Scientific name	Authority	First published in
Magnolia angustifolia	Millais	Magnolias : 55, 83 (1927)
Magnolia elliptica	Link	Handbuch 2: 375 (1829)
Magnolia exoniensis	hort. ex Millais	Magnolias : 59 (1927)
Magnolia ferruginea	hort. ex W.Watson	Bull. Misc. Inform. Kew 1889(36): 305. [Dec 1889]
Magnolia foetida	(L.) Sarg.	Gard. & Forest 2: 615 (1889)
Magnolia foetida f. margarettae	Ashe	Torreya 31: 37 (1931)
Magnolia foetida f. parvifolia	Ashe	Torreya 31: 37 (1931)
Magnolia galissoniensis	hort. ex Millais	Magnolias : 60 (1927)
Magnolia glabra	P.Parm.	Bull. Sci. France Belgique 27: 251 (1895 publ. 1896)
Magnolia gloriosa	Millais	Magnolias : 61 (1927)
Magnolia grandiflora var. elliptica	Aiton	Hort. Kew. 2: 251 (1789)
Magnolia grandiflora var. exoniensis	Loudon	Arbor. Frutic. Brit. 1: 261. 1839
Magnolia grandiflora f. galissoniensis	K.Koch	Dendrologie 1: 368 1869
Magnolia grandiflora var. lanceolata	Aiton	Hortus Kew. 2: 251 (1789)
Magnolia grandiflora f. lanceolata	(Aiton) Rehder	Bibl. Cult. Trees 180 1949
Magnolia grandiflora var. obovata	Aiton	Hort. Kew. 2: 251 (1789)
Magnolia hartwegii	hort.	ex Gard. Kew i. Polypet. (1894) 17.
Magnolia hartwicus	hort.	ex Gard. Kew i. Polypet. (1894) 17.
Magnolia lacunosa	Raf.	Autik. Bot. : 78 (1840)
Magnolia lanceolata	Link	Handbuch 2: 375 (1829)
Magnolia longifolia	Sweet	Hort. Brit. : 11 (1826)
Magnolia maxima	Lodd. ex G.Don	Hort. Brit. : 226 (1830)
Magnolia microphylla	Ser.	Fl. Jard. 3: 226. 1849 (1849)
Magnolia praecox	Millais	Magnolias : 69 (1927)
Magnolia pravertiana	Millais	Magnolias : 69 (1927)
Magnolia rotundifolia	Millais	Magnolias : 70 (1927)
Magnolia stricta	hort.	ex Gard. Kew i. Polypet. (1894) 17.
Magnolia tardiflora	Ser.	Fl. Jard. 3: 226. 1849 (1849)
Magnolia tomentosa	Ser.	Fl. Jard. 3: 226. 1849 (1849)
Magnolia virginiana var. foetida	L.	Sp. Pl. : 536 (1753)
Magnolia virginiana var. grisea	L.	Sp. Pl. : 536 (1753)
Magnolia grandiflora var. ferruginea	Sims	Bot. Mag. 45: t. 1952 (1817)
Magnolia grandiflora var. rotundifolia	Sweet ex Loudon	Arbor. Frutic. Brit. 1: 261. 1838
Magnolia grandiflora var. angustifolia	Loudon	Arbor. Frutic. Brit. 1: 261. 1838
Magnolia grandiflora var. praecox	Loudon	Arbor. Frutic. Brit. 1: 261. 1838
Magnolia umbrella var. maxima	(Lodd. ex G.Don) P.Parm.	Bull. Sci. France Belgique 27: 253. 1896
Magnolia ferruginea	hort. ex W.Watson	Bull. Misc. Inform. Kew 1889: 305 (1889)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	bull-bay
English	bull bay
English	big-laurel
English	evergreen magnolia
English	southern magnolia
Arabic	مغنولية كبيرة الزهر
Arabic	مغنوليا كبيرة
Arabic	مانوليا
Arabic	ماغنوليا كبيرة الأزهار
Azerbaijani	İriçiçək maqnoliya
Belarusian	Магнолія буйнакветкавая
Bulgarian	Едроцветна магнолия
Bengali	উদয়পদ্ম
Bengali	হিমচাঁপা
Catalan	magnòlia
Czech	šácholan velkokvětý
German	immergrüne magnolie
dty	रूख कमल
Persian	مگنولیای جنوبی
Finnish	kuningasmagnolia
French	laurier tulipier
French	laurier-tulipier
French	magnolier à grandes fleurs
Galician	magnolio común
Galician	magnolio
Hebrew	מגנוליה גדולת פרחים
Hindi	हिम चम्पा
Croatian	velecvjetna magnolija
Upper Sorbian	wulkokwětkaty lilijowc
Hungarian	nagyvirágú liliomfa
Hungarian	örökzöld liliomfa
Armenian	խոշորածաղիկ մագնոլիա
Japanese	泰山木
Japanese	タイサンボク
Japanese	広玉蘭
Japanese	大山木
Japanese	タイザンボク
Georgian	დიდყვავილა მაგნოლია
Korean	태산목
Macedonian	крупноцветна магнолија
Malayalam	മഗ്നോലിയ ഗ്രാൻഡിഫ്ളോറ
Burmese	တတိုင်းမွှေး
Norwegian Bokmål	oksemagnolia
Nepali	रूख कमल
Punjab	سدا ہرا میگنولیا
Portuguese	magnólia-branca
Portuguese	magnólia branca
Russian	Магнолия крупноцветковая
Slovenian	velecvetna magnolija
Swedish	kungsmagnolia
Tamil	மக்னோலியா கிராண்டிஃபுளோரா
udm	Бадӟым сяськаё магнолия
Ukrainian	Магнолія великоквіткова
Chinese	荷花木兰
Chinese	荷花玉兰
Chinese	荷花玉蘭
Chinese	洋玉兰
Chinese	广玉兰

