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Croton gratissimus

Croton gratissimus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644036ba2daf3071508121
Scientific name Croton gratissimus
Authority Burch.
First published in Trav. S. Africa 2: 263 (1824)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Oxydectes gratissima Kuntze Revis. Gen. Pl. 2: 611 (1891)

Common names Top

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Language Common/alternative name
English lavender croton
English laventelkoorsbessie
Afrikaans laventelkoorsbessie
French oxydectes amabilis
French oxydectes welwitschiana
French oxydectes zambesica

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Croton gratissimus var. gratissimus Unknown
Croton gratissimus var. subgratissimus (Prain) Burtt Davy Man. Pl. Transvaal : 301 (1932)

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Caprivi Strip
      • Kwazulu-Natal
      • Namibia
      • Northern Provinces
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Ivory Coast
      • Mali
      • Nigeria
      • Senegal
      • Sierra Leone
    • West-central Tropical Africa
      • Cameroon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000931164
Tropicos 12802900
KEW urn:lsid:ipni.org:names:342614-1
The Plant List kew-50054
Open Tree Of Life 528092
NCBI Taxonomy 316784
IUCN Red List 146220792
IPNI 342614-1
iNaturalist 583075
GBIF 3058727
Freebase /m/0gyx6fr
EPPO CVNGG
EOL 1147149
USDA GRIN 12412
Wikipedia Croton_gratissimus
CMAUP NPO5608

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
Targeting RNA modifications with pharmacological agents: New frontiers in cancer therapy Guan A, Wong JJ Cancer Med 28-Mar-2024
PMCID:PMC10974741
doi:10.1002/cam4.6989
PMID:38545841
Preserving Ethnoveterinary Medicine (EVM) along the Transhumance Routes in Southwestern Angola: Synergies between International Cooperation and Academic Research Solazzo D, Moretti MV, Tchamba JJ, Rafael MF, Tonini M, Fico G, Basterrecea T, Levi S, Marini L, Bruschi P Plants (Basel) 28-Feb-2024
PMCID:PMC10933900
doi:10.3390/plants13050670
PMID:38475516
Nature’s Green Potential: Anticancer Properties of Plants of the Euphorbiaceae Family Jiménez-González V, Kowalczyk T, Piekarski J, Szemraj J, Rijo P, Sitarek P Cancers (Basel) 25-Dec-2023
PMCID:PMC10778523
doi:10.3390/cancers16010114
PMID:38201542
Indigenous knowledge and use of medicinal plants for ethnoveterinary within the North West Province, South Africa Ndou RV, Materechera SA, Mwanza M, Otang-Mbeng W, Ijane MF Front Vet Sci 22-Nov-2023
PMCID:PMC10703488
doi:10.3389/fvets.2023.1273562
PMID:38076569
Phytochemical Properties of Croton gratissimus Burch (Lavender Croton) Herbal Tea and Its Protective Effect against Iron-Induced Oxidative Hepatic Injury Ncume PV, Salau VF, Mtshali S, Olofinsan KA, Erukainure OL, Matsabisa MG Plants (Basel) 10-Aug-2023
PMCID:PMC10459045
doi:10.3390/plants12162915
PMID:37631127
Chemistry and Bioactivity of Croton Essential Oils: Literature Survey and Croton hirtus from Vietnam Luu-dam NA, Le CV, Satyal P, Le TM, Bui VH, Vo VH, Ngo GH, Bui TC, Nguyen HH, Setzer WN Molecules 03-Mar-2023
PMCID:PMC10005233
doi:10.3390/molecules28052361
PMID:36903605
Comparison study of Beninese and Chinese herbal medicines in treating COVID-19 Houeze EA, Wang Y, Zhou Q, Zhang H, Wang X J Ethnopharmacol 10-Feb-2023
PMCID:PMC9911150
doi:10.1016/j.jep.2023.116172
PMID:36773790
Histochemical Analysis and Ultrastructure of Trichomes and Laticifers of Croton gratissimus Burch. var. gratissimus (Euphorbiaceae) Naidoo D, Naidoo Y, Naidoo G, Kianersi F, Dewir YH Plants (Basel) 08-Feb-2023
PMCID:PMC9964807
doi:10.3390/plants12040772
PMID:36840119
First Report on the Chemical Composition, Antioxidant Capacity, and Preliminary Toxicity to Artemia salina L. of Croton campinarensis Secco, A. Rosário & PE Berry (Euphorbiaceae) Essential Oil, and In Silico Study da Costa LS, de Moraes ÂA, Cruz JN, Mali SN, Almeida LQ, do Nascimento LD, Ferreira OO, Varela EL, Percário S, de Oliveira MS, Andrade EH Antioxidants (Basel) 06-Dec-2022
