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Rothmannia globosa

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 UUID643feb4066689983345519
Scientific name Rothmannia globosa
Authority (Hochst.) Keay
First published in Bull. Jard. Bot. État Bruxelles 28: 56 (1958)

Ethnobotanical Use Top

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General Uses Top

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Food and beverages (non-medicinal):
The fruits are edible berries eaten fresh or processed, notably as jam.

Synonyms Top

Scientific name Authority First published in
Gardenia globosa Hochst. Flora 25: 237 (1842)
Gardenia gerrardiana Sond.

Common names Top

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Language Common/alternative name
Afrikaans septemberklokkies
Chinese 九月钟花
Chinese 九月鍾花

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
  • Africa
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
      • Northern Provinces

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000298233
Tropicos 27904725
KEW urn:lsid:ipni.org:names:765125-1
The Plant List kew-180041
Open Tree Of Life 3878139
NCBI Taxonomy 1237791
IUCN Red List 146454675
IPNI 765125-1
iNaturalist 431565
GBIF 2906181
Freebase /m/04yfcwj
EOL 1105492
USDA GRIN 103295
Wikipedia Rothmannia_globosa

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
A Comparative Study of the Anatomy of Leaf Domatia in Gardenia thunbergia Thunb., Rothmannia capensis Thunb., and Rothmannia globosa (Hochst.) Keay (Rubiaceae) Situngu S, Barker NP Plants (Basel) 16-Nov-2022
PMCID:PMC9696783
doi:10.3390/plants11223126
PMID:36432855
Iridoids in rothmannia globosa Søren Rosendal Jensen Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80266-6

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 / Monoterpenoids / Iridoids and derivatives
(+)-Genipin 442424 Click to see 226.23 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
Methyl (1r,2r,6s)-2-hydroxy-9-(hydroxymethyl)-3-oxabicyclo[4.3.0]nona-4,8-diene-5-carboxylate 40491677 Click to see 226.23 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
methyl (1R,4R,7S,8R,9S,11S)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.04,11]undec-5-ene-8-carboxylate 101936009 Click to see 242.22 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
methyl (1R,4R,7S,8S,9S,11S)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.04,11]undec-5-ene-8-carboxylate 101936008 Click to see 242.22 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
methyl (1S,4R,7S,8R,9S,11S)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.04,11]undec-5-ene-8-carboxylate 163042985 Click to see COC(=O)C1C2C=CC3(C2C(OC3)OC1O)O 242.22 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
methyl (1S,4R,7S,8S,9S,11S)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.04,11]undec-5-ene-8-carboxylate 163042990 Click to see COC(=O)C1C2C=CC3(C2C(OC3)OC1O)O 242.22 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
methyl (1S,4S,7R,8R,9S,11S)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.04,11]undec-5-ene-8-carboxylate 163187270 Click to see 242.22 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
methyl (1S,4S,7R,8S,9S,11S)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.04,11]undec-5-ene-8-carboxylate 163042989 Click to see COC(=O)C1C2C=CC3(C2C(OC3)OC1O)O 242.22 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
methyl (1S,7S,8R,9S,11S)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.04,11]undec-5-ene-8-carboxylate 163187269 Click to see 242.22 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
Methyl 1-hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 23340 Click to see 226.23 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
Methyl 4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.04,11]undec-5-ene-8-carboxylate 74318243 Click to see COC(=O)C1C2C=CC3(C2C(OC3)OC1O)O 242.22 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
5-chloro-2-(4-(2-(2-hydroxyethoxy)ethyl)piperazin-1-yl)-N-(6-(3-methoxybenzamido)pyridin-3-yl)isonicotinamide 13848072 Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
6alpha-Hydroxygeniposide; Deacetylasperulosidic acid methyl ester 3515876 Click to see COC(=O)C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
Deacetyl asperulosidic acid methyl ester 6325021 Click to see COC(=O)C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
Gardenoside 442423 Click to see COC(=O)C1=COC(C2C1C=CC2(CO)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
Geniposide 107848 Click to see 388.40 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
methyl (1R,4aS,7aS)-7-(hydroxymethyl)-1-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 154496622 Click to see 388.40 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
methyl (1R,4aS,7S,7aS)-7-hydroxy-7-methyl-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 162910840 Click to see 390.40 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
methyl (1S,4aR,5R,7aR)-5-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 162957154 Click to see COC(=O)C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
methyl (1S,4aR,7R,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylate 129384808 Click to see COC(=O)C1=COC(C2C1C=CC2(CO)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
methyl (1S,4aR,7S,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylate 161728207 Click to see 404.40 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
methyl (4aR,7aS)-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 137706142 Click to see 388.40 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
methyl (4aR,7S,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylate 138113473 Click to see 404.40 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
Methyl 7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 3515873 Click to see 388.40 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
methyl 7-hydroxy-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylate 100058 Click to see 404.40 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
Mussaenoside 182423 Click to see 390.40 unknown https://doi.org/10.1016/S0031-9422(00)80266-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3S,4R,5R,6S)-2-ethoxy-6-(hydroxymethyl)oxane-3,4,5-triol 133645885 Click to see 208.21 unknown https://doi.org/10.1016/S0031-9422(00)80266-6

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