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Salvia lasiantha

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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 UUID643febc4c3822825215482
Scientific name Salvia lasiantha
Authority Benth.
First published in Labiat. Gen. Spec. : 276 (1833)

Description Top

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Synonyms Top

Scientific name Authority First published in
Salvia altimitrata Epling Repert. Spec. Nov. Regni Veg. Beih. 110: 108. 1938
Salvia chrysantha M.Martens & Galeotti Bull. Acad. Roy. Sci. Bruxelles 11(2): 72 (1844)
Salvia lantanifolia M.Martens & Galeotti Bull. Acad. Roy. Sci. Bruxelles 11(2): 69 (1844)
Salvia pittieri Briq. ex T.Durand & Pittier Bull. Soc. Roy. Bot. Belgique xxx. 1891 (1892) 237.
Salvia populifolia Fernald Proc. Amer. Acad. Arts 35: 530. 1900

Common names Top

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Language Common/alternative name
Arabic قصعين أشعث الأزهار

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Central America
      • Costa Rica
      • Guatemala
      • Honduras

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000301375
Tropicos 17603322
KEW urn:lsid:ipni.org:names:456525-1
The Plant List kew-182990
Open Tree Of Life 574339
NCBI Taxonomy 392668
IPNI 456525-1
iNaturalist 277915
GBIF 3898253
CMAUP NPO9980

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
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
Floral Diversity and Pollen Transfer Mechanisms in Bird-pollinated Salvia Species Wester P, Claßen-Bockhoff R Ann Bot 22-May-2007
PMCID:PMC2735312
doi:10.1093/aob/mcm036
PMID:17522077
Staminal Evolution in the Genus Salvia (Lamiaceae): Molecular Phylogenetic Evidence for Multiple Origins of the Staminal Lever Walker JB, Sytsma KJ Ann Bot 22-Aug-2006
PMCID:PMC2735309
doi:10.1093/aob/mcl176
PMID:16926227
Lasianthin, a neo-clerodane diterpenoid from Salvia lasiantha Ana-Adela Sánchez, Baldomero Esquivel, Agapita Pera, Jorge Cárdenas, Manuel Soriano-García, Alfredo Toscano, Lydia Rodriguez-Hahn Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81437-5

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
Daniellic acid 6955052 Click to see CC12CCCC(C1CCC(=C)C2CCC3=COC=C3)(C)C(=O)O 316.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
8-(3,7-Dimethylocta-2,6-dienyl)-7-hydroxychromen-2-one 78151388 Click to see CC(=CCCC(=CCC1=C(C=CC2=C1OC(=O)C=C2)O)C)C 298.40 unknown via CMAUP database
Ostruthin 5281420 Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)C)C 298.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(2R,3S,4R,4aR,8aR)-3,4,8,8a-tetramethyl-6-oxo-4-[2-(5-oxo-2H-furan-3-yl)ethyl]-2,3,4a,5-tetrahydro-1H-naphthalen-2-yl] acetate 162933971 Click to see CC1C(CC2(C(C1(C)CCC3=CC(=O)OC3)CC(=O)C=C2C)C)OC(=O)C 374.50 unknown https://doi.org/10.1016/S0031-9422(00)81437-5
[3,4,8,8a-tetramethyl-6-oxo-4-[2-(5-oxo-2H-furan-3-yl)ethyl]-2,3,4a,5-tetrahydro-1H-naphthalen-2-yl] acetate 162933970 Click to see CC1C(CC2(C(C1(C)CCC3=CC(=O)OC3)CC(=O)C=C2C)C)OC(=O)C 374.50 unknown https://doi.org/10.1016/S0031-9422(00)81437-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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)81437-5
> 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)81437-5
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)81437-5
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
3-(3-Methyl-2-butenoyl)-1H-indole 11805712 Click to see CC(=CC(=O)C1=CNC2=CC=CC=C21)C 199.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown via CMAUP database
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Dihydroluvangetin 11482357 Click to see CC1(CCC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)OC)C 260.28 unknown via CMAUP database
Xanthyletin 65188 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 228.24 unknown via CMAUP database

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