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Xylopia parviflora

Xylopia parviflora - 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 UUID643ffbb9a39c1819730383
Scientific name Xylopia parviflora
Authority Spruce
First published in J. Proc. Linn. Soc., Bot. 5: 6 (1860)

Description Top

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Synonyms Top

Scientific name Authority First published in
Xylopia neglecta R.E.Fr. Kongl. Svenska Vetensk. Acad. Handl. , n.s., 34(5): 31 (1900)

Common names Top

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Language Common/alternative name
English xylopia holtzii
Afrikaans xylopia holtzii
Quechua kutu kara kaspi
Quechua pukuna kara kaspi
Quechua qutu qara k'aspi
Quechua phukuna qara k'aspi

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
    • Northern South America
      • French Guiana
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000428914
Tropicos 1601379
INPN 732567
KEW urn:lsid:ipni.org:names:76217-1
The Plant List kew-2468174
Open Tree Of Life 1030229
NCBI Taxonomy 992813
IUCN Red List 137024286
IPNI 76217-1
iNaturalist 431749
GBIF 3157027
EOL 304404
USDA GRIN 474690
Wikipedia Xylopia_parviflora

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
Woody Species Composition, Structure, and Status of Regeneration in Pugnido Forest, Gambella Region, Western Ethiopia Masresha G, Melkamu Y, Mulu G Scientifica (Cairo) 04-Apr-2024
PMCID:PMC11008979
doi:10.1155/2024/3961434
PMID:38605976
Coffee leaf extract exhibits anti-obesity property and improves lipid metabolism in high-fat diet-induced C57BL6 obese mice Patil S, Das M, Kumar GS, Murthy PS 3 Biotech 18-Jul-2023
PMCID:PMC10353976
doi:10.1007/s13205-023-03698-6
PMID:37476547
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Anti-Inflammatory, Antioxidant Activities, and Phytochemical Characterization of Edible Plants Exerting Synergistic Effects in Human Gastric Epithelial Cells Atchan AP, Monthe OC, Tchamgoue AD, Singh Y, Shivashankara ST, Selvi MK, Agbor GA, Magni P, Piazza S, Manjappara UV, Kuiate JR, Dell’Agli M Antioxidants (Basel) 27-Feb-2023
PMCID:PMC10045632
doi:10.3390/antiox12030591
PMID:36978842
Chronic Gastric Ulcer Healing Actions of the Aqueous Extracts of Staple Plant Foods of the North-West, Adamawa, and West Regions of Cameroon Mikwangock HD, Tamfu AN, Amang AP, Siwe GT, Mezui C, Kucukaydin S, Enow-Orock EG, Tan PV Biomed Res Int 09-Jan-2023
PMCID:PMC9842419
doi:10.1155/2023/2657278
PMID:36654868
Chemical composition, antibacterial efficacy, and antioxidant capacity of essential oil and oleoresin from Monodora myristica and Tetrapleura tetraptera in Southeast Nigeria Okechukwu QN, Ugwuona FU, Ofoedu CE, Juchniewicz S, Okpala CO Sci Rep 18-Nov-2022
PMCID:PMC9674670
doi:10.1038/s41598-022-23161-5
PMID:36400870
