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Salvia sahendica

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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 UUID643febed8eb04099675479
Scientific name Salvia sahendica
Authority Boiss. & Buhse
First published in Nouv. Mém. Soc. Imp. Naturalistes Moscou 12: 172 (1860)

Description Top

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Synonyms Top

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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

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Database ID/link to page
World Flora Online wfo-0000302220
Tropicos 100254217
KEW urn:lsid:ipni.org:names:457174-1
The Plant List kew-183784
Open Tree Of Life 6083535
NCBI Taxonomy 1933756
IPNI 457174-1
GBIF 3888503

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
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
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
Diterpenoids from Roots of Salvia lachnocalyx; In-silico and In-vitro Toxicity against Human Cancer Cell Lines Hadavand Mirzaei H, Firuzi O, Jassbi AR Iran J Pharm Res 01-Sep-2020
PMCID:PMC8019878
doi:10.22037/ijpr.2019.15429.13095
PMID:33841524
Antiprotozoal activity of diterpenoids isolated from Zhumeria majdae- absolute configuration by circular dichroism Zadali R, Nejad Ebrahimi S, Tofighi Z, Es-haghi A, Hamburger M, Kaiser M, D’ Ambola M, De Tommasi N, Hadjiakhoondi A Daru 11-May-2020
PMCID:PMC7704868
doi:10.1007/s40199-020-00345-w
PMID:32394309
Iranian Medicinal Plants: From Ethnomedicine to Actual Studies Buso P, Manfredini S, Reza Ahmadi-Ashtiani H, Sciabica S, Buzzi R, Vertuani S, Baldisserotto A Medicina (Kaunas) 26-Feb-2020
PMCID:PMC7143749
doi:10.3390/medicina56030097
PMID:32110920
Antiplasmodial natural products: an update Tajuddeen N, Van Heerden FR Malar J 05-Dec-2019
PMCID:PMC6896759
doi:10.1186/s12936-019-3026-1
PMID:31805944
MicroRNA-Mediated Health-Promoting Effects of Phytochemicals Kang H Int J Mol Sci 23-May-2019
PMCID:PMC6566171
doi:10.3390/ijms20102535
PMID:31126043
Tracking leading anti-Candida compounds in plant samples; Plumbago europaea Sobhani M, Abbas-Mohammadi M, Ebrahimi SN, Aliahmadi A Iran J Microbiol 01-Jun-2018
PMCID:PMC6087695
PMID:30112157
Salvia Species as Sources of Natural Products with Antiprotozoal Activity Llurba-Montesino N, Schmidt TJ Int J Mol Sci 16-Jan-2018
PMCID:PMC5796210
doi:10.3390/ijms19010264
PMID:29337909
Signaling pathway cross talk in Alzheimer’s disease Godoy JA, Rios JA, Zolezzi JM, Braidy N, Inestrosa NC Cell Commun Signal 28-Mar-2014
PMCID:PMC3977891
doi:10.1186/1478-811X-12-23
PMID:24679124
Composition of the Essential Oil of<i>Salvia sahendica</i>Boiss. &amp; Buhse. Abdolhossein Rustaiyan, Hossein Komeillizadeh, Shiva Masoudi, Amir-Reza Jassbi Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1997.9700820
In vitro cytotoxic activity of abietane diterpenes from Peltodon longipes as well as Salvia miltiorrhiza and Salvia sahendica. Fronza M, Murillo R, Ślusarczyk S, Adams M, Hamburger M, Heinzmann B, Laufer S, Merfort I Bioorg Med Chem 15-Aug-2011
doi:10.1016/J.BMC.2011.06.067
PMID:21775156
Sesterterpenoids and other constituents of Salvia sahendica. Moghaddam FM, Farimani MM, Seirafi M, Taheri S, Khavasi HR, Sendker J, Proksch P, Wray V, Edrada R J Nat Prod 24-Sep-2010
doi:10.1021/NP1002516
PMID:20735065
Salvileucolide methylester, a sesterterpene from Salvia Sahendica Firouz Matloubi Moghaddam, Behzad Zaynizadeh, Peter Rüedi Elsevier BV 01-May-2003
doi:10.1016/0031-9422(95)00027-5

