Scientific name	Authority	First published in
Magnolia conspicua var. purpurascens	Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 17: 419 (1872)
Magnolia denudata var. elongata	Rehder & E.H.Wilson	Pl. Wilson. 1: 402 (1913)
Magnolia denudata var. purpurascens	(Maxim.) Rehder & E.H.Wilson	Pl. Wilson. 1: 401 1913
Magnolia denudata var. pyramidalis	T.B.Chao & Zhi X.Chen	J. Henan Agric. Coll. 17(4): 11 (1983)
Magnolia diva	Stapf ex Dandy	Magnolias : 51, 120 (1927)
Magnolia elongata	Millais	Magnolias : 59 (1927)
Magnolia heptapeta f. purpurascens	(Maxim.) H.Ohba	J. Jap. Bot. 55: 190 (1980)
Magnolia purpurascens	(Maxim.) Makino	J. Jap. Bot. vi. No. 4, 8 (1929).
Magnolia sprengeri var. diva	(Stapf ex Dandy) Stapf	Bot. Mag. 153: t. 9116. 1927 (1927)
Magnolia sprengeri var. elongata	(Rehder & E.H.Wilson) Johnstone	Asiatic Magnolias Cult. 87. 1955
Magnolia denudata var. dilutipurpurascens	Z.W.Xie & Z.Z.Zhao	Acta Pharm. Sin. 22: 778 (1987)
Yulania denudata var. pubescens	D.L.Fu, T.B.Chao & G.H.Tian	J. Wuhan Bot. Res. 22: 327 (2004)
Yulania sprengeri	(Pamp.) D.L.Fu	J. Wuhan Bot. Res. 19: 198 (2001)
Magnolia wufengensis	L.Y.Ma & L.R.Wang	Bull. Bot. Res., Harbin 26: 4 (2006)
Yulania denudata var. elongata	(Rehder & E.H.Wilson) D.L.Fu & T.B.Chao	Bull. Bot. Res., Harbin 26: 35 (2006)
Yulania denudata var. flava	D.L.Fu, T.B.Chao & Zhi X.Chen	Bull. Bot. Res., Harbin 26: 35 (2006)
Yulania denudata subsp. pubescens	(D.L.Fu, T.B.Chao & G.H.Tian) D.L.Fu, T.B.Chao & G.H.Tian	Bull. Bot. Res., Harbin 26: 36 (2006)
Yulania denudata var. purpurascens	(Maxim.) D.L.Fu, T.B.Chao & G.H.Tian	Bull. Bot. Res., Harbin 26: 35 (2006)
Yulania denudata var. pyramidalis	(T.B.Chao & Zhi X.Chen) D.L.Fu, T.B.Chao & Zhi X.Chen	Bull. Bot. Res., Harbin 26: 35 (2006)
Magnolia wufengensis var. multitepala	L.Y.Ma & L.R.Wang	Bull. Bot. Res., Harbin 26: 516 (2006)
Yulania verrucata	D.L.Fu, T.B.Chao & S.S.Chen	Bull. Bot. Res., Harbin 30: 641 (2010)
Yulania denudata var. purpurascens	(Maxim.) D.L.Fu
Magnolia verrucata	(D.L.Fu, T.B.Chao & S.S.Chen) C.B.Callaghan & Png	Bot. Stud. (Taipei) 54-53: 3 (2013)

Common names Top

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Filter by language:

Language	Common/alternative name
Arabic	ماغنوليا سبرنغرية
Arabic	مغنولية سبرنغرية
koi	Шпренгер магнолия
udm	Шпренгер магнолия
Chinese	武当木兰
Chinese	湖北木兰
Chinese	迎春树
Chinese	武当玉兰
Chinese	武當玉蘭

