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Schumanniophyton problematicum

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 UUID643fec7693602532766186
Scientific name Schumanniophyton problematicum
Authority (A.Chev.) Aubrév.
First published in Fl. Forest. Côte d'Ivoire , ed. 2, 3: 255 (1959)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Assidora problematica A.Chev. Compt. Rend. Hebd. Séances Acad. Sci. 226: 1117 (1948)

Common names Top

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Language Common/alternative name
Armenian Շումաննիոֆիթոն պրոբլեմատիկում

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-0000307164
Tropicos 50109170
KEW urn:lsid:ipni.org:names:766235-1
The Plant List kew-188462
Open Tree Of Life 3877868
NCBI Taxonomy 2708974
IUCN Red List 34819
IPNI 766235-1
iNaturalist 443409
GBIF 2899640
Freebase /m/02xcyfg
EOL 1109765
USDA GRIN 467795
Wikipedia Schumanniophyton_problematicum

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 Pharmacological Implications of Flavopiridol: An Updated Overview Joshi H, Tuli HS, Ranjan A, Chauhan A, Haque S, Ramniwas S, Bhatia GK, Kandari D Molecules 10-Nov-2023
PMCID:PMC10673037
doi:10.3390/molecules28227530
PMID:38005250
Anti-leishmanial and Anti-inflammatory Agents from Endophytes: A Review Toghueo RM Nat Prod Bioprospect 28-Sep-2019
PMCID:PMC6814666
doi:10.1007/s13659-019-00220-5
PMID:31564050
Anticancer Alkaloids from Trees: Development into Drugs Isah T Pharmacogn Rev 01-Jul-2016
PMCID:PMC5214563
doi:10.4103/0973-7847.194047
PMID:28082790
The Chromone Alkaloid, Rohitukine, Affords Anti-Cancer Activity via Modulating Apoptosis Pathways in A549 Cell Line and Yeast Mitogen Activated Protein Kinase (MAPK) Pathway Safia, Kamil M, Jadiya P, Sheikh S, Haque E, Nazir A, Lakshmi V, Mir SS PLoS One 25-Sep-2015
PMCID:PMC4583253
doi:10.1371/journal.pone.0137991
PMID:26405812
Secondary Metabolites from Rubiaceae Species Martins D, Nunez CV Molecules 22-Jul-2015
PMCID:PMC6331836
doi:10.3390/molecules200713422
PMID:26205062
Chromone and Flavonoid Alkaloids: Occurrence and Bioactivity Khadem S, Marles RJ Molecules 27-Dec-2011
PMCID:PMC6268529
doi:10.3390/molecules17010191
PMID:22202807
High performance liquid chromatographic analysis of chromone alkaloids from <i>Schumanniophyton</i> species Peter J. Houghton, Tibebe Z. Woldemariam Wiley 07-Mar-2007
doi:10.1002/PCA.2800040103
On the contents of schumanniophyton problematicum (rubiaceae) Emil Schlittler, Ulrich Spitaler Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(01)94896-8

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 / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,3R,4R,5S,6S)-6-[[(3S,4aS,6aS,6bS,8aS,11S,12R,12aR,14aR,14bS)-12-hydroxy-4,4,6a,6b,11,12,14b-heptamethyl-8a-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 163023957 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1(C)O)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O 811.00 unknown https://doi.org/10.1016/S0040-4039(01)94896-8
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
(4S)-4-(5,7-dihydroxy-2-methyl-4-oxochromen-6-yl)piperidin-2-one 163069945 Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)C3CCNC(=O)C3)O 289.28 unknown https://doi.org/10.1016/S0040-4039(01)94896-8
Noreugenin 5375252 Click to see 192.17 unknown https://doi.org/10.1002/PCA.2800040103
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
8,12-Dihydroxy-4-methyl-3,11-dioxa-15-azatetracyclo[8.8.0.02,7.013,18]octadeca-1(10),2(7),4,8-tetraene-6,14-dione 9883434 Click to see CC1=CC(=O)C2=C(O1)C3=C(C=C2O)OC(C4C3CCNC4=O)O 317.29 unknown https://doi.org/10.1002/PCA.2800040103
> Organoheterocyclic compounds / Piperidines / Phenylpiperidines
(4S)-4-(5,7-dihydroxy-2-methyl-4-oxochromen-6-yl)-1-methylpiperidin-2-one 162898496 Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)C3CCN(C(=O)C3)C)O 303.31 unknown https://doi.org/10.1016/S0040-4039(01)94896-8
4-(5,7-Dihydroxy-2-methyl-4-oxochromen-6-yl)-1-methylpiperidin-2-one 162898495 Click to see 303.31 unknown https://doi.org/10.1016/S0040-4039(01)94896-8
4-(5,7-Dihydroxy-2-methyl-4-oxochromen-6-yl)piperidin-2-one 163069944 Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)C3CCNC(=O)C3)O 289.28 unknown https://doi.org/10.1016/S0040-4039(01)94896-8
5,7-Dihydroxy-8-(3-hydroxy-1-methyl-4-piperidinyl)-2-methyl-4H-1-benzopyran-4-one 5387431 Click to see 305.32 unknown https://doi.org/10.1002/PCA.2800040103
Rohitukine 13422573 Click to see CC1=CC(=O)C2=C(O1)C(=C(C=C2O)O)C3CCN(CC3O)C 305.32 unknown https://doi.org/10.1002/PCA.2800040103
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1002/PCA.2800040103
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
14-Methyl-9,13-dioxa-5-azatetracyclo[8.8.0.02,7.012,17]octadeca-1,3,6,10,12(17),14-hexaene-8,16,18-trione 13892290 Click to see CC1=CC(=O)C2=C(O1)C=C3C(=C4C=CNC=C4C(=O)O3)C2=O 295.25 unknown https://doi.org/10.1002/PCA.2800040103

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