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

Suggest a correction or add new data!

Start at 4°C for 3 months, then warm to 20°C for another 3 months.

Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.

remove pulpy coat with detergent washes; germination unlikely if dried by just 20%, store seeds @ 4°C

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - East Himalaya

Northern America click to expand
- Mexico
  - Mexico Central
- South-central U.S.A.
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Arkansas
  - Florida
  - Georgia
  - Kentucky
  - Louisiana
  - Maryland
  - Mississippi
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia

Southern America click to expand
- Caribbean
  - Cuba
  - Dominican Republic
  - Puerto Rico
- Southern South America
  - Juan Fernández Islands

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000233174
UNII	OON62ADO4M
Florida Plant Atlas	3766
Flora of Alabama	2597
Cornell Woody Plants	355
USDA Plants	MAGR4
UConn	274
Tropicos	19300008
INPN	107141
Flora of Italy	1260
KEW	urn:lsid:ipni.org:names:554723-1
The Plant List	kew-117615
Missouri Botanical Garden	282515
PFAF	Magnolia grandiflora
PaleoBotany	27059
PaleoBotany	111704
Open Tree Of Life	622553
Observations.org	127100
NCBI Taxonomy	3406
Nature Serve	2.146090
IUCN Red List	193948
IPNI	554723-1
iNaturalist	83074
IFPNI	ECE202D9-EC41-294F-32CB-DF834317DB14
GBIF	3153283
Freebase	/m/02hd99
FEIS	plants/tree/maggra
EPPO	MAGGR
EOL	1154991
Elurikkus	209991
Calflora (Californian flora)	9363
USDA GRIN	23108
Wikipedia	Magnolia_grandiflora

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

Apple crown and collar canker and necrosis caused by Cytospora balanejica sp. nov. in Iran

Azizi R, Ghosta Y, Ahmadpour A

Sci Rep

19-Mar-2024

PMCID:	PMC10951349
doi:	10.1038/s41598-024-57235-3
PMID:	38504125

Role of STAT3 in cancer cell epithelial-mesenchymal transition (Review)

Zhang G, Hou S, Li S, Wang Y, Cui W

Int J Oncol

13-Mar-2024

PMCID:	PMC11000535
doi:	10.3892/ijo.2024.5636
PMID:	38488027

Sesquiterpene lactones as emerging biomolecules to cease cancer by targeting apoptosis

Hsu CY, Rajabi S, Hamzeloo-Moghadam M, Kumar A, Maresca M, Ghildiyal P

Front Pharmacol

11-Mar-2024

PMCID:	PMC10961375
doi:	10.3389/fphar.2024.1371002
PMID:	38529189

Pharmacological potential of micheliolide: A focus on anti-inflammatory and anticancer activities

