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Gardenia sootepensis

Gardenia sootepensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Gardenia sootepensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Gardenia sootepensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Gardenia sootepensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Gardenia sootepensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64403cc3032fb299694712
Scientific name Gardenia sootepensis
Authority Hutch.
First published in Bull. Misc. Inform. Kew 1911: 392 (1911)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 山栀子
Chinese 栀子花
Chinese 大黄栀子
Chinese 糯帅聋
Chinese 麦托罗

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
  • Asia-tropical
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000971172
Tropicos 27910085
KEW urn:lsid:ipni.org:names:751253-1
The Plant List kew-88455
Open Tree Of Life 189668
NCBI Taxonomy 1233751
IPNI 751253-1
iNaturalist 431062
GBIF 5335111
EOL 1103536
USDA GRIN 312754

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
Discovery of teliospores of a Cape jasmine rust fungus, Hemileia gardeniae-floridae (Pucciniales), and its occurrence in Thailand Ono Y, Okane I, Unartngam J, Ayawong C Mycoscience 20-Sep-2021
PMCID:PMC9733717
doi:10.47371/mycosci.2021.06.003
PMID:37089462
Advancing urban ethnopharmacology: a modern concept of sustainability, conservation and cross-cultural adaptations of medicinal plant lore in the urban environment Dutta T, Anand U, Saha SC, Mane AB, Prasanth DA, Kandimalla R, Proćków J, Dey A Conserv Physiol 16-Sep-2021
PMCID:PMC8448427
doi:10.1093/conphys/coab073
PMID:34548925
Seed Rain, Soil Seed Bank, and Seedling Emergence Indicate Limited Potential for Self-Recovery in a Highly Disturbed, Tropical, Mixed Deciduous Forest Chalermsri A, Ampornpan LA, Purahong W Plants (Basel) 20-Oct-2020
PMCID:PMC7589040
doi:10.3390/plants9101391
PMID:33092026
Evolutionary correlation of water-related traits between different structures of Dendrobium plants Sun M, Feng CH, Liu ZY, Tian K Bot Stud 16-May-2020
PMCID:PMC7230118
doi:10.1186/s40529-020-00292-4
PMID:32417994
A Review on the Phytochemistry, Pharmacology, Pharmacokinetics and Toxicology of Geniposide, a Natural Product Shan M, Yu S, Yan H, Guo S, Xiao W, Wang Z, Zhang L, Ding A, Wu Q, Li SF Molecules 10-Oct-2017
PMCID:PMC6151614
doi:10.3390/molecules22101689
PMID:28994736
Secondary Metabolites from Rubiaceae Species Martins D, Nunez CV Molecules 22-Jul-2015
PMCID:PMC6331836
doi:10.3390/molecules200713422
PMID:26205062
Cytotoxic 3,4-seco-cycloartane triterpenes from Gardenia sootepensis. Nuanyai T, Sappapan R, Teerawatananond T, Muangsin N, Pudhom K J Nat Prod 01-Jun-2009
doi:10.1021/NP900156K
PMID:19456120
Crystal and molecular structure of bicuculline C. Gorinsky, D. S. Moss Springer Science and Business Media LLC 26-Mar-2005
doi:10.1007/BF01321855
A sesquiterpene from Gardenia sootepensis Vatcharin Rukachaisirikul, Sam-aung Naovanit, Walter C. Taylor, William A. Bubb, Pimchit Dampawan Elsevier BV 30-Apr-2003
doi:10.1016/S0031-9422(97)01108-4
Novel cytotoxic ring-a seco-cycloartane triterpenes from Gardenia coronaria and G. sootepensis Gloria L. Silva, Roberto R. Gil, Baoliang Cui, Heebyung Chai, Thawatchai Santisuk, Ekarath Srisook, Vichai Reutrakul, Patoomratana Tuchinda, Smaisukh Sophasan, Suparp Sujarit, Suchart Upatham, Sean M. Lynn, John E. Farthing, Shi-Lin Yang, Jane A. Lewis, Melanie J. O'Neill, Norman R. Farnsworth, Geoffrey A. Cordell, John M. Pezzuto, A.Douglas Kinghorn Elsevier BV 04-Mar-2003
doi:10.1016/S0040-4020(96)01003-4

