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Clausena anisata

Clausena anisata - 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 UUID6440119d67f7a470258311
Scientific name Clausena anisata
Authority (Willd.) Hook.f.
First published in Niger Fl. : 256 (1849)

Description Top

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Synonyms Top

Scientific name Authority First published in
Myaris inaequalis C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 470 (1845)
Amyris anisata Willd. Sp. Pl., ed. 4 , 2: 337 (1799)
Amyris dentata Willd. Sp. Pl., ed. 4 , 2: 337 (1799)
Amyris inaequalis Spreng. Syst. Veg. 2: 218 (1825)
Amyris nana Roxb. Fl. Ind. ed. 1832 , 2: 249 (1832)
Amyris suffruticosa Roxb. Fl. Ind. 2: 250 (1824)
Clausena abyssinica Engl. Veg. Erde 9(III 1): 757 (1915)
Clausena anisata var. mollis Engl. Pflanzenw. Ost-Afrikas C: 228 1895
Clausena anisata var. multijuga Welw. ex Hiern Cat. Afr. Pl. 1: 116 1896
Clausena anisata var. paucijuga (Kurz) Molino Bull. Mus. Natl. Hist. Nat., B, Adansonia 16: 132 (1994)
Clausena bergeyckiana De Wild. & T.Durand Bull. Herb. Boissier , sér. 2, 1: 743 (1901)
Clausena dentata (Willd.) M.Roem. Fam. Nat. Syn. Monogr. 1: 44 (1846)
Clausena dentata var. dunniana (H.Lév.) Swingle J. Wash. Acad. Sci. 30: 82 1940
Clausena dentata var. nana (Roxb.) N.P.Balakr. Bull. Bot. Surv. India 22: 173 (1980 publ. 1982)
Clausena dentata var. pubescens (Wight & Arn.) N.P.Balakr. Bull. Bot. Surv. India 22: 173 (1980 publ. 1982)
Clausena dentata var. robusta Yu.Tanaka J. Bot. 68: 228 1930
Clausena dunniana H.Lév. Repert. Spec. Nov. Regni Veg. 11: 67 (1912)
Clausena dunniana var. robusta (Tan.) C.C.Huang Acta Phytotax. Sin. 16(2): 85 (1978)
Clausena inaequalis (DC.) Benth. Niger Fl. : 257 (1849)
Clausena longipes Craib Bull. Misc. Inform. Kew 1926: 340 (1926)
Clausena nana Wight & Arn. Prodr. Fl. Ind. Orient. : 96 (1834)
Clausena odorata C.C.Huang Acta Phytotax. Sin. 8: 92 (1959)
Clausena pobeguinii Pobég. Essai Fl. Guinée Franç. : 318 (1906)
Clausena pubescens Wight & Arn. Prodr. Fl. Ind. Orient. : 96 (1834)
Clausena suffruticosa (Roxb.) Wight & Arn. Prodr. Fl. Ind. Orient. : 96 (1834)
Clausena vestita D.D.Tao Acta Bot. Yunnan. 6: 73 (1984)
Clausena wightii M.Roem. Fam. Nat. Syn. Monogr. 1: 44 (1846)
Clausena willdenowii Wight & Arn. Prodr. Fl. Ind. Orient. 1: 96. 1834 [10 Oct 1834]
Cookia dulcis Bedd. Madras J. Lit. Sci. , n.s., 22: 73 (1861)
Elaphrium inaequale DC. Prodr. [A. P. de Candolle] 1: 724. 1824 [mid Jan 1824]
Fagarastrum anisatum G.Don Gen. Hist. 2: 87 (1832)
Fagarastrum inaequale G.Don Gen. Hist. 2: 87 (1832)
Icica dentata DC. Prodr. 2: 78 (1825)
Clausena suffruticosa var. paucijuga Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 44(3): 133 1875
Clausena inaequalis var. abyssinica Engl.