Chemical Profiling and Molecular Docking Study of Agathophora alopecuroides Amin E, Abdel-Bakky MS, Mohammed HA, Hassan MH Life (Basel) 11-Nov-2022
PMCID:PMC9696702
doi:10.3390/life12111852
PMID:36430987
The Antiplasmodial Potential of Medicinal Plants Used in the Cameroonian Pharmacopoeia: An Updated Systematic Review and Meta-Analysis Tepa AG, Ambassa P, Ayong LS, Biapa Nya PC, Pieme CA Evid Based Complement Alternat Med 08-Oct-2022
PMCID:PMC9569203
doi:10.1155/2022/4661753
PMID:36254175
In vitro anticholinesterase potential of some spices consumed in Cameroon and their protective effects on hydrogen peroxide-mediated oxidative stress damage in SK-N-SH cells Dibacto RE, Ngoumen DJ, Ella FA, Nanhah JV, Ambamba BD, Hagbe PV, Fonkoua M, Mandob DE, Minka RS, Ngondi JL IBRO Neurosci Rep 13-Jul-2022
PMCID:PMC9305342
doi:10.1016/j.ibneur.2022.07.001
PMID:35874495
The neuroprotective effect of Xylopia parviflora against aluminum chloride-induced neurotoxicity in rats Kemadjou Dibacto RE, Akamba Ambamba BD, Ella FA, Biyegue Nyangono CF, Kamga Nanhah JV, Fonkoua M, Minka RS, Ngondi JL Heliyon 06-Jul-2022
PMCID:PMC9287802
doi:10.1016/j.heliyon.2022.e09896
PMID:35855984
Polyphenol-Rich Extracts of Xylopia and Aframomum Species Show Metabolic Benefits by Lowering Hepatic Lipid Accumulation in Diet-Induced Obese Mice Nwakiban Atchan AP, Shivashankara ST, Piazza S, Tchamgoue AD, Beretta G, Dell’Agli M, Magni P, Agbor GA, Kuiaté JR, Manjappara UV ACS Omega 30-Mar-2022
PMCID:PMC9016817
doi:10.1021/acsomega.2c00050
PMID:35449947
Hydroethanolic Extract of Prunus domestica L.: Metabolite Profiling and In Vitro Modulation of Molecular Mechanisms Associated to Cardiometabolic Diseases Ullah H, Sommella E, Santarcangelo C, D’Avino D, Rossi A, Dacrema M, Minno AD, Di Matteo G, Mannina L, Campiglia P, Magni P, Daglia M Nutrients 14-Jan-2022
PMCID:PMC8778072
doi:10.3390/nu14020340
PMID:35057523
Jatrorrhizine: A Review of Sources, Pharmacology, Pharmacokinetics and Toxicity Zhong F, Chen Y, Chen J, Liao H, Li Y, Ma Y Front Pharmacol 13-Jan-2022
PMCID:PMC8793695
doi:10.3389/fphar.2021.783127
PMID:35095493
Essential Oils from Zingiber striolatum Diels Attenuate Inflammatory Response and Oxidative Stress through Regulation of MAPK and NF-κB Signaling Pathways Huang Z, Xie L, Xu Y, Zhao K, Li X, Zhong J, Lu Y, Xu X, Goodin S, Zhang K, Zhang L, Li C, Zheng X Antioxidants (Basel) 19-Dec-2021
PMCID:PMC8698606
doi:10.3390/antiox10122019
PMID:34943122
Cameroonian Spice Extracts Modulate Molecular Mechanisms Relevant to Cardiometabolic Diseases in SW 872 Human Liposarcoma Cells Atchan Nwakiban AP, Passarelli A, Da Dalt L, Olivieri C, Demirci TN, Piazza S, Sangiovanni E, Carpentier-Maguire E, Martinelli G, Shivashankara ST, Manjappara UV, Tchamgoue AD, Agbor GA, Kuiate JR, Daglia M, Dell’Agli M, Magni P Nutrients 26-Nov-2021
PMCID:PMC8706885
doi:10.3390/nu13124271
PMID:34959824

