Salvia ballotiflora - Unknown
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Internal ID UUID643feb9773584679413503
Scientific name Salvia ballotiflora
Authority Benth.
First published in Labiat. Gen. Spec. : 270 (1833)

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Synonyms Top

Scientific name Authority First published in
Salvia ballotiflora var. eulaliae Fernald Proc. Amer. Acad. Arts 35: 522. 1900 as ballotaeflora
Salvia laxa Benth. Prodr. 12: 313 (1848)

Common names Top

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Language Common/alternative name
English shrubby blue sage

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 Northeast
    • South-central U.S.A.
      • Texas

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000300387
USDA Plants SABA5
Tropicos 17601683
KEW urn:lsid:ipni.org:names:455736-1
The Plant List kew-182081
Open Tree Of Life 582965
NCBI Taxonomy 268890
Nature Serve 2.153514
IPNI 455736-1
iNaturalist 168376
GBIF 2927043
Freebase /m/0bmb8mz
EPPO SALBF
EOL 579394
Wikipedia Salvia_ballotiflora

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
Structure, Absolute Configuration, Antiproliferative and Phytotoxic Activities of Icetexane and Abietane Diterpenoids from Salvia carranzae and Chemotaxonomic Implications Bustos-Brito C, Torres-Medicis JP, Bedolla-García BY, Zamudio S, Ramírez-Apan T, Macías-Rubalcava ML, Quijano L, Esquivel B Molecules 09-Mar-2024
PMCID:PMC10975418
doi:10.3390/molecules29061226
PMID:38542863
Immunomodulatory Activity of Diterpenes over Innate Immunity and Cytokine Production in a Human Alveolar Epithelial Cell Line Infected with Mycobacterium tuberculosis Hernández-Herrera AD, Luna-Herrera J, del Rocío González-Martínez M, Prieto-Hinojosa AI, Turcios-Esquivel AM, Castillo-Maldonado I, Delgadillo-Guzmán D, Ramírez-Moreno A, Bustos-Brito C, Esquivel B, Vega-Menchaca MD, Pedroza-Escobar D Curr Mol Pharmacol 24-Mar-2023
PMCID:PMC10240657
doi:10.2174/1874467215666221005115007
PMID:36200155
The Dual Benefit of Plant Essential Oils against Tuta absoluta Ben Abdallah S, Riahi C, Vacas S, Navarro-Llopis V, Urbaneja A, Pérez-Hedo M Plants (Basel) 21-Feb-2023
PMCID:PMC10005231
doi:10.3390/plants12050985
PMID:36903846
Recent Developments with Icetexane Natural Products Naeini AA, Ziegelmeier AA, Chain WJ Chem Biodivers 08-Nov-2022
PMCID:PMC11067433
doi:10.1002/cbdv.202200793
PMID:36215180
New Diterpenes with Potential Antitumoral Activity Isolated from Plants in the Years 2017–2022 Forzato C, Nitti P Plants (Basel) 29-Aug-2022
PMCID:PMC9460660
doi:10.3390/plants11172240
PMID:36079622
The Effect and Related Mechanism of Action of Astragalus Compatible with Curcumin against Colon Cancer Metastasis in Mice Wu J, Tang D Gastroenterol Res Pract 10-Jun-2022
PMCID:PMC9205740
doi:10.1155/2022/9578307
PMID:35721822
Review of Whole Plant Extracts With Activity Against Herpes Simplex Viruses In Vitro and In Vivo Garber A, Barnard L, Pickrell C J Evid Based Integr Med 16-Feb-2021
PMCID:PMC7894602
doi:10.1177/2515690X20978394
PMID:33593082
Anti-inflammatory and antitumor activities of the chloroform extract and anti-inflammatory effect of the three diterpenes isolated from Salvia ballotiflora Benth Campos-Xolalpa N, Alonso-Castro ÁJ, Ortíz-Sanchez E, Zapata-Morales JR, González-Chávez MM, Pérez S BMC Complement Med Ther 07-Jan-2021
PMCID:PMC7791881
doi:10.1186/s12906-020-03179-w
PMID:33413289
An In Vitro Evaluation of the Molecular Mechanisms of Action of Medical Plants from the Lamiaceae Family as Effective Sources of Active Compounds against Human Cancer Cell Lines Sitarek P, Merecz-Sadowska A, Śliwiński T, Zajdel R, Kowalczyk T Cancers (Basel) 13-Oct-2020
PMCID:PMC7601952
doi:10.3390/cancers12102957
PMID:33066157
Functional group and diversity analysis of BIOFACQUIM: A Mexican natural product database Sánchez-Cruz N, Pilón-Jiménez BA, Medina-Franco JL F1000Res 08-Jun-2020
PMCID:PMC6993822
doi:10.12688/f1000research.21540.1
PMID:32047598
Insecticidal and Genotoxic effects of some indigenous plant extracts in Culex quinquefasciatus Say Mosquitoes Zulhussnain M, Zahoor MK, Rizvi H, Zahoor MA, Rasul A, Ahmad A, Majeed HN, Rasul A, Ranian K, Jabeen F Sci Rep 22-Apr-2020
PMCID:PMC7176662
doi:10.1038/s41598-020-63815-w
PMID:32321960
Opportunities and Scope for Botanical Extracts and Products for the Management of Fall Armyworm (Spodoptera frugiperda) for Smallholders in Africa Rioba NB, Stevenson PC Plants (Basel) 06-Feb-2020
PMCID:PMC7076698
doi:10.3390/plants9020207
PMID:32041322
Medicinal Plants in the Prevention and Treatment of Colon Cancer Aiello P, Sharghi M, Mansourkhani SM, Ardekan AP, Jouybari L, Daraei N, Peiro K, Mohamadian S, Rezaei M, Heidari M, Peluso I, Ghorat F, Bishayee A, Kooti W Oxid Med Cell Longev 04-Dec-2019
PMCID:PMC7187726
doi:10.1155/2019/2075614
PMID:32377288
Structure, Absolute Configuration, and Antiproliferative Activity of Abietane and Icetexane Diterpenoids from Salvia ballotiflora. Esquivel B, Bustos-Brito C, Sánchez-Castellanos M, Nieto-Camacho A, Ramírez-Apan T, Joseph-Nathan P, Quijano L Molecules 18-Oct-2017
PMCID:PMC6151488
doi:10.3390/MOLECULES22101690
PMID:29057832
Structure, Absolute Configuration, and Antiproliferative Activity of Abietane and Icetexane Diterpenoids from Salvia ballotiflora Esquivel B, Bustos-Brito C, Sánchez-Castellanos M, Nieto-Camacho A, Ramírez-Apan T, Joseph-Nathan P, Quijano L Molecules 11-Oct-2017
PMCID:PMC6151488
doi:10.3390/molecules22101690
PMID:29057832

