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Salvia hypoleuca

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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
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Details Top

Internal ID UUID643febbd7e008333756023
Scientific name Salvia hypoleuca
Authority Benth.
First published in Prodr. 12: 279 (1848)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Arabic قصعين أبيض شاحب

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000301234
Tropicos 17600590
KEW urn:lsid:ipni.org:names:456414-1
The Plant List kew-182860
Open Tree Of Life 576937
NCBI Taxonomy 1294397
IPNI 456414-1
GBIF 3899789

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
Molecular Pathways of Rosmarinic Acid Anticancer Activity in Triple-Negative Breast Cancer Cells: A Literature Review Konstantinou EK, Panagiotopoulos AA, Argyri K, Panoutsopoulos GI, Dimitriou M, Gioxari A Nutrients 19-Dec-2023
PMCID:PMC10780465
doi:10.3390/nu16010002
PMID:38201832
Chemical composition, cholinesterase, and α-glucosidase inhibitory activity of the essential oils of some Iranian native Salvia species Gharehbagh HJ, Ebrahimi M, Dabaghian F, Mojtabavi S, Hariri R, Saeedi M, Faramarzi MA, Khanavi M BMC Complement Med Ther 03-Jun-2023
PMCID:PMC10239571
doi:10.1186/s12906-023-04004-w
PMID:37270541
Middle East Medicinal Plants in the Treatment of Diabetes: A Review Abu-Odeh AM, Talib WH Molecules 31-Jan-2021
PMCID:PMC7867005
doi:10.3390/molecules26030742
PMID:33572627
Molecular mechanism of the anti-diabetic activity of an identified oligosaccharide from Rosa canina Bahrami G, Miraghaee SS, Mohammadi B, Bahrami MT, Taheripak G, Keshavarzi S, Babaei A, Sajadimajd S, Hatami R Res Pharm Sci 20-Feb-2020
PMCID:PMC7053289
doi:10.4103/1735-5362.278713
PMID:32180815
Antidiabetic Potential of Medicinal Plants and Their Active Components Salehi B, Ata A, V. Anil Kumar N, Sharopov F, Ramírez-Alarcón K, Ruiz-Ortega A, Abdulmajid Ayatollahi S, Valere Tsouh Fokou P, Kobarfard F, Amiruddin Zakaria Z, Iriti M, Taheri Y, Martorell M, Sureda A, N. Setzer W, Durazzo A, Lucarini M, Santini A, Capasso R, Adrian Ostrander E, -ur-Rahman A, Iqbal Choudhary M, C. Cho W, Sharifi-Rad J Biomolecules 30-Sep-2019
PMCID:PMC6843349
doi:10.3390/biom9100551
PMID:31575072
Phytochemical profile, anti-oxidant, anti-inflammatory, and anti-proliferative activities of Pogostemon deccanensis essential oils Kumar V, Shriram V, Bhagat R, Khare T, Kapse S, Kadoo N 3 Biotech 04-Jan-2019
PMCID:PMC6320326
doi:10.1007/s13205-018-1560-0
PMID:30622869
Notes: Exudate Flavonoids of Some Salvia and a Trichostema Species Eckhard Wollenweber, Marion Dörr, Abdolhossein Rustaiyan, James N. Roitman, Earl H. Graven Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1992-9-1025
Tracking leading anti-Candida compounds in plant samples; Plumbago europaea Sobhani M, Abbas-Mohammadi M, Ebrahimi SN, Aliahmadi A Iran J Microbiol 01-Jun-2018
PMCID:PMC6087695
PMID:30112157
Molecullar and biochemical effect of alcohlic extract of Alpinia galanga on rat spermatogenesis process Mazaheri M, Shahdadi V, Nazari Boron A Iran J Reprod Med 01-Nov-2014
PMCID:PMC4330656
PMID:25709632
Cytotoxic, Antioxidant and Antimicrobial Activities and Phenolic Contents of Eleven Salvia Species from Iran Firuzi O, Miri R, Asadollahi M, Eslami S, Jassbi AR Iran J Pharm Res 01-Sep-2013
PMCID:PMC3920696
PMID:24523760
Terpenes From the Root of Salvia hypoleuca Benth Saeidnia S, Ghamarinia M, Gohari AR, Shakeri A Daru 24-Oct-2012
PMCID:PMC3556016
doi:10.1186/2008-2231-20-66
PMID:23351362
Comparative study of rosmarinic acid content in some plants of Labiatae family Shekarchi M, Hajimehdipoor H, Saeidnia S, Gohari AR, Hamedani MP Pharmacogn Mag 01-Jan-2012
PMCID:PMC3307200
doi:10.4103/0973-1296.93316
PMID:22438661
Sesterterpenes from Salvia hypoleuca Abdolhossein Rustaiyan, Akram Niknejad, Lilly Nazarians, Jasmin Jakupovic, Ferdinand Bohlmann Elsevier BV 03-Jan-2008
doi:10.1016/S0031-9422(82)85076-0
Further sesterterpenes from Salvia hypoleuca A. Rustaiyan, S. Koussari Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80440-0
Polyphenolics of Salvia--a review. Lu Y, Foo LY Phytochemistry 01-Jan-2002
doi:10.1016/S0031-9422(01)00415-0
PMID:11809447

