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Rudgea jasminoides

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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 UUID643feb5906279677289324
Scientific name Rudgea jasminoides
Authority (Cham.) Müll.Arg.
First published in Flora 59: 452 (1879)

Description Top

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Synonyms Top

Scientific name Authority First published in
Uragoga jasminioides (Cham.) Kuntze Revis. Gen. Pl. 2: 960 (1891)
Coffea jasminoides Cham. Linnaea 9: 222 (1834)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Rudgea jasminoides subsp. corniculata (Benth.) Zappi Kew Bull. 58: 525 (2003)
Rudgea jasminoides subsp. jasminoides Unknown
Rudgea jasminoides subsp. micrantha Zappi Kew Bull. 58: 526 (2003)
Rudgea jasminoides subsp. nervosa Zappi & Anunc. Kew Bull. 58: 526 (2003)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000298798
Tropicos 27902414
INPN 887448
KEW urn:lsid:ipni.org:names:765493-1
The Plant List kew-180574
Open Tree Of Life 3875052
NCBI Taxonomy 2072289
IUCN Red List 148755903
IPNI 765493-1
iNaturalist 538242
GBIF 2910527
EOL 1107512

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
Metabolite profiles of callus and cell suspension cultures of mangosteen Jamil SZ, Rohani ER, Baharum SN, Noor NM 3 Biotech 17-Jul-2018
PMCID:PMC6049810
doi:10.1007/s13205-018-1336-6
PMID:30034986
Secondary Metabolites from Rubiaceae Species Martins D, Nunez CV Molecules 22-Jul-2015
PMCID:PMC6331836
doi:10.3390/molecules200713422
PMID:26205062
New limonoids from Hortia oreadica and unexpected coumarin from H. superba using chromatography over cleaning Sephadex with sodium hypochlorite. Severino VG, de Freitas SD, Braga PA, Forim MR, das G F da Silva MF, Fernandes JB, Vieira PC, Venâncio T Molecules 12-Aug-2014
PMCID:PMC6271672
doi:10.3390/MOLECULES190812031
PMID:25120055
Characterization of 10 microsatellite loci for Bathysa australis (Rubiaceae) Reis TS, Ciampi-Guillardi M, Baldauf C, Souza AP, dos Santos FA Appl Plant Sci 31-Oct-2013
PMCID:PMC4103462
doi:10.3732/apps.1300055
PMID:25202500
químicos das folhas de Qualea grandiflora: atribuição dos dados de RMN de dois flavonóides glicosilados acilados diastereoisoméricos Mariane Cruz Costa Ayres, Samuel Portela Escórcio, Danielly Albuquerque da Costa, Mariana H. Chaves, Gerardo Magela Vieira Júnior, Alberto J. Cavalheiro FapUNIFESP (SciELO) 15-Oct-2008
doi:10.1590/S0100-40422008000600038
Complete Assignments of ¹H and 13C-NMR Spectra of the 3,4-seco-Triterpene Canaric Acid isolated from Rudgea jasminoides Marcia N. Lopes, Fabiano C. Mazza, Maria Claudia M. Young, Vanderlan da S. Bolzani FapUNIFESP (SciELO) 25-Apr-2005
doi:10.1590/S0103-50531999000300013

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 / Triterpenoids
(1S,2R,4aS,6aS,6bR,10S,12aR,12bR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid 13073350 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/10.1590/S0100-40422008000600038
(4aS,6aS,6bR,10S,12aR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 3010929 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1590/S0100-40422008000600038
3-[(3S,4S,5R,8R,9R,10R,13R,14R,15R)-4,9,10,13-tetramethyl-3,15-bis(prop-1-en-2-yl)-2,3,5,6,7,8,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-4-yl]propanoic acid 20055797 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC(C4(C)CCC(=O)O)C(=C)C)C)C 440.70 unknown https://doi.org/10.1590/S0103-50531999000300013
3-[(3S,4S,5R,8R,9R,13R,14R,15R)-4,9,10,13-tetramethyl-3,15-bis(prop-1-en-2-yl)-2,3,5,6,7,8,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-4-yl]propanoic acid 163193214 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC(C4(C)CCC(=O)O)C(=C)C)C)C 440.70 unknown https://doi.org/10.1590/S0103-50531999000300013
3-[4,9,10,13-tetramethyl-3,15-bis(prop-1-en-2-yl)-2,3,5,6,7,8,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-4-yl]propanoic acid 73657090 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC(C4(C)CCC(=O)O)C(=C)C)C)C 440.70 unknown https://doi.org/10.1590/S0103-50531999000300013
methyl 3-[(3S,4S,5R,8R,9R,10R,13R,14R,15S)-4,9,10,13-tetramethyl-3,15-bis(prop-1-en-2-yl)-2,3,5,6,7,8,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-4-yl]propanoate 162909070 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC(C4(C)CCC(=O)OC)C(=C)C)C)C 454.70 unknown https://doi.org/10.1590/S0103-50531999000300013
methyl 3-[(3S,4S,5R,8R,9R,13R,14R,15S)-4,9,10,13-tetramethyl-3,15-bis(prop-1-en-2-yl)-2,3,5,6,7,8,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-4-yl]propanoate 163189823 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC(C4(C)CCC(=O)OC)C(=C)C)C)C 454.70 unknown https://doi.org/10.1590/S0103-50531999000300013
methyl 3-[4,9,10,13-tetramethyl-3,15-bis(prop-1-en-2-yl)-2,3,5,6,7,8,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-4-yl]propanoate 73821080 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC(C4(C)CCC(=O)OC)C(=C)C)C)C 454.70 unknown https://doi.org/10.1590/S0103-50531999000300013
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1590/S0103-50531999000300013
https://doi.org/10.1590/S0100-40422008000600038
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/10.1590/S0103-50531999000300013
https://doi.org/10.1590/S0100-40422008000600038
> 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/10.1590/S0103-50531999000300013
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1590/S0103-50531999000300013
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271672/

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