Scientific name	Authority	First published in
Podophyllum emodi	Wall. ex Hook.f. & Thomson	Fl. Ind. [Hooker f. & Thomson] 1: 232. 1855
Sinopodophyllum emodi	T.S.Ying	Acta Phytotax. Sin. 17(1): 16 (1979)
Sinopodophyllum hexandrum	(Royle) T.S.Ying	Fl. Xizang. 2: 119. 1985
Podophyllum emodi var. chinense	Sprague	Bot. Mag. 146: t. 8850 (1920)
Dysosma emodi	(Wall. ex Royle) M.Hiroe	Pl. Basho's & Buson's Hokku Lit. 8: 328 (1973)
Podophyllum sikkimense	R.Chatterjee & Mukerjee	Rec. Bot. Surv. India 16(2): 48 (1953)
Podophyllum emodi var. hexandrum	(Royle) R.Chatterjee & Mukerjee	Rec. Bot. Surv. India 16(2): 45 (1953)
Podophyllum hexandrum var. chinense	(Sprague) Stearn ex Cubey	Hanburyana 3: 81 (2008)
Sinopodophyllum hexandrum var. emodi	(Wall., Hook.f. & Thomson) J.M.H.Shaw	Hanburyana 4: 36 (2009)
Sinopodophyllum hexandrum var. chinense	(Sprague) Stearn ex J.M.H.Shaw & Cubey	Hanburyana 4: 37 (2009)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	himalayan mayapple
Azerbaijani	podophyllum emodi
Azerbaijani	himalay podofili
German	himalaya-maiapfel
Estonian	himaalaja jalgleht
Swedish	indiskt fotblad
Chinese	桃儿七
Chinese	桃兒七

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

Begin at 20°C for 6 weeks, cool to 4°C for 6 weeks, then gradually increase to 10°C over 6 weeks. If no germination, the cycle is repeated.

Germination Improved by GA3: Gibberellic Acid(GA3) is a plant growth hormone that can break dormancy and improve germination rates for seeds that are otherwise difficult to sprout.

Pulpy Coat Inhibits Germination: Seeds with a pulpy or fleshy outer coat need to have this material removed by soaking and rinsing in clean water daily for about a week. The inhibitory substances in the pulp are thus washed away, and germination rates improve.

hydrophilic, some may start to germinate after 3 weeks of warmth

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
  - Qinghai
  - Tibet
- Western Asia
  - Afghanistan

Asia-tropical click to expand
- Indian Subcontinent
  - East Himalaya
  - Nepal
  - Pakistan
  - West Himalaya

Europe click to expand
- Middle Europe
  - Czechoslovakia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000397412
UNII	0E1BZ0WZXH
USDA Plants	POHE16
Tropicos	3500028
KEW	urn:lsid:ipni.org:names:327192-2
PFAF	Podophyllum hexandrum
IPNI	327192-2
GBIF	3033840
EPPO	PDLHE
Elurikkus	6414
USDA GRIN	105098
Wikipedia	Podophyllum_hexandrum
CMAUP	NPO10903
CMAUP	NPO14752

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)!

Title

Authors

Publication

Released

IDs

On the improvement of the podophyllotoxin production by phenylpropanoid precursor feeding to cell cultures of Podophyllum hexandrum Royle

Wim van Uden, Niesko Pras, Theo M. Malingré

Springer Science and Business Media LLC

14-Jul-2014

doi:	10.1007/BF00034435

Biochemical composition and antioxidant capacity of extracts from Podophyllum hexandrum rhizome.

Li M, Zhou L, Yang D, Li T, Li W

BMC Complement Altern Med

22-Dec-2012

PMCID:	PMC3542176
doi:	10.1186/1472-6882-12-263
PMID:	23259745

Production of podophyllotoxin by plant cell cultures of Podophyllum hexandrum in bioreactor

Saurabh Chattopadhyay, Ashok K. Srivastava, Sant S. Bhojwani, Virendra S. Bisaria

Elsevier BV

01-Jan-2012

doi:	10.1016/S1389-1723(02)80017-2

Three new cytotoxic aryltetralin lignans from Sinopodophyllum emodi.