PMCID:PMC9774510
doi:10.3390/antiox11122410
PMID:36552618
Volatile Profiling of Magnolia champaca Accessions by Gas Chromatography Mass Spectrometry Coupled with Chemometrics Sahoo C, Champati BB, Dash B, Jena S, Ray A, Panda PC, Nayak S, Sahoo A Molecules 27-Oct-2022
PMCID:PMC9658739
doi:10.3390/molecules27217302
PMID:36364127
Medicinal plants used for the management of respiratory diseases in Zimbabwe: Review and perspectives potential management of COVID-19 Nyagumbo E, Pote W, Shopo B, Nyirenda T, Chagonda I, Mapaya RJ, Maunganidze F, Mavengere WN, Mawere C, Mutasa I, Kademeteme E, Maroyi A, Taderera T, Bhebhe M Phys Chem Earth (2002) 21-Sep-2022
PMCID:PMC9489988
doi:10.1016/j.pce.2022.103232
PMID:36161239
Ethnoveterinary Practices and Ethnobotanical Knowledge on Plants Used against Cattle Diseases among Two Communities in South Africa Chakale MV, Asong JA, Struwig M, Mwanza M, Aremu AO Plants (Basel) 05-Jul-2022
PMCID:PMC9268905
doi:10.3390/plants11131784
PMID:35807736
Essential Oils in Respiratory Mycosis: A Review Zuzarte M, Salgueiro L Molecules 28-Jun-2022
PMCID:PMC9268412
doi:10.3390/molecules27134140
PMID:35807386
Study on South African Indigenous Teas—Antioxidant Potential, Nutritional Content, and Hypoxia-Induced Cyclooxygenase Inhibition on U87 MG Cell Line Matsabisa MG, Bala A, Tripathy S, Digashu MM, Rautenbach F, Dassarma B, Erhabor JO, Braga FC, Mukherjee PK, Tang M, Kang Y Molecules 30-May-2022
PMCID:PMC9181930
doi:10.3390/molecules27113505
PMID:35684442
Ethnopharmacological Study of Medicinal Plants Used for the Treatment of Cardiovascular Diseases and Their Associated Risk Factors in sub-Saharan Africa Odukoya JO, Odukoya JO, Mmutlane EM, Ndinteh DT Plants (Basel) 23-May-2022
PMCID:PMC9143319
doi:10.3390/plants11101387
PMID:35631812

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 / Benzene and substituted derivatives / Benzoic acids and derivatives
N-Formyl-4-hydroxybenzamide 71370414 Click to see C1=CC(=CC=C1C(=O)NC=O)O 165.15 unknown via CMAUP database
N-Formylbenzamide 151196 Click to see C1=CC=C(C=C1)C(=O)NC=O 149.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
4-Hydroxybenzamide 65052 Click to see C1=CC(=CC=C1C(=O)N)O 137.14 unknown via CMAUP database
Benzamide, N-[(2S)-2-hydroxy-2-phenylethyl]- 6542363 Click to see C1=CC=C(C=C1)C(CNC(=O)C2=CC=CC=C2)O 241.28 unknown via CMAUP database
> Lignans, neolignans and related compounds / Cyclobutane lignans
[(1R,2R,3S,4S)-2-(2,4-dihydroxybenzoyl)-3,4-diphenylcyclobutyl]-(2,4-dihydroxyphenyl)methanone 102228233 Click to see C1=CC=C(C=C1)C2C(C(C2C(=O)C3=C(C=C(C=C3)O)O)C(=O)C4=C(C=C(C=C4)O)O)C5=CC=CC=C5 480.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(8-Hydroxy-4a,8-dimethyl-2-propan-2-yl-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-yl) 3-(3-hydroxyphenyl)prop-2-enoate 163008764 Click to see CC(C)C1CCC2(CCCC(C2C1OC(=O)C=CC3=CC(=CC=C3)O)(C)O)C 386.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.05.014
Platambin 613194 Click to see CC(C)C1CCC2(C(CCC(=C)C2C1O)O)C 238.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.05.014
Voleneol 14137570 Click to see CC(C)C1CCC2(C(CCC(=C)C2C1O)O)C 238.37 unknown https://doi.org/10.1021/NP2002012
https://doi.org/10.1016/J.PHYTOCHEM.2010.05.014
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(13S)-7,11-dimethyl-4-prop-1-en-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),4,6,10-tetraen-15-one 162847981 Click to see CC1=CC=C(CCC2=CC(CC(=CCC1)C)OC2=O)C(=C)C 298.40 unknown https://doi.org/10.1021/NP2002012
(13S)-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),4,6,10-tetraen-15-one 163086272 Click to see CC1=CC=C(CCC2=CC(CC(=CCC1)C)OC2=O)C(C)C 300.40 unknown https://doi.org/10.1021/NP2002012