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Yohimbine alkaloids
(1S,12S,15R,18S,19S,20S)-18-hydroxy-19-methoxycarbonyl-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-12-carboxylic acid 163188031 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CC(N3C2)C(=O)O)C5=CC=CC=C5N4)O 398.50 unknown https://doi.org/10.1021/NP900156K
https://doi.org/10.1016/S0040-4020(96)01003-4
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown https://doi.org/10.1016/S0031-9422(97)01108-4
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown https://doi.org/10.1016/S0031-9422(97)01108-4
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/S0031-9422(97)01108-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(8S,8aS)-5-(2-hydroxypropan-2-yl)-3,8-dimethyl-6,7,8,8a-tetrahydro-1H-azulen-2-one 15380738 Click to see CC1CCC(=CC2=C(C(=O)CC12)C)C(C)(C)O 234.33 unknown https://doi.org/10.1016/S0031-9422(97)01108-4
5-(2-hydroxypropan-2-yl)-3,8-dimethyl-6,7,8,8a-tetrahydro-1H-azulen-2-one 162906099 Click to see CC1CCC(=CC2=C(C(=O)CC12)C)C(C)(C)O 234.33 unknown https://doi.org/10.1016/S0031-9422(97)01108-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-[(1R,3S,4S,8S,10R,11R,14S,15S)-11,15-dimethyl-14-[(2S)-6-methylhept-5-en-2-yl]-5-methylidene-6-oxo-7-oxapentacyclo[8.7.0.01,3.04,8.011,15]heptadecan-3-yl]propanoic acid 162875585 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CC5C(C3(C4)CCC(=O)O)C(=C)C(=O)O5)C)C 468.70 unknown https://doi.org/10.1021/NP900156K
3-[(1R,3S,4S,8S,10R,11R,14S,15S)-11,15-dimethyl-5-methylidene-14-[(E,2S)-6-methyl-7-oxohept-5-en-2-yl]-6-oxo-7-oxapentacyclo[8.7.0.01,3.04,8.011,15]heptadecan-3-yl]propanoic acid 162860654 Click to see CC(CCC=C(C)C=O)C1CCC2(C1(CCC34C2CC5C(C3(C4)CCC(=O)O)C(=C)C(=O)O5)C)C 482.60 unknown https://doi.org/10.1021/NP900156K
3-[(1R,4S,5S,8R,9R,12R,13S)-4,8-dimethyl-5-[(2S)-6-methylhept-5-en-2-yl]-12-prop-1-en-2-yl-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 162864191 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)C)C)C 440.70 unknown https://doi.org/10.1021/NP900156K
3-[(1R,4S,5S,8R,9R,12S,13S)-12-(3-hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-[(2S)-6-methylhept-5-en-2-yl]-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 162876568 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)CO)C)C 456.70 unknown https://doi.org/10.1021/NP900156K
3-[(1S,4R,5R,8S,9R,12R,13R)-12-(3-hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-[(2R)-6-methylhept-5-en-2-yl]-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 44566394 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)CO)C)C 456.70 unknown https://doi.org/10.1021/NP900156K
3-[11,15-Dimethyl-14-(6-methylhept-5-en-2-yl)-5-methylidene-6-oxo-7-oxapentacyclo[8.7.0.01,3.04,8.011,15]heptadecan-3-yl]propanoic acid 56680935 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CC5C(C3(C4)CCC(=O)O)C(=C)C(=O)O5)C)C 468.70 unknown https://doi.org/10.1021/NP900156K
3-[11,15-Dimethyl-5-methylidene-14-(6-methyl-7-oxohept-5-en-2-yl)-6-oxo-7-oxapentacyclo[8.7.0.01,3.04,8.011,15]heptadecan-3-yl]propanoic acid 76393292 Click to see CC(CCC=C(C)C=O)C1CCC2(C1(CCC34C2CC5C(C3(C4)CCC(=O)O)C(=C)C(=O)O5)C)C 482.60 unknown https://doi.org/10.1021/NP900156K
3-[12-(3-Hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-(6-methylhept-5-en-2-yl)-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 92030288 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)CO)C)C 456.70 unknown https://doi.org/10.1021/NP900156K
3-[4,8-Dimethyl-5-(6-methylhept-5-en-2-yl)-12-prop-1-en-2-yl-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 56664437 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)C)C)C 440.70 unknown https://doi.org/10.1021/NP900156K
Coronalolide 6479499 Click to see CC(CCC=C(C)C=O)C1CCC2(C1(CCC34C2CC5C(C3(C4)CCC(=O)O)C(=C)C(=O)O5)C)C 482.60 unknown https://doi.org/10.1021/NP900156K
Coronalolide methyl ester 5468948 Click to see CC(CCC=C(C)C=O)C1CCC2(C1(CCC34C2CC5C(C3(C4)CCC(=O)OC)C(=C)C(=O)O5)C)C 496.70 unknown https://doi.org/10.1016/S0040-4020(96)01003-4
https://doi.org/10.1021/NP900156K
