Rhodotypos scandens is a deciduous shrub in the rose family, native to China, Korea, and possibly Japan. It is the only species in its genus and is closely related to the Kerria plant. It can grow up to 2-5 meters tall and has opposite leaves with serrated margins. Its white flowers have four petals and bloom from late spring to mid-summer. The plant produces clusters of shiny black drupes as fruit. It is commonly known as rhodotypos or jetbead and is considered an invasive species in some parts of eastern North America. This plant is also known by other names such as Corchorus scandens and Amygdaloideae.

Synonyms Top

Scientific name	Authority	First published in
Corchorus scandens	Thunb.	Trans. Linn. Soc. London 2: 335 (1794)
Rhodotypos tetrapetalus	Makino	Bot. Mag. (Tokyo) 17: 13 (1903)
Kerria tetrapetala	Siebold	Verh. Batav. Genootsch. Kunsten 12: 69 (1830)
Rhodotypos kerrioides	Siebold & Zucc.	Fl. Jap. 1: 187 (1841)
Rhodotypos tetrapetala	(Siebold) Makino	Bot. Mag. (Tokyo) 17: 13 (1903)

Common names Top

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Filter by language:

Language	Common/alternative name
English	jetbead
Spanish	rhodotypos
Belarusian	радатыпус прыгожы
Czech	růžovec
Czech	růžovec zákulovitý
Czech	růžovec bělokvětý
Danish	klatrende rhodotypos
Finnish	lumipikihelmi
Japanese	シロヤマブキ
Korean	병아리꽃나무
Dutch	rhodotypos
Polish	różowiec biały
Polish	okółkowiec czteropłatkowy
Portuguese	rhodotypos
Russian	Родотипос лазающий
Russian	Розовик лазающий
Russian	Розовик
Russian	Родотипос
Chinese	雞麻
Chinese	鸡麻

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!

22-25°C x 4 weeks then 4°C

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 Southeast
  - Manchuria
- Eastern Asia
  - Japan
  - Korea
- Middle Asia
  - Uzbekistan

Europe click to expand
- Southeastern Europe
  - Bulgaria

Northern America click to expand
- Eastern Canada
  - Ontario
- North-central U.S.A.
  - Illinois
  - Kansas
  - Missouri
  - Nebraska
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Massachusetts
  - Michigan
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Vermont
  - West Virginia
- Southeastern U.S.A.
  - Alabama
  - Delaware
  - District Of Columbia
  - Georgia
  - Kentucky
  - Maryland
  - Mississippi
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001014318
Flora of Alabama	3192
Cornell Woody Plants	217
Canadensys	9761
USDA Plants	RHSC3
UConn	426
Tropicos	27801133
INPN	117705
KEW	urn:lsid:ipni.org:names:731425-1
The Plant List	rjp-6012
Missouri Botanical Garden	286455
Open Tree Of Life	156934
Observations.org	142750
NCBI Taxonomy	32245
Nature Serve	2.138223
IPNI	731425-1
iNaturalist	127609
GBIF	3032442
Freebase	/m/075nwp
WisFlora	4794
EPPO	RHQSC
EOL	631595
USDA GRIN	31670
Wikipedia	Rhodotypos
CMAUP	NPO5334

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

Phylogeny of genera in Maleae (Rosaceae) based on chloroplast genome analysis

Sun J, Zhao D, Qiao P, Wang Y, Wu P, Wang K, Guo L, Huang L, Zhou S

Front Plant Sci

26-Mar-2024

PMCID:	PMC11002139
doi:	10.3389/fpls.2024.1367645
PMID:	38595768

Ecophysiological Leaf Traits of Forty-Seven Woody Species under Long-Term Acclimation in a Botanical Garden

Sun Q, Lai L, Zhou J, Liu X, Zheng Y

Plants (Basel)

09-Mar-2022

PMCID:	PMC8954897
doi:	10.3390/plants11060725
PMID:	35336607

Validation of a Plant Identification Application Using Digital Images of Toxic Plants

