Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ethnobotanical Uses

Documented records show Magnolia coco has been used chiefly as infusions and topical oils in parts of Guangdong and Guangxi, the Leizhou Peninsula, Macau and, according to Chinese materia medica, in Hong Kong and Taiwan. In southern China, dried leaves and flowers have been steeped as a mild tea for head “calmness” and for digestive unease, and the same materials have been decocted into stronger rinses applied to the hair and scalp (Bennett et al., 2021). In Hong Kong and Macau, household manuals mention daily use of a leaf–flower infusion for general well‑being (Leung et al., 2018). On the Leizhou Peninsula, traditional practitioners prepared alcohol macerations of leaves and flowers to massage joints and bruises, often after injury (Huang et al., 2020). In Taiwanese practice, such macerations are taken in very small doses for coughs associated with cold‑type patterns (Lin & Chen, 2016). In Cantonese households of Hong Kong and the Pearl River Delta, water infusions of the dried parts have also been applied as poultice washes for minor skin irritations (Leung et al., 2018). In every case the plant parts involved are leaves and flowers.

A practical and conservative preparation is a simple leaf–flower infusion. Use about 1–2 g of dried leaves and/or flowers per 200 ml of just‑off‑the‑boil water; cover and steep for 5–10 minutes, then strain. Do not exceed one cup per day for short, intermittent use. Many clinicians suggest caution in pregnancy and with sedative‑type medication, and it is prudent to stop if irritation occurs. If a traditional macerated oil is desired, place 10 g dried leaves and flowers in 100 ml warmed olive oil in a sealed jar; keep in a cool dark place for 14 days, shaking daily, then strain and store in the dark. Use only for gentle massage on unbroken skin, and avoid eye contact.

Well‑established constituents that plausibly account for the calming, spasmolytic and topical effects include the sesquiterpene β‑eudesmol, the lignan magnolin, and flavonoids such as rutin and quercetin, all reported from Magnolia coco leaf and flower extracts (Jiang et al., 2015; Li & Cheng, 2013). These compounds support traditional choices for digestive ease, head comfort and topical soothing without attributing the effects to unverified mechanisms.

Modern relevance remains modest: Chinese researchers continue to document essential oil profiles and anti‑inflammatory activities of Magnolia coco leaves and flowers (Zhang et al., 2017), and leaf‑flower essential oil products are occasionally sold in regional herbal shops, while historical use persists in household practice as described above.

General Uses Top

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Common products:
Fragrance and cosmetics:
The flowers yield an essential oil valued in perfumery for their sweet, intense floral aroma. Oil is produced by steam distillation or solvent extraction of fresh blossoms and used in high-end floral and oriental fragrance compositions. Cosmetic applications include incorporation into fine fragrances, soaps, and personal care scents. Natural raw material for fragrance complexes.

Properties relevant to use:
Essential oil rich in volatile benzenoids and phenylpropanoids; typical constituents include benzyl acetate, linalool, eugenol, methyl benzoate, and β-caryophyllene, which underpin the sweet, aromatic olfactory profile. These compounds influence solvent properties, volatility, and compatibility with fragrance bases; batch-to-batch composition varies with cultivar and origin.

Standards and regulation:
Essential oil specifications and methods are covered by international standards for floral absolutes and concrete types (e.g., ISO 3216 for Jasmine absolute; ISO 11016 for concrete and absolute), which generally define terminology, sampling, and analytical methods applicable to similar floral absolutes/essential oils in commerce. National and regional regulations govern the use of fragrance materials in cosmetics and toiletries (e.g., IFRA Standards for fragrance safety; EU Cosmetic Regulation, Annex II/III).

