Database	ID/link to page
World Flora Online	wfo-0000970374
Tropicos	1400017
KEW	urn:lsid:ipni.org:names:975426-1
The Plant List	kew-8768
Open Tree Of Life	942012
NCBI Taxonomy	63089
IUCN Red List	200681
IPNI	975426-1
iNaturalist	437275
GBIF	3659006
EOL	6874710
Wikipedia	Ancistrocladus_korupensis
CMAUP	NPO2073

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

Naphthylisoquinoline alkaloids: novel agents against the causative pathogens of eumycetoma and actinomycetoma—en route to broad-spectrum antimycetomal drugs

Khalid SA, Abd Algaffar S, Tajuddeen N, Lombe BK, Bringmann G

Antimicrob Agents Chemother

11-Apr-2024

PMCID:	PMC11064494
doi:	10.1128/aac.01612-23
PMID:	38602413

On the Efficiency of the Density Functional Theory (DFT)-Based Computational Protocol for 1H and 13C Nuclear Magnetic Resonance (NMR) Chemical Shifts of Natural Products: Studying the Accuracy of the pecS-n (n = 1, 2) Basis Sets

Rusakov YY, Semenov VA, Rusakova IL

Int J Mol Sci

27-Sep-2023

PMCID:	PMC10572908
doi:	10.3390/ijms241914623
PMID:	37834068

Role of phytocompounds as the potential anti-viral agent: an overview

Mohanty SS, Sahoo CR, Paidesetty SK, Padhy RN

Naunyn Schmiedebergs Arch Pharmacol

09-May-2023

PMCID:	PMC10169142
doi:	10.1007/s00210-023-02517-2
PMID:	37160482

Alkaloids as potential antivirals. A comprehensive review

Faisal S, Badshah SL, Kubra B, Emwas AH, Jaremko M

Nat Prod Bioprospect

04-Jan-2023

PMCID:	PMC9812014
doi:	10.1007/s13659-022-00366-9
PMID:	36598588

Biosynthesis Investigations of Terpenoid, Alkaloid, and Flavonoid Antimicrobial Agents Derived from Medicinal Plants

Huang W, Wang Y, Tian W, Cui X, Tu P, Li J, Shi S, Liu X

Antibiotics (Basel)

09-Oct-2022

PMCID:	PMC9598646
doi:	10.3390/antibiotics11101380
PMID:	36290037

The naturally‐derived alkaloids as a potential treatment for COVID‐19: A scoping review

Gonzalez BL, de Oliveira NC, Ritter MR, Tonin FS, Melo EB, Sanches AC, Fernandez‐Llimos F, Petruco MV, de Mello JC, Chierrito D, de Medeiros Araújo DC

Phytother Res

30-Mar-2022

PMCID:	PMC9111026
doi:	10.1002/ptr.7442
PMID:	35355337

Potential Antiviral Action of Alkaloids

Abookleesh FL, Al-Anzi BS, Ullah A

Molecules

28-Jan-2022

PMCID:	PMC8839337
doi:	10.3390/molecules27030903
PMID:	35164173

In Vitro Selective Antibacterial and Antiproliferative Effects of Ethanolic Extracts from Cambodian and Philippine Plants Used in Folk Medicine for Diarrhea Treatment

Kudera T, Fiserova B, Korytakova M, Doskocil I, Salmonova H, Tulin EE, Nguon S, Bande MM, Kokoska L

Front Pharmacol

26-Nov-2021

PMCID:	PMC8661004
doi:	10.3389/fphar.2021.746808
PMID:	34899301

African and Asian Medicinal Plants as a Repository for Prospective Antiviral Metabolites Against HIV-1 and SARS CoV-2: A Mini Review

Anywar G, Akram M, Chishti MA

Front Pharmacol

25-Aug-2021

PMCID:	PMC8424073
doi:	10.3389/fphar.2021.703837
PMID:	34512337

Anti-HIV reverse transcriptase plant polyphenolic natural products with in silico inhibitory properties on seven non-structural proteins vital in SARS-CoV-2 pathogenesis

de Leon VN, Manzano JA, Pilapil DY IV, Fernandez RA, Ching JK, Quimque MT, Agbay JC, Notarte KI, Macabeo AP

