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Salvia limbata

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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 UUID643febc68b4d6658668906
Scientific name Salvia limbata
Authority C.A.Mey.
First published in Verz. Pfl. Casp. Meer. : 86 (1831)

Description Top

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Synonyms Top

Scientific name Authority First published in
Salvia chrysadenia Freyn Bull. Herb. Boissier , sér. 2, 1: 279 (1901)
Salvia flexuosa Schrank Syll. Pl. Nov. 2: 57 (1826)
Salvia polyadenia Boiss. & Heldr. Diagn. Pl. Orient. 5: 7 (1844)

Common names Top

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Language Common/alternative name
Russian Шалфей окаймлённый

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
    • Caucasus
      • Transcaucasus
    • Western Asia
      • Iran
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000301445
Tropicos 17600594
KEW urn:lsid:ipni.org:names:456572-1
The Plant List kew-183053
Open Tree Of Life 5921567
Observations.org 132025
NCBI Taxonomy 1685713
IPNI 456572-1
GBIF 3897571
Elurikkus 435987
USDA GRIN 419465

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
Molecular Pathways of Rosmarinic Acid Anticancer Activity in Triple-Negative Breast Cancer Cells: A Literature Review Konstantinou EK, Panagiotopoulos AA, Argyri K, Panoutsopoulos GI, Dimitriou M, Gioxari A Nutrients 19-Dec-2023
PMCID:PMC10780465
doi:10.3390/nu16010002
PMID:38201832
Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens Kernou ON, Azzouz Z, Madani K, Rijo P Molecules 22-May-2023
PMCID:PMC10220798
doi:10.3390/molecules28104243
PMID:37241981
Seed priming with essential oils for sustainable wheat agriculture in semi-arid region Oğuz MÇ, Oğuz E, Güler M PeerJ 27-Mar-2023
PMCID:PMC10062347
doi:10.7717/peerj.15126
PMID:37009155
Chemical Analysis and Investigation of Biological Effects of Salvia officinalis Essential Oils at Three Phenological Stages Assaggaf HM, Naceiri Mrabti H, Rajab BS, Attar AA, Alyamani RA, Hamed M, El Omari N, El Menyiy N, Hazzoumi Z, Benali T, Al-Mijalli SH, Zengin G, AlDhaheri Y, Eid AH, Bouyahya A Molecules 12-Aug-2022
PMCID:PMC9415112
doi:10.3390/molecules27165157
PMID:36014393
Exploration of Lamiaceae in Cardio Vascular Diseases and Functional Foods: Medicine as Food and Food as Medicine Chakrabartty I, Mohanta YK, Nongbet A, Mohanta TK, Mahanta S, Das N, Saravanan M, Sharma N Front Pharmacol 14-Jun-2022
PMCID:PMC9237463
doi:10.3389/fphar.2022.894814
PMID:35774598