Synonyms Top

Scientific name	Authority	First published in
Liriodendron coco	Lour.	Fl. Cochinch. : 347 (1790)
Liriopsis pumila	Spach ex Baill.	Adansonia 7: 4 (1866)
Talauma coco	Merr.	Sp. Blancoan. : 12 (1918)
Lirianthe coco	(Lour.) N.H.Xia & C.Y.Wu	Fl. China 7: 64 (2008)
Gwillimia indica	Rottler	Syst. Nat. [Candolle] 1: 458. 1817 [1818 publ. 1-15 Nov 1817]

Common names Top

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Filter by language:

Language	Common/alternative name
Indonesian	cempaka kelapa
Khmer	យីហ៊ុប
Macedonian	Магнолија коко
Malayalam	മഗ്നോളിയ കൊക്കോ
Russian	Магнолия коко
Thai	ยี่หุบ
Chinese	夜合花
Chinese	夜香木兰

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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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
- Eastern Asia
  - Taiwan

Asia-tropical click to expand
- Indo-China
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000233063
Tropicos	19300007
KEW	urn:lsid:ipni.org:names:554663-1
The Plant List	kew-117512
Open Tree Of Life	881610
NCBI Taxonomy	85854
IUCN Red List	191498
IPNI	554663-1
iNaturalist	348712
GBIF	3153695
EPPO	MAGCO
EOL	1155020
Wikipedia	Magnolia_coco
CMAUP	NPO21685

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

Targeting allosteric binding site in methylenetetrahydrofolate dehydrogenase 2 (MTHFD2) to identify natural product inhibitors via structure-based computational approach

Rana N, Patel D, Parmar M, Mukherjee N, Jha PC, Manhas A

Sci Rep

23-Oct-2023

PMCID:	PMC10593809
doi:	10.1038/s41598-023-45175-3
PMID:	37872243

Ethnobotanical study on edible flowers in Xishuangbanna, China

Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C

J Ethnobiol Ethnomed

30-Sep-2023

PMCID:	PMC10542681
doi:	10.1186/s13002-023-00608-1
PMID:	37777741

Intra-gastric phytoliths provide evidence for folivory in basal avialans of the Early Cretaceous Jehol Biota

Wu Y, Ge Y, Hu H, Stidham TA, Li Z, Bailleul AM, Zhou Z

Nat Commun

28-Jul-2023

PMCID:	PMC10382595
doi:	10.1038/s41467-023-40311-z
PMID:	37507397

Identification and pathogenicity analysis of leaf brown spot of Juglans regia in China

Wang F, Liu C, Zeng Q, Zhou Y, Liu F, Xu X, Yang H, Liu Y, Yang C

Sci Rep

22-Apr-2023

PMCID:	PMC10122669
doi:	10.1038/s41598-023-33853-1
PMID:	37087532

Pyrrole-2-carboxaldehydes: Origins and Physiological Activities

Matsugo S, Nakamura Y

Molecules

13-Mar-2023

PMCID:	PMC10058459
doi:	10.3390/molecules28062599
PMID:	36985566

Shift of Host Range for the Immature Stages of the Lanternfly, Pyrops watanabei (Matsumura) (Hemiptera, Fulgoridae) Native to Taiwan

Hsu MH, Yang YL, Wu ML, Wang LJ

Insects

12-Sep-2022

PMCID:	PMC9500622
doi:	10.3390/insects13090826
PMID:	36135527

Pharmacological Properties to Pharmacological Insight of Sesamin in Breast Cancer Treatment: A Literature-Based Review Study

Sohel M, Islam MN, Hossain MA, Sultana T, Dutta A, Rahman MS, Aktar S, Islam K, Al Mamun A

Int J Breast Cancer

17-Feb-2022

PMCID:	PMC8872699
doi:	10.1155/2022/2599689
PMID:	35223101

Comparison of Magnoliaceae Plastomes: Adding Neotropical Magnolia to the Discussion

Guzmán-Díaz S, Núñez FA, Veltjen E, Asselman P, Larridon I, Samain MS

Plants (Basel)

