PlantaeDB Logo
Login Sign-up

Isodon oresbius

We don't have an image yet. Upload an image!

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 UUID643fdf80d5eed677410649
Scientific name Isodon oresbius
Authority Kudô
First published in Mem. Fac. Sci. Taihoku Imp. Univ. 2: 120 (1929)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Plectranthus oresbius W.W.Sm. Notes Roy. Bot. Gard. Edinburgh 9: 118 (1916)
Rabdosia oresbia (W.W.Sm.) H.Hara J. Jap. Bot. 47: 198 (1972)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Chinese 山地香茶菜

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000217929
Tropicos 17607207
KEW urn:lsid:ipni.org:names:448600-1
The Plant List kew-102998
Open Tree Of Life 5800862
NCBI Taxonomy 1504648
IPNI 448600-1
GBIF 5608899
EOL 2898974

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
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
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
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
Short Chain (≤C4) Esterification Increases Bioavailability of Rosmarinic Acid and Its Potency to Inhibit Vascular Smooth Muscle Cell Proliferation Blažević T, Reznicek G, Ding L, Yang G, Haiss P, Heiss EH, Dirsch VM, Liu R Front Pharmacol 21-Jan-2021
PMCID:PMC7859449
doi:10.3389/fphar.2020.609756
PMID:33551811
Molecular and morphological evidence for a new species of Isodon (Lamiaceae) from southern China Chen YP, Huang CZ, Zhao Y, Xiang CL Plant Divers 14-Jul-2020
PMCID:PMC7987569
doi:10.1016/j.pld.2020.06.004
PMID:33778225
Structure and cytotoxicity of diterpenoids from Isodon adenolomus. Zhao W, Pu JX, Du X, Su J, Li XN, Yang JH, Xue YB, Li Y, Xiao WL, Sun HD J Nat Prod 27-May-2011
doi:10.1021/NP200140J
PMID:21534539
ent-Kaurene diterpenoids from Isodon oresbius. Xiang W, Li RT, Wang ZY, Li SH, Zhao QS, Zhang HJ, Sun HD Phytochemistry 01-Apr-2004
doi:10.1016/J.PHYTOCHEM.2004.02.022
PMID:15110700
Flavonoids from Isodon oresbius Huang Hao, Sun Handong, Zhao Shouxun Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(96)00084-2
Phenolic Compounds of <i>Isodon oresbius</i> Hao Huang, Han-Dong Sun, Ming-Shi Wang, Shou-Xun Zhao American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/NP960430W
Terpenoids from Isodon grandifolia var. Atuntzensis Wu Shun-Hua, Zhang Hong-Jie, Lin Zhong-Wen, Sun Han-Dong Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90740-4
A New Rosmarinic Acid Derivative from Isodon oresbius. Huang H, Chao QR, Tan RX, Sun HD, Wang DC, Ma J, Zhao SX Planta Med 01-Feb-1999
doi:10.1055/S-2006-960451
PMID:17260244

