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Santolina oblongifolia

Santolina oblongifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fd3b735a89185245492
Scientific name Santolina oblongifolia
Authority Boiss.
First published in Diagn. Pl. Orient. , ser. 2, 3: 18 (1856)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Spanish manzanilla de gredos

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Santolina oblongifolia subsp. oblongifolia
Santolina oblongifolia subsp. obtusifolia (Willk.) Rivas Mart. Anales Inst. Bot. Cavanilles 32(2): 1542 (1975)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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-0000134303
Tropicos 2701204
KEW urn:lsid:ipni.org:names:241978-1
The Plant List gcc-95096
Open Tree Of Life 992381
Observations.org 136118
NCBI Taxonomy 634960
IUCN Red List 202990
IPNI 241978-1
iNaturalist 443266
GBIF 3125931
EPPO SNTOB
USDA GRIN 475438

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
Design and Development of COX-II Inhibitors: Current Scenario and Future Perspective Chahal S, Rani P, Kiran, Sindhu J, Joshi G, Ganesan A, Kalyaanamoorthy S, Mayank, Kumar P, Singh R, Negi A ACS Omega 09-May-2023
PMCID:PMC10210234
doi:10.1021/acsomega.3c00692
PMID:37251190
The role of nanocomposites against biofilm infections in humans Varma A, Warghane A, Dhiman NK, Paserkar N, Upadhye V, Modi A, Saini R Front Cell Infect Microbiol 28-Feb-2023
PMCID:PMC10011468
doi:10.3389/fcimb.2023.1104615
PMID:36926513
Edible Flowers Used in Some Countries of the Mediterranean Basin: An Ethnobotanical Overview Motti R, Paura B, Cozzolino A, de Falco B Plants (Basel) 28-Nov-2022
PMCID:PMC9736219
doi:10.3390/plants11233272
PMID:36501312
An Overview of Biofilm Formation–Combating Strategies and Mechanisms of Action of Antibiofilm Agents Asma ST, Imre K, Morar A, Herman V, Acaroz U, Mukhtar H, Arslan-Acaroz D, Shah SR, Gerlach R Life (Basel) 23-Jul-2022
PMCID:PMC9394423
doi:10.3390/life12081110
PMID:35892912
Hedycaryol – Central Intermediates in Sesquiterpene Biosynthesis, Part II Xu H, Dickschat JS Chemistry 21-Mar-2022
PMCID:PMC9310801
doi:10.1002/chem.202200405
PMID:35239190
Recent Development in Micropropagation Techniques for Rare Plant Species Chokheli VA, Dmitriev PA, Rajput VD, Bakulin SD, Azarov AS, Varduni TV, Stepanenko VV, Tarigholizadeh S, Singh RK, Verma KK, Minkina TM Plants (Basel) 08-Dec-2020
PMCID:PMC7764825
doi:10.3390/plants9121733
PMID:33302534
Protective Effects of Licochalcone A Ameliorates Obesity and Non-Alcoholic Fatty Liver Disease Via Promotion of the Sirt-1/AMPK Pathway in Mice Fed a High-Fat Diet Liou CJ, Lee YK, Ting NC, Chen YL, Shen SC, Wu SJ, Huang WC Cells 11-May-2019
PMCID:PMC6562591
doi:10.3390/cells8050447
PMID:31083505
Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J Int J Mol Sci 14-May-2018
PMCID:PMC5983620
doi:10.3390/ijms19051459
PMID:29757986
Scopolin ameliorates high-fat diet induced hepatic steatosis in mice: potential involvement of SIRT1-mediated signaling cascades in the liver Yoo A, Narayan VP, Hong EY, Whang WK, Park T Sci Rep 22-May-2017
PMCID:PMC5440403
doi:10.1038/s41598-017-02416-6
PMID:28533555
Strategies for combating bacterial biofilms: A focus on anti-biofilm agents and their mechanisms of action Roy R, Tiwari M, Donelli G, Tiwari V Virulence 31-Mar-2017
PMCID:PMC5955472
doi:10.1080/21505594.2017.1313372
PMID:28362216
Chemical composition, antibacterial and antifungal activities of flowerhead and root essential oils of Santolina chamaecyparissus L., growing wild in Tunisia Bel Hadj Salah-Fatnassi K, Hassayoun F, Cheraif I, Khan S, Jannet HB, Hammami M, Aouni M, Harzallah-Skhiri F Saudi J Biol Sci 26-Mar-2016
PMCID:PMC5415143
doi:10.1016/j.sjbs.2016.03.005
PMID:28490960
Medical Ethnobotany in Europe: From Field Ethnography to a More Culturally Sensitive Evidence-Based CAM? Quave CL, Pardo-de-Santayana M, Pieroni A Evid Based Complement Alternat Med 30-Jul-2012
PMCID:PMC3413992
doi:10.1155/2012/156846
PMID:22899952
Revised structures for the bejarols from Santolina oblongifolia J. De Pascual Teresa, I.S. Bellido, M.S. González, S. Vicente Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84974-2
Nerolidol-5,8-oxides from the essential oil of santolina oblongifolia J. De Pascual-T, S. Vicente, M.S. González, I.S. Bellido Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80154-5
Tetracyclic triterpenes and nerolidol derivatives from Santolina oblongifolia J. De Pascual Teresa, I.S. Bellido, M.S. González, S. Vicente Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)94526-6

