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Cedrelopsis grevei

Cedrelopsis grevei - 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 UUID64401001b1498860132856
Scientific name Cedrelopsis grevei
Authority Baill. & Courchet
First published in Ann. Inst. Colon. Marseille , sér. 2, 4: 56 (1906)

Description Top

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Cedrelopsis grevei is a plant that is found in dry, subarid, and subhumid climates in the provinces of Toliara, Mahajanga, and Antsiranana in Madagascar. It can grow up to 2-9 meters in height and has a diameter of 0.2 to 1.5 meters. The leaves of this plant are 12-20 cm long and 6-8 cm wide. The stem bark and leaves of this plant are used to produce essential oil, which is used in traditional medicine to treat malaria, fever, and muscular fatigue. The wood of this plant is also used for construction purposes. It is considered to be of Least Concern in terms of conservation status. It is also known by the synonym Katafa crassisepalum Costantin & Poiss.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
French acajou blanc de madagascar
French katrafay
Malagasy katrafay

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000592509
UNII 66PD1T04O0
Tropicos 20400916
KEW urn:lsid:ipni.org:names:577813-1
The Plant List kew-2707298
PFAF Cedrelopsis grevei
Open Tree Of Life 582617
NCBI Taxonomy 864332
IUCN Red List 70102674
IPNI 577812-1
iNaturalist 485215
GBIF 3990259
Freebase /m/0j7jsjs
EOL 5226749
Wikipedia Cedrelopsis_grevei

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
Discovering Potential Compounds for Venous Disease Treatment through Virtual Screening and Network Pharmacology Approach Barrera-Vázquez OS, Escobar-Ramírez JL, Santiago-Mejía J, Carrasco-Ortega OF, Magos-Guerrero GA Molecules 05-Dec-2023
PMCID:PMC10745828
doi:10.3390/molecules28247937
PMID:38138427
In vitro and in silico prediction of antibacterial interaction between essential oils via graph embedding approach Yabuuchi H, Hayashi K, Shigemoto A, Fujiwara M, Nomura Y, Nakashima M, Ogusu T, Mori M, Tokumoto SI, Miyai K Sci Rep 02-Nov-2023
PMCID:PMC10622510
doi:10.1038/s41598-023-46377-5
PMID:37919469
Evaluation of Senna tora (L.) Roxb. leaves as source of bioactive molecules with antioxidant, anti-inflammatory and antibacterial potential Rahman MM, Al Noman MA, Khatun S, Alam R, Shetu MM, Talukder EK, Imon RR, Biswas MY, Anis-Ul-Haque KM, Uddin MJ, Akhter S Heliyon 19-Jan-2023
PMCID:PMC9898628
doi:10.1016/j.heliyon.2023.e12855
PMID:36747926
Active Compounds with Medicinal Potential Found in Maxillariinae Benth. (Orchidaceae Juss.) Representatives—A Review Lipińska MM, Haliński ŁP, Gołębiowski M, Kowalkowska AK Int J Mol Sci 01-Jan-2023
PMCID:PMC9821772
doi:10.3390/ijms24010739
PMID:36614181
Essential Oils against Sarcoptes scabiei Nardoni S, Mancianti F Molecules 19-Dec-2022
PMCID:PMC9788335
doi:10.3390/molecules27249067
PMID:36558200
Beyond the Bark: An Overview of the Chemistry and Biological Activities of Selected Bark Essential Oils Graf M, Stappen I Molecules 27-Oct-2022