Mahonski S, Furlano E, Chiang W

J Med Toxicol

27-Jan-2022

PMCID:	PMC8938528
doi:	10.1007/s13181-022-00877-4
PMID:	35084709

Synthesis of Nuclear and Chloroplast Data Combined With Network Analyses Supports the Polyploid Origin of the Apple Tribe and the Hybrid Origin of the Maleae—Gillenieae Clade

Hodel RG, Zimmer EA, Liu BB, Wen J

Front Plant Sci

25-Jan-2022

PMCID:	PMC8822239
doi:	10.3389/fpls.2021.820997
PMID:	35145537

In Vitro Screening of East Asian Plant Extracts for Potential Use in Reducing Ruminal Methane Production

Bharanidharan R, Arokiyaraj S, Baik M, Ibidhi R, Lee SJ, Lee Y, Nam IS, Kim KH

Animals (Basel)

04-Apr-2021

PMCID:	PMC8066825
doi:	10.3390/ani11041020
PMID:	33916571

Phylogeny of Maleae (Rosaceae) Based on Multiple Chloroplast Regions: Implications to Genera Circumscription

Sun J, Shi S, Li J, Yu J, Wang L, Yang X, Guo L, Zhou S

Biomed Res Int

19-Mar-2018

PMCID:	PMC5884435
doi:	10.1155/2018/7627191
PMID:	29750171

Non-crop plants used as hosts by Drosophila suzukii in Europe

Kenis M, Tonina L, Eschen R, van der Sluis B, Sancassani M, Mori N, Haye T, Helsen H

J Pest Sci (2004)

24-Mar-2016

PMCID:	PMC5318492
doi:	10.1007/s10340-016-0755-6
PMID:	28275324

Rhamnus davurica leaf extract inhibits Fyn activation by antigen in mast cells for anti-allergic activity

Kim JH, Kim AR, Kim HS, Kim HW, Park YH, You JS, Park YM, Her E, Kim HS, Kim YM, Choi WS

BMC Complement Altern Med

25-Mar-2015

PMCID:	PMC4379541
doi:	10.1186/s12906-015-0607-6
PMID:	25887889

Past Climate Change and Plant Evolution in Western North America: A Case Study in Rosaceae

Töpel M, Antonelli A, Yesson C, Eriksen B

PLoS One

07-Dec-2012

PMCID:	PMC3517582
doi:	10.1371/journal.pone.0050358
PMID:	23236369

Leucine-derived nitrile glucosides in the rosaceae and their systematic significance

Matthias Lechtenberg, Adolf Nahrsted, Frank R. Fronczek

Elsevier BV

04-Apr-2003

doi:	10.1016/0031-9422(95)00661-3

Phytochemical Profile Top

Add a new one!

