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Isodon scoparius

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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 UUID643fdf82df48c919052816
Scientific name Isodon scoparius
Authority (C.Y.Wu & H.W.Li) H.Hara
First published in J. Jap. Bot. 60: 236 (1985)

Description Top

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Synonyms Top

Scientific name Authority First published in
Rabdosia scoparia C.Y.Wu & H.W.Li Fl. Yunnanica 1: 777 (1977)

Common names Top

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Language Common/alternative name
Chinese 帚状香茶菜

Subspecies (abbr. subsp./ssp.) Top

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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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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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000217960
Tropicos 17607230
KEW urn:lsid:ipni.org:names:915160-1
The Plant List kew-103024
Open Tree Of Life 1017555
NCBI Taxonomy 662927
IPNI 915160-1
GBIF 5608855
EOL 2898986
CMAUP NPO18028

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
Ethnobotanical, Phytochemical, and Pharmacological Properties of the Subfamily Nepetoideae (Lamiaceae) in Inflammatory Diseases Ortiz-Mendoza N, Martínez-Gordillo MJ, Martínez-Ambriz E, Basurto-Peña FA, González-Trujano ME, Aguirre-Hernández E Plants (Basel) 02-Nov-2023
PMCID:PMC10648697
doi:10.3390/plants12213752
PMID:37960108
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
Isolation and HPLC Quantitative Determination of 5α-Reductase Inhibitors from Tectona grandis L.f. Leaf Extract Insumrong K, Ingkaninan K, Waranuch N, Tanuphol N, Wisuitiprot W, Promgool T, Suphrom N Molecules 30-Apr-2022
PMCID:PMC9101728
doi:10.3390/molecules27092893
PMID:35566245
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
Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes Lautié E, Russo O, Ducrot P, Boutin JA Front Pharmacol 07-Apr-2020
PMCID:PMC7154113
doi:10.3389/fphar.2020.00397
PMID:32317969
A database-driven approach identifies additional diterpene synthase activities in the mint family (Lamiaceae) Johnson SR, Bhat WW, Bibik J, Turmo A, Hamberger B, Hamberger B J Biol Chem 29-Nov-2018
PMCID:PMC6349103
doi:10.1074/jbc.RA118.006025
PMID:30498089
Bioactive ent-kaurane diterpenoids from Isodon rubescens. Zhang YY, Jiang HY, Liu M, Hu K, Wang WG, Du X, Li XN, Pu JX, Sun HD Phytochemistry 01-Nov-2017
doi:10.1016/J.PHYTOCHEM.2017.08.009
PMID:28869908
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-Kaurane diterpenoids from Isodon scoparius. Zhao Y, Pu JX, Huang SX, Wu YL, Yang LB, Xiao WL, Han QB, Chen GQ, Sun HD J Nat Prod 01-Jan-2009
doi:10.1021/NP800484J
PMID:19072209
<i>ent</i>‐Clerodanoids from <i>Isodon scoparius</i> Wei Xiang, Rong‐Tao Li, Qi‐Shi Song, Zhi Na, Han‐Dong Sun Wiley 24-Nov-2004
doi:10.1002/HLCA.200490257