Uddin J, Fatima M, Riaz A, Kamal GM, Muhsinah AB, Ahmed AR, Iftikhar R

Heliyon

05-Mar-2024

PMCID:	PMC10944196
doi:	10.1016/j.heliyon.2024.e27299
PMID:	38496875

Comparative analysis of chloroplast and mitochondrial genomes of sweet potato provides evidence of gene transfer

Li G, Zhang H, Lin Z, Li H, Xu G, Xu Y, Ji R, Luo W, Qiu Y, Qiu S, Tang H

Sci Rep

24-Feb-2024

PMCID:	PMC10894244
doi:	10.1038/s41598-024-55150-1
PMID:	38402284

Study of summer microclimate and PM2.5 concentration in campus plant communities

Jiang Y, Liu C, Wen C, Long Y

Sci Rep

09-Feb-2024

PMCID:	PMC10853255
doi:	10.1038/s41598-024-52508-3
PMID:	38332000

Co-Delivery of Gemcitabine and Honokiol by Lipid Bilayer-Coated Mesoporous Silica Nanoparticles Enhances Pancreatic Cancer Therapy via Targeting Depletion of Tumor Stroma

Liu D, Wang L, Li H, Li D, Zhou J, Wang J, Zhang Q, Cai D

Molecules

31-Jan-2024

PMCID:	PMC10856273
doi:	10.3390/molecules29030675
PMID:	38338418

Morphological and Phylogenetic Analyses Reveal Three New Species of Didymella (Didymellaceae, Pleosporales) from Jiangxi, China

Luo X, Hu Y, Xia J, Zhang K, Ma L, Xu Z, Ma J

J Fungi (Basel)

18-Jan-2024

PMCID:	PMC10821193
doi:	10.3390/jof10010075
PMID:	38248984

Commodity risk assessment of Corylus avellana plants from the UK

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P

EFSA J

12-Jan-2024

PMCID:	PMC10784871
doi:	10.2903/j.efsa.2024.8495
PMID:	38222930

Role of SIRT3 in bone homeostasis and its application in preventing and treating bone diseases

Xu K, Li J, Wen R, Chang B, Cheng Y, Yi X

Front Pharmacol

20-Dec-2023

PMCID:	PMC10773770
doi:	10.3389/fphar.2023.1248507
PMID:	38192409

Seamless integration of sewer system topology and tree location data: An algorithm to diagnose the potential impact of tree roots on pipes and propose rearrangement solutions

Martínez D, Bergillos S, Corominas L, Comas-Cufí M, Calle E

Heliyon

07-Dec-2023

PMCID:	PMC10758799
doi:	10.1016/j.heliyon.2023.e23382
PMID:	38169737

Insect α-Amylases and Their Application in Pest Management

Wang B, Huang D, Cao C, Gong Y

Molecules

01-Dec-2023

PMCID:	PMC10708458
doi:	10.3390/molecules28237888
PMID:	38067617

Phylogenetics Study to Compare Chloroplast Genomes in Four Magnoliaceae Species

Zhao J, Chen H, Li G, Jumaturti MA, Yao X, Hu Y

Curr Issues Mol Biol

16-Nov-2023

PMCID:	PMC10670740
doi:	10.3390/cimb45110578
PMID:	37998755

Cell Membrane Sialome: Sialic Acids as Therapeutic Targets and Regulators of Drug Resistance in Human Cancer Management

Jastrząb P, Narejko K, Car H, Wielgat P

Cancers (Basel)

22-Oct-2023

PMCID:	PMC10604966
doi:	10.3390/cancers15205103
PMID:	37894470

Octadecadienoate derivatives from Michelia champaca seed extract as potential larvicide and pupicide against Dengue vector Aedes albopictus