Zanthoxylum engleri P.G.Waterman Taxon 23: 365 (1975)

Common names Top

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Language Common/alternative name
Afrikaans perdepis
Amharic ልምጭ
Malayalam സുഗന്ധവേപ്പ്
Chinese 香黄皮

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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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

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Database ID/link to page
World Flora Online wfo-0000608620
Tropicos 28101180
KEW urn:lsid:ipni.org:names:772111-1
The Plant List kew-2724765
Open Tree Of Life 907390
NCBI Taxonomy 159034
IUCN Red List 146453629
IPNI 772112-1
iNaturalist 342748
GBIF 6434280
Freebase /m/0100ds5f
EPPO CUSAN
EOL 47126209
USDA GRIN 10807
Wikipedia Clausena_anisata
CMAUP NPO18135
CMAUP NPO23120
CMAUP NPO28622
CMAUP NPO29109

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
Traditional lore on the healing effects of therapeutic plants used by the local communities around Simien Mountains National Park, northwestern Ethiopia Seraw E, Melkamu Y, Masresha G J Ethnobiol Ethnomed 17-Apr-2024
PMCID:PMC11025143
doi:10.1186/s13002-024-00678-9
PMID:38632559
Phytochemical screening and insecticidal activities of some medicinal plants against the maize weevil, Sitophilus zeamais (Motschulsky) (Coleoptera: Curculionidae) Gindaba A, Negeri M, Abdisa B, Nemo R, Kitila C Sci Rep 15-Apr-2024
PMCID:PMC11018737
doi:10.1038/s41598-024-59207-z
PMID:38622206
Wetland vegetation composition and ecology of Lake Abaya in southern Ethiopia Gojamme DU PLoS One 10-Apr-2024
PMCID:PMC11006174
doi:10.1371/journal.pone.0301795
PMID:38598506
Oral hygiene practices and associated factors among rural communities in northwest Ethiopia Gizaw Z, Demissie NG, Gebrehiwot M, Bitew BD, Nigusie A BMC Oral Health 09-Mar-2024
PMCID:PMC10924987
doi:10.1186/s12903-024-04049-4
PMID:38461252
Development and Assessment of SNP Genotyping Arrays for Citrus and Its Close Relatives Hiraoka Y, Ferrante SP, Wu GA, Federici CT, Roose ML Plants (Basel) 29-Feb-2024
PMCID:PMC10935022
doi:10.3390/plants13050691
PMID:38475537
Ethnobotanical study of traditional medicinal plants used by the local Gamo people in Boreda Abaya District, Gamo Zone, southern Ethiopia Zemede J, Mekuria T, Ochieng CO, Onjalalaina GE, Hu GW J Ethnobiol Ethnomed 28-Feb-2024
PMCID:PMC10900619
doi:10.1186/s13002-024-00666-z
PMID:38419092
Evaluation of packaging, labels, and some physicochemical properties of herbal antimalarial products on the Ghanaian market Amekyeh H, Kumadoh D, Adongo DW, Orman E, Abubakar S, Dwamena A, Aggrey MO Heliyon 28-Feb-2024
PMCID:PMC10920373
doi:10.1016/j.heliyon.2024.e27032
PMID:38463810
Exploring the benefits of wild plants in dietary nutrition: investigating perspectives, choices, health impacts and sustainable practices Anwar T, Qureshi H, Shahzadi S, Siddiqi EH, Ali HM, Abdelhamid MM, Nazim M BMC Complement Med Ther 14-Feb-2024
PMCID:PMC10865668
doi:10.1186/s12906-024-04379-4
PMID:38355544
Next Generation Sequencing, and Development of a Pipeline as a Tool for the Detection and Discovery of Citrus Pathogens to Facilitate Safer Germplasm Exchange Keremane M, Singh K, Ramadugu C, Krueger RR, Skaggs TH Plants (Basel) 30-Jan-2024
PMCID:PMC10856814
doi:10.3390/plants13030411
PMID:38337944
Ethnobotanical and ethnopharmacological survey of medicinal tree species used in the treatment of diseases by forest-fringe communities of Southwestern Ghana Asigbaase M, Adusu D, Musah AA, Anaba L, Nsor CA, Abugre S, Derkyi M Heliyon 14-Dec-2023
PMCID:PMC10788458
doi:10.1016/j.heliyon.2023.e23645
PMID:38226220
The vegetation of Holocene coastal dunes of the Cape south coast, South Africa Cowling RM, Cawthra H, Privett S, Grobler BA PeerJ 12-Dec-2023
PMCID:PMC10722985
doi:10.7717/peerj.16427
PMID:38107568
Management strategies and floristic diversity in agroforestry practices of northwestern Ethiopia Tebkew M, Asfaw Z, Worku A Heliyon 21-Oct-2023
