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Salvia pomifera

Salvia pomifera - 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 UUID643febe00d5a3472799030
Scientific name Salvia pomifera
Authority L.
First published in Sp. Pl. : 24 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Crolocos pomifera Raf. Fl. Tellur. 3: 93 (1837)

Common names Top

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Language Common/alternative name
English apple-bearing sage
Arabic خوخ بري
German apfel-salbei
German kreta-salbei
German apfeltragender salbei

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Salvia pomifera subsp. calycina (Sm.) Hayek Repert. Spec. Nov. Regni Veg. Beih. 30(2): 306 (1929)
Salvia pomifera subsp. pomifera Unknown

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-0000301968
Tropicos 17600605
KEW urn:lsid:ipni.org:names:456985-1
The Plant List kew-183545
Open Tree Of Life 618972
Observations.org 139168
NCBI Taxonomy 396869
IPNI 456985-1
iNaturalist 513848
GBIF 3891602
EPPO SALPM
Elurikkus 434814
USDA GRIN 404844

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
Comparative transcriptomics of two Salvia subg. Perovskia species contribute towards molecular background of abietane-type diterpenoid biosynthesis Bielecka M, Stafiniak M, Pencakowski B, Ślusarczyk S, Jastrzębski JP, Paukszto Ł, Łaczmański Ł, Gharibi S, Matkowski A Sci Rep 06-Feb-2024
PMCID:PMC10847172
doi:10.1038/s41598-024-53510-5
PMID:38321199
Identification of Volatile Compounds and Terpene Synthase (TPS) Genes Reveals ZcTPS02 Involved in β-Ocimene Biosynthesis in Zephyranthes candida Wei G, Xu Y, Xu M, Shi X, Wang J, Feng L Genes (Basel) 30-Jan-2024
PMCID:PMC10887521
doi:10.3390/genes15020185
PMID:38397175
Climate Change Dependence in Ex Situ Conservation of Wild Medicinal Plants in Crete, Greece Bariotakis M, Georgescu L, Laina D, Koufaki M, Souma M, Douklias S, Giannakakis KA, Chouli KN, Paoli L, Loppi S, Karousou R, Smykal P, Castanas E, Pirintsos SA Biology (Basel) 11-Oct-2023
PMCID:PMC10604457
doi:10.3390/biology12101327
PMID:37887037
Functional divergence of CYP76AKs shapes the chemodiversity of abietane-type diterpenoids in genus Salvia Hu J, Qiu S, Wang F, Li Q, Xiang CL, Di P, Wu Z, Jiang R, Li J, Zeng Z, Wang J, Wang X, Zhang Y, Fang S, Qiao Y, Ding J, Jiang Y, Xu Z, Chen J, Chen W Nat Commun 04-Aug-2023
PMCID:PMC10403556
doi:10.1038/s41467-023-40401-y
PMID:37542034
Engineered production of isoprene from the model green microalga Chlamydomonas reinhardtii Yahya RZ, Wellman GB, Overmans S, Lauersen KJ Metab Eng Commun 23-Mar-2023
PMCID:PMC10063407
doi:10.1016/j.mec.2023.e00221
PMID:37006831
Biocontrol Activity of Aromatic and Medicinal Plants and Their Bioactive Components against Soil-Borne Pathogens Greff B, Sáhó A, Lakatos E, Varga L Plants (Basel) 05-Feb-2023