Dutta M, Chandra G

BMC Res Notes

12-Sep-2023

PMCID:	PMC10498518
doi:	10.1186/s13104-023-06487-9
PMID:	37700379

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
> Alkaloids and derivatives / Aporphines
(-)-N-nornuciferine	624491	Click to see COC1=C(C2=C3C(CC4=CC=CC=C42)NCCC3=C1)OC	281.30	unknown	https://doi.org/10.1248/YAKUSHI1947.87.9_1134
(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/10.1021/NP50021A009
(R)-Roemerine	235224	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3	279.30	unknown	https://doi.org/10.1007/BF02234867
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/10.1248/YAKUSHI1947.87.9_1134
1,2-Methylenedioxynoraporphine	3462225	Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5	265.31	unknown	https://doi.org/10.1080/14786410902906959
16-Methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,9,11,14(19),15,17-octaen-13-one	162847121	Click to see CC1=CC2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O	289.30	unknown	https://doi.org/10.1080/14786410902906959
Anolobine	164710	Click to see C1CNC2CC3=C(C=CC(=C3)O)C4=C2C1=CC5=C4OCO5	281.30	unknown	https://doi.org/10.1248/YAKUSHI1947.87.9_1134
Anonaine	160597	Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5	265.31	unknown	https://doi.org/10.1080/14786410902906959 https://doi.org/10.1055/S-2007-986794 https://doi.org/10.1021/NP50021A009
Lanuginosine	97622	Click to see COC1=CC2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O	305.30	unknown	https://doi.org/10.1055/S-2007-986794
Liriodenine	10144	Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53	275.26	unknown	https://doi.org/10.1055/S-2007-986794 https://doi.org/10.1080/14786410902906959 https://doi.org/10.11110/KJPT.1985.15.3.145 https://doi.org/10.1248/YAKUSHI1947.87.9_1134 https://doi.org/10.1590/S0100-46702007000300002 https://doi.org/10.1007/BF02234867
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/10.1055/S-2007-986794 https://doi.org/10.1021/NP50021A009
Menisperine	30358	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/10.1021/NP50021A009
N-Nornuciferine	12313579	Click to see COC1=C(C2=C3C(CC4=CC=CC=C42)NCCC3=C1)OC	281.30	unknown	https://doi.org/10.1248/YAKUSHI1947.87.9_1134
Roemerine	119204	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3	279.30	unknown	https://doi.org/10.11110/KJPT.1985.15.3.145 https://doi.org/10.1007/BF02234867
> 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	https://doi.org/10.1007/S10600-010-9591-8
> Benzenoids / Naphthalenes
Naphthalene	931	Click to see C1=CC=C2C=CC=CC2=C1	128.17	unknown	https://doi.org/10.1016/0031-9422(96)00082-9
> Benzenoids / Phenols / Methoxyphenols
1,2,3-Propanetriol, 1-(4-hydroxy-3,5-dimethoxyphenyl)-, (1R,2R)-rel-	14237630	Click to see COC1=CC(=CC(=C1O)OC)C(C(CO)O)O	244.24	unknown	https://doi.org/10.1007/S10600-010-9591-8
Syringaldehyde	8655	Click to see COC1=CC(=CC(=C1O)OC)C=O	182.17	unknown	https://doi.org/10.1007/S10600-010-9591-8
threo-Syringoylglycerol	14237629	Click to see COC1=CC(=CC(=C1O)OC)C(C(CO)O)O	244.24	unknown	https://doi.org/10.1007/S10600-010-9591-8
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptacosane	11636	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC	380.70	unknown	https://doi.org/10.1515/ZNC-1992-7-805
Nonacosane	12409	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC	408.80	unknown	https://doi.org/10.1515/ZNC-1992-7-805
> Lignans, neolignans and related compounds / Furanoid lignans
Medioresinol	181681	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC	388.40	unknown	https://doi.org/10.1016/S0031-9422(00)80557-9
Syringaresinol, (+)-	443023	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1016/S0031-9422(00)80557-9
