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Lavandula angustifolia subsp. angustifolia

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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 UUID643fe08cbecf3583666040
Scientific name Lavandula angustifolia subsp. angustifolia
First published in Unknown

Description Top

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Common names Top

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Language Common/alternative name
English lavandula angustifolia angustifolia

Varieties (abbr. var.) Top

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No variety added yet.

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000224117
Tropicos 17602416
INPN 137161
KEW urn:lsid:ipni.org:names:77171433-1
Open Tree Of Life 893883
Observations.org 119257
NCBI Taxonomy 1211581
iNaturalist 413974
GBIF 7307884
USDA GRIN 453619

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
Lavandoside from Lavandula spica flowers V. A. Kurkin, M. Lamrini, S. G. Klochkov Springer Science and Business Media LLC 29-Aug-2008
doi:10.1007/S10600-008-9005-3
Flavonoids of Lavandula spica flowers V. A. Kurkin, M. Lamrini Springer Science and Business Media LLC 23-Feb-2008
doi:10.1007/S10600-007-0236-5
Anxiolytic effects of lavender oil inhalation on open-field behaviour in rats. Shaw D, Annett JM, Doherty B, Leslie JC Phytomedicine 01-Sep-2007
doi:10.1016/J.PHYMED.2007.03.007
PMID:17482442
Analysis of the lactone fraction of lavender oil (Lavandula vera D. C.) Rien. Timmer, Roelof. Ter Heide, Pieter J. De Valois, Henk J. Wobben American Chemical Society (ACS) 10-Mar-2005
doi:10.1021/JF60197A009
New Carbonyl Compounds in the High‐Boiling Fraction of Lavender Oil. 1st Communication Roman Kaiser, Dietmar Lamparsky Wiley 28-Dec-2004
doi:10.1002/HLCA.19830660623
Supercritical-fluid extraction of essential oil from Turkish lavender flowers Nalan Adaşoğlu, Salih Dinçer, Esen Bolat Elsevier BV 27-Nov-2004
doi:10.1016/0896-8446(94)90045-0
Rosmarinic acid from Lavandula vera MM cell culture E. Kovatcheva, A. Pavlov, I. Koleva, M. Ilieva, M. Mihneva Elsevier BV 04-Apr-2003
doi:10.1016/S0031-9422(96)00426-8
The activity of volatile compounds fromLavandula angustifolia againstPsoroptes cuniculi S. Perrucci, G. Macchioni, P. C. Cioni, G. Flamini, I. Morelli, F. Taccini Wiley 10-Sep-2002
doi:10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
HPLC/DAD ANALYSIS OF PHENOLIC COMPOUNDS FROM LAVENDER AND ITS APPLICATION TO QUALITY CONTROL F. M. Areias, P. Valentão, P. B. Andrade, M. M. Moreira, J. Amaral, R. M. Seabra Informa UK Limited 26-Jul-2002
doi:10.1081/JLC-100100510
Biotransformation of monoterpenoids by suspension cultures of Lavandula angustifolia Graham J. Lappin, John D. Stride, John Tampion Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82334-1
Biosynthesis of the coumarins IV. The formation of coumarin and herniarin in lavender Stewart A. Brown Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82973-8
Pigment formation by callus of Lavandula angustifolia Derik V. Banthorpe, Hilary J. Bilyard, David G. Watson Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80692-5
2-N-Phenylaminonaphthalene from Lavandula vera G Papanov Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80631-7
2-N-Phenylaminonaphthalene from Lavandula vera Georgi Y. Papanov, Eszter Gacs-Baitz, Peter Y. Malakov Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(85)80053-4
Triterpenoids from lavandula spica G Papanov, P Bozov, P Malakov Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80309-3