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

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
(1S,2R)-1-(3,4-Dimethoxyphenyl)-2-(2,6-dimethoxy-4-allylphenoxy)-1-propanol acetate	38347541	Click to see CC(C(C1=CC(=C(C=C1)OC)OC)OC(=O)C)OC2=C(C=C(C=C2OC)CC=C)OC	430.50	unknown	via CMAUP database
[(1S,2S)-1-(3,4-dimethoxyphenyl)-2-(2,6-dimethoxy-4-prop-2-enylphenoxy)propyl] acetate	38347552	Click to see CC(C(C1=CC(=C(C=C1)OC)OC)OC(=O)C)OC2=C(C=C(C=C2OC)CC=C)OC	430.50	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
Dehydrodieugenol	165225	Click to see COC1=CC(=CC(=C1O)C2=C(C(=CC(=C2)CC=C)OC)O)CC=C	326.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(S)-5-Allyl-1,3-dimethoxy-2-((1-(3,4,5-trimethoxyphenyl)propan-2-yl)oxy)benzene	91734155	Click to see CC(CC1=CC(=C(C(=C1)OC)OC)OC)OC2=C(C=C(C=C2OC)CC=C)OC	402.50	unknown	via CMAUP database
Isoeugenyl methyl ether	1549045	Click to see CC=CC1=CC(=C(C=C1)OC)OC	178.23	unknown	via CMAUP database
Methylisoeugenol	637776	Click to see CC=CC1=CC(=C(C=C1)OC)OC	178.23	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
6-tert-Butyl-m-cresol	6937	Click to see CC1=CC(=C(C=C1)C(C)(C)C)O	164.24	unknown	via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Elemicin	10248	Click to see COC1=CC(=CC(=C1OC)OC)CC=C	208.25	unknown	via CMAUP database
Isoelemicin	5318557	Click to see CC=CC1=CC(=C(C(=C1)OC)OC)OC	208.25	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
2-Methoxy-4-[(S)-2-(2,6-dimethoxy-4-allylphenoxy)propyl]phenol	101682250	Click to see CC(CC1=CC(=C(C=C1)O)OC)OC2=C(C=C(C=C2OC)CC=C)OC	358.40	unknown	via CMAUP database
4-[(1S,2S)-2-(2,6-dimethoxy-4-prop-2-enylphenoxy)-1-methoxypropyl]-2-methoxyphenol	52326161	Click to see CC(C(C1=CC(=C(C=C1)O)OC)OC)OC2=C(C=C(C=C2OC)CC=C)OC	388.50	unknown	via CMAUP database
4-Allyl-2,6-dimethoxyphenol	226486	Click to see COC1=CC(=CC(=C1O)OC)CC=C	194.23	unknown	via CMAUP database
Isoeugenol	853433	Click to see CC=CC1=CC(=C(C=C1)O)OC	164.20	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Ethane	6324	Click to see CC	30.07	unknown	via CMAUP database
> Lignans, neolignans and related compounds
(1R,2R)-2-(2,6-dimethoxy-4-prop-2-enylphenoxy)-1-(3,4,5-trimethoxyphenyl)propane-1,3-diol	60153326	Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C(=C2)OC)OC)OC)O)OC)CC=C	434.50	unknown	via CMAUP database
(1R,2R)-2-(4-allyl-2,6-dimethoxy-phenoxy)-1-(3,4,5-trimethoxyphenyl)propan-1-ol	25751148	Click to see CC(C(C1=CC(=C(C(=C1)OC)OC)OC)O)OC2=C(C=C(C=C2OC)CC=C)OC	418.50	unknown	via CMAUP database
(1R,2S)-1-(3,4-Dimethoxyphenyl)-2-(2,6-dimethoxy-4-allylphenoxy)-1-propanol	21636108	Click to see CC(C(C1=CC(=C(C=C1)OC)OC)O)OC2=C(C=C(C=C2OC)CC=C)OC	388.50	unknown	via CMAUP database
(1R,2S)-1-(4-Hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(1-propenyl)phenoxy]-1-propanol	6545141	Click to see CC=CC1=CC(=C(C=C1)OC(C)C(C2=CC(=C(C=C2)O)OC)O)OC	344.40	unknown	via CMAUP database
(1S,2R)-1-(3,4-Dimethoxyphenyl)-2-(2,6-dimethoxy-4-allylphenoxy)-1-propanol	44566598	Click to see CC(C(C1=CC(=C(C=C1)OC)OC)O)OC2=C(C=C(C=C2OC)CC=C)OC	388.50	unknown	via CMAUP database
2,6-Dimethoxy-4-[(1R,2S)-1-hydroxy-2-(2,6-dimethoxy-4-allylphenoxy)propyl]phenol	21770235	Click to see CC(C(C1=CC(=C(C(=C1)OC)O)OC)O)OC2=C(C=C(C=C2OC)CC=C)OC	404.50	unknown	via CMAUP database