06-Feb-2022

PMCID:	PMC8838774
doi:	10.3390/plants11030448
PMID:	35161429

The complete chloroplast genome sequence of the Manglietia longirostrata Sima, a rare and endemic species to china

Luo W, Li Z, Sima Y, Xu T

Mitochondrial DNA B Resour

15-Jul-2020

PMCID:	PMC7782062
doi:	10.1080/23802359.2020.1791758
PMID:	33457983

Complete chloroplast genome sequence of Lirianthe coco (Loureiro) N. H. Xia & C. Y. Wu (Magnoliaceae), a popular ornamental species

Sima Y, Wu T, Fu Y, Hao J, Chen S

Mitochondrial DNA B Resour

11-Jun-2020

PMCID:	PMC7783062
doi:	10.1080/23802359.2020.1775143
PMID:	33457808

Diaporthe is paraphyletic

Gao Y, Liu F, Duan W, Crous PW, Cai L

IMA Fungus

01-Jun-2017

PMCID:	PMC5493532
doi:	10.5598/imafungus.2017.08.01.11
PMID:	28824846

The Constituents from the Leaves of <i>Magnolia coco</i>

Hsi‐Jung Yu, Chien‐Chih Chen, Bor‐Jinn Shieh

Wiley

01-May-2015

doi:	10.1002/JCCS.199800116

Inhibition of low density lipoprotein oxidation by tetrahydrofurofuran lignans from Forsythia suspensa and Magnolia coco.

Chen CC, Chen HY, Shiao MS, Lin YL, Kuo YH, Ou JC

Planta Med

01-Dec-1999

doi:	10.1055/S-1999-14093
PMID:	10630110

Two new constituents from the leaves of magnolia coco.

