Scientific name	Authority	First published in
Oxydectes caudata	Kuntze	Revis. Gen. Pl. 2: 611 (1891)
Oxydectes denticulata	Kuntze	Revis. Gen. Pl. 2: 609 (1891)
Croton aromaticus	Gaertn.	Fruct. Sem. Pl. 2: 119 (1790)
Croton caudatus var. denticulatus	Müll.Arg.	Prodr. 15(2): 599 (1866)
Croton caudatus var. harmandii	Gagnep.	Fl. Indo-Chine : 277 (1925)
Croton caudatus var. malaccanus	Hook.f.	Fl. Brit. India 5: 389 (1887)
Croton caudatus var. oblongifolius	Müll.Arg.	Prodr. 15(2): 600 (1866)
Croton caudatus var. obovoideus	N.P.Balakr. & Chakrab.	Bull. Bot. Surv. India 25: 190 (1983 publ. 1985)
Croton denticulatus	Blume	Bijdr. Fl. Ned. Ind. : 603 (1826)
Croton drupaceus	Roxb.	Fl. Ind. ed. 1832 , 3: 684 (1832)
Croton malvifolius	Griff.	Itin. Pl. Khasyah Mts. : 200 (1848)
Croton racemosus	Burm.f.	Fl. Indica : 206 (1768)
Croton caudatus var. hispidus	Hook.f.	Fl. Brit. India 5: 389 (1887)
Croton caudatus var. ruminatus	Hook.f.	Fl. Brit. India 5: 389 (1887)
Croton caudatus var. globosus	Hook.f.	Fl. Brit. India 5: 389 (1887)
Croton caudatus var. tomentosus	Hook.f.	Fl. Brit. India 5: 389 (1887)

Common names Top

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Filter by language:

Language	Common/alternative name
Malay	pokok angguk-angguk
Malay	angguk-angguk
Chinese	卵叶巴豆
Chinese	卵叶巴豆*(柳叶巴豆）
Chinese	毛叶巴豆
Chinese	毛叶巴豆树

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

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

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

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Christmas Island
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Philippines
  - Sulawesi
  - Sumatera

Australasia click to expand
- Australia
  - Queensland

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000927601
Tropicos	50077335
KEW	urn:lsid:ipni.org:names:342252-1
The Plant List	kew-49567
Open Tree Of Life	426170
NCBI Taxonomy	323037
IPNI	342252-1
iNaturalist	427404
GBIF	3057531
EOL	1147376
USDA GRIN	12403
CMAUP	NPO6330

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

Nature’s Green Potential: Anticancer Properties of Plants of the Euphorbiaceae Family

Jiménez-González V, Kowalczyk T, Piekarski J, Szemraj J, Rijo P, Sitarek P

Cancers (Basel)

25-Dec-2023

PMCID:	PMC10778523
doi:	10.3390/cancers16010114
PMID:	38201542

A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes

Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B

Molecules

21-Dec-2023

PMCID:	PMC10780140
doi:	10.3390/molecules29010060
PMID:	38202643

Indoor metabolites and chemicals outperform microbiome in classifying childhood asthma and allergic rhinitis

Sun Y, Tang H, Du S, Chen Y, Ou Z, Zhang M, Chen Z, Tang Z, Zhang D, Chen T, Xu Y, Li J, Norback D, Hashim JH, Hashim Z, Shao J, Fu X, Zhao Z

Eco Environ Health

22-Aug-2023

PMCID:	PMC10902507
doi:	10.1016/j.eehl.2023.08.001
PMID:	38435359

Larvicidal Activities of Allium sativum L. and Zingiber officinale Rosc. Extracts against Filariasis Vectors in Hadiya Zone, Ethiopia

Assemie A, Gemeda T

Biomed Res Int

31-May-2023

PMCID:	PMC10247325
doi:	10.1155/2023/6636837
PMID:	37292452

4-Chlorophenol adsorption from water solutions by activated carbon functionalized with amine groups: response surface method and artificial neural networks

Tazik M, Dehghani MH, Yaghmaeian K, Nazmara S, Salari M, Mahvi AH, Nasseri S, Soleimani H, Karri RR

