138857792 Click to see CN1CCC2(C1NC3=CC=CC=C32)C45CCN(C4NC6=CC=CC=C56)C 346.50 unknown https://doi.org/10.1055/S-2006-962098
3a,3'a(1H,1'H):7',3''a(1''H)-Terpyrrolo[2,3-b]indole, 2,2',2'',3,3',3'',8,8',8'',8a,8'a,8''a-dodecahydro-1,1',1''-trimethyl- 161244 Click to see CN1CCC2(C1NC3=CC=CC=C32)C4=C5C(=CC=C4)C6(CCN(C6N5)C)C78CCN(C7NC9=CC=CC=C89)C 518.70 unknown https://doi.org/10.1055/S-2006-962098
isopsychotridine C 129011146 Click to see CN1CCC2(C1NC3=CC=CC=C32)C4=C5C(=CC=C4)C6(CCN(C6N5)C)C7=C8C(=CC=C7)C9(CCN(C9N8)C)C1=C2C(=CC=C1)C1(CCN(C1N2)C)C12CCN(C1NC1=CC=CC=C21)C 863.10 unknown https://doi.org/10.1055/S-2007-969496
https://doi.org/10.1055/S-2007-969491
Meso-chimonanthine 11727714 Click to see CN1CCC2(C1NC3=CC=CC=C32)C45CCN(C4NC6=CC=CC=C56)C 346.50 unknown https://doi.org/10.1016/0031-9422(91)83062-P
Psychotridine 171175 Click to see CN1CCC2(C1NC3=CC=CC=C32)C4=C5C(=CC=C4)C6(CCN(C6N5)C)C7=C8C(=CC=C7)C9(CCN(C9N8)C)C12CCN(C1NC1=C(C=CC=C21)C12CCN(C1NC1=CC=CC=C21)C)C 863.10 unknown https://doi.org/10.1055/S-2006-962098
https://doi.org/10.1055/S-2007-969251
https://doi.org/10.1055/S-2007-969491
https://doi.org/10.1055/S-2007-969496
Quadrigemine A 172448 Click to see CN1CCC2(C1NC3=CC=CC=C32)C4=C5C(=CC=C4)C6(CCN(C6N5)C)C78CCN(C7NC9=C(C=CC=C89)C12CCN(C1NC1=CC=CC=C21)C)C 690.90 unknown https://doi.org/10.1055/S-2006-962098
https://doi.org/10.1055/S-2007-969496
https://doi.org/10.1055/S-2007-969491
https://doi.org/10.1055/S-2007-969251
Quadrigemine B 635745 Click to see CN1CCC2(C1NC3=CC=CC=C32)C4=C5C(=CC=C4)C6(CCN(C6N5)C)C7=C8C(=CC=C7)C9(CCN(C9N8)C)C12CCN(C1NC1=CC=CC=C21)C 690.90 unknown https://doi.org/10.1055/S-2007-969251
https://doi.org/10.1055/S-2007-969491
https://doi.org/10.1055/S-2006-962098
https://doi.org/10.1055/S-2007-969496
SureCN1006038 118701325 Click to see CN1CCC2(C1NC3=CC=CC=C32)C4=C5C(=CC=C4)C6(CCN(C6N5)C)C78CCN(C7NC9=CC=CC=C89)C 518.70 unknown https://doi.org/10.1055/S-2006-962098
> Organoheterocyclic compounds / Quinolines and derivatives / Aminoquinolines and derivatives
(+)-Calycanthine 264115 Click to see CN1CCC23C4NC5=CC=CC=C5C2(C1NC6=CC=CC=C36)CCN4C 346.50 unknown https://doi.org/10.1016/0031-9422(91)83062-P
(1R,9R,13R,21R)-10,22-dimethyl-8,10,20,22-tetrazahexacyclo[11.11.0.01,21.02,7.09,13.014,19]tetracosa-2,4,6,14,16,18-hexaene 162999645 Click to see CN1CCC23C1NC4=CC=CC=C4C25CCN(C5NC6=CC=CC=C36)C 346.50 unknown https://doi.org/10.1016/0031-9422(91)83062-P
5,10b:11,4b-Bis(iminoethano)dibenzo[c,h][2,6]naphthyridine,5,6,11,12-tetrahydro-13,18-dimethyl-, (4bS,5R,10bS,11R) 5479813 Click to see CN1CCC23C4NC5=CC=CC=C5C2(C1NC6=CC=CC=C36)CCN4C 346.50 unknown https://doi.org/10.1016/0031-9422(91)83062-P
Calycanthine 5392245 Click to see CN1CCC23C4NC5=CC=CC=C5C2(C1NC6=CC=CC=C36)CCN4C 346.50 unknown https://doi.org/10.1055/S-2006-960040
https://doi.org/10.1016/0031-9422(91)83062-P
iso-Calycanthine 101618942 Click to see CC1CNC2C13C4=CC=CC=C4NC5C3(CCN5C)C6=CC=CC=C6N2 346.50 unknown https://doi.org/10.1016/0031-9422(91)83062-P
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
(R)-Hispaglabridin A 4484221 Click to see CC(=CCC1=C(C=CC(=C1O)C2CC3=C(C4=C(C=C3)OC(C=C4)(C)C)OC2)O)C 392.50 unknown https://doi.org/10.1016/0031-9422(91)83062-P

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