PlantaeDB Logo
Login Sign-up

Isodon excisus

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 UUID643fdf7cab7b5838106353
Scientific name Isodon excisus
Authority Kudô
First published in Mem. Fac. Sci. Taihoku Imp. Univ. 2: 133 (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 excisus Maxim. Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 213 (1859)
Rabdosia excisa (Maxim.) H.Hara J. Jap. Bot. 47: 195 (1972)
Rabdosia excisa f. albiflora (Sakata) H.Hara J. Jap. Bot. 47: 195 (1972)
Rabdosia excisa var. chiisanensis (Nakai) Murata Acta Phytotax. Geobot. 40: 100 (1989)
Stachys polygonatum H.Lév. Repert. Spec. Nov. Regni Veg. 9: 449 (1911)
Amethystanthus excisus var. coreanus Nakai Bot. Mag. (Tokyo) 48: 788. 1934
Amethystanthus excisus (Maxim.) Nakai Bot. Mag. (Tokyo) 48: 787 (1934)
Amethystanthus excisus f. albiflorus Sakata Acta Phytotax. Geobot. 7: 16 1938
Amethystanthus excisus var. chiisanensis Nakai Bot. Mag. (Tokyo) 48: 788 1934
Rabdosia umbrosa var. coreana (T.B.Lee) Y.N.Lee Fl. Korea 1: 696 (1996)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Chinese 野苏子
Chinese 尾叶香茶菜
Chinese 高丽花
Chinese 龟叶草

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
  • Asia-temperate
    • China
      • China North-central
      • Manchuria
    • Eastern Asia
      • Korea
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000217853
Tropicos 17607188
KEW urn:lsid:ipni.org:names:448575-1
The Plant List kew-102927
Open Tree Of Life 624040
NCBI Taxonomy 705303
IPNI 448575-1
iNaturalist 565880
GBIF 5609026
EOL 2898941
CMAUP NPO17628

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
Natural Products as Anticancer Agents: Current Status and Future Perspectives Naeem A, Hu P, Yang M, Zhang J, Liu Y, Zhu W, Zheng Q Molecules 30-Nov-2022
PMCID:PMC9737905
doi:10.3390/molecules27238367
PMID:36500466
Temporal Variation Dominates in Local Carabid Beetle Communities in Korean Mountains Park Y, Jang T, Kim J, Kim SK, Kim IK, Kim CJ, Takami Y Insects 12-Nov-2021
PMCID:PMC8624729
doi:10.3390/insects12111019
PMID:34821819
Manipulation of Dietary Intake on Changes in Circulating Testosterone Concentrations Zamir A, Ben-Zeev T, Hoffman JR Nutrients 25-Sep-2021
PMCID:PMC8538516
doi:10.3390/nu13103375
PMID:34684376
In Silico Studies of Lamiaceae Diterpenes with Bioinsecticide Potential against Aphis gossypii and Drosophila melanogaster Rodrigues GC, dos Santos Maia M, Silva Cavalcanti AB, de Sousa NF, Scotti MT, Scotti L Molecules 02-Feb-2021
PMCID:PMC7867283
doi:10.3390/molecules26030766
PMID:33540716
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
Mechanistic Pathways and Molecular Targets of Plant-Derived Anticancer ent-Kaurane Diterpenes Sarwar MS, Xia YX, Liang ZM, Tsang SW, Zhang HJ Biomolecules 16-Jan-2020
PMCID:PMC7023344
doi:10.3390/biom10010144
PMID:31963204
Human Cytochrome P450 Enzymes 5-51 as Targets of Drugs and Natural and Environmental Compounds: Mechanisms, Induction, and Inhibition—Toxic Effects and Benefits Rendic S, Guengerich FP Drug Metab Rev 01-Aug-2018
PMCID:PMC6421578
doi:10.1080/03602532.2018.1483401
PMID:30717606
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
All that glitters is not Ramularia Videira SI, Groenewald JZ, Braun U, Shin HD, Crous PW Stud Mycol 29-Jun-2016
PMCID:PMC4986539
doi:10.1016/j.simyco.2016.06.001
PMID:27570325