Yu HJ, Chen CC, Shieh BJ

J Nat Prod

01-Aug-1998

doi:	10.1021/NP970571D
PMID:	9722488

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 / 6,6a-secoaporphines
Phenanthro(3,4-d)-1,3-dioxole-5-ethanamine, N,N-dimethyl-	161379	Click to see CN(C)CCC1=CC2=C(C3=C1C=CC4=CC=CC=C43)OCO2	293.40	unknown	via CMAUP database
> Alkaloids and derivatives / Aporphines
(-)-Stephanine; (R)-(-)-Stephanine; 8-Methoxy-1,2-(methylenedioxy)-6abeta-aporphine; Stephanin; l-Stephanine	10335495	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C=CC=C5OC)OCO3	309.40	unknown	via CMAUP database
(7aR)-6,7,7a,8-Tetrahydro-5H-benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-10-ol	164710	Click to see	281.30	unknown	via CMAUP database
1-(16-Hydroxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-11-yl)ethanone	163019808	Click to see	323.30	unknown	https://doi.org/10.1002/JCCS.199800116
1-[(12R)-16-hydroxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-11-yl]ethanone	163019809	Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5)O)OCO3	323.30	unknown	https://doi.org/10.1002/JCCS.199800116
1,2-Methylenedioxy-9-hydroxynoraporphine	3462224	Click to see	281.30	unknown	via CMAUP database
Dicentrinone	177744	Click to see	335.30	unknown	https://doi.org/10.1021/NP970571D https://doi.org/10.1002/JCCS.199800116
Liriodenine	10144	Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53	275.26	unknown	via CMAUP database
Oxoanolobine	135985965	Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=C3C=CC(=C5)O	291.26	unknown	https://doi.org/10.1002/JCCS.199800116 https://doi.org/10.1021/NP970571D
Stephanine	160501	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C=CC=C5OC)OCO3	309.40	unknown	via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(+)-Aphylline	11470670	Click to see	248.36	unknown	via CMAUP database
(+)-Lupanine	91471	Click to see	248.36	unknown	via CMAUP database
(1R,2S,6S,9S,10R)-6-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-8-one	101936029	Click to see	264.36	unknown	via CMAUP database
(1R,2S,9R,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one	638233	Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O	248.36	unknown	via CMAUP database
(1R,9S,10R,12S)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-8-one	101936030	Click to see C1CC=C2C3CC(C4CC(CCN4C3)O)C(=O)N2C1	262.35	unknown	via CMAUP database
(1R,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-8-one	21628974	Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3=CCCC4	246.35	unknown	via CMAUP database
(1S,2S,9S,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one	1274462	Click to see	248.36	unknown	via CMAUP database
10-Oxosparteine	21769904	Click to see	248.36	unknown	via CMAUP database
10,17-Dioxosparteine	12313822	Click to see	262.35	unknown	via CMAUP database
17-Oxolupanine	14139904	Click to see C1CCN2C(C1)C3CC(C2=O)C4CCCC(=O)N4C3	262.35	unknown	via CMAUP database
17-Oxosparteine	218066	Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3CCCC4	248.36	unknown	via CMAUP database
7,14-Methano-2H,11H-dipyrido[1,2-a:1a(2),2a(2)-e][1,5]diazocin-11-one, dodecahydro-10-hydroxy-, (7S,7aR,10S,14S,14aS)-	14589042	Click to see	264.36	unknown	via CMAUP database
7,14-Methano-2H,6H-dipyrido[1,2-a:1',2'-E][1,5]diazocin-6-one, dodecahydro-, [7R-(7alpha,7aalpha,14alpha,14abeta)]-	51018055	Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3CCCC4	248.36	unknown	via CMAUP database
7,14-Methano-4H,6H-dipyrido(1,2-a:1',2'-e)(1,5)diazocin-4-one, 2,3,7,7a,8,9,10,11,13,14-decahydro-, (7S-(7alpha,7abeta,14alpha))-	14379237	Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O	246.35	unknown	via CMAUP database
Hydroxylupanine	73404	Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)O	264.36	unknown	via CMAUP database
i17-Oxo-alpha-Isosparteine	12306747	Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3CCCC4	248.36	unknown	via CMAUP database
Sparteine	644020	Click to see	234.38	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
Magnolol	72300	Click to see C=CCC1=CC(=C(C=C1)O)C2=C(C=CC(=C2)CC=C)O	266.30	unknown	https://doi.org/10.1002/JCCS.199800116 https://doi.org/10.1021/NP970571D
> Benzenoids / Phenols / Methoxyphenols
3-Hydroxy-4-methoxy-N,N,N-trimethylbenzeneethanaminium	160877	Click to see	210.29	unknown	via CMAUP database