PMCID:PMC10632684
doi:10.1016/j.heliyon.2023.e20963
PMID:37954387
Potential of medicinal plants as antimalarial agents: a review of work done at Kenya Medical Research Institute Irungu B, Okari E, Nyangi M, Njeru S, Koech L Front Pharmacol 20-Oct-2023
PMCID:PMC10623325
doi:10.3389/fphar.2023.1268924
PMID:37927601
Ethnobotanical Study of Medicinal Plants Used against Human Diseases in Zuway Dugda District, Ethiopia Megersa M, Nedi T, Belachew S Evid Based Complement Alternat Med 18-Oct-2023
PMCID:PMC10599937
doi:10.1155/2023/5545294
PMID:37886427
Sabinene: A New Green Solvent Used in the Synthesis of Thiazolo[5,4-b]pyridines by Thermal or Microwave Activation Messire G, Ferreira V, Caillet E, Bodin L, Auville A, Berteina-Raboin S Molecules 03-Oct-2023
PMCID:PMC10574264
doi:10.3390/molecules28196924
PMID:37836766

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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(+)-epi-Vittatine 12304132 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown via CMAUP database
(1R,13R,15S,18R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 40469675 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
(1S,11S,13S,15R,18R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 101297739 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown via CMAUP database
(1S,13R,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 42579248 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
[(1S,13R,15R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-yl] acetate 101935954 Click to see CC(=O)OC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 313.30 unknown via CMAUP database
3-O-Acetylhamayne 443671 Click to see CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 329.30 unknown via CMAUP database
Crinamidine 399204 Click to see COC1=C2CN3CCC4(C3CC(C5C4O5)O)C2=CC6=C1OCO6 317.34 unknown via CMAUP database
Crinamin 73620 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
O-Demethylhaemanthamine 44445844 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown via CMAUP database
Vittatine 443693 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Lycorine 72378 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
(1S,11S,13R,16S,18R)-11-ethoxy-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraene 15483834 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4N(CC5O1)C)OC)OCO3 359.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
4-Propoxybenzoic acid 138500 Click to see CCCOC1=CC=C(C=C1)C(=O)O 180.20 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
p-Anisic acid 7478 Click to see COC1=CC=C(C=C1)C(=O)O 152.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
p-Anisaldehyde 31244 Click to see COC1=CC=C(C=C1)C=O 136.15 unknown https://doi.org/10.1016/0031-9422(89)80056-1
> Benzenoids / Phenol ethers
4-[(3-Methylbut-2-en-1-yl)oxy]benzaldehyde 10921323 Click to see CC(=CCOC1=CC=C(C=C1)C=O)C 190.24 unknown https://doi.org/10.1080/10412905.2000.9712209
Dictagymnin 85845705 Click to see CC(=CCOC1=CC=C(C=C1)CC=C)C 202.29 unknown https://doi.org/10.1080/10412905.2000.9712209
> Benzenoids / Phenol ethers / Anisoles
Anethole 637563 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown https://doi.org/10.1016/0031-9422(89)80056-1
Anethole, (Z)- 1549040 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown via CMAUP database
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 148.20 unknown https://doi.org/10.1021/NP50053A046
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2R,4aS,10aR)-7-isopropyl-1,1,4a-trimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-2,6-diol 10913694 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)C)O)C)O 302.50 unknown via CMAUP database
(2S,4aS,10aR)-1,1,4a-trimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-2,7-diol 53494908 Click to see CC1(C2CCC3=C(C2(CCC1O)C)C=CC(=C3)O)C 260.40 unknown via CMAUP database
