Food and beverages (non-medicinal):
The fresh leaves are used in Brazil as a culinary herb and flavoring in regional dishes; leaves have been recorded as edible and as condiments for fish and other foods. Processing involves washing, chopping or crushing to release aroma, and adding as a fresh or briefly cooked seasoning. Brazilian research has characterized the leaf essential oil, confirming its distinct aroma profile.

Industrial and craft applications:
The essential oil is obtained from leaves and stems by steam distillation for analytical and flavoring purposes. Quantitative GC analyses report the major constituents typically include dillapiole, (E)-nerolidol, myristicin, safrole, p-mentha-1,5-dien-8-ol, and α-bisabolol, depending on chemotype and origin. Chemical data supports differentiation among Piper species and chemotypes in quality control and identity testing for flavor preparations.

Colorants and tanning:
No reliable industrial records of use as a natural colorant or tannin source for this species.

Wood and fiber:
No reliable records of timber or bast/leaf-fiber utilization; it is a small understory shrub.

Fragrance and cosmetics:
The leaf oil is used in trace amounts as a natural flavor/fragrance ingredient; its composition (rich in phenylpropanoids and sesquiterpenes) informs olfactory notes. Regulatory status varies by jurisdiction; the 2017 RIFM compendium lists Piper extracts in the category of “perfume raw materials” with varying restrictions.

Properties relevant to use:
Dillapiole-rich chemotypes yield oils with high concentrations of dillapiole (often >50% in some analyses). Other chemotypes display higher levels of (E)-nerolidol and myristicin. Oil density and refractive index data are available in Brazilian GC studies; these parameters aid analytical fingerprinting and batch-to-batch consistency.

Standards and regulation:
Natural flavor compositions containing Piper extracts are typically evaluated under general food and cosmetics regulations (e.g., ANVISA in Brazil; EU Regulation 1334/2008 for flavoring substances; IFRA standards for fragrance materials). National limits and safety assessments apply to individual constituents (e.g., safrole and myristicin) and to finished products in which these extracts are used.

Sustainability and sourcing:
The species is collected in the wild; conservation strategies are not specified in the available literature. Cultivation status is not documented; no post-harvest or agronomic guidance is reported in the cited sources.

References: Santos et al. (Química Nova, 1997); Sawaya et al. (Journal of Essential Oil Research, 2006); Mesquita et al. (Química Nova, 2005); RIFM (Fragrance Materials Compendium, 2017).

Synonyms Top

Scientific name	Authority	First published in
Piper fulvescens	C.DC.	Mém. Soc. Phys. Genève 32(2): 7 (1893)
Piper pallescens	C.DC.	Linnaea 37: 362 (1872)
Piper fulvescens var. subglabrum	C.DC.	Mém. Soc. Phys. Genève 31(1: 2): 8 (1893)
Piper regnellii var. pallescens	(C.DC.) Yunck.	Bol. Inst. Bot. (São Paulo) 3: 119 (1966)
Artanthe regnellii	Miq.	Linnaea 22: 574 (1849)
Piper epunctulatum	C.DC.	Prodr. 16(1): 338 (1869)
Piper flabellinerve	C.DC.	Beibl. Bot. Jahrb. Syst. 65: 26 (1900)
Piper fulvescens var. geraense	C.DC.	Notizbl. Bot. Gart. Berlin-Dahlem 6: 436 1917
Piper fulvescens var. igatimiana	C.DC.	Bull. Herb. Boissier , sér. 2, 3: 400 (1903)
Piper fulvescens var. velutinum	C.DC.	Mém. Soc. Phys. Genève 31(1: 2): 8 (1893)
Piper regnellii var. glabrius	C.DC.	Candollea 1: 273 (1923)
Piper regnellii var. parvifolium	C.DC.	Candollea 1: 273 (1923)

Common names Top

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No common names added yet.