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000233420
UNII	AQ5EB00DT0
Tropicos	19300332
KEW	urn:lsid:ipni.org:names:554854-1
The Plant List	kew-117850
Open Tree Of Life	91684
Observations.org	461046
NCBI Taxonomy	86737
IUCN Red List	194009
IPNI	554854-1
iNaturalist	440100
GBIF	3152927
Freebase	/m/0drkw8
EPPO	MAGSP
EOL	1154918
Elurikkus	366196
USDA GRIN	23143
Wikipedia	Magnolia_sprengeri
CMAUP	NPO25197

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

Differential distribution shifts in two subregions of East Asian subtropical evergreen broadleaved forests—a case of Magnoliaceae

Wu HY, Liu YH, He QX, Ye JW, Tian B

Front Plant Sci

23-Jan-2024

PMCID:	PMC10844446
doi:	10.3389/fpls.2023.1326207
PMID:	38322424

Integrative traditional Chinese medicine treatment for children with obstructive sleep apnea

Lai WY, Wei CC, Lin CH, Hang LW, Shih YH, Huang FW, Yen HR

J Tradit Complement Med

07-Aug-2023

PMCID:	PMC10785241
doi:	10.1016/j.jtcme.2023.08.002
PMID:	38223810

Anticancer Potentials of the Lignan Magnolin: A Systematic Review

Bhuia MS, Wilairatana P, Chowdhury R, Rakib AI, Kamli H, Shaikh A, Coutinho HD, Islam MT

Molecules

23-Apr-2023

PMCID:	PMC10180476
doi:	10.3390/molecules28093671
PMID:	37175081

Systematic analysis and expression of Gossypium 2ODD superfamily highlight the roles of GhLDOXs responding to alkali and other abiotic stress in cotton

Jiang T, Cui A, Cui Y, Cui R, Han M, Zhang Y, Fan Y, Huang H, Feng X, Lei Y, Liu X, Ni K, Zhang H, Xu N, Wang J, Sun L, Rui C, Wang J, Wang S, Chen X, Lu X, Wang D, Guo L, Zhao L, Hao F, Ye W

BMC Plant Biol

04-Mar-2023

PMCID:	PMC9985220
doi:	10.1186/s12870-023-04133-x
PMID:	36869319

Suitability of botanical extracts as components of complex mixtures used in herbal tea infusions—challenges and opportunities

Brendler T, Brinckmann JA, Daoust M, He H, Masé G, Steffan K, Williams M

Front Pharmacol

07-Nov-2022

PMCID:	PMC9676638
doi:	10.3389/fphar.2022.1013340
PMID:	36419619

Heat production and volatile biosynthesis are linked via alternative respiration in Magnolia denudata during floral thermogenesis

Wang R, Chen L, Jia Y, Liu L, Sun L, Liu Y, Li Y

Front Plant Sci

14-Oct-2022

PMCID:	PMC9614359
doi:	10.3389/fpls.2022.955665
PMID:	36311085

Novel Insights into Floral Thermogenesis: In Vivo Analyses of Mitochondrial Dynamics in Nelumbo nucifera Flowers

Li R, Li J, Wang S, Wang R

Int J Mol Sci

08-Oct-2022

PMCID:	PMC9570085
doi:	10.3390/ijms231911950
PMID:	36233249

Traditional Chinese medicine together with high-dose vitamin C improves the therapeutic effect of western medicine against COVID-19

Yang X, Wang Y, Liu Y, Shang L, Cheng Z, Fang L, Zhang J, Feng Y, Zhang K, Jiang S, He X

Am J Transl Res

15-Jan-2022

PMCID:	PMC8829592
PMID:	35173870

Comparative Transcriptome Analysis Identifies Key Regulatory Genes Involved in Anthocyanin Metabolism During Flower Development in Lycoris radiata

Wang N, Shu X, Zhang F, Zhuang W, Wang T, Wang Z

Front Plant Sci

15-Dec-2021

PMCID:	PMC8715008
doi:	10.3389/fpls.2021.761862
PMID:	34975946

Crosstalk of Multi-Omics Platforms with Plants of Therapeutic Importance

Pandita D, Pandita A, Wani SH, Abdelmohsen SA, Alyousef HA, Abdelbacki AM, Al-Yafrasi MA, Al-Mana FA, Elansary HO