(2S,4aS,10aR)-1,1,4a-trimethyl-6-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,7-diol 102194918 Click to see CC(C)C1=C(C=C2CCC3C(C(CCC3(C2=C1)C)O)(C)C)O 302.50 unknown via CMAUP database
(2S,4aS,10aR)-7-(2-hydroxypropan-2-yl)-1,1,4a-trimethyl-2,3,4,9,10,10a-hexahydrophenanthren-2-ol 53496760 Click to see CC1(C2CCC3=C(C2(CCC1O)C)C=CC(=C3)C(C)(C)O)C 302.50 unknown via CMAUP database
(4aR,7R,10aS)-1,3,4,5,6,7,8,9,10,10a-Decahydro-7-hydroxy-1,1-dimethyl-7-(1-methylethyl)-4a(2H)-phenanthrenecarboxylic acid 101787485 Click to see CC(C)C1(CCC2=C(C1)CCC3C2(CCCC3(C)C)C(=O)O)O 320.50 unknown via CMAUP database
(4aR)-6,10-dihydroxy-7-(2-hydroxypropan-2-yl)-1,1,4a-trimethyl-3,4-dihydro-2H-phenanthren-9-one 15480773 Click to see CC1(CCCC2(C1=C(C(=O)C3=CC(=C(C=C32)O)C(C)(C)O)O)C)C 330.40 unknown via CMAUP database
(4bS,8S,8aR)-8-(hydroxymethyl)-4b,8-dimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-1-ol 102194912 Click to see CC(C)C1=C(C2=C(C=C1)C3(CCCC(C3CC2)(C)CO)C)O 302.50 unknown via CMAUP database
1-[(4aS,9S)-5,6-dihydroxy-7-(1-methoxy-1-methyl-ethyl)-1,1,4a-trimethyl-2,3,4,9-tetrahydrophenanthren-9-yl]propan-2-one 53494907 Click to see CC(=O)CC1C=C2C(CCCC2(C3=C(C(=C(C=C13)C(C)(C)OC)O)O)C)(C)C 386.50 unknown via CMAUP database
15hia Hydroxyhai 20-deoxocarnosol 102194917 Click to see CC1(CCCC23C1CC(C4=CC(=C(C(=C42)O)O)C(C)(C)O)OC3)C 332.40 unknown via CMAUP database
3beta-Acetoxyabieta-8,11,13-triene-12-ol 21668708 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)C)OC(=O)C)C)O 344.50 unknown via CMAUP database
Graciliflorin F 102194915 Click to see CC(=O)OC1CCC2(C3=CC(=C(C=C3C(=O)C(=C2C1(C)C)O)C(C)(C)O)O)C 388.50 unknown via CMAUP database
Isolophanthin B 53496761 Click to see CC1(C2CCC3=C(C2(CCC1O)C)C=CC(=C3)C(C)(C)OC)C 316.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1016/0031-9422(75)85267-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
Dunniana acid B 11067173 Click to see CC1CCC2(C(C1(C)CCC(C)CC(=O)O)CC(=C2C)C=O)C 320.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/0031-9422(75)85267-8
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/0031-9422(75)85267-8
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Acetyl aleuritolic acid 161616 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
6-(3,7-Dimethylocta-2,6-dienyl)-7-hydroxychromen-2-one 5357655 Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)C)C 298.40 unknown via CMAUP database
7-[(2E,5S)-5-hydroxy-3,7-dimethylocta-2,6-dienoxy]chromen-2-one 25763649 Click to see CC(=CC(CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)O)C 314.40 unknown https://doi.org/10.1021/NP50062A003
Anisocoumarin H 14376449 Click to see CC(=CC(CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)O)C 314.40 unknown https://doi.org/10.1021/NP50062A003
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
Limonin 179651 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown https://doi.org/10.1021/NP50064A027
Zapoterin 441812 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)C(CC4(C35C(O5)C(=O)OC4C6=COC=C6)C)O)C)C 470.50 unknown https://doi.org/10.1021/NP50064A027
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,5R,8S,10S,13R,14S,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-4,5,5,6-tetramethylhept-6-en-2-yl]-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 101316920 Click to see CC(CC(C)C(C)(C)C(=C)C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(95)00047-B
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
Clausenolide 5458600 Click to see CC1(C2CC(=O)C3(C(C2(C(O1)(C)O)C)C(CC4(C35C(O5)C(=O)OC4C6=COC=C6)C)O)C)C 460.50 unknown https://doi.org/10.1021/NP50064A027
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 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
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasterol glucoside 6602508 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
