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Chromolaena laevigata

Chromolaena laevigata - 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 UUID643fcf7991892973171391
Scientific name Chromolaena laevigata
Authority (Lam.) R.M.King & H.Rob.
First published in Phytologia 20(3): 202 (1970)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eupatorium laevigatum Griseb. Abh. Königl. Ges. Wiss. Göttingen 19: 167 (1874)
Eupatorium australe Thunb. Pl. Bras. 2: 26. 1818
Eupatorium laevigatum f. lilacinum Kuntze Revis. Gen. Pl. 3[3]: 147 (1898)
Eupatorium psiadiaefolium DC. Prodr. 5: 144. 1836.
Osmia propinqua Sch.Bip. Jahresber. Pollichia 22-24: 252 (1866)
Eupatorium laevigatum var. longepetiolatum Hassl. Repert. Spec. Nov. Regni Veg. 14: 282 (1916)
Eupatorium alternans DC. Prodr. 5: 144 (1836)
Eupatorium resinosum Poepp. & Endl. Nov. Gen. Sp. Pl. iii. 54.
Chrysocoma punctata Vell. Florae Fluminensis 313 1825
Eupatorium laevigatum var. arenarium Baker Fl. Bras. 6(2): 287 (1876)
Osmia alternans Sch.Bip. Jahresber. Pollichia 22-24: 252 (1866)
Chrysocoma punctata Steud. Nomencl. Bot. 1: 358 (1840)
Eupatorium psiadiifolium var. latifolium DC. Prodr. 5: 145 (1836)
Eupatorium laevigatum f. albiflorum Kuntze Revis. Gen. Pl. 3[3]: 147 (1898)
Eupatorium laevigatum f. flavidum Kuntze Revis. Gen. Pl. 3[3]: 147 (1898)
Eupatorium osseanum Sch.Bip. ex Baker Fl. Bras. 6(2): 287 (1876)
Eupatorium propinquum DC. Prodr. 5: 146 (1836)
Eupatorium psiadiifolium DC. Prodr. 5: 146 (1836)
Eupatorium laevigatum Lam. Encycl. 2: 408 (1788)
Osmia laevigata Sch.Bip. Jahresber. Pollichia 22-24: 252 (1866)
Eupatorium laevigatum var. squamulosa Hieron. Bot. Jahrb. Syst. 22(4-5): 747 (1897)
Eupatorium laevigatum var. submembranacea Hieron. Bot. Jahrb. Syst. 22(4-5): 748 (1897)
Chromolaena laevigata var. arenaria (Baker) S.E.Freire & Ariza Fl. Vasc. Argent. 7(1): 335 (2014)
Chromolaena laevigata var. submembranacea (Hieron.) S.E.Freire & Ariza Fl. Vasc. Argent. 7(1): 336 (2014)

Common names Top

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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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Southeast
    • Northeastern U.S.A.
      • New York
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Trinidad-Tobago
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000090695
Tropicos 2711358
INPN 733075
KEW urn:lsid:ipni.org:names:57414-2
The Plant List gcc-46981
Open Tree Of Life 5739721
NCBI Taxonomy 1745036
IPNI 57414-2
iNaturalist 288987
GBIF 3087662
CMAUP NPO11000

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
Anti-Leishmania compounds can be screened using Leishmania spp. expressing red fluorescence (tdTomato) Cruz MG, Santi AM, de Morais-Teixeira E, Caldeira AS, de Siqueira EP, Oliveira E, Alves TM, Murta SM Antimicrob Agents Chemother 08-Dec-2023
PMCID:PMC10777850
doi:10.1128/aac.00509-23
PMID:38063403
Aspergillus flavus YRB2 from Thymelaea hirsuta (L.) Endl., a non-aflatoxigenic endophyte with ability to overexpress defense-related genes against Fusarium root rot of maize Rashad YM, Abdalla SA, Shehata AS BMC Microbiol 30-Sep-2022
PMCID:PMC9524039
doi:10.1186/s12866-022-02651-6
PMID:36175855
Pharmacology and Phytochemistry of Ecuadorian Medicinal Plants: An Update and Perspectives Armijos C, Ramírez J, Salinas M, Vidari G, Suárez AI Pharmaceuticals (Basel) 11-Nov-2021
PMCID:PMC8624270
doi:10.3390/ph14111145
PMID:34832927
Chromolaena laevigata (Asteraceae) as a source of endophytic non-aflatoxigenic Aspergillus flavus: chemical profile in different culture conditions and biological applications Balbinot RB, de Oliveira JA, Bernardi DI, Polli AD, Polonio JC, Cabral MR, Zanqueta ÉB, Endo EH, Meneguello JE, Cardoso RF, Azevedo JL, Dias Filho BP, Nakamura TU, do Carmo MR, Sarragiotto MH, Pamphile JA, Baldoqui DC Braz J Microbiol 30-Apr-2021
PMCID:PMC8324641
doi:10.1007/s42770-021-00502-6
PMID:33929720
