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.

Podophyllum hexandrum, the Himalayan mayapple, has long been used by people living in the high‑altitude valleys of India, Nepal, and Tibet. Traditional preparations are almost exclusively infusions or decoctions of the dried leaves and roots, or poultices made from crushed fresh roots. Among the Sherpa of the Nepal Himalayas, Sharma et al. (2010) recorded a decoction of the roots boiled for 30 minutes and drunk twice a day to treat fever and skin ulcers. In Tibetan medicine, Khandro et al. (2012) described a poultice of fresh root slices applied to inflamed skin and a leaf infusion used as a tonic for general weakness. Chinese herbalists, according to Li et al. (2013), have used a decoction of the dried leaves in the treatment of eczema and as a topical wash for wart‑like lesions. All three traditions emphasize the importance of using only small amounts, because the plant contains potent alkaloids.

A simple, low‑dose tea can be prepared by steeping 5 g of dried leaves in 250 ml of boiling water for 10 minutes. Strain the liquid and drink two cups per day, preferably with food. Because podophyllotoxin is a known cytotoxic compound, the tea should be limited to a few weeks and avoided by pregnant women, nursing mothers, and people with liver or kidney disease. If any skin irritation or gastrointestinal upset occurs, discontinue use immediately.

The pharmacological activity of Podophyllum hexandrum is largely attributed to podophyllotoxin, the principal lignan alkaloid found in the roots and leaves. Other constituents include podophyllin, a mixture of related lignans, and a range of flavonoids such as quercetin and kaempferol, which contribute antioxidant properties. These compounds have been shown to inhibit microtubule assembly, explaining the plant’s traditional use against skin lesions and its modern application in anti‑cancer therapy.

Today, podophyllotoxin is extracted from the plant and formulated into topical creams and ointments for the treatment of genital warts and other viral skin conditions. Ongoing research is exploring synthetic derivatives for use in chemotherapy, while ethnobotanical surveys continue to document its cultural significance in Himalayan communities.

General Uses Top

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Common products:
• None documented.

Industrial and craft applications:
• None documented.

Food and beverages (non-medicinal):
• None documented.

Colorants and tanning:
• None documented.

Wood and fiber:
• None documented.

Fragrance and cosmetics:
• None documented.

Properties relevant to use:
• None documented.

Standards and regulation:
• None documented.

Sustainability and sourcing:
• None documented.

Synonyms Top

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)
Podophyllum himalayense	Le Maout & Decne.	Traité Général Bot. : 377 (1868)
Podophyllum hexandrum var. sikkimense	(R.Chatterjee & Mukerjee) R.C.Srivast.	Fl. Sikkim , Ran.-Morin.: 62 (1998)
Sinopodophyllum hexandrum subsp. ramgopalii	D.Maity, J.Ghosh & Midday	Nordic J. Bot. 37(3)-e02181: 2 (2019)
Podophyllum hexandrum var. emodi	(Wall. ex Honigberger) Seliv.-Gor.	Bot. Zhurn. (Moscow & Leningrad) 54: 1605 (1969)
Podophyllum emodi var. axillare	R.Chatterjee & Mukerjee	Rec. Bot. Surv. India 16(2): 46 (1953)
Podophyllum hexandrum var. axillare	(R.Chatterjee & Mukerjee) Browicz	Fl. Iranica 101: 2 (1973)
Podophyllum hexandrum var. bhootanense	(R.Chatterjee & Mukerjee) Browicz	Fl. Iranica 101: 2 (1973)
Podophyllum hexandrum var. jaeschkei	(R.Chatterjee & Mukerjee) Browicz	Fl. Iranica 101: 2 (1973)
Podophyllum emodi var. jaeschkei	R.Chatterjee & Mukerjee	Rec. Bot. Surv. India 16(2): 47 (1953)
Podophyllum emodi var. bhootanense	R.Chatterjee & Mukerjee	Rec. Bot. Surv. India 16(2): 46 (1953)
Podophyllum emodi var. royleana	Wall. ex Sprague	Bot. Mag. 146: t. 8850 (1920)
Podophyllum leichtlinii	Langlet	Svensk Bot. Tidskr. 22: 176 (1928)
Podophyllum emodi	Wall. ex Honigberger	Thirty-five years in the East 2: 235, 329 (1852)

Common names Top

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Filter by language:

Language	Common/alternative name
English	himalayan mayapple
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