Sci Rep

15-May-2023

PMCID:	PMC10185562
doi:	10.1038/s41598-023-35117-4
PMID:	37188708

Siwalik plant megafossil diversity in the Eastern Himalayas: A review

Khan MA, Mahato S, Spicer RA, Spicer TE, Ali A, Hazra T, Bera S

Plant Divers

17-Dec-2022

PMCID:	PMC10311196
doi:	10.1016/j.pld.2022.12.003
PMID:	37397603

Phytochemical Screening and Isolation of New Ent-Clerodane Diterpenoids from Croton guatemalensis Lotsy

Escandón-Rivera SM, Andrade-Cetto A, Rosas-Ramírez DG, Arreguín-Espinosa R

Plants (Basel)

18-Nov-2022

PMCID:	PMC9692395
doi:	10.3390/plants11223159
PMID:	36432893

Antileishmanial Activities of Medicinal Herbs and Phytochemicals In Vitro and In Vivo: An Update for the Years 2015 to 2021

Hassan AA, Khalid HE, Abdalla AH, Mukhtar MM, Osman WJ, Efferth T

Molecules

04-Nov-2022

PMCID:	PMC9656935
doi:	10.3390/molecules27217579
PMID:	36364404

Synbiotic Effects of Fermented Rice on Human Health and Wellness: A Natural Beverage That Boosts Immunity

Fuloria S, Mehta J, Talukdar MP, Sekar M, Gan SH, Subramaniyan V, Rani NN, Begum MY, Chidambaram K, Nordin R, Maziz MN, Sathasivam KV, Lum PT, Fuloria NK

Front Microbiol

13-Jul-2022

PMCID:	PMC9325588
doi:	10.3389/fmicb.2022.950913
PMID:	35910609

Combining DNA and HPTLC profiles to differentiate a pain relief herb, Mallotus repandus, from plants sharing the same common name, “Kho-Khlan”

Thongkhao K, Tungphatthong C, Pichetkun V, Gaewtongliam S, Wiwatcharakornkul W, Sukrong S

PLoS One

09-Jun-2022

PMCID:	PMC9200221
doi:	10.1371/journal.pone.0268680
PMID:	35679267

Recent Advances in the Development of Noble Metal NPs for Cancer Therapy

Zhao R, Xiang J, Wang B, Chen L, Tan S

Bioinorg Chem Appl

28-Jan-2022

PMCID:	PMC8816609
doi:	10.1155/2022/2444516
PMID:	35126483

Hepatoprotective Plants from Bangladesh: A Biophytochemical Review and Future Prospect

Rouf R, Ghosh P, Uzzaman MR, Sarker DK, Zahura FT, Uddin SJ, Muhammad I

Evid Based Complement Alternat Med

31-Aug-2021

PMCID:	PMC8423546
doi:	10.1155/2021/1633231
PMID:	34504532

The Potential of Traditional Knowledge to Develop Effective Medicines for the Treatment of Leishmaniasis

Passero LF, Brunelli ED, Sauini T, Amorim Pavani TF, Jesus JA, Rodrigues E

Front Pharmacol

08-Jun-2021

PMCID:	PMC8248671
doi:	10.3389/fphar.2021.690432
PMID:	34220515

Evaluation of the Antioxidant and Antimicrobial Activities of Ethyl Acetate Extract of Saccharomyces cerevisiae

Makky EA, AlMatar M, Mahmood MH, Ting OW, Qi WZ

Food Technol Biotechnol

01-Jun-2021

PMCID:	PMC8284104
doi:	10.17113/ftb.59.02.21.6658
PMID:	34316274

Bioremediation and pharmacological applications of gold nanoparticles synthesized from plant materials