PMCID:PMC9958657
doi:10.3390/plants12040706
PMID:36840053
Uncovering a miltiradiene biosynthetic gene cluster in the Lamiaceae reveals a dynamic evolutionary trajectory Bryson AE, Lanier ER, Lau KH, Hamilton JP, Vaillancourt B, Mathieu D, Yocca AE, Miller GP, Edger PP, Buell CR, Hamberger B Nat Commun 20-Jan-2023
PMCID:PMC9860074
doi:10.1038/s41467-023-35845-1
PMID:36670101
GC-MS and LC-DAD-MS Phytochemical Profiling for Characterization of Three Native Salvia Taxa from Eastern Mediterranean with Antiglycation Properties Gkioni MD, Zeliou K, Dimaki VD, Trigas P, Lamari FN Molecules 22-Dec-2022
PMCID:PMC9821822
doi:10.3390/molecules28010093
PMID:36615289
Can Molecularly Engineered Plant Galls Help to Ease the Problem of World Food Shortage (and Our Dependence on Pollinating Insects)? Meyer-Rochow VB Foods 12-Dec-2022
PMCID:PMC9777877
doi:10.3390/foods11244014
PMID:36553755
Combined analysis of transcriptomics and metabolomics revealed complex metabolic genes for diterpenoids biosynthesis in different organs of Anoectochilus roxburghii Wei Y, Zhang J, Qi K, Li Y, Chen Y Chin Herb Med 21-Nov-2022
PMCID:PMC10230631
doi:10.1016/j.chmed.2022.11.002
PMID:37265764
From Traditional Ethnopharmacology to Modern Natural Drug Discovery: A Methodology Discussion and Specific Examples Pirintsos S, Panagiotopoulos A, Bariotakis M, Daskalakis V, Lionis C, Sourvinos G, Karakasiliotis I, Kampa M, Castanas E Molecules 24-Jun-2022
PMCID:PMC9268545
doi:10.3390/molecules27134060
PMID:35807306
Quantifying Cardinal Temperatures of Chia (Salvia hispanica L.) Using Non-Linear Regression Models Cabrera-Santos D, Ordoñez-Salanueva CA, Sampayo-Maldonado S, Campos JE, Orozco-Segovia A, Flores-Ortiz CM Plants (Basel) 22-Apr-2022
PMCID:PMC9105696
doi:10.3390/plants11091142
PMID:35567143
Tanshinones: Leading the way into Lamiaceae labdane-related diterpenoid biosynthesis Wang Z, Peters RJ Curr Opin Plant Biol 20-Feb-2022
PMCID:PMC8940693
doi:10.1016/j.pbi.2022.102189
PMID:35196638
Phytochemical profile, antioxidant, antiproliferative, and enzyme inhibition-docking analyses of Salvia ekimiana Celep & Doğan Karatoprak GŞ, Göger F, Çelik İ, Budak Ü, Akkol EK, Aschner M S Afr J Bot 09-Oct-2021
PMCID:PMC8863303
doi:10.1016/j.sajb.2021.09.033
PMID:35210693
Phytochemical Study and In Vitro Screening Focusing on the Anti-Aging Features of Various Plants of the Greek Flora Sklirou AD, Angelopoulou MT, Argyropoulou A, Chaita E, Boka VI, Cheimonidi C, Niforou K, Mavrogonatou E, Pratsinis H, Kalpoutzakis E, Aligiannis N, Kletsas D, Trougakos IP, Skaltsounis AL Antioxidants (Basel) 28-Jul-2021
PMCID:PMC8389045
doi:10.3390/antiox10081206
PMID:34439454