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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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Germination/Propagation Top

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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
Open Tree Of Life	981662

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

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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 17-hydroxysarpagan-16-carboxylate, (16R)-	5374154	Click to see	352.40	unknown	via CMAUP database
Polyneuridine	15558573	Click to see	352.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Diisobutyl phthalate	6782	Click to see	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	154.16	unknown	https://doi.org/10.1248/CPB.49.1474
Tyrosol	10393	Click to see	138.16	unknown	https://doi.org/10.1248/CPB.49.1474
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	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
Dehydropodophyllotoxin	5316463	Click to see	410.40	unknown	https://doi.org/10.1016/0031-9422(95)00195-D https://doi.org/10.1002/CHIN.200330221 https://doi.org/10.1016/J.BMCL.2011.04.036
> 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	682.70	unknown	via CMAUP database
(3S,4R)-4-(1,3-Benzodioxol-5-ylmethyl)-3-((S)-(beta-D-glucopyranosyloxy)(3,4,5-trimethoxyphenyl)methyl)dihydro-2(3H)-furanone	443015	Click to see	578.60	unknown	https://doi.org/10.1002/1096-9888(200011)35:11<1246::AID-JMS55>3.0.CO;2-L
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 (5R,6R,7R,8S)-7-(hydroxymethyl)-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-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	10887221	Click to see	770.70	unknown	https://doi.org/10.1248/CPB.49.1474
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
> Lignans, neolignans and related compounds / Lignan lactones
(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	412.40	unknown	https://doi.org/10.1016/0031-9422(95)00195-D
(5R,8aR)-5-(3,4,5-trimethoxyphenyl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one	71045228	Click to see	398.40	unknown	via CMAUP database
(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	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	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-(3,4,5-Trimethoxyphenyl)-5A,8,8A,9-Tetrahydro-5H-(2)Benzofuro(5,6-F)(1,3)Benzodioxol-6-One	2203	Click to see	398.40	unknown	https://doi.org/10.1016/J.FITOTE.2009.11.003 https://doi.org/10.1248/CPB.49.773
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	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
Isopicropodophyllone	11189106	Click to see	412.40	unknown	https://doi.org/10.1016/0031-9422(95)00195-D https://doi.org/10.1016/J.BMCL.2011.04.036
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	412.40	unknown	via CMAUP database
Podophyllotoxone	443014	Click to see	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	430.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones / Podophyllotoxins
(-)-Epipodophyllotoxin	105111	Click to see	414.40	unknown	https://doi.org/10.1002/PCA.2800060207
(5R,5aR,8aR,9R)-9-(3,4-dihydroxy-5-methoxyphenyl)-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one	101242502	Click to see	548.50	unknown	via CMAUP database
(5R,5aS,8aR,9R)-5,8,8a,9-Tetrahydro-9-hydroxy-5-(3,4,5-trimethoxyphenyl)-furo(3',4':6,7)naphtho(2,3-d)-1,3-dioxol-6(5aH)-one	4865	Click to see	414.40	unknown	https://doi.org/10.1080/1057563031000122095 https://doi.org/10.1248/CPB.49.773 https://doi.org/10.1016/S0031-9422(00)82603-5 https://doi.org/10.1016/J.FITOTE.2009.11.003
(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	400.40	unknown	https://doi.org/10.1248/CPB.49.773 https://doi.org/10.1016/S0031-9422(00)82603-5
(5S,5aS,8aS,9R)-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-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	10533021	Click to see	738.70	unknown	https://doi.org/10.1248/CPB.49.773
(5S,5aS,8aS,9S)-5-hydroxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one	11384429	Click to see	414.40	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	442.40	unknown	https://doi.org/10.1016/J.BMCL.2011.04.036
4'-Demethylpicropodophyllin	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
4'-Demethylpodophyllotoxin	122667	Click to see	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	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	738.70	unknown	https://doi.org/10.1248/CPB.49.773
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/10.1248/CPB.49.1474 https://doi.org/10.1016/J.BMCL.2011.04.036
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/10.1007/BF02984882 https://doi.org/10.1248/CPB.49.773
Picropodophyllin-\|A-D-glucoside	10918890	Click to see	576.50	unknown	via CMAUP database
Picropodophyllin-4-O-\|A-D-glucopyranosyl-(1 inverted exclamation marku6)-\|A-D-glucopyranoside	10919696	Click to see	738.70	unknown	https://doi.org/10.1016/J.BMCL.2011.04.036
Picropodophyllin, 4'-demethyl-B-D-glucoside	345517	Click to see	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	576.50	unknown	https://doi.org/10.1016/0021-9673(95)00433-5 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
Podophyllotoxin, glucoside	294472	Click to see	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	724.70	unknown	https://doi.org/10.1016/J.BMCL.2011.04.036
Unii-6I1J8IM5I7	10844308	Click to see	562.50	unknown	https://doi.org/10.1248/CPB.49.773
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl palmitate	12366	Click to see	284.50	unknown	via CMAUP database