Elucidating the Ramularia eucalypti species complex Videira SI, Groenewald JZ, Kolecka A, van Haren L, Boekhout T, Crous PW Persoonia 20-Nov-2014
PMCID:PMC4510271
doi:10.3767/003158515X685670
PMID:26240445
Dimeric ent-kaurane diterpenoids from Isodon excisus. Hong SS, Lee SA, Lee C, Han XH, Choe S, Kim N, Lee D, Lee CK, Kim Y, Hong JT, Lee MK, Hwang BY J Nat Prod 28-Nov-2011
doi:10.1021/NP200439N
PMID:22066578
Pyrrolidinone diterpenoid from Isodon excisus and inhibition of nitric oxide production in lipopolysaccharide-induced macrophage RAW264.7 cells. Hong SS, Lee SA, Kim N, Hwang JS, Han XH, Lee MK, Jung JK, Hong JT, Kim Y, Lee D, Hwang BY Bioorg Med Chem Lett 15-Feb-2011
doi:10.1016/J.BMCL.2010.11.095
PMID:21273070
Inhibitors of Microglial Neurotoxicity: Focus on Natural Products Choi DK, Koppula S, Suk K Molecules 25-Jan-2011
PMCID:PMC6259841
doi:10.3390/molecules16021021
PMID:21350391
Phylogenetic lineages in the Capnodiales Crous PW, Schoch CL, Hyde KD, Wood AR, Gueidan C, de Hoog GS, Groenewald JZ Stud Mycol 01-Jan-2009
PMCID:PMC2816965
doi:10.3114/sim.2009.64.02
PMID:20169022
Natural Products as Aromatase Inhibitors Balunas MJ, Su B, Brueggemeier RW, Kinghorn AD Anticancer Agents Med Chem 01-Aug-2008
PMCID:PMC3074486
PMID:18690828

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
4-Hydroxy-3,5-dimethoxybenzoate 54694262 Click to see COC1=CC(=CC(=C1[O-])OC)C(=O)O 197.16 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Catechols
(1R,5S,7S)-3-[(3,4-dihydroxyphenyl)-hydroxymethylidene]-6,6-dimethyl-1,7-bis(3-methylbut-3-enyl)-5-[(2,4,4-trimethylcyclohexen-1-yl)methyl]bicyclo[3.3.1]nonane-2,4,9-trione 102283888 Click to see CC1=C(CCC(C1)(C)C)CC23C(=O)C(=C(C4=CC(=C(C=C4)O)O)O)C(=O)C(C2=O)(CC(C3(C)C)CCC(=C)C)CCC(=C)C 602.80 unknown https://doi.org/10.1021/NP060638+
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
(10E,12E,14E,16S)-16-hydroxy-9-oxooctadeca-10,12,14-trienoic acid 22956671 Click to see CCC(C=CC=CC=CC(=O)CCCCCCCC(=O)O)O 308.40 unknown https://doi.org/10.1016/J.BMCL.2010.11.095
(16S)-16-hydroxy-9-oxooctadeca-10,12,14-trienoic acid 91478638 Click to see CCC(C=CC=CC=CC(=O)CCCCCCCC(=O)O)O 308.40 unknown https://doi.org/10.1016/J.BMCL.2010.11.095
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(15-Acetyloxy-3,8,11-trihydroxy-5,5,9-trimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 14414556 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(C2C1(C)C)O)C(C4=C)OC(=O)C)O)C)O 436.50 unknown https://doi.org/10.1016/J.BMCL.2010.11.095
(1R,2R,4R,5S,8S,9R,10S,13S,16R)-2,8,16-trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 10066480 Click to see CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)CO 350.40 unknown https://doi.org/10.1021/NP030357R
(1R,2R,4R,8S,9R,10S,13R)-2,8,16-trihydroxy-9-(hydroxymethyl)-5,5-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 146014674 Click to see CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)CO)O)C 350.40 unknown https://doi.org/10.1021/NP030357R
https://doi.org/10.1016/0031-9422(91)83072-S
(1R,2R,4R,8S,9R,10S,13S,16R)-2,8,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.0^{1,10.0^{4,9]hexadecan-15-one 13945496 Click to see CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)C 334.40 unknown https://doi.org/10.1021/NP030357R
(1R,2R,4R,8S,9R,10S,13S,16S)-2,8,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 162871586 Click to see CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)C 334.40 unknown https://doi.org/10.1016/S0031-9422(01)00245-X