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3S,4R,5S,6S)-2-[4-[(3R,3aS,6R,6aS)-6-hydroxy-6-(4-hydroxy-3,5-dimethoxyphenyl)-3,3a,4,6a-tetrahydro-1H-furo[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	154496961	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)(C5=CC(=C(C(=C5)OC)O)OC)O	596.60	unknown	https://doi.org/10.1016/S0031-9422(00)85062-1
[5-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-4-(hydroxymethyl)oxolan-3-yl]-(4-hydroxy-3,5-dimethoxyphenyl)methanone	5319199	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C(C(CO3)C(=O)C4=CC(=C(C(=C4)OC)O)OC)CO	596.60	unknown	https://doi.org/10.1016/S0031-9422(00)85062-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
[(2R)-2,3-dihydroxypropyl] 24-hydroxytetracosanoate	162960853	Click to see C(CCCCCCCCCCCC(=O)OCC(CO)O)CCCCCCCCCCCO	458.70	unknown	https://doi.org/10.1007/S10600-010-9591-8
Tetracosanoic acid, 24-hydroxy-, 2,3-dihydroxypropyl ester	10072879	Click to see C(CCCCCCCCCCCC(=O)OCC(CO)O)CCCCCCCCCCCO	458.70	unknown	https://doi.org/10.1007/S10600-010-9591-8
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
[(2R)-2,3-dihydroxypropyl] tetracosanoate	163004763	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)OCC(CO)O	442.70	unknown	https://doi.org/10.1007/S10600-010-9591-8
2,3-Dihydroxypropyl tetracosanoate	14542801	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)OCC(CO)O	442.70	unknown	https://doi.org/10.1007/S10600-010-9591-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Cyclocolorenone	160491	Click to see CC1CCC2C(C2(C)C)C3=C(C(=O)CC13)C	218.33	unknown	https://doi.org/10.1021/JF00049A013 https://doi.org/10.1021/JF00006A036
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
[3-Acetyloxy-2-(4-ethenyl-2-hydroxy-4-methyl-3-prop-1-en-2-ylcyclohexyl)-2-hydroxypropyl] acetate	162999724	Click to see CC(=C)C1C(C(CCC1(C)C=C)C(COC(=O)C)(COC(=O)C)O)O	354.40	unknown	https://doi.org/10.1055/S-2001-14326
[3-acetyloxy-2-[(1R,2R,3S,4S)-4-ethenyl-2-hydroxy-4-methyl-3-prop-1-en-2-ylcyclohexyl]-2-hydroxypropyl] acetate	162999725	Click to see CC(=C)C1C(C(CCC1(C)C=C)C(COC(=O)C)(COC(=O)C)O)O	354.40	unknown	https://doi.org/10.1055/S-2001-14326
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
[2-[(3R,3aS,4S,5R,8R,8aR)-3,4,8-trihydroxy-3,8-dimethyl-1,2,3a,4,5,6,7,8a-octahydroazulen-5-yl]-3-acetyloxy-2-hydroxypropyl] acetate	101128712	Click to see CC(=O)OCC(COC(=O)C)(C1CCC(C2CCC(C2C1O)(C)O)(C)O)O	388.50	unknown	https://doi.org/10.1055/S-2001-14326
[3-Acetyloxy-2-hydroxy-2-(3,4,8-trihydroxy-3,8-dimethyl-1,2,3a,4,5,6,7,8a-octahydroazulen-5-yl)propyl] acetate	162911038	Click to see CC(=O)OCC(COC(=O)C)(C1CCC(C2CCC(C2C1O)(C)O)(C)O)O	388.50	unknown	https://doi.org/10.1055/S-2001-14326
2-(3,4,8-Trihydroxy-3,8-dimethyl-1,2,3a,4,5,6,7,8a-octahydroazulen-5-yl)prop-2-enyl acetate	163023246	Click to see CC(=O)OCC(=C)C1CCC(C2CCC(C2C1O)(C)O)(C)O	312.40	unknown	https://doi.org/10.1055/S-2001-14326
2-[(3R,3aS,4S,5S,8R,8aS)-3,4,8-trihydroxy-3,8-dimethyl-1,2,3a,4,5,6,7,8a-octahydroazulen-5-yl]prop-2-enyl acetate	101128710	Click to see CC(=O)OCC(=C)C1CCC(C2CCC(C2C1O)(C)O)(C)O	312.40	unknown	https://doi.org/10.1055/S-2001-14326
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,2R,4S,7S,9R,12S)-4,9-dimethyl-13-methylidene-3,8,15-trioxatetracyclo[10.3.0.02,4.07,9]pentadecan-14-one	101151058	Click to see CC12CCC3C(C4C(O4)(CCC1O2)C)OC(=O)C3=C	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)85062-1
(1S,2S,4R,7R,11S)-7-hydroperoxy-4-methyl-8,12-dimethylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradecan-13-one	154497187	Click to see CC12CCC(C(=C)CCC3C(C1O2)OC(=O)C3=C)OO	280.32	unknown	https://doi.org/10.1021/JO01336A041
