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Salvia blepharophylla

Salvia blepharophylla - Unknown
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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
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Details Top

Internal ID UUID643feb9a0ede2921242404
Scientific name Salvia blepharophylla
Authority Brandegee ex Epling
First published in Repert. Spec. Nov. Regni Veg. Beih. 110: 314. 1939

Description Top

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Salvia blepharophylla, also known as eyelash-leaved sage, is a perennial plant native to the Mexican states of San Luis Potosí and Tamaulipas. Its name comes from the Greek word for "with leaves fringed like eyelashes". This plant has a creeping growth habit and can quickly spread through stolons. It produces bright red flowers with an orange undertone, measuring 2.5 cm in length. The flowers are arranged in loose whorls and spaced about 2.5 cm apart on inflorescences that can reach up to 30 cm in length. When in full bloom, the plant can reach a height of 45 cm.

Synonyms Top

No known synonyms.

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000300457
Tropicos 17605257
KEW urn:lsid:ipni.org:names:226438-2
The Plant List kew-182145
Open Tree Of Life 1074406
NCBI Taxonomy 933122
IPNI 307380-2
iNaturalist 477081
GBIF 3883534
Freebase /m/05b2txz
EOL 6341723
USDA GRIN 467884
Wikipedia Salvia_blepharophylla

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
Green Synthesis of Novel Silver Nanoparticles Using Salvia blepharophylla and Salvia greggii: Antioxidant and Antidiabetic Potential and Effect on Foodborne Bacterial Pathogens Geremew A, Gonzalles J III, Peace E, Woldesenbet S, Reeves S, Brooks N Jr, Carson L Int J Mol Sci 11-Jan-2024
PMCID:PMC10815671
doi:10.3390/ijms25020904
PMID:38255978
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
In Silico Studies of Lamiaceae Diterpenes with Bioinsecticide Potential against Aphis gossypii and Drosophila melanogaster Rodrigues GC, dos Santos Maia M, Silva Cavalcanti AB, de Sousa NF, Scotti MT, Scotti L Molecules 02-Feb-2021
PMCID:PMC7867283
doi:10.3390/molecules26030766
PMID:33540716
Tools to Tie: Flower Characteristics, VOC Emission Profile, and Glandular Trichomes of Two Mexican Salvia Species to Attract Bees Giuliani C, Giovanetti M, Lupi D, Mesiano MP, Barilli R, Ascrizzi R, Flamini G, Fico G Plants (Basel) 25-Nov-2020
PMCID:PMC7760984
doi:10.3390/plants9121645
PMID:33255733
A botanic garden as a tool to combine public perception of nature and life-science investigations on native/exotic plants interactions with local pollinators Giovanetti M, Giuliani C, Boff S, Fico G, Lupi D PLoS One 20-Feb-2020
PMCID:PMC7032708
doi:10.1371/journal.pone.0228965
PMID:32078664
α-Glucosidase Inhibitors from Salvia circinata. Flores-Bocanegra L, González-Andrade M, Bye R, Linares E, Mata R J Nat Prod 26-May-2017
doi:10.1021/ACS.JNATPROD.7B00155
PMID:28422509
Clerodane diterpenes: sources, structures, and biological activities Li R, Morris-Natschke SL, Lee KH Nat Prod Rep 18-Jul-2016
PMCID:PMC5154363
doi:10.1039/c5np00137d
PMID:27433555
Mechanosensitivity below Ground: Touch-Sensitive Smell-Producing Roots in the Shy Plant Mimosa pudica Musah RA, Lesiak AD, Maron MJ, Cody RB, Edwards D, Fowble KL, Dane AJ, Long MC Plant Physiol 09-Dec-2015
PMCID:PMC4734582
doi:10.1104/pp.15.01705
PMID:26661932
Polyphenolic profile and biological activity of Salvia splendens leaves. Moharram FA, Marzouk MS, El-Shenawy SM, Gaara AH, El Kady WM J Pharm Pharmacol 01-Nov-2012
doi:10.1111/J.2042-7158.2012.01544.X
PMID:23058056
Morphology and Histochemistry of the Glandular Trichomes of Lippia scaberrima (Verbenaceae) Combrinck S, Du Plooy GW, McCrindle RI, Botha BM Ann Bot 27-Apr-2007
PMCID:PMC3243582
doi:10.1093/aob/mcm064
PMID:17468110
Subject Index N/A 01-Jan-2005
PMCID:PMC7148952
doi:10.1016/S1572-5995(05)80049-3
Light, Conventional and Environmental Scanning Electron Microscopy of the Trichomes of Cucurbita pepo subsp. pepo var. styriaca and Histochemistry of Glandular Secretory Products KOLB D, MÜLLER M Ann Bot 11-Aug-2004
PMCID:PMC4242234
doi:10.1093/aob/mch180
PMID:15306562
Changes in Leaf Trichomes and Epicuticular Flavonoids during Leaf Development in Three Birch Taxa VALKAMA E, SALMINEN JP, KORICHEVA J, PIHLAJA K Ann Bot 28-Jun-2004
PMCID:PMC4242156
doi:10.1093/aob/mch131
PMID:15238348
UV‐B is Required for Normal Development of Oil Glands in Ocimum basilicum L. (Sweet Basil) IOANNIDIS D, BONNER L, JOHNSON CB Ann Bot 01-Oct-2002
PMCID:PMC4240378
doi:10.1093/aob/mcf212
PMID:12324268
Clerodane diterpenoids from Salvia blepharophylla Angela Bisio, Nadia Fontana, Giovanni Romussi, Giovanni Ciarallo, Nunziatina De Tommasi, Cosimo Pizza, Angelo Mugnoli Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00324-6