Antimicrobial Potential of Essential Oils from Cerrado Plants against Multidrug−Resistant Foodborne Microorganisms de Jesus GS, Micheletti AC, Padilha RG, de Souza de Paula J, Alves FM, Leal CR, Garcez FR, Garcez WS, Yoshida NC Molecules 21-Jul-2020
PMCID:PMC7397120
doi:10.3390/molecules25143296
PMID:32708062
Improving classification of pollen grain images of the POLEN23E dataset through three different applications of deep learning convolutional neural networks Sevillano V, Aznarte JL PLoS One 14-Sep-2018
PMCID:PMC6138340
doi:10.1371/journal.pone.0201807
PMID:30216353
Chemical Composition, Antimicrobial and Antioxidant Activities of Essential Oils from Two Avicennia schaueriana Stapf & Leechm. Ex Moldenke (Acanthaceae) Populations Machado KN, Kaneko TM, Young MC, Murakami C, Cordeiro I, Moreno PR Medicines (Basel) 01-May-2017
PMCID:PMC5590062
doi:10.3390/medicines4020026
PMID:28930241
Feature Extraction and Machine Learning for the Classification of Brazilian Savannah Pollen Grains Gonçalves AB, Souza JS, da Silva GG, Cereda MP, Pott A, Naka MH, Pistori H PLoS One 08-Jun-2016
PMCID:PMC4898734
doi:10.1371/journal.pone.0157044
PMID:27276196
The Essential oil of<i>Eupatorium laevigatum</i> Alaide B. de Oliveira, Fernando Carazza, L. Scott Ramos, José Guilherme S. Maia Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1990.9697816
Notiz über ein neues Germacranolid aus <i>Chromolaena glaberrima</i> (DC) K. et R. Ferdinand Bohlmann, Lothar Fiedler Wiley 29-Jun-2007
doi:10.1002/CBER.19781110139
Isodaucane derivatives, norsesquiterpenes and clerodanes from chromolaena laevigata L.N. Misra, J. Jakupovic, F. Bohlmann, G. Schmeda-hirschmann Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)96789-4
Neue cadinen-derivate und andere inhaltsstoffe aus Chromolaena-arten Ferdinand Bohlmann, Christa Zdero, Robert M. King, Harold Robinson Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(79)80129-6

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
(+)-Elwesine 70697964 Click to see C1CC23CCN(C2CC1O)CC4=CC5=C(C=C34)OCO5 273.33 unknown via CMAUP database
(+)-epi-Vittatine 12304132 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown via CMAUP database
(11S,13beta,19S)-1,2-Didehydrocrinan-3alpha,11-diol 5282088 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown via CMAUP database
(1R,13S,15R,18R)-9,15-dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 92211489 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 331.40 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
11-Epicrinamine 5281172 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
11-O-Methylcrinamine 101493050 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)OC 315.40 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
Crinamin 73620 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
Crinine 398937 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown via CMAUP database
Hamayne 443670 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown via CMAUP database
Powellin 443669 Click to see COC1=C2CN3CCC4(C3CC(C=C4)O)C2=CC5=C1OCO5 301.34 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 / Galanthamine-type amaryllidaceae alkaloids
[(1S,12S,14R)-4-acetyl-9-methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-14-yl] acetate 21826143 Click to see CC(=O)N1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)OC(=O)C 357.40 unknown via CMAUP database
Epinorgalanthamine 443721 Click to see COC1=C2C3=C(CNCCC34C=CC(CC4O2)O)C=C1 273.33 unknown via CMAUP database
Galantamine 9651 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown via CMAUP database
Norgalanthamine 9838394 Click to see COC1=C2C3=C(CNCCC34C=CC(CC4O2)O)C=C1 273.33 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
(1S,17S,18S,19R)-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,15-tetraene-17,18-diol 7060909 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown via CMAUP database
[(1S,17S,18S,19S)-17-hydroxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,15-tetraen-18-yl] hexadecanoate 54764247 Click to see CCCCCCCCCCCCCCCC(=O)OC1C(C=C2CCN3C2C1C4=CC5=C(C=C4C3)OCO5)O 525.70 unknown via CMAUP database