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 acid esters
(2-Hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl) 3-methylbutanoate 163019294 Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)CC(C)C 298.30 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
[(2E,5R,9S)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] 3-methylbutanoate 163019297 Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)CC(C)C 298.30 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
[(1R,2R,6S,7R,10S)-2-(hydroxymethyl)-6,9-dimethyl-6-tricyclo[5.4.0.02,10]undec-8-enyl]methanol 163006654 Click to see CC1=CC2C3CC1C3(CCCC2(C)CO)CO 236.35 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
[2-(Hydroxymethyl)-6,9-dimethyl-6-tricyclo[5.4.0.02,10]undec-8-enyl]methanol 85526779 Click to see CC1=CC2C3CC1C3(CCCC2(C)CO)CO 236.35 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(10-Hydroxy-2,6,10-trimethyl-8-oxododeca-2,6,11-trien-4-yl) acetate 162896611 Click to see CC(=CC(CC(=CC(=O)CC(C)(C=C)O)C)OC(=O)C)C 294.40 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
(2R)-2-methyl-1-[(2R,6R)-4-methyl-2-(2-methylprop-1-enyl)-3,6-dihydro-2H-pyran-6-yl]but-3-en-2-ol 25110934 Click to see CC1=CC(OC(C1)C=C(C)C)CC(C)(C=C)O 236.35 unknown https://doi.org/10.1016/S0031-9422(00)84974-2
(2R)-2-methyl-1-[(2S,6R)-4-methyl-2-(2-methylprop-1-enyl)-3,6-dihydro-2H-pyran-6-yl]but-3-en-2-ol 163023374 Click to see CC1=CC(OC(C1)C=C(C)C)CC(C)(C=C)O 236.35 unknown https://doi.org/10.1016/S0031-9422(00)84974-2
(2S)-2-methyl-1-[(2S,6R)-4-methyl-2-(2-methylprop-1-enyl)-3,6-dihydro-2H-pyran-6-yl]but-3-en-2-ol 102392465 Click to see CC1=CC(OC(C1)C=C(C)C)CC(C)(C=C)O 236.35 unknown https://doi.org/10.1016/S0031-9422(00)84974-2
(3,11-Dihydroxy-3,7,11-trimethyldodeca-1,6,9-trien-5-yl) acetate 162926781 Click to see CC(=CC(CC(C)(C=C)O)OC(=O)C)CC=CC(C)(C)O 296.40 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
(3E,6E,8S,10R)-2,6,10-trimethyldodeca-3,6,11-triene-2,8,10-triol 162847766 Click to see CC(=CC(CC(C)(C=C)O)O)CC=CC(C)(C)O 254.36 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
(3R,5S,6E,9S)-3,7,11-trimethyldodeca-1,6,10-triene-3,5,9-triol 163035366 Click to see CC(=CC(CC(=CC(CC(C)(C=C)O)O)C)O)C 254.36 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
(8-Acetyloxy-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl) acetate 163040517 Click to see CC(=CC(CC(=CC(CC(C)(C=C)O)OC(=O)C)C)OC(=O)C)C 338.40 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
(8,10-Dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl) acetate 92012847 Click to see CC(=CC(CC(=CC(CC(C)(C=C)O)O)C)OC(=O)C)C 296.40 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
[(3R,5S,6E,9E)-3,11-dihydroxy-3,7,11-trimethyldodeca-1,6,9-trien-5-yl] acetate 162926782 Click to see CC(=CC(CC(C)(C=C)O)OC(=O)C)CC=CC(C)(C)O 296.40 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
[(4S,6E,10R)-10-hydroxy-2,6,10-trimethyl-8-oxododeca-2,6,11-trien-4-yl] acetate 162896612 Click to see CC(=CC(CC(=CC(=O)CC(C)(C=C)O)C)OC(=O)C)C 294.40 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
[(4S,6E,8S,10R)-8-acetyloxy-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl] acetate 14707122 Click to see CC(=CC(CC(=CC(CC(C)(C=C)O)OC(=O)C)C)OC(=O)C)C 338.40 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
[(4S,6E,8S,10R)-8,10-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl] acetate 14167377 Click to see CC(=CC(CC(=CC(CC(C)(C=C)O)O)C)OC(=O)C)C 296.40 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
1-[(1S,3aR,7S,7aR)-4-methyl-7-propan-2-yl-2,3,3a,6,7,7a-hexahydro-1H-inden-1-yl]ethanone 162939837 Click to see CC1=CCC(C2C1CCC2C(=O)C)C(C)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)80154-5
2-methyl-1-[4-methyl-2-(2-methylprop-1-enyl)-3,6-dihydro-2H-pyran-6-yl]but-3-en-2-ol 163023373 Click to see CC1=CC(OC(C1)C=C(C)C)CC(C)(C=C)O 236.35 unknown https://doi.org/10.1016/S0031-9422(00)84974-2
3,7,11-Trimethyldodeca-1,6,10-triene-3,5,9-triol 163035365 Click to see CC(=CC(CC(=CC(CC(C)(C=C)O)O)C)O)C 254.36 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
cis-Bejarol 6429172 Click to see CC1=CC(OC(C1)C=C(C)C)CC(C)(C=C)O 236.35 unknown https://doi.org/10.1016/S0031-9422(00)84974-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,5R,8R,9R,10R,13R,14R,17R)-17-[(E,2S)-6-hydroxy-6-methylhept-4-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 163056367 Click to see CC(CC=CC(C)(C)O)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C 444.70 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