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 / Terpene lactones / Diterpene lactones
methyl (1R,4aS,5R,6R,8S,8aR)-5-[(4S)-4-hydroperoxy-3-methylidene-5-[(2S)-3-methyl-5-oxo-2H-furan-2-yl]pentyl]-6,8-dihydroxy-1,4a,6-trimethyl-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 163043078 Click to see CC1=CC(=O)OC1CC(C(=C)CCC2C3(CCCC(C3C(CC2(C)O)O)(C)C(=O)OC)C)OO 480.60 unknown https://doi.org/10.1016/0031-9422(88)80440-0
methyl (1R,4aS,5R,6R,8S,8aR)-5-[(E,3R)-3-hydroperoxy-3-methyl-5-[(2S)-3-methyl-5-oxo-2H-furan-2-yl]pent-4-enyl]-6,8-dihydroxy-1,4a,6-trimethyl-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 162864748 Click to see CC1=CC(=O)OC1C=CC(C)(CCC2C3(CCCC(C3C(CC2(C)O)O)(C)C(=O)OC)C)OO 480.60 unknown https://doi.org/10.1016/0031-9422(88)80440-0
methyl (1R,4aS,5R,6R,8S,8aR)-5-[3-[(3R,4aS,7aR)-7a-methyl-6-oxo-3,4,4a,7-tetrahydrofuro[3,2-c][1,2]dioxin-3-yl]but-3-enyl]-6,8-dihydroxy-1,4a,6-trimethyl-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 162895153 Click to see CC12CCCC(C1C(CC(C2CCC(=C)C3CC4C(CC(=O)O4)(OO3)C)(C)O)O)(C)C(=O)OC 480.60 unknown https://doi.org/10.1016/0031-9422(88)80440-0
methyl (1R,4aS,5R,6R,8S,8aR)-6,8-dihydroxy-1,4a,6-trimethyl-5-[(E)-3-methyl-5-[(2S)-3-methyl-5-oxo-2H-furan-2-yl]pent-3-enyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 162994837 Click to see CC1=CC(=O)OC1CC=C(C)CCC2C3(CCCC(C3C(CC2(C)O)O)(C)C(=O)OC)C 448.60 unknown https://doi.org/10.1016/S0031-9422(82)85076-0
methyl 5-[3-(7a-methyl-6-oxo-3,4,4a,7-tetrahydrofuro[3,2-c][1,2]dioxin-3-yl)but-3-enyl]-6,8-dihydroxy-1,4a,6-trimethyl-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 14108829 Click to see CC12CCCC(C1C(CC(C2CCC(=C)C3CC4C(CC(=O)O4)(OO3)C)(C)O)O)(C)C(=O)OC 480.60 unknown https://doi.org/10.1016/0031-9422(88)80440-0
methyl 5-[3-hydroperoxy-3-methyl-5-(3-methyl-5-oxo-2H-furan-2-yl)pent-4-enyl]-6,8-dihydroxy-1,4a,6-trimethyl-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 162864747 Click to see CC1=CC(=O)OC1C=CC(C)(CCC2C3(CCCC(C3C(CC2(C)O)O)(C)C(=O)OC)C)OO 480.60 unknown https://doi.org/10.1016/0031-9422(88)80440-0
methyl 5-[4-hydroperoxy-3-methylidene-5-(3-methyl-5-oxo-2H-furan-2-yl)pentyl]-6,8-dihydroxy-1,4a,6-trimethyl-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 14108827 Click to see CC1=CC(=O)OC1CC(C(=C)CCC2C3(CCCC(C3C(CC2(C)O)O)(C)C(=O)OC)C)OO 480.60 unknown https://doi.org/10.1016/0031-9422(88)80440-0
methyl 6,8-dihydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2H-furan-2-yl)pent-3-enyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 73189502 Click to see CC1=CC(=O)OC1CC=C(C)CCC2C3(CCCC(C3C(CC2(C)O)O)(C)C(=O)OC)C 448.60 unknown https://doi.org/10.1016/S0031-9422(82)85076-0
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S,4R,8S,9R,10R,12R)-10-hydroxy-4,8,10-trimethyl-9-[(E)-3-methyl-5-[(2R)-3-methyl-5-oxo-2H-furan-2-yl]pent-3-enyl]-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 156010972 Click to see CC1=CC(=O)OC1CC=C(C)CCC2C3(CCCC4(C3C(CC2(C)O)OC4=O)C)C 416.50 unknown https://doi.org/10.1016/S0031-9422(82)85076-0
(1S,4R,8S,9R,10R,12R)-10-hydroxy-4,8,10-trimethyl-9-[2-[(2R,3R)-2-methyl-3-[(Z)-(3-methyl-5-oxofuran-2-ylidene)methyl]oxiran-2-yl]ethyl]-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 163190570 Click to see CC1=CC(=O)OC1=CC2C(O2)(C)CCC3C4(CCCC5(C4C(CC3(C)O)OC5=O)C)C 430.50 unknown https://doi.org/10.1016/0031-9422(88)80440-0
