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Salvia wagneriana

Salvia wagneriana - 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 UUID643fec0280a2e147690671
Scientific name Salvia wagneriana
Authority Pol.
First published in Linnaea 41: 591 (1878)

Description Top

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Synonyms Top

Scientific name Authority First published in
Salvia albopileata Epling in Woodson & Schery Ann. Missouri Bot. Gard. 27: 337. 1940
Salvia tonduzii Briq. Annuaire Conserv. Jard. Bot. Genève 2: 157. 1898

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Nicaragua
      • Panamá

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000302627
Tropicos 17601344
KEW urn:lsid:ipni.org:names:457527-1
The Plant List kew-184157
Open Tree Of Life 6083678
NCBI Taxonomy 2039552
IPNI 457527-1
iNaturalist 285167
GBIF 3883845
Freebase /m/05p9q49
EOL 6341539
Wikipedia Salvia_wagneriana

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
From Plant to Chemistry: Sources of Active Opioid Antinociceptive Principles for Medicinal Chemistry and Drug Design Turnaturi R, Piana S, Spoto S, Costanzo G, Reina L, Pasquinucci L, Parenti C Molecules 14-Oct-2023
PMCID:PMC10609244
doi:10.3390/molecules28207089
PMID:37894567
Phylogenomics of Salvia L. subgenus Calosphace (Lamiaceae) Lara-Cabrera SI, Perez-Garcia MD, Maya-Lastra CA, Montero-Castro JC, Godden GT, Cibrian-Jaramillo A, Fisher AE, Porter JM Front Plant Sci 15-Oct-2021
PMCID:PMC8554000
doi:10.3389/fpls.2021.725900
PMID:34721456
1-O-Acetylgeopyxin A, a derivative of a fungal metabolite, blocks tetrodotoxin-sensitive voltage-gated sodium, calcium channels and neuronal excitability which correlates with inhibition of neuropathic pain Zhou Y, Cai S, Gomez K, Wijeratne EM, Ji Y, Bellampalli SS, Luo S, Moutal A, Gunatilaka AA, Khanna R Mol Brain 11-May-2020
PMCID:PMC7216607
doi:10.1186/s13041-020-00616-2
PMID:32393368
New clerodane diterpenoids from Salvia miniata Fernald (Lamiaceae) A Bisio, G Romussi, E Russo, S Cafaggi, D Fraternale, N De Tommasi Georg Thieme Verlag KG 05-Aug-2008
doi:10.1055/S-0028-1084389
Triterpenoids from Salvia wagneriana. Bisio A, De Tommasi N, Romussi G Pharmazie 01-Apr-2004
doi:10.1002/CHIN.200431151
PMID:15125580

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 / Diterpenoids / Colensane and clerodane diterpenoids
(+)-Hardwickiic Acid 15559627 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C(=O)O)C 316.40 unknown https://doi.org/10.1055/S-0028-1084389
Hardwickiic acid 15559629 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C(=O)O)C 316.40 unknown https://doi.org/10.1055/S-0028-1084389
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(4aR,5S,6R,8aR)-5-[2-[(1R,2R,6S,9R,11S,13R,14S,17S,18S)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.02,6.02,17.06,14.09,13]henicosa-15,19-dien-20-yl]ethyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid 162966717 Click to see CC1CCC2(C(C1(C)CCC3=CC4C5C=CC6C7(CC(OC7(CCC68C5(C3O4)C(=O)OC8)C)C9=COC=C9)C)CCC=C2C(=O)O)C 642.80 unknown https://doi.org/10.1055/S-0028-1084389
5-[2-[11-(Furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.02,6.02,17.06,14.09,13]henicosa-15,19-dien-20-yl]ethyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid 162966714 Click to see CC1CCC2(C(C1(C)CCC3=CC4C5C=CC6C7(CC(OC7(CCC68C5(C3O4)C(=O)OC8)C)C9=COC=C9)C)CCC=C2C(=O)O)C 642.80 unknown https://doi.org/10.1055/S-0028-1084389
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3R,3aR,5aR,5bR,7aR,11aS,11bR,12R,13aR,13bR)-1,3,12-trihydroxy-1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydrocyclopenta[a]chrysen-9-one 12110562 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)C(CC4C3(CCC5(C4C(CC5O)(C(C)(C)O)O)C)C)O)C)C 490.70 unknown https://doi.org/10.1002/CHIN.200431151
(1S,3R,3aR,5aR,5bR,7aR,9S,11aS,11bR,12R,13aR,13bR)-1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-tetradecahydro-2H-cyclopenta[a]chrysene-1,3,9,12-tetrol 12110563 Click to see CC1(C2CCC3(C(C2(CCC1O)C)C(CC4C3(CCC5(C4C(CC5O)(C(C)(C)O)O)C)C)O)C)C 492.70 unknown https://doi.org/10.1002/CHIN.200431151
1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-tetradecahydro-2H-cyclopenta[a]chrysene-1,3,9,12-tetrol 163044390 Click to see CC1(C2CCC3(C(C2(CCC1O)C)C(CC4C3(CCC5(C4C(CC5O)(C(C)(C)O)O)C)C)O)C)C 492.70 unknown https://doi.org/10.1002/CHIN.200431151
1,3,12-Trihydroxy-1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydrocyclopenta[a]chrysen-9-one 163023958 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)C(CC4C3(CCC5(C4C(CC5O)(C(C)(C)O)O)C)C)O)C)C 490.70 unknown https://doi.org/10.1002/CHIN.200431151
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 19-oxosteroids
(1R,4S,7R,9S,14R)-7-[(1R,2R,6S,9R,11S,13R,14S,17S,18S)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.02,6.02,17.06,14.09,13]henicosa-15,19-dien-20-yl]-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadeca-10,12-diene-5,15-dione 163056956 Click to see CC12CCC34COC(=O)C35C(C=CC4C1(CC(O2)C6=COC=C6)C)C7C=C(C5O7)C8CC9(C(CCC12C9=CC=CC1C(=O)OC2)C(=O)O8)C 666.80 unknown https://doi.org/10.1055/S-0028-1084389
7-[11-(Furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.02,6.02,17.06,14.09,13]henicosa-15,19-dien-20-yl]-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadeca-10,12-diene-5,15-dione 163056955 Click to see CC12CCC34COC(=O)C35C(C=CC4C1(CC(O2)C6=COC=C6)C)C7C=C(C5O7)C8CC9(C(CCC12C9=CC=CC1C(=O)OC2)C(=O)O8)C 666.80 unknown https://doi.org/10.1055/S-0028-1084389
> Organoheterocyclic compounds / Naphthopyrans
(1S,7R,9R,10R)-7-(furan-3-yl)-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadeca-3,13-diene-5,15-dione 162872747 Click to see CC12CC(OC(=O)C1=CCC34C2CCC=C3C(=O)OC4)C5=COC=C5 340.40 unknown https://doi.org/10.1055/S-0028-1084389
7-(Furan-3-yl)-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadeca-3,13-diene-5,15-dione 162872746 Click to see CC12CC(OC(=O)C1=CCC34C2CCC=C3C(=O)OC4)C5=COC=C5 340.40 unknown https://doi.org/10.1055/S-0028-1084389

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