(1R,2R,4S,9R,10S,12S,13R,16R)-2,12,16-trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 45271374 Click to see CC1(CCCC2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)C)CO 350.40 unknown via CMAUP database
(1R,2S,5S,8R,9S,11R,15S,18R)-9,15,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 10315734 Click to see CC1(CCC(C23C1CC(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)C 348.40 unknown https://doi.org/10.1021/NP030357R
(1R,4R,9R,10S)-2,8,12,16-tetrahydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 137795540 Click to see CC1(CCC(C2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)C)O)C 350.40 unknown https://doi.org/10.1016/0031-9422(91)83072-S
https://doi.org/10.1021/NP030357R
(1S,2R,4R,8S,9R,12S,13S,16S)-2,8,12-trihydroxy-5,5-dimethyl-18-methylidene-11-oxapentacyclo[11.3.2.01,12.04,9.09,16]octadecan-17-one 101345678 Click to see CC1(CCC(C23C1CC(C45C2CCC(C4(OC3)O)C(=C)C5=O)O)O)C 348.40 unknown https://doi.org/10.1021/NP030357R
(1S,2S,5S,8S,9R,11R,15S,16S,18R)-15,18-dihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 102371731 Click to see CC1(CCC(C23C1CC(C45C2CCC(C4O)C(=C)C5=O)OC3OC)O)C 362.50 unknown https://doi.org/10.1016/0031-9422(91)83072-S
(1S,4R,5S,8S,9R,10S,13S,16R)-8,16-dihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 45270538 Click to see CC1(CCC(C2(C1CCC34C2CCC(C3O)C(=C)C4=O)C)O)CO 334.40 unknown https://doi.org/10.1021/NP030357R
(2,8,16-Trihydroxy-5,5-dimethyl-14-methylidene-15-oxo-9-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methyl acetate 3847003 Click to see CC(=O)OCC12C3CCC4C(C3(C(CC1C(CCC2O)(C)C)O)C(=O)C4=C)O 392.50 unknown https://doi.org/10.1021/NP030357R
(2,8,16-Trihydroxy-5,9-dimethyl-14-methylidene-15-oxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methyl acetate 75048976 Click to see CC(=O)OCC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)C 392.50 unknown https://doi.org/10.1021/NP030357R
(2R,4S,8S,9R,10S,12S,16S)-2,8,12,16-tetrahydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 50987574 Click to see CC1(CCC(C2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)C)O)C 350.40 unknown via CMAUP database
(2R,4S,9R,10R)-2,16-dihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-6,15-dione 50987570 Click to see CC1(C2CC(C34C(C2(CCC1=O)C)CCC(C3O)C(=C)C4=O)O)C 332.40 unknown via CMAUP database
(3,11-Dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 13874227 Click to see CC(=O)OC1CCC2(C3C(CC4CC3(CC(C2C1(C)C)O)C(=O)C4=C)O)C 376.50 unknown https://doi.org/10.1021/NP060638+
(3,8,11-Trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 13874231 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(C2C1(C)C)O)C(=O)C4=C)O)C)O 392.50 unknown https://doi.org/10.1021/NP060638+
(4R,10S,16R)-2,8,12,16-tetrahydroxy-9-(hydroxymethyl)-5,5-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 5320877 Click to see CC1(CCC(C2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)CO)O)C 366.40 unknown https://doi.org/10.1021/NP030357R
(6-Acetyloxy-3,8,15-trihydroxy-5,5,9-trimethyl-14-methylidene-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 14219410 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3)O)(C)C)OC(=O)C)O)C)C(C2=C)O 436.50 unknown https://doi.org/10.1021/NP060638+