Lycorine O1,O2-di-(beta-D-glucopyranoside) 101529183 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5OC6C(C(C(C(O6)CO)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)OCO4 611.60 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
Crinasiadine 442850 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC=C4NC3=O 239.23 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
Sekisanolin 5321780 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
16,19-Dimethoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(21),2,4(8),9,13,15,17,19-octaene 25051817 Click to see COC1=C2C=C3C4=CC5=C(C=C4CC[N+]3=CC2=C(C=C1)OC)OCO5 336.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Ethylparaben 8434 Click to see CCOC(=O)C1=CC=C(C=C1)O 166.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Aminobenzaldehyde 11158 Click to see C1=CC(=CC=C1C=O)N 121.14 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthols and derivatives
1-(2-Hydroxy-4,7-dimethylnaphthalen-1-yl)ethanone 85519538 Click to see CC1=CC2=C(C=C1)C(=CC(=C2C(=O)C)O)C 214.26 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(Z)-5-[(1R,2S,3R,4R,4aR,8aR)-3-acetyloxy-1,2,4a,5-tetramethyl-4-(2-methylpropoxy)-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-enoic acid 162854396 Click to see CC1C(C(C2(C(C1(C)CCC(=CC(=O)O)C)CCC=C2C)C)OCC(C)C)OC(=O)C 434.60 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
5-[3-Acetyloxy-1,2,4a,5-tetramethyl-4-(2-methylpropoxy)-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-enoic acid 162854395 Click to see CC1C(C(C2(C(C1(C)CCC(=CC(=O)O)C)CCC=C2C)C)OCC(C)C)OC(=O)C 434.60 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(5R,5aS)-1,5,8-trimethyl-4,5,5a,6-tetrahydrobenzo[e][1]benzofuran 163106147 Click to see CC1CC2=C(C(=CO2)C)C3=CC(=CCC13)C 214.30 unknown https://doi.org/10.1016/0031-9422(79)80129-6
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697816
1-Ethenyl-1,2-dimethyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane 5317024 Click to see CC(=C1CCC(C(C1)(C)C(=C)C)(C)C=C)C 218.38 unknown https://doi.org/10.1080/10412905.1990.9697816
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane 6432312 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697816
alpha-Curcumene 92139 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697816
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
beta-Cubebene 93081 Click to see CC1CCC(C2C13C2C(=C)CC3)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697816
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697816
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
Chromolaenin 11745938 Click to see CC1CC2=C(C(=CO2)C)C3=C1C=CC(=C3)C 212.29 unknown https://doi.org/10.1002/CBER.19781110139
Dehydrochromolaenin 12309959 Click to see CC1=CC2=C(C=C1)C(=CC3=C2C(=CO3)C)C 210.27 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(3S,3aR,8aR)-8a-methyl-8-oxo-3-propan-2-yl-1,2,3,3a,6,7-hexahydroazulene-5-carbaldehyde 11770398 Click to see CC(C)C1CCC2(C1C=C(CCC2=O)C=O)C 234.33 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
8-hydroxy-8a-methyl-3-propan-2-yl-2,3,3a,6,7,8-hexahydro-1H-azulene-5-carbaldehyde 14446663 Click to see CC(C)C1CCC2(C1C=C(CCC2O)C=O)C 236.35 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
8a-Methyl-8-oxo-3-propan-2-yl-1,2,3,3a,6,7-hexahydroazulene-5-carbaldehyde 14446657 Click to see CC(C)C1CCC2(C1C=C(CCC2=O)C=O)C 234.33 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
aphanamol II 44566761 Click to see CC(C)C1CCC2(C1C=C(CCC2O)C=O)C 236.35 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Lactiflorenol 102113807 Click to see CC(C)C1=CC2C(CCC2(C)O)C(=C)CC1 220.35 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,3aR,9bR)-3a-hydroxy-1,5,8-trimethyl-1,9b-dihydrobenzo[e][1]benzofuran-2-one 163043223 Click to see CC1C2C3=C(C=CC(=C3)C)C(=CC2(OC1=O)O)C 244.28 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