Cells

23-May-2021

PMCID:	PMC8224614
doi:	10.3390/cells10061296
PMID:	34071113

Targeted enrichment of novel chloroplast-based probes reveals a large-scale phylogeny of 412 bamboos

Wang J, Mu W, Yang T, Song Y, Hou YG, Wang Y, Gao Z, Liu X, Liu H, Zhao H

BMC Plant Biol

05-Feb-2021

PMCID:	PMC7863319
doi:	10.1186/s12870-020-02779-5
PMID:	33546593

Complete chloroplast genome sequence and phylogenetic analysis of Annona reticulata

Niu YF, Li KX, Liu J

Mitochondrial DNA B Resour

09-Oct-2020

PMCID:	PMC7782357
doi:	10.1080/23802359.2020.1829131
PMID:	33458233

Quality standard of traditional Chinese medicines: comparison between European Pharmacopoeia and Chinese Pharmacopoeia and recent advances

Leong F, Hua X, Wang M, Chen T, Song Y, Tu P, Chen XJ

Chin Med

28-Jul-2020

PMCID:	PMC7388521
doi:	10.1186/s13020-020-00357-3
PMID:	32742301

Identification of the Genes Involved in Anthocyanin Biosynthesis and Accumulation in Taxus chinensis

Zhang L, Sun X, Wilson IW, Shao F, Qiu D

Genes (Basel)

28-Nov-2019

PMCID:	PMC6947853
doi:	10.3390/genes10120982
PMID:	31795268

Integrated Metabolome and Transcriptome Analysis Uncovers the Role of Anthocyanin Metabolism in Michelia maudiae