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

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Southern South America
  - Argentina Northeast
  - Paraguay

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000485253
Tropicos	25000864
KEW	urn:lsid:ipni.org:names:683057-1
The Plant List	kew-2567651
Open Tree Of Life	5321898
NCBI Taxonomy	1427529
IPNI	683057-1
GBIF	7305320
EOL	5481987
CMAUP	NPO16141

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

UHPLC-HRMS/MS Chemical Fingerprinting of the Bioactive Partition from Cultivated Piper aduncum L.

de Luna AV, Fagundes TD, Ramos YJ, de Araújo MH, Muzitano MF, Calixto SD, Simão TL, de Queiroz GA, Guimarães EF, Marques AM, Moreira DD

Molecules

09-Apr-2024

PMCID:	PMC11051932
doi:	10.3390/molecules29081690
PMID:	38675510

Chemical profile and biological properties of the Piper corcovadense C.DC. essential oil

Henrique Fontoura B, Cristina Perin E, Paula Buratto A, Francisco Schreiner J, Menezes Cavalcante K, Dias Teixeira S, Manica D, Antônio Narzetti R, Bruno da Silva G, Dulce Bagatini M, Luiza Cadorin Oldoni T, Teresinha Carpes S

Saudi Pharm J

12-Feb-2024

PMCID:	PMC10879029
doi:	10.1016/j.jsps.2024.101993
PMID:	38384478

Essential Oils in Cervical Cancer: Narrative Review on Current Insights and Future Prospects

Abd Rashid N, Mohamad Najib NH, Abdul Jalil NA, Teoh SL

Antioxidants (Basel)

13-Dec-2023

PMCID:	PMC10740549
doi:	10.3390/antiox12122109
PMID:	38136228

Preliminary Study on the Antibacterial Activities and Antibacterial Guided Fractionation of Some Common Medicinal Plants Practices in Itum Bahal, Kathmandu Valley of Nepal

Bhandari R, Pant D, Kathayat KS, Bhattarai R, Barakoti H, Pandey J, Jamarkatel-Pandit N

ScientificWorldJournal

21-Sep-2023

PMCID:	PMC10539093
doi:	10.1155/2023/7398866
PMID:	37780640

Novel transungual drug delivery system for treating onychomycosis

Sharma S, Chopra H, Pahwa R, Emran TB, Singh I

Int J Surg

01-Mar-2023

PMCID:	PMC10389512
doi:	10.1097/JS9.0000000000000041
PMID:	36906788

Exploring Synthetic Dihydrobenzofuran and Benzofuran Neolignans as Antiprotozoal Agents against Trypanosoma cruzi

Pagotti MC, Dias HJ, Candido AC, Oliveira TA, Borges A, Oliveira ND, Lopes CD, Orenha RP, Parreira RL, Crotti AE, Magalhães LG

Pharmaceutics

24-Feb-2023

PMCID:	PMC10052957
doi:	10.3390/pharmaceutics15030754
PMID:	36986617

Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review

Salazar-Gómez A, Alonso-Castro AJ

Pharmaceuticals (Basel)

31-Aug-2022

PMCID:	PMC9505834
doi:	10.3390/ph15091095
PMID:	36145316

Secondary plant metabolites as potent drug candidates against antimicrobial-resistant pathogens

Keita K, Darkoh C, Okafor F

SN Appl Sci

08-Jul-2022

PMCID:	PMC9264742
doi:	10.1007/s42452-022-05084-y
PMID:	35821909

Natural compounds based chemotherapeutic against Chagas disease and leishmaniasis: mitochondrion as a strategic target

Lazarin-Bidóia D, Garcia FP, Ueda-Nakamura T, Silva SD, Nakamura CV

Mem Inst Oswaldo Cruz

30-Mar-2022

PMCID:	PMC8970591
doi:	10.1590/0074-02760220396
PMID:	35352776

20th IUPAB International Congress, 45th SBBf Congress and 50th Annual Meeting of SBBq: Poster Abstracts

N/A

Biophys Rev

28-Oct-2021

PMCID:	PMC8551951
doi:	10.1007/s12551-021-00845-2

Natural-Product-Based Solutions for Tropical Infectious Diseases

Adegboye O, Field MA, Kupz A, Pai S, Sharma D, Smout MJ, Wangchuk P, Wong Y, Loiseau C

Clin Microbiol Rev

08-Sep-2021

PMCID:	PMC8673330
doi:	10.1128/CMR.00348-20
PMID:	34494873

Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review

Xu Y, Liang B, Kong C, Sun Z

Biomed Res Int

08-Sep-2021

PMCID:	PMC8448615
doi:	10.1155/2021/9910365
PMID:	34541000

Ontogenetic Changes in the Chemical Profiles of Piper Species

Gaia AM, Yamaguchi LF, Guerrero-Perilla C, Kato MJ

Plants (Basel)