Sun YJ, Li ZL, Chen H, Liu XQ, Zhou W, Hua HM

Bioorg Med Chem Lett

15-Jun-2011

doi:	10.1016/J.BMCL.2011.04.036
PMID:	21570846

Indian Podophyllum

Ramgopal Chatterjee

Springer Science and Business Media LLC

04-Dec-2010

doi:	10.1007/BF02984882

A new cytotoxic flavonoid from the fruit of Sinopodophyllum hexandrum.

Kong Y, Xiao JJ, Meng SC, Dong XM, Ge YW, Wang RF, Shang MY, Cai SQ

Fitoterapia

01-Jul-2010

doi:	10.1016/J.FITOTE.2009.11.003
PMID:	19909799

Quantitative determination of podophyllotoxin and related compounds in <i>podophyllum</i> species by reverse phase high performance liquid chromatography

Jairo K. Bastos, Wlodzimierz J. Kopycki, Charles L. Burandt, N. P. Dhammika Nanayakkara, James D. McChesney

Wiley

08-Mar-2007

doi:	10.1002/PCA.2800060207

New Lignan Glycosides from Chinese Medicinal Plant, Sinopodophillum emodi

Changqi Zhao, Akito Nagatsu, Keiichiro Hatano, Naohiro Shirai, Setsuko Kato, Yukio Ogihara

Wiley

29-Jun-2005

doi:	10.1002/CHIN.200330221

Cytotoxicity of in vitro produced podophyllotoxin from Podophyllum hexandrum on human cancer cell line.

Chattopadhyay S, Bisaria VS, Panda AK, Srivastava AK

Nat Prod Res

01-Feb-2004

doi:	10.1080/1057563031000122095
PMID:	14974618

Antifungal aryltetralin lignans from leaves of Podophyllum hexandrum

Atta-ur-Rahman, M. Ashraf, M. Iqbal Choudhary, Habib-ur-Rehman, M.H. Kazmi

Elsevier BV

23-Apr-2003

doi:	10.1016/0031-9422(95)00195-D

Preparative Separation of Chemical Ingredients from Podophyllum emodii var. Chinensis Sprague by High-Speed Countercurrent Chromatography

S.M. Zhang, Q.Y. Ou

Elsevier BV

07-Oct-2002

doi:	10.1006/MCHJ.1995.1079

Biosynthetic relationship of aryltetralin lactone lignans to dibenzylbutyrolactone lignans

Widad M. Kamil, Paul M. Dewick

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(86)80072-3

Biosynthesis of podophyllum lignans—i. cinnamic acid precursors of podophyllotoxin in podophyllum hexandrum