J Genet Eng Biotechnol

16-Jul-2021

PMCID:	PMC8284420
doi:	10.1186/s43141-021-00206-2
PMID:	34272647

New species and records of Trichoderma isolated as mycoparasites and endophytes from cultivated and wild coffee in Africa

del Carmen H. Rodríguez M, Evans HC, de Abreu LM, de Macedo DM, Ndacnou MK, Bekele KB, Barreto RW

Sci Rep

11-Mar-2021

PMCID:	PMC7952591
doi:	10.1038/s41598-021-84111-1
PMID:	33707461

Emerging paradigms of viral diseases and paramount role of natural resources as antiviral agents

Sagaya Jansi R, Khusro A, Agastian P, Alfarhan A, Al-Dhabi NA, Arasu MV, Rajagopal R, Barcelo D, Al-Tamimi A

Sci Total Environ

07-Nov-2020

PMCID:	PMC7833357
doi:	10.1016/j.scitotenv.2020.143539
PMID:	33234268

Bioactive Natural Antivirals: An Updated Review of the Available Plants and Isolated Molecules

Mohan S, Elhassan Taha MM, Makeen HA, Alhazmi HA, Al Bratty M, Sultana S, Ahsan W, Najmi A, Khalid A

Molecules

22-Oct-2020

PMCID:	PMC7659943
doi:	10.3390/molecules25214878
PMID:	33105694

Antimicrobial Importance of Medicinal Plants in Nigeria

Ugboko HU, Nwinyi OC, Oranusi SU, Fatoki TH, Omonhinmin CA

ScientificWorldJournal

22-Sep-2020

PMCID:	PMC7528132
doi:	10.1155/2020/7059323
PMID:	33029108

Structure-Activity-Relationship and Mechanistic Insights for Anti-HIV Natural Products

