Scientific name	Authority	First published in
Arischrada multicaulis	(Vahl) Pobed.	Novosti Sist. Vyssh. Rast. 9: 247 (1972)
Salvia bodeana	Bunge	Labiat. Persic. : 42 (1873)
Salvia pinardi	Boiss.	Diagn. Pl. Orient. 12: 59 (1853)
Salvia rascheyana	Boiss.	Diagn. Pl. Orient. 12: 58 (1853)
Salvia szovitsiana	Bunge	Labiat. Persic. : 43 (1873)
Schraderia acetabulosa	(Vahl) Pobed.	Fl. URSS 21: 369 (1954)
Stiefia multicaulis	(Vahl) Soják	Cas. Nár. Mus., Odd. Prír. 152: 22 (1983)

Common names Top

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Filter by language:

Language	Common/alternative name
Arabic	قصعين متعدد السوق
Persian	مریمگلی پرساقه
Hebrew	מרווה רחבת-גביע

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

Asia-temperate click to expand
- Western Asia
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Sinai
  - Turkey

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000301657
Tropicos	17600598
KEW	urn:lsid:ipni.org:names:456747-1
The Plant List	kew-183253
Open Tree Of Life	5921568
Observations.org	134998
NCBI Taxonomy	1685714
IPNI	456747-1
iNaturalist	493013
GBIF	3895293
Freebase	/m/0bxzj4h
EOL	6342652
Elurikkus	435566
Wikipedia	Salvia_multicaulis

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

Chromosome Doubling Enhances Biomass and Carotenoid Content in Lycium chinense

Zhang R, Rao S, Wang Y, Qin Y, Qin K, Chen J

Plants (Basel)

02-Feb-2024

PMCID:	PMC10857560
doi:	10.3390/plants13030439
PMID:	38337972

In Vitro Antibacterial, Antioxidant, Anticholinesterase, and Antidiabetic Activities and Chemical Composition of Salvia balansae

Mokhtar A, Souhila T, Nacéra B, Amina B, Alghonaim MI, Öztürk M, Alsalamah SA, Miara MD, Boufahja F, Bendif H

Molecules

27-Nov-2023

PMCID:	PMC10708212
doi:	10.3390/molecules28237801
PMID:	38067531

Establishing the Relationship Between Flavonoid Content, Mycorrhization, and Soil Nutritional Content in Different Species of the Genus Passiflora in Colombia

Hernández-Martínez AX, Lozano-Puentes HS, Camacho-Montealegre CM, Costa GM, Díaz-Ariza LA

ACS Omega

19-Oct-2023

PMCID:	PMC10620891
doi:	10.1021/acsomega.3c05606
PMID:	37929148

Screening of 20 species from Lamiaceae family based on phytochemical analysis, antioxidant activity and HPLC profiling

Moshari-Nasirkandi A, Alirezalu A, Alipour H, Amato J

Sci Rep

09-Oct-2023

PMCID:	PMC10562417
doi:	10.1038/s41598-023-44337-7
PMID:	37813985

Current State of Knowledge Regarding WHO High Priority Pathogens—Resistance Mechanisms and Proposed Solutions through Candidates Such as Essential Oils: A Systematic Review

Romanescu M, Oprean C, Lombrea A, Badescu B, Teodor A, Constantin GD, Andor M, Folescu R, Muntean D, Danciu C, Dalleur O, Batrina SL, Cretu O, Buda VO

Int J Mol Sci

04-Jun-2023

PMCID:	PMC10253476
doi:	10.3390/ijms24119727
PMID:	37298678

Chemical composition, cholinesterase, and α-glucosidase inhibitory activity of the essential oils of some Iranian native Salvia species

Gharehbagh HJ, Ebrahimi M, Dabaghian F, Mojtabavi S, Hariri R, Saeedi M, Faramarzi MA, Khanavi M