David E. Jackson, Paul M. Dewick

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)82603-5

Aryltetralin lignans from Podophyllum hexandrum and Podophyllum peltatum

David E. Jackson, Paul M. Dewick

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)82628-X

Biosynthesis of lignans in Forsythia intermedia

Maiada M.A. Rahman, Paul M. Dewick, David E. Jackson, John A. Lucas

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(90)85025-B

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 / Macroline alkaloids
methyl (1S,12S,13R,14S,15E)-15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate	15558573	Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)(CO)C(=O)OC	352.40	unknown	via CMAUP database
Methyl 17-hydroxysarpagan-16-carboxylate, (16R)-	5374154	Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)(CO)C(=O)OC	352.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Diisobutyl phthalate	6782	Click to see CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C	278.34	unknown	via CMAUP database
Diisooctyl phthalate	33934	Click to see CC(C)CCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC(C)C	390.60	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,4,5-Trimethoxybenzoic acid	8357	Click to see COC1=CC(=CC(=C1OC)OC)C(=O)O	212.20	unknown	https://doi.org/10.1007/BF02984882
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Hydroxytyrosol	82755	Click to see C1=CC(=C(C=C1CCO)O)O	154.16	unknown	https://doi.org/10.1248/CPB.49.1474
Tyrosol	10393	Click to see C1=CC(=CC=C1CCO)O	138.16	unknown	https://doi.org/10.1248/CPB.49.1474
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
4'-Demethyldehydropodophyllotoxin	15232507	Click to see COC1=CC(=CC(=C1O)OC)C2=C3C(=C(C4=CC5=C(C=C42)OCO5)O)COC3=O	396.30	unknown	https://doi.org/10.1016/J.BMCL.2011.04.036 https://doi.org/10.1016/0031-9422(95)00195-D
Tetradehydropodophyllotoxin	5316463	Click to see COC1=CC(=CC(=C1OC)OC)C2=C3C(=C(C4=CC5=C(C=C42)OCO5)O)COC3=O	410.40	unknown	https://doi.org/10.1016/J.BMCL.2011.04.036 https://doi.org/10.1002/CHIN.200330221 https://doi.org/10.1016/0031-9422(95)00195-D
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[(3S,3aR,6R,6aR)-6-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	13991182	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)OC6C(C(C(C(O6)CO)O)O)O	682.70	unknown	via CMAUP database
(5R)-5beta-(3,4,5-Trimethoxyphenyl)-7alpha-(hydroxymethyl)-8alpha-(6-O-beta-D-glucopyranosyl-beta-D-glucopyranosyloxy)-5,6,7,8-tetrahydronaphtho[2,3-d]-1,3-dioxole-6beta-carboxylic acid methyl ester	10887221	Click to see COC1=CC(=CC(=C1OC)OC)C2C(C(C(C3=CC4=C(C=C23)OCO4)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)CO)C(=O)OC	770.70	unknown	https://doi.org/10.1248/CPB.49.1474
4'-Demethyldeoxypodophyllotoxin beta-D-glucopyranoside	12311205	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4C(CC5=CC6=C(C=C35)OCO6)COC4=O	546.50	unknown	https://doi.org/10.1016/J.BMCL.2011.04.036
Methyl 7-(hydroxymethyl)-8-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-(3,4,5-trimethoxyphenyl)-5,6,7,8-tetrahydrobenzo[f][1,3]benzodioxole-6-carboxylate	85303190	Click to see COC1=CC(=CC(=C1OC)OC)C2C(C(C(C3=CC4=C(C=C23)OCO4)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)CO)C(=O)OC	770.70	unknown	https://doi.org/10.1248/CPB.49.1474
Podorhizol beta-D-glucoside	443015	Click to see COC1=CC(=CC(=C1OC)OC)C(C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)OC5C(C(C(C(O5)CO)O)O)O	578.60	unknown	https://doi.org/10.1002/1096-9888(200011)35:11<1246::AID-JMS55>3.0.CO;2-L
> Lignans, neolignans and related compounds / Lignan lactones
(-)-Deoxypodophyllotoxin	2203	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O	398.40	unknown	https://doi.org/10.1016/J.FITOTE.2009.11.003 https://doi.org/10.1248/CPB.49.773
(3aR,4R,9R,9aR)-4,6,7-trihydroxy-9-(3,4,5-trimethoxyphenyl)-3a,4,9,9a-tetrahydro-3H-benzo[f]isobenzofuran-1-one	3010625	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC(=C(C=C24)O)O)O	402.40	unknown	https://doi.org/10.1016/J.BMCL.2011.04.036
(5aS,8aS,9S)-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-[2]benzofuro[5,6-f][1,3]benzodioxole-5,8-dione	25208172	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(=O)C4=CC5=C(C=C24)OCO5	412.40	unknown	https://doi.org/10.1016/0031-9422(95)00195-D