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 / Phenols / Benzenediols / Catechols
3,4-Dihydroxyphenyllactic acid methyl ester 10584634 Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)O 212.20 unknown https://doi.org/10.1021/NP960430W
https://doi.org/10.1055/S-2006-960451
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2S,4S,5R,7R,8S,9S,10S,11R)-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecane-4,7,9,10-tetrol 21577380 Click to see CC1(CCCC23C1C(C(C45C2CC(C(C4)C(=C)C5O)O)(OC3)O)O)C 350.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
https://doi.org/10.1016/S0031-9422(00)90740-4
(1R,2S,4S,5R,7S,8S,9S,10S,11R)-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecane-4,7,9,10-tetrol 162853422 Click to see CC1(CCCC23C1C(C(C45C2CC(C(C4)C(=C)C5O)O)(OC3)O)O)C 350.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
(1S,2S,5R,7R,8S,9S,10S,11R,15R)-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecane-7,9,10,15-tetrol 101306711 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4)C(=C)C5O)(OC3)O)O)O)C 350.40 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
(3,9,10,15-Tetrahydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl)methyl acetate 77916064 Click to see CC(=O)OCC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)O)C 422.50 unknown https://doi.org/10.1021/NP200140J
https://doi.org/10.1016/S0031-9422(00)90740-4
(7,10-Diacetyloxy-9-hydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl) acetate 163033789 Click to see CC(=O)OC1CCC(C2C13COC(C2OC(=O)C)(C45C3CCC(C4)C(=C)C5OC(=O)C)O)(C)C 476.60 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
(7,9-Dihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-10-yl) acetate 162883592 Click to see CC(=O)OC1C2C(CCCC23COC1(C45C3CCC(C4)C(=C)C5O)O)(C)C 376.50 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
(7,9,10,15-Tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-3-yl) acetate 14109082 Click to see CC(=O)OC1CC2CC3(C1C45COC3(C(C4C(CCC5O)(C)C)O)O)C(C2=C)O 408.50 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
(8,10-Dihydroxy-13,13-dimethyl-7-methylidene-4,18-dioxahexacyclo[8.6.2.16,9.01,12.02,9.03,5]nonadecan-11-yl) acetate 72791610 Click to see CC(=O)OC1C2C(CCCC23COC1(C45C3C6C(O6)C(C4)C(=C)C5O)O)(C)C 390.50 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
[(1R,2S,3R,5S,6R,8R,9R,10S,11S,12R)-8,10-dihydroxy-13,13-dimethyl-7-methylidene-4,18-dioxahexacyclo[8.6.2.16,9.01,12.02,9.03,5]nonadecan-11-yl] acetate 162863132 Click to see CC(=O)OC1C2C(CCCC23COC1(C45C3C6C(O6)C(C4)C(=C)C5O)O)(C)C 390.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
[(1R,2S,3R,5S,6R,8R,9S,10S,11S,12R)-8,10-dihydroxy-13,13-dimethyl-7-methylidene-4,18-dioxahexacyclo[8.6.2.16,9.01,12.02,9.03,5]nonadecan-11-yl] acetate 21577379 Click to see CC(=O)OC1C2C(CCCC23COC1(C45C3C6C(O6)C(C4)C(=C)C5O)O)(C)C 390.50 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
[(1R,2S,3R,5S,8R,9R,10S,11S,12R)-8,10-dihydroxy-13,13-dimethyl-7-methylidene-4,18-dioxahexacyclo[8.6.2.16,9.01,12.02,9.03,5]nonadecan-11-yl] acetate 163187154 Click to see CC(=O)OC1C2C(CCCC23COC1(C45C3C6C(O6)C(C4)C(=C)C5O)O)(C)C 390.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
[(1R,2S,3R,5S,8S,9S,10S,11R,12R,15S)-3,9,10,15-tetrahydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl]methyl acetate 15213241 Click to see CC(=O)OCC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)O)C 422.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
[(1R,2S,3S,5S,7R,8S,9S,10S,11R,15S)-7,9,10,15-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-3-yl] acetate 101306770 Click to see CC(=O)OC1CC2CC3(C1C45COC3(C(C4C(CCC5O)(C)C)O)O)C(C2=C)O 408.50 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
https://doi.org/10.1055/S-2006-960451
https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
[(1R,2S,5R,7R,8S,9S,10S,11R)-7,9-dihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-10-yl] acetate 101735666 Click to see CC(=O)OC1C2C(CCCC23COC1(C45C3CCC(C4)C(=C)C5O)O)(C)C 376.50 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
[(1S,2S,3S,5S,8S,9S,10S,11R,12R,15S)-3,9,10,15-tetrahydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl]methyl acetate 162850546 Click to see CC(=O)OCC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
[(1S,2S,5R,7R,8S,9S,10S,11R,12R,15S)-7,9,10,15-tetrahydroxy-12-methyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl]methyl acetate 10835290 Click to see CC(=O)OCC1(CCC(C23C1C(C(C45C2CCC(C4)C(=C)C5O)(OC3)O)O)O)C 408.50 unknown https://doi.org/10.1055/S-2006-960451
