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Machilus zuihoensis

Machilus zuihoensis - 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 UUID64404767370da018741893
Scientific name Machilus zuihoensis
Authority Hayata
First published in J. Coll. Sci. Imp. Univ. Tokyo 30(1): 244 (1911)

Description Top

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Synonyms Top

Scientific name Authority First published in
Persea zuihoensis (Hayata) H.L.Li Woody Fl. Taiwan : 227 (1963)
Machilus zuihoensis f. longipaniculata (Hayata) Tang S.Liu & J.C.Liao Annual Taiwan Mus. 14: 20 1971

Common names Top

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Language Common/alternative name
tay atalaw
Chinese 香楠
Chinese 香润楠
Chinese 瑞芳楠

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
Machilus zuihoensis var. mushaensis (F.Y.Lu) Y.C.Liu Trees Taiwan : 157 (1988)
Machilus zuihoensis var. zuihoensis Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001071809
Tropicos 17805636
KEW urn:lsid:ipni.org:names:466282-1
The Plant List tro-17805636
Open Tree Of Life 36198
Observations.org 458459
NCBI Taxonomy 337466
IUCN Red List 175597744
IPNI 466282-1
iNaturalist 574576
GBIF 4177730
EOL 5395041
Elurikkus 481108
CMAUP NPO4130

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
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Gastroprotective effects of Machilus zuihoensis Hayata bark against acidic ethanol-induced gastric ulcer in mice Huang SC, Wu WJ, Lee YJ, Tsai MS, Yan XZ, Lin HC, Lai PY, Wang KT, Liao JW, Tsai JC, Wang SH J Tradit Complement Med 31-May-2023
PMCID:PMC10492164
doi:10.1016/j.jtcme.2023.05.006
PMID:37693097
Exogenous application of melatonin to mitigate drought stress-induced oxidative damage in Phoebe sheareri seedlings Li G, Li Y, Zhu Y, Zheng W, Li M, Hu J, Fei Y, Zhu S PeerJ 17-Apr-2023
PMCID:PMC10117382
doi:10.7717/peerj.15159
PMID:37090109
Chemical characteristics of the sesquiterpenes and diterpenes from Lauraceae family and their multifaceted health benefits: A review Feng H, Jiang Y, Cao H, Shu Y, Yang X, Zhu D, Shao M Heliyon 07-Dec-2022
PMCID:PMC9801090
doi:10.1016/j.heliyon.2022.e12013
PMID:36590503
Shift of Host Range for the Immature Stages of the Lanternfly, Pyrops watanabei (Matsumura) (Hemiptera, Fulgoridae) Native to Taiwan Hsu MH, Yang YL, Wu ML, Wang LJ Insects 12-Sep-2022
PMCID:PMC9500622
doi:10.3390/insects13090826
PMID:36135527
Four New Pale-Spored Species of Xylaria (Xylariaceae, Xylariales) with a Key to Worldwide Species on Fallen Fruits and Seeds Ma H, Song Z, Pan X, Qu Z, Yang Z, Li Y, Zhu A Biology (Basel) 08-Jun-2022
PMCID:PMC9220042
doi:10.3390/biology11060885
PMID:35741406
Host Plants of the Immature Stages of the Invasive Longan Lanternfly, Pyrops candelaria (L.) (Hemiptera, Fulgoridae) in Taiwan Hsu MH, Yang YL, Wu ML, Wang LJ Insects 12-Nov-2021
PMCID:PMC8618601
doi:10.3390/insects12111022
PMID:34821821
Anti-COVID-19 drug candidates: A review on potential biological activities of natural products in the management of new coronavirus infection Prasansuklab A, Theerasri A, Rangsinth P, Sillapachaiyaporn C, Chuchawankul S, Tencomnao T J Tradit Complement Med 29-Dec-2020
PMCID:PMC7833040
doi:10.1016/j.jtcme.2020.12.001
PMID:33520683
Tree mortality in response to typhoon-induced floods and mudslides is determined by tree species, size, and position in a riparian Formosan gum forest in subtropical Taiwan Tzeng HY, Wang W, Tseng YH, Chiu CA, Kuo CC, Tsai ST PLoS One 05-Jan-2018
PMCID:PMC5755898
doi:10.1371/journal.pone.0190832
PMID:29304149
Mycosphaerellaceae – Chaos or clarity? Videira SI, Groenewald JZ, Nakashima C, Braun U, Barreto RW, de Wit PJ, Crous PW Stud Mycol 28-Sep-2017
PMCID:PMC5693839
doi:10.1016/j.simyco.2017.09.003
PMID:29180830
Characteristics of tropical human-modified forests after 20 years of natural regeneration Loo LC, Song GZ, Chao KJ Bot Stud 30-Aug-2017
PMCID:PMC5578950
doi:10.1186/s40529-017-0190-x
PMID:28861854
Potential biotechnological capabilities of cultivable mycobiota from carwash effluents Sibanda T, Selvarajan R, Tekere M, Nyoni H, Meddows‐Taylor S Microbiologyopen 17-Jul-2017
PMCID:PMC5635173
doi:10.1002/mbo3.498
PMID:28714266
HMGB1 in Health and Disease Kang R, Chen R, Zhang Q, Hou W, Wu S, Cao L, Huang J, Yu Y, Fan XG, Yan Z, Sun X, Wang H, Wang Q, Tsung A, Billiar TR, Zeh HJ III, Lotze MT, Tang D Mol Aspects Med 08-Jul-2014
PMCID:PMC4254084
doi:10.1016/j.mam.2014.05.001
PMID:25010388
A new genus, two new species and a new record of subfamily Cecidophyinae (Acari, Eriophyidae) from China Wang GQ, Wei SG, Yang D Zookeys 05-Apr-2012
PMCID:PMC3332006
doi:10.3897/zookeys.180.2641
PMID:22539903
Anti-Inflammatory and Free Radial Scavenging Activities of the Constituents Isolated from Machilus zuihoensis Mao YW, Tseng HW, Liang WL, Chen IS, Chen ST, Lee MH Molecules 10-Nov-2011
PMCID:PMC6264439
doi:10.3390/molecules16119451
PMID:22075574