(6-Acetyloxy-8-hydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 163047622 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC3)C(C(CC4O)OC(=O)C)(C)C)C)C(=O)C2=C 418.50 unknown https://doi.org/10.1021/NP060638+
(6-Acetyloxy-8-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 14219409 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(=O)C3)(C)C)OC(=O)C)O)C)C(=O)C2=C 432.50 unknown https://doi.org/10.1021/NP060638+
(8,11-Dihydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 14414558 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(=O)C2C1(C)C)C(=O)C4=C)O)C)O 390.50 unknown https://doi.org/10.1016/J.BMCL.2010.11.095
[(1R,2R,4R,8S,9R,10S,12S,13S,16R)-2,8,16-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-12-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 13193213 Click to see CC(=O)OC1CC2C3(C(CCC(C3CC(C24C(C1C(=C)C4=O)O)O)(C)C)O)C 392.50 unknown https://doi.org/10.1246/CL.1981.753
https://doi.org/10.1021/NP030357R
[(1R,4R,6S,8S,9R,10S,11R,13S)-8,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162870763 Click to see CC(=O)OC1CC(C2(C(C1(C)C)CCC34C2C(CC(C3)C(=C)C4=O)O)C)O 376.50 unknown https://doi.org/10.1021/NP060638+
[(1R,4S,5R,6R,9R,10S,11R,13S,15R)-6,11,15-trihydroxy-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate 162870761 Click to see CC(=O)OCC1(C2CCC34CC(CC(C3C2(CCC1O)C)O)C(=C)C4O)C 378.50 unknown https://doi.org/10.1021/NP060638+
[(1R,4S,5R,6S,9R,10S,11R,13S)-11-hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162885244 Click to see CC(=O)OC1CCC2(C(C1(C)CO)CCC34C2C(CC(C3)C(=C)C4=O)O)C 376.50 unknown https://doi.org/10.1021/NP060638+
[(1R,4S,5R,9R,10S,11R,13S)-11-hydroxy-5,9-dimethyl-14-methylidene-6,15-dioxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate 162946321 Click to see CC(=O)OCC1(C2CCC34CC(CC(C3C2(CCC1=O)C)O)C(=C)C4=O)C 374.50 unknown https://doi.org/10.1021/NP060638+
[(1S,2S,5R,6S,7S,8S,10S,11R,15R)-10-acetyloxy-6,7,9,15-tetrahydroxy-12,12-dimethyl-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-6-yl]methyl acetate 102004643 Click to see CC(=O)OCC1(C2CCC3C(C2)(C1O)C4(C(C5C3(CO4)C(CCC5(C)C)O)OC(=O)C)O)O 468.50 unknown via CMAUP database
[(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 via CMAUP database
[(1S,3S,4R,6S,8R,9R,10S,11R,13S)-3,8,11-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162887309 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(C2C1(C)C)O)C(=O)C4=C)O)C)O 392.50 unknown https://doi.org/10.1021/NP060638+
[(1S,3S,4R,6S,8R,9R,10S,11R,13S)-8-acetyloxy-3,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162933079 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(C2C1(C)C)O)C(=O)C4=C)O)C)OC(=O)C 434.50 unknown https://doi.org/10.1021/NP060638+
[(1S,3S,4R,6S,8S,9R,10R,11S,13S,15R)-15-acetyloxy-3,8,11-trihydroxy-5,5,9-trimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 163030495 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(C2C1(C)C)O)C(C4=C)OC(=O)C)O)C)O 436.50 unknown https://doi.org/10.1016/J.BMCL.2010.11.095
[(1S,3S,4R,6S,8S,9R,10S,11R,13S)-3,6,8-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162932886 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3)O)(C)C)O)O)C)C(=O)C2=C 392.50 unknown https://doi.org/10.1021/NP060638+
[(1S,4S,9S,10R)-2,8,16-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-12-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 137705109 Click to see CC(=O)OC1CC2C3(C(CCC(C3CC(C24C(C1C(=C)C4=O)O)O)(C)C)O)C 392.50 unknown https://doi.org/10.1021/NP030357R
