Salvia kronenburgii

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Details Top

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

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Western Asia
  - Turkey

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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,11R,12S,12aR,14bS)-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	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
[(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,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/NP030359B https://doi.org/10.1021/NP990165P
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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Salvia kronenburgii

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