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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see COC(=O)C1=CC=C(C=C1)O 152.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
> Benzenoids / Benzene and substituted derivatives / Toluenes
(2R,3R)-2-[(3R,5S)-3,5-dimethyl-2-methylidene-6-[[(2R,3R)-3-(4-methylphenyl)oxiran-2-yl]methyl]hept-6-enyl]-3-(4-methylphenyl)oxirane 162908942 Click to see CC1=CC=C(C=C1)C2C(O2)CC(=C)C(C)CC(C)C(=C)CC3C(O3)C4=CC=C(C=C4)C 416.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
(2S,3S)-2-[(3R,5S)-3,5-dimethyl-2-methylidene-6-[[(2S,3S)-3-(4-methylphenyl)oxiran-2-yl]methyl]hept-6-enyl]-3-(4-methylphenyl)oxirane 162908941 Click to see CC1=CC=C(C=C1)C2C(O2)CC(=C)C(C)CC(C)C(=C)CC3C(O3)C4=CC=C(C=C4)C 416.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
2-[3,5-Dimethyl-2-methylidene-6-[[3-(4-methylphenyl)oxiran-2-yl]methyl]hept-6-enyl]-3-(4-methylphenyl)oxirane 72830626 Click to see CC1=CC=C(C=C1)C2C(O2)CC(=C)C(C)CC(C)C(=C)CC3C(O3)C4=CC=C(C=C4)C 416.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
Machillene 11395937 Click to see CC1=CC=C(C=C1)C2C(O2)CC(=C)C(C)CC(C)C(=C)CC3C(O3)C4=CC=C(C=C4)C 416.60 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3,5-dimethoxyphenyl)- 119216 Click to see COC1=CC(=CC(=C1O)OC)C=CC=O 208.21 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
N-Trans-feruloyltramine 5280537 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
Sinapaldehyde 5280802 Click to see COC1=CC(=CC(=C1O)OC)C=CC=O 208.21 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1080/14786410802401432
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol, (+)- 443023 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
methyl (E)-2-[(1S)-1-hydroxy-2-oxopropyl]icos-2-enoate 162899477 Click to see CCCCCCCCCCCCCCCCCC=C(C(C(=O)C)O)C(=O)OC 396.60 unknown https://doi.org/10.1002/1522-2675(200207)85:7<1909::AID-HLCA1909>3.0.CO;2-1
methyl (Z)-2-[(1R)-1-hydroxy-2-oxopropyl]icos-2-enoate 129716173 Click to see CCCCCCCCCCCCCCCCCC=C(C(C(=O)C)O)C(=O)OC 396.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
Methyl 2-(1-hydroxy-2-oxopropyl)icos-2-enoate 85088347 Click to see CCCCCCCCCCCCCCCCCC=C(C(C(=O)C)O)C(=O)OC 396.60 unknown https://doi.org/10.1002/1522-2675(200207)85:7<1909::AID-HLCA1909>3.0.CO;2-1
https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
Secomahubanolide 101741814 Click to see CCCCCCCCCCCCCCCCCC=C(C(C(=O)C)O)C(=O)OC 396.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
DL-alpha-Tocopherol 2116 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,2R,4S)-4-[(1S)-1,5-Dimethyl-4-hexenyl]-1-methylcyclohexane-1,2,4-triol 10967106 Click to see CC(CCC=C(C)C)C1(CCC(C(C1)O)(C)O)O 256.38 unknown https://doi.org/10.1002/1522-2675(200207)85:7<1909::AID-HLCA1909>3.0.CO;2-1
1-Methyl-4-(6-methylhept-5-en-2-yl)cyclohexane-1,2,4-triol 85349295 Click to see CC(CCC=C(C)C)C1(CCC(C(C1)O)(C)O)O 256.38 unknown https://doi.org/10.1002/1522-2675(200207)85:7<1909::AID-HLCA1909>3.0.CO;2-1
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
5-(1-Hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-3-methylpenta-2,4-dienoic acid 287291 Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)O)C)O)(C)C 264.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
Abscisic acid 5280896 Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)O)C)O)(C)C 264.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496016 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/J.PHYTOCHEM.2005.03.020
(3beta,5alpha,6beta,24R)-Stigmastane-3,5,6-triol 634760 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C)C(C)C 448.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1080/14786410802401432
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
https://doi.org/10.1080/14786410802401432
6beta-Hydroxystigmast-4-en-3-one 9823926 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 428.70 unknown via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1080/14786410802401432
https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
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/J.PHYTOCHEM.2005.03.020
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/J.PHYTOCHEM.2005.03.020