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
(+)-Norpurpureine 15286670 Click to see COC1=C(C=C2C(=C1)CC3C4=C(CCN3)C(=C(C(=C24)OC)OC)OC)OC 371.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(12S)-17,18,19-trimethoxy-13,13-dimethyl-5,7-dioxa-13-azoniapentacyclo[10.7.1.02,10.04,8.016,20]icosa-1(19),2,4(8),9,16(20),17-hexaene 101731569 Click to see C[N+]1(CCC2=C3C1CC4=CC5=C(C=C4C3=C(C(=C2OC)OC)OC)OCO5)C 384.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
(12S)-17,18,19-trimethoxy-5,7-dioxa-13-azapentacyclo[10.7.1.02,10.04,8.016,20]icosa-1(19),2,4(8),9,16(20),17-hexaene 163009713 Click to see COC1=C(C(=C2C3=CC4=C(C=C3CC5C2=C1CCN5)OCO4)OC)OC 355.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(12S)-18,19-dimethoxy-5,7-dioxa-13-azapentacyclo[10.7.1.02,10.04,8.016,20]icosa-1(20),2,4(8),9,16,18-hexaene 14395308 Click to see COC1=C(C2=C3C(CC4=CC5=C(C=C42)OCO5)NCCC3=C1)OC 325.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(6aS)-1,2-dimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-10,11-diol 101426476 Click to see COC1=C(C2=C3C(CC4=C2C(=C(C=C4)O)O)NCCC3=C1)OC 313.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(6aS)-1,2,3,10-tetramethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-11-ol 163036988 Click to see COC1=C(C2=C(CC3C4=C(CCN3)C(=C(C(=C42)OC)OC)OC)C=C1)O 357.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(6aS)-1,2,3,10-tetramethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-9-ol 101426478 Click to see COC1=C(C=C2CC3C4=C(CCN3)C(=C(C(=C4C2=C1)OC)OC)OC)O 357.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(6aS)-1,2,3,9,10-pentamethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline 15726908 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2OC)OC)OC)OC)OC 385.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(6aS)-1,2,3,9,10-pentamethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium 101731567 Click to see C[N+]1(CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2OC)OC)OC)OC)OC)C 400.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
(6As)-11-hydroxy-1,2,10-trimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinolinium 161487 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC)C 356.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
[6aS,(+)]-5,6,6a,7-Tetrahydro-1,2,9,10-tetramethoxy-4H-dibenzo[de,g]quinoline 11348415 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)OC)NCCC3=C1)OC 341.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
1,10-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,9-diol 248507 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)O 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
1,10-Dimethoxy-6a-alpha-noraporphine-2,9-diol 628557 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C(=C(C=C4CCN3)O)OC)O 313.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
1,2-dimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-10,11-diol 90863813 Click to see COC1=C(C2=C3C(CC4=C2C(=C(C=C4)O)O)NCCC3=C1)OC 313.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
1,2-Methylenedioxy-9-hydroxynoraporphine 3462224 Click to see C1CNC2CC3=C(C=CC(=C3)O)C4=C2C1=CC5=C4OCO5 281.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
1,2-Methylenedioxy-9-methoxynoraporphine 431059 Click to see COC1=CC2=C(C=C1)C3=C4C(C2)NCCC4=CC5=C3OCO5 295.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
1,2-Methylenedioxynoraporphine 3462225 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
1,2,10-Trimethoxy-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinolin-9-ol 267400 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
1,2,3,10-tetramethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-9-ol 162922313 Click to see COC1=C(C=C2CC3C4=C(CCN3)C(=C(C(=C4C2=C1)OC)OC)OC)O 357.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
16-Methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-18-ol 14604488 Click to see COC1=CC2=C(C(=C1)O)C3=C4C(C2)NCCC4=CC5=C3OCO5 311.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
17,18,19-Trimethoxy-5,7-dioxa-13-azapentacyclo[10.7.1.02,10.04,8.016,20]icosa-1(19),2,4(8),9,16(20),17-hexaene 163009712 Click to see COC1=C(C(=C2C3=CC4=C(C=C3CC5C2=C1CCN5)OCO4)OC)OC 355.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
18,19-Dimethoxy-5,7-dioxa-13-azapentacyclo[10.7.1.02,10.04,8.016,20]icosa-1(19),2,4(8),9,16(20),17-hexaen-17-ol 75968593 Click to see COC1=C2C3=CC4=C(C=C3CC5C2=C(CCN5)C(=C1OC)O)OCO4 341.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
2,10-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,9-diol 98369 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
4,15,16-Trimethoxy-10-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(16),2,4,6,13(17),14-hexaen-3-ol 5320211 Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)OC)C=C1)O 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Anolobine 164710 Click to see C1CNC2CC3=C(C=CC(=C3)O)C4=C2C1=CC5=C4OCO5 281.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Anonaine 160597 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Boldine 10154 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)O 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
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/J.PHYTOCHEM.2006.07.011
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/J.PHYTOCHEM.2006.07.011
Corytuberine, pentahydrate 347379 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Fissistigine A 14604489 Click to see COC1=CC2=C(C(=C1)O)C3=C4C(C2)NCCC4=CC5=C3OCO5 311.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Glaucine 16754 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC 355.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Laurolitsine 22179 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C(=C(C=C4CCN3)O)OC)O 313.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Laurotetanine 31415 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Magnoflorine 73337 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C 342.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
