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Hernandia sonora

Hernandia sonora - 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 UUID6440204a9fd0f690430273
Scientific name Hernandia sonora
Authority L.
First published in Sp. Pl. : 981 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Hernandia peltata Sessé & Moc. Fl. Mexic., ed. 2 213. 1894
Hernandezia sonora (L.) Hoffmanns. Verz. Pfl.-Kult. 219. 1824
Hernandia sonora var. guadeloupensis Meisn. Prodr. 15(1): 264 (1864)

Common names Top

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Language Common/alternative name
English mago
Finnish karibianrakkomarja
Chinese 血桐
Chinese 莲叶桐

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southwest
  • Southern America
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000720618
USDA Plants HESO
Tropicos 15300019
INPN 448460
KEW urn:lsid:ipni.org:names:316357-2
The Plant List kew-2846858
Open Tree Of Life 1035519
NCBI Taxonomy 482941
IPNI 316357-2
iNaturalist 278899
GBIF 3034104
EOL 487372
USDA GRIN 18918
CMAUP NPO18997

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
The rhizosphere and root selections intensify fungi-bacteria interaction in abiotic stress-resistant plants Huang F, Lei M, Li W PeerJ 15-Apr-2024
PMCID:PMC11025542
doi:10.7717/peerj.17225
PMID:38638154
The root enrichment of bacteria is consistent across different stress-resistant plant species Huang F, Zhu C, Huang M, Song X, Peng A PeerJ 17-Jan-2023
PMCID:PMC9854377
doi:10.7717/peerj.14683
PMID:36684671
Chemistry and Biological Activities of Naturally Occurring and Structurally Modified Podophyllotoxins Jin L, Song Z, Cai F, Ruan L, Jiang R Molecules 30-Dec-2022
PMCID:PMC9822336
doi:10.3390/molecules28010302
PMID:36615496
Establishing community-wide DNA barcode references for conserving mangrove forests in China Mao X, Xie W, Li X, Shi S, Guo Z BMC Plant Biol 04-Dec-2021
PMCID:PMC8642986
doi:10.1186/s12870-021-03349-z
PMID:34863107
8-, 9-, and 11-Aryloxy Dimeric Aporphines and Their Pharmacological Activities Ali G, Cuny GD Molecules 27-Jul-2021
PMCID:PMC8347945
doi:10.3390/molecules26154521
PMID:34361671
Strengthening Structures in the Petiole–Lamina Junction of Peltate Leaves Wunnenberg J, Rjosk A, Neinhuis C, Lautenschläger T Biomimetics (Basel) 02-Apr-2021
PMCID:PMC8167582
doi:10.3390/biomimetics6020025
PMID:33918405
Identification and Quantification of Phenolic Compounds from Mexican Oregano (Lippia graveolens HBK) Hydroethanolic Extracts and Evaluation of Its Antioxidant Capacity Cortés-Chitala MD, Flores-Martínez H, Orozco-Ávila I, León-Campos C, Suárez-Jacobo Á, Estarrón-Espinosa M, López-Muraira I Molecules 29-Jan-2021
PMCID:PMC7866295
doi:10.3390/molecules26030702
PMID:33572779
Invasive rat eradication strongly impacts plant recruitment on a tropical atoll Wolf CA, Young HS, Zilliacus KM, Wegmann AS, McKown M, Holmes ND, Tershy BR, Dirzo R, Kropidlowski S, Croll DA PLoS One 17-Jul-2018
PMCID:PMC6049951
doi:10.1371/journal.pone.0200743
PMID:30016347
Data-mining of potential antitubercular activities from molecular ingredients of traditional Chinese medicines Jamal S, Scaria V PeerJ 17-Jul-2014
PMCID:PMC4106188
doi:10.7717/peerj.476
PMID:25081126
Taxonomy, distribution, and natural history of flying foxes (Chiroptera, Pteropodidae) in the Mortlock Islands and Chuuk State, Caroline Islands Buden DW, Helgen KM, Wiles GJ Zookeys 29-Oct-2013
PMCID:PMC3817444
doi:10.3897/zookeys.345.5840
PMID:24194666
TIPdb: A Database of Anticancer, Antiplatelet, and Antituberculosis Phytochemicals from Indigenous Plants in Taiwan Lin YC, Wang CC, Chen IS, Jheng JL, Li JH, Tung CW ScientificWorldJournal 12-May-2013
PMCID:PMC3666282
doi:10.1155/2013/736386
PMID:23766708
Subject Index N/A 01-Jan-2005
PMCID:PMC7148952
doi:10.1016/S1572-5995(05)80049-3
Antineoplastic agents. 522. Hernandia peltata (Malaysia) and Hernandia nymphaeifolia (Republic of Maldives). Pettit GR, Meng Y, Gearing RP, Herald DL, Pettit RK, Doubek DL, Chapuis JC, Tackett LP J Nat Prod 01-Feb-2004
doi:10.1021/NP030125S
PMID:14987061
The Plant Communities and Environmental Gradients of Pitcairn Island: The Significance of Invasive Species and the Need for Conservation Management KINGSTON N, WALDREN S Ann Bot 01-Jul-2003
PMCID:PMC4243631
doi:10.1093/aob/mcg106
PMID:12824069
Alkaloids from Hernandia sonora Ih-Sheng Chen, Jih-Jung Chen, Ian-Lih Tsai Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(95)00280-K

