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Salvia kronenburgii

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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 UUID643febc30bf04283483630
Scientific name Salvia kronenburgii
Authority Rech.f.
First published in Oesterr. Bot. Z. 99: 50 (1952)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000301338
Tropicos 100253825
KEW urn:lsid:ipni.org:names:456488-1
The Plant List kew-182957
Open Tree Of Life 5801009
NCBI Taxonomy 1642914
IPNI 456488-1
GBIF 3898658

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
Natural Compounds of Salvia L. Genus and Molecular Mechanism of Their Biological Activity Zhumaliyeva G, Zhussupova A, Zhusupova GE, Błońska-Sikora E, Cerreto A, Omirbekova N, Zhunusbayeva Z, Gemejiyeva N, Ramazanova M, Wrzosek M, Ross SA Biomedicines 27-Nov-2023
PMCID:PMC10740457
doi:10.3390/biomedicines11123151
PMID:38137372
The Antibacterial and Wound Healing Properties of Natural Products: A Review on Plant Species with Therapeutic Potential against Staphylococcus aureus Wound Infections Morguette AE, Bartolomeu-Gonçalves G, Andriani GM, Bertoncini GE, de Castro IM, Spoladori LF, Bertão AM, Tavares ER, Yamauchi LM, Yamada-Ogatta SF Plants (Basel) 29-May-2023
PMCID:PMC10255540
doi:10.3390/plants12112147
PMID:37299127
Herbal Products and Their Active Constituents for Diabetic Wound Healing—Preclinical and Clinical Studies: A Systematic Review Herman A, Herman AP Pharmaceutics 14-Jan-2023
PMCID:PMC9865817
doi:10.3390/pharmaceutics15010281
PMID:36678910
Phytochemistry and Biological Activity of Medicinal Plants in Wound Healing: An Overview of Current Research Vitale S, Colanero S, Placidi M, Di Emidio G, Tatone C, Amicarelli F, D’Alessandro AM Molecules 01-Jun-2022
PMCID:PMC9182061
doi:10.3390/molecules27113566
PMID:35684503
Recent Applications of Capillary Electrophoresis in the Determination of Active Compounds in Medicinal Plants and Pharmaceutical Formulations Gackowski M, Przybylska A, Kruszewski S, Koba M, Mądra-Gackowska K, Bogacz A Molecules 07-Jul-2021
PMCID:PMC8307982
doi:10.3390/molecules26144141
PMID:34299418
Potential Synergistic Action of Bioactive Compounds from Plant Extracts against Skin Infecting Microorganisms Sitarek P, Merecz-Sadowska A, Kowalczyk T, Wieczfinska J, Zajdel R, Śliwiński T Int J Mol Sci 19-Jul-2020
PMCID:PMC7403983
doi:10.3390/ijms21145105
PMID:32707732
The MTT viability assay yields strikingly false-positive viabilities although the cells are killed by some plant extracts KARAKAŞ D, ARI F, ULUKAYA E Turk J Biol 18-Dec-2017
PMCID:PMC6353273
doi:10.3906/biy-1703-104
PMID:30814856
Highly hydroxylated triterpenes from Salvia kronenburgii. Topçu G, Türkmen Z, Ulubelen A, Schilling JK, Kingston DG J Nat Prod 01-Jan-2004
doi:10.1021/NP030359B
PMID:14738403
Terpenoids from <i>Salvia</i> <i>kronenburgii</i> Gülaçtı Topçu, Ayhan Ulubelen American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/NP990165P
Terpenoids from Salvia palaestina Ayhan Ulubelen, Mahmut Miski, Candan Johansson, Esther Lee, Tom J. Mabry, Stephen A. Matlin Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81143-7

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
> Benzenoids / Naphthalenes