Lang X, Li N, Li L, Zhang S

Int J Genomics

03-Nov-2019

PMCID:	PMC6874964
doi:	10.1155/2019/4393905
PMID:	31781588

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
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	via CMAUP database
Magnoflorine iodide, (+)-(RG)	131664584	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)[O-])OC)C.I	469.30	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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
2-O-(4-Hydroxybenzoyl)-6-O-(galloyl)-beta-D-glucopyranose	102086065	Click to see C1=CC(=CC=C1C(=O)OC2C(C(C(OC2O)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	452.40	unknown	via CMAUP database
2,6-di-O-galloyl-beta-glucose	14034262	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O	484.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Styrenes
4-Ethylstyrene	18940	Click to see CCC1=CC=C(C=C1)C=C	132.20	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Magnosprengerine	161861	Click to see CN(C)CCC1=CC(=C(C=C1)O)OC	195.26	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
1,3,5,5-Tetramethyl-1,3-cyclohexadiene	78453	Click to see CC1=CC(=CC(C1)(C)C)C	136.23	unknown	via CMAUP database
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Epimagnolin A	21722943	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC)OC	416.50	unknown	via CMAUP database
(+)-Eudesmin	73117	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC	386.40	unknown	via CMAUP database
(+)-Fargesin	5320622	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC	370.40	unknown	via CMAUP database
(3R,3aR,6S,6aR)-3-(3,4-dimethoxyphenyl)-6-(3,4,5-trimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan	10454576	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC)OC	416.50	unknown	via CMAUP database
1,4-Bis(3,4-dimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan	234823	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC	386.40	unknown	via CMAUP database
Demethoxyaschantin	12697524	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC	370.40	unknown	via CMAUP database
Eudesmine	325601	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC	386.40	unknown	via CMAUP database
Fargesin	10926754	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC	370.40	unknown	via CMAUP database
Kobusin	182278	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC	370.40	unknown	via CMAUP database
Medioresinol dimethyl ether	169234	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC)OC	416.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Citronellol	7793	Click to see CC(CCC=C(C)C)CCO	156.26	unknown	via CMAUP database
beta-CITRONELLOL, (+/-)-	8842	Click to see CC(CCC=C(C)C)CCO	156.26	unknown	via CMAUP database
beta-CITRONELLOL, (R)-	101977	Click to see CC(CCC=C(C)C)CCO	156.26	unknown	via CMAUP database
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
Linalool, (+)-	67179	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene	440966	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
(-)-Fenchone	82229	Click to see CC1(C2CCC(C2)(C1=O)C)C	152.23	unknown	via CMAUP database
(-)-Sabinene	11051711	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	via CMAUP database
(+)-4-Carene	71351627	Click to see CC1CC2C(C2(C)C)C=C1	136.23	unknown	via CMAUP database
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
(+)-Bornyl acetate	6950274	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
(+)-Camphene	92221	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
(+)-Fenchone	1201521	Click to see CC1(C2CCC(C2)(C1=O)C)C	152.23	unknown	via CMAUP database
(1R,2S,4R)-(+)-Bornyl acetate	443131	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
(1S,2R,4S)-(-)-Bornyl acetate	442460	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
(1S)-1,3,3-Trimethylbicyclo[2.2.1]heptan-2-one	12049113	Click to see CC1(C2CCC(C2)(C1=O)C)C	152.23	unknown	via CMAUP database
(1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene	12223113	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
(2S,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl acetate	44630108	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
(4R)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-one	16213045	Click to see CC1(C2CCC(C2)(C1=O)C)C	152.23	unknown	via CMAUP database
(R)-Fenchone; L-(-)-Fenchone; L-Fenchone; l-Fenchone	2794921	Click to see CC1(C2CCC(C2)(C1=O)C)C	152.23	unknown	via CMAUP database
4,7,7-Trimethylbicyclo[4.1.0]hept-2-ene	530422	Click to see CC1CC2C(C2(C)C)C=C1	136.23	unknown	via CMAUP database
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	via CMAUP database
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)-	17868	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	via CMAUP database
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
Bornyl acetate, (-)-	93009	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
Camphor (synthetic)	159055	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
d-2-Bornanone	9543187	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
d-Camphor	230921	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
Fargesone C	14130915	Click to see CC(C(=O)C1=CC2=C(C=C1)OCO2)C3(C=C(C(=O)C=C3OC)CC=C)OC	370.40	unknown	via CMAUP database
