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Salvia reptans

Salvia reptans - 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 UUID643febe8d4d4d065000020
Scientific name Salvia reptans
Authority Jacq.
First published in Pl. Hort. Schoenbr. 3: 38 (1798)

Description Top

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Salvia reptans is a perennial herb that is commonly found in the mountains of Trans-Pecos in Texas, as well as in Mexico and Guatemala. It prefers dry stream beds and gravelly soils. This plant was introduced into horticulture in the 19th century and was previously known by different names, alluding to its slender leaves. The name "reptans" refers to its creeping growth habit. There are two forms of this plant - one that is commonly grown in gardens and has lax or decumbent stems, and another that is native to western Texas and grows upright. The variety "glabra" can also be found growing wild in Texas. In gardens, Salvia reptans can reach a width of 3 feet or more, with thin black stems that can make a groundcover. The leaves are narrow and mistletoe-green in color, while the flowers are small with blue corollas and dark calyces.

Synonyms Top

Scientific name Authority First published in
Salvia angustifolia Cav. Icon. 4: 9 (1797)
Salvia angustifolia var. glabra Briq. Bull. Herb. Boissier 7: 570 (1899)
Salvia leptophylla Benth. Labiat. Gen. Spec. : 249 (1833)
Salvia linearis Sessé & Moc. Naturaleza (Mexico City) ser. 2, 2, app. 6. 1892 Fl. Mex
Salvia linifolia M.Martens & Galeotti Bull. Acad. Roy. Sci. Bruxelles 11(2): 70 (1844)
Salvia virgata Ortega Nov. Rar. Pl. Descr. Dec. : 3 (1797)
Salvia reptans var. reptans Jacq.
Salvia angustifolia var. glabra A.Gray Syn. Fl. N. Amer. 2(1): 369. 1878

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Northeast
      • Mexico Southeast
      • Mexico Southwest
    • South-central U.S.A.
      • Texas

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000302122
Tropicos 50207314
KEW urn:lsid:ipni.org:names:457104-1
The Plant List kew-183690
Open Tree Of Life 3882829
NCBI Taxonomy 2026526
IPNI 457104-1
iNaturalist 287591
GBIF 3889656
Freebase /m/05myh5t
Wikipedia Salvia_reptans

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
Antimicrobial Diterpenes from Salvia reptans Mariano Martínez-Vázquez, Patricia Miranda, Norma A. Valencia, Maria Luisa Torres, René Miranda, Jorge Cárdenas, Manuel Salmón Informa UK Limited 25-Mar-2003
doi:10.1076/PHBI.36.2.77.4611
Clerodane and seco-clerodane diterpenoids from Salvia reptans Baldomero Esquivel, Obdulia Esquivel, Jorge Cárdenas, Ana Adela Sánchez, T.P. Ramamoorthy, Rubén Alfredo Toscano, Lydia Rodríguez-Hahn Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83644-Z

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
Horminone 2751795 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2O)(C)C)C)O 332.40 unknown https://doi.org/10.1076/PHBI.36.2.77.4611
Taxoquinone 99965 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2O)(C)C)C)O 332.40 unknown https://doi.org/10.1076/PHBI.36.2.77.4611
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Hydroxyolean-12-en-28-oic acid 619166 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/10.1016/0031-9422(91)83644-Z
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0031-9422(91)83644-Z
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/10.1016/0031-9422(91)83644-Z
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0031-9422(91)83644-Z
> 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/10.1016/0031-9422(91)83644-Z
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/10.1016/0031-9422(91)83644-Z
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/10.1016/0031-9422(91)83644-Z
> Organoheterocyclic compounds / Isocoumarans / Isobenzofuranones / Phthalides
4-[(3R,4S,5S)-3-[2-(furan-3-yl)-2-oxoethyl]-4,5-dimethyl-2-oxooxolan-3-yl]-3H-2-benzofuran-1-one 162951045 Click to see CC1C(OC(=O)C1(CC(=O)C2=COC=C2)C3=CC=CC4=C3COC4=O)C 354.40 unknown https://doi.org/10.1016/0031-9422(91)83644-Z
4-[3-[2-(furan-3-yl)-2-oxoethyl]-4,5-dimethyl-2-oxooxolan-3-yl]-3H-2-benzofuran-1-one 14866175 Click to see CC1C(OC(=O)C1(CC(=O)C2=COC=C2)C3=CC=CC4=C3COC4=O)C 354.40 unknown https://doi.org/10.1016/0031-9422(91)83644-Z
7-[(3R,4S,5S)-3-[2-(furan-3-yl)-2-oxoethyl]-4,5-dimethyl-2-oxooxolan-3-yl]-3H-2-benzofuran-1-one 101607177 Click to see CC1C(OC(=O)C1(CC(=O)C2=COC=C2)C3=CC=CC4=C3C(=O)OC4)C 354.40 unknown https://doi.org/10.1016/0031-9422(91)83644-Z
> Organoheterocyclic compounds / Naphthopyrans
(1S,4S,7R,9R,10S,11R,13S,15S)-7-(furan-3-yl)-9-methyl-6,12,17-trioxapentacyclo[8.8.0.01,15.04,9.011,13]octadecane-5,16-dione 14866174 Click to see CC12CC(OC(=O)C1CCC34C2C5C(O5)CC3C(=O)OC4)C6=COC=C6 358.40 unknown https://doi.org/10.1016/0031-9422(91)83644-Z
7-(Furan-3-yl)-9-methyl-6,12,17-trioxapentacyclo[8.8.0.01,15.04,9.011,13]octadecane-5,16-dione 14866173 Click to see CC12CC(OC(=O)C1CCC34C2C5C(O5)CC3C(=O)OC4)C6=COC=C6 358.40 unknown https://doi.org/10.1016/0031-9422(91)83644-Z
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/0031-9422(91)83644-Z

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