Akintelu SA, Yao B, Folorunso AS

Heliyon

29-Mar-2021

PMCID:	PMC8035509
doi:	10.1016/j.heliyon.2021.e06591
PMID:	33869841

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
galloyl(-3)[galloyl(-6)]b-Glc	44421782	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O	484.40	unknown	via CMAUP database
Methyl gallate	7428	Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O	184.15	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(1S,3aR,4S,6aR)-Tetrahydro-1-(4-hydroxy-3-methoxyphenyl)-4-[4-(6-O-galloyl-beta-D-glucopyranosyloxy)-3-methoxyphenyl]-1H,3H-furo[3,4-c]furan	44470458	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)COC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)O)OC)O	672.60	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	486614	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)O	520.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(1S,5R,8R)-8-[(3R)-3-(6-O-Galloyl-beta-D-glucopyranosyloxy)butyl]-1,5-dimethyl-6-oxabicyclo[3.2.1]octane-3-one	101503539	Click to see CC(CCC1C2(CC(=O)CC1(OC2)C)C)OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O	540.60	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(Z)-hex-3-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	5318045	Click to see CCC=CCCOC1C(C(C(C(O1)CO)O)O)O	262.30	unknown	via CMAUP database
(4R)-4-[(3R)-3-(6-O-Galloyl-beta-D-glucopyranosyloxy)-1-butenyl]3,5,5-trimethyl-2-cyclohexene-1-one	44184344	Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)(C)C	522.50	unknown	via CMAUP database
(6R,9R)-3-Oxo-alpha-ionol glucoside	9820702	Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C	370.40	unknown	via CMAUP database
2-Hexenyl-beta-glucopyranoside	6450053	Click to see CCCC=CCOC1C(C(C(C(O1)CO)O)O)O	262.30	unknown	via CMAUP database
3Eec4Q65S4	21630888	Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C	370.40	unknown	via CMAUP database
icariside B5	14135399	Click to see CC1=CC(=O)CC(C1(CCC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	388.50	unknown	via CMAUP database
Lauroside E	101367898	Click to see CC(CCC1C(=CC(=O)CC1(C)C)CO)OC2C(C(C(C(O2)CO)O)O)O	388.50	unknown	via CMAUP database
Macarangioside A	16062725	Click to see CC1=CC(=O)CC(C1(CCC(C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)(C)C	540.60	unknown	via CMAUP database
Macarangioside D	101412231	Click to see CC(C=CC1C(=CC(=O)CC1(C)C)CO)OC2C(C(C(C(O2)CO)O)O)O	386.40	unknown	via CMAUP database
Macarangioside F	44470459	Click to see CC(CCC1C2(CC(=O)CC1(OC2)C)C)OC3C(C(C(C(O3)CO)O)O)O	388.50	unknown	via CMAUP database
Mallophenol B	11156928	Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)(C)C	538.50	unknown	via CMAUP database
Roseoside	9930064	Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	386.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Euphorbiasteroid	15940183	Click to see CC1CC2(C(C1OC(=O)CC3=CC=CC=C3)C(C4(CCC5C(C5(C)C)C=C(C2=O)C)CO4)OC(=O)C)OC(=O)C	552.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
5-[(1S,2R,4aR,8aS)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-ol	71446681	Click to see CC1CCC2(C(C1(C)CCC(=CCO)C)CCC=C2C)C	290.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
blumenol B	14135402	Click to see CC1=CC(=O)CC(C1(CCC(C)O)O)(C)C	226.31	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	via CMAUP database
beta-Amyrone	12306160	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C	424.70	unknown	via CMAUP database
Epifriedelanol	119242	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	428.70	unknown	via CMAUP database
Friedelanol	101341	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	428.70	unknown	via CMAUP database
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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	11870456	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
5alpha-Stigmastane-3,6-dione	13992092	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CCC(=O)C4)C)C)C(C)C	428.70	unknown	via CMAUP database
6beta-Hydroxystigmast-4-en-3-one	9823926	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C	428.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(1R,6R)-1-[(S)-3-Hydroxybutyl]-2,2-dimethyl-7-oxaspiro[5.2]octane-4-one	5319213	Click to see CC(CCC1C(CC(=O)CC12CO2)(C)C)O	226.31	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxepanes
4-[(1R,3R,5S,8R)-3-hydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]butan-2-one	11424667	Click to see CC(=O)CCC1C2(CC(CC1(OC2)C)O)C	226.31	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / 3-pyridinecarbonitriles
