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Thamnosma rhodesica

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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 UUID643ffea6b67f7183488730
Scientific name Thamnosma rhodesica
Authority (Baker f.) Mendonça
First published in Fl. Zambes. 2: 183 (1963)

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
    • South Tropical Africa
      • Zimbabwe
    • Southern Africa
      • Botswana

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000455269
Tropicos 28100712
KEW urn:lsid:ipni.org:names:775386-1
Open Tree Of Life 123379
NCBI Taxonomy 675746
IPNI 775386-1
iNaturalist 595337
GBIF 3835929
CMAUP NPO28975

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
Evolution of Acridines and Xanthenes as a Core Structure for the Development of Antileishmanial Agents Silva CF, Pinto DC, Fernandes PA, Silva AM Pharmaceuticals (Basel) 26-Jan-2022
PMCID:PMC8879592
doi:10.3390/ph15020148
PMID:35215261
Computational study to discover potent phytochemical inhibitors against drug target, squalene synthase from Leishmania donovani Wadanambi PM, Mannapperuma U Heliyon 31-May-2021
PMCID:PMC8188062
doi:10.1016/j.heliyon.2021.e07178
PMID:34141935
Antileishmanial and antifungal acridone derivatives from the roots of Thamnosma rhodesica. Ahua KM, Ioset JR, Ransijn A, Mauël J, Mavi S, Hostettmann K Phytochemistry 01-Apr-2004
doi:10.1016/J.PHYTOCHEM.2003.12.020
PMID:15081302

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
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
(2R)-2-[(2S)-1,2-dihydroxypropan-2-yl]-5-hydroxy-11-methyl-1,2-dihydrofuro[2,3-c]acridin-6-one 162890122 Click to see CC(CO)(C1CC2=C(O1)C=C(C3=C2N(C4=CC=CC=C4C3=O)C)O)O 341.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.020
(2R)-5-hydroxy-11-methyl-2-prop-1-en-2-yl-1,2-dihydrofuro[2,3-c]acridin-6-one 11623705 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2N(C4=CC=CC=C4C3=O)C)O 307.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.020
1-Hydroxy-10-methylacridone 5376484 Click to see CN1C2=C(C(=CC=C2)O)C(=O)C3=CC=CC=C31 225.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.020
Gravacridonediol 5317836 Click to see CC(CO)(C1CC2=C(O1)C=C(C3=C2N(C4=CC=CC=C4C3=O)C)O)O 341.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.020
methyl (2R)-2,3-dihydroxy-2-[(2R)-5-hydroxy-11-methyl-6-oxo-1,2-dihydrofuro[2,3-c]acridin-2-yl]propanoate 162955295 Click to see CN1C2=CC=CC=C2C(=O)C3=C1C4=C(C=C3O)OC(C4)C(CO)(C(=O)OC)O 385.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.020
Rhodesiacridone 10430166 Click to see CN1C2=CC=CC=C2C(=O)C3=C1C4=C(C=C3O)OC(C4)C(CO)(C(=O)OC)O 385.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.020
Rutacridone 5281849 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2N(C4=CC=CC=C4C3=O)C)O 307.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.020
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
2-(2-Hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one 604512 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.020
Marmesin 334704 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.020
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.020
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
(Rac)-Byakangelicin 616063 Click to see CC(C)(C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)O)O 334.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.020
9-[(2S)-2,3-dihydroxy-3-methylbutoxy]-4-methoxyfuro[3,2-g]chromen-7-one 5315583 Click to see CC(C)(C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)O)O 334.30 unknown via CMAUP database
Byakangelicin 10211 Click to see CC(C)(C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)O)O 334.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.020
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
9-Methoxy-5-(3-methylbut-2-enoxy)furo[3,2-g]chromen-7-one 53398727 Click to see CC(=CCOC1=CC(=O)OC2=C1C=C3C=COC3=C2OC)C 300.30 unknown via CMAUP database
Cnidilin 821449 Click to see CC(=CCOC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC)C 300.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.020
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.020
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
QUERCETIN 3-O-beta-D-GLUCURONIDE METHYL ESTER 21722016 Click to see COC(=O)C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 492.40 unknown via CMAUP database
Querciturone 5274585 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-8-O-glucuronides
HYPOLAETIN 8-O-beta-D-GLUCURONIDE 14887605 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown via CMAUP database
ISOSCUTELLAREIN 8-O-beta-D-GLUCURONIDE 14332450 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O 462.40 unknown via CMAUP database
ISOSCUTELLAREIN 8-O-beta-D-GLUCURONIDE 6''-METHYL ESTER 44566911 Click to see COC(=O)C1C(C(C(C(O1)OC2=C(C=C(C3=C2OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O)O 476.40 unknown via CMAUP database
theograndin I 11156985 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)OS(=O)(=O)O)O)O 542.40 unknown via CMAUP database
Theograndin II 11272944 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)OS(=O)(=O)O)O)O)O 558.40 unknown via CMAUP database

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