28-May-2021

PMCID:	PMC8227164
doi:	10.3390/plants10061085
PMID:	34071315

Antimicrobial and Anti-Biofilm Activities of Citrus sinensis and Moringa oleifera Against the Pathogenic Pseudomonas aeruginosa and Staphylococcus aureus

Zubair M

Cureus

28-Dec-2020

PMCID:	PMC7839279
doi:	10.7759/cureus.12337
PMID:	33520533

Overview of Antifungal Drugs against Paracoccidioidomycosis: How Do We Start, Where Are We, and Where Are We Going?

do Carmo Silva L, de Oliveira AA, de Souza DR, Barbosa KL, Freitas e Silva KS, Carvalho Júnior MA, Rocha OB, Lima RM, Santos TG, Soares CM, Pereira M

J Fungi (Basel)

19-Nov-2020

PMCID:	PMC7712482
doi:	10.3390/jof6040300
PMID:	33228010

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 / Lupin alkaloids / Anagyrine-type alkaloids
(-)-Thermopsine	638234	Click to see	244.33	unknown	via CMAUP database
(1R,9R,10R,12R)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one	15939858	Click to see	260.33	unknown	via CMAUP database
Anagyrine	5351589	Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O	244.33	unknown	via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
N-Methylcytisine	670971	Click to see	204.27	unknown	via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
Mamanine	3085182	Click to see	262.35	unknown	via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(-)-Sophocarpine	115269	Click to see	246.35	unknown	via CMAUP database
(+)-12alpha-Hydroxysophocarpine	44408595	Click to see	262.35	unknown	via CMAUP database
(+)-Sophoranol	12442899	Click to see	264.36	unknown	via CMAUP database
(1R,2R,5S,9S,17S)-5-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	10659287	Click to see C1CC2CN3C(CCC(C3=O)O)C4C2N(C1)CCC4	264.36	unknown	via CMAUP database
(1R,2R,9R,13R,17S)-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	21586634	Click to see C1CC2C3CCC[N+]4(C3C(CCC4)CN2C(=O)C1)[O-]	264.36	unknown	via CMAUP database
(1R,2R,9R,17S)-7,13-Diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one	21763818	Click to see	246.35	unknown	via CMAUP database
(1R,2R,9S,15S,17S)-15-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one	12133310	Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CC(C4)O	262.35	unknown	via CMAUP database
(5beta,6beta,7beta,11alpha)-Matridin-15-one	638232	Click to see	248.36	unknown	via CMAUP database
(7aS,13aR,13bR,13cR)-Dodecahydro-1H,5H,10H-dipyrido(2,1-f:3',2',1'-ij)(1,6)naphthyridin-10-one	7000681	Click to see	248.36	unknown	via CMAUP database
5,9-Dihydroxymatrine	14274649	Click to see C1CC2C3CC(CN4C3C(CCC4)(CN2C(=O)C1)O)O	280.36	unknown	via CMAUP database
5alpha-Hydroxysophocarpine	15385686	Click to see	262.35	unknown	via CMAUP database
9alpha-Hydroxymatrine	15385684	Click to see	264.36	unknown	via CMAUP database
Isomatrine	5271984	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	via CMAUP database
Matridin-15-one, 12,13-didehydro-	3041752	Click to see C1CC2CN3C(C=CCC3=O)C4C2N(C1)CCC4	246.35	unknown	via CMAUP database
Matrine	91466	Click to see	248.36	unknown	via CMAUP database
Sophoridine	165549	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(+)-Lupanine	91471	Click to see	248.36	unknown	via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Anethole	637563	Click to see	148.20	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(1S,6R,7R)-7-[(1S)-1,2-dihydroxyethyl]-6-hydroxy-1-(4-hydroxyphenyl)-4,8-dioxaspiro[4.4]nonane-3,9-dione	193664	Click to see	324.28	unknown	https://doi.org/10.1055/S-2001-18838 https://doi.org/10.1590/S0102-695X2005000300006
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1055/S-2001-18363
Myrcene	31253	Click to see	136.23	unknown	https://doi.org/10.1055/S-2001-18363 https://doi.org/10.1590/S0102-695X2005000300006 https://doi.org/10.1016/S0378-8741(01)00211-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene	7463	Click to see	134.22	unknown	https://doi.org/10.1055/S-2001-18363
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
Sabinene	18818	Click to see	136.23	unknown	https://doi.org/10.1055/S-2001-18363
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1055/S-2001-18363
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1055/S-2001-18363
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1055/S-2001-18363
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	5315592	Click to see	222.37	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
