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Cassipourea gummiflua

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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 UUID64400f9b691d4769210512
Scientific name Cassipourea gummiflua
Authority Tul.
First published in Ann. Sci. Nat., Bot. , sér. 4, 6: 123 (1856)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cassipourea glabra Alston Wiss. Erg. Deut. Zentr.-Afr. Exped., Bot. 2: 274 (1922)
Cassipourea gummiflua var. mannii (Hook.f. ex Oliv.) J.Lewis Kew Bull. 10: 147 1955
Cassipourea gummiflua var. ugandensis (Stapf) J.Lewis Kew Bull. 10: 147 1955
Cassipourea gummiflua subsp. ugandensis (Stapf) Lye Lidia 4: 92 (1998)
Cassipourea gummiflua var. verticillata (N.E.Br.) J.Lewis Kew Bull. 10: 147 1955
Cassipourea mannii Engl. Bot. Jahrb. Syst. 54: 369 (1917)
Cassipourea paradoxa Alston Wiss. Erg. Deut. Zentr.-Afr. Exped., Bot. 2: 275 (1922)
Cassipourea redslobii Engl. Bot. Jahrb. Syst. 54: 368 (1917)
Cassipourea ugandensis (Stapf) Engl. Veg. Erde 9(III 2): 673 (1921)
Cassipourea verticillata N.E.Br. Bull. Misc. Inform. Kew 1894: 5 (1894)
Dactylopetalum gummifluum Baill. Adansonia 3: 22 (1862)
Dactylopetalum mannii Hook.f. ex Oliv. Fl. Trop. Afr. 2: 412 (1871)
Dactylopetalum sessiliflorum Benth. J. Proc. Linn. Soc., Bot. 3: 79 (1859)
Dactylopetalum ugandense Stapf J. Linn. Soc., Bot. 37: 515 (1906)
Dactylopetalum verticillatum Schinz Bull. Herb. Boissier 5: 866 (1897)
Cassipourea verticillata f. decussata Engl. Bot. Jahrb. Syst. 54: 369 1917
Richea gummiflua (Tul.) Baill. Hist. pl. Madag., Atlas (1891) t. 323.
Dactylopetalum gummifluum (Tul.) B.D.Jacks. Index Kew. 2: 709 1893

Common names Top

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Language Common/alternative name
Afrikaans grootblaaruiehout

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
      • Kenya
      • Tanzania
      • Uganda
    • South Tropical Africa
      • Angola
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
      • Swaziland
    • West Tropical Africa
      • Ivory Coast
      • Nigeria
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Madagascar
      • Seychelles

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000589636
Tropicos 27600040
KEW urn:lsid:ipni.org:names:719638-1
The Plant List kew-2704467
Open Tree Of Life 5233423
NCBI Taxonomy 1237416
IUCN Red List 61957203
IPNI 719638-1
iNaturalist 133564
GBIF 3873856
EPPO CUEGM
EOL 5541210

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
Analysis of Three Species of Cassipourea Traditionally Used for Hypermelanosis in Selected Provinces in South Africa Mpofana N, Yalo M, Gqaleni N, Dlova NC, Hussein AA Int J Mol Sci 23-Dec-2023
PMCID:PMC10779010
doi:10.3390/ijms25010237
PMID:38203415
Ethnopharmacology, Phytochemistry, and Global Distribution of Mangroves―A Comprehensive Review Nabeelah Bibi S, Fawzi MM, Gokhan Z, Rajesh J, Nadeem N, R.R. RK, R.D.D.G. A, Pandian SK Mar Drugs 18-Apr-2019
PMCID:PMC6520788
doi:10.3390/md17040231
PMID:31003533
Methylated A-type proanthocyanidins and related metabolites from Cassipourea gummiflua. Drewes SE, Taylor CW Phytochemistry 01-Sep-1994
doi:10.1016/0031-9422(94)85098-4
PMID:7765632
Rhizophoraceae Alkaloids. 1. Four sulphur-containing bases from Cassipourea spp. Wright WG, Warren FL J Chem Soc Perkin 1 01-Jan-1970
doi:10.1039/J39670000283
PMID:6068752