6-(4-Hydroxyphenyl)-1,3-benzodioxole-5-carbaldehyde 15549895 Click to see C1OC2=C(O1)C=C(C(=C2)C=O)C3=CC=C(C=C3)O 242.23 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
Leptorumol 56683359 Click to see CC1=C(C(=C2C(=C1O)C(=O)C=CO2)C)O 206.19 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
N-Desmethyl-8alpha-ethoxypretazettine 15483835 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4NCC5O1)OC)OCO3 345.40 unknown via CMAUP database
N-Desmethyl-8beta-ethoxypretazettine 15483836 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4NCC5O1)OC)OCO3 345.40 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(1R)-1-[(2S)-3,3-dimethyloxiran-2-yl]-5-methoxy-1,6-dihydrofuro[3,4-c]carbazol-3-one 162900793 Click to see CC1(C(O1)C2C3=C4C5=CC=CC=C5NC4=C(C=C3C(=O)O2)OC)C 323.30 unknown https://doi.org/10.1021/NP800735M
(1R)-5-methoxy-1-(2-methylprop-1-enyl)-1,6-dihydrofuro[3,4-c]carbazol-3-one 163004987 Click to see CC(=CC1C2=C3C4=CC=CC=C4NC3=C(C=C2C(=O)O1)OC)C 307.30 unknown https://doi.org/10.1021/NP800735M
(2R)-2-(2-hydroxypropan-2-yl)-6-methoxy-2,7-dihydro-1H-pyrano[3,4-c]carbazol-4-one 24809257 Click to see CC(C)(C1CC2=C3C4=CC=CC=C4NC3=C(C=C2C(=O)O1)OC)O 325.40 unknown https://doi.org/10.1248/CPB.46.344
(2R)-6-hydroxy-2-prop-1-en-2-yl-2,7-dihydro-1H-pyrano[3,4-c]carbazol-4-one 24809260 Click to see CC(=C)C1CC2=C3C4=CC=CC=C4NC3=C(C=C2C(=O)O1)O 293.30 unknown https://doi.org/10.1248/CPB.46.344
(2R)-6-methoxy-2-prop-1-en-2-yl-2,7-dihydro-1H-pyrano[3,4-c]carbazol-4-one 24809259 Click to see CC(=C)C1CC2=C3C4=CC=CC=C4NC3=C(C=C2C(=O)O1)OC 307.30 unknown https://doi.org/10.1248/CPB.46.344
1-(3,3-Dimethyloxiran-2-yl)-5-methoxy-1,6-dihydrofuro[3,4-c]carbazol-3-one 44178674 Click to see CC1(C(O1)C2C3=C4C5=CC=CC=C5NC4=C(C=C3C(=O)O2)OC)C 323.30 unknown https://doi.org/10.1021/NP800735M
1-Hydroxy-6-methoxy-3-methylcarbazole 10353685 Click to see CC1=CC2=C(C(=C1)O)NC3=C2C=C(C=C3)OC 227.26 unknown https://doi.org/10.1016/0031-9422(95)00047-B
1-Hydroxy-9H-carbazole-3-carbaldehyde 611174 Click to see C1=CC=C2C(=C1)C3=C(N2)C(=CC(=C3)C=O)O 211.22 unknown https://doi.org/10.1021/NP100654M
https://doi.org/10.1248/CPB.46.344
https://doi.org/10.1016/S0031-9422(00)97778-1
1,6-dimethoxy-3-methyl-9H-carbazole 10354321 Click to see CC1=CC2=C(C(=C1)OC)NC3=C2C=C(C=C3)OC 241.28 unknown https://doi.org/10.1016/0031-9422(95)00047-B
2-Hydroxy-7-methoxy-9H-carbazole-3-carbaldehyde 189687 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=C(C(=C3)C=O)O 241.24 unknown via CMAUP database
2-methoxy-9H-carbazole-3-carbaldehyde 6483032 Click to see COC1=CC2=C(C=C1C=O)C3=CC=CC=C3N2 225.24 unknown https://doi.org/10.1021/NP800735M
3-methyl-9H-carbazol-2-ol 3459141 Click to see CC1=CC2=C(C=C1O)NC3=CC=CC=C32 197.23 unknown via CMAUP database
3-Methylcarbazole 20746 Click to see CC1=CC2=C(C=C1)NC3=CC=CC=C32 181.23 unknown https://doi.org/10.1016/S0031-9422(00)97778-1
5-Methoxy-1-(2-methylprop-1-enyl)-1,6-dihydrofuro[3,4-c]carbazol-3-one 44178760 Click to see CC(=CC1C2=C3C4=CC=CC=C4NC3=C(C=C2C(=O)O1)OC)C 307.30 unknown https://doi.org/10.1021/NP800735M
9H-Carbazole-3-carboxaldehyde, 2,7-dimethoxy- 5317755 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=C(C(=C3)C=O)OC 255.27 unknown via CMAUP database
clausamine A 9994522 Click to see CC(=C)C1CC2=C3C4=CC=CC=C4NC3=C(C=C2C(=O)O1)O 293.30 unknown https://doi.org/10.1248/CPB.46.344
Clausamine B 10662509 Click to see CC(=C)C1CC2=C3C4=CC=CC=C4NC3=C(C=C2C(=O)O1)OC 307.30 unknown https://doi.org/10.1021/NP800735M
clausamine C 10448976 Click to see CC(C)(C1CC2=C3C4=CC=CC=C4NC3=C(C=C2C(=O)O1)OC)O 325.40 unknown https://doi.org/10.1248/CPB.46.344
https://doi.org/10.1021/NP800735M
Clausamine D 10041876 Click to see CC(=CCC1=C2C3=CC=CC=C3NC2=C(C=C1C(=O)OC)OC)C 323.40 unknown https://doi.org/10.1021/NP800735M
https://doi.org/10.1021/NP990285X
clausamine E 10759519 Click to see CC(C)(C=CC1=C2C3=CC=CC=C3NC2=C(C=C1C(=O)OC)OC)O 339.40 unknown https://doi.org/10.1021/NP800735M
https://doi.org/10.1021/NP990285X