(3S,5R,8R,9R,10R,13R,14R,17S)-17-[(4E)-6-hydroxy-6-methylhepta-1,4-dien-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 44285137 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC4C(=C)CC=CC(C)(C)O)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
[(3S,5R,8R,9R,10R,13S,14R,17R)-17-hydroxy-4,4,8,10,14-pentamethyl-17-(6-methylhepta-1,6-dien-2-yl)-1,2,3,5,6,7,9,11,12,13,15,16-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 163012049 Click to see CC(=C)CCCC(=C)C1(CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C)O 484.80 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
[17-Hydroxy-4,4,8,10,14-pentamethyl-17-(6-methylhepta-1,6-dien-2-yl)-1,2,3,5,6,7,9,11,12,13,15,16-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 163012048 Click to see CC(=C)CCCC(=C)C1(CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C)O 484.80 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
[4,4,8,10,14-pentamethyl-17-(6-methylhepta-1,5-dien-2-yl)-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 14137679 Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
17-(6-hydroxy-6-methylhept-4-en-2-yl)-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 163056365 Click to see CC(CC=CC(C)(C)O)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C 444.70 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
17-(6-hydroxy-6-methylhepta-1,4-dien-2-yl)-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 74969663 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC4C(=C)CC=CC(C)(C)O)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
Dammara-20,24-dien-3 beta-ol 13893944 Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
Dammaradienol 13893946 Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
Dammaradienyl acetate 14137680 Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
Friedelanol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(2-Hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl) acetate 327392 Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 256.25 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
(2E,5R,9R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-ol 162897102 Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)O 214.22 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
(2E,5R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-diene 44575221 Click to see CC#CC#CC=C1C=CC2(O1)CC=CO2 198.22 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
[(2E,5R,9S)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate 162983961 Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 256.25 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
[(2Z,5R,9S)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate 162983963 Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 256.25 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
2-Hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-diene 327390 Click to see CC#CC#CC=C1C=CC2(O1)CC=CO2 198.22 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
> Organoheterocyclic compounds / Heteroaromatic compounds
2-(4-Thiophen-2-ylbut-1-en-3-ynyl)furan 78384933 Click to see C1=COC(=C1)C=CC#CC2=CC=CS2 200.26 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
2-[(Z)-4-thiophen-2-ylbut-1-en-3-ynyl]furan 5317432 Click to see C1=COC(=C1)C=CC#CC2=CC=CS2 200.26 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
(10S)-5,7-dioxo-1,3,6,8-tetrazatricyclo[6.3.1.04,12]dodeca-2,4(12)-diene-10-carboxylic acid 163187483 Click to see C1C(CN2C3=C(C(=O)NC2=O)N=CN31)C(=O)O 236.18 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
> Organoheterocyclic compounds / Naphthopyrans
5,13,13-Trimethyl-9,18-dioxapentacyclo[8.6.2.12,6.01,12.010,19]nonadeca-2(19),3,5-trien-14-ol 162851735 Click to see CC1=C2CCOC34C2=C(C=C1)C5(CCC(C(C5C3)(C)C)O)CO4 314.40 unknown https://doi.org/10.1016/S0031-9422(00)94526-6
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-Methoxycoumarin 10748 Click to see COC1=CC2=C(C=C1)C=CC(=O)O2 176.17 unknown https://doi.org/10.1021/NP960422F
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1021/NP960422F
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1021/NP960422F
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1021/NP960422F

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