Kaur R, Sharma P, Gupta GK, Ntie-Kang F, Kumar D

Molecules

29-Apr-2020

PMCID:	PMC7249135
doi:	10.3390/molecules25092070
PMID:	32365518

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Methyl 4-hydroxy-3,5-dimethoxybenzoate	70164	Click to see COC1=CC(=CC(=C1O)OC)C(=O)OC	212.20	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
Justin C	10814927	Click to see CC(=O)OCC(CC1=CC(=C(C=C1)OC)OC)C(CC2=CC(=C(C(=C2)OC)O)OC)COC(=O)C	490.50	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Episyringaresinol	101663451	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	via CMAUP database
4-[(3aR,6S,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol	17750970	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	via CMAUP database
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 / Prenol lipids / Terpene lactones / Quassinoids
(1S,2S,6R,7S,8R,12R,14S,15S,19S,20R)-7,10-dihydroxy-17-methoxy-7,15,19,20-tetramethyl-3,5,11-trioxapentacyclo[10.7.1.02,6.08,20.014,19]icos-16-en-18-one	101921953	Click to see CC1C=C(C(=O)C2(C1CC3C4(C2C5C(C(C4CC(O3)O)(C)O)OCO5)C)C)OC	408.50	unknown	https://doi.org/10.1016/S0031-9422(00)95222-1
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
Theophylline	2153	Click to see CN1C2=C(C(=O)N(C1=O)C)NC=N2	180.16	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Naphthylisoquinolines
(1R,3R)-5-[3-[4-[(1S,3S)-6,8-dihydroxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-5-yl]-1-hydroxy-8-methoxy-6-methylnaphthalen-2-yl]-4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl]-1,2,3-trimethyl-3,4-dihydro-1H-isoquinoline-6,8-diol	162850040	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(N(C(C8=C(C=C7O)O)C)C)C)O	770.90	unknown	https://doi.org/10.1016/S0040-4020(97)00502-4
(1R,3R)-5-[3-[4-[(1S,3S)-6,8-dihydroxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-5-yl]-1-hydroxy-8-methoxy-6-methylnaphthalen-2-yl]-4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-6,8-diol	44592719	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(NC(C8=C(C=C7O)O)C)C)O	756.90	unknown	https://doi.org/10.1016/S0003-2670(97)00141-4 https://doi.org/10.1002/(SICI)1099-1565(199705)8:3<120::AID-PCA345>3.0.CO;2-4 https://doi.org/10.1021/JM00116A011 https://doi.org/10.1016/0021-9673(94)00923-6 https://doi.org/10.1300/J044V03N02_07 https://doi.org/10.1021/JM00038A003 https://doi.org/10.1007/BF02908220
(1R,3R)-5-[4-hydroxy-3-[1-hydroxy-4-[(3R)-6-hydroxy-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-5-yl]-8-methoxy-6-methylnaphthalen-2-yl]-5-methoxy-7-methylnaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-6,8-diol	392426	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(NC(C8=C(C=C7O)OC)C)C)O	770.90	unknown	https://doi.org/10.1016/S0040-4020(97)00502-4 https://doi.org/10.1021/NP9700679
(1R,3S)-5-(4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl)-1,2,3-trimethyl-3,4-dihydro-1H-isoquinoline-6,8-diol	10069155	Click to see CC1CC2=C(C(=CC(=C2C(N1C)C)O)O)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C	393.50	unknown	https://doi.org/10.1021/JO00100A042 https://doi.org/10.1016/0021-9673(94)00923-6
(1R)-5-(4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-6,8-diol	392423	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C	379.40	unknown	https://doi.org/10.1016/0021-9673(94)00923-6 https://doi.org/10.1021/JO00100A042
(1S,3S)-5-(4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-6,8-diol	101060354	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C	379.40	unknown	https://doi.org/10.1021/JO00100A042
(1S,3S)-5-(5-hydroxy-4-methoxy-7-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-6-ol	162883093	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)O)C3=C4C=C(C=C(C4=C(C=C3)OC)O)C	393.50	unknown	https://doi.org/10.1016/S0040-4020(97)00502-4
(1S,3S)-5-[4-hydroxy-3-[1-hydroxy-4-[(1S,3R)-6-hydroxy-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-5-yl]-8-methoxy-6-methylnaphthalen-2-yl]-5-methoxy-7-methylnaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-6,8-diol	163032469	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(NC(C8=C(C=C7O)OC)C)C)O	770.90	unknown	https://doi.org/10.1016/S0040-4020(97)00502-4