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see C1=CC=C(C(=C1)C(=O)O)O 138.12 unknown https://doi.org/10.1002/HLCA.200490257
> Benzenoids / Naphthalenes / Naphthoquinones
Chimaphilin 101211 Click to see CC1=CC2=C(C=C1)C(=O)C=C(C2=O)C 186.21 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(E)-5-[(1R,4aR,8aR)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-2-enoic acid 14733517 Click to see CC1=CCC2C(CCCC2(C1CCC(=CC(=O)O)C)C)(C)C 304.50 unknown https://doi.org/10.1002/HLCA.200490257
5-(2,5,5,8a-Tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-enoic acid 78131064 Click to see CC1=CCC2C(CCCC2(C1CCC(=CC(=O)O)C)C)(C)C 304.50 unknown https://doi.org/10.1002/HLCA.200490257
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(E,5R)-5-[(1S,2R,4aR,8aS)-1,2,4a-trimethyl-5-methylidene-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]-5-acetyloxy-3-methylpent-2-enoic acid 12148005 Click to see CC1CCC2(C(C1(C)C(CC(=CC(=O)O)C)OC(=O)C)CCCC2=C)C 362.50 unknown https://doi.org/10.1002/HLCA.200490257
5-acetyloxy-5-(1,2,4a-trimethyl-5-methylidene-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl)-3-methylpent-2-enoic acid 78096331 Click to see CC1CCC2(C(C1(C)C(CC(=CC(=O)O)C)OC(=O)C)CCCC2=C)C 362.50 unknown https://doi.org/10.1002/HLCA.200490257
methyl (E,5R)-5-[(1S,2R,4aR,5S,8aR)-5-hydroxy-1,2,4a,5-tetramethyl-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]-5-hydroxy-3-methylpent-2-enoate 102212886 Click to see CC1CCC2(C(C1(C)C(CC(=CC(=O)OC)C)O)CCCC2(C)O)C 352.50 unknown https://doi.org/10.1002/HLCA.200490257
methyl 5-hydroxy-5-(5-hydroxy-1,2,4a,5-tetramethyl-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl)-3-methylpent-2-enoate 163028147 Click to see CC1CCC2(C(C1(C)C(CC(=CC(=O)OC)C)O)CCCC2(C)O)C 352.50 unknown https://doi.org/10.1002/HLCA.200490257
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1'R,2'R,4'S,9'S,10'R,12'R,13'S,16'R)-2',12',16'-trihydroxy-5',5',9'-trimethylspiro[oxirane-2,14'-tetracyclo[11.2.1.01,10.04,9]hexadecane]-11',15'-dione 102283754 Click to see CC1(CCCC2(C1CC(C34C2C(=O)C(C(C3O)C5(C4=O)CO5)O)O)C)C 364.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
(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/NP800484J
(1R,2R,4R,5S,9S,10R,13S,15R,16R)-2,15,16-trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-11-one 102283758 Click to see CC1(CCCC2(C1CC(C34C2C(=O)CC(C3O)C(=C)C4O)O)C)CO 350.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
(1R,2R,4R,5S,9S,10R,13S,16R)-2,16-dihydroxy-5-(hydroxymethyl)-14-(methoxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-11,15-dione 102283757 Click to see CC1(CCCC2(C1CC(C34C2C(=O)CC(C3O)C(C4=O)COC)O)C)CO 380.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
(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/10.1021/NP800484J
(1R,2R,4R,9R,10R,11S,13S,15R,16R)-2,11,15,16-tetrahydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-8-one 25209067 Click to see CC1(CCC(=O)C2(C1CC(C34C2C(CC(C3O)C(=C)C4O)O)O)C)C 350.40 unknown https://doi.org/10.1021/NP800484J
(1R,2R,4R,9R,10S,11R,12R,13R,16R)-2,11,12,16-tetrahydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 163092523 Click to see CC1(CCCC2(C1CC(C34C2C(C(C(C3O)C(=C)C4=O)O)O)O)C)C 350.40 unknown https://doi.org/10.1021/NP800484J
(1R,2R,4R,9R,10S,12R,13R,16R)-2,12,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-11,15-dione 162944669 Click to see CC1(CCCC2(C1CC(C34C2C(=O)C(C(C3O)C(=C)C4=O)O)O)C)C 348.40 unknown https://doi.org/10.1021/NP800484J
(1R,2R,4R,9R,12R,13R,16R)-2,12,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-11,15-dione 163185305 Click to see CC1(CCCC2(C1CC(C34C2C(=O)C(C(C3O)C(=C)C4=O)O)O)C)C 348.40 unknown https://doi.org/10.1021/NP800484J
(1R,2R,4S,5S,9R,10S,11S,13S,16R)-2,11,16-trihydroxy-5,9-dimethyl-14-methylidene-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carbaldehyde 25195036 Click to see CC1(CCCC2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)C=O 348.40 unknown https://doi.org/10.1021/NP800484J
(1R,2R,4S,5S,9R,10S,12R,13R,14R,16R)-2,12,16-trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-(3-oxobutyl)tetracyclo[11.2.1.01,10.04,9]hexadecane-11,15-dione 45273127 Click to see CC(=O)CCC1C2C(C(=O)C3C4(CCCC(C4CC(C3(C2O)C1=O)O)(C)CO)C)O 422.50 unknown https://doi.org/10.1021/NP800484J