https://doi.org/10.1016/0031-9422(91)83072-S
[11-Hydroxy-5,9-dimethyl-14-methylidene-15-oxo-5-[(5-oxopyrrolidin-2-yl)oxymethyl]-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 75599925 Click to see CC(=O)OC1CCC2(C(C1(C)COC3CCC(=O)N3)CCC45C2C(CC(C4)C(=C)C5=O)O)C 459.60 unknown https://doi.org/10.1016/J.BMCL.2010.11.095
1,7,12,14-Tetrahydroxykaur-16-en-15-one (1alpha,7alpha,12alpha,14R) 174150 Click to see CC1(CCC(C2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)C)O)C 350.40 unknown https://doi.org/10.1021/NP030357R
https://doi.org/10.1016/0031-9422(91)83072-S
2,12,16-Trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 14563761 Click to see CC1(CCCC2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)C)CO 350.40 unknown https://doi.org/10.1021/NP030357R
2,12,16-Trihydroxy-9-(hydroxymethyl)-5,5-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 73657179 Click to see CC1(CCCC2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)CO)C 350.40 unknown https://doi.org/10.1021/NP030357R
2,16-Dihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 72742985 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)CO 334.40 unknown https://doi.org/10.1016/0031-9422(92)90064-W
https://doi.org/10.1016/0031-9422(92)80450-S
2,16-Dihydroxy-5,9-bis(hydroxymethyl)-5-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 73657180 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)CO)CO 350.40 unknown https://doi.org/10.1021/NP030357R
2,8,12-Trihydroxy-5,5-dimethyl-18-methylidene-11-oxapentacyclo[11.3.2.01,12.04,9.09,16]octadecan-17-one 73657178 Click to see CC1(CCC(C23C1CC(C45C2CCC(C4(OC3)O)C(=C)C5=O)O)O)C 348.40 unknown https://doi.org/10.1021/NP030357R
2,8,12,16-Tetrahydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 13193212 Click to see CC1(CCC(C2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)C)O)C 350.40 unknown https://doi.org/10.1246/CL.1981.753
https://doi.org/10.1021/NP030357R
2,8,12,16-Tetrahydroxy-9-(hydroxymethyl)-5,5-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 14466843 Click to see CC1(CCC(C2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)CO)O)C 366.40 unknown https://doi.org/10.1021/NP030357R
2,8,16-Trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 73657181 Click to see CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)CO 350.40 unknown https://doi.org/10.1021/NP030357R
3,11-Dihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-6,15-dione 162843643 Click to see CC1(C2C(CC34CC(CC(C3C2(CCC1=O)C)O)C(=C)C4=O)O)C 332.40 unknown https://doi.org/10.1021/NP060638+
3beta,11beta-Diacetoxy-1alpha-hydroxykaura-16-ene-6,15-dione 442041 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(=O)C2C1(C)C)C(=O)C4=C)O)C)OC(=O)C 432.50 unknown https://doi.org/10.1021/NP060638+
https://doi.org/10.1007/BF02976453
7beta-Hydroxykaur-16-en-19-oic acid 101526595 Click to see CC12CCCC(C1CC(C34C2CCC(C3)C(=C)C4)O)(C)C(=O)O 318.40 unknown via CMAUP database
8,16-Dihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 56671376 Click to see CC1(CCC(C2(C1CCC34C2CCC(C3O)C(=C)C4=O)C)O)CO 334.40 unknown via CMAUP database
Acetylsventenic acid 102004542 Click to see CC(=O)OC1CC2C(CCCC2(C)C(=O)O)(C3C14CC(CC3)C(=C)C4)C 360.50 unknown via CMAUP database