(1S,3aR,9bR)-3a-methoxy-1,5,8-trimethyl-1,9b-dihydrobenzo[e][1]benzofuran-2-one 162955827 Click to see CC1C2C3=C(C=CC(=C3)C)C(=CC2(OC1=O)OC)C 258.31 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
3a-Hydroxy-1,5,8-trimethyl-1,9b-dihydrobenzo[e][1]benzofuran-2-one 163043222 Click to see CC1C2C3=C(C=CC(=C3)C)C(=CC2(OC1=O)O)C 244.28 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
3a-Methoxy-1,5,8-trimethyl-1,9b-dihydrobenzo[e][1]benzofuran-2-one 162955826 Click to see CC1C2C3=C(C=CC(=C3)C)C(=CC2(OC1=O)OC)C 258.31 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / 1,3-dicarbonyl compounds / Beta-diketones
1-acetyl-4,7-dimethyl-3,4,4a,5,6,7,8,8a-octahydro-1H-naphthalen-2-one 101416430 Click to see CC1CCC2C(CC(=O)C(C2C1)C(=O)C)C 222.32 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(1R,5R,6S)-6-[(3S)-2-methyl-6-oxoheptan-3-yl]bicyclo[3.1.0]hexan-2-one 15954590 Click to see CC(C)C(CCC(=O)C)C1C2C1C(=O)CC2 222.32 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
6-(2-Methyl-6-oxoheptan-3-yl)bicyclo[3.1.0]hexan-2-one 73205688 Click to see CC(C)C(CCC(=O)C)C1C2C1C(=O)CC2 222.32 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
Chromolaevanedione 25084009 Click to see CC(C)C(CCC(=O)C)C1C2C1C(=O)CC2 222.32 unknown https://doi.org/10.1016/S0040-4020(01)96789-4
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(-)-8-Demethylmaritidine 443683 Click to see COC1=C(C=C2CN3CCC4(C3CC(C=C4)O)C2=C1)O 273.33 unknown via CMAUP database
(4aS,10bR)-Noroxomaritidine 11184826 Click to see COC1=C(C=C2CN3CCC4(C3CC(=O)C=C4)C2=C1)O 271.31 unknown via CMAUP database
1-Epideacetylbowdensine 443673 Click to see COC1=C2CN3CCC4(C3CCC(C4O)O)C2=CC5=C1OCO5 319.40 unknown via CMAUP database
1-Epijosephinine 70697961 Click to see CC(=O)OC1CCC2C3(C1O)CCN2CC4=CC5=C(C=C34)OCO5 331.40 unknown via CMAUP database
1-O-Acetylbulbisine 70698017 Click to see CC(=O)OC1C(CCC2C13CCN2CC4=C(C5=C(C=C34)OCO5)OC)O 361.40 unknown via CMAUP database
2-O-Acetylbulbisine 56928078 Click to see CC(=O)OC1CCC2C3(C1O)CCN2CC4=C(C5=C(C=C34)OCO5)OC 361.40 unknown via CMAUP database
2-O-Acetylcrinamabine 70697942 Click to see CC(=O)OC1CCC2(C3(C1O)CCN2CC4=CC5=C(C=C34)OCO5)O 347.40 unknown via CMAUP database
3-O-Acetyl-8-O-demethylmaritidine 52937473 Click to see CC(=O)OC1CC2C3(CCN2CC4=CC(=C(C=C43)OC)O)C=C1 315.40 unknown via CMAUP database
4a-Dehydroxycrinamabine 398935 Click to see C1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C(C1O)O 289.33 unknown via CMAUP database
7-Methoxycrinamabine 70698020 Click to see COC1=C2CN3CCC4(C2=CC5=C1OCO5)C3(CCC(C4O)O)O 335.40 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
9-Methoxy-10-hydroxy-4aalpha,6-dihydro-5alpha,10balpha-ethanophenanthridine-3(4H)-one 11140214 Click to see COC1=C(C2=C(CN3CCC24C3CC(=O)C=C4)C=C1)O 271.31 unknown via CMAUP database
CID 3738100 3738100 Click to see C1C[N+]2=CC3=CC4=C(C=C3C5=CC(=CC1=C52)[O-])OCO4 265.26 unknown via CMAUP database
Crinamabine 15378991 Click to see C1CC2(C3(CCN2CC4=CC5=C(C=C43)OCO5)C(C1O)O)O 305.32 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
Maritinamine 11818191 Click to see COC1=C(C=C2CN3CCC4(C3CC(CC4)O)C2=C1)O 275.34 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
Siculine 11208052 Click to see COC1=C(C=C2CN3CCC4(C3CC(C=C4)O)C2=C1)O 273.33 unknown via CMAUP database
Ungeremine 159646 Click to see C1C[N+]2=CC3=CC4=C(C=C3C5=CC(=CC1=C52)O)OCO4 266.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-Caffeoyltyramine 9994897 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC(=C(C=C2)O)O)O 299.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Paprazine 5372945 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone 688857 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
(S)-2-(3-Hydroxy-4-methoxyphenyl)chroman-7-ol 44257179 Click to see COC1=C(C=C(C=C1)C2CCC3=C(O2)C=C(C=C3)O)O 272.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4'-Hydroxy-7-methoxyflavan 185609 Click to see COC1=CC2=C(CCC(O2)C3=CC=C(C=C3)O)C=C1 256.30 unknown via CMAUP database

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