(8aR)-4-hydroxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one	5320458	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)O)COC3=O	414.40	unknown	https://doi.org/10.1016/S0031-9422(00)82628-X
4-Deoxypodophyllotoxin	101256	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O	398.40	unknown	via CMAUP database
4'-Demethyldeoxypodophyllotoxin	160705	Click to see COC1=CC(=CC(=C1O)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O	384.40	unknown	https://doi.org/10.1248/CPB.49.773 https://doi.org/10.1016/J.BMCL.2011.04.036 https://doi.org/10.1016/J.FITOTE.2009.11.003
5-(4-hydroxy-3,5-dimethoxyphenyl)-5,8,8a,9-tetrahydrofuro[3',4':6,7]naphtho[2,3-d][1,3]dioxol-6(5aH)-one	1689	Click to see COC1=CC(=CC(=C1O)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O	384.40	unknown	https://doi.org/10.1016/J.FITOTE.2009.11.003 https://doi.org/10.1248/CPB.49.773
alpha-Peltatin	92129	Click to see COC1=CC(=CC(=C1O)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)O)COC3=O	400.40	unknown	via CMAUP database
d,l-Isopodophyllotoxone	323439	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(=O)C4=CC5=C(C=C24)OCO5	412.40	unknown	https://doi.org/10.1016/0031-9422(95)00195-D
Deoxypodophyllotoxin	345501	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O	398.40	unknown	https://doi.org/10.1248/CPB.49.773 https://doi.org/10.1016/S0031-9422(00)82604-7 https://doi.org/10.1016/J.FITOTE.2009.11.003 https://doi.org/10.1002/1096-9888(200011)35:11<1246::AID-JMS55>3.0.CO;2-L https://doi.org/10.1016/J.BMCL.2011.04.036 https://doi.org/10.1002/CHIN.200330221
Desoxypodophyllotoxin	71045228	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O	398.40	unknown	via CMAUP database
Isopicropodophyllone	11189106	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(=O)C4=CC5=C(C=C24)OCO5	412.40	unknown	https://doi.org/10.1016/J.BMCL.2011.04.036 https://doi.org/10.1016/0031-9422(95)00195-D
Naphtho(2,3-c)furan-1(3H)-one, 3a,4,9,9a-tetrahydro-4,6,7-trihydroxy-9-(4-hydroxy-3,5-dimethoxyphenyl)-, (3aR,4R,9R,9aR)-	468863	Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC(=C(C=C24)O)O)O	388.40	unknown	https://doi.org/10.1016/J.BMCL.2011.04.036
Picropodopyllotoxone	3083574	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(=O)C4=CC5=C(C=C24)OCO5	412.40	unknown	via CMAUP database
Podophyllotoxone	443014	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(=O)C4=CC5=C(C=C24)OCO5	412.40	unknown	https://doi.org/10.1016/S0031-9422(00)82604-7 https://doi.org/10.1002/1096-9888(200011)35:11<1246::AID-JMS55>3.0.CO;2-L
Sikkimotoxin	3010626	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC(=C(C=C24)OC)OC)O	430.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones / Podophyllotoxins
(+)-Podophyllotoxin	11384429	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O	414.40	unknown	via CMAUP database
(5R,5aR,8aS,9R)-5-hydroxy-9-(4-hydroxy-3,5-dimethoxy-phenyl)-5a,6,8a,9-tetrahydro-5H-isobenzofuro[6,5-f][1,3]benzodioxol-8-one	456051	Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O	400.40	unknown	https://doi.org/10.1248/CPB.49.773
(5R)-5beta-(3,4,5-Trimethoxyphenyl)-9alpha-(6-O-beta-D-glucopyranosyl-beta-D-glucopyranosyloxy)-5,5abeta,6,8,8aalpha,9-hexahydrofuro[3',4':6,7]naphtho[2,3-d]-1,3-dioxole-6-one	10533021	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O	738.70	unknown	https://doi.org/10.1248/CPB.49.773
(5R)-5beta-(3,4,5-Trimethoxyphenyl)-9beta-(beta-D-glucopyranosyloxy)-5,5abeta,6,8,8abeta,9-hexahydrofuro[3',4':6,7]naphtho[2,3-d]-1,3-dioxole-6-one	10918890	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O	576.50	unknown	via CMAUP database
(5R)-9beta-(6-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyloxy)-5beta-(3,4,5-trimethoxyphenyl)-5,5abeta,6,8,8abeta,9-hexahydrofuro[3',4':6,7]naphtho[2,3-d]-1,3-dioxole-6-one	10919696	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O	738.70	unknown	https://doi.org/10.1016/J.BMCL.2011.04.036
(5S,5aR,8aR,9R)-5-hydroxy-9-(4-hydroxy-3,5-dimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one	500181	Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O	400.40	unknown	https://doi.org/10.1248/CPB.49.773 https://doi.org/10.1016/S0031-9422(00)82603-5
