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Salvia dianthera

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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 UUID643febab04092411348115
Scientific name Salvia dianthera
Authority Roth ex Roem. & Schult.
First published in Syst. Veg., ed. 15 bis 1: 263 (1817)

Description Top

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Synonyms Top

Scientific name Authority First published in
Meriandra abyssinica F.Muell. Select Pl. , ed. 2: 130 (1876)
Meriandra bengalensis (Roxb.) Benth. Edwards's Bot. Reg. 15: t. 1282 (1829)
Salvia bengalensis Roxb. Fl. Ind. ed. 1832 , 1: 145 (1832)
Salvia stachydea J.G.Klein ex Schult. Mant. 1: 216 (1822)

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000300855
Tropicos 100253634
KEW urn:lsid:ipni.org:names:456098-1
Open Tree Of Life 619544
NCBI Taxonomy 392636
IPNI 456098-1
iNaturalist 919188
GBIF 3904071
Wikipedia Salvia_dianthera

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
Plant Species as Potential Forage for Honey Bees in the Al-Baha Mountain Region in Southwestern Saudi Arabia Al-Ghamdi AA, Al-Sagheer NA Plants (Basel) 22-Mar-2023
PMCID:PMC10058344
doi:10.3390/plants12061402
PMID:36987090
The Botanical, Chemical and Ethnobotanical Diversity of Southern African Lamiaceae Rattray RD, Van Wyk BE Molecules 18-Jun-2021
PMCID:PMC8233991
doi:10.3390/molecules26123712
PMID:34207006
Natural plant species inventory of hotspot areas in Arabian Peninsula: Southwest Al-Baha region, Saudi Arabia Al-Namazi AA, Al-Khulaidi AW, Algarni S, Al-Sagheer NA Saudi J Biol Sci 04-Mar-2021
PMCID:PMC8176062
doi:10.1016/j.sjbs.2021.02.076
PMID:34121869
Inhibitory evaluation of Curculigo latifolia on α-glucosidase, DPP (IV) and in vitro studies in antidiabetic with molecular docking relevance to type 2 diabetes mellitus Zabidi NA, Ishak NA, Hamid M, Ashari SE, Mohammad Latif MA J Enzyme Inhib Med Chem 29-Nov-2020
PMCID:PMC7717572
doi:10.1080/14756366.2020.1844680
PMID:33249946
Analysis of Chemical Composition and Assessment of Cytotoxic, Antimicrobial, and Antioxidant Activities of the Essential Oil of Meriandra dianthera Growing in Saudi Arabia Mothana RA, Nasr FA, Khaled JM, AL-Zharani M, Noman OM, Abutaha N, Al-Rehaily AJ, Almarfadi OM, Kumar A, Kurkcuoglu M Molecules 22-Jul-2019
PMCID:PMC6680587
doi:10.3390/molecules24142647
PMID:31336582
In Vitro Inhibition of α-Amylase and α-Glucosidase by Extracts from Psiadia punctulata and Meriandra bengalensis Kidane Y, Bokrezion T, Mebrahtu J, Mehari M, Gebreab YB, Fessehaye N, Achila OO Evid Based Complement Alternat Med 16-Jul-2018
PMCID:PMC6077584
doi:10.1155/2018/2164345
PMID:30108648
Human-Forest interfaces in Hugumburda-Gratkhassu National Forest Priority Area, North-eastern Ethiopia Kidane L, Nemomissa S, Bekele T J Ethnobiol Ethnomed 23-Feb-2018
PMCID:PMC5824611
doi:10.1186/s13002-018-0218-7
PMID:29471862
Main vegetation types and plant species diversity along an altitudinal gradient of Al Baha region, Saudi Arabia Al-Aklabi A, Al-Khulaidi AW, Hussain A, Al-Sagheer N Saudi J Biol Sci 03-Mar-2016
PMCID:PMC5109499
doi:10.1016/j.sjbs.2016.02.007
PMID:27872563
Assessment of wild leafy vegetables traditionally consumed by the ethnic communities of Manipur, northeast India Thongam B, Konsam S, Handique AK J Ethnobiol Ethnomed 29-Jan-2016
PMCID:PMC4731935
doi:10.1186/s13002-016-0080-4
PMID:26822996
A Survey of Chemical Compositions and Biological Activities of Yemeni Aromatic Medicinal Plants Chhetri BK, Awadh Ali NA, Setzer WN Medicines (Basel) 28-May-2015
PMCID:PMC5533162
doi:10.3390/medicines2020067
PMID:28930202
Why Africa matters: evolution of Old World Salvia (Lamiaceae) in Africa Will M, Claßen-Bockhoff R Ann Bot 01-Jul-2014
PMCID:PMC4071099
doi:10.1093/aob/mcu081
PMID:24966353
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
Sesquiterpenoid constituents of Meriandra benghalensis (Labiatae). X-ray structure analysis Aurea Perales, Martin Martinez-Ripoll, Jose Fayos, Giuseppe Savona, Maurizio Bruno, Benjamin Rodriguez American Chemical Society (ACS) 12-Mar-2005
doi:10.1021/JO00174A030
Abietane and 20-nor-abietane diterpenoids from the root of Meriandra benghalensis Maria C. de la Torre, Maurizio Bruno, Benjamín Rodríguez, Guiseppe Savona Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97561-7