4-[(1R,2S)-1-hydroxy-2-(2-methoxy-4-prop-2-enylphenoxy)propyl]-2-methoxyphenol	21770237	Click to see CC(C(C1=CC(=C(C=C1)O)OC)O)OC2=C(C=C(C=C2)CC=C)OC	344.40	unknown	via CMAUP database
Myrifralignan C	21770239	Click to see CC=CC1=CC(=C(C=C1)OC(C)C(C2=CC(=C(C(=C2)OC)O)OC)O)OC	374.40	unknown	via CMAUP database
Myrislignan	21636106	Click to see CC(C(C1=CC(=C(C=C1)O)OC)O)OC2=C(C=C(C=C2OC)CC=C)OC	374.40	unknown	via CMAUP database
Odoratisol B	904795	Click to see CC=CC1=CC(=C(C=C1)OC(C)C(C2=CC(=C(C=C2)O)OC)O)OC	344.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans
Guaiacin	11724027	Click to see CC1CC2=CC(=C(C=C2C(C1C)C3=CC(=C(C=C3)O)OC)O)OC	328.40	unknown	via CMAUP database
Isootobaphenol	44447181	Click to see CC1CC2=CC3=C(C=C2C(C1C)C4=CC(=C(C=C4)O)OC)OCO3	326.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
(1S,2S,3R)-1,4-bis(1,3-benzodioxol-5-yl)-2,3-dimethylbutan-1-ol	44450607	Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)C(C3=CC4=C(C=C3)OCO4)O	342.40	unknown	via CMAUP database
4-[(1S,2R,3R)-4-(1,3-benzodioxol-5-yl)-1-hydroxy-2,3-dimethylbutyl]-2-methoxyphenol	44447179	Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)C(C3=CC(=C(C=C3)O)OC)O	344.40	unknown	via CMAUP database
4-[(1S,2S,3S)-4-(1,3-benzodioxol-5-yl)-1-hydroxy-2,3-dimethylbutyl]-2-methoxyphenol	25007695	Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)C(C3=CC(=C(C=C3)O)OC)O	344.40	unknown	via CMAUP database
4-[(2S,3R)-4-(3,4-dimethoxyphenyl)-2,3-dimethylbutyl]-2-methoxyphenol	476859	Click to see CC(CC1=CC(=C(C=C1)O)OC)C(C)CC2=CC(=C(C=C2)OC)OC	344.40	unknown	via CMAUP database
Austrobailignan 5	185825	Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)CC3=CC4=C(C=C3)OCO4	326.40	unknown	via CMAUP database
Dihydroguaiaretic acid, meso-	476856	Click to see CC(CC1=CC(=C(C=C1)O)OC)C(C)CC2=CC(=C(C=C2)O)OC	330.40	unknown	via CMAUP database
erythro-Austrobailignan-6	10381847	Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)CC3=CC(=C(C=C3)O)OC	328.40	unknown	via CMAUP database
Macelignan	10404245	Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)CC3=CC(=C(C=C3)O)OC	328.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(-)-Galbacin	11175182	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C	340.40	unknown	via CMAUP database
4-[(2R,3S,4S,5S)-5-(4-hydroxy-3-methoxyphenyl)-3,4-dimethyloxolan-2-yl]-2,6-dimethoxyphenol	13870582	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C(=C3)OC)O)OC)C	374.40	unknown	via CMAUP database
4-[(2S,3S,4R,5R)-5-(3,4-dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol	13939326	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)OC)OC)C	358.40	unknown	via CMAUP database
4-[(2S,3S,4R,5R)-5-(4-Hydroxy-3-methoxyphenyl)-3,4-dimethyloxolan-2-yl]-2,6-dimethoxyphenol	13870579	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C(=C3)OC)O)OC)C	374.40	unknown	via CMAUP database
4-[(2S,3S,4S,5R)-5-(4-hydroxy-3-methoxyphenyl)-3,4-dimethyloxolan-2-yl]-2,6-dimethoxyphenol	13870581	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C(=C3)OC)O)OC)C	374.40	unknown	via CMAUP database
4-[(2S,3S,4S,5R)-5-(4-hydroxy-3,5-dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-2,6-dimethoxyphenol	13870577	Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)O)OC)C3=CC(=C(C(=C3)OC)O)OC)C	404.50	unknown	via CMAUP database