PMCID:PMC9654741
doi:10.3390/molecules27217295
PMID:36364121
Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T Molecules 09-Sep-2022
PMCID:PMC9501561
doi:10.3390/molecules27185858
PMID:36144591
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
In vitro efficacy of essential oils against Sarcoptes scabiei Andriantsoanirina V, Guillot J, Ratsimbason M, Mekhloufi G, Randriamialinoro F, Ranarivelo L, Ariey F, Durand R Sci Rep 03-May-2022
PMCID:PMC9065015
doi:10.1038/s41598-022-11176-x
PMID:35504935
Hedycaryol – Central Intermediates in Sesquiterpene Biosynthesis, Part II Xu H, Dickschat JS Chemistry 21-Mar-2022
PMCID:PMC9310801
doi:10.1002/chem.202200405
PMID:35239190
Phytochemical Screening, In Vitro and In Silico Studies of Volatile Compounds from Petroselinum crispum (Mill) Leaves Grown in Saudi Arabia Foudah AI, Alqarni MH, Alam A, Salkini MA, Ross SA, Yusufoglu HS Molecules 29-Jan-2022
PMCID:PMC8840193
doi:10.3390/molecules27030934
PMID:35164196
Chemical investigation and screening of anti-cancer potential of Syzygium aromaticum L. bud (clove) essential oil nanoemulsion Abadi AV, Karimi E, Oskoueian E, Mohammad GR, Shafaei N 3 Biotech 27-Jan-2022
PMCID:PMC8795257
doi:10.1007/s13205-022-03117-2
PMID:35127304
Volatile Organic Compounds Emitted by Aspergillus flavus Strains Producing or Not Aflatoxin B1 Josselin L, De Clerck C, De Boevre M, Moretti A, Jijakli MH, Soyeurt H, Fauconnier ML Toxins (Basel) 06-Oct-2021
PMCID:PMC8539470
doi:10.3390/toxins13100705
PMID:34678998
Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F Malar J 25-Aug-2021
PMCID:PMC8390284
doi:10.1186/s12936-021-03866-0
PMID:34433465
Natural Products from Madagascar, Socio-Cultural Usage, and Potential Applications in Advanced Biomedicine: A Concise Review Mesa CL, Ranalison O, Randriantseheno LN, Risuleo G Molecules 27-Jul-2021
PMCID:PMC8348691
doi:10.3390/molecules26154507
PMID:34361660

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 / Phenol ethers / Anisoles
6-Chloro-7-hydroxy-9-methoxy-13-methyl-12,19-dioxatricyclo[14.2.1.05,10]nonadeca-5,7,9-triene-3,11-dione 163001476 Click to see CC1CCC2CCC(O2)CC(=O)CC3=C(C(=CC(=C3C(=O)O1)OC)O)Cl 382.80 unknown https://doi.org/10.1016/S0031-9422(02)00675-1
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,1aR,2aS,5R,6R,6aS,7aS)-1,6,6a-trimethyldecahydro-1,2a-methanocyclopropa[b]naphthalen-5-ol 91710043 Click to see CC1C(CCC23C1(CC4C(C2)C4(C3)C)C)O 220.35 unknown https://doi.org/10.1002/MRC.1577
https://doi.org/10.1002/MRC.1394
(1R,4R,5R,6S,8S,9R,10R)-5,6,9-trimethyltetracyclo[7.2.1.01,6.08,10]dodecan-4-ol 162907936 Click to see CC1C(CCC23C1(CC4C(C2)C4(C3)C)C)O 220.35 unknown https://doi.org/10.1002/MRC.1394
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
(3R,5aR,9S,9aS)-2,2,5a,9-Tetramethyloctahydro-2H-3,9a-methanobenzo[b]oxepine 521889 Click to see CC1CCCC2(C13CC(CC2)C(O3)(C)C)C 222.37 unknown https://doi.org/10.1002/MRC.1394
Dihydroagarofuran. cis- 90478975 Click to see CC1CCCC2(C13CC(CC2)C(O3)(C)C)C 222.37 unknown https://doi.org/10.1002/MRC.1394