[(1S,2S,5R,7R,8S,9S,10S,11R,15R)-7-acetyloxy-9,15-dihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-10-yl] acetate 101297736 Click to see CC(=O)OC1C2C(CCC(C23COC1(C45C3CCC(C4)C(=C)C5OC(=O)C)O)O)(C)C 434.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
https://doi.org/10.1016/S0031-9422(00)90740-4
[(1S,2S,5R,7R,8S,9S,10S,11R,15R)-7,10-diacetyloxy-9-hydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate 163033790 Click to see CC(=O)OC1CCC(C2C13COC(C2OC(=O)C)(C45C3CCC(C4)C(=C)C5OC(=O)C)O)(C)C 476.60 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
[(1S,2S,5S,7R,8S,10S,11R,15R)-7-acetyloxy-9,15-dihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-10-yl] acetate 102004540 Click to see CC(=O)OC1C2C(CCC(C23COC1(C45C3CCC(C4)C(=C)C5OC(=O)C)O)O)(C)C 434.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
[(2S,3R,5S,8S,9S,10S,11R,12R,15S)-3,9,10,15-tetrahydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl]methyl acetate 163193666 Click to see CC(=O)OCC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)O)C 422.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
12,12-Dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecane-4,7,9,10-tetrol 73803061 Click to see CC1(CCCC23C1C(C(C45C2CC(C(C4)C(=C)C5O)O)(OC3)O)O)C 350.40 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
12,12-Dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecane-7,9,10,15-tetrol 73298984 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4)C(=C)C5O)(OC3)O)O)O)C 350.40 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
Adenolin B 70698031 Click to see CC(=O)OCC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)O)C 422.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
CID 101306849 101306849 Click to see CC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)O)C 364.40 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
Effusanin E 24721137 Click to see CC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)O)C 364.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
Lasiodonin 12305578 Click to see CC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)O)C 364.40 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
Trichokaurin 12444495 Click to see CC(=O)OC1C2C(CCC(C23COC1(C45C3CCC(C4)C(=C)C5OC(=O)C)O)O)(C)C 434.50 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1S,1'R,5S,6S,7S,9S)-7-hydroxy-2',2'-dimethyl-10-methylidene-2,11-dioxospiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,6'-cyclohexane]-1'-carbaldehyde 162926634 Click to see CC1(CCCC2(C1C=O)COC(=O)C34C2C(CC(C3)C(=C)C4=O)O)C 346.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
(1S,4S,8R,12S,13S,16S)-9,14-dihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione 137705233 Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(=O)C5=C)C(=O)O2)O)C 362.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
(6,7'-Dihydroxy-3a-methyl-10'-methylidene-2',11'-dioxospiro[1,3,4,5,6,7a-hexahydro-2-benzofuran-7,5'-3-oxatricyclo[7.2.1.01,6]dodecane]-1-yl) acetate 78201215 Click to see CC(=O)OC1C2C(CCC(C23COC(=O)C45C3C(CC(C4)C(=C)C5=O)O)O)(CO1)C 420.50 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
[(1R,1'S,3aR,6R,6'R,7S,7'R,7aR,9'S)-6,7'-dihydroxy-3a-methyl-10'-methylidene-2',11'-dioxospiro[1,3,4,5,6,7a-hexahydro-2-benzofuran-7,5'-3-oxatricyclo[7.2.1.01,6]dodecane]-1-yl] acetate 162951273 Click to see CC(=O)OC1C2C(CCC(C23COC(=O)C45C3C(CC(C4)C(=C)C5=O)O)O)(CO1)C 420.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
[(1S,1'S,3aR,6R,6'S,7S,7'R,7aR,9'S)-6,7'-dihydroxy-3a-methyl-10'-methylidene-2',11'-dioxospiro[1,3,4,5,6,7a-hexahydro-2-benzofuran-7,5'-3-oxatricyclo[7.2.1.01,6]dodecane]-1-yl] acetate 101735664 Click to see CC(=O)OC1C2C(CCC(C23COC(=O)C45C3C(CC(C4)C(=C)C5=O)O)O)(CO1)C 420.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
6,9-Dihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione 3721623 Click to see CC1(C(CC2C3(C1C(OC3)O)C4CCC5CC4(C(=O)C5=C)C(=O)O2)O)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
9,14-Dihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione 430943 Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(=O)C5=C)C(=O)O2)O)C 362.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
https://doi.org/10.1016/S0031-9422(00)90740-4
CID 13241283 13241283 Click to see CC1(CCCC2(C1C=O)COC(=O)C34C2C(CC(C3)C(=C)C4=O)O)C 346.40 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
Enmein 352542 Click to see CC1(C(CC2C3(C1C(OC3)O)C4CCC5CC4(C(=O)C5=C)C(=O)O2)O)C 362.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
https://doi.org/10.1016/S0031-9422(00)90740-4