(1S,2S,4R,7R,9S,12S)-4,9-dimethyl-13-methylidene-3,8,15-trioxatetracyclo[10.3.0.02,4.07,9]pentadecan-14-one	13895611	Click to see CC12CCC3C(C4C(O4)(CCC1O2)C)OC(=O)C3=C	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)85062-1
(3aS,7R,10E,11aS)-7-hydroperoxy-10-methyl-3,6-dimethylidene-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-2-one	13895608	Click to see CC1=CC2C(CCC(=C)C(CC1)OO)C(=C)C(=O)O2	264.32	unknown	https://doi.org/10.1021/JO01336A041
Artemorin	5281428	Click to see CC1=CC2C(CCC(=C)C(CC1)O)C(=C)C(=O)O2	248.32	unknown	https://doi.org/10.1021/JO01336A041
Epoxyparthenolide	154933	Click to see CC12CCC3C(C4C(O4)(CCC1O2)C)OC(=O)C3=C	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)85062-1
Peroxyparthenolide	325148	Click to see CC12CCC(C(=C)CCC3C(C1O2)OC(=O)C3=C)OO	280.32	unknown	https://doi.org/10.1021/JO01336A041
Verlotorin	13895607	Click to see CC1=CC2C(CCC(=C)C(CC1)OO)C(=C)C(=O)O2	264.32	unknown	https://doi.org/10.1021/JO01336A041
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
6-hydroxy-5a,9-dimethyl-3-methylidene-4,5,6,7,8,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one	14414342	Click to see CC1=C2C3C(CCC2(C(CC1)O)C)C(=C)C(=O)O3	248.32	unknown	https://doi.org/10.1016/0031-9422(79)80039-4
Magnolialide	636954	Click to see CC1=C2C3C(CCC2(C(CC1)O)C)C(=C)C(=O)O3	248.32	unknown	https://doi.org/10.1016/0031-9422(79)80039-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1aR,7aS,10aS,10bS)-1a,5-dimethyl-8-methylidene-2,3,6,7,7a,8,10a,10b-octahydrooxireno[9,10]cyclodeca[1,2-b]furan-9(1aH)-one	6473881	Click to see CC1=CCCC2(C(O2)C3C(CC1)C(=C)C(=O)O3)C	248.32	unknown	https://doi.org/10.1016/J.BSE.2007.06.009 https://doi.org/10.1016/0031-9422(96)00082-9 https://doi.org/10.1016/S0031-9422(00)85062-1
(1R,2S,4S,11S)-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one	162942114	Click to see CC1=CCCC2(C(O2)C3C(CC1)C(=C)C(=O)O3)C	248.32	unknown	https://doi.org/10.1002/PS.1337
(1R,2S,4S,7E,11S)-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one	25880675	Click to see CC1=CCCC2(C(O2)C3C(CC1)C(=C)C(=O)O3)C	248.32	unknown	https://doi.org/10.1002/PS.1337
(1R,4R,6R,9E,11R)-4-(hydroxymethyl)-9-methyl-14-methylidene-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-13-one	162875438	Click to see CC1=CC2C(CCC3(C(O3)CC1)CO)C(=C)C(=O)O2	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)80557-9
(1S,2R,4R,7E,11R)-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one	124463365	Click to see CC1=CCCC2(C(O2)C3C(CC1)C(=C)C(=O)O3)C	248.32	unknown	https://doi.org/10.1016/S0031-9422(00)80557-9 https://doi.org/10.1016/S0031-9422(00)85062-1 https://doi.org/10.1021/JF00049A013
(1S,2R,4R,7E,11S)-8-(hydroxymethyl)-4-methyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one	52918137	Click to see CC12CCC=C(CCC3C(C1O2)OC(=O)C3=C)CO	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)80557-9
(1S,2S,4R,7E,11S)-8-(hydroxymethyl)-4-methyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one	10754094	Click to see CC12CCC=C(CCC3C(C1O2)OC(=O)C3=C)CO	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)80557-9
(1S,2S,4S,11S)-8-(hydroxymethyl)-4-methyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one	162941644	Click to see CC12CCC=C(CCC3C(C1O2)OC(=O)C3=C)CO	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)80557-9
(1S,2S,4S,7Z,11S)-8-(hydroxymethyl)-4-methyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one	163189704	Click to see CC12CCC=C(CCC3C(C1O2)OC(=O)C3=C)CO	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)80557-9
(1S,4R,6R,9E,11R)-4-(hydroxymethyl)-9-methyl-14-methylidene-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-13-one	11369084	Click to see CC1=CC2C(CCC3(C(O3)CC1)CO)C(=C)C(=O)O2	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)80557-9