CID 102004538 102004538 Click to see CC1(CCCC2(C1CCC34C2CCC(C3O)C(C4)(C)O)C=O)C 320.50 unknown via CMAUP database
CID 3819 3819 Click to see CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)CO)O)C 350.40 unknown https://doi.org/10.1021/NP030357R
Excisanin 15011613 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)CO 334.40 unknown https://doi.org/10.1016/0031-9422(92)90064-W
https://doi.org/10.1016/0031-9422(92)80450-S
https://doi.org/10.1016/0031-9422(91)83072-S
Excisanin A 11772488 Click to see CC1(CCC(C2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)C)O)C 350.40 unknown https://doi.org/10.1246/CL.1981.753
https://doi.org/10.1021/NP030357R
Excisanin B 367618 Click to see CC(=O)OC1CC2C3(C(CCC(C3CC(C24C(C1C(=C)C4=O)O)O)(C)C)O)C 392.50 unknown https://doi.org/10.1021/NP030357R
https://doi.org/10.1016/0031-9422(91)83072-S
Excisanin D 44575548 Click to see CC(=O)OCC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)C 392.50 unknown https://doi.org/10.1016/S0031-9422(96)00738-8
https://doi.org/10.1021/NP030357R
Excisanin E 101712256 Click to see CC(=O)OCC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)CO)O)C 408.50 unknown via CMAUP database
Excisanin F 10594940 Click to see CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)CO)O)C=O 364.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
https://doi.org/10.1021/NP970155T
Excisanin G 10714063 Click to see CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(C4=O)CO)O)CO)O)C 368.50 unknown https://doi.org/10.1021/NP970155T
Excisanin H 10066342 Click to see CC1(CCC(C23C1CC(C45C2CCC(C4(OC3)O)C(=C)C5=O)O)O)C 348.40 unknown https://doi.org/10.1021/NP030357R
Excisanin I 10360537 Click to see CC1(CCCC2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)CO)C 350.40 unknown https://doi.org/10.1021/NP030357R
Excisanin J 10405621 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)CO)CO 350.40 unknown https://doi.org/10.1021/NP030357R
excisusin A 16215553 Click to see CC(=O)OC1CCC2(C(C1(C)CO)CCC34C2C(CC(C3)C(=C)C4=O)O)C 376.50 unknown https://doi.org/10.1021/NP060638+
excisusin B 16215554 Click to see CC(=O)OC1CC(C2(C(C1(C)C)CCC34C2C(CC(C3)C(=C)C4=O)O)C)O 376.50 unknown https://doi.org/10.1021/NP060638+
excisusin C 16215670 Click to see CC(=O)OCC1(C2CCC34CC(CC(C3C2(CCC1O)C)O)C(=C)C4O)C 378.50 unknown https://doi.org/10.1021/NP060638+
excisusin D 16215671 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3)O)(C)C)O)O)C)C(=O)C2=C 392.50 unknown https://doi.org/10.1021/NP060638+
excisusin E 16215672 Click to see CC(=O)OCC1(C2CCC34CC(CC(C3C2(CCC1=O)C)O)C(=C)C4=O)C 374.50 unknown https://doi.org/10.1021/NP060638+
Excisusin F 53323644 Click to see CC(=O)OC1CCC2(C(C1(C)COC3CCC(=O)N3)CCC45C2C(CC(C4)C(=C)C5=O)O)C 459.60 unknown https://doi.org/10.1016/J.BMCL.2010.11.095
Henryin 11741244 Click to see CC(=O)OCC12C3CCC4C(C3(C(CC1C(CCC2O)(C)C)O)C(=O)C4=C)O 392.50 unknown https://doi.org/10.1021/NP030357R
inflexanin A 13874229 Click to see CC(=O)OC1CCC2(C3C(CC4CC3(CC(C2C1(C)C)O)C(=O)C4=C)O)C 376.50 unknown https://doi.org/10.1021/NP060638+
inflexanin B 44421638 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(C2C1(C)C)O)C(=O)C4=C)O)C)O 392.50 unknown https://doi.org/10.1021/NP060638+
inflexarabdonin A 44421642 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3)O)(C)C)OC(=O)C)O)C)C(C2=C)O 436.50 unknown https://doi.org/10.1021/NP060638+