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 / Aporphines
(12S)-4,6,19,21-tetraoxa-13-azahexacyclo[10.10.1.02,10.03,7.016,23.018,22]tricosa-1(23),2(10),3(7),8,16,18(22)-hexaene 821351 Click to see C1CNC2CC3=C(C4=C2C1=CC5=C4OCO5)C6=C(C=C3)OCO6 309.30 unknown https://doi.org/10.1016/0031-9422(95)00280-K
16-Hydroxy-4,15-dimethoxy-10-methyl-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,4,7,9(17),13,15-hexaene-3,6-dione 162843626 Click to see CN1CCC2=CC(=C(C3=C4C(=CC1=C23)C(=O)C=C(C4=O)OC)O)OC 339.30 unknown https://doi.org/10.1055/S-2006-959366
18,19-Dimethoxy-5,7-dioxa-13-azapentacyclo[10.7.1.02,10.04,8.016,20]icosa-1(20),2,4(8),9,11,16,18-heptaene-11-carbaldehyde 15765196 Click to see COC1=C(C2=C3C(=C1)CCNC3=C(C4=CC5=C(C=C42)OCO5)C=O)OC 351.40 unknown https://doi.org/10.1016/0031-9422(95)00280-K
4,15,16-Trimethoxy-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,4,7,9(17),13,15-hexaene-3,6-dione 10830917 Click to see COC1=CC(=O)C2=CC3=C4C(=CC(=C(C4=C2C1=O)OC)OC)CCN3 339.30 unknown https://doi.org/10.1055/S-2006-959366
4,5-Dimethoxy-2-[(4,15,16-trimethoxy-10-methyl-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,3,5,7,9(17),13,15-heptaen-5-yl)oxy]benzaldehyde 15765197 Click to see CN1CCC2=CC(=C(C3=C4C=C(C(=CC4=CC1=C23)OC5=CC(=C(C=C5C=O)OC)OC)OC)OC)OC 503.50 unknown https://doi.org/10.1016/0031-9422(95)00280-K
4,6,19,21-Tetraoxa-13-azahexacyclo[10.10.1.02,10.03,7.016,23.018,22]tricosa-1,3(7),8,10,12(23),16,18(22)-heptaene-11-carbaldehyde 15765195 Click to see C1CNC2=C3C1=CC4=C(C3=C5C(=C2C=O)C=CC6=C5OCO6)OCO4 335.30 unknown https://doi.org/10.1016/0031-9422(95)00280-K
4,6,19,21-Tetraoxa-13-azahexacyclo[10.10.1.02,10.03,7.016,23.018,22]tricosa-1,3(7),8,10,12(23),16,18(22)-heptaene-13-carbaldehyde 9997062 Click to see C1CN(C2=C3C1=CC4=C(C3=C5C(=C2)C=CC6=C5OCO6)OCO4)C=O 335.30 unknown https://doi.org/10.1016/0031-9422(95)00280-K
Atheroline 21222 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC(=C(C=C42)OC)O)OC 337.30 unknown https://doi.org/10.1016/0031-9422(95)00280-K
Boldine 2-methyl ether 16573 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC 341.40 unknown https://doi.org/10.1016/0031-9422(95)00280-K
Corytuberine 160500 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC 327.40 unknown https://doi.org/10.1016/0031-9422(95)00280-K
Hernandaline 12310422 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC5=CC(=C(C=C5C=O)OC)OC)OC)OC 505.60 unknown via CMAUP database
Hernandonine 500428 Click to see C1OC2=C(O1)C3=C(C=C2)C(=O)C4=NC=CC5=CC6=C(C3=C54)OCO6 319.30 unknown https://doi.org/10.1016/0031-9422(95)00280-K
Hernangerine 497804 Click to see COC1=C(C=CC2=C1C3=C4C(C2)NCCC4=CC5=C3OCO5)O 311.30 unknown https://doi.org/10.1016/0031-9422(95)00280-K
Hernovine 10425723 Click to see COC1=C(C=CC2=C1C3=C4C(C2)NCCC4=CC(=C3OC)O)O 313.30 unknown via CMAUP database
Isocorydione 10689393 Click to see CN1CCC2=CC(=C(C3=C4C(=CC1=C23)C(=O)C=C(C4=O)OC)OC)OC 353.40 unknown https://doi.org/10.1055/S-2006-959366
N-Methyl hernangerin 497829 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)O)OC)OCO3 325.40 unknown https://doi.org/10.1016/0031-9422(95)00280-K
> Benzenoids / Phenols / Methoxyphenols
Isovanillin 12127 Click to see COC1=C(C=C(C=C1)C=O)O 152.15 unknown https://doi.org/10.1016/0031-9422(95)00280-K
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Epieudesmin 7299790 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1021/NP030125S