[(5aalpha,8abeta)-5beta-(3,4-Dihydroxy-5-methoxyphenyl)-5,5a,6,8,8a,9-hexahydro-6-oxofuro[3',4':6,7]naphtho[2,3-d]-1,3-dioxole-9beta-yl]beta-D-glucopyranoside	101242502	Click to see COC1=CC(=CC(=C1O)O)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O	548.50	unknown	via CMAUP database
[4-[(5R,5aR,8aR,9R)-5-hydroxy-8-oxo-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-9-yl]-2,6-dimethoxyphenyl] acetate	53359026	Click to see CC(=O)OC1=C(C=C(C=C1OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O)OC	442.40	unknown	https://doi.org/10.1016/J.BMCL.2011.04.036
4'-Demethylpodophyllotoxin	122667	Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O	400.40	unknown	https://doi.org/10.1016/0031-9422(86)80072-3 https://doi.org/10.1006/MCHJ.1995.1079 https://doi.org/10.1016/J.BMCL.2011.04.036 https://doi.org/10.1002/1096-9888(200011)35:11<1246::AID-JMS55>3.0.CO;2-L https://doi.org/10.1016/0031-9422(91)84194-W https://doi.org/10.1016/S0031-9422(00)82603-5 https://doi.org/10.1248/CPB.49.773 https://doi.org/10.1016/0021-9673(95)00433-5
4'-Demthylpodophyllotoxin beta-D-glucoside	170385	Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O	562.50	unknown	https://doi.org/10.1248/CPB.49.773 https://doi.org/10.1016/0031-9422(90)85342-D https://doi.org/10.1016/J.BMCL.2011.04.036
5-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one	85175252	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O	738.70	unknown	https://doi.org/10.1248/CPB.49.773
5-hydroxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one	4865	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O	414.40	unknown	https://doi.org/10.1080/1057563031000122095 https://doi.org/10.1016/J.FITOTE.2009.11.003 https://doi.org/10.1016/S0031-9422(00)82603-5 https://doi.org/10.1248/CPB.49.773
6I1J8IM5I7	10844308	Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O	562.50	unknown	https://doi.org/10.1248/CPB.49.773
Epipodophyllotoxin	105111	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O	414.40	unknown	https://doi.org/10.1002/PCA.2800060207
Lignan P	159949	Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O	562.50	unknown	https://doi.org/10.1016/J.BMCL.2011.04.036 https://doi.org/10.1248/CPB.49.1474
Picropodophyllin	72435	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O	414.40	unknown	https://doi.org/10.1248/CPB.49.773 https://doi.org/10.1007/BF02984882
Picropodophyllin, 4'-demethyl-B-D-glucoside	345517	Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O	562.50	unknown	https://doi.org/10.1248/CPB.49.773 https://doi.org/10.1016/0031-9422(90)85342-D https://doi.org/10.1248/CPB.49.1474
Podofilox	10607	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O	414.40	unknown	https://doi.org/10.1016/0031-9422(90)85025-B https://doi.org/10.1007/BF02984882 https://doi.org/10.1248/CPB.49.773 https://doi.org/10.1006/MCHJ.1995.1079 https://doi.org/10.1016/S0031-9422(00)82604-7 https://doi.org/10.1016/J.FITOTE.2009.11.003 https://doi.org/10.1016/0031-9422(86)80072-3 https://doi.org/10.1016/S0031-9422(00)82603-5 https://doi.org/10.1002/1096-9888(200011)35:11<1246::AID-JMS55>3.0.CO;2-L https://doi.org/10.1016/J.BMCL.2011.04.036 https://doi.org/10.1016/S1389-1723(02)80017-2 https://doi.org/10.1080/10575630108041286 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542176/ https://doi.org/10.1080/1057563031000122095 https://doi.org/10.1007/BF00034435 https://doi.org/10.1002/CHIN.200330221
Podophyllotoxin glucoside	161177	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O	576.50	unknown	https://doi.org/10.1248/CPB.49.773 https://doi.org/10.1016/J.BMCL.2011.04.036 https://doi.org/10.1016/0031-9422(90)85342-D https://doi.org/10.1016/0021-9673(95)00433-5
Podophyllotoxin, glucoside	294472	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O	576.50	unknown	https://doi.org/10.1248/CPB.49.773 https://doi.org/10.1016/0031-9422(90)85342-D
sinolignan A	54581698	Click to see CC(=O)OCC1C(C(C(C(O1)OC2C3COC(=O)C3C(C4=CC5=C(C=C24)OCO5)C6=CC(=C(C(=C6)OC)OC)OC)O)O)O	618.60	unknown	https://doi.org/10.1016/J.BMCL.2011.04.036
sinolignan B	54581699	Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O	724.70	unknown	https://doi.org/10.1016/J.BMCL.2011.04.036