Inflexarabdonin D 53324240 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(C2C1(C)C)O)C(C4=C)OC(=O)C)O)C)O 436.50 unknown https://doi.org/10.1016/J.BMCL.2010.11.095
Inflexarabdonin E 53324930 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(=O)C2C1(C)C)C(=O)C4=C)O)C)O 390.50 unknown https://doi.org/10.1016/J.BMCL.2010.11.095
inflexarabdonin G 44421637 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC3)C(C(CC4O)OC(=O)C)(C)C)C)C(=O)C2=C 418.50 unknown https://doi.org/10.1021/NP060638+
inflexarabdonin I 44421635 Click to see CC1(C2C(CC34CC(CC(C3C2(CCC1=O)C)O)C(=C)C4=O)O)C 332.40 unknown https://doi.org/10.1021/NP060638+
Inflexin 10502865 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(=O)C3)(C)C)OC(=O)C)O)C)C(=O)C2=C 432.50 unknown https://doi.org/10.1021/NP060638+
https://doi.org/10.1007/BF02976453
Inflexinol 44421641 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3)O)(C)C)OC(=O)C)O)C)C(=O)C2=C 434.50 unknown https://doi.org/10.1021/NP060638+
Kamebakaurin 13945489 Click to see CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)CO)O)C 350.40 unknown https://doi.org/10.1021/NP030357R
Kamebanin 12004580 Click to see CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)C 334.40 unknown https://doi.org/10.1021/NP030357R
https://doi.org/10.1016/0031-9422(91)83072-S
rabdokunmin C 14563762 Click to see CC1(CCCC2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)C)CO 350.40 unknown https://doi.org/10.1021/NP030357R
Rabdoserrin B 14466844 Click to see CC1(CCC(C2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)CO)O)C 366.40 unknown https://doi.org/10.1021/NP030357R
Wangzaozin A 70691853 Click to see CC1(C(CCC2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)C 334.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
1-O-(2,3,19,23-Tetrahydroxy-28-oxours-12-en-28-yl)hexopyranose 44566341 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O 666.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1S,2R,5S,8S,9R,11R,15S,18R)-15,18-dihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecane-7,16-dione 44575567 Click to see CC1(CCC(C23C1CC(C45C2CCC(C4O)C(=C)C5=O)OC3=O)O)C 346.40 unknown https://doi.org/10.1021/NP030357R
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aS,6aS,6bR,8aR,10R,11R,12aR,14bS)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 11887403 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 via CMAUP database
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Asiatic Acid 119034 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O 488.70 unknown via CMAUP database
Biexcisusin A, (rel)- 57393032 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3)O)(C)C)OC(=O)C)O)C)C(=O)C2(CCC5(C6CC(C7C8(C(CC(C(C8C(CC7(C6)C5=O)O)(C)C)OC(=O)C)OC(=O)C)C)O)O)O 903.10 unknown https://doi.org/10.1021/NP200439N
Biexcisusin B, (rel)- 57398302 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3)O)(C)C)OC(=O)C)O)C)C5=C2CCC6(O5)C7CC(C8C9(C(CC(C(C9C(CC8(C7)C6=O)O)(C)C)OC(=O)C)O)C)OC(=O)C 869.00 unknown https://doi.org/10.1021/NP200439N
Biexcisusin C, (rel)- 57399961 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3)O)(C)C)OC(=O)C)O)C)C(=O)OC5(CCC2=O)C6CC(C7C8(C(CC(C(C8C(CC7(C6)C5=O)O)(C)C)OC(=O)C)O)C)OC(=O)C 901.00 unknown https://doi.org/10.1021/NP200439N
Biexcisusin D, (rel)- 57403476 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3)O)(C)C)OC(=O)C)O)C)C(=O)OC5(CCC2=O)C6CC(C7C8(C(CC(C(C8C(=O)CC7(C6)C5=O)(C)C)OC(=O)C)O)C)OC(=O)C 899.00 unknown https://doi.org/10.1021/NP200439N