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.2000.9712167
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1,4a-Dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl)methanol 107171 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)CO)C 286.50 unknown https://doi.org/10.1016/S0031-9422(00)97560-5
(1,4a-dimethyl-9-oxo-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-1-yl)methyl acetate 163072054 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)COC(=O)C)C 342.50 unknown https://doi.org/10.1016/S0031-9422(00)89809-X
(3R,4aS,10aS)-3-hydroxy-7-(2-hydroxypropan-2-yl)-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 101666185 Click to see CC1(CC(CC2(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)C)O)C 316.40 unknown https://doi.org/10.1016/S0031-9422(00)89809-X
(3S,4aS,10aR)-3-hydroxy-7-(2-hydroxypropan-2-yl)-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 163082289 Click to see CC1(CC(CC2(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)C)O)C 316.40 unknown https://doi.org/10.1016/S0031-9422(00)89809-X
(3S,4aS,10aS)-3-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 101635446 Click to see CC(C)C1=CC2=C(C=C1)C3(CC(CC(C3CC2=O)(C)C)O)C 300.40 unknown https://doi.org/10.1016/S0031-9422(00)89809-X
https://doi.org/10.1016/S0031-9422(00)97560-5
(6-Hydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl)methyl acetate 73050282 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)COC(=O)C)C)O 344.50 unknown https://doi.org/10.1016/S0031-9422(00)97560-5
[(1R,4aS,10aR)-1,4a-dimethyl-9-oxo-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-1-yl]methyl acetate 101666186 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)COC(=O)C)C 342.50 unknown https://doi.org/10.1016/S0031-9422(00)89809-X
[(1R,4aS,10aS)-1,4a-dimethyl-9-oxo-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-1-yl]methyl acetate 163072055 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)COC(=O)C)C 342.50 unknown https://doi.org/10.1016/S0031-9422(00)89809-X
1,1,4a-Trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-3-ol 162862729 Click to see CC(C)C1=CC2=C(C=C1)C3(CC(CC(C3CC2)(C)C)O)C 286.50 unknown https://doi.org/10.1016/S0031-9422(00)97560-5
3-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 163081456 Click to see CC(C)C1=CC2=C(C=C1)C3(CC(CC(C3CC2=O)(C)C)O)C 300.40 unknown https://doi.org/10.1016/S0031-9422(00)97560-5
3-hydroxy-7-(2-hydroxypropan-2-yl)-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 163082288 Click to see CC1(CC(CC2(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)C)O)C 316.40 unknown https://doi.org/10.1016/S0031-9422(00)89809-X
5-Hydroxy-6-methoxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid 73816012 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)O)OC 346.50 unknown https://doi.org/10.1016/S0031-9422(00)97560-5
Dehydroabietinol 15586718 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)CO)C 286.50 unknown https://doi.org/10.1016/S0031-9422(00)97560-5
https://doi.org/10.1016/S0031-9422(00)89809-X
Pomiferin B 21632842 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)COC(=O)C)C)O 344.50 unknown https://doi.org/10.1016/S0031-9422(00)89809-X
https://doi.org/10.1016/S0031-9422(00)97560-5
Pomiferin C 21632854 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)O)OC 346.50 unknown https://doi.org/10.1016/S0031-9422(00)89809-X
https://doi.org/10.1016/S0031-9422(00)97560-5
Pomiferin D 101635445 Click to see CC(C)C1=CC2=C(C=C1)C3(CC(CC(C3CC2)(C)C)O)C 286.50 unknown https://doi.org/10.1016/S0031-9422(00)89809-X
https://doi.org/10.1016/S0031-9422(00)97560-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
[(1R,2R,6S,10R,11R,13S,14R,15R)-13-acetyloxy-8-formyl-1-hydroxy-4,12,12,15-tetramethyl-5-oxo-14-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] 2-(methylamino)benzoate 162901456 Click to see CC1C(C2(C(C2(C)C)C3C1(C4C=C(C(=O)C4CC(=C3)C=O)C)O)OC(=O)C)OC(=O)C5=CC=CC=C5NC 521.60 unknown https://doi.org/10.1016/S0031-9422(00)97560-5
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.2000.9712167
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1080/10412905.2000.9712167
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.2000.9712167
3-Thujanone 11027 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1992.9698143
beta-Thujone 91456 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1992.9698143
https://doi.org/10.1080/10412905.2000.9712167
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1080/10412905.2000.9712167
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1080/10412905.2000.9712167
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1080/10412905.2000.9712167
Thujone 261491 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1992.9698143
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1080/10412905.2000.9712167
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrene B 5281519 Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.2000.9712167
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aS,6aR,6bR,8aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicen-3-ol 15560617 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)CO)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)89809-X
(6aR,6bR,8aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol 145706026 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97560-5
23-Hydroxygermanicone 101665855 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(=O)C5(C)CO)C)C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(00)89809-X
4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-2,4a,5,6,6a,7,8,9,10,13,14,14a-dodecahydro-1H-picen-3-one 163013662 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(=O)C5(C)CO)C)C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(00)89809-X
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97560-5
Erythrodiol 101761 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)89809-X
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97560-5
Methyl oleanolate 92900 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC)C 470.70 unknown https://doi.org/10.1016/S0031-9422(00)97560-5
Moronic acid 489941 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C(=O)O)C 454.70 unknown https://doi.org/10.1016/S0031-9422(00)89809-X
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/10.1016/S0031-9422(00)97560-5
Urs-12-en-3beta-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97560-5
> 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/10.1016/S0031-9422(00)97560-5
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/10.1016/S0031-9422(00)97560-5
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/10.1016/S0031-9422(00)97560-5
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
Isoamyl alcohol 31260 Click to see CC(C)CCO 88.15 unknown https://doi.org/10.1080/10412905.2000.9712167

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