(4E,6E,10E,13S)-7,11-dimethyl-4-prop-1-en-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),4,6,10-tetraen-15-one 163186578 Click to see CC1=CC=C(CCC2=CC(CC(=CCC1)C)OC2=O)C(=C)C 298.40 unknown https://doi.org/10.1021/NP2002012
(4E,6E,10E,13S)-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),4,6,10-tetraen-15-one 163195490 Click to see CC1=CC=C(CCC2=CC(CC(=CCC1)C)OC2=O)C(C)C 300.40 unknown https://doi.org/10.1021/NP2002012
(4R,13S)-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,7,10-tetraen-15-one 163193016 Click to see CC1=CCC=C(C=CC(CCC2=CC(C1)OC2=O)C(C)C)C 300.40 unknown https://doi.org/10.1021/NP2002012
(4R,5E,7R,10E,13S)-4,7-dihydroxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 163185033 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)(C(C)C)O)(C)O 334.40 unknown https://doi.org/10.1021/NP2002012
(4R,5E,7R,10R,13S)-4,7,10-trihydroxy-7-methyl-11-methylidene-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5-dien-15-one 163186786 Click to see CC(C)C1(CCC2=CC(CC(=C)C(CCC(C=C1)(C)O)O)OC2=O)O 350.40 unknown https://doi.org/10.1021/NP2002012
(4R,5E,7R,10S,13S)-4,7,10-trihydroxy-7-methyl-11-methylidene-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5-dien-15-one 163193360 Click to see CC(C)C1(CCC2=CC(CC(=C)C(CCC(C=C1)(C)O)O)OC2=O)O 350.40 unknown https://doi.org/10.1021/NP2002012
(4R,5E,7S,10E,13S)-4-hydroxy-7-methoxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 163194504 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)(C(C)C)O)(C)OC 348.50 unknown https://doi.org/10.1021/NP2002012
(4R,5E,7S,10E,13S)-4,7-dihydroxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 163187582 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)(C(C)C)O)(C)O 334.40 unknown https://doi.org/10.1021/NP2002012
(4R,5E,7S,13R)-7-hydroxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 162869661 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)C(C)C)(C)O 318.40 unknown https://doi.org/10.1021/NP2002012
(4R,5E,7S,9E,11R,13S)-4,7,11-trihydroxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,9-trien-15-one 163186703 Click to see CC(C)C1(CCC2=CC(CC(C=CCC(C=C1)(C)O)(C)O)OC2=O)O 350.40 unknown https://doi.org/10.1021/NP2002012
(4R,7R,10R,13S)-4,7,10-trihydroxy-7-methyl-11-methylidene-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5-dien-15-one 162889431 Click to see CC(C)C1(CCC2=CC(CC(=C)C(CCC(C=C1)(C)O)O)OC2=O)O 350.40 unknown https://doi.org/10.1021/NP2002012
(4R,7R,10S,13S)-4,7,10-trihydroxy-7-methyl-11-methylidene-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5-dien-15-one 162889433 Click to see CC(C)C1(CCC2=CC(CC(=C)C(CCC(C=C1)(C)O)O)OC2=O)O 350.40 unknown https://doi.org/10.1021/NP2002012
(4R,7R,13S)-4,7-dihydroxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 163011599 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)(C(C)C)O)(C)O 334.40 unknown https://doi.org/10.1021/NP2002012
(4R,7R,13S)-7-methoxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 163190701 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)C(C)C)(C)OC 332.50 unknown https://doi.org/10.1021/NP2002012
(4R,7S,11R,13S)-4,7,11-trihydroxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,9-trien-15-one 163050939 Click to see CC(C)C1(CCC2=CC(CC(C=CCC(C=C1)(C)O)(C)O)OC2=O)O 350.40 unknown https://doi.org/10.1021/NP2002012
(4R,7S,13S)-4-hydroxy-7-methoxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 163051200 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)(C(C)C)O)(C)OC 348.50 unknown https://doi.org/10.1021/NP2002012
(4R,7S,13S)-4,7-dihydroxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 163011595 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)(C(C)C)O)(C)O 334.40 unknown https://doi.org/10.1021/NP2002012
(4R,7S,13S)-7-hydroxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 163189864 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)C(C)C)(C)O 318.40 unknown https://doi.org/10.1021/NP2002012