N-Methyllaurotetanine; NSC 247506; NSC 247564 631015 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC 341.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Norglaucin 30835 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)OC)NCCC3=C1)OC 341.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Norisocorydine 12313549 Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)OC)C=C1)O 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Nornantenine 3084228 Click to see COC1=C(C2=C3C(CC4=CC5=C(C=C42)OCO5)NCCC3=C1)OC 325.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Norpurpureine 98472 Click to see COC1=C(C=C2C(=C1)CC3C4=C(CCN3)C(=C(C(=C24)OC)OC)OC)OC 371.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Purpureine 98473 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2OC)OC)OC)OC)OC 385.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
S-(+)-3-hydroxynornantenine 52943336 Click to see COC1=C2C3=CC4=C(C=C3CC5C2=C(CCN5)C(=C1OC)O)OCO4 341.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
S-(+)-N-methylcorydine 52949574 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC)C 356.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
Xanthoplanine 14262868 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC)C 356.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
Michelalbine 10378981 Click to see C1CNC2C(C3=CC=CC=C3C4=C2C1=CC5=C4OCO5)O 281.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Norushinsunine 5319820 Click to see C1CNC2C(C3=CC=CC=C3C4=C2C1=CC5=C4OCO5)O 281.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
> Alkaloids and derivatives / Pavine alkaloids
(-)-Norargemonine 288121 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)OC 341.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(1S,9S)-5,12-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene-4,13-diol 12300156 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(1S,9S)-5,12,13-trimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaen-4-ol 10882393 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)OC 341.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Bisnorargemonine 288120 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
> Alkaloids and derivatives / Proaporphines
(+)-Stepharine 193686 Click to see COC1=C(C2=C3C(CC24C=CC(=O)C=C4)NCCC3=C1)OC 297.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Glaziovina 73426 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)O)OC 297.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Glaziovine 65631 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)O)OC 297.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Stepharine 98455 Click to see COC1=C(C2=C3C(CC24C=CC(=O)C=C4)NCCC3=C1)OC 297.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Suavedol 442245 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)O)OC 297.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
2,10,11-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-3-ol 12309269 Click to see COC1=C(C=C2CN3CCC4=CC(=C(C=C4C3CC2=C1)OC)O)OC 341.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
CID 12305144 12305144 Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=CC(=C(C=C4C2)OC)O)O)OC 342.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
Discretine 821491 Click to see COC1=C(C=C2CN3CCC4=CC(=C(C=C4C3CC2=C1)OC)O)OC 341.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Palmatine 19009 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)OC)OC 352.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
Phellodendrine 3081405 Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=CC(=C(C=C4C2)OC)O)O)OC 342.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
Stepharanine 10358881 Click to see COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC(=C(C4=C3)OC)O)O 324.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Tyramine 5610 Click to see C1=CC(=CC=C1CCN)O 137.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
4-Hydroxyphenylacetaldehyde 440113 Click to see C1=CC(=CC=C1CC=O)O 136.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
> Benzenoids / Benzene and substituted derivatives / Phenylpyruvic acid derivatives
4-Hydroxyphenylpyruvic acid 979 Click to see C1=CC(=CC=C1CC(=O)C(=O)O)O 180.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
> Benzenoids / Phenols / Benzenediols / Catechols / Catecholamines and derivatives
Dopamine 681 Click to see C1=CC(=C(C=C1CCN)O)O 153.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Excisanin H 10066342 Click to see CC1(CCC(C23C1CC(C45C2CCC(C4(OC3)O)C(=C)C5=O)O)O)C 348.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1989.9697790
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1989.9697790
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.1989.9697790
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1080/10412905.1989.9697790
> Organoheterocyclic compounds / Dihydroisoquinolines
6,7-Dimethoxy-3,4-dihydroisoquinoline 30058 Click to see COC1=C(C=C2C=NCCC2=C1)OC 191.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
Pycnarrhine 20056242 Click to see C[N+]1=CC2=CC(=C(C=C2CC1)OC)O 192.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
> Organoheterocyclic compounds / Isoquinolines and derivatives
2-Hydroxy-3,10-dimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-11-one 101731566 Click to see COC1=CC2=CN3CCC4=CC(=C(C=C4C3=CC2=CC1=O)O)OC 323.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
6,7-Dimethoxyisoquinoline 177578 Click to see COC1=C(C=C2C=NC=CC2=C1)OC 189.21 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(+)-O-Methylarmepavine 11067397 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC)OC)OC 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(1R)-1-[(4-hydroxyphenyl)methyl]-7-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-8-ol 101677941 Click to see C[N+]1(CCC2=C(C1CC3=CC=C(C=C3)O)C(=C(C=C2)OC)O)C 314.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
(1S)-1-[(3-hydroxy-4-methoxyphenyl)methyl]-7-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol 9862290 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)OC)O 329.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(1S)-1-[(4-hydroxyphenyl)methyl]-7-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-8-ol 173713 Click to see C[N+]1(CCC2=C(C1CC3=CC=C(C=C3)O)C(=C(C=C2)OC)O)C 314.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