(1S,4R,8S,9R,10R,12R)-10-hydroxy-4,8,10-trimethyl-9-[2-[(2R,3S)-2-methyl-3-[(Z)-(3-methyl-5-oxofuran-2-ylidene)methyl]oxiran-2-yl]ethyl]-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 163190569 Click to see CC1=CC(=O)OC1=CC2C(O2)(C)CCC3C4(CCCC5(C4C(CC3(C)O)OC5=O)C)C 430.50 unknown https://doi.org/10.1016/0031-9422(88)80440-0
(1S,4R,8S,9R,10R,12R)-10-hydroxy-4,8,10-trimethyl-9-[2-[(2S,3R)-2-methyl-3-[(Z)-(3-methyl-5-oxofuran-2-ylidene)methyl]oxiran-2-yl]ethyl]-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 163189463 Click to see CC1=CC(=O)OC1=CC2C(O2)(C)CCC3C4(CCCC5(C4C(CC3(C)O)OC5=O)C)C 430.50 unknown https://doi.org/10.1016/0031-9422(88)80440-0
(1S,4R,8S,9R,10R,12R)-10-hydroxy-9-[(E)-4-[(1S,5R)-5-hydroxy-3-methyl-2-oxocyclopent-3-en-1-yl]-3-methylbut-3-enyl]-4,8,10-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 163035108 Click to see CC1=CC(C(C1=O)C=C(C)CCC2C3(CCCC4(C3C(CC2(C)O)OC4=O)C)C)O 416.50 unknown https://doi.org/10.1016/0031-9422(88)80440-0
(1S,4R,8S,9R,10R,12R)-9-[(4R)-4-hydroperoxy-3-methylidene-5-[(2S)-3-methyl-5-oxo-2H-furan-2-yl]pentyl]-10-hydroxy-4,8,10-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 163193731 Click to see CC1=CC(=O)OC1CC(C(=C)CCC2C3(CCCC4(C3C(CC2(C)O)OC4=O)C)C)OO 448.50 unknown https://doi.org/10.1016/0031-9422(88)80440-0
10-Hydroxy-4,8,10-trimethyl-9-[2-[2-methyl-3-[(3-methyl-5-oxofuran-2-ylidene)methyl]oxiran-2-yl]ethyl]-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 162950842 Click to see CC1=CC(=O)OC1=CC2C(O2)(C)CCC3C4(CCCC5(C4C(CC3(C)O)OC5=O)C)C 430.50 unknown https://doi.org/10.1016/0031-9422(88)80440-0
10-hydroxy-4,8,10-trimethyl-9-[3-methyl-5-(3-methyl-5-oxo-2H-furan-2-yl)pent-3-enyl]-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 162940542 Click to see CC1=CC(=O)OC1CC=C(C)CCC2C3(CCCC4(C3C(CC2(C)O)OC4=O)C)C 416.50 unknown https://doi.org/10.1016/S0031-9422(82)85076-0
10-Hydroxy-9-[4-(5-hydroxy-3-methyl-2-oxocyclopent-3-en-1-yl)-3-methylbut-3-enyl]-4,8,10-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 163035107 Click to see CC1=CC(C(C1=O)C=C(C)CCC2C3(CCCC4(C3C(CC2(C)O)OC4=O)C)C)O 416.50 unknown https://doi.org/10.1016/0031-9422(88)80440-0
9-[4-hydroperoxy-3-methylidene-5-(3-methyl-5-oxo-2H-furan-2-yl)pentyl]-10-hydroxy-4,8,10-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 14108816 Click to see CC1=CC(=O)OC1CC(C(=C)CCC2C3(CCCC4(C3C(CC2(C)O)OC4=O)C)C)OO 448.50 unknown https://doi.org/10.1016/0031-9422(88)80440-0
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R,3R,4S,5S,6R)-2-[3-[2-(1,3-benzodioxol-5-yl)-7-methoxy-1-benzofuran-5-yl]propoxy]-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 10651516 Click to see COC1=CC(=CC2=C1OC(=C2)C3=CC4=C(C=C3)OCO4)CCCOC5C(C(C(C(O5)COC6C(C(C(CO6)O)O)O)O)O)O 620.60 unknown https://doi.org/10.1016/0031-9422(88)80440-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
https://doi.org/10.1515/ZNC-1992-9-1025
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
7-O-Methylluteolin 5318214 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 300.26 unknown https://doi.org/10.1515/ZNC-1992-9-1025

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