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
[(1R,2S,3S,4S,6R,7S,9R,14R,16R,17R)-3-hydroxy-4-methoxy-2,6,14,17-tetramethyl-11-oxo-14-[(5-oxo-2H-furan-3-yl)methyl]-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-12-en-16-yl] acetate 21576502 Click to see CC1CC(C(C2(C1CC3C4(C2C(CC(C4=CC(=O)O3)(C)CC5=CC(=O)OC5)OC(=O)C)C)C)O)OC 502.60 unknown https://doi.org/10.1016/S0031-9422(03)00342-X
[3-hydroxy-4-methoxy-2,6,14,17-tetramethyl-11-oxo-14-[(5-oxo-2H-furan-3-yl)methyl]-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-12-en-16-yl] acetate 73802633 Click to see CC1CC(C(C2(C1CC3C4(C2C(CC(C4=CC(=O)O3)(C)CC5=CC(=O)OC5)OC(=O)C)C)C)O)OC 502.60 unknown https://doi.org/10.1016/S0031-9422(03)00342-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aS,6aR,6aR,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,14a-tetradecahydropicen-3-ol 154497735 Click to see CC1(CCC2(CCC3(C(C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(03)00342-X
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0040-4020(99)00653-5
https://doi.org/10.1016/S0031-9422(03)00342-X
https://doi.org/10.1016/S0031-9422(02)00440-5
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(02)00440-5
https://doi.org/10.1016/S0031-9422(03)00342-X
https://doi.org/10.1016/S0040-4020(99)00653-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.1016/S0031-9422(03)00342-X
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 https://doi.org/10.1016/S0031-9422(03)00342-X
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
[(1S,2S,4R,5Z,9S,10S)-2-hydroxy-2,6,9-trimethyl-9-(4-methylpent-3-enyl)-4-bicyclo[8.1.0]undec-5-enyl] acetate 162852609 Click to see CC1=CC(CC(C2CC2C(CC1)(C)CCC=C(C)C)(C)O)OC(=O)C 348.50 unknown https://doi.org/10.1016/S0031-9422(02)00675-1
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans / Precocenes
1-(5-Hydroxy-7-methoxy-2,2-dimethylchromen-8-yl)-3-phenylprop-2-en-1-one 73088815 Click to see CC1(C=CC2=C(O1)C(=C(C=C2O)OC)C(=O)C=CC3=CC=CC=C3)C 336.40 unknown https://doi.org/10.1016/S0031-9422(02)00675-1
Cedreprenone 11759486 Click to see CC1(C=CC2=C(O1)C(=C(C=C2O)OC)C(=O)C=CC3=CC=CC=C3)C 336.40 unknown https://doi.org/10.1016/S0031-9422(02)00675-1
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxy-2-methyl-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one 12310443 Click to see CC1=CC(=O)C2=C(C=C(C(=C2O1)CC=C(C)C)O)O 260.28 unknown https://doi.org/10.1016/S0031-9422(03)00342-X
https://doi.org/10.1016/S0031-9422(00)97377-1
Peucenin 68477 Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)CC=C(C)C)O 260.28 unknown https://doi.org/10.1016/S0031-9422(03)00342-X
https://doi.org/10.1016/S0031-9422(00)97377-1
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
(9R,10S)-9,10-dihydroxy-5-methoxy-2,8,8-trimethyl-9,10-dihydropyrano[2,3-h]chromen-4-one 163031662 Click to see CC1=CC(=O)C2=C(C=C3C(=C2O1)C(C(C(O3)(C)C)O)O)OC 306.31 unknown https://doi.org/10.1016/S0031-9422(03)00342-X