(4S,13S)-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,7,10-tetraen-15-one 162869670 Click to see CC1=CCC=C(C=CC(CCC2=CC(C1)OC2=O)C(C)C)C 300.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.05.014
(4S,5E,7R,10E,13S)-7-hydroxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 163189863 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)C(C)C)(C)O 318.40 unknown https://doi.org/10.1021/NP2002012
https://doi.org/10.1016/J.PHYTOCHEM.2010.05.014
(4S,5E,7S,10E,13S)-7-hydroxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 163188165 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)C(C)C)(C)O 318.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.05.014
(4S,5E,7S,10E,13S)-7-methoxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 163193793 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)C(C)C)(C)OC 332.50 unknown https://doi.org/10.1021/NP2002012
(4S,7R,11R,13S)-4,7,11-trihydroxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,9-trien-15-one 163188340 Click to see CC(C)C1(CCC2=CC(CC(C=CCC(C=C1)(C)O)(C)O)OC2=O)O 350.40 unknown https://doi.org/10.1021/NP2002012
(4S,7R,13S)-4-hydroxy-7-methoxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 163185929 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)(C(C)C)O)(C)OC 348.50 unknown https://doi.org/10.1021/NP2002012
(4S,7R,13S)-4,7-dihydroxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 163187583 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)(C(C)C)O)(C)O 334.40 unknown https://doi.org/10.1021/NP2002012
(4S,7R,13S)-7-hydroxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 162869662 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)C(C)C)(C)O 318.40 unknown https://doi.org/10.1021/NP2002012
https://doi.org/10.1016/J.PHYTOCHEM.2010.05.014
(4S,7S,10R,13S)-4,7,10-trihydroxy-7-methyl-11-methylidene-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5-dien-15-one 163185542 Click to see CC(C)C1(CCC2=CC(CC(=C)C(CCC(C=C1)(C)O)O)OC2=O)O 350.40 unknown https://doi.org/10.1021/NP2002012
(4S,7S,10S,13S)-4,7,10-trihydroxy-7-methyl-11-methylidene-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5-dien-15-one 163186787 Click to see CC(C)C1(CCC2=CC(CC(=C)C(CCC(C=C1)(C)O)O)OC2=O)O 350.40 unknown https://doi.org/10.1021/NP2002012
(4S,7S,13S)-4,7-dihydroxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 163187579 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)(C(C)C)O)(C)O 334.40 unknown https://doi.org/10.1021/NP2002012
(4S,7S,13S)-7-hydroxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 162869664 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)C(C)C)(C)O 318.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.05.014
(4S,7S,13S)-7-methoxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,10-trien-15-one 162973358 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)C(C)C)(C)OC 332.50 unknown https://doi.org/10.1021/NP2002012
(6E,8S,13S)-8-methoxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),4,6,10-tetraen-15-one 162943863 Click to see CC1=CCC(C(=CC=C(CCC2=CC(C1)OC2=O)C(C)C)C)OC 330.50 unknown https://doi.org/10.1021/NP2002012
(8R,13S)-8-methoxy-7,11-dimethyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),4,6,10-tetraen-15-one 163195263 Click to see CC1=CCC(C(=CC=C(CCC2=CC(C1)OC2=O)C(C)C)C)OC 330.50 unknown https://doi.org/10.1021/NP2002012
7,11-Dimethyl-4-prop-1-en-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),4,6,10-tetraen-15-one 76416383 Click to see CC1=CC=C(CCC2=CC(CC(=CCC1)C)OC2=O)C(=C)C 298.40 unknown https://doi.org/10.1021/NP2002012
rel-(+)-(1R,4S,10R)-4-hydroxycembra-2E,7E,11Z-trien-20,10-olide 46872827 Click to see CC1=CCCC(C=CC(CCC2=CC(C1)OC2=O)C(C)C)(C)O 318.40 unknown https://doi.org/10.1021/NP2002012