Biexcisusin E, (rel)- 57403477 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(=O)C3)(C)C)OC(=O)C)O)C)C(=O)OC5(CCC2=O)C6CC(C7C8(C(CC(C(C8C(CC7(C6)C5=O)O)(C)C)OC(=O)C)O)C)OC(=O)C 899.00 unknown https://doi.org/10.1021/NP200439N
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown via CMAUP database
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/BF02976453
Ursolic acid (Malol) 49867942 Click to see CC1CC(C2CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
Solasodine 442985 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1 413.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 52940117 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 via CMAUP database
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 via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
4-(3,7-Dimethyl-2,6-octadienyl)-3-hydroxy-6-methyl-9H-carbazole 14635307 Click to see CC1=CC2=C(C=C1)NC3=C2C(=C(C=C3)O)CC=C(C)CCC=C(C)C 333.50 unknown https://doi.org/10.1246/CL.1981.753
https://doi.org/10.1021/NP030357R
> Organoheterocyclic compounds / Oxepanes
6-(3-Hydroxybut-1-enyl)-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol 539381 Click to see CC(C=CC12C(CC(CC1(O2)C)O)(C)C)O 226.31 unknown https://doi.org/10.1016/J.BMCL.2010.11.095
Corchoionol A 10656857 Click to see CC(C=CC12C(CC(CC1(O2)C)O)(C)C)O 226.31 unknown https://doi.org/10.1016/J.BMCL.2010.11.095
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(E)-3-(4-hydroxy-3-methoxyphenyl)-N-[(2S)-2-(4-hydroxyphenyl)-2-methoxyethyl]prop-2-enamide 643362 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCC(C2=CC=C(C=C2)O)OC)O 343.40 unknown https://doi.org/10.1021/NP000604G
3-(4-hydroxy-3-methoxyphenyl)-N-[2-(4-hydroxyphenyl)-2-methoxyethyl]acrylamide 68977241 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCC(C2=CC=C(C=C2)O)OC)O 343.40 unknown https://doi.org/10.1021/NP000604G
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
methyl (3S)-3-(3,4-dihydroxyphenyl)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxypropanoate 10452024 Click to see COC(=O)CC(C1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 374.30 unknown https://doi.org/10.1021/NP000604G
Methyl 3-(3,4-dihydroxyphenyl)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoate 73809375 Click to see COC(=O)CC(C1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 374.30 unknown https://doi.org/10.1021/NP000604G
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)prop-2-enoate 54710367 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)[O-] 179.15 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxychromen-4-one 57339948 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(OC4O)CO)O)O)O)O 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(2,3-Dihydroxyphenyl)-5,7-dihydroxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 53399169 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=C(C(=CC=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,4R,5S)-3,4,5-trihydroxy-6-[[(2R,4R,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 24211973 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Pedalitin 31161 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)O 316.26 unknown via CMAUP database

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.