Fenchone	14525	Click to see CC1(C2CCC(C2)(C1=O)C)C	152.23	unknown	via CMAUP database
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	via CMAUP database
Sabinene	10887971	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol	443162	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	via CMAUP database
(-)-Terpinen-4-ol	5325830	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
(+)-Terpinen-4-ol	2724161	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	via CMAUP database
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	via CMAUP database
beta-Terpinene	66841	Click to see CC(C)C1=CCC(=C)CC1	136.23	unknown	via CMAUP database
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Amorphene	12306052	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	via CMAUP database
(-)-alpha-Cubebene	86609	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	via CMAUP database
(+)-alpha-Muurolene	12306049	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	via CMAUP database
(+)-beta-Caryophyllene	20831623	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
(+)-Gamma-cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	via CMAUP database
(4Z)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene	5322111	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
(Z)-3-methyl-4-(2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one	5356787	Click to see CC1=CCCC(C1C=C(C)C(=O)C)(C)C	206.32	unknown	via CMAUP database
(Z)-caryophyllene	6429301	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
1-epi-Bicyclosesquiphellandrene	521496	Click to see CC1CCC(C2=CC(=C)CCC12)C(C)C	204.35	unknown	via CMAUP database
1-Methyl-4-(1-methylethylidene)-2-(1-methylvinyl)-1-vinylcyclohexane	94254	Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C	204.35	unknown	via CMAUP database
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene	101708	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	via CMAUP database
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	via CMAUP database
3-Methyl-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-3-buten-2-one	5372174	Click to see CC1=CCCC(C1C=C(C)C(=O)C)(C)C	206.32	unknown	via CMAUP database
3,4-Dihydrocadalene	528708	Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C	200.32	unknown	via CMAUP database
4-Isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydro-1-naphthalenol	519662	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
alpha-Cadinol #1	6431302	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
alpha-Panasinsene	578929	Click to see CC1=CCCC2(C13CC(C3CC2)(C)C)C	204.35	unknown	via CMAUP database
alpha-Patchoulene	521710	Click to see CC1CCC23C1CC(C2(C)C)CC=C3C	204.35	unknown	via CMAUP database
beta-Cadinene	10657	Click to see CC1=CCC2C(C1)C(CC=C2C)C(C)C	204.35	unknown	via CMAUP database
Cadina-1,4-diene	6427091	Click to see CC1CCC(C2C1=CCC(=C2)C)C(C)C	204.35	unknown	via CMAUP database
Cadina-4,9-diene	91748288	Click to see CC1CCC2C(=CCC(C2=C1)C(C)C)C	204.35	unknown	via CMAUP database
Calamenene	6429077	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	via CMAUP database
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Caryophyllene,alpha + beta mixt.	5354499	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
Cubenol	11770062	Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C	222.37	unknown	via CMAUP database
epi-Cubenol	519857	Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C	222.37	unknown	via CMAUP database
Epizonarene	595385	Click to see CC1CCC(=C2C1CCC(=C2)C)C(C)C	204.35	unknown	via CMAUP database
Farnesal	5280598	Click to see CC(=CCCC(=CCCC(=CC=O)C)C)C	220.35	unknown	via CMAUP database
Isocaryophyllene	5281522	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
tau-Muurolol	6432221	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
trans-Muurola-4(14),5-diene	91747125	Click to see CC1CCC(C2=CC(=C)CCC12)C(C)C	204.35	unknown	via CMAUP database
Tricyclo[4.4.0.0(2,7)]dec-3-ene, 1,3-dimethyl-8-(1-methylethyl)-, stereoisomer	6432119	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
(7S,7aS)-1,1,7,7a-tetramethyl-2,3,5,6,7,7b-hexahydro-1aH-cyclopropa[a]naphthalene	6432176	Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C	204.35	unknown	via CMAUP database
Calarene	28481	Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7R,7aS,7bS)-1,1,7-Trimethyl-4-methylenedecahydro-1H-cyclopropa[e]azulen-7-ol	6432706	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	via CMAUP database
1H-Cycloprop[e]azulen-7-ol, decahydro-1,1,7-trimethyl-4-methylene-, [1ar-(1aalpha,4aalpha,7beta,7abeta,7balpha)]-	6432640	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	via CMAUP database
1H-Cycloprop[e]azulene, 1a,2,3,4,4a,5,6,7b-octahydro-1,1,4,7-tetramethyl-, (1aR,4R,4aR,7bS)-	521243	Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C	204.35	unknown	via CMAUP database
beta-Spathulenol	522266	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	via CMAUP database
Ent-Spathulenol	13854255	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	via CMAUP database
Spathulenol	92231	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