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
7,10-Dihydroxytetradec-5-en-8-ynoic acid 74318833 Click to see CCCCC(C#CC(C=CCCCC(=O)O)O)O 254.32 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151488/
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
[(1R,4aS,10aR)-5,6-dihydroxy-1,4a-dimethyl-9-oxo-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-1-yl]methyl acetate 162820090 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)COC(=O)C)C)O)O 374.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151488/
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(9,10,15-Trihydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl)methyl acetate 75052824 Click to see CC(=O)OCC1(CCC(C23C1C(C(C45C2CCC(C4)C(=C)C5=O)(OC3)O)O)O)C 406.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151488/
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Calyculin H 44576179 Click to see CC1C(CC2(C(C(C(O2)C(CC(C(C)C(C(C)C=C(C)C(=CC=CC(=CC#N)C)C)O)O)OC)OP(=O)(O)O)(C)C)OC1CC=CC3=COC(=N3)C(C)CC(C)NC(=O)C(C(C(COC)N(C)C)O)O)O 1023.20 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151488/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R)-1-[(1R,3aS,5aR,11aS,11bS)-3a,11a-dimethyl-1,2,3,4,5,5a,6,11b-octahydrocyclopenta[c]xanthen-1-yl]-2-methylpropan-1-ol 162929114 Click to see CC(C)C(C1CCC2(C1C3(C(CC2)CC4=CC=CC=C4O3)C)C)O 328.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151488/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
1,4a-dimethyl-7-prop-1-en-2-yl-3,4,5,6,8,8a-hexahydro-2H-naphthalene-1,2,6,7-tetrol 85272961 Click to see CC(=C)C1(CC2C(CCC(C2(C)O)O)(CC1O)C)O 270.36 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151488/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
Withaphysalin M 10096775 Click to see CC1=C(C(=O)OC(C1)C2(C3CCC4C3(CCC5C4CC6C7(C5(C(=O)C=CC7O)C)O6)C(=O)O2)C)C 482.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151488/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
8-[2-(1-carboxy-2-methylpropyl)-4,6-dihydroxy-1-oxo-3H-isoindol-5-yl]-2,6-dimethylocta-2,6-dienoic acid 162876876 Click to see CC(C)C(C(=O)O)N1CC2=C(C(=C(C=C2C1=O)O)CC=C(C)CCC=C(C)C(=O)O)O 431.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151488/
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
Sandorinic Acid C 11048975 Click to see CC1(C2CCC3=C(C2(CCC1=O)C)CC(C4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)O)C 470.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151488/
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
(1S,11S,12S)-4,5,7-trihydroxy-12-methyl-6-propan-2-yl-16-oxatetracyclo[10.3.2.01,11.03,8]heptadeca-3(8),4,6-triene-9,17-dione 162962056 Click to see CC(C)C1=C(C2=C(CC34CCCC(C3CC2=O)(C(=O)O4)C)C(=C1O)O)O 360.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151488/
> Organoheterocyclic compounds / Azaspirodecane derivatives
methyl (1S,2'S,5S,11R,12R,15R)-2'-ethyl-2'-hydroxy-3-methylspiro[3-azatetracyclo[6.5.1.11,5.011,14]pentadec-8(14)-ene-15,5'-oxane]-12-carboxylate 162974597 Click to see CCC1(CCC2(CO1)C3CCC4=C5C2(CC(C5CC4)C(=O)OC)CN(C3)C)O 389.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151488/

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