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 / Pyrrolizidines
2,3,12,13-Tetrathia-9,16-diazapentacyclo[12.6.0.04,11.05,9.016,20]icosane 12302510 Click to see C1CC2C3C(CN2C1)SSC4CN5CCCC5C4SS3 346.60 unknown https://doi.org/10.1039/J39670000283
Cassipourine 101821144 Click to see C1CC2C3C(CN2C1)SSC4CN5CCCC5C4SS3 346.60 unknown https://doi.org/10.1039/J39670000283
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1R,5R,6R,13S,21R)-5,13-bis(4-hydroxyphenyl)-17-methoxy-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,19,21-tetrol 162946174 Click to see COC1=CC(=C2C3C(C(OC2=C1)(OC4=C3C5=C(CC(C(O5)C6=CC=C(C=C6)O)O)C(=C4)O)C7=CC=C(C=C7)O)O)O 558.50 unknown https://doi.org/10.1016/0031-9422(94)85098-4
(1R,5S,6R,13S,21R)-5,13-bis(4-hydroxyphenyl)-17-methoxy-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,19,21-tetrol 162946173 Click to see COC1=CC(=C2C3C(C(OC2=C1)(OC4=C3C5=C(CC(C(O5)C6=CC=C(C=C6)O)O)C(=C4)O)C7=CC=C(C=C7)O)O)O 558.50 unknown https://doi.org/10.1016/0031-9422(94)85098-4
(1R,5S,6R,13S,21R)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 162923888 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown https://doi.org/10.1016/0031-9422(94)85098-4
(2S,2''S,3S,3''R,4S)-3,4',5,7-Tetrahydroxyflavan(2->7,4->8)-3,4',5,7-tetrahydroxyflavan 4023574 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown https://doi.org/10.1016/0031-9422(94)85098-4
5,13-Bis(4-hydroxyphenyl)-17-methoxy-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,19,21-tetrol 162946172 Click to see COC1=CC(=C2C3C(C(OC2=C1)(OC4=C3C5=C(CC(C(O5)C6=CC=C(C=C6)O)O)C(=C4)O)C7=CC=C(C=C7)O)O)O 558.50 unknown https://doi.org/10.1016/0031-9422(94)85098-4
Lqrhgtvffpmwcg-lsbowgmisa- 13259907 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown https://doi.org/10.1016/0031-9422(94)85098-4
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
2-(4-Hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 282014 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC=C(C=C3)O)O 274.27 unknown https://doi.org/10.1016/0031-9422(94)85098-4
Afzelechin 442154 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC=C(C=C3)O)O 274.27 unknown https://doi.org/10.1016/0031-9422(94)85098-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-[[5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl]oxy]-6-methyloxane-3,4,5-triol 74977160 Click to see CC1C(C(C(C(O1)OC2CC3=C(C=C(C=C3OC2C4=CC=C(C=C4)O)O)O)O)O)O 420.40 unknown https://doi.org/10.1016/0031-9422(94)85098-4
Afzelechin 3-O-alpha-L-rhamnopyranoside 44257060 Click to see CC1C(C(C(C(O1)OC2CC3=C(C=C(C=C3OC2C4=CC=C(C=C4)O)O)O)O)O)O 420.40 unknown https://doi.org/10.1016/0031-9422(94)85098-4
Afzelechin 3-rhamnoside 44584170 Click to see CC1C(C(C(C(O1)OC2CC3=C(C=C(C=C3OC2C4=CC=C(C=C4)O)O)O)O)O)O 420.40 unknown https://doi.org/10.1016/0031-9422(94)85098-4
Afzelin 5316673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(94)85098-4
Kaempferol-3-O-rhamnoside 5835713 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(94)85098-4

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