(9S,10R)-9,10-dihydroxy-5-methoxy-2,8,8-trimethyl-9,10-dihydropyrano[2,3-h]chromen-4-one 163031663 Click to see CC1=CC(=O)C2=C(C=C3C(=C2O1)C(C(C(O3)(C)C)O)O)OC 306.31 unknown https://doi.org/10.1016/S0031-9422(00)97377-1
5-Methoxy-2,8,8-trimethyl-9,10-dihydropyrano[2,3-h]chromen-4-one 13147261 Click to see CC1=CC(=O)C2=C(C=C3C(=C2O1)CCC(O3)(C)C)OC 274.31 unknown https://doi.org/10.1016/S0031-9422(00)97377-1
9,10-Dihydroxy-5-methoxy-2,8,8-trimethyl-9,10-dihydropyrano[2,3-h]chromen-4-one 163031661 Click to see CC1=CC(=O)C2=C(C=C3C(=C2O1)C(C(C(O3)(C)C)O)O)OC 306.31 unknown https://doi.org/10.1016/S0031-9422(00)97377-1
Alloptaeroxylin 12305984 Click to see CC1=CC(=O)C2=C(O1)C3=C(C=C2O)OC(C=C3)(C)C 258.27 unknown https://doi.org/10.1016/S0031-9422(03)00342-X
https://doi.org/10.1016/S0031-9422(00)97377-1
Greveichromenol 71450427 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)CO)C 274.27 unknown https://doi.org/10.1016/S0031-9422(00)97377-1
https://doi.org/10.1016/S0031-9422(03)00342-X
Perforatin A 441968 Click to see CC1=CC(=O)C2=C(C=C3C(=C2O1)C=CC(O3)(C)C)OC 272.29 unknown https://doi.org/10.1016/S0031-9422(00)97377-1
> Organoheterocyclic compounds / Benzoxepines
(8S)-5,8-dihydroxy-8-(hydroxymethyl)-2-methyl-9H-pyrano[3,2-h][1]benzoxepin-4-one 163040968 Click to see CC1=CC(=O)C2=C(C3=C(C=C2O1)OCC(C=C3)(CO)O)O 290.27 unknown https://doi.org/10.1016/S0031-9422(00)97377-1
5-Hydroxy-8-(hydroxymethyl)-2-methyl-6,9-dihydropyrano[3,2-h][1]benzoxepin-4-one 12314734 Click to see CC1=CC(=O)C2=C(C3=C(C=C2O1)OCC(=CC3)CO)O 274.27 unknown https://doi.org/10.1016/S0031-9422(02)00440-5
Ptaeroglycol 441981 Click to see CC1=CC(=O)C2=C(C3=C(C=C2O1)OCC(C=C3)(CO)O)O 290.27 unknown https://doi.org/10.1016/S0031-9422(02)00440-5
https://doi.org/10.1016/S0031-9422(00)97377-1
Ptaeroxylin 3646533 Click to see CC1=CCC2=C(C=C3C(=C2O)C(=O)C=C(O3)C)OC1 258.27 unknown https://doi.org/10.1016/S0031-9422(03)00342-X
> Organoheterocyclic compounds / Oxepanes
(1R,5R,11R,12S,15R,16S)-16-[(2S)-2-hydroxy-5-oxo-2H-furan-3-yl]-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.01,12.05,11]octadec-9-ene-3,8,18-trione 162909957 Click to see CC1(C2CC(=O)CC34C(C2(C=CC(=O)O1)C)CCC(C3=O)(C(O4)C5=CC(=O)OC5O)C)C 444.50 unknown https://doi.org/10.1016/S0031-9422(03)00342-X
(1R,5R,11S,12R,15R,16R)-16-(furan-3-yl)-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.01,12.05,11]octadec-9-ene-3,8,18-trione 101036586 Click to see CC1(C2CC(=O)CC34C(C2(C=CC(=O)O1)C)CCC(C3=O)(C(O4)C5=COC=C5)C)C 412.50 unknown https://doi.org/10.1016/S0040-4020(99)00653-5
https://doi.org/10.1016/S0031-9422(03)00342-X
(1R,5R,11S,12R,15R,16R)-16-[(2S)-2-hydroxy-5-oxo-2H-furan-3-yl]-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.01,12.05,11]octadec-9-ene-3,8,18-trione 21576501 Click to see CC1(C2CC(=O)CC34C(C2(C=CC(=O)O1)C)CCC(C3=O)(C(O4)C5=CC(=O)OC5O)C)C 444.50 unknown https://doi.org/10.1016/S0031-9422(03)00342-X
(1S,5R,11S,12R,15S,16S)-16-(furan-3-yl)-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.01,12.05,11]octadec-9-ene-3,8,18-trione 162907434 Click to see CC1(C2CC(=O)CC34C(C2(C=CC(=O)O1)C)CCC(C3=O)(C(O4)C5=COC=C5)C)C 412.50 unknown https://doi.org/10.1016/S0031-9422(03)00342-X