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(4aR,5'R,7R,8R,8aS)-5'-[(2R)-2-hydroxy-5-oxo-2H-furan-4-yl]-4,7-dimethylspiro[1,4a,5,6,7,8a-hexahydronaphthalene-8,3'-oxolane]-2,2'-dione 102588560 Click to see CC1CCC2C(C13CC(OC3=O)C4=CC(OC4=O)O)CC(=O)C=C2C 346.40 unknown https://doi.org/10.1021/NP2002012
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R,22R)-10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-ene-11,22-diol 44253988 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6O)C)C)C)C)(C)CO)O 472.70 unknown via CMAUP database
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R,22R)-10-(hydroxymethyl)-22-methoxy-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-11-ol 44253989 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6OC)C)C)C)C)(C)CO)O 486.70 unknown via CMAUP database
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R)-11-hydroxy-10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-22-one 102482971 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6=O)C)C)C)C)(C)CO)O 470.70 unknown via CMAUP database
(2R,4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bR)-10-hydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylic acid 21594159 Click to see CC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)(C)C(=O)O 472.70 unknown via CMAUP database
(2R,4aS,6aR,6aS,6bR,8aR,9S,12aR,14bR)-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-2-carboxylic acid 44253990 Click to see CC12CCC(CC1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)CO)C)(C)C(=O)O 470.70 unknown via CMAUP database
(3S,4S,4aR,6aR,6bS,8aR,9R,11R,12aS,14aR,14bR)-4,11-bis(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,9-diol 14335966 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC(CC5O)(C)CO)C)C)C)(C)CO)O 474.70 unknown via CMAUP database
24-Hydroxy-beta-amyrin 14167253 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C)C 442.70 unknown via CMAUP database
5-Glutinen-3-ol 12309493 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1021/NP2002012
alpha-Glutinol 12309496 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1021/NP2002012
Glutinol 9932254 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1021/NP2002012
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1021/NP2002012
https://doi.org/10.1016/J.PHYTOCHEM.2010.05.014
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.05.014
Melilotigenin B 91895471 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)C)C 454.70 unknown via CMAUP database
Melilotigenin C 10551785 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)C)C 456.70 unknown via CMAUP database
Soyasapogenol B 115012 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C 458.70 unknown via CMAUP database
Soyasapogenol E 13632872 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)O)C)C 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(8R,9S,10R,13R,14S,17R)-10,13,14-trimethyl-17-[(2R)-6-methylhept-3-en-2-yl]-2,6,7,8,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-one 162886821 Click to see CC(C)CC=CC(C)C1CCC2(C1(CCC3C2CCC4=CC(=O)CCC34C)C)C 396.60 unknown https://doi.org/10.1021/NP2002012
(8R,9S,10R,13R,14S,17R)-10,13,14-trimethyl-17-[(E,2R)-6-methylhept-3-en-2-yl]-2,6,7,8,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-one 163188595 Click to see CC(C)CC=CC(C)C1CCC2(C1(CCC3C2CCC4=CC(=O)CCC34C)C)C 396.60 unknown https://doi.org/10.1021/NP2002012
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-Ethylcholesta-4,22-dien-3-one 12611206 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 410.70 unknown https://doi.org/10.1021/NP2002012
> Organoheterocyclic compounds / Benzopyrans
Oxytropisoflavan B 46918734 Click to see COC1=C(C(=C(C=C1)C2CC3(CCC(=O)C=C3OC2)O)O)OC 320.30 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(4R,13R)-11-methyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,7,10-tetraen-15-one 162955521 Click to see CC1=CCC=CC=CC(CCC2=CC(C1)OC2=O)C(C)C 286.40 unknown https://doi.org/10.1021/NP2002012