Sitostenone 579897 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
Stigmastane-3beta,5alpha,6beta-triol 3036251 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C)C(C)C 448.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1080/14786410802401432
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(2R,3aR,6E,6aS)-2-heptadecyl-3a-methyl-6-octadecylidene-6aH-furo[2,3-d][1,3]dioxol-5-one 10258508 Click to see CCCCCCCCCCCCCCCCCC=C1C2C(OC(O2)CCCCCCCCCCCCCCCCC)(OC1=O)C 633.00 unknown https://doi.org/10.1002/1522-2675(200207)85:7<1909::AID-HLCA1909>3.0.CO;2-1
(2R,3S,4R,5R)-2-butoxy-2-(hydroxymethyl)oxane-3,4,5-triol 50914217 Click to see CCCCOC1(C(C(C(CO1)O)O)O)CO 236.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
2-Butoxy-2-(hydroxymethyl)oxane-3,4,5-triol 13059905 Click to see CCCCOC1(C(C(C(CO1)O)O)O)CO 236.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
2-heptadecyl-3a-methyl-6-octadecylidene-6aH-furo[2,3-d][1,3]dioxol-5-one 162873638 Click to see CCCCCCCCCCCCCCCCCC=C1C2C(OC(O2)CCCCCCCCCCCCCCCCC)(OC1=O)C 633.00 unknown https://doi.org/10.1002/1522-2675(200207)85:7<1909::AID-HLCA1909>3.0.CO;2-1
4-Hydroxy-5-methoxy-5-methyl-3-octadecylideneoxolan-2-one 85095532 Click to see CCCCCCCCCCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 396.60 unknown https://doi.org/10.1002/1522-2675(200207)85:7<1909::AID-HLCA1909>3.0.CO;2-1
Machicolide A 10023683 Click to see CCCCCCCCCCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 396.60 unknown https://doi.org/10.1002/1522-2675(200207)85:7<1909::AID-HLCA1909>3.0.CO;2-1
Machicolide B 10069345 Click to see CCCCCCCCCCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 396.60 unknown https://doi.org/10.1002/1522-2675(200207)85:7<1909::AID-HLCA1909>3.0.CO;2-1
> Organoheterocyclic compounds / Azolidines / Imidazolidines / Hydantoins
4,6-Dehydro-1,2,4,5-tetrahydro-2,5-dioxopilocarpin 11499651 Click to see CCC1C(COC1=O)C=C2C(=O)NC(=O)N2C 238.24 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
[(1S,2S)-1-(1,3-benzodioxol-5-yl)-2-methyl-3-oxobutyl] 1,3-benzodioxole-5-carboxylate 162973074 Click to see CC(C(C1=CC2=C(C=C1)OCO2)OC(=O)C3=CC4=C(C=C3)OCO4)C(=O)C 370.40 unknown https://doi.org/10.1080/14786410802401432
[1-(1,3-Benzodioxol-5-yl)-2-methyl-3-oxobutyl] 1,3-benzodioxole-5-carboxylate 162973073 Click to see CC(C(C1=CC2=C(C=C1)OCO2)OC(=O)C3=CC4=C(C=C3)OCO4)C(=O)C 370.40 unknown https://doi.org/10.1080/14786410802401432
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
3-(1-Methoxyoctadecyl)-5-methylidenefuran-2-one 91056912 Click to see CCCCCCCCCCCCCCCCCC(C1=CC(=C)OC1=O)OC 378.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
3-[(1R)-1-methoxyoctadecyl]-5-methylidenefuran-2-one 162961586 Click to see CCCCCCCCCCCCCCCCCC(C1=CC(=C)OC1=O)OC 378.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
> Organoheterocyclic compounds / Oxolanes
4-Hydroxy-5-methylidene-3-octadecylideneoxolan-2-one 370916 Click to see CCCCCCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 364.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
Isophilippinolide A 11210739 Click to see CCCCCCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 364.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
Zuihoenalide 101741815 Click to see CCCCCCCCCCCCCCCCC(=C1C(C(=C)OC1=O)O)C 364.60 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
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1-methylquinolin-2-one 182073 Click to see CN1C2=CC=CC=C2C(=CC1=O)OC 189.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-feruloyltyramine; Moupinamide 125213 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.020
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(8S)-5-hydroxy-8-prop-1-en-2-yl-8,9-dihydrofuro[2,3-h]chromen-2-one 44310181 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC(=O)C=C3)O 244.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
3-(1,1-Dimethylallyl)scopoletin 5377569 Click to see CC(C)(C=C)C1=CC2=CC(=C(C=C2OC1=O)O)OC 260.28 unknown via CMAUP database
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database

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