16-(2-hydroxy-5-oxo-2H-furan-3-yl)-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.01,12.05,11]octadec-9-ene-3,8,18-trione 73802632 Click to see CC1(C2CC(=O)CC34C(C2(C=CC(=O)O1)C)CCC(C3=O)(C(O4)C5=CC(=O)OC5O)C)C 444.50 unknown https://doi.org/10.1016/S0031-9422(03)00342-X
16-(Furan-3-yl)-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.01,12.05,11]octadec-9-ene-3,8,18-trione 162907433 Click to see CC1(C2CC(=O)CC34C(C2(C=CC(=O)O1)C)CCC(C3=O)(C(O4)C5=COC=C5)C)C 412.50 unknown https://doi.org/10.1016/S0040-4020(99)00653-5
https://doi.org/10.1016/S0031-9422(03)00342-X
> Phenylpropanoids and polyketides / Coumarins and derivatives
2H-1-Benzopyran-2-one, 6,7-dimethoxy-8-(3-methyl-2-butenyl)- 155937 Click to see CC(=CCC1=C2C(=CC(=C1OC)OC)C=CC(=O)O2)C 274.31 unknown https://doi.org/10.1016/S0031-9422(02)00440-5
https://doi.org/10.1055/S-2003-37717
6,7-dimethoxy-5-(3-methylbut-2-en-1-yl)-2H-chromen-2-one 642899 Click to see CC(=CCC1=C2C=CC(=O)OC2=CC(=C1OC)OC)C 274.31 unknown https://doi.org/10.1016/S0367-326X(03)00181-3
https://doi.org/10.1016/S0031-9422(02)00440-5
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1016/S0031-9422(03)00342-X
https://doi.org/10.1055/S-2003-37717
https://doi.org/10.1016/S0367-326X(03)00181-3
https://doi.org/10.1016/S0031-9422(02)00440-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
2H-1-Benzopyran-2-one, 6-hydroxy-7-methoxy-5-(3-methyl-2-butenyl)- 12144100 Click to see CC(=CCC1=C2C=CC(=O)OC2=CC(=C1O)OC)C 260.28 unknown https://doi.org/10.1016/S0367-326X(03)00181-3
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1016/S0367-326X(03)00181-3
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Cedrelopsin 12302592 Click to see CC(=CCC1=C2C(=CC(=C1O)OC)C=CC(=O)O2)C 260.28 unknown https://doi.org/10.1016/S0031-9422(02)00440-5
https://doi.org/10.1016/S0367-326X(03)00181-3
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
6-Methoxy-8,8-dimethyl-9,10-dihydropyrano[2,3-h]chromen-2-one 90655369 Click to see CC1(CCC2=C3C(=CC(=C2O1)OC)C=CC(=O)O3)C 260.28 unknown https://doi.org/10.1016/S0367-326X(03)00181-3
Braylin 618370 Click to see CC1(C=CC2=C3C(=CC(=C2O1)OC)C=CC(=O)O3)C 258.27 unknown https://doi.org/10.1055/S-2003-37717
Cedrecoumarin A 10263845 Click to see CC1(C=CC2=C(O1)C(=CC3=C2C=CC(=O)O3)O)C 244.24 unknown https://doi.org/10.1016/S0031-9422(03)00342-X
https://doi.org/10.1016/S0031-9422(02)00440-5
https://doi.org/10.1055/S-2003-37717
Norbraylin 10105863 Click to see CC1(C=CC2=C3C(=CC(=C2O1)O)C=CC(=O)O3)C 244.24 unknown https://doi.org/10.1016/S0031-9422(02)00440-5
https://doi.org/10.1055/S-2003-37717
> Phenylpropanoids and polyketides / Coumarins and derivatives / p-Dioxolo[2,3-g]coumarins
(2S)-5-methoxy-2-prop-1-en-2-yl-2,3-dihydropyrano[2,3-g][1,4]benzodioxin-7-one 129360519 Click to see CC(=C)C1COC2=C(O1)C=C3C=CC(=O)OC3=C2OC 274.27 unknown https://doi.org/10.1016/S0367-326X(03)00181-3
2-Prop-1-en-2-yl-2,3-dihydropyrano[2,3-g][1,4]benzodioxin-7-one 5018929 Click to see CC(=C)C1COC2=C(O1)C=C3C=CC(=O)OC3=C2 244.24 unknown https://doi.org/10.1016/S0367-326X(03)00181-3