Malloapeltine	45079694	Click to see COC1=C(C=[N+](C=C1)[O-])C#N	150.13	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R)-2beta-[3-Methoxy-4-(beta-D-glucopyranosyloxy)phenyl]-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydrobenzofuran-3alpha-methanol	10625848	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)CCCO	522.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Scopolin	439514	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	354.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 2-prenylated flavans / 2-prenylated flavanones
(2S)-2-[2-(3,7-dimethylocta-2,6-dienyl)-3,4-dihydroxyphenyl]-5,7-dihydroxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	91152580	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)O)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)C)C	492.60	unknown	via CMAUP database
(2S)-2-[2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3-hydroxy-4-methoxyphenyl]-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one	11351463	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)OC)C2CC(=O)C3=C(C=C(C=C3O2)OC)O)C)C	452.50	unknown	via CMAUP database
(2S)-2-[2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3-hydroxy-4-methoxyphenyl]-5-hydroxy-7-methoxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	11375844	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)OC)C2CC(=O)C3=C(C(=C(C=C3O2)OC)CC=C(C)C)O)C)C	520.70	unknown	via CMAUP database
(2S)-2-[2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,4-dimethoxyphenyl]-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one	11476850	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1OC)OC)C2CC(=O)C3=C(C=C(C=C3O2)OC)O)C)C	466.60	unknown	via CMAUP database
(2S)-2-[2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,4-dimethoxyphenyl]-5-hydroxy-7-methoxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	11466771	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1OC)OC)C2CC(=O)C3=C(C(=C(C=C3O2)OC)CC=C(C)C)O)C)C	534.70	unknown	via CMAUP database
3',4'-Dihydro-5,7,8'-trihydroxy-2'alpha-methyl-6-(3-methyl-2-butenyl)-2'-(4-methyl-1,3-pentadienyl)-2alpha,5'-bi[2H-1-benzopyran]-4(3H)-one	25155065	Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=C4CCC(OC4=C(C=C3)O)(C)C=CC=C(C)C)O)C	490.60	unknown	via CMAUP database
3',4'-Dihydro-5,7,8'-trihydroxy-2'beta-methyl-6-(3-methyl-2-butenyl)-2'-(4-methyl-1,3-pentadienyl)-2alpha,5'-bi[2H-1-benzopyran]-4(3H)-one	25155334	Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=C4CCC(OC4=C(C=C3)O)(C)C=CC=C(C)C)O)C	490.60	unknown	via CMAUP database
Macaflavanone F	25155066	Click to see CC(=CCCC1(CCC2=C(C=CC(=C2O1)O)C3CC(=O)C4=C(O3)C=C(C(=C4O)CC=C(C)C)O)C)C	492.60	unknown	via CMAUP database
Macaflavanone G	25155335	Click to see CC(=CCCC1(CCC2=C(C=CC(=C2O1)O)C3CC(=O)C4=C(O3)C=C(C(=C4O)CC=C(C)C)O)C)C	492.60	unknown	via CMAUP database
nymphaeol B	10387631	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)O)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C)C	424.50	unknown	via CMAUP database
nymphaeol C	10323393	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)O)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)C)C	492.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-2-(3,4-dimethoxyphenyl)-6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one	11294269	Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC(=C(C=C3)OC)OC)OC)C)C	466.60	unknown	via CMAUP database
(2S)-5,7-dihydroxy-2-[(2R)-8-hydroxy-2-methyl-2-(4-methylpent-3-enyl)chromen-5-yl]-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	25155068	Click to see CC(=CCCC1(C=CC2=C(C=CC(=C2O1)O)C3CC(=O)C4=C(O3)C=C(C(=C4O)CC=C(C)C)O)C)C	490.60	unknown	via CMAUP database
Macaflavanone C	25155069	Click to see CC(=CCCC1(C=CC2=C(C=CC(=C2O1)O)C3CC(=O)C4=C(O3)C=C(C(=C4O)CC=C(C)C)O)C)C	490.60	unknown	via CMAUP database
Nymphaeol A	639465	Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3)O)O)O)C)C	424.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-(beta-D-Arabinopyranosyloxy)-5,7-dihydroxy-2-(3,4-dihydroxyphenyl)-4H-1-benzopyran-4-one	21722017	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	via CMAUP database
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
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	via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,4-di-O-galloyl-alpha-d-glucopyranose	14605152	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(OC(C(C2O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)CO	484.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	via CMAUP database
Geraniin	3001497	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	via CMAUP database
Punicafolin	5320800	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O	938.70	unknown	via CMAUP database

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Croton caudatus

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