(1S,4R,6R,9Z,11R)-4-(hydroxymethyl)-9-methyl-14-methylidene-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-13-one	101630461	Click to see CC1=CC2C(CCC3(C(O3)CC1)CO)C(=C)C(=O)O2	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)80557-9
(3aS,6E,11aR)-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one	133640194	Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C	232.32	unknown	https://doi.org/10.1021/JO01336A041 https://doi.org/10.1016/S0031-9422(00)80557-9 https://doi.org/10.1021/JF00049A013
4-(Hydroxymethyl)-9-methyl-14-methylidene-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-13-one	72819991	Click to see CC1=CC2C(CCC3(C(O3)CC1)CO)C(=C)C(=O)O2	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)80557-9
8-(Hydroxymethyl)-4-methyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one	75953564	Click to see CC12CCC=C(CCC3C(C1O2)OC(=O)C3=C)CO	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)80557-9
CID 4692	4692	Click to see CC1=CCCC2(C(O2)C3C(CC1)C(=C)C(=O)O3)C	248.32	unknown	https://doi.org/10.1016/S0031-9422(00)85062-1 https://doi.org/10.1016/0031-9422(96)00082-9
Costunolide	5281437	Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C	232.32	unknown	https://doi.org/10.1021/JF00049A013 https://doi.org/10.1021/JO01336A041
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
6,9-Dihydroxy-6,9-dimethyl-3-methylidene-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one	13305018	Click to see CC1(CCC2C(C3C1CCC3(C)O)OC(=O)C2=C)O	266.33	unknown	https://doi.org/10.1016/S0031-9422(00)85062-1 https://doi.org/10.1055/S-2001-14326
Magnograndiolide	5319198	Click to see CC1(CCC2C(C3C1CCC3(C)O)OC(=O)C2=C)O	266.33	unknown	https://doi.org/10.1016/S0031-9422(00)85062-1 https://doi.org/10.1055/S-2001-14326
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1007/S10600-010-9591-8
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/10.1007/S10600-010-9591-8
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[2-[3-Acetyloxy-6-(acetyloxymethyl)-4,5-dihydroxyoxan-2-yl]oxy-4-hydroxy-3-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]-5-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxymethyl]oxolan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate	73091566	Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC)COC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C)O)O	924.80	unknown	https://doi.org/10.1016/S0031-9422(00)80557-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol	154497544	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	https://doi.org/10.1016/0031-9422(79)80039-4
(2S,3R,4S,5S,6R)-2-(3-hydroxy-4,5-dimethoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol	71719415	Click to see COC1=CC(=CC(=C1OC)O)OC2C(C(C(C(O2)CO)O)O)O	332.30	unknown	https://doi.org/10.1007/S10600-010-9591-8
2-(3-Hydroxy-4,5-dimethoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol	78157783	Click to see COC1=CC(=CC(=C1OC)O)OC2C(C(C(C(O2)CO)O)O)O	332.30	unknown	https://doi.org/10.1007/S10600-010-9591-8
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol	323959	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	https://doi.org/10.1590/S0100-46702007000300002
Eleutheroside B	5316860	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	https://doi.org/10.1016/0031-9422(79)80039-4
> Organoheterocyclic compounds / Furopyrans
Abyssomicin D	139583150	Click to see CC1CC(C(=C2C(=O)OC34C25C(C1=O)CC3C(C(O5)C(C4)C)O)O)C	348.40	unknown	https://doi.org/10.1016/S0031-9422(00)80557-9
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone	8417	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC	206.19	unknown	https://doi.org/10.1016/S0031-9422(00)80557-9

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Magnolia grandiflora

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