A Comprehensive Review of Rosmarinic Acid: From Phytochemistry to Pharmacology and Its New Insight Guan H, Luo W, Bao B, Cao Y, Cheng F, Yu S, Fan Q, Zhang L, Wu Q, Shan M Molecules 20-May-2022
PMCID:PMC9143754
doi:10.3390/molecules27103292
PMID:35630768
Therapeutic benefits of Salvia species: A focus on cancer and viral infection Ezema CA, Ezeorba TP, Aguchem RN, Okagu IU Heliyon 13-Jan-2022
PMCID:PMC8819530
doi:10.1016/j.heliyon.2022.e08763
PMID:35146151
A comparison of artificial intelligence techniques for predicting hyperforin content in Hypericum perforatum L. in different ecological habitats Saffariha M, Jahani A, Jahani R Plant Direct 24-Nov-2021
PMCID:PMC8611508
doi:10.1002/pld3.363
PMID:34849453
Phytomedicine from Middle Eastern Countries: An Alternative Remedy to Modern Medicine against Candida spp Infection Alam MZ, Ahmad Khan MS Evid Based Complement Alternat Med 14-Jul-2021
PMCID:PMC8298167
doi:10.1155/2021/6694876
PMID:34335836
Middle East Medicinal Plants in the Treatment of Diabetes: A Review Abu-Odeh AM, Talib WH Molecules 31-Jan-2021
PMCID:PMC7867005
doi:10.3390/molecules26030742
PMID:33572627
Prediction of hypericin content in Hypericum perforatum L. in different ecological habitat using artificial neural networks Saffariha M, Jahani A, Jahani R, Latif S Plant Methods 26-Jan-2021
PMCID:PMC7836460
doi:10.1186/s13007-021-00710-z
PMID:33499873
Seed germination prediction of Salvia limbata under ecological stresses in protected areas: an artificial intelligence modeling approach Saffariha M, Jahani A, Potter D BMC Ecol 29-Aug-2020
PMCID:PMC7456011
doi:10.1186/s12898-020-00316-4
PMID:32861248
Antidiabetic Potential of Medicinal Plants and Their Active Components Salehi B, Ata A, V. Anil Kumar N, Sharopov F, Ramírez-Alarcón K, Ruiz-Ortega A, Abdulmajid Ayatollahi S, Valere Tsouh Fokou P, Kobarfard F, Amiruddin Zakaria Z, Iriti M, Taheri Y, Martorell M, Sureda A, N. Setzer W, Durazzo A, Lucarini M, Santini A, Capasso R, Adrian Ostrander E, -ur-Rahman A, Iqbal Choudhary M, C. Cho W, Sharifi-Rad J Biomolecules 30-Sep-2019
PMCID:PMC6843349
doi:10.3390/biom9100551
PMID:31575072
The Health-Benefits and Phytochemical Profile of Salvia apiana and Salvia farinacea var. Victoria Blue Decoctions Afonso AF, Pereira OR, Fernandes ÂS, Calhelha RC, Silva AM, Ferreira IC, Cardoso SM Antioxidants (Basel) 25-Jul-2019
PMCID:PMC6721217
doi:10.3390/antiox8080241
PMID:31349575
Phytochemicals in Helicobacter pylori Infections: What Are We Doing Now? Salehi B, Sharopov F, Martorell M, Rajkovic J, Ademiluyi AO, Sharifi-Rad M, Fokou PV, Martins N, Iriti M, Sharifi-Rad J Int J Mol Sci 10-Aug-2018
PMCID:PMC6121492
doi:10.3390/ijms19082361
PMID:30103451