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl palmitate	12366	Click to see CCCCCCCCCCCCCCCC(=O)OCC	284.50	unknown	via CMAUP database
Palmitic acid, 2-(octadecyloxy)ethyl ester	545613	Click to see CCCCCCCCCCCCCCCCCCOCCOC(=O)CCCCCCCCCCCCCCC	553.00	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(Z)-9,10-dideuteriooctadec-9-enoic acid	13011408	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	284.50	unknown	via CMAUP database
9-Hexadecenoic acid	5282745	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	via CMAUP database
9-Octadecenoic acid	965	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542176/
Elaidic Acid	637517	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
Oleic Acid	445639	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	via CMAUP database
Palmitoleic Acid	445638	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	via CMAUP database
Palmitolinoleic acid	4668	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542176/
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
3,7-Dimethylocta-2,6-dienyl formate	7779	Click to see CC(=CCCC(=CCOC=O)C)C	182.26	unknown	via CMAUP database
Geranyl acetate	1549026	Click to see CC(=CCCC(=CCOC(=O)C)C)C	196.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Stearyl Alcohol	8221	Click to see CCCCCCCCCCCCCCCCCCO	270.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542176/
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
(9Z,12Z)-Ethyl octadeca-9,12-dienoate	11001	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC	308.50	unknown	via CMAUP database
ethyl (9E,12E)-octadeca-9,12-dienoate	5365672	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC	308.50	unknown	via CMAUP database
Ethyl Linoleate	5282184	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC	308.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(3R,5E)-2,6-dimethylocta-1,5,7-trien-3-ol	92256191	Click to see CC(=C)C(CC=C(C)C=C)O	152.23	unknown	via CMAUP database
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	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
(+)-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
(1R)-5-propan-2-ylbicyclo[3.1.0]hex-2-ene-2-carbaldehyde	92469857	Click to see CC(C)C12CC=C(C1C2)C=O	150.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-Terpinen-4-ol	5325830	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
(-)-trans-Carveol	94221	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	via CMAUP database
(+)-Terpinen-4-ol	2724161	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
(1R)-1-Isopropenyl-4-methyl-3-cyclohexene-1beta-ol	16059268	Click to see CC1=CCC(CC1)(C(=C)C)O	152.23	unknown	via CMAUP database
(1S)-3-Methyl-6alpha-isopropyl-3-cyclohexene-1beta-ol	21604552	Click to see CC1=CCC(C(C1)O)C(C)C	154.25	unknown	via CMAUP database
3-Cyclohexene-1-methanol, alpha,alpha,4-trimethyl-, 1-acetate, (1R)-	11469649	Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C	196.29	unknown	via CMAUP database
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	via CMAUP database
Carvone, (-)-	439570	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	via CMAUP database
cis-p-Mentha-1(7),8-dien-2-ol	6429040	Click to see CC(=C)C1CCC(=C)C(C1)O	152.23	unknown	via CMAUP database
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
trans-1(7),8-p-Menthadien-2-ol	6428442	Click to see CC(=C)C1CCC(=C)C(C1)O	152.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Retinoids
Retinol	445354	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CCO)C)C	286.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542176/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Calamenene	11298625	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	via CMAUP database
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	via CMAUP database
beta-(Z)-Elemenone	22211636	Click to see CC(=C1CC(C(CC1=O)(C)C=C)C(=C)C)C	218.33	unknown	via CMAUP database
beta-Farnesene	5281517	Click to see CC(=CCCC(=CCCC(=C)C=C)C)C	204.35	unknown	via CMAUP database
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(-)-Alloaromadendrene	10899740	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	via CMAUP database