Clausine E 5315951 Click to see COC(=O)C1=CC2=C(C(=C1)O)NC3=CC=CC=C32 241.24 unknown https://doi.org/10.1248/CPB.46.344
Clausine F 132514 Click to see CC(=CCC1=C2C3=CC=CC=C3NC2=C(C=C1C(=O)OC)O)C 309.40 unknown https://doi.org/10.1248/CPB.46.344
https://doi.org/10.1021/NP800735M
Clausine H 5315952 Click to see COC1=CC2=C(C=C1)C3=CC(=C(C=C3N2)OC)C(=O)OC 285.29 unknown via CMAUP database
Clausine K 504070 Click to see COC1=CC2=C(C=C1)C3=CC(=C(C=C3N2)OC)C(=O)O 271.27 unknown via CMAUP database
Clausine O 11241634 Click to see C1=CC2=C(C=C1O)NC3=C2C=C(C(=C3)O)C=O 227.21 unknown via CMAUP database
Clauszoline K 10537169 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=CC(=C3)C=O 225.24 unknown via CMAUP database
Ekeberginine 10379640 Click to see CC(=CCC1=C2C3=CC=CC=C3NC2=C(C=C1C=O)OC)C 293.40 unknown https://doi.org/10.1248/CPB.46.344
https://doi.org/10.1016/S0031-9422(00)97778-1
Girinimbine 96943 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=CC=CC=C42 263.30 unknown https://doi.org/10.1016/S0031-9422(00)97778-1
Heptaphylline 5318015 Click to see CC(=CCC1=C(C(=CC2=C1NC3=CC=CC=C32)C=O)O)C 279.30 unknown https://doi.org/10.1016/S0031-9422(00)97778-1
Methyl 3-carbazolecarboxylate 504069 Click to see COC(=O)C1=CC2=C(C=C1)NC3=CC=CC=C32 225.24 unknown https://doi.org/10.1248/CPB.46.344
methyl 4-[(E)-3-hydroperoxy-3-methylbut-1-enyl]-1-methoxy-9H-carbazole-3-carboxylate 10665878 Click to see CC(C)(C=CC1=C2C3=CC=CC=C3NC2=C(C=C1C(=O)OC)OC)OO 355.40 unknown https://doi.org/10.1021/NP990285X
Mukonal 504068 Click to see C1=CC=C2C(=C1)C3=C(N2)C=C(C(=C3)C=O)O 211.22 unknown https://doi.org/10.1021/NP800735M
Mukonidine 10999153 Click to see COC(=O)C1=C(C=C2C(=C1)C3=CC=CC=C3N2)O 241.24 unknown https://doi.org/10.1021/NP800735M
Ulofabczpkmtrn-cmdggobgsa- 10829895 Click to see CC(C)(C=CC1=C2C3=CC=CC=C3NC2=C(C=C1C(=O)OC)O)O 325.40 unknown https://doi.org/10.1021/NP800735M
https://doi.org/10.1021/NP990285X
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1S,13R)-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,14,16-pentaene 21723147 Click to see COC1=C2CN3CCC4(C3C=CC=C4)C2=CC5=C1OCO5 283.32 unknown via CMAUP database
1-Epideacetylbowdensine 443673 Click to see COC1=C2CN3CCC4(C3CCC(C4O)O)C2=CC5=C1OCO5 319.40 unknown via CMAUP database
7H-Pyrrolo(3,2,1-de)phenanthridin-7-one, 10-hydroxy-9-methoxy- 5488695 Click to see COC1=C(C=C2C3=CC=CC4=C3N(C=C4)C(=O)C2=C1)O 265.26 unknown via CMAUP database
Hippacine 10015025 Click to see C1=CC2=C3C(=C1)C4=CC(=C(C=C4C(=O)N3C=C2)O)O 251.24 unknown via CMAUP database
Hippadine 100605 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC5=C4N(C3=O)C=C5 263.25 unknown via CMAUP database
Pratorimine 181937 Click to see COC1=C(C=C2C(=C1)C3=CC=CC4=C3N(C2=O)C=C4)O 265.26 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown via CMAUP database
Gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
3,4-Dimethoxy-1-methylquinolin-2(1H)-one 14335230 Click to see CN1C2=CC=CC=C2C(=C(C1=O)OC)OC 219.24 unknown https://doi.org/10.1016/S0031-9422(00)97778-1
4-Methoxy-1-methylquinolin-2-one 182073 Click to see CN1C2=CC=CC=C2C(=CC1=O)OC 189.21 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines / 4-phenyltetrahydroisoquinolines
Cherylline 90075 Click to see CN1CC(C2=CC(=C(C=C2C1)O)OC)C3=CC=C(C=C3)O 285.34 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
(2E)-N-methyl-3-phenyl-N-[(E)-2-phenylethenyl]prop-2-enamide 11242495 Click to see CN(C=CC1=CC=CC=C1)C(=O)C=CC2=CC=CC=C2 263.30 unknown https://doi.org/10.1016/S0031-9422(00)84114-X
> Phenylpropanoids and polyketides / Coumarins and derivatives
2-[7-Methoxy-3-(2-methylbut-3-en-2-yl)-2-oxochromen-6-yl]acetaldehyde 14259049 Click to see CC(C)(C=C)C1=CC2=CC(=C(C=C2OC1=O)OC)CC=O 286.32 unknown https://doi.org/10.1016/0031-9422(89)80056-1
https://doi.org/10.1016/S0031-9422(00)97778-1
7-(3-Methylbut-2-enoxy)-8-(3-methyl-2-oxo-butyl)chromen-2-one 14376446 Click to see CC(C)C(=O)CC1=C(C=CC2=C1OC(=O)C=C2)OCC=C(C)C 314.40 unknown https://doi.org/10.1021/NP50062A003