Nodosin 10248089 Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(=O)C5=C)C(=O)O2)O)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
Oreskaurin A 643551 Click to see CC(=O)OC1C2C(CCC(C23COC(=O)C45C3C(CC(C4)C(=C)C5=O)O)O)(CO1)C 420.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
https://doi.org/10.1016/S0031-9422(00)90740-4
Sculponeatin D 73075 Click to see CC1(C(CC2C3(C1C(OC3)O)C4CCC5CC4(C(=O)C5=C)C(=O)O2)O)C 362.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
Trichorabdal A 13241286 Click to see CC1(CCCC2(C1C=O)COC(=O)C34C2C(CC(C3)C(=C)C4=O)O)C 346.40 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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/10.1055/S-2006-960451
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/10.1055/S-2006-960451
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Butyl 3-(3,4-dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoate 73038698 Click to see CCCCOC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 416.40 unknown https://doi.org/10.1055/S-2006-960451
Butyl Rosmarinate 11953776 Click to see CCCCOC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 416.40 unknown https://doi.org/10.1055/S-2006-960451
methyl 3-(3,4-dihydroxyphenyl)-2-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxypropanoate 10548299 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC(CC2=CC(=C(C=C2)O)O)C(=O)OC)O 388.40 unknown https://doi.org/10.1021/NP960430W
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/10.1055/S-2006-960451
https://doi.org/10.1021/NP960430W
Rosmarinic Acid Methyl Ester 3012090 Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 374.30 unknown https://doi.org/10.1021/NP960430W
https://doi.org/10.1055/S-2006-960451
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1021/NP960430W
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1021/NP960430W
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1021/NP960430W
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-Dihydroxyphenyl)-6,8-dihydroxychromen-4-one 162882699 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=CC(=C3)O)O)O)O 286.24 unknown https://doi.org/10.1016/0031-9422(96)00084-2
6,7,4'-Trihydroxyflavone 10355753 Click to see C1=CC(=CC=C1C2=CC(=O)C3=CC(=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/0031-9422(96)00084-2
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/10.1016/0031-9422(96)00084-2
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/10.1016/0031-9422(96)00084-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 5378180 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(00)90740-4
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 154497677 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
https://doi.org/10.1016/S0031-9422(00)90740-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1055/S-2006-960451
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2006-960451
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/0031-9422(96)00084-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
6,7,8-Trihydroxy-5-methoxy-2-phenyl-2,3-dihydrochromen-4-one 74819437 Click to see COC1=C(C(=C(C2=C1C(=O)CC(O2)C3=CC=CC=C3)O)O)O 302.28 unknown https://doi.org/10.1016/0031-9422(96)00084-2
6,7,8-Trihydroxy-5-methoxyflavanone 42608124 Click to see COC1=C(C(=C(C2=C1C(=O)CC(O2)C3=CC=CC=C3)O)O)O 302.28 unknown https://doi.org/10.1016/0031-9422(96)00084-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxychroman-4-one 348130 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(96)00084-2
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/0031-9422(96)00084-2
5-Hydroxy-7-methoxyflavanone 4101463 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/0031-9422(96)00084-2
Pinostrobin 6950539 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/0031-9422(96)00084-2
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(96)00084-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(S)-5-Hydroxy-7,8-dimethoxy-2-phenylchroman-4-one 13963771 Click to see COC1=C(C2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)O)OC 300.30 unknown https://doi.org/10.1016/0031-9422(96)00084-2
5-Hydroxy-7,8-dimethoxyflavanone 13963770 Click to see COC1=C(C2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)O)OC 300.30 unknown https://doi.org/10.1016/0031-9422(96)00084-2
Dihydrowogonin 11491431 Click to see COC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(96)00084-2
S-Dihydrowogonin 10265977 Click to see COC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(96)00084-2

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.