1,4-Bis(3,4-dimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan 234823 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1021/NP030125S
5-[(3aR,6aR)-6-(3,4,5-trimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-1,3-benzodioxole 137706650 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5 400.40 unknown https://doi.org/10.1055/S-2006-958149
https://doi.org/10.1021/NP030125S
5-[(4r)-4-(3,4,5-Trimethoxyphenyl)tetrahydro-1h,3h-furo[3,4-c]furan-1-yl]-1,3-benzodioxole 374872 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5 400.40 unknown via CMAUP database
Epiaschantin 10408679 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5 400.40 unknown https://doi.org/10.1021/NP030125S
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3S,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(R)-hydroxy-(3,4,5-trimethoxyphenyl)methyl]oxolan-2-one 173676 Click to see COC1=CC(=CC(=C1OC)OC)C(C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)O 416.40 unknown https://doi.org/10.1021/NP030125S
[(R)-[(3S,4R)-4-[(7-methoxy-1,3-benzodioxol-5-yl)methyl]-2-oxooxolan-3-yl]-(3,4,5-trimethoxyphenyl)methyl] acetate 162876897 Click to see CC(=O)OC(C1C(COC1=O)CC2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C(=C4)OC)OC)OC 488.50 unknown https://doi.org/10.1055/S-2006-960779
[[4-[(7-Methoxy-1,3-benzodioxol-5-yl)methyl]-2-oxooxolan-3-yl]-(3,4,5-trimethoxyphenyl)methyl] acetate 162876896 Click to see CC(=O)OC(C1C(COC1=O)CC2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C(=C4)OC)OC)OC 488.50 unknown https://doi.org/10.1055/S-2006-960779
4-[(2H-1,3-Benzodioxol-5-yl)methyl]-3-[hydroxy(3,4,5-trimethoxyphenyl)methyl]oxolan-2-one 323437 Click to see COC1=CC(=CC(=C1OC)OC)C(C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)O 416.40 unknown https://doi.org/10.1021/NP030125S
Yatein 442835 Click to see COC1=CC(=CC(=C1OC)OC)CC2C(COC2=O)CC3=CC4=C(C=C3)OCO4 400.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
(-)-Deoxypodophyllotoxin 2203 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O 398.40 unknown https://doi.org/10.1055/S-2006-960779
https://doi.org/10.1021/NP030125S
(5R,5aR,8aR)-4-methoxy-5-(3,4,5-trimethoxyphenyl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one 10251969 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C(=C24)OC)OCO5)COC3=O 428.40 unknown https://doi.org/10.1055/S-2006-960779
4-methoxy-5-(3,4,5-trimethoxyphenyl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one 5259729 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C(=C24)OC)OCO5)COC3=O 428.40 unknown https://doi.org/10.1055/S-2006-960779
Deoxypodophyllotoxin 345501 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O 398.40 unknown https://doi.org/10.1055/S-2006-960779
> Lignans, neolignans and related compounds / Lignan lactones / Podophyllotoxins
(5R,5aR,8aR,9R)-9-hydroxy-4-methoxy-5-(3,4,5-trimethoxyphenyl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one 163188639 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C(=C24)OC)OCO5)O 444.40 unknown https://doi.org/10.1055/S-2006-960779
[(5R,5aR,8aR,9R)-4-methoxy-6-oxo-5-(3,4,5-trimethoxyphenyl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-9-yl] acetate 162991371 Click to see CC(=O)OC1C2COC(=O)C2C(C3=C(C4=C(C=C13)OCO4)OC)C5=CC(=C(C(=C5)OC)OC)OC 486.50 unknown https://doi.org/10.1055/S-2006-960779
[4-methoxy-6-oxo-5-(3,4,5-trimethoxyphenyl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-9-yl] acetate 22297316 Click to see CC(=O)OC1C2COC(=O)C2C(C3=C(C4=C(C=C13)OCO4)OC)C5=CC(=C(C(=C5)OC)OC)OC 486.50 unknown https://doi.org/10.1055/S-2006-960779