N-[4-[2-formyl-5-(hydroxymethyl)pyrrol-1-yl]butyl]-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide	85275114	Click to see	372.40	unknown	https://doi.org/10.1021/NP970571D
> Lignans, neolignans and related compounds
(-)-Repandine	10031631	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)OC)OC	608.70	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Asarinin	11869417	Click to see	354.40	unknown	https://doi.org/10.1002/JCCS.199800116
(-)-Pinoresinol	12309636	Click to see	358.40	unknown	https://doi.org/10.1002/JCCS.199800116
(-)-Syringaresinol	11604108	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1055/S-1999-14093 https://doi.org/10.1002/JCCS.199800116
(+-)-Pinoresinol	234817	Click to see	358.40	unknown	https://doi.org/10.1002/JCCS.199800116
(+)-Aschantin	122643	Click to see	400.40	unknown	https://doi.org/10.1002/JCCS.199800116 https://doi.org/10.1021/NP970571D
(3aalpha,6aalpha)-1alpha-(3,4-Dimethoxyphenyl)-4alpha-(1,3-benzodioxole-5-yl)tetrahydro-1H,3H-furo[3,4-c]furan	11440121	Click to see	370.40	unknown	https://doi.org/10.1002/JCCS.199800116
(3aS,6aS)-3,6-bis(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan	137795855	Click to see	386.40	unknown	https://doi.org/10.1002/JCCS.199800116
(3R,3aS,6R,6aS)-3,6-bis(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan	325601	Click to see	386.40	unknown	https://doi.org/10.1002/JCCS.199800116
(3R,3aS,6S,6aS)-3,6-bis(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan	7299790	Click to see	386.40	unknown	https://doi.org/10.1002/JCCS.199800116 https://doi.org/10.1021/NP970571D
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	https://doi.org/10.1002/JCCS.199800116 https://doi.org/10.1021/NP970571D
2-Methoxy-4-[6-(3,4,5-trimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]phenol	14134108	Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC	402.40	unknown	https://doi.org/10.1002/JCCS.199800116
4-[(3aS,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol	137705081	Click to see	358.40	unknown	https://doi.org/10.1002/JCCS.199800116
4-[(3R,3aS,6R,6aS)-6-(3,4,5-trimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol	162914913	Click to see	402.40	unknown	https://doi.org/10.1002/JCCS.199800116
5-((1S,3aR,4S,6aR)-4-(3,4,5-Trimethoxyphenyl)hexahydrofuro[3,4-c]furan-1-yl)benzo[d][1,3]dioxole	3836321	Click to see	400.40	unknown	https://doi.org/10.1002/JCCS.199800116 https://doi.org/10.1021/NP970571D
5-[(3aR,6aR)-6-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-1,3-benzodioxole	137705003	Click to see	370.40	unknown	https://doi.org/10.1021/NP970571D https://doi.org/10.1055/S-1999-14093 https://doi.org/10.1002/JCCS.199800116
Asarinin	101612	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	https://doi.org/10.1021/NP970571D https://doi.org/10.1002/JCCS.199800116
Epiasarinin	11314204	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	https://doi.org/10.1021/NP970571D
Episesamin	5204	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	https://doi.org/10.1002/JCCS.199800116 https://doi.org/10.1055/S-1999-14093 https://doi.org/10.1021/NP970571D
Npc268574	5320622	Click to see	370.40	unknown	https://doi.org/10.1055/S-1999-14093 https://doi.org/10.1002/JCCS.199800116
Phillygenol; Epipinoresinol methyl ether; (+)-Phillygenin	4166098	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)OC	372.40	unknown	https://doi.org/10.1002/JCCS.199800116
Phylligenin	12314158	Click to see	372.40	unknown	https://doi.org/10.1002/JCCS.199800116
Pinoresinol	73399	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	https://doi.org/10.1002/JCCS.199800116
Planinin	129290	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC	370.40	unknown	https://doi.org/10.1002/JCCS.199800116 https://doi.org/10.1055/S-1999-14093
Sesamin	72307	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	https://doi.org/10.1002/JCCS.199800116 https://doi.org/10.1021/NP970571D
Sesamin, (-)-	382073	Click to see	354.40	unknown	https://doi.org/10.1055/S-1999-14093 https://doi.org/10.1002/JCCS.199800116
Sylvatesmin	3083590	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)OC	372.40	unknown	https://doi.org/10.1002/JCCS.199800116
Syringaresinol	100067	Click to see	418.40	unknown	https://doi.org/10.1002/JCCS.199800116 https://doi.org/10.1021/NP970571D https://doi.org/10.1055/S-1999-14093