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 / Naphthols and derivatives
(2R)-2-hydroxy-1-(7-hydroxy-2-methyl-6-propan-2-ylnaphthalen-1-yl)-4-methylpent-3-en-1-one 163022977 Click to see CC1=C(C2=CC(=C(C=C2C=C1)C(C)C)O)C(=O)C(C=C(C)C)O 312.40 unknown https://doi.org/10.1016/0031-9422(95)00754-7
[1-(7-Hydroxy-2-methyl-6-propan-2-ylnaphthalen-1-yl)-4-methyl-1-oxopent-3-en-2-yl] acetate 101999881 Click to see CC1=C(C2=CC(=C(C=C2C=C1)C(C)C)O)C(=O)C(C=C(C)C)OC(=O)C 354.40 unknown https://doi.org/10.1016/0031-9422(96)00248-8
2-Hydroxy-1-(7-hydroxy-2-methyl-6-propan-2-ylnaphthalen-1-yl)-4-methylpent-3-en-1-one 10828927 Click to see CC1=C(C2=CC(=C(C=C2C=C1)C(C)C)O)C(=O)C(C=C(C)C)O 312.40 unknown https://doi.org/10.1016/0031-9422(95)00754-7
> Benzenoids / Naphthalenes / Naphthoquinones
12-Hydroxysapriparaquinone 369176 Click to see CC1=C(C2=C(C=C1)C(=C(C(=O)C2=O)C(C)C)O)CCC=C(C)C 312.40 unknown https://doi.org/10.1016/0031-9422(95)00754-7
2-[1-Hydroxy-6-methyl-5-(4-methylpent-3-enyl)-3,4-dioxonaphthalen-2-yl]propanal 101999880 Click to see CC1=C(C2=C(C=C1)C(=C(C(=O)C2=O)C(C)C=O)O)CCC=C(C)C 326.40 unknown https://doi.org/10.1016/0031-9422(96)00248-8
8-(2-Hydroxy-4-methylpent-3-enyl)-7-methyl-3-propan-2-ylnaphthalene-1,2-dione 10781412 Click to see CC1=C(C2=C(C=C1)C=C(C(=O)C2=O)C(C)C)CC(C=C(C)C)O 312.40 unknown https://doi.org/10.1016/0031-9422(95)00754-7
8-[(2R)-2-hydroxy-4-methylpent-3-enyl]-7-methyl-3-propan-2-ylnaphthalene-1,2-dione 162965230 Click to see CC1=C(C2=C(C=C1)C=C(C(=O)C2=O)C(C)C)CC(C=C(C)C)O 312.40 unknown https://doi.org/10.1016/0031-9422(95)00754-7
> Benzenoids / Phenols / Benzenediols / Resorcinols
2-[[(1S,2S,4aR,8aR)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methyl]-5-methylbenzene-1,3-diol 24881205 Click to see CC1=CC(=C(C(=C1)O)CC2C3(CCCC(C3CCC2(C)O)(C)C)C)O 346.50 unknown https://doi.org/10.1016/0031-9422(96)00248-8
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
1-(7,8,8a-trihydroxy-2-methyl-6-propan-2-yl-1H-naphthalen-1-yl)-4-hydroxy-4-methylpentan-3-one 15786258 Click to see CC1=CC=C2C=C(C(=C(C2(C1CCC(=O)C(C)(C)O)O)O)O)C(C)C 348.40 unknown https://doi.org/10.1016/0031-9422(95)00754-7
1-[(1R,8aS)-7,8,8a-trihydroxy-2-methyl-6-propan-2-yl-1H-naphthalen-1-yl]-4-hydroxy-4-methylpentan-3-one 162871381 Click to see CC1=CC=C2C=C(C(=C(C2(C1CCC(=O)C(C)(C)O)O)O)O)C(C)C 348.40 unknown https://doi.org/10.1016/0031-9422(95)00754-7
5-(7,8,8a-trihydroxy-2-methyl-6-propan-2-yl-1H-naphthalen-1-yl)-2-methylpent-1-en-3-one 15786259 Click to see CC1=CC=C2C=C(C(=C(C2(C1CCC(=O)C(=C)C)O)O)O)C(C)C 330.40 unknown https://doi.org/10.1016/0031-9422(95)00754-7
5-[(1R,8aS)-7,8,8a-trihydroxy-2-methyl-6-propan-2-yl-1H-naphthalen-1-yl]-2-methylpent-1-en-3-one 163188266 Click to see CC1=CC=C2C=C(C(=C(C2(C1CCC(=O)C(=C)C)O)O)O)C(C)C 330.40 unknown https://doi.org/10.1016/0031-9422(95)00754-7
7-Isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene 86869 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C)C 270.50 unknown https://doi.org/10.1016/0031-9422(96)00248-8
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/10.1016/0031-9422(96)00248-8
Abietatriene 6432211 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C)C 270.50 unknown https://doi.org/10.1016/0031-9422(96)00248-8
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1016/0031-9422(96)00248-8
> 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/10.1016/0031-9422(96)00248-8
(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/10.1016/0031-9422(96)00248-8
beta-Spathulenol 522266 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/0031-9422(96)00248-8
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/0031-9422(96)00248-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[7-Hydroxy-10-methyl-4-(2-methylbutanoyloxy)-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-6-yl]methyl 2-methylbutanoate 162896784 Click to see CCC(C)C(=O)OCC1=CC(C2C(CC(=CCC1O)C)OC(=O)C2=C)OC(=O)C(C)CC 448.50 unknown https://doi.org/10.1016/0031-9422(95)00754-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(E)-1-[(3R,4aR,6aR,10aS,10bR)-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-3-yl]pent-1-en-3-one 162979102 Click to see CCC(=O)C=CC1(CCC2C3(CCCC(C3CCC2(O1)C)(C)C)C)C 346.50 unknown https://doi.org/10.1016/0031-9422(96)00248-8
1-(3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-3-yl)pent-1-en-3-one 162979101 Click to see CCC(=O)C=CC1(CCC2C3(CCCC(C3CCC2(O1)C)(C)C)C)C 346.50 unknown https://doi.org/10.1016/0031-9422(96)00248-8