7-[(2S,3R)-2,3-dihydroxy-3-methyl-4-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]butoxy]-8-methoxychromen-2-one 163023835 Click to see CC1CC(OC1=O)CC(C)(C(COC2=C(C3=C(C=C2)C=CC(=O)O3)OC)O)O 392.40 unknown https://doi.org/10.1016/0031-9422(91)85155-S
7-[2,3-Dihydroxy-3-methyl-4-(4-methyl-5-oxooxolan-2-yl)butoxy]-8-methoxychromen-2-one 15693462 Click to see CC1CC(OC1=O)CC(C)(C(COC2=C(C3=C(C=C2)C=CC(=O)O3)OC)O)O 392.40 unknown https://doi.org/10.1016/0031-9422(91)85155-S
7-Methoxy-3-(2-methylbut-3-en-2-yl)-6-(3-methylbut-2-enyl)chromen-2-one 5317839 Click to see CC(=CCC1=C(C=C2C(=C1)C=C(C(=O)O2)C(C)(C)C=C)OC)C 312.40 unknown https://doi.org/10.1016/0031-9422(89)80056-1
8-(2,3-Dihydroxy-3-methylbutyl)-7-(3-methylbut-2-enoxy)chromen-2-one 14376448 Click to see CC(=CCOC1=C(C2=C(C=C1)C=CC(=O)O2)CC(C(C)(C)O)O)C 332.40 unknown https://doi.org/10.1021/NP50062A003
8-[(2S)-2,3-dihydroxy-3-methylbutyl]-7-(3-methylbut-2-enoxy)chromen-2-one 163091088 Click to see CC(=CCOC1=C(C2=C(C=C1)C=CC(=O)O2)CC(C(C)(C)O)O)C 332.40 unknown https://doi.org/10.1021/NP50062A003
8-[(3,3-Dimethyloxiran-2-yl)methyl]-7-(3-methylbut-2-enoxy)chromen-2-one 14376447 Click to see CC(=CCOC1=C(C2=C(C=C1)C=CC(=O)O2)CC3C(O3)(C)C)C 314.40 unknown https://doi.org/10.1021/NP50062A003
8-[[(2S)-3,3-dimethyloxiran-2-yl]methyl]-7-(3-methylbut-2-enoxy)chromen-2-one 163087142 Click to see CC(=CCOC1=C(C2=C(C=C1)C=CC(=O)O2)CC3C(O3)(C)C)C 314.40 unknown https://doi.org/10.1021/NP50062A003
8-methoxy-7-[[(2R,3S)-3-methyl-3-[[(2S,4R)-4-methyl-5-oxooxolan-2-yl]methyl]oxiran-2-yl]methoxy]chromen-2-one 162979389 Click to see CC1CC(OC1=O)CC2(C(O2)COC3=C(C4=C(C=C3)C=CC(=O)O4)OC)C 374.40 unknown https://doi.org/10.1016/0031-9422(91)85155-S
8-Methoxy-7-[[3-methyl-3-[(4-methyl-5-oxooxolan-2-yl)methyl]oxiran-2-yl]methoxy]chromen-2-one 15693461 Click to see CC1CC(OC1=O)CC2(C(O2)COC3=C(C4=C(C=C3)C=CC(=O)O4)OC)C 374.40 unknown https://doi.org/10.1016/0031-9422(91)85155-S
CID 13343541 13343541 Click to see CC(=C)C(CC1=C(C=CC2=C1OC(=O)C=C2)OC)O 260.28 unknown https://doi.org/10.1016/0031-9422(89)80056-1
Coumarin deriv 5776876 Click to see CC1=CC(OC1=O)CC(=CCOC2=CC3=C(C=C2)C=CC(=O)O3)C 326.30 unknown https://doi.org/10.1021/NP50062A003
Isomeranzin 473252 Click to see CC(C)C(=O)CC1=C(C=CC2=C1OC(=O)C=C2)OC 260.28 unknown https://doi.org/10.1016/0031-9422(89)80056-1
Osthol 10228 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)OC)C 244.28 unknown https://doi.org/10.1016/0031-9422(75)85267-8
https://doi.org/10.1016/0031-9422(89)80056-1
Triphasiol 157953 Click to see CC(C)C(=O)CC1=C(C=CC2=C1OC(=O)C=C2)OCC(C(C)(C)O)O 348.40 unknown https://doi.org/10.1021/NP50062A003
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Pimpinellin 4825 Click to see COC1=C(C2=C(C=CO2)C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1016/0031-9422(75)85267-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(+)-Oxypeucedanin 928465 Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 286.28 unknown https://doi.org/10.1080/15287398409530517
(2S)-2-(2-hydroxypropan-2-yl)-6-[2-[(2S)-oxiran-2-yl]propan-2-yl]-2,3-dihydrofuro[3,2-g]chromen-7-one 162914355 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=C(C(=O)O3)C(C)(C)C4CO4)O 330.40 unknown https://doi.org/10.1016/S0031-9422(00)97778-1
(2S)-6-[(3S)-3,4-dihydroxy-2-methylbutan-2-yl]-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one 162998313 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=C(C(=O)O3)C(C)(C)C(CO)O)O 348.40 unknown https://doi.org/10.1016/S0031-9422(00)97778-1
2-(2-Hydroxypropan-2-yl)-6-[2-(oxiran-2-yl)propan-2-yl]-2,3-dihydrofuro[3,2-g]chromen-7-one 14259052 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=C(C(=O)O3)C(C)(C)C4CO4)O 330.40 unknown https://doi.org/10.1016/0031-9422(89)80056-1