(1S,3S)-5-[4-hydroxy-3-[1-hydroxy-4-[(3R)-6-hydroxy-8-methoxy-1,3-dimethyl-3,4-dihydroisoquinolin-5-yl]-8-methoxy-6-methylnaphthalen-2-yl]-5-methoxy-7-methylnaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-6,8-diol	163046853	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(N=C(C8=C(C=C7O)OC)C)C)O	768.90	unknown	https://doi.org/10.1016/S0040-4020(97)00502-4
(1S)-1,2,3,4-Tetrahydro-8-methoxy-1alpha,3beta-dimethyl-5-[(aR)-4,5-dimethoxy-2-methyl-1-naphthalenyl]isoquinoline-6-ol	4332940	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC	407.50	unknown	via CMAUP database
(1S)-5-[3-[4-[(1S)-6,8-dihydroxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-5-yl]-1-hydroxy-8-methoxy-6-methylnaphthalen-2-yl]-4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-6,8-diol	5459215	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(NC(C8=C(C=C7O)O)C)C)O	756.90	unknown	https://doi.org/10.1016/S0003-2670(97)00141-4 https://doi.org/10.1021/JM00038A003 https://doi.org/10.1016/0021-9673(94)00923-6 https://doi.org/10.1021/JM00116A011 https://doi.org/10.1002/(SICI)1099-1565(199705)8:3<120::AID-PCA345>3.0.CO;2-4
(2R,3S,4S,5S,6R)-2-[[(3R)-7-(4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-3,4-dihydroisoquinolin-6-yl]oxy]-6-methyloxane-3,4,5-triol	21583389	Click to see CC1CC2=CC(=C(C(=C2C(=N1)C)OC)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C)OC5C(C(C(C(O5)C)O)O)O	537.60	unknown	https://doi.org/10.1016/S0040-4020(97)00502-4
(3R)-5-[4-hydroxy-3-[1-hydroxy-4-[(3R)-6-hydroxy-8-methoxy-1,3-dimethyl-3,4-dihydroisoquinolin-7-yl]-8-methoxy-6-methylnaphthalen-2-yl]-5-methoxy-7-methylnaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-6,8-diol	135958385	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C(C=C8CC(N=C(C8=C7OC)C)C)O)O	768.90	unknown	https://doi.org/10.1016/S0960-894X(98)00304-7
(3R)-7-(4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-3,4-dihydro-2H-isoquinolin-6-one	5469776	Click to see CC1CC2=CC(=O)C(=C(C2=C(N1)C)OC)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C	391.50	unknown	https://doi.org/10.1016/S0040-4020(97)00502-4
(3R)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol	375943	Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O	377.50	unknown	https://doi.org/10.1016/S0031-9422(00)97574-5
(3R)-7-[3-[4-[(1R,3R)-6,8-dihydroxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-5-yl]-1-hydroxy-8-methoxy-6-methylnaphthalen-2-yl]-4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl]-8-methoxy-1,3-dimethyl-3,4-dihydro-2H-isoquinolin-6-one	5481816	Click to see CC1CC2=CC(=O)C(=C(C2=C(N1)C)OC)C3=C4C=C(C=C(C4=C(C(=C3)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(NC(C8=C(C=C7O)O)C)C)O)O)OC)C	768.90	unknown	https://doi.org/10.1016/S0960-894X(98)00304-7
5-[3-[4-(6,8-dihydroxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-5-yl)-1-hydroxy-8-methoxy-6-methylnaphthalen-2-yl]-4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl]-1,2,3-trimethyl-3,4-dihydro-1H-isoquinoline-6,8-diol	4187	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(N(C(C8=C(C=C7O)O)C)C)C)O	770.90	unknown	https://doi.org/10.1021/NP9700679
5-[3-[4-(6,8-Dihydroxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-5-yl)-1-hydroxy-8-methoxy-6-methylnaphthalen-2-yl]-4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-6,8-diol	4185	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(NC(C8=C(C=C7O)O)C)C)O	756.90	unknown	https://doi.org/10.1021/JM00038A003 https://doi.org/10.1016/0021-9673(94)00923-6 https://doi.org/10.1016/S0003-2670(97)00141-4 https://doi.org/10.1663/0013-0001(2006)60[386:NOEP]2.0.CO;2 https://doi.org/10.1021/NP9700679 https://doi.org/10.1300/J044V03N02_07 https://doi.org/10.1002/(SICI)1099-1565(199705)8:3<120::AID-PCA345>3.0.CO;2-4 https://doi.org/10.1021/JM00116A011
5-[4'-(6,8-Dihydroxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-5-yl)-1,1'-dihydroxy-8,8'-dimethoxy-6,6'-dimethyl[2,2'-binaphthalen]-4-yl]-8-methoxy-1,3-dimethyl-3,4-dihydroisoquinolin-6(2H)-one	5469775	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=CC(=C6C=C(C=C(C6=C5O)OC)C)C7=C8CC(NC(=C8C(=CC7=O)OC)C)C	768.90	unknown	https://doi.org/10.1021/NP9700679 https://doi.org/10.1016/S0040-4020(97)00502-4
Ancistrobertsonine C	10410728	Click to see CC1CC2=C(C(=CC(=C2C(N1C)C)OC)OC)C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C	435.60	unknown	via CMAUP database