(1aR,4R,4aS,7S,7aS,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol	42433470	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	via CMAUP database
(1aR,7S,7aS,7bR)-1,1,4,7-tetramethyl-1a,2,3,5,6,7,7a,7b-octahydrocyclopropa[e]azulene	11074500	Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C	204.35	unknown	via CMAUP database
(1aR)-1abeta,2,3,4,4a,5,6,7,7aalpha,7bbeta-Decahydro-1,1,4beta,7beta-tetramethyl-1H-cyclopropa[e]azulene-4abeta-ol	100922590	Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O	222.37	unknown	via CMAUP database
(1aS,4aS,7R,7aR,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene	94249462	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	via CMAUP database
Palustrol (Ledum)	9794494	Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O	222.37	unknown	via CMAUP database
Viridiflorene	10910653	Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(3S,4aR,6aR,6aS,8aR,12aS,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol	7093194	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid	7163172	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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Trihydroxy bile acids, alcohols and derivatives
5beta-Cholanic acid-3alpha,7alpha,12alpha-triol ethyl ester	536919	Click to see CCOC(=O)CCC(C)C1CCC2C1(C(CC3C2C(CC4C3(CCC(C4)O)C)O)O)C	436.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542176/
Ethyl cholate	6452096	Click to see CCOC(=O)CCC(C)C1CCC2C1(C(CC3C2C(CC4C3(CCC(C4)O)C)O)O)C	436.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24R)-Methylcholest-5-en-3beta-ol	6428659	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	via CMAUP database
22,23-Dihydrobrassicasterol	5283637	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	via CMAUP database
5-Cholestene-3-ol, 24-methyl-	312822	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542176/
Campesterol	173183	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	6432744	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
(3S,8S,9S,10R,13R,14S,17S)-17-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	1738061	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/J.FITOTE.2009.11.003
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/J.FITOTE.2009.11.003
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/10.1016/J.FITOTE.2009.11.003
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/10.1016/J.FITOTE.2009.11.003
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron	88113319	Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O	192.12	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
3,7-Octadien-2-ol, 2-methyl-6-methylene-, (E)-	5363351	Click to see CC(C)(C=CCC(=C)C=C)O	152.23	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
alpha-D-Glucopyranoside, beta-D-fructofuranosyl	91692850	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
Sucrose	5988	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
Sucrose NF	46782954	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[2-methoxy-4-(1,2,3-trihydroxypropyl)phenoxy]oxane-3,4,5-triol	101713170	Click to see COC1=C(C=CC(=C1)C(C(CO)O)O)OC2C(C(C(C(O2)CO)O)O)O	376.36	unknown	https://doi.org/10.1248/CPB.49.1474
(2R,3S,4S,5R,6S)-2-[[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[4-(2-hydroxyethyl)phenoxy]oxane-3,4,5-triol	10961007	Click to see C1=CC(=CC=C1CCO)OC2C(C(C(C(O2)COC3C(C(C(O3)CO)O)O)O)O)O	432.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexanal	102288	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	via CMAUP database
D-Allose	439507	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	via CMAUP database
L-Galactose	24749	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Octoses
d-Gala-l-ido-octonic amide	552061	Click to see C(C(C(C(C(C(C(C(=O)N)O)O)O)O)O)O)O	255.22	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542176/
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Alpha-branched alpha,beta-unsaturated ketones
2-Methyl-6-methylene-1,7-octadien-3-one	93231	Click to see CC(=C)C(=O)CCC(=C)C=C	150.22	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1S,5R)-5-propan-2-ylbicyclo[3.1.0]hex-3-en-2-one	21626600	Click to see CC(C)C12CC1C(=O)C=C2	136.19	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