BMC Complement Med Ther

03-Jun-2023

PMCID:	PMC10239571
doi:	10.1186/s12906-023-04004-w
PMID:	37270541

Drying temperatures affect the qualitative–quantitative variation of aromatic profiling in Anethum graveolens L. ecotypes as an industrial–medicinal–vegetable plant

Farmanpour Kalalagh K, Mohebodini M, Fattahi R, Beyraghdar Kashkooli A, Davarpanah Dizaj S, Salehifar F, Mokhtari AM

Front Plant Sci

12-May-2023

PMCID:	PMC10214840
doi:	10.3389/fpls.2023.1137840
PMID:	37251761

The variability of phenolic constituents and antioxidant properties among wild populations of Ziziphora clinopodioides Lam

Taheri A, Ganjeali A, Arefi-Oskouie A, Çirak C, Cheniany M

Physiol Mol Biol Plants

30-Jan-2023

PMCID:	PMC9981857
doi:	10.1007/s12298-023-01283-y
PMID:	36875730

Comparison of antibacterial and antioxidant potentials of pure and nanoemulsified Nepeta pogonosperma essential oil

Sharifi K, Sharifi A

Food Sci Nutr

28-Dec-2022

PMCID:	PMC10084963
doi:	10.1002/fsn3.3210
PMID:	37051348

Preparation and characterization of geraniol nanoemulsions and its antibacterial activity

Feng X, Feng K, Zheng Q, Tan W, Zhong W, Liao C, Liu Y, Li S, Hu W

Front Microbiol

29-Nov-2022

PMCID:	PMC9745324
doi:	10.3389/fmicb.2022.1080300
PMID:	36523845

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

7-Acetoxyhorminone from Salvia multicaulis Vahl. as Promising Inhibitor of 3-Hydroxy-3-methylglutaryl Coenzyme A (HMG-CoA) Reductase

Yigitkan S, Ertas A, Salmas RE, Firat M, Orhan IE

Pharmaceuticals (Basel)

04-Feb-2022

PMCID:	PMC8880194
doi:	10.3390/ph15020198
PMID:	35215310

Ethnomedicinal Plants of Hasankeyf (Batman-Turkey)

Yeşil Y, İnal İ

Front Pharmacol

11-Mar-2021

PMCID:	PMC7990790
doi:	10.3389/fphar.2020.624710
PMID:	33776756

Phytotoxic Effects of Plant Essential Oils: A Systematic Review and Structure-Activity Relationship Based on Chemometric Analyses

Abd-ElGawad AM, El Gendy AE, Assaeed AM, Al-Rowaily SL, Alharthi AS, Mohamed TA, Nassar MI, Dewir YH, Elshamy AI

Plants (Basel)

25-Dec-2020

PMCID:	PMC7823517
doi:	10.3390/plants10010036
PMID:	33375618

Taming the pandemic? The importance of homemade plant-based foods and beverages as community responses to COVID-19

Pieroni A, Vandebroek I, Prakofjewa J, Bussmann RW, Paniagua-Zambrana NY, Maroyi A, Torri L, Zocchi DM, Dam AT, Khan SM, Ahmad H, Yeşil Y, Huish R, Pardo-de-Santayana M, Mocan A, Hu X, Boscolo O, Sõukand R

J Ethnobiol Ethnomed

09-Dec-2020

PMCID:	PMC7724619
doi:	10.1186/s13002-020-00426-9
PMID:	33298108

Phytochemical Profile Top

Add a new one!