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
> Benzenoids / Naphthalenes / Naphthoquinones
Sahandinone 56666274 Click to see CC1=C(C2=C(C=C1)C(=O)C(=CC2=O)C(C)C)CCC=C(C)C 296.40 unknown https://doi.org/10.1016/J.BMC.2011.06.067
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,8aS)-1-[(3R)-3-hydroxy-3-methylpent-4-enyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol 73114 Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C 308.50 unknown https://doi.org/10.1016/0031-9422(95)00027-5
[1R-[1alpha(R*),2beta,4abeta,8aalpha]]-2-hydroxy-alpha,2,5,5,8a-pentamethyl-alpha-vinyldecahydronaphthalene-1-propan-1-ol 7093249 Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C 308.50 unknown https://doi.org/10.1016/0031-9422(95)00027-5
1-Naphthalenepropanol, alpha-ethenyldecahydro-2-hydroxy-alpha,2,5,5,8a-pentamethyl-, [1R-[1alpha(R*),2beta,4abeta,8aalpha]]- 521332 Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C 308.50 unknown https://doi.org/10.1016/0031-9422(95)00027-5
https://doi.org/10.1021/NP1002516
13-Episclareol 56842011 Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C 308.50 unknown https://doi.org/10.1016/0031-9422(95)00027-5
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/J.BMC.2011.06.067
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/J.BMC.2011.06.067
Sclareol 163263 Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C 308.50 unknown https://doi.org/10.1021/NP1002516
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.1997.9700820
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1997.9700820
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1997.9700820
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1997.9700820
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.1997.9700820
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1997.9700820
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1080/10412905.1997.9700820
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1997.9700820
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1997.9700820
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1080/10412905.1997.9700820
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)- 89316 Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700820
delta-Elemene 12309449 Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700820
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1080/10412905.1997.9700820
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1080/10412905.1997.9700820
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700820
Bicyclogermacrene 5315347 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700820
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700820
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700820
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
methyl (1R,4aS,5R,6R,8S,8aR)-6,8-dihydroxy-1,4a,6-trimethyl-5-[(E)-3-methyl-5-[(2S)-3-methyl-5-oxo-2H-furan-2-yl]pent-3-enyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 162994837 Click to see CC1=CC(=O)OC1CC=C(C)CCC2C3(CCCC(C3C(CC2(C)O)O)(C)C(=O)OC)C 448.60 unknown https://doi.org/10.1016/0031-9422(95)00027-5
methyl 6,8-dihydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2H-furan-2-yl)pent-3-enyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 73189502 Click to see CC1=CC(=O)OC1CC=C(C)CCC2C3(CCCC(C3C(CC2(C)O)O)(C)C(=O)OC)C 448.60 unknown https://doi.org/10.1016/0031-9422(95)00027-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
2,3-Dihydroxyolean-12-en-28-oic acid 3694932 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/NP1002516
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/10.1021/NP1002516
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/NP1002516
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/NP1002516