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4bS,8aS,10R)-10-hydroxy-3-methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-1,4-dione 71676389 Click to see CC(C)C1=C(C(=O)C2=C(C1=O)C(CC3C2(CCCC3(C)C)C)O)OC 346.50 unknown https://doi.org/10.1016/S0031-9422(00)97561-7
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/10.1016/S0031-9422(00)97561-7
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/10.1016/S0031-9422(00)97561-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
1,6,6-Trimethyl-1,2,6,7,8,9-hexahydrophenanthro[1,2-b]furan-10,11-dione 496348 Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C 296.40 unknown https://doi.org/10.1016/S0031-9422(00)97561-7
Cryptotanshinone 160254 Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C 296.40 unknown https://doi.org/10.1016/S0031-9422(00)97561-7
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Camphor (synthetic) 159055 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1021/JO00174A030
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,5R,6S,9R,10S)-5-methyl-2-propan-2-yl-11-oxatricyclo[7.2.1.01,6]dodecane-5,9,10-triol 101318104 Click to see CC(C)C1CCC(C2C13CC(CC2)(C(O3)O)O)(C)O 270.36 unknown https://doi.org/10.1021/JO00174A030
(1R,8S,11R)-1,11-dihydroxy-8-methyl-11-propan-2-yl-2-oxatricyclo[6.3.1.04,12]dodeca-4(12),6-dien-5-one 101318103 Click to see CC(C)C1(CCC2(C=CC(=O)C3=C2C1(OC3)O)C)O 264.32 unknown https://doi.org/10.1021/JO00174A030
(1R,8S,11S)-1,11-dihydroxy-8-methyl-11-propan-2-yl-2-oxatricyclo[6.3.1.04,12]dodeca-4(12),6-dien-5-one 163023757 Click to see CC(C)C1(CCC2(C=CC(=O)C3=C2C1(OC3)O)C)O 264.32 unknown https://doi.org/10.1021/JO00174A030
(1S,9R,12R)-1-hydroxy-9-methyl-12-propan-2-yl-2,3-dioxatricyclo[7.3.1.05,13]trideca-5(13),7-dien-6-one 162932051 Click to see CC(C)C1CCC2(C=CC(=O)C3=C2C1(OOC3)O)C 264.32 unknown https://doi.org/10.1021/JO00174A030
(1S,9S,12S)-1-hydroxy-9-methyl-12-propan-2-yl-2,3-dioxatricyclo[7.3.1.05,13]trideca-5(13),7-dien-6-one 101982332 Click to see CC(C)C1CCC2(C=CC(=O)C3=C2C1(OOC3)O)C 264.32 unknown https://doi.org/10.1021/JO00174A030
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bR)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 7163260 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1021/JO00174A030
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 51892422 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/10.1021/JO00174A030
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1021/JO00174A030
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1021/JO00174A030
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/10.1021/JO00174A030
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/10.1021/JO00174A030
Ursolic acid acetate 6475119 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1021/JO00174A030
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 11-oxosteroids
17-Hydroxycryptotanshinone 23252570 Click to see CC1(CCCC2=C1C=CC3=C2C(=O)C(=O)C4=C3OCC4CO)C 312.40 unknown https://doi.org/10.1016/S0031-9422(00)97561-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Penduletin 5320462 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)OC 344.30 unknown https://doi.org/10.1021/JO00174A030

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