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
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
Heptyl 4-(4-heptoxycarbonylphenyl)benzoate	15378965	Click to see CCCCCCCOC(=O)C1=CC=C(C=C1)C2=CC=C(C=C2)C(=O)OCCCCCCC	438.60	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
> Benzenoids / Benzene and substituted derivatives / Cumenes
8-Hydroxy-3,3-dimethyl-7-propan-2-yl-2,3a,4,5-tetrahydrobenzo[g]azulen-1-one	85273221	Click to see CC(C)C1=C(C=C2C=C3C(CCC2=C1)C(CC3=O)(C)C)O	284.40	unknown	https://doi.org/10.1021/NP990458I
Salvimultine	10803003	Click to see CC(C)C1=C(C=C2C=C3C(CCC2=C1)C(CC3=O)(C)C)O	284.40	unknown	https://doi.org/10.1021/NP990458I
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
(4As,4br,7r,9r)-4b,9-dihydroxy-1,1,4a,7-tetramethyl-7-vinyl-3,4,6,9,10,10a-hexahydrophenanthrene-2,5-dione	467788	Click to see CC1(C2CC(C3=CC(CC(=O)C3(C2(CCC1=O)C)O)(C)C=C)O)C	332.40	unknown	https://doi.org/10.1021/NP9700681
7-Ethenyl-4b,9-dihydroxy-1,1,4a,7-tetramethyl-3,4,6,9,10,10a-hexahydrophenanthrene-2,5-dione	73805598	Click to see CC1(C2CC(C3=CC(CC(=O)C3(C2(CCC1=O)C)O)(C)C=C)O)C	332.40	unknown	https://doi.org/10.1021/NP9700681
Salvipimarone	21582617	Click to see CC1(C2CC(C3=CC(CC(=O)C3(C2(CCC1=O)C)O)(C)C=C)O)C	332.40	unknown	https://doi.org/10.1021/NP9700681
> Benzenoids / Tetralins
CID 9906686	9906686	Click to see CC1(CC2=C(C(=O)C1)C34C(C5=C(C(C3(O4)C=C2)O)C(=CC=C5)OC)O)O	356.40	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(+)-Pisiferal	13785026	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C=O)O	300.40	unknown	https://doi.org/10.1021/NP9700681
(1S,4aS,10aR)-6-hydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde	101103460	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C=O)C)O	300.40	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
(4aS,10aR)-6-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one	11700871	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(=O)C3(C)C)C)O	300.40	unknown	https://doi.org/10.1021/NP9700681
(4aS,10aR)-8-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one	15378963	Click to see CC(C)C1=C(C=C2C(=C1O)CCC3C2(CCC(=O)C3(C)C)C)OC	330.50	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
(4aS,10aS)-6-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,9,10,10a-tetrahydro-2H-phenanthren-4-one	15241260	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(C(=O)CCC3(C)C)C)O	300.40	unknown	https://doi.org/10.1021/NP9700681
(4bR,8aR)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-1,3,4-triol	101219048	Click to see CC(C)C1=C(C2=C(C(=C1O)O)C3(CCCC(C3C=C2)(C)C)C)O	316.40	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
(4bS,8aS)-3-hydroxy-4b,8,8-trimethyl-2-propan-2-yl-6,7,8a,10-tetrahydro-5H-phenanthren-9-one	14165057	Click to see CC(C)C1=C(C=C2C(=C1)CC(=O)C3C2(CCCC3(C)C)C)O	300.40	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
10-Hydroxy-3-methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,10-tetrahydrophenanthrene-1,4-dione	78187759	Click to see CC(C)C1=C(C(=O)C2=C(C1=O)C(C=C3C2(CCCC3(C)C)C)O)OC	344.40	unknown	https://doi.org/10.1021/NP9700681
12-Demethylmulticaulin	467783	Click to see CC1=C(C2=C(C=C1)C3=CC(=C(C=C3C=C2)C(C)C)O)C	264.40	unknown	https://doi.org/10.1021/NP9700681
12-Methyl-5-dehydroacetylhorminone	467787	Click to see CC(C)C1=C(C(=O)C2=C(C1=O)C(C=C3C2(CCCC3(C)C)C)OC(=O)C)OC	386.50	unknown	https://doi.org/10.1021/NP9700681
12-Methyl-5-dehydrohorminone	467786	Click to see CC(C)C1=C(C(=O)C2=C(C1=O)C(C=C3C2(CCCC3(C)C)C)O)OC	344.40	unknown	https://doi.org/10.1021/NP9700681
18-Oxoferruginol	52946772	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C=O)C)O	300.40	unknown	https://doi.org/10.1021/NP9700681
6-Hydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde	14323964	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C=O)C)O	300.40	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