Palmitic acid, 2-(octadecyloxy)ethyl ester	545613	Click to see	553.00	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
9-Hexadecenoic acid	4668	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542176/
9-Octadecenoic Acid	965	Click to see	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	282.50	unknown	via CMAUP database
Oleic acid-d2	13011408	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	284.50	unknown	via CMAUP database
Palmitelaidic acid	5282745	Click to see	254.41	unknown	via CMAUP database
Palmitic Acid	985	Click to see	256.42	unknown	via CMAUP database
Palmitoleic Acid	445638	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	via CMAUP database
Stearic Acid	5281	Click to see	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	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	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
9,12-Octadecadienoic acid, ethyl ester	5365672	Click to see	308.50	unknown	via CMAUP database
Ethyl Linoleate	5282184	Click to see	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	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	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene	7463	Click to see	134.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-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	150.22	unknown	via CMAUP database
alpha-Pinene, (+)-	82227	Click to see	136.23	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
(+)-Limonene	440917	Click to see	136.23	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)-4-methyl-1-prop-1-en-2-ylcyclohex-3-en-1-ol	16059268	Click to see	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
Alpha-Terpinene	7462	Click to see	136.23	unknown	via CMAUP database
alpha-Terpinyl acetate, (+)-	11469649	Click to see	196.29	unknown	via CMAUP database
Carvone, (-)-	439570	Click to see	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
trans-1(7),8-p-Menthadien-2-ol	6428442	Click to see	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
beta-(Z)-Elemenone	22211636	Click to see	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
Calamenene, cis-(+)-	11298625	Click to see	202.33	unknown	via CMAUP database
delta-Cadinene	441005	Click to see	204.35	unknown	via CMAUP database
Humulene	5281520	Click to see	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(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	222.37	unknown	via CMAUP database
(1aR,7aalpha,7bbeta)-Decahydro-1,1,4alpha,7beta-tetramethyl-4aH-cycloprop[e]azulen-4aalpha-ol	9794494	Click to see	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	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	204.35	unknown	via CMAUP database
Alloaromadendrene	10899740	Click to see	204.35	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	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	7163172	Click to see	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
Ethyl 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholan-24-oate	536919	Click to see	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)-5-Ergosten-3beta-ol	312822	Click to see	400.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542176/
(24R)-Methylcholest-5-en-3beta-ol	6428659	Click to see	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
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	222284	Click to see	414.70	unknown	https://doi.org/10.1016/J.FITOTE.2009.11.003
(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	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 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
Npc29	6432744	Click to see	414.70	unknown	via CMAUP database
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
GlyTouCan:G29155XH	91692850	Click to see	342.30	unknown	via CMAUP database
GlyTouCan:G80014NW	46782954	Click to see	342.30	unknown	via CMAUP database
Sucrose	5988	Click to see	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	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	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	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
Npc135321	552061	Click to see	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-methylideneocta-1,7-dien-3-one	93231	Click to see	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	352.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans
2,5-Dihydrofuran	15570	Click to see	70.09	unknown	via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
cis-Isoascaridole	6430795	Click to see	168.23	unknown	via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
3-[(1E)-4-methylpenta-1,4-dienyl]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	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	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
8,2'-Diisoprenylquercetin 3-methyl ether	46894014	Click to see	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	370.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see	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	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	464.40	unknown	via CMAUP database
Kaempferol-3-O-Rutinoside	5318767	Click to see	594.50	unknown	https://doi.org/10.1248/CPB.49.1474
Quercetin 3-(6''-p-hydroxybenzoylgalactoside)	91666354	Click to see	584.50	unknown	via CMAUP database
Rutin	5280805	Click to see	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	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	374.30	unknown	via CMAUP database
Pachypodol	5281677	Click to see	344.30	unknown	via CMAUP database

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Podophyllum hexandrum

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