> 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/10.1021/NP1002516
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/10.1021/NP1002516
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP1002516
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP1002516
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(10-Acetyloxy-4,8,10-trimethyl-3-oxo-2-oxatricyclo[6.3.1.04,12]dodecan-9-yl)acetic acid 75244352 Click to see CC(=O)OC1(CC2C3C(C1CC(=O)O)(CCCC3(C(=O)O2)C)C)C 338.40 unknown https://doi.org/10.1021/NP1002516
2-[(1S,4R,8S,9R,10R,12R)-10-acetyloxy-4,8,10-trimethyl-3-oxo-2-oxatricyclo[6.3.1.04,12]dodecan-9-yl]acetic acid 46938758 Click to see CC(=O)OC1(CC2C3C(C1CC(=O)O)(CCCC3(C(=O)O2)C)C)C 338.40 unknown https://doi.org/10.1021/NP1002516
> Organoheterocyclic compounds / Benzofurans
6-Hydroxy-4,4,7a-trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one 14334 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1021/NP1002516
Loliolide 100332 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1021/NP1002516
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S,4R,8S,9R,10R,12R)-9-[(E,3R)-3-hydroperoxy-3-methyl-5-[(2S)-3-methyl-5-oxo-2H-furan-2-yl]pent-4-enyl]-10-hydroxy-4,8,10-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 102429721 Click to see CC1=CC(=O)OC1C=CC(C)(CCC2C3(CCCC4(C3C(CC2(C)O)OC4=O)C)C)OO 448.50 unknown https://doi.org/10.1021/NP1002516
(1S,4R,8S,9R,10R,12S)-10-hydroxy-4,8,10-trimethyl-9-[(E)-3-methyl-5-[(2S)-3-methyl-5-oxo-2H-furan-2-yl]pent-3-enyl]-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 162940543 Click to see CC1=CC(=O)OC1CC=C(C)CCC2C3(CCCC4(C3C(CC2(C)O)OC4=O)C)C 416.50 unknown https://doi.org/10.1021/NP1002516
10-hydroxy-4,8,10-trimethyl-9-[3-methyl-5-(3-methyl-5-oxo-2H-furan-2-yl)pent-3-enyl]-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 162940542 Click to see CC1=CC(=O)OC1CC=C(C)CCC2C3(CCCC4(C3C(CC2(C)O)OC4=O)C)C 416.50 unknown https://doi.org/10.1021/NP1002516
9-[3-hydroperoxy-3-methyl-5-(3-methyl-5-oxo-2H-furan-2-yl)pent-4-enyl]-10-hydroxy-4,8,10-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 75244349 Click to see CC1=CC(=O)OC1C=CC(C)(CCC2C3(CCCC4(C3C(CC2(C)O)OC4=O)C)C)OO 448.50 unknown https://doi.org/10.1021/NP1002516
> Organoheterocyclic compounds / Naphthofurans
(1S,2R,6R,8S,11R,15R)-1,6,11-trimethyl-5,9-dioxatetracyclo[6.6.1.02,6.011,15]pentadecane-4,10-dione 46938757 Click to see CC12CCCC3(C1C(CC4(C2CC(=O)O4)C)OC3=O)C 278.34 unknown https://doi.org/10.1021/NP1002516
1,6,11-Trimethyl-5,9-dioxatetracyclo[6.6.1.02,6.011,15]pentadecane-4,10-dione 75244351 Click to see CC12CCCC3(C1C(CC4(C2CC(=O)O4)C)OC3=O)C 278.34 unknown https://doi.org/10.1021/NP1002516
> Organoheterocyclic compounds / Naphthopyrans
(E)-3-[(1S,2R,5S,7R,9S,12R,16R)-1,5,7,12-tetramethyl-11-oxo-6,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadecan-5-yl]prop-2-enoic acid 46938756 Click to see CC1(CCC2C3(CCCC4(C3C(CC2(O1)C)OC4=O)C)C)C=CC(=O)O 362.50 unknown https://doi.org/10.1021/NP1002516
3-(1,5,7,12-Tetramethyl-11-oxo-6,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadecan-5-yl)prop-2-enoic acid 75244350 Click to see CC1(CCC2C3(CCCC4(C3C(CC2(O1)C)OC4=O)C)C)C=CC(=O)O 362.50 unknown https://doi.org/10.1021/NP1002516
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1021/NP1002516
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1021/NP1002516
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1021/NP1002516
Ladanein 3084066 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O 314.29 unknown https://doi.org/10.1021/NP1002516
Salvigenin 161271 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown https://doi.org/10.1016/0031-9422(95)00027-5
https://doi.org/10.1021/NP1002516

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