methyl 3-[(1R,3R,4S,8S,10S,11S,14S,15R)-11,15-dimethyl-5-methylidene-14-[(E,2S)-6-methyl-7-oxohept-5-en-2-yl]-6-oxo-7-oxapentacyclo[8.7.0.01,3.04,8.011,15]heptadecan-3-yl]propanoate 71720331 Click to see CC(CCC=C(C)C=O)C1CCC2(C1(CCC34C2CC5C(C3(C4)CCC(=O)OC)C(=C)C(=O)O5)C)C 496.70 unknown https://doi.org/10.1021/NP900156K
methyl 3-[(1R,3S,4S,8S,10R,11R,14S,15S)-11,15-dimethyl-14-[(2S)-6-methylhept-5-en-2-yl]-5-methylidene-6-oxo-7-oxapentacyclo[8.7.0.01,3.04,8.011,15]heptadecan-3-yl]propanoate 162923912 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CC5C(C3(C4)CCC(=O)OC)C(=C)C(=O)O5)C)C 482.70 unknown https://doi.org/10.1021/NP900156K
methyl 3-[(1R,3S,4S,8S,10R,11R,14S,15S)-14-[(E,2S)-7-hydroxy-6-methylhept-5-en-2-yl]-11,15-dimethyl-5-methylidene-6-oxo-7-oxapentacyclo[8.7.0.01,3.04,8.011,15]heptadecan-3-yl]propanoate 162996265 Click to see CC(CCC=C(C)CO)C1CCC2(C1(CCC34C2CC5C(C3(C4)CCC(=O)OC)C(=C)C(=O)O5)C)C 498.70 unknown https://doi.org/10.1021/NP900156K
methyl 3-[(1R,4S,5S,8R,9R,12S,13S)-12-(3-hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-[(2S)-6-methylhept-5-en-2-yl]-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoate 163195171 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)OC)C(=C)CO)C)C 470.70 unknown https://doi.org/10.1021/NP900156K
methyl 3-[(1R,4S,5S,8R,9R,12S,13S)-12-(3-hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-[(E,2S)-6-methyl-7-oxohept-5-en-2-yl]-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoate 163060538 Click to see CC(CCC=C(C)C=O)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)OC)C(=C)CO)C)C 484.70 unknown https://doi.org/10.1021/NP900156K
Methyl 3-[11,15-dimethyl-14-(6-methylhept-5-en-2-yl)-5-methylidene-6-oxo-7-oxapentacyclo[8.7.0.01,3.04,8.011,15]heptadecan-3-yl]propanoate 56660460 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CC5C(C3(C4)CCC(=O)OC)C(=C)C(=O)O5)C)C 482.70 unknown https://doi.org/10.1021/NP900156K
Methyl 3-[12-(3-hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-(6-methyl-7-oxohept-5-en-2-yl)-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoate 74941993 Click to see CC(CCC=C(C)C=O)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)OC)C(=C)CO)C)C 484.70 unknown https://doi.org/10.1021/NP900156K
Methyl 3-[12-(3-hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-(6-methylhept-5-en-2-yl)-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoate 56674600 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)OC)C(=C)CO)C)C 470.70 unknown https://doi.org/10.1021/NP900156K
Methyl 3-[14-(7-hydroxy-6-methylhept-5-en-2-yl)-11,15-dimethyl-5-methylidene-6-oxo-7-oxapentacyclo[8.7.0.01,3.04,8.011,15]heptadecan-3-yl]propanoate 74941992 Click to see CC(CCC=C(C)CO)C1CCC2(C1(CCC34C2CC5C(C3(C4)CCC(=O)OC)C(=C)C(=O)O5)C)C 498.70 unknown https://doi.org/10.1021/NP900156K
Secaubryenol 16099423 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)CO)C)C 456.70 unknown https://doi.org/10.1021/NP900156K
Sootepin A 44179867 Click to see CC(CCC=C(C)CO)C1CCC2(C1(CCC34C2CC5C(C3(C4)CCC(=O)OC)C(=C)C(=O)O5)C)C 498.70 unknown https://doi.org/10.1021/NP900156K
Sootepin B 44179868 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CC5C(C3(C4)CCC(=O)O)C(=C)C(=O)O5)C)C 468.70 unknown https://doi.org/10.1021/NP900156K
Sootepin C 44179866 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)OC)C(=C)CO)C)C 470.70 unknown https://doi.org/10.1021/NP900156K
Sootepin D 44179869 Click to see CC(CCC=C(C)C=O)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)OC)C(=C)CO)C)C 484.70 unknown https://doi.org/10.1021/NP900156K
Sootepin E 44179870 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)C)C)C 440.70 unknown https://doi.org/10.1021/NP900156K
Tubiferolide methyl ester 516547 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CC5C(C3(C4)CCC(=O)OC)C(=C)C(=O)O5)C)C 482.70 unknown https://doi.org/10.1021/NP900156K
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Quinide 101711082 Click to see C1C(C(C2CC1(C(=O)O2)O)O)O 174.15 unknown https://doi.org/10.1007/BF01321855
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7,3'-Trihydroxy-6,4',5'-trimethoxyflavone 5496475 Click to see COC1=CC(=CC(=C1OC)O)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 360.30 unknown https://doi.org/10.1016/S0031-9422(97)01108-4
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1016/S0031-9422(97)01108-4

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