15-Demethyl plumieride	453214	Click to see COC(=O)C1=COC(C2C1C=CC23C=C(C(=O)O3)CO)OC4C(C(C(C(O4)CO)O)O)O	456.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-hydroperoxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol	25136231	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)OO	444.70	unknown	via CMAUP database
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-hydroperoxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol	25136233	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)OO	444.70	unknown	via CMAUP database
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a,9-diol	15838686	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)O	428.70	unknown	via CMAUP database
Asiatic Acid	119034	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O	488.70	unknown	via CMAUP database
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	via CMAUP database
Betulinaldehyde	99615	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O	440.70	unknown	via CMAUP database
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	via CMAUP database
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
Ursolic aldehyde	14423521	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C=O	440.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Platanic Acid	64980	Click to see CC(=O)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	458.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
3,7-Dimethyl-1,7-octadien-3-ol	69016	Click to see CC(=C)CCCC(C)(C=C)O	154.25	unknown	via CMAUP database
Linalool, oxide	102611	Click to see CC(=CCCC(C)(C1CO1)O)C	170.25	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Pimentol	9917512	Click to see COC1=C(C(=CC(=C1)CC=C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O	494.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Fargesone A	442838	Click to see CC1C(OC2C1(C(=CC(=O)C2CC=C)OC)OC)C3=CC4=C(C=C3)OCO4	372.40	unknown	via CMAUP database
Futoenone	9819306	Click to see CC1C(CC2CC13C=C(C(=O)C=C3O2)OC)C4=CC5=C(C=C4)OCO5	340.40	unknown	https://doi.org/10.1016/J.JCHROMB.2011.10.023
> Organoheterocyclic compounds / Benzofurans
(1S,8R,10S,11R)-3-methoxy-11-methyl-10-(3,4,5-trimethoxyphenyl)-7-oxatricyclo[6.3.1.01,6]dodeca-2,5-dien-4-one	91895474	Click to see CC1C(CC2CC13C=C(C(=O)C=C3O2)OC)C4=CC(=C(C(=C4)OC)OC)OC	386.40	unknown	via CMAUP database
Maglifloenone	21723002	Click to see CC1C(CC2CC13C=C(C(=O)C=C3O2)OC)C4=CC(=C(C(=C4)OC)OC)OC	386.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Furopyrans
Cocculin	6473767	Click to see CC(=C)C1C2C3C4(C(C1C(=O)O2)(CC5C4(O5)C(=O)O3)O)C.CC12C3C4C(C(C1(CC5C2(O5)C(=O)O3)O)C(=O)O4)C(C)(C)O	602.60	unknown	via CMAUP database
Picrotoxin	31304	Click to see CC(=C)C1C2C3C4(C(C1C(=O)O2)(CC5C4(O5)C(=O)O3)O)C.CC12C3C4C(C(C1(CC5C2(O5)C(=O)O3)O)C(=O)O4)C(C)(C)O	602.60	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-[(7-hydroxy-6-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-1-yl)methyl]phenolate	5319196	Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)[O-])O)OC)C	313.40	unknown	via CMAUP database
Magnoline	362563	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CCN5C)OC)O)O)O)OC	596.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxanes
Eucalyptol	2758	Click to see CC1(C2CCC(O1)(CC2)C)C	154.25	unknown	via CMAUP database
Rose oxide	27866	Click to see CC1CCOC(C1)C=C(C)C	154.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
2-Hydrazino-nicotinic acid	585323	Click to see C1=CC(=C(N=C1)NN)C(=O)O	153.14	unknown	via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
2-[(2R,5S)-5-ethenyl-5-methyloxolan-2-yl]propan-2-ol	6428573	Click to see CC1(CCC(O1)C(C)(C)O)C=C	170.25	unknown	via CMAUP database
Linalool oxide	22310	Click to see CC1(CCC(O1)C(C)(C)O)C=C	170.25	unknown	via CMAUP database
trans-Linalool oxide	6432254	Click to see CC1(CCC(O1)C(C)(C)O)C=C	170.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	via CMAUP database
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	12304323	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	51402820	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	via CMAUP database
5,7-dihydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one	51402816	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O	464.40	unknown	via CMAUP database
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
Leucoside	44566720	Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O	580.50	unknown	via CMAUP database
O-Quercetin 3-(2-O-xylopyranosylglucopyranoside)	101138141	Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O	596.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,6-bis-O-galloyl-beta-D-glucose	440221	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	484.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
3-O-Methylellagic acid 4-O-rhamnoside	16720461	Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)OC)O)O)O	462.40	unknown	via CMAUP database
3,3'-Di-O-methylellagic acid	5488919	Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)OC)O)O	330.24	unknown	via CMAUP database
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	via CMAUP database

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Magnolia sprengeri

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