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Lydenburgia cassinoides

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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 UUID64405b3490b25637064555
Scientific name Lydenburgia cassinoides
Authority N.Robson
First published in Bol. Soc. Brot. , sér. 2, 39: 35 (1965)

Description Top

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Synonyms Top

Scientific name Authority First published in
Catha cassinoides (N.Robson) Codd Bothalia ix. 124 (1966).
Catha transvaalensis Codd Bothalia 10: 365 (1971)

Common names Top

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Language Common/alternative name
English sekhukhuni bushman's tea
Afrikaans sekhukhuni boesmanstee

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-0001292628
Tropicos 6600464
KEW urn:lsid:ipni.org:names:161770-1
The Plant List tro-6600464
Open Tree Of Life 55968
NCBI Taxonomy 353136
IPNI 161770-1
iNaturalist 589502
GBIF 5579636
EOL 5226403

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
Isolation and structure of vaalens-1, -3, -5, and -7. Sesquiterpene esters of Catha transvaalensis Codd (Celastraceae): X-ray molecular structure of vaalens-5 Michael J. Begley, Leslie Crombie, W. Mary L. Crombie, Dane Toplis, Donald A. Whiting Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19900002841
Vaalens sesquiterpenes of Catha transvaalensis; structure of vaalens-5 using the COLOC n.m.r. pulse sequence Leslie Crombie, Robert A. Fleming, Dane Toplis, Donald A. Whiting Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19890001700
Three triterpenes and other terpenoids from Catha cassinoides C. Betancor, R. Freire, A.G. Gonzalez, J.A. Salazar, C. Pascard, T. Prange Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)83019-6
Iguesterin, a new quinonoid triterpene from Catha cassinoides Antonio G. González, Cosme G. Francisco, Raimundo Freire, Rosendo Hernández, José A. Salazar, Ernesto Suárez Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(75)85188-0

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 / Sesquiterpenoids / Agarofurans
(5,12-Diacetyloxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl) 3-phenylprop-2-enoate 163052136 Click to see CC(=O)OC1CCC(C23C1(C(CC(C2OC(=O)C)C(O3)(C)C)OC(=O)C=CC4=CC=CC=C4)C)(C)O 500.60 unknown https://doi.org/10.1039/P19900002841
[(1S,2S,4S,5R,6R,7S,9R,12R)-4,12-diacetyloxy-2-hydroxy-5-(2-hydroxyacetyl)oxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] (E)-3-phenylprop-2-enoate 163185385 Click to see CC(=O)OC1CC(C23C(C(CC(C2(C1OC(=O)CO)C)OC(=O)C=CC4=CC=CC=C4)C(O3)(C)C)OC(=O)C)(C)O 574.60 unknown https://doi.org/10.1039/P19900002841
[(1S,2S,5S,6S,7S,9R,12R)-12-acetyloxy-2-hydroxy-5-(2-hydroxyacetyl)oxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] (E)-3-phenylprop-2-enoate 163191393 Click to see CC(=O)OC1C2CC(C3(C1(C(CCC3OC(=O)CO)(C)O)OC2(C)C)C)OC(=O)C=CC4=CC=CC=C4 516.60 unknown https://doi.org/10.1039/P19900002841
[(1S,2S,5S,6S,7S,9R,12R)-5,12-diacetyloxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] (E)-3-phenylprop-2-enoate 163186095 Click to see CC(=O)OC1CCC(C23C1(C(CC(C2OC(=O)C)C(O3)(C)C)OC(=O)C=CC4=CC=CC=C4)C)(C)O 500.60 unknown https://doi.org/10.1039/P19900002841
[12-Acetyloxy-2-hydroxy-5-(2-hydroxyacetyl)oxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] 3-phenylprop-2-enoate 162904168 Click to see CC(=O)OC1C2CC(C3(C1(C(CCC3OC(=O)CO)(C)O)OC2(C)C)C)OC(=O)C=CC4=CC=CC=C4 516.60 unknown https://doi.org/10.1039/P19890001700
https://doi.org/10.1039/P19900002841
[4,12-Diacetyloxy-2-hydroxy-5-(2-hydroxyacetyl)oxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] 3-phenylprop-2-enoate 162843228 Click to see CC(=O)OC1CC(C23C(C(CC(C2(C1OC(=O)CO)C)OC(=O)C=CC4=CC=CC=C4)C(O3)(C)C)OC(=O)C)(C)O 574.60 unknown https://doi.org/10.1039/P19900002841
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
1-(3-Hydroxyprop-1-en-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 14108935 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(80)83019-6
24-Nor-D:A-friedooleana-1(10),5,7-tetraen-29-oic acid, 3-hydroxy-2-oxo-, methyl ester 264268 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O 464.60 unknown https://doi.org/10.1016/0031-9422(75)85188-0
29-Hydroxyfriedelan-3-one 14108943 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(80)83019-6
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(80)83019-6
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0031-9422(80)83019-6
D:A-Friedooleanan-3-one, 29-hydroxy-, (20alpha)- 588284 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(80)83019-6
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(80)83019-6
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(80)83019-6
Hennadiol 489919 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(80)83019-6
Octandronic acid 14108946 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)C 456.70 unknown https://doi.org/10.1016/0031-9422(80)83019-6
Octandronol 14108942 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(80)83019-6
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(80)83019-6
Polpunonic acid 343427 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)C 456.70 unknown https://doi.org/10.1016/0031-9422(80)83019-6
Pristimerin 159516 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O 464.60 unknown https://doi.org/10.1016/0031-9422(75)85188-0
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0031-9422(80)83019-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(80)83019-6
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(80)83019-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1S,2S,4S,5R,6R,7S,9R,12R)-4,12-diacetyloxy-5-(2-acetyloxyacetyl)oxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] (E)-3-phenylprop-2-enoate 163193494 Click to see CC(=O)OCC(=O)OC1C(CC(C23C1(C(CC(C2OC(=O)C)C(O3)(C)C)OC(=O)C=CC4=CC=CC=C4)C)(C)O)OC(=O)C 616.70 unknown https://doi.org/10.1039/P19900002841
[4,12-Diacetyloxy-5-(2-acetyloxyacetyl)oxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] 3-phenylprop-2-enoate 162992715 Click to see CC(=O)OCC(=O)OC1C(CC(C23C1(C(CC(C2OC(=O)C)C(O3)(C)C)OC(=O)C=CC4=CC=CC=C4)C)(C)O)OC(=O)C 616.70 unknown https://doi.org/10.1039/P19900002841
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(6aS,6bS,8aS,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-8,9,12,12a,13,14-hexahydro-7H-picen-2-one 46881919 Click to see CC1=CCC2(CCC3(C4=CC=C5C(=C(C(=O)C=C5C4(CCC3(C2C1)C)C)O)C)C)C 404.60 unknown https://doi.org/10.1016/0031-9422(75)85188-0
3-Hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione 3527193 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C 420.60 unknown https://doi.org/10.1016/0031-9422(75)85188-0
3-Hydroxy-4,6b,8a,11,12b,14a-hexamethyl-7,8,8a,9,12,12a,12b,13,14,14a-decahydropicen-2(6bh)-one 162727 Click to see CC1=CCC2(CCC3(C4=CC=C5C(=C(C(=O)C=C5C4(CCC3(C2C1)C)C)O)C)C)C 404.60 unknown https://doi.org/10.1016/0031-9422(75)85188-0
Tingenone 101520 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C 420.60 unknown https://doi.org/10.1016/0031-9422(75)85188-0

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