(1R,2R,4S,5S,9R,10S,12R,13S,16R)-2,12,16-trihydroxy-5,9-dimethyl-14-methylidene-11,15-dioxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carbaldehyde 163010750 Click to see CC1(CCCC2(C1CC(C34C2C(=O)C(C(C3O)C(=C)C4=O)O)O)C)C=O 362.40 unknown https://doi.org/10.1021/NP800484J
(1R,2R,4S,5S,9R,10S,13S,14S,16R)-2,16-dihydroxy-5-(hydroxymethyl)-14-(methoxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-11,15-dione 25208915 Click to see CC1(CCCC2(C1CC(C34C2C(=O)CC(C3O)C(C4=O)COC)O)C)CO 380.50 unknown https://doi.org/10.1021/NP800484J
(1R,2R,4S,9S,10R,12S,13R,16R)-2,12,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 102283762 Click to see CC1(CCCC2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)C)C 334.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
(1R,2R,4S,9S,10S,11S,13S,15R,16R)-2,11,15,16-tetrahydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-8-one 102283761 Click to see CC1(CCC(=O)C2(C1CC(C34C2C(CC(C3O)C(=C)C4O)O)O)C)C 350.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
(1R,2S,4R,9R,10S,11S,13S,16R)-2,11,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-8,15-dione 16081683 Click to see CC1(CCC(=O)C2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)C 348.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
(1R,2S,4R,9R,10S,11S,13S,16S)-2,11,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-8,15-dione 163056612 Click to see CC1(CCC(=O)C2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)C 348.40 unknown https://doi.org/10.1021/NP800484J
(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/J.PHYTOCHEM.2017.08.009
(1S,2R,4S,5S,9R,10S,13S,15R,16R)-2,15,16-trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-11-one 163068736 Click to see CC1(CCCC2(C1CC(C34C2C(=O)CC(C3O)C(=C)C4O)O)C)CO 350.40 unknown https://doi.org/10.1021/NP800484J
(1S,2R,4S,5S,9R,13S,15R,16R)-2,15,16-trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-11-one 163185773 Click to see CC1(CCCC2(C1CC(C34C2C(=O)CC(C3O)C(=C)C4O)O)C)CO 350.40 unknown https://doi.org/10.1021/NP800484J
(7,9,10,18-Tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl) acetate 13919285 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4O)C(=C)C5O)O)(C)C 408.50 unknown https://doi.org/10.1021/NP200140J
[(1R,2R,4R,9R,10S,11R,12R,13S,16R)-2,11,12-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-16-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162868359 Click to see CC(=O)OC1C2C(C(C3C1(C(CC4C3(CCCC4(C)C)C)O)C(=O)C2=C)O)O 392.50 unknown https://doi.org/10.1021/NP800484J
[(1R,4S,9S,10R,11R,12R,13S,15R,16R)-11,12,16-trihydroxy-5,5,9-trimethyl-14-methylidene-2-oxo-15-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 102283756 Click to see CC(=O)OC1C(=C)C2C(C(C3C1(C2O)C(=O)CC4C3(CCCC4(C)C)C)O)O 392.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
[(1S,2R,4R,9R,10S,11R,12R,13R,16R)-11,12,16-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-2-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 163036297 Click to see CC(=O)OC1CC2C(CCCC2(C3C14C(C(C(C3O)O)C(=C)C4=O)O)C)(C)C 392.50 unknown https://doi.org/10.1021/NP800484J
[(1S,2S,5S,7R,8R,9S,10S,11R,15S,18R)-7,9,10,18-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate 162966019 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4O)C(=C)C5O)O)(C)C 408.50 unknown https://doi.org/10.1021/NP800484J
[(1S,4R,9R,10S,11R,12R,13R,15R,16S)-11,12,16-trihydroxy-5,5,9-trimethyl-14-methylidene-2-oxo-15-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162916333 Click to see CC(=O)OC1C(=C)C2C(C(C3C1(C2O)C(=O)CC4C3(CCCC4(C)C)C)O)O 392.50 unknown https://doi.org/10.1021/NP800484J
[(2S,5S,9S,10R,11R,15S,18R)-7,9,10,18-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate 102090489 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4O)C(=C)C5O)O)(C)C 408.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
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/NP800484J
2-[(1R,2R,4R,5S,8S,9R,10S,13S,16R)-2,8,16-trihydroxy-5,9-dimethyl-14-methylidene-11,15-dioxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]acetaldehyde 101402142 Click to see CC1(CCC(C2(C1CC(C34C2C(=O)CC(C3O)C(=C)C4=O)O)C)O)CC=O 376.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