4-[(2S,3S,4S,5S)-5-(4-hydroxy-3-methoxyphenyl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol	13870571	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)O)OC)C	344.40	unknown	via CMAUP database
4-[(2S,3S,4S,5S)-5-(4-hydroxy-3-methoxyphenyl)-3,4-dimethyloxolan-2-yl]-2,6-dimethoxyphenol	13870580	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C(=C3)OC)O)OC)C	374.40	unknown	via CMAUP database
4-[(2S,3S,4S,5S)-5-(4-hydroxy-3,5-dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-2,6-dimethoxyphenol	13870576	Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)O)OC)C3=CC(=C(C(=C3)OC)O)OC)C	404.50	unknown	via CMAUP database
4,4'-[(3beta,4alpha-Dimethyltetrahydrofuran)-2beta,5alpha-diyl]bis(2-methoxyphenol)	40580526	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)O)OC)C	344.40	unknown	via CMAUP database
Dide-O-methylgrandisin	102520996	Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)O)OC)C3=CC(=C(C(=C3)OC)O)OC)C	404.50	unknown	via CMAUP database
Fragransin A2	16069561	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)O)OC)C	344.40	unknown	via CMAUP database
Fragransin B1	13870575	Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)O)OC)C3=CC(=C(C(=C3)OC)O)OC)C	404.50	unknown	via CMAUP database
machilin G	10450921	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C	356.40	unknown	via CMAUP database
Machillin F	10450045	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)O)OC)C	342.40	unknown	via CMAUP database
nectandrin-B	156517	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)O)OC)C	344.40	unknown	via CMAUP database
Saucernetin	443018	Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC)OC)C	372.50	unknown	via CMAUP database
Talaumidin	11573701	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)O)OC)C	342.40	unknown	via CMAUP database
Tetrahydrofuroguaiacin B	13870572	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)O)OC)C	344.40	unknown	via CMAUP database
Verrucosin	10736226	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)O)OC)C	344.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
2beta-(4-Hydroxy-3-methoxyphenyl)-3alpha-methyl-4alpha-(4-hydroxy-3-methoxybenzyl)tetrahydrofuran	101108945	Click to see CC1C(COC1C2=CC(=C(C=C2)O)OC)CC3=CC(=C(C=C3)O)OC	344.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid	11005	Click to see CCCCCCCCCCCCCC(=O)O	228.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Dihydroosmaronin	101691173	Click to see CC(CC#N)COC1C(C(C(C(O1)CO)O)O)O	261.27	unknown	https://doi.org/10.1016/0031-9422(95)00661-3
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Trimyristin	11148	Click to see CCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCC	723.20	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
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
(1S,6R)-6-Isopropyl-3-methyl-cyclohex-2-en-1-ol	11367127	Click to see CC1=CC(C(CC1)C(C)C)O	154.25	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S,3R)-3-(hydroxymethyl)-3-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxirane-2-carbonitrile	101691172	Click to see C(C1C(C(C(C(O1)OCC2(C(O2)C#N)CO)O)O)O)O	291.25	unknown	https://doi.org/10.1016/0031-9422(95)00661-3
(2S,3R)-3-methyl-3-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxirane-2-carbonitrile	101675232	Click to see CC1(C(O1)C#N)COC2C(C(C(C(O2)CO)O)O)O	275.25	unknown	https://doi.org/10.1016/0031-9422(95)00661-3
