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Gymnosporia putterlickioides subsp. putterlickioides

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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
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Details Top

Internal ID UUID64406acca600a120659590
Scientific name Gymnosporia putterlickioides subsp. putterlickioides

Description Top

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Common names Top

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Varieties (abbr. var.) 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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001441315
KEW urn:lsid:ipni.org:names:77230333-1
iNaturalist 599509
GBIF 7265742

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)!
Title Authors Publication Released IDs
Antiplasmodial sesquiterpene alkaloids from the roots of Maytenus mekongensis. Lhinhatrakool T, Prabpai S, Kongsaeree P, Sutthivaiyakit S J Nat Prod 24-Jun-2011
doi:10.1021/NP200014K
PMID:21634414
Bioactive sesquiterpene pyridine alkaloids from Maytenus aquifolium Joaquim Corsino, Vanderlan da Silva Bolzani, Ana Maria S. Pereira, Suzelei Castro França, Maysa Furlan Elsevier BV 01-May-2003
doi:10.1016/S0031-9422(97)00824-8
Dihydroagarofuran sesquiterpene alkaloids from Maytenus putterlickoides. Schaneberg BT, Green DK, Sneden AT J Nat Prod 01-May-2001
doi:10.1021/NP010041O
PMID:11374957

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
[(1R,3R,13R,14S,17R,18S,19R,20R,21S,22S,23S,24S,25R)-18,21,22,24-tetraacetyloxy-20-(acetyloxymethyl)-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-19-yl] benzoate 162968439 Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C6=CC=CC=C6)OC(=O)C)C 867.80 unknown https://doi.org/10.1021/NP010041O
[(1R,3S,13R,14S,17R,18S,19S,20S,21R,22S,23S,24S,25R)-18,21,22,24-tetraacetyloxy-20-(acetyloxymethyl)-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-19-yl] benzoate 133562434 Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C6=CC=CC=C6)OC(=O)C)C 867.80 unknown https://doi.org/10.1021/NP010041O
[18,21,22,24-Tetraacetyloxy-20-(acetyloxymethyl)-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-19-yl] benzoate 14635608 Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C6=CC=CC=C6)OC(=O)C)C 867.80 unknown https://doi.org/10.1021/NP200014K
Aquifoliunine EIV 85368858 Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C6=CN=CC=C6)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C 868.80 unknown https://doi.org/10.1016/S0031-9422(97)00824-8
Mayteine 3086511 Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C6=CC=CC=C6)OC(=O)C)C 867.80 unknown https://doi.org/10.1021/NP010041O

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