(4R,5E,7E,10E,13R)-11-methyl-4-propan-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,7,10-tetraen-15-one 163188442 Click to see CC1=CCC=CC=CC(CCC2=CC(C1)OC2=O)C(C)C 286.40 unknown https://doi.org/10.1021/NP2002012
> Organoheterocyclic compounds / Indoles and derivatives / Benzoylindoles
(3-Hydroxyindol-1-yl)-(3-hydroxyphenyl)methanone 46850207 Click to see C1=CC=C2C(=C1)C(=CN2C(=O)C3=CC(=CC=C3)O)O 253.25 unknown via CMAUP database
(3-Hydroxyindol-1-yl)-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]methanone 46850206 Click to see CC(=CCC1=C(C=CC(=C1)C(=O)N2C=C(C3=CC=CC=C32)O)O)C 321.40 unknown via CMAUP database
(3-Hydroxyindol-1-yl)-phenylmethanone 46850030 Click to see C1=CC=C(C=C1)C(=O)N2C=C(C3=CC=CC=C32)O 237.25 unknown via CMAUP database
(4-Hydroxy-3-methoxyindol-1-yl)-(4-hydroxyphenyl)methanone 46850205 Click to see COC1=CN(C2=C1C(=CC=C2)O)C(=O)C3=CC=C(C=C3)O 283.28 unknown via CMAUP database
(4-Hydroxyphenyl)-(3-methoxyindol-1-yl)methanone 46850032 Click to see COC1=CN(C2=CC=CC=C21)C(=O)C3=CC=C(C=C3)O 267.28 unknown via CMAUP database
Oxytrofalcatin B 46850031 Click to see C1=CC=C2C(=C1)C(=CN2C(=O)C3=CC=C(C=C3)O)O 253.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone 688857 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown via CMAUP database
Liquiritigenin 114829 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown via CMAUP database
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> 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 via CMAUP database
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
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
3-[(2S,3R,4S,5R,6R)-4,5-Dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 10919701 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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 740.70 unknown via CMAUP database
3-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one 60200223 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)O)O)O)O)O 608.50 unknown via CMAUP database
3-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 10865825 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)COC6C(C(C(C(O6)C)O)OC7C(C(C(CO7)O)O)O)O)O)O)O)O)O 872.80 unknown via CMAUP database
3-[6-O-(3-O-beta-D-Xylopyranosyl-alpha-L-rhamnopyranosyl)-beta-D-galactopyranosyloxy]-4',5,7-trihydroxyflavone 21668680 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)OC6C(C(C(CO6)O)O)O)O 726.60 unknown via CMAUP database
Biorobin 15944778 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
Oxytroflavoside A 60200065 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)COC(=O)CC(C)(CC(=O)O)O)O)O)O)O)O 752.70 unknown via CMAUP database
Oxytroflavoside B 60200066 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)O)OC(=O)CC(C)(CC(=O)O)O)O)O)O 752.70 unknown via CMAUP database
Oxytroflavoside C 60200220 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)OC(=O)CC(C)(CC(=O)O)O)O)O)O)O 752.70 unknown via CMAUP database
Oxytroflavoside D 60200221 Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC)C4=CC=C(C=C4)O)O)O)O)O 606.50 unknown via CMAUP database
Oxytroflavoside E 60200222 Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC)C4=CC=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O 768.70 unknown via CMAUP database
Oxytroflavoside G 60200370 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 754.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 3-O-[alpha-L-rhamnopyranosyl(1->2)-beta-D-galactopyranosyl]-7-O-alpha-L-rhamnopyranoside 57397583 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)CO)O)O)O)O)O 740.70 unknown via CMAUP database
Robinin 5281693 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O 740.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-2-(4-hydroxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one 14157884 Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=C(C=C3)O 270.28 unknown via CMAUP database