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
> Benzenoids / Naphthalenes
N-Phenyl-2-naphthylamine 8679 Click to see C1=CC=C(C=C1)NC2=CC3=CC=CC=C3C=C2 219.28 unknown https://doi.org/10.1016/0031-9422(85)80053-4
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1016/S0031-6989(88)80836-1
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
Octatriene, dimethyl- 6434062 Click to see CC(C)C=CC=C(C)C=C 136.23 unknown https://doi.org/10.1515/ZNC-1991-11-1223
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
Neryl acetate 1549025 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives / Jasmonic acids
methyl {3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl}acetate 5319693 Click to see CCC=CCC1C(CCC1=O)CC(=O)OC 224.30 unknown https://doi.org/10.1002/HLCA.19830660623
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
[(2R)-1-hydroxy-5-methyl-2-prop-1-en-2-ylhex-4-enyl] acetate 129819800 Click to see CC(=CCC(C(O)OC(=O)C)C(=C)C)C 212.28 unknown https://doi.org/10.1515/ZNC-1991-11-1223
beta-CITRONELLOL, (+/-)- 8842 Click to see CC(CCC=C(C)C)CCO 156.26 unknown https://doi.org/10.1016/S0031-9422(00)82334-1
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1515/ZNC-1991-11-1223
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(00)82334-1
https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
https://doi.org/10.1016/S0031-6989(88)80836-1
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1016/S0031-6989(88)80836-1
https://doi.org/10.1515/ZNC-1991-11-1223
https://doi.org/10.1016/0896-8446(94)90045-0
https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
https://doi.org/10.1016/J.PHYMED.2007.03.007
Linalyl acetate 8294 Click to see CC(=CCCC(C)(C=C)OC(=O)C)C 196.29 unknown https://doi.org/10.1016/0896-8446(94)90045-0
https://doi.org/10.1016/J.PHYMED.2007.03.007
https://doi.org/10.1515/ZNC-1991-11-1223
https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
Linalyl propionate 61098 Click to see CCC(=O)OC(C)(CCC=C(C)C)C=C 210.31 unknown https://doi.org/10.1515/ZNC-1991-11-1223
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1016/S0031-6989(88)80836-1
https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
> 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/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
https://doi.org/10.1016/S0031-6989(88)80836-1
https://doi.org/10.1016/0896-8446(94)90045-0
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
https://doi.org/10.1016/0896-8446(94)90045-0
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1515/ZNC-1991-11-1223
https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
https://doi.org/10.1016/S0031-6989(88)80836-1
https://doi.org/10.1016/0896-8446(94)90045-0
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
https://doi.org/10.1016/S0031-6989(88)80836-1
Fenchone 14525 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown https://doi.org/10.1016/0896-8446(94)90045-0
> 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/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1515/ZNC-1991-11-1223
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
Perillyl alcohol 10819 Click to see CC(=C)C1CCC(=CC1)CO 152.23 unknown https://doi.org/10.1016/S0031-9422(00)82334-1
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1515/ZNC-1991-11-1223
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4E,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-en-3-one 5352042 Click to see CC1=CCCC(=C)C2CC(C2CC1=O)(C)C 218.33 unknown https://doi.org/10.1002/HLCA.19830660623
beta-Cadinene 10657 Click to see CC1=CCC2C(C1)C(CC=C2C)C(C)C 204.35 unknown https://doi.org/10.1016/0896-8446(94)90045-0
beta-Ionone 638014 Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C 192.30 unknown https://doi.org/10.1002/HLCA.19830660623
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-6989(88)80836-1
https://doi.org/10.1515/ZNC-1991-11-1223
https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<5::AID-PTR758>3.0.CO;2-W
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1515/ZNC-1991-11-1223
gamma-Bisabolene, (Z)- 3033866 Click to see CC1=CCC(=C(C)CCC=C(C)C)CC1 204.35 unknown https://doi.org/10.1515/ZNC-1991-11-1223
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-formyloxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 21729656 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC=O)C)C)C2C1C)C)C(=O)O 484.70 unknown https://doi.org/10.1016/0031-9422(92)80309-3
(1S,2R,4aS,6aS,6aS,6bR,8aR,12aR,14bR)-1,2,6a,6b,9,9,12a-heptamethyl-10-oxo-1,2,3,4,5,6,6a,7,8,8a,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 131632297 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C(=O)O 454.70 unknown https://doi.org/10.1016/0031-9422(92)80309-3
10-formyloxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 73826747 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC=O)C)C)C2C1C)C)C(=O)O 484.70 unknown https://doi.org/10.1016/0031-9422(92)80309-3
3-Hydroxy-11-ursen-28,13-olide 21606663 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)O)(C)C)C)C 454.70 unknown https://doi.org/10.1016/0031-9422(92)80309-3
3-Oxo-12-ursen-28-oic acid 13893949 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C(=O)O 454.70 unknown https://doi.org/10.1016/0031-9422(92)80309-3