2,11,16-Trihydroxy-5,9-dimethyl-14-methylidene-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carbaldehyde 56681662 Click to see CC1(CCCC2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)C=O 348.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
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/10.1016/J.PHYTOCHEM.2017.08.009
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/10.1021/NP800484J
Excisanin K 45270538 Click to see CC1(CCC(C2(C1CCC34C2CCC(C3O)C(=C)C4=O)C)O)CO 334.40 unknown https://doi.org/10.1021/NP800484J
henryine A 16046182 Click to see CC1(CCCC2(C1CC(C34C2C(=O)CC(C3O)C(=C)C4=O)O)C)CO 348.40 unknown https://doi.org/10.1021/NP800484J
https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
Isoscoparin D 25208913 Click to see CC1(CCCC2(C1CC(C34C2C(=O)C(C(C3O)C5(C4=O)CO5)O)O)C)C 364.40 unknown https://doi.org/10.1021/NP800484J
Isoscoparin E 102283755 Click to see CC(=O)OC1CC2C(CCCC2(C3C14C(C(C(C3O)O)C(=C)C4=O)O)C)(C)C 392.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
Isoscoparin F 25209066 Click to see CC(=O)OC1C(=C)C2C(C(C3C1(C2O)C(=O)CC4C3(CCCC4(C)C)C)O)O 392.50 unknown https://doi.org/10.1021/NP800484J
Isoscoparin H 25209064 Click to see CC1(CCCC2(C1CC(C34C2C(=O)CC(C3O)C(=C)C4O)O)C)CO 350.40 unknown https://doi.org/10.1021/NP800484J
Isoscoparin J 102283760 Click to see CC1(CCCC2(C1CC(C34C2C(=O)CC(C3O)C(=C)C4=O)O)C)CC=O 360.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
Isoscoparin L 25195034 Click to see CC1(CCCC2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)C)C 334.40 unknown https://doi.org/10.1021/NP800484J
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/10.1016/J.PHYTOCHEM.2017.08.009
https://doi.org/10.1021/NP800484J
Lasiokaurinol 45272267 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4O)C(=C)C5O)O)(C)C 408.50 unknown https://doi.org/10.1021/NP800484J
phyllostachysin D 16081682 Click to see CC1(CCCC2(C1CC(C34C2C(=O)C(C(C3O)C(=C)C4=O)O)O)C)C 348.40 unknown https://doi.org/10.1021/NP800484J
https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
phyllostachysin F 16081680 Click to see CC1(CCCC2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)C 334.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
https://doi.org/10.1021/NP800484J
PhyllostachysinH 16081681 Click to see CC1(CCC(C2(C1CCC34C2C(CC(C3O)C(=C)C4=O)O)C)O)C 334.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
https://doi.org/10.1021/NP800484J
rabdoinflexin B 14466855 Click to see CC1(CCC(C2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)O)C 350.40 unknown https://doi.org/10.1021/NP800484J
https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
Rabdokunmin A 14563758 Click to see CC(=O)OC1C2C(C(C3C1(C(CC4C3(CCCC4(C)C)C)O)C(=O)C2=C)O)O 392.50 unknown https://doi.org/10.1021/NP800484J
https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
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/NP800484J
https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
Rabdokunmin D 45267139 Click to see CC1(CCCC2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)CO 350.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
https://doi.org/10.1021/NP800484J
rabdoloxin A 45271373 Click to see CC1(CCCC2(C1CC(C34C2C(=O)C(C(C3O)C(=C)C4=O)O)O)C)CO 364.40 unknown https://doi.org/10.1021/NP800484J
Rabdoloxin B 25195035 Click to see CC1(CCCC2(C1CC(C34C2C(C(C(C3O)C(=C)C4=O)O)O)O)C)C 350.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2017.08.009
https://doi.org/10.1021/NP800484J
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
CID 3838010 3838010 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown https://doi.org/10.1002/HLCA.200490257
Pomolic acid 382831 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown https://doi.org/10.1002/HLCA.200490257
> 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/10.1002/HLCA.200490257
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/10.1002/HLCA.200490257
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/10.1002/HLCA.200490257
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/10.1002/HLCA.200490257
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Isohomoarbutin 5318573 Click to see CC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1002/HLCA.200490257

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