(1S,13S)-13-hydroxy-1,8,13-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-3,5(14),6,8-tetraene-2,10-dione 10495322 Click to see CC1=C2C(=O)CCC(C3(C2=C(C=C1)C=C(C3=O)C(C)C)C)(C)O 312.40 unknown https://doi.org/10.1016/S0031-9422(00)81143-7
> Benzenoids / Naphthalenes / Naphthoquinones
12-Hydroxysapriparaquinone 369176 Click to see CC1=C(C2=C(C=C1)C(=C(C(=O)C2=O)C(C)C)O)CCC=C(C)C 312.40 unknown https://doi.org/10.1016/S0031-9422(00)81143-7
4-Hydroxy-7-methyl-8-(4-methylpent-4-enyl)-3-propan-2-ylnaphthalene-1,2-dione 821448 Click to see CC1=C(C2=C(C=C1)C(=C(C(=O)C2=O)C(C)C)O)CCCC(=C)C 312.40 unknown https://doi.org/10.1016/S0031-9422(00)81143-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4bS,8aR)-4-hydroxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-3,9-dione 92163171 Click to see CC(C)C1=CC2=CC(=O)C3C(CCCC3(C2=C(C1=O)O)C)(C)C 314.40 unknown https://doi.org/10.1021/NP990165P
14-deoxycoleon U 10735190 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C(=C3C2(CCCC3(C)C)C)O)O)O 330.40 unknown https://doi.org/10.1016/S0031-9422(00)81143-7
4-Hydroxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-3,9-dione 275527 Click to see CC(C)C1=CC2=CC(=O)C3C(CCCC3(C2=C(C1=O)O)C)(C)C 314.40 unknown https://doi.org/10.1021/NP990165P
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1016/S0031-9422(00)81143-7
Royleanone 442084 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2)(C)C)C)O 316.40 unknown https://doi.org/10.1016/S0031-9422(00)81143-7
Taxodione 73588 Click to see CC(C)C1=CC2=CC(=O)C3C(CCCC3(C2=C(C1=O)O)C)(C)C 314.40 unknown https://doi.org/10.1016/S0031-9422(00)81143-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
Kronenquinone 135496383 Click to see CC1=C(C(=C(C2=C1C=CC3=C2C(=O)C(=O)C(=C3O)C(C)C)O)O)C 326.30 unknown https://doi.org/10.1016/S0031-9422(00)81143-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1,14-dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl) acetate 73819956 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(C(CC(C5(C)C)OC(=O)C)O)C)C)O)C2C1C)C)C 500.80 unknown https://doi.org/10.1021/NP990165P
(1,2-Dihydroxy-4,4,6a,6b,8a,11,11,12,14b-nonamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl) acetate 163029374 Click to see CC1C2C3=CC=C4C(C3(CCC2(CCC1(C)C)C)C)(CCC5C4(C(C(C(C5(C)C)OC(=O)C)O)O)C)C 512.80 unknown https://doi.org/10.1021/NP030359B
(1,2-Dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-14-oxo-1,2,3,4a,5,6,7,8,9,10,11,12,12a,14a-tetradecahydropicen-3-yl) acetate 22298368 Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(C(C(C(C5(C)C)OC(=O)C)O)O)C)C)C2C1C)C)C 514.70 unknown https://doi.org/10.1021/NP030359B
(1,2-dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a-dodecahydro-1H-picen-3-yl) acetate 73100533 Click to see CC1CCC2(CCC3(C(=CC=C4C3(CCC5C4(C(C(C(C5(C)C)OC(=O)C)O)O)C)C)C2C1C)C)C 498.70 unknown https://doi.org/10.1021/NP030359B
(1R,2S,3R,4aS,6aR,6aS,6bR,8aR,10S,12aS,13S,14bR)-1,2,4a,6a,6b,9,9,12a-octamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-3,10,13-triol 162873925 Click to see CC1C(C2C3=CC(C4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C)C)C)(C)C)O)C)O)C 458.70 unknown https://doi.org/10.1021/NP030359B
(1R,3R,4aS,6aR,6bS,8aR,11R,12S,12aR,14R,14aS,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-1,3,14-triol 101000531 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(C(CC(C5(C)C)O)O)C)C)O)C2C1C)C)C 458.70 unknown https://doi.org/10.1021/NP990165P
