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Strychnos mellodora

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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 UUID644058e0423ba776186410
Scientific name Strychnos mellodora
Authority S.Moore
First published in J. Linn. Soc., Bot. 40: 147 (1911)

Description Top

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Synonyms Top

No known synonyms.

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Tanzania
    • South Tropical Africa
      • Mozambique
      • Zimbabwe

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001273372
Tropicos 50263867
KEW urn:lsid:ipni.org:names:547322-1
The Plant List tro-50263867
Open Tree Of Life 5145450
NCBI Taxonomy 1343448
IUCN Red List 34640
IPNI 547322-1
iNaturalist 444012
GBIF 5645409
Freebase /m/02y_nqk
USDA GRIN 35849
Wikipedia Strychnos_mellodora

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
In vivo antimalarial activity of crude extracts and solvent fractions of leaves of Strychnos mitis in Plasmodium berghei infected mice Fentahun S, Makonnen E, Awas T, Giday M BMC Complement Altern Med 05-Jan-2017
PMCID:PMC5217609
doi:10.1186/s12906-016-1529-7
PMID:28056932
Plant-Derived Antimalarial Agents: New Leads and Efficient Phytomedicines. Part II. Non-Alkaloidal Natural Products Batista R, de Jesus Silva Júnior A, de Oliveira AB Molecules 13-Aug-2009
PMCID:PMC6254980
doi:10.3390/molecules14083037
PMID:19701144
Rigorous Biogenetic Network for a Group of Indole Alkaloids Derived from Strictosidine Szabó LF Molecules 27-Aug-2008
PMCID:PMC6245392
doi:10.3390/molecules13081875
PMID:18794791
Alkaloids and a pimarane diterpenoid from Strychnos vanprukii. Thongphasuk P, Suttisri R, Bavovada R, Verpoorte R Phytochemistry 01-Oct-2003
doi:10.1016/S0031-9422(03)00508-9
PMID:14559288
β-Carboline glucoalkaloids from Strychnos mellodora V BRANDT, M TITS, A GEERLINGS, M FREDERICH, J PENELLE, C DELAUDE, R VERPOORTE, L ANGENOT Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00129-6
Glucoindole alkaloids from stem bark of Strychnos mellodora. Tits M, Brandt V, Wauters JN, Delaude C, Llabres G, Angenot L Planta Med 01-Feb-1996
doi:10.1055/S-2006-957807
PMID:17252413