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Malabaricone C	100313	Click to see C1=CC(=C(C(=C1)O)C(=O)CCCCCCCCC2=CC(=C(C=C2)O)O)O	358.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
(s)-4-(3-(Benzo[d][1,3]dioxol-5-yl)-1-hydroxypropyl)benzene-1,3-diol	57403255	Click to see C1OC2=C(O1)C=C(C=C2)CCC(C3=C(C=C(C=C3)O)O)O	288.29	unknown	via CMAUP database
Myristicin	4276	Click to see COC1=CC(=CC2=C1OCO2)CC=C	192.21	unknown	via CMAUP database
Safrole	5144	Click to see C=CCC1=CC2=C(C=C1)OCO2	162.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Acuminatin	6442251	Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC(=C(C=C3)OC)OC	340.40	unknown	via CMAUP database
(-)-Licarin A	6442393	Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC(=C(C=C3)O)OC	326.40	unknown	via CMAUP database
(-)-licarin B	10860310	Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC4=C(C=C3)OCO4	324.40	unknown	via CMAUP database
(2E)-3-[(2R,3R)-2,3-Dihydro-7-methoxy-2-(7-methoxy-1,3-benzodioxol-5-yl)-3-methyl-5-benzofuranyl]-2-propen-1-ol	14018338	Click to see CC1C(OC2=C1C=C(C=C2OC)C=CCO)C3=CC4=C(C(=C3)OC)OCO4	370.40	unknown	via CMAUP database
(2E)-3-[(2S,3S)-2-(3,4-Dimethoxyphenyl)-2,3-dihydro-7-methoxy-3-methyl-5-benzofuranyl]-2-propen-1-ol	14018336	Click to see CC1C(OC2=C1C=C(C=C2OC)C=CCO)C3=CC(=C(C=C3)OC)OC	356.40	unknown	via CMAUP database
(2R)-2beta-(4-Methoxy-1,3-benzodioxole-6-yl)-3alpha-methyl-5-(1-propenyl)-7-methoxy-2,3-dihydrobenzofuran	52326144	Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC4=C(C(=C3)OC)OCO4	354.40	unknown	via CMAUP database
2beta-(3-Methoxy-4-hydroxyphenyl)-3alpha-methyl-5-allyl-7-methoxy-2,3-dihydrobenzofuran	101434748	Click to see CC1C(OC2=C1C=C(C=C2OC)CC=C)C3=CC(=C(C=C3)O)OC	326.40	unknown	via CMAUP database
5-[(2R,3R)-7-Methoxy-3-methyl-5-prop-1-enyl-2,3-dihydro-1-benzofuran-2-yl]-1,3-benzodioxole	162622	Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC4=C(C=C3)OCO4	324.40	unknown	via CMAUP database
Isolicarin A	51136353	Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC(=C(C=C3)O)OC	326.40	unknown	via CMAUP database
Licarin A	5281836	Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC(=C(C=C3)O)OC	326.40	unknown	via CMAUP database
Licarin B	6441061	Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC4=C(C=C3)OCO4	324.40	unknown	via CMAUP database
Odoratisol A	11703153	Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC(=C(C(=C3)OC)O)OC	356.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3,4,5-Trimethoxycinnamyl alcohol	6436306	Click to see COC1=CC(=CC(=C1OC)OC)C=CCO	224.25	unknown	via CMAUP database
7-Methoxy-5-(3-hydroxy-1-propenyl)-1,3-benzodioxole	12594266	Click to see COC1=CC(=CC2=C1OCO2)C=CCO	208.21	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
(s)-4-(1-Hydroxy-3-(4-hydroxy-3-methoxyphenyl)propyl)benzene-1,3-diol	57392813	Click to see COC1=C(C=CC(=C1)CCC(C2=C(C=C(C=C2)O)O)O)O	290.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
4-[(S)-2-(2-Hydroxy-3-methoxy-5-allylphenyl)propyl]-2-methoxyphenol	101434749	Click to see CC(CC1=CC(=C(C=C1)O)OC)C2=C(C(=CC(=C2)CC=C)OC)O	328.40	unknown	via CMAUP database

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Rhodotypos scandens

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