2,2'-Benzylidenebis(3-methylbenzofuran)	631793	Click to see CC1=C(OC2=CC=CC=C12)C(C3=CC=CC=C3)C4=C(C5=CC=CC=C5O4)C	352.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans
2,5-Dihydrofuran	15570	Click to see C1C=CCO1	70.09	unknown	via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
cis-Isoascaridole	6430795	Click to see CC(C)C12CCC(C=C1)(OO2)C	168.23	unknown	via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
3-(4-Methyl-1,4-pentadienyl)furan	101409012	Click to see CC(=C)CC=CC1=COC=C1	148.20	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthofurans / Furanonaphthodioxoles
5-Hydroxy-9-(4-hydroxy-3,5-dimethoxyphenyl)-[1]benzofuro[6,5-f][1,3]benzodioxol-8-one	163105345	Click to see COC1=CC(=CC(=C1O)OC)C2=C3C(=O)COC3=C(C4=CC5=C(C=C42)OCO5)O	396.30	unknown	https://doi.org/10.1016/0031-9422(95)00195-D
> Organoheterocyclic compounds / Oxepanes
cis-Carvenone oxide	6430794	Click to see CC1CCC2(C(C1=O)O2)C(C)C	168.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin	5281417	Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O	340.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Fraxetin	5273569	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)O	208.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(1R,2R,3S,4R,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexoxy]chromen-4-one	15959354	Click to see C1C(C(C(C(C1OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O)CO	462.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 2-prenylated flavones
2-[3,4-Dihydroxy-2-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-3-methoxy-8-(3-methylbut-2-enyl)chromen-4-one	46894014	Click to see CC(=CCC1=C(C=CC(=C1O)O)C2=C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)OC)C	452.50	unknown	https://doi.org/10.1016/J.FITOTE.2009.11.003
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
8-Prenylkaempferol	5318624	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C	354.40	unknown	https://doi.org/10.1016/J.FITOTE.2009.11.003
8-Prenylquercetin	9799499	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)O)C	370.40	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	https://doi.org/10.1248/CPB.49.1474 https://doi.org/10.1006/MCHJ.1995.1079 https://doi.org/10.1016/J.FITOTE.2009.11.003
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	https://doi.org/10.1007/BF02984882 https://doi.org/10.1248/CPB.49.1474 https://doi.org/10.1006/MCHJ.1995.1079 https://doi.org/10.1016/J.FITOTE.2009.11.003
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-[3,4-dihydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]-3,5,7-trihydroxychromen-4-one	100952311	Click to see C1C(C(C(C(O1)OC2=CC(=CC(=C2O)O)C3=C(C(=O)C4=C(C=C(C=C4O3)O)O)O)O)O)O	450.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
6''-Acetylhyperin	25230434	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	506.40	unknown	via CMAUP database
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1248/CPB.49.1474
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
Isoquercetin	5280804	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
Kaempferol-3-O-rutinoside	5318767	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O	594.50	unknown	https://doi.org/10.1248/CPB.49.1474
Quercetin 3-(6''-p-hydroxybenzoylgalactoside)	91666354	Click to see C1=CC(=CC=C1C(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O	584.50	unknown	via CMAUP database
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1248/CPB.49.1474 https://doi.org/10.1016/J.FITOTE.2009.11.003
Vitamin P	5293655	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1016/J.FITOTE.2009.11.003
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
8-Demethyleucalyptin	15715157	Click to see CC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)OC)OC	312.30	unknown	via CMAUP database
Myricetin 3,7,3',5'-tetramethyl ether	44259713	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)OC)O)OC)O	374.30	unknown	via CMAUP database
Pachypodol	5281677	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)OC)O	344.30	unknown	via CMAUP database

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Podophyllum hexandrum

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top