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 / Triterpenoids
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/S0031-9422(99)00324-6
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/S0031-9422(99)00324-6
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S,7R,9S,10R,14R)-7-(furan-3-yl)-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,8]heptadeca-4(8),12-diene-5,15-dione 162848767 Click to see CC1C2CC=CC3C2(CCC4=C1C(OC4=O)C5=COC=C5)COC3=O 340.40 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
(1S,7S,9R,10S,14R)-7-(furan-3-yl)-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,8]heptadeca-4(8),12-diene-5,15-dione 162848768 Click to see CC1C2CC=CC3C2(CCC4=C1C(OC4=O)C5=COC=C5)COC3=O 340.40 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
(1S,9R,10S,14R)-7-(furan-3-yl)-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,8]heptadeca-4(8),12-diene-5,15-dione 15479020 Click to see CC1C2CC=CC3C2(CCC4=C1C(OC4=O)C5=COC=C5)COC3=O 340.40 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
7-(Furan-3-yl)-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,8]heptadeca-4(8),12-diene-5,15-dione 162848766 Click to see CC1C2CC=CC3C2(CCC4=C1C(OC4=O)C5=COC=C5)COC3=O 340.40 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
> Organoheterocyclic compounds / Naphthopyrans
(1S,3S,4S,7R,8S,9R,10R,14R)-7-(furan-3-yl)-3-hydroxy-9-methyl-6,16-dioxapentacyclo[8.7.0.01,14.04,8.04,9]heptadec-12-ene-5,15-dione 162955888 Click to see CC12C3CC=CC4C3(CC(C15C2C(OC5=O)C6=COC=C6)O)COC4=O 356.40 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
(1S,3S,4S,7R,8S,9S,10R,14R)-7-(furan-3-yl)-3-hydroxy-9-methyl-6,16-dioxapentacyclo[8.7.0.01,14.04,8.04,9]heptadec-12-ene-5,15-dione 15479019 Click to see CC12C3CC=CC4C3(CC(C15C2C(OC5=O)C6=COC=C6)O)COC4=O 356.40 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
7-(Furan-3-yl)-3-hydroxy-9-methyl-6,16-dioxapentacyclo[8.7.0.01,14.04,8.04,9]heptadec-12-ene-5,15-dione 162955887 Click to see CC12C3CC=CC4C3(CC(C15C2C(OC5=O)C6=COC=C6)O)COC4=O 356.40 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)-8-(3,4,5-Trihydroxyoxan-2-Yl)Chromen-4-One 3550102 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2R,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 49794094 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 5378180 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 154497677 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
Schaftoside 442658 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
(2S,3S,4R,5S,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 154497005 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
Quercetin 3-glucuronide 12004528 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
https://doi.org/10.1016/S0031-9422(01)00415-0
Querciturone 5274585 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14704553 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 154497326 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
Quercetin 3-O-robinobioside 10371536 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
Rhamnetin 3-O-|A-D-glucopyranoside 14704554 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
Vitamin P 5293655 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Nuchensin 373260 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O)O 330.29 unknown https://doi.org/10.1016/S0031-9422(99)00324-6
Pedalitin 31161 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)O 316.26 unknown https://doi.org/10.1111/J.2042-7158.2012.01544.X
https://doi.org/10.1016/S0031-9422(99)00324-6
https://doi.org/10.1021/ACS.JNATPROD.7B00155

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