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
> Alkaloids and derivatives / Harmala alkaloids
1,2-Dimethyl-4a,9-dihydropyrido[3,4-b]indole 163106776 Click to see CC1=C2C(C=CN1C)C3=CC=CC=C3N2 198.26 unknown https://doi.org/10.1016/S0031-9422(99)00129-6
2H-Pyrido(3,4-b)indole, 1,2-dimethyl- 184129 Click to see CC1=C2C(=C3C=CC=CC3=N2)C=CN1C 196.25 unknown https://doi.org/10.1016/S0031-9422(99)00129-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
1-(3-Methyl-2-butenoyl)-6-apiosylglucose 74029762 Click to see CC(=CC(=O)OC1C(C(C(C(O1)COC2C(C(CO2)(CO)O)O)O)O)O)C 394.37 unknown https://doi.org/10.1016/S0031-9422(99)00129-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2S,3R,4S)-3-ethenyl-4-[(2-methylpyrido[3,4-b]indol-1-yl)methyl]-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylic acid 163191299 Click to see CN1C=CC2=C3C=CC=CC3=NC2=C1CC4C(C(OC=C4C(=O)O)OC5C(C(C(C(O5)CO)O)O)O)C=C 526.50 unknown https://doi.org/10.1016/S0031-9422(99)00129-6
1-[[(2S,3R,4R)-3-ethenyl-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]methyl]-9H-pyrido[3,4-b]indole-3-carboxylic acid 162998836 Click to see COC(=O)C1=COC(C(C1CC2=C3C(=CC(=N2)C(=O)O)C4=CC=CC=C4N3)C=C)OC5C(C(C(C(O5)CO)O)O)O 570.50 unknown https://doi.org/10.1016/S0031-9422(99)00129-6
1-[[(2S,3R,4S)-3-ethenyl-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]methyl]-9H-pyrido[3,4-b]indole-3-carboxylic acid 21577866 Click to see COC(=O)C1=COC(C(C1CC2=C3C(=CC(=N2)C(=O)O)C4=CC=CC=C4N3)C=C)OC5C(C(C(C(O5)CO)O)O)O 570.50 unknown https://doi.org/10.1016/S0031-9422(99)00129-6
3-ethenyl-4-[(2-methylpyrido[3,4-b]indol-1-yl)methyl]-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylic acid 163195772 Click to see CN1C=CC2=C3C=CC=CC3=NC2=C1CC4C(C(OC=C4C(=O)O)OC5C(C(C(C(O5)CO)O)O)O)C=C 526.50 unknown https://doi.org/10.1016/S0031-9422(99)00129-6
Dolichantoside 10437390 Click to see CN1CCC2=C(C1CC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C)NC5=CC=CC=C25 544.60 unknown https://doi.org/10.1016/S0031-9422(99)00129-6
https://doi.org/10.1055/S-2006-957807
Isodolichantoside 21579183 Click to see CN1CCC2=C(C1CC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C)NC5=CC=CC=C25 544.60 unknown https://doi.org/10.1016/S0031-9422(99)00129-6
methyl (2S,3R,4R)-3-ethenyl-4-[[(1S)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl]methyl]-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 154497529 Click to see COC(=O)C1=COC(C(C1CC2C3=C(CCN2)C4=CC=CC=C4N3)C=C)OC5C(C(C(C(O5)CO)O)O)O 530.60 unknown https://doi.org/10.1055/S-2006-957807
methyl (2S,3S,4S)-3-ethenyl-4-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]-2-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 162936915 Click to see CN1CCC2=C(C1CC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C)NC5=CC=CC=C25 544.60 unknown https://doi.org/10.1055/S-2006-957807
methyl 3-ethenyl-4-(2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-ylmethyl)-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 3262516 Click to see COC(=O)C1=COC(C(C1CC2C3=C(CCN2)C4=CC=CC=C4N3)C=C)OC5C(C(C(C(O5)CO)O)O)O 530.60 unknown https://doi.org/10.1055/S-2006-957807
methyl 3-ethenyl-4-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 73803915 Click to see CN1CCC2=C(C1CC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C)NC5=CC=CC=C25 544.60 unknown https://doi.org/10.1055/S-2006-957807
https://doi.org/10.1016/S0031-9422(99)00129-6
Palicoside 10029943 Click to see CN1CCC2=C(C1CC3C(C(OC=C3C(=O)O)OC4C(C(C(C(O4)CO)O)O)O)C=C)NC5=CC=CC=C25 530.60 unknown https://doi.org/10.1016/S0031-9422(99)00129-6
https://doi.org/10.1016/S0031-9422(03)00508-9
https://doi.org/10.1055/S-2006-957807
Strictosidine 161336 Click to see COC(=O)C1=COC(C(C1CC2C3=C(CCN2)C4=CC=CC=C4N3)C=C)OC5C(C(C(C(O5)CO)O)O)O 530.60 unknown https://doi.org/10.1016/S0031-9422(99)00129-6
https://doi.org/10.1055/S-2006-957807
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1R,3S,4R,6S,7S,8R,12R)-4-(hydroxymethyl)-1,8-dimethyl-12-propan-2-yltricyclo[9.3.0.03,7]tetradec-10-ene-6,8-diol 139588901 Click to see CC(C)C1CCC2(C1=CCC(C3C(CC(C3C2)CO)O)(C)O)C 322.50 unknown https://doi.org/10.1016/S0031-9422(99)00129-6
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
2,3,4-Trihydroxybutyl 3-(4-methoxy-6-oxopyran-2-yl)but-2-enoate 78163264 Click to see CC(=CC(=O)OCC(C(CO)O)O)C1=CC(=CC(=O)O1)OC 314.29 unknown https://doi.org/10.1016/S0031-9422(99)00129-6
https://doi.org/10.1055/S-2006-957807
https://doi.org/10.1016/S0031-9422(03)00508-9

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