Ancistrobertsonine D	10476498	Click to see CC1CC2=CC(=C(C(=C2C(N1)C)OC)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O	407.50	unknown	via CMAUP database
Ancistrobrevine A	443776	Click to see CC1CC2=CC(=C(C(=C2C(N1C)C)OC)C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C)OC	435.60	unknown	via CMAUP database
Ancistrocladine	161741	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC	407.50	unknown	https://doi.org/10.1016/S0031-9422(00)97574-5
Ancistrocline	158203	Click to see CC1CC2=C(C(=CC(=C2C(N1C)C)OC)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC	421.50	unknown	via CMAUP database
Ancistrocongoline A	392424	Click to see CC1CC2=C(C(=CC(=C2C(N1C)C)O)O)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C	393.50	unknown	https://doi.org/10.1016/0021-9673(94)00923-6 https://doi.org/10.1021/JO00100A042
Ancistrotectorine	179169	Click to see CC1CC2=CC(=C(C(=C2C(N1C)C)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O)OC	421.50	unknown	via CMAUP database
Dioncophylline A	443773	Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O	377.50	unknown	https://doi.org/10.1016/S0031-9422(00)97574-5
Korundamine A	479267	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C(C=C8CC(N=C(C8=C7OC)C)C)O)O	768.90	unknown	https://doi.org/10.1016/S0960-894X(98)00304-7
Korupensamine A	392421	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C	379.40	unknown	https://doi.org/10.1016/0021-9673(94)00923-6 https://doi.org/10.1016/S0040-4020(97)00502-4 https://doi.org/10.1021/JO00100A042
Korupensamine C	392422	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C	393.50	unknown	https://doi.org/10.1016/0021-9673(94)00923-6 https://doi.org/10.1021/JO00100A042
Korupensamine E	392425	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)O)C3=C4C=C(C=C(C4=C(C=C3)OC)O)C	393.50	unknown	https://doi.org/10.1021/NP9700679 https://doi.org/10.1016/S0040-4020(97)00502-4
Michellamine A	454909	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(NC(C8=C(C=C7O)O)C)C)O	756.90	unknown	https://doi.org/10.1021/NP9700679 https://doi.org/10.1021/JM00038A003
Michellamine A	453654	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(NC(C8=C(C=C7O)O)C)C)O	756.90	unknown	via CMAUP database
Michellamine D	468217	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(NC(C8=C(C=C7O)OC)C)C)O	770.90	unknown	https://doi.org/10.1021/NP9700679
Michellamine E	10350236	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(N(C(C8=C(C=C7O)O)C)C)C)O	770.90	unknown	https://doi.org/10.1021/NP9700679
Michellamine F	392428	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(N=C(C8=C(C=C7O)OC)C)C)O	768.90	unknown	https://doi.org/10.1021/NP9700679
N-Methyl Michellamine B	392427	Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(N(C(C8=C(C=C7O)O)C)C)C)O	770.90	unknown	https://doi.org/10.1016/S0040-4020(97)00502-4 https://doi.org/10.1021/NP9700679
Yaoundamine A	392429	Click to see CC1CC2=CC(=C(C(=C2C(=N1)C)OC)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C)O	391.50	unknown	https://doi.org/10.1016/S0040-4020(97)00502-4
Yaoundamine B	392430	Click to see CC1CC2=CC(=C(C(=C2C(=N1)C)OC)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C)OC5C(C(C(C(O5)C)O)O)O	537.60	unknown	https://doi.org/10.1016/S0040-4020(97)00502-4
> Organoheterocyclic compounds / Tetrahydroisoquinolines
Gentrymine A	392419	Click to see CC1CC2=C(C(N1C)C)C(=CC(=C2)OC)O	221.29	unknown	https://doi.org/10.1016/00404-0399(50)0884F-
Gentrymine B	392420	Click to see CC1CC2=C(C([N+]1(C)C)C)C(=CC(=C2)OC)O	236.33	unknown	https://doi.org/10.1016/00404-0399(50)0884F-
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-Methoxycoumarin	10748	Click to see COC1=CC2=C(C=C1)C=CC(=O)O2	176.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechin	73160	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-olate luteolin-7-olate(1-)	25201972	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)[O-]	285.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Rhamnetin-3-olate	54758607	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)[O-])C3=CC(=C(C=C3)O)O)O	315.25	unknown	via CMAUP database

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Ancistrocladus korupensis

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