(2,11-Dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl) acetate 72787829 Click to see CC1C2C3=CC=C4C(C3(CCC2(CCC1(C)O)C)C)(CCC5C4(CC(C(C5(C)C)OC(=O)C)O)C)C 498.70 unknown https://doi.org/10.1021/NP030359B
(2,14-dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl) acetate 163070396 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C)O)C)C)O)C2C1C)C)C 500.80 unknown https://doi.org/10.1021/NP030359B
(2R,3R,4aR,6aR,6bS,8aR,11R,12S,12aR,14R,14aR,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-2,3,14-triol 21670090 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)O)C2C1C)C)C 458.70 unknown https://doi.org/10.1021/NP990165P
(3,14-dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,6,7,8,9,10,11,12,12a,14,14a-dodecahydro-1H-picen-2-yl) acetate 73819955 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CC=C5C4(CC(C(C5(C)C)O)OC(=O)C)C)C)O)C2C1C)C)C 498.70 unknown https://doi.org/10.1021/NP990165P
(3R,4aS,6aR,6aR,6bR,8aR,10S,12aS,13S,14bR)-2,2,4a,6a,6b,9,9,12a-octamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-3,10,13-triol 162977718 Click to see CC1(CC2C3=CC(C4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C)C)C)(C)C)O)C)O)C 458.70 unknown https://doi.org/10.1021/NP030359B
(3R,4aS,6aR,6aS,6bR,8aR,10S,12aS,13R,14bR)-2,2,4a,6a,6b,9,9,12a-octamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-3,10,13-triol 44575562 Click to see CC1(CC2C3=CC(C4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C)C)C)(C)C)O)C)O)C 458.70 unknown https://doi.org/10.1021/NP030359B
[(1S,2R,3R,4aS,6aR,6bS,8aR,11R,12S,12aR,14aS,14bS)-1,2-dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-14-oxo-1,2,3,4a,5,6,7,8,9,10,11,12,12a,14a-tetradecahydropicen-3-yl] acetate 21600000 Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(C(C(C(C5(C)C)OC(=O)C)O)O)C)C)C2C1C)C)C 514.70 unknown https://doi.org/10.1021/NP030359B
[(1S,2R,3R,4aS,6aR,6bS,8aR,11R,12S,12aR,14R,14aS,14bS)-1,2,14-trihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] acetate 22212738 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(C(C(C(C5(C)C)OC(=O)C)O)O)C)C)O)C2C1C)C)C 516.80 unknown https://doi.org/10.1021/NP030359B
[(1S,2R,3R,4aS,6aR,6bS,8aR,12aR,14R,14aS,14bS)-1,2,14-trihydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 44575565 Click to see CC(=O)OC1C(C(C2(C(C1(C)C)CCC3(C2C(C=C4C3(CCC5(C4CC(CC5)(C)C)C)C)O)C)C)O)O 516.80 unknown https://doi.org/10.1021/NP030359B
[(1S,2R,3R,4aS,6aS,6bR,8aR,12aR,14bS)-1,2-dihydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl] acetate 21594132 Click to see CC(=O)OC1C(C(C2(C(C1(C)C)CCC3(C2=CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)O)O 498.70 unknown https://doi.org/10.1021/NP030359B
[(1S,2R,3R,4aS,6aS,6bR,8aR,12R,12aR,14bS)-1,2-dihydroxy-4,4,6a,6b,8a,11,11,12,14b-nonamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl] acetate 163029375 Click to see CC1C2C3=CC=C4C(C3(CCC2(CCC1(C)C)C)C)(CCC5C4(C(C(C(C5(C)C)OC(=O)C)O)O)C)C 512.80 unknown https://doi.org/10.1021/NP030359B
[(2R,3R,4aR,6aR,6bS,8aR,11R,12S,12aR,14R,14aR,14bS)-2,14-dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] acetate 163070397 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C)O)C)C)O)C2C1C)C)C 500.80 unknown https://doi.org/10.1021/NP030359B