6-(1,1-Dimethylallyl)-2-(1-hydroxy-1-methylethyl)-2,3-dihydro-7H-furo[3,2-G]chromen-7-one 5287846 Click to see CC(C)(C=C)C1=CC2=CC3=C(C=C2OC1=O)OC(C3)C(C)(C)O 314.40 unknown https://doi.org/10.1016/0031-9422(75)85267-8
6-(3,4-Dihydroxy-2-methylbutan-2-yl)-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one 14259053 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=C(C(=O)O3)C(C)(C)C(CO)O)O 348.40 unknown https://doi.org/10.1016/0031-9422(89)80056-1
Chalepin 119066 Click to see CC(C)(C=C)C1=CC2=CC3=C(C=C2OC1=O)OC(C3)C(C)(C)O 314.40 unknown https://doi.org/10.1080/15287398409530517
https://doi.org/10.1016/0031-9422(89)80056-1
https://doi.org/10.1016/0031-9422(75)85267-8
Clausenacoumarine 6439823 Click to see CC1=CC(OC1=O)CC(=CCOC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 366.40 unknown https://doi.org/10.1016/S0031-9422(00)84114-X
Isogosferol 148619 Click to see CC(=C)C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O 286.28 unknown https://doi.org/10.1016/0031-9422(89)80056-1
Isoimperatorin 68081 Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C 270.28 unknown https://doi.org/10.1016/0031-9422(89)80056-1
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown https://doi.org/10.1016/S0031-9422(00)84114-X
https://doi.org/10.1016/0031-9422(75)85267-8
https://doi.org/10.1016/0031-9422(89)80056-1
https://doi.org/10.1021/NP50062A003
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1016/0031-9422(89)80056-1
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-hydroxypsoralens
Xanthotoxol 65090 Click to see C1=CC(=O)OC2=C(C3=C(C=CO3)C=C21)O 202.16 unknown https://doi.org/10.1016/S0031-9422(00)84114-X
https://doi.org/10.1016/0031-9422(89)80056-1
https://doi.org/10.1016/0031-9422(75)85267-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown https://doi.org/10.1016/0031-9422(75)85267-8
https://doi.org/10.1016/0031-9422(89)80056-1
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Anisocoumarin B 14259051 Click to see CC(=CCOC1=CC(=C2C=CC(=O)OC2=C1)O)C 246.26 unknown https://doi.org/10.1016/0031-9422(89)80056-1
https://doi.org/10.1016/S0031-9422(00)97778-1
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Gravelliferone 14133589 Click to see CC(=CCC1=C(C=C2C(=C1)C=C(C(=O)O2)C(C)(C)C=C)O)C 298.40 unknown https://doi.org/10.1016/0031-9422(89)80056-1
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1016/0031-9422(75)85267-8
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1016/0031-9422(75)85267-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthoxyletin 66548 Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C=CC(=O)O3)C 258.27 unknown https://doi.org/10.1016/0031-9422(89)80056-1
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
3,5,7-Trihydroxy-8-(4-hydroxyphenyl)-2-methyl-2-(4-methylpent-3-enyl)-3,4,7,8-tetrahydropyrano[3,2-g]chromen-6-one 73306723 Click to see CC(=CCCC1(C(CC2=C(C3=C(C=C2O1)OC(C(C3=O)O)C4=CC=C(C=C4)O)O)O)C)C 440.50 unknown https://doi.org/10.1016/S0031-9422(00)84114-X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
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
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3',4'-Dihydroxy-7-methoxyflavan 14157886 Click to see COC1=CC2=C(CCC(O2)C3=CC(=C(C=C3)O)O)C=C1 272.29 unknown via CMAUP database
5,2'-Dihydroxy-7-methoxy-6,8-dimethylflavone 44257614 Click to see CC1=C(C2=C(C(=C1OC)C)OC(=CC2=O)C3=CC=CC=C3O)O 312.30 unknown via CMAUP database
Guibourtinidol-7-methyl ether 15549896 Click to see COC1=CC2=C(CC(C(O2)C3=CC=C(C=C3)O)O)C=C1 272.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2S)-7-hydroxy-8-methoxy-2-phenyl-2,3-dihydrochromen-4-one 15549894 Click to see COC1=C(C=CC2=C1OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
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
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
4-Hydroxy-2',4'-dimethoxydihydrochalcone 15549893 Click to see COC1=CC(=C(C=C1)C(=O)CCC2=CC=C(C=C2)O)OC 286.32 unknown via CMAUP database

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