(1S)-5,6,7-trimethoxy-1-[(4-methoxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinoline 162906358 Click to see COC1=CC=C(C=C1)CC2C3=CC(=C(C(=C3CCN2)OC)OC)OC 343.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(1S)-6-methoxy-1-[(4-methoxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinolin-7-ol 24944443 Click to see COC1=CC=C(C=C1)CC2C3=CC(=C(C=C3CCN2)OC)O 299.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(1S)-6,7-dimethoxy-1-[(4-methoxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinolin-5-ol 162872722 Click to see COC1=CC=C(C=C1)CC2C3=CC(=C(C(=C3CCN2)O)OC)OC 329.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(6R)-4-methoxy-6-[(4-methoxyphenyl)methyl]-6,7,8,9-tetrahydro-[1,3]dioxolo[4,5-f]isoquinoline 162979113 Click to see COC1=CC=C(C=C1)CC2C3=CC(=C4C(=C3CCN2)OCO4)OC 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(R)-Coclaurine 440989 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O 285.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(R)-N-Methylcoclaurine 440595 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC 299.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(R)-Reticuline 440586 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(S)-3'-Hydroxy-N-methylcoclaurine 440591 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)O)O)O)OC 315.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
(S)-Laudanine 821396 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)OC)OC 343.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(S)-N-Methylcoclaurine 440584 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC 299.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
(S)-Norcoclaurine 440927 Click to see C1CNC(C2=CC(=C(C=C21)O)O)CC3=CC=C(C=C3)O 271.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
1-[(3-hydroxy-4-methoxyphenyl)methyl]-7-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol 74218772 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)OC)O 329.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
1-[(3-hydroxy-4-methoxyphenyl)methyl]-7-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-6-ol 12144635 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)OC)O)C 344.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
1-[[4-[2-Hydroxy-5-[(7-hydroxy-6-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl]phenoxy]phenyl]methyl]-6-methoxy-1,2,3,4-tetrahydroisoquinolin-7-ol 13895817 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CCN5)OC)O)O)O 568.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
1,2-Dehydroreticuline 440930 Click to see C[N+]1=C(C2=CC(=C(C=C2CC1)OC)O)CC3=CC(=C(C=C3)OC)O 328.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
4-Methoxy-6-[(4-methoxyphenyl)methyl]-6,7,8,9-tetrahydro-[1,3]dioxolo[4,5-f]isoquinoline 101426481 Click to see COC1=CC=C(C=C1)CC2C3=CC(=C4C(=C3CCN2)OCO4)OC 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
5,6,7-Trimethoxy-1-[(4-methoxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinoline 157218 Click to see COC1=CC=C(C=C1)CC2C3=CC(=C(C(=C3CCN2)OC)OC)OC 343.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
6-Methoxy-1-[(4-methoxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinolin-7-ol 487554 Click to see COC1=CC=C(C=C1)CC2C3=CC(=C(C=C3CCN2)OC)O 299.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
6,7-Dimethoxy-1-[(4-methoxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinolin-5-ol 157209 Click to see COC1=CC=C(C=C1)CC2C3=CC(=C(C(=C3CCN2)O)OC)OC 329.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Coclaurine 160487 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O 285.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
Codamine 20056510 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)O)OC 343.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Csh 068 259676 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC)OC)OC 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
dl-Codamine 89421 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)O)OC 343.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Juzirine 3085285 Click to see COC1=C(C=C2C(=C1)C=CN=C2CC3=CC=C(C=C3)O)O 281.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Laudanine 92732 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)OC)OC 343.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Lindoldhamine (R,R) 10370752 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CCN5)OC)O)O)O 568.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Longifolonine 442312 Click to see COC1=C(C=C2C(=C1)CCN=C2C(=O)C3=CC=C(C=C3)O)O 297.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Lotusine 5274587 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)OC)O)C 314.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
Machiline 281691 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O 285.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
N-Methylcoclaurine 2752274 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC 299.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
O-Methylarmepavine, (R)- 821338 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC)OC)OC 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Reticulin 10233 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Reticuline 439653 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
Tembetarine 167718 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC)C 344.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
2,10,11-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 10246448 Click to see COC1=CC2=CC3=C4C=C(C(=O)C=C4CCN3C=C2C=C1OC)OC 337.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 10065647 Click to see COC1=C(C2=CN3CCC4=CC(=O)C(=CC4=C3C=C2C=C1)OC)OC 337.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010
Thalifoline 89048 Click to see CN1CCC2=CC(=C(C=C2C1=O)O)OC 207.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.07.011
> Organoheterocyclic compounds / Tetrahydroisoquinolines
Litcubine 85243417 Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)O)OC 328.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.12.010

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