[(2R,3R,4aR,6aS,6bR,8aS,11S,12R,12aR,14bS)-2,11-dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl] acetate 21600001 Click to see CC1C2C3=CC=C4C(C3(CCC2(CCC1(C)O)C)C)(CCC5C4(CC(C(C5(C)C)OC(=O)C)O)C)C 498.70 unknown https://doi.org/10.1021/NP030359B
[(2R,3R,6aR,6bS,8aR,11R,12S,12aR,14R,14aS,14bR)-3,14-dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,6,7,8,9,10,11,12,12a,14,14a-dodecahydro-1H-picen-2-yl] acetate 21670087 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CC=C5C4(CC(C(C5(C)C)O)OC(=O)C)C)C)O)C2C1C)C)C 498.70 unknown https://doi.org/10.1021/NP990165P
https://doi.org/10.1021/NP030359B
1,2,4a,6a,6b,9,9,12a-octamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-3,10,13-triol 75048981 Click to see CC1C(C2C3=CC(C4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C)C)C)(C)C)O)C)O)C 458.70 unknown https://doi.org/10.1021/NP030359B
1beta,3beta,11alpha,-Tetrahydroxy-urs-12-ene 404646 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(C(C(C(C5(C)C)O)O)O)C)C)O)C2C1C)C)C 474.70 unknown https://doi.org/10.1021/NP990165P
https://doi.org/10.1021/NP030359B
2,2,4a,6a,6b,9,9,12a-Octamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-3,10,13-triol 74323912 Click to see CC1(CC2C3=CC(C4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C)C)C)(C)C)O)C)O)C 458.70 unknown https://doi.org/10.1021/NP030359B
3beta-Acetoxyurs-9(11),12-diene-1beta,2alpha-diol 21600002 Click to see CC1CCC2(CCC3(C(=CC=C4C3(CCC5C4(C(C(C(C5(C)C)OC(=O)C)O)O)C)C)C2C1C)C)C 498.70 unknown https://doi.org/10.1021/NP030359B
3beta,11alpha,21Alphatrihydroxyurs-12-ene 44575561 Click to see CC1C(C2C3=CC(C4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C)C)C)(C)C)O)C)O)C 458.70 unknown https://doi.org/10.1021/NP030359B
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-1,2,3,14-tetrol 23132230 Click to see CC1(CCC2(CCC3(C(=CC(C4C3(CCC5C4(C(C(C(C5(C)C)O)O)O)C)C)O)C2C1)C)C)C 474.70 unknown https://doi.org/10.1021/NP990165P
https://doi.org/10.1021/NP030359B
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-1,2,3,14-tetrol 23132226 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(C(C(C(C5(C)C)O)O)O)C)C)O)C2C1C)C)C 474.70 unknown https://doi.org/10.1021/NP990165P
https://doi.org/10.1021/NP030359B
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-1,3,14-triol 73106019 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(C(CC(C5(C)C)O)O)C)C)O)C2C1C)C)C 458.70 unknown https://doi.org/10.1021/NP990165P
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-2,3,14-triol 23132201 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)O)C2C1C)C)C 458.70 unknown https://doi.org/10.1021/NP990165P
Olean-12-ene-1,2,3,11-tetrol, (1beta,2alpha,3beta,11alpha)- 21670086 Click to see CC1(CCC2(CCC3(C(=CC(C4C3(CCC5C4(C(C(C(C5(C)C)O)O)O)C)C)O)C2C1)C)C)C 474.70 unknown https://doi.org/10.1021/NP990165P
https://doi.org/10.1021/NP030359B
Urs-12-ene-1beta,3alpha,11alpha-triol 3-acetate 101000530 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(C(CC(C5(C)C)OC(=O)C)O)C)C)O)C2C1C)C)C 500.80 unknown https://doi.org/10.1021/NP990165P
> 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/10.1021/NP030359B
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/10.1021/NP030359B
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
Phialophoriol 72193405 Click to see CC1CC(C2=C1C3=C(C(=CC(=C3)OC)O)C(=O)O2)O 262.26 unknown https://doi.org/10.1021/NP990165P

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