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/10.1016/0031-9422(96)00248-8
3-methoxy-4,4,10,13,14-pentamethyl-17-(5,5,6-trimethylhept-6-en-2-yl)-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene 162989253 Click to see CC(CCC(C)(C)C(=C)C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)OC)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(96)00248-8
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/10.1016/0031-9422(96)00248-8
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/10.1016/0031-9422(96)00248-8
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/10.1007/BF00570866
https://doi.org/10.1016/0031-9422(96)00248-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
6-[(17-Carboxy-18-hydroxy-17,21-dimethyl-10-azapentacyclo[11.8.0.03,11.04,9.016,21]henicosa-1(13),2,4,6,8,11-hexaen-12-yl)sulfonyl]-18-hydroxy-17,21-dimethyl-10-azapentacyclo[11.8.0.03,11.04,9.016,21]henicosa-1,3(11),4(9),5,7,12-hexaene-17-carboxylic acid 139586887 Click to see CC12CCC(C(C1CCC3=CC4=C(C=C23)C5=C(N4)C=CC(=C5)S(=O)(=O)C6=C7C(=CC8=C6CCC9C8(CCC(C9(C)C(=O)O)O)C)C1=CC=CC=C1N7)(C)C(=O)O)O 788.90 unknown https://doi.org/10.1016/0031-9422(95)00754-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(95)00754-7
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/10.1016/0031-9422(95)00754-7
https://doi.org/10.1016/0031-9422(96)00248-8
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/10.1016/0031-9422(95)00754-7
https://doi.org/10.1016/0031-9422(96)00248-8
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/10.1016/0031-9422(96)00248-8
https://doi.org/10.1016/0031-9422(95)00754-7
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(95)00754-7
> Organoheterocyclic compounds / Naphthopyrans
(6S,14R,18S)-6,10,10,14,15,20-hexamethyl-21-oxahexacyclo[17.3.2.01,18.02,15.05,14.06,11]tetracosan-20-ol 5316485 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C46CCC5C(OC6)(C)O)C)C)C)C 428.70 unknown https://doi.org/10.1016/0031-9422(95)00754-7
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-rosmarinic acid 639655 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1080/14786411003766912
3-(3,4-Dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoic acid 5099 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1080/14786411003766912
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-[4-Hydroxy-2,6-bis(3-methylbut-2-enyl)phenyl]prop-2-enoic acid 162967528 Click to see CC(=CCC1=CC(=CC(=C1C=CC(=O)O)CC=C(C)C)O)C 300.40 unknown https://doi.org/10.1016/0031-9422(96)00248-8
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1007/BF00570866
> 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/10.1007/BF00570866
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/BF00570866
https://doi.org/10.1016/0031-9422(96)00248-8
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1016/0031-9422(96)00248-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14656729 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1080/14786411003766912
2-(3,4-Dihydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14656728 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1080/14786411003766912
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1007/BF00570866
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00570866
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown https://doi.org/10.1016/0031-9422(96)00248-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupatilin 5273755 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 344.30 unknown https://doi.org/10.1016/0031-9422(96)00248-8
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown https://doi.org/10.1016/0031-9422(95)00754-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
7-O-Methylluteolin 5318214 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 300.26 unknown https://doi.org/10.1080/14786411003766912
Cirsiliol 160237 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC 330.29 unknown https://doi.org/10.1080/14786411003766912
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/10.1080/14786411003766912
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/10.1080/14786411003766912
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(96)00248-8
https://doi.org/10.1016/0031-9422(95)00754-7
https://doi.org/10.1080/14786411003766912

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