5-hydroxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one 4865 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 414.40 unknown https://doi.org/10.1055/S-2006-960779
5-Methoxypodophyllotoxin 3035544 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=C(C5=C(C=C24)OCO5)OC)O 444.40 unknown https://doi.org/10.1055/S-2006-960779
9-hydroxy-4-methoxy-5-(3,4,5-trimethoxyphenyl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one 117939676 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C(=C24)OC)OCO5)O 444.40 unknown https://doi.org/10.1055/S-2006-960779
Acetylepipodophyllotoxin 225920 Click to see CC(=O)OC1C2COC(=O)C2C(C3=CC4=C(C=C13)OCO4)C5=CC(=C(C(=C5)OC)OC)OC 456.40 unknown https://doi.org/10.1055/S-2006-960779
Picropodophyllin 72435 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 414.40 unknown https://doi.org/10.1055/S-2006-960779
Podofilox 10607 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 414.40 unknown https://doi.org/10.1055/S-2006-960779
Podophyllotoxin acetate 164791 Click to see CC(=O)OC1C2COC(=O)C2C(C3=CC4=C(C=C13)OCO4)C5=CC(=C(C(=C5)OC)OC)OC 456.40 unknown https://doi.org/10.1055/S-2006-960779
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,7R,10S,13R,14R,16S,19S,20S)-19-(furan-3-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 99641980 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 via CMAUP database
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 via CMAUP database
> 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
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
Isobauerenol 3084367 Click to see CC1CCC2(CCC3(C4=C(CCC3(C2C1C)C)C5(CCC(C(C5CC4)(C)C)O)C)C)C 426.70 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives
6,7-Dimethoxyisoquinoline 177578 Click to see COC1=C(C=C2C=NC=CC2=C1)OC 189.21 unknown https://doi.org/10.1016/0031-9422(95)00280-K
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(+)-Malekulatine 10439456 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)OC4=CC(=C(C=C4CC5C6=CC(=C(C=C6CCN5C)OC)O)OC)OC)OC 670.80 unknown https://doi.org/10.1016/0031-9422(95)00280-K
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
N-Methylcorydaldine 303906 Click to see CN1CCC2=CC(=C(C=C2C1=O)OC)OC 221.25 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown via CMAUP database
Isodictamnine 442913 Click to see CN1C2=CC=CC=C2C(=O)C3=C1OC=C3 199.20 unknown via CMAUP database
Kokusaginine 10227 Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
Maculine 68232 Click to see COC1=C2C=COC2=NC3=CC4=C(C=C31)OCO4 243.21 unknown via CMAUP database
Maculosidine 68222 Click to see COC1=CC2=C(C(=C1)OC)N=C3C(=C2OC)C=CO3 259.26 unknown via CMAUP database
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Rutacultin 182049 Click to see CC(C)(C=C)C1=CC2=CC(=C(C=C2OC1=O)OC)OC 274.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(R)-6-(1,1-Dimethyl-allyl)-2-(1-hydroxy-1-methyl-ethyl)-2,3-dihydro-furo[3,2-g]chromen-7-one 17753871 Click to see CC(C)(C=C)C1=CC2=CC3=C(C=C2OC1=O)OC(C3)C(C)(C)O 314.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
(3R)-3-hydroxy-2,2-dimethyl-7-(2-methylbut-3-en-2-yl)-3,4-dihydropyrano[3,2-g]chromen-8-one 92470573 Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=C(C(=O)O3)C(C)(C)C=C)O)C 314.40 unknown via CMAUP database

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