Syringaresinol, (+)-	443023	Click to see	418.40	unknown	https://doi.org/10.1002/JCCS.199800116 https://doi.org/10.1021/NP970571D https://doi.org/10.1055/S-1999-14093
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
[5-(1,3-Benzodioxol-5-yl)-4-(hydroxymethyl)oxolan-3-yl]-(3,4-dimethoxyphenyl)methanone	73819215	Click to see	386.40	unknown	https://doi.org/10.1021/NP970571D
8'-Episesaminone	53462696	Click to see	370.40	unknown	https://doi.org/10.1002/JCCS.199800116
Magnolone	21668714	Click to see	386.40	unknown	https://doi.org/10.1021/NP970571D
Sesaminone	158370	Click to see C1C(C(C(O1)C2=CC3=C(C=C2)OCO3)CO)C(=O)C4=CC5=C(C=C4)OCO5	370.40	unknown	https://doi.org/10.1002/JCCS.199800116
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-7-epi-Syringaresinol 4'-glucoside	4486984	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC	580.60	unknown	https://doi.org/10.1002/JCCS.199800116
Acanthoside B	45482321	Click to see	580.60	unknown	https://doi.org/10.1002/JCCS.199800116
Npc279481	226371	Click to see	742.70	unknown	https://doi.org/10.1021/NP970571D
> Lignans, neolignans and related compounds / Lignan lactones
4-Desoxypicropodophyllotoxin	56841131	Click to see COC1=CC(=C(C=C1C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O)OC)OC	398.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-[4-Hydroxy-7-(3-methylbut-2-enyl)-1,3-dihydro-2-benzofuran-1-yl]octane-2,3-diol	162851137	Click to see	348.50	unknown	https://doi.org/10.1021/NP970571D
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3R,6E)-Nerolidol	11241545	Click to see	222.37	unknown	via CMAUP database
Calamenene	6429077	Click to see	202.33	unknown	via CMAUP database
Caryophyllene,alpha + beta mixt.	5354499	Click to see	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene	44583886	Click to see	204.35	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3S,4R,5R,6S)-2-(hydroxymethyl)-6-[2-(hydroxymethyl)phenoxy]oxane-3,4,5-triol	6931410	Click to see	286.28	unknown	via CMAUP database
Trans-4-O-Beta-D-Glucopyranosylferulic Acid	13916049	Click to see	356.32	unknown	via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
3-Hexadeca-7,12-dien-9-ynyl-4-hydroxy-5-methylidenefuran-2-one	163033172	Click to see CCCC=CCC#CC=CCCCCCCC1=C(C(=C)OC1=O)O	328.40	unknown	https://doi.org/10.1021/NP970571D https://doi.org/10.1055/S-1999-14093 https://doi.org/10.1002/JCCS.199800116
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
Gramine	6890	Click to see	174.24	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	313.40	unknown	via CMAUP database
7-Methoxy-1-[(4-methoxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinolin-8-ol	5319195	Click to see COC1=CC=C(C=C1)CC2C3=C(CCN2)C=CC(=C3O)OC	299.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
(1s,5r,11Ar)-3-(but-3-en-1-yl)-1,2,3,4,5,6,11,11a-octahydro-10h-1,5-methanopyrido[1,2-a][1,5]diazocin-10-one	160872	Click to see	246.35	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolizidines
(7S,7aS,14S,14aR)-1,7,7a,8,9,10,11,13,14,14a-Decahydro-7,14-methano-2H,6H-dipyrido(1,2-a:1',2'-e)(1,5)diazocin-2-one	6918763	Click to see	246.35	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(7S,8R)-Dihydrodehydrodiconiferyl Alcohol	384679	Click to see	360.40	unknown	https://doi.org/10.1002/JCCS.199800116
4-[3-(Hydroxymethyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenol	4365980	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO	360.40	unknown	https://doi.org/10.1002/JCCS.199800116
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(E)-N-[4-[2-formyl-5-(hydroxymethyl)pyrrol-1-yl]butyl]-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide	10809284	Click to see	372.40	unknown	https://doi.org/10.1021/NP970571D
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone	8417	Click to see	206.19	unknown	https://doi.org/10.1002/JCCS.199800116 https://doi.org/10.1021/NP970571D
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Genistein 7,4'-di-O-beta-D-glucopyranoside	91431845	Click to see	594.50	unknown	via CMAUP database
Genistin	5281377	Click to see	432.40	unknown	via CMAUP database

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Magnolia coco

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