(R,S)-7-Methoxy-2-phenyl-chroman-4-one 688883 Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=CC=C3 254.28 unknown via CMAUP database
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 via CMAUP database
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one 26088035 Click to see C1C(C(=O)C2=C(O1)C=C(C=C2)O)CC3=CC=C(C=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(6aR)-9,10-Dimethoxy-6aalpha,11aalpha-dihydro-6H-benzofuro[3,2-c][1]benzopyran-3,8-diol 46918735 Click to see COC1=C(C=C2C3COC4=C(C3OC2=C1OC)C=CC(=C4)O)O 316.30 unknown via CMAUP database
(l)-Edunol 182148 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=CC5=C(C=C34)OCO5)C 352.40 unknown via CMAUP database
Maackiain 91510 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein 5281708 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O 254.24 unknown via CMAUP database
Pseudobaptigenin 5281805 Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)O 282.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavanquinones
5-[(3R)-7-hydroxy-3,4-dihydro-2H-chromen-3-yl]-2,3-dimethoxycyclohexa-2,5-diene-1,4-dione 10403457 Click to see COC1=C(C(=O)C(=CC1=O)C2CC3=C(C=C(C=C3)O)OC2)OC 316.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Daidzein-4'-glucoside 49862229 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown via CMAUP database
Sophoricoside 5321398 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)OC4C(C(C(C(O4)CO)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-Methoxydaidzein 5319422 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(R)-Isomucronulatol 10380176 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O)OC 302.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
(3R)-2',3',7-trihydroxy-4'-methoxyisoflavan 15939757 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O)O 288.29 unknown via CMAUP database
2H-1-Benzopyran-7-ol, 3,4-dihydro-3-(3-hydroxy-2,4-dimethoxyphenyl)-, (3R)- 13873811 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)OC)O 302.32 unknown via CMAUP database
Calycosin 5280448 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2'-Hydroxybiochanin A 5282075 Click to see COC1=CC(=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O 300.26 unknown via CMAUP database
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Isoformononetin 3764 Click to see COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=C(C=C3)O 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',4'-Dihydroxydihydrochalcone 586491 Click to see C1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2)O)O 242.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2-Hydroxy-4-methoxyphenyl)-3-phenylprop-2-en-1-one 265720 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=CC=C2)O 254.28 unknown via CMAUP database
1-(2,4-Dihydroxyphenyl)-3-phenylprop-2-en-1-one 344530 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 240.25 unknown via CMAUP database
2-Propen-1-one, 1-(2-hydroxy-4-methoxyphenyl)-3-(4-hydroxyphenyl)- 592216 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O 270.28 unknown via CMAUP database
2',4'-Dihydroxychalcone 5376979 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 240.25 unknown via CMAUP database
Acrylophenone, 2',4'-dihydroxy-3-(p-methoxyphenyl)- 166795 Click to see COC1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 270.28 unknown via CMAUP database
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown via CMAUP database
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
2',4',4-Trihydroxy-3'-prenylchalcone 193568 Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C 324.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
1-(4-Hydroxy-2-methoxyphenyl)-3-phenylprop-2-en-1-one 71442332 Click to see COC1=C(C=CC(=C1)O)C(=O)C=CC2=CC=CC=C2 254.28 unknown via CMAUP database

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