3Alpha-Hydroxyurs-12-En-28-Oic Acid 7163177 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(92)80309-3
3beta-Hydroxy-28,13-ursanolide 131752032 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5CCC4(C2C1C)OC3=O)C)O)(C)C)C)C 456.70 unknown https://doi.org/10.1016/0031-9422(92)80309-3
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0031-9422(92)80309-3
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/0031-9422(92)80309-3
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0031-9422(92)80309-3
CID 4450096 4450096 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)O)(C)C)C)C 454.70 unknown https://doi.org/10.1016/0031-9422(92)80309-3
Lup-20(29)-ene-3beta,28-diol 221023 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/0031-9422(92)80309-3
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(92)80309-3
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/10.1016/0031-9422(92)80309-3
Ursonic Acid 9890209 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C(=O)O 454.70 unknown https://doi.org/10.1016/0031-9422(92)80309-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Macdougallin 23258271 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3=C2CC(C4C3(CCC(C4)O)C)O)C)C 416.70 unknown https://doi.org/10.1016/S0031-9422(00)80692-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(4-Hydroxyphenoxy)-6-[3-(4-hydroxyphenyl)prop-2-enoxymethyl]oxane-3,4,5-triol 162890773 Click to see C1=CC(=CC=C1C=CCOCC2C(C(C(C(O2)OC3=CC=C(C=C3)O)O)O)O)O 404.40 unknown https://doi.org/10.1016/S0031-9422(00)80692-5
3-(3-Methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoic acid 73021256 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 356.32 unknown https://doi.org/10.1007/S10600-008-9005-3
Lavandoside 13916049 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 356.32 unknown https://doi.org/10.1007/S10600-008-9005-3
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
4,12,12-Trimethyl-5-oxatricyclo[8.2.0.0^{4,6}]dodecan-9-one 3440569 Click to see CC1(CC2C1CCC3(C(O3)CCC2=O)C)C 222.32 unknown https://doi.org/10.1002/HLCA.19830660623
> Organoheterocyclic compounds / Lactones / Delta valerolactones
delta-Decalactone 12810 Click to see CCCCCC1CCCC(=O)O1 170.25 unknown https://doi.org/10.1021/JF60197A009
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
2(3H)-Furanone, 5-ethenyldihydro-5-methyl- 102550 Click to see CC1(CCC(=O)O1)C=C 126.15 unknown https://doi.org/10.1021/JF60197A009
5-Methyl-4-hexanolide 13382542 Click to see CC(C)C1CCC(=O)O1 128.17 unknown https://doi.org/10.1021/JF60197A009
alpha-Methyl-gamma-butyrolactone 98323 Click to see CC1CCOC1=O 100.12 unknown https://doi.org/10.1021/JF60197A009
gamma-Butyrolactone 7302 Click to see C1CC(=O)OC1 86.09 unknown https://doi.org/10.1021/JF60197A009
Gamma-Decalactone 12813 Click to see CCCCCCC1CCC(=O)O1 170.25 unknown https://doi.org/10.1021/JF60197A009
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
3,4-Dihydrocoumarin 660 Click to see C1CC(=O)OC2=CC=CC=C21 148.16 unknown https://doi.org/10.1021/JF60197A009
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Rosmarinic acid 5281792 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/10.1016/S0031-9422(96)00426-8
https://doi.org/10.1081/JLC-100100510
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
2-Hydroxycinnamic acid, (2E)- 637540 Click to see C1=CC=C(C(=C1)C=CC(=O)O)O 164.16 unknown https://doi.org/10.1081/JLC-100100510
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(96)00426-8
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1016/S0031-9422(96)00426-8
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/S0031-9422(96)00426-8
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Cinnamyl alcohol 5315892 Click to see C1=CC=C(C=C1)C=CCO 134.17 unknown https://doi.org/10.1016/S0031-9422(00)82334-1
Phenylallyl alcohol 308 Click to see C1=CC=C(C=C1)C=CCO 134.17 unknown https://doi.org/10.1016/S0031-9422(00)82334-1
> 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/10.1016/0031-9422(85)80053-4
https://doi.org/10.1139/O65-027
https://doi.org/10.1016/S0031-9422(00)82973-8
https://doi.org/10.1016/S0031-9422(00)80631-7
https://doi.org/10.1081/JLC-100100510
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown https://doi.org/10.1021/JF60197A009
https://doi.org/10.1016/S0031-9422(00)82973-8
https://doi.org/10.1081/JLC-100100510
> 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/10.1081/JLC-100100510
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/10.1081/JLC-100100510
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5385553 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/S10600-007-0236-5
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/10.1081/JLC-100100510
Luteolin 7-galactoside 5291488 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/S10600-007-0236-5
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
Flavylium, 3,3',4',5,5',7-hexahydroxy- 128853 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O 303.24 unknown https://doi.org/10.1016/S0031-9422(00)80692-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Malvidin 159287 Click to see COC1=CC(=CC(=C1O)OC)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O 331.30 unknown https://doi.org/10.1016/S0031-9422(00)80692-5

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