8-Methoxyobliquin 131676095 Click to see CC(=C)C1COC2=C(O1)C=C3C=CC(=O)OC3=C2OC 274.27 unknown https://doi.org/10.1016/S0367-326X(03)00181-3
Obliquin 6708593 Click to see CC(=C)C1COC2=C(O1)C=C3C=CC(=O)OC3=C2 244.24 unknown https://doi.org/10.1016/S0367-326X(03)00181-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one 689011 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown https://doi.org/10.1016/S0031-9422(02)00675-1
5,7-Dimethoxyflavanone 378567 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown https://doi.org/10.1016/S0031-9422(02)00675-1
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Uvangoletin 6483649 Click to see COC1=CC(=CC(=C1C(=O)CCC2=CC=CC=C2)O)O 272.29 unknown https://doi.org/10.1016/S0031-9422(02)00675-1
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-[(3R)-3,5-dihydroxy-7-methoxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]-3-phenylprop-2-en-1-one 162963488 Click to see CC1(C(CC2=C(C(=C(C=C2O1)OC)C(=O)C=CC3=CC=CC=C3)O)O)C 354.40 unknown https://doi.org/10.1016/S0031-9422(02)00675-1
(E)-1-[(3S)-3,5-dihydroxy-7-methoxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]-3-phenylprop-2-en-1-one 162963489 Click to see CC1(C(CC2=C(C(=C(C=C2O1)OC)C(=O)C=CC3=CC=CC=C3)O)O)C 354.40 unknown https://doi.org/10.1016/S0031-9422(02)00675-1
1-(2,4-Dihydroxy-6-methoxyphenyl)-3-phenylprop-2-en-1-one 154102 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown https://doi.org/10.1016/S0031-9422(02)00675-1
1-(3,5-Dihydroxy-7-methoxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-3-phenylprop-2-en-1-one 74819235 Click to see CC1(C(CC2=C(C(=C(C=C2O1)OC)C(=O)C=CC3=CC=CC=C3)O)O)C 354.40 unknown https://doi.org/10.1016/S0031-9422(02)00675-1
6'-Hydroxy-2',4'-dimethoxychalcone 242589 Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=CC=C2)O 284.31 unknown https://doi.org/10.1016/S0031-9422(02)00675-1
Cardamonin 641785 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown https://doi.org/10.1016/S0031-9422(02)00675-1
Flavokawain B 5356121 Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=CC=C2)O 284.31 unknown https://doi.org/10.1016/S0031-9422(02)00675-1
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
(E)-1-[(2R)-4,6-dihydroxy-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-7-yl]-3-phenylprop-2-en-1-one 163057968 Click to see CC(=CCC1=C(C(=C2C(=C1O)CC(O2)C(C)(C)O)C(=O)C=CC3=CC=CC=C3)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(02)00675-1
(E)-1-[(2S)-4,6-dihydroxy-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-7-yl]-3-phenylprop-2-en-1-one 637297 Click to see CC(=CCC1=C(C(=C2C(=C1O)CC(O2)C(C)(C)O)C(=O)C=CC3=CC=CC=C3)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(02)00675-1
1-[4,6-Dihydroxy-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-7-yl]-3-phenylprop-2-en-1-one 20979925 Click to see CC(=CCC1=C(C(=C2C(=C1O)CC(O2)C(C)(C)O)C(=O)C=CC3=CC=CC=C3)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(02)00675-1

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