8-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one	73193330	Click to see CC(C)C1=C(C=C2C(=C1O)CCC3C2(CCC(=O)C3(C)C)C)OC	330.50	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
Abieta-9(11),8(14),12-trien-12-ol	521330	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
Cryptanol	184179	Click to see CC(C)C1=C(C2=C(C(=C1O)O)C3(CCCC(C3C=C2)(C)C)C)O	316.40	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
Ferruginol	442027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
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/10.1021/NP9700681
Indigoferabietone	504479	Click to see CC(C)C1=C(C(=O)C2=C(C1=O)C(C=C3C2(CCCC3(C)C)C)OC(=O)C)OC	386.50	unknown	https://doi.org/10.1021/NP9700681
Manool	3034394	Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)C	290.50	unknown	https://doi.org/10.1021/NP9700681
Multicaulin	467782	Click to see CC1=C(C2=C(C=C1)C3=CC(=C(C=C3C=C2)C(C)C)OC)C	278.40	unknown	https://doi.org/10.1021/NP9700681
Sempervirol	12442761	Click to see CC(C)C1=C(C=C2CCC3C(CCCC3(C2=C1)C)(C)C)O	286.50	unknown	https://doi.org/10.1021/NP9700681
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/10.1021/NP9700681
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
12-Demethylmultiorthoquinone	467785	Click to see CC1=C2C=CC3=C(C2=CC(=C1C)O)C(=O)C(=O)C(=C3)C(C)C	294.30	unknown	https://doi.org/10.1021/NP9700681
Multiorthoquinone	467784	Click to see CC1=C2C=CC3=C(C2=CC(=C1C)OC)C(=O)C(=O)C(=C3)C(C)C	308.40	unknown	https://doi.org/10.1021/NP9700681
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
8-Hydroxy-12-oxoabieta-9(11),13-dien-20-oic 8,20-lactone	70698284	Click to see CC(C)C1=CC23CCC4C(CCCC4(C2=CC1=O)C(=O)O3)(C)C	314.40	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol	225688	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
alpha-Amyrenyl acetate	92842	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C	468.80	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
alpha-Amyrin	73170	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1021/NP9700681 https://doi.org/10.1016/S0031-9422(97)00540-2
alpha-Amyrin acetate	293754	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C	468.80	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
Lup-20(29)-en-3-ol, (3beta)-	521518	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
Lup-20(29)-en-3-one	323075	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C	424.70	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
Lupenone	92158	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C	424.70	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1021/NP9700681 https://doi.org/10.1016/S0031-9422(97)00540-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(22e)-Ergosta-5,22-dien-3-one	134691564	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C	396.60	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
17-(5,6-Dimethylhept-3-en-2-yl)-10,13-dimethyl-1,2,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one	85632475	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C	396.60	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
Brassicasterone	133655762	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C	396.60	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
> 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(97)00540-2
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(97)00540-2
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/S0031-9422(97)00540-2
Stigmast-4-en-3-one	5484202	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
Stigmast-4-en-3-one, (24S)-	579897	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
Me-bAla(2-OH,3-heptyl)-DL-Tyr-DL-N(Me)Leu-DL-Pro-DL-Tyr-OMe	163129860	Click to see CCCCCCCC(C(C(=O)NC(CC1=CC=C(C=C1)O)C(=O)N(C)C(CC(C)C)C(=O)N2CCCC2C(=O)NC(CC3=CC=C(C=C3)O)C(=O)OC)O)NC	782.00	unknown	https://doi.org/10.1016/S0031-9422(97)00540-2

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Salvia multicaulis

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

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