delta-Cadinene	441005	Click to see	204.35	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
gamma-Muurolene	12313020	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
Ishwarane	14619932	Click to see	204.35	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
Nerolidol	5284507	Click to see	222.37	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2 https://doi.org/10.1055/S-2001-18363
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol	91746597	Click to see	222.37	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene	91746456	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	97032059	Click to see	220.35	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	5321422	Click to see	220.35	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
1H-Cycloprop(e)azulene, decahydro-1,1,7-trimethyl-4-methylene-, (1aR-(1aalpha,4abeta,7alpha,7abeta,7balpha))-	91354	Click to see	204.35	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
Npc239037	101716	Click to see	222.37	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(+)-Bicyclogermacrene	5315347	Click to see	204.35	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene	44583886	Click to see	204.35	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene	91723653	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1016/S0378-8741(01)00211-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Illudanes and illudins / Melleolides and analogues
Armillyl orsellinate	14707323	Click to see CC1=CC(=CC(=C1C(=O)OC2CC3(C2=C(C(C4C3CC(C4)(C)C)O)CO)C)O)O	402.50	unknown	https://doi.org/10.1016/S0031-9422(99)00177-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylate	21636205	Click to see	1251.40	unknown	via CMAUP database
Soyasaponin I	122097	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O	943.10	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid	9476	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
Neochlorogenic acid	5280633	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
> Organoheterocyclic compounds / Azoles / Imidazoles
2,4-Dimethylimidazole	70259	Click to see	96.13	unknown	via CMAUP database
4-Methylimidazole	13195	Click to see	82.10	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
(1S,12R,13R,20S)-13,20-dimethoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,17-tetraen-16-one	10831417	Click to see	346.30	unknown	via CMAUP database
(1S,12R,13S,20S)-13-hydroxy-20-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,17-tetraen-16-one	10496772	Click to see	332.30	unknown	via CMAUP database
Apiole	10659	Click to see	222.24	unknown	https://doi.org/10.1016/S0031-9422(99)00177-6
Dillapiol	10231	Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC	222.24	unknown	https://doi.org/10.1016/S0031-9422(99)00177-6
Myristicin	4276	Click to see	192.21	unknown	https://doi.org/10.1016/S0031-9422(99)00177-6
> Organoheterocyclic compounds / Coumarans
Kushecarpin A	10495761	Click to see	318.32	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines
(-)-Sophoramine	169014	Click to see	244.33	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(3S)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-ium-3-carboxylate	6920044	Click to see C1C([NH2+]CC2=C1C3=CC=CC=C3N2)C(=O)[O-]	216.24	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Pyridinones
(+)-Kuraramine	46187187	Click to see CN1CC(CC(C1)C2=CC=CC(=O)N2)CO	222.28	unknown	via CMAUP database
6-[(3R,5R)-5-(hydroxymethyl)-1-methylpiperidin-3-yl]-1H-pyridin-2-one	101665417	Click to see	222.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+)-Conocarpan	6474521	Click to see	266.30	unknown	https://doi.org/10.1055/S-2001-18838
(2S,3R)-2-(4-hydroxyphenyl)-3-methyl-2,3-dihydro-1-benzofuran-5-carbaldehyde	101040753	Click to see CC1C(OC2=C1C=C(C=C2)C=O)C3=CC=C(C=C3)O	254.28	unknown	https://doi.org/10.1016/S0031-9422(99)00177-6
(E)-4-[3-Methyl-5-(1-propen-1-yl)-2-benzofuryl]phenol	3001232	Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC=C(C=C3)O	264.30	unknown	https://doi.org/10.1248/BPB.29.2126 https://doi.org/10.1016/S0031-9422(99)00177-6 https://doi.org/10.1055/S-2001-18838
2-(2,4-Dihydroxy-5-prenylphenyl)-5,6-methylenedioxybenzofuran	15953774	Click to see CC(=CCC1=CC(=C(C=C1O)O)C2=CC3=CC4=C(C=C3O2)OCO4)C	338.40	unknown	via CMAUP database
2-(4-Hydroxyphenyl)-3-methyl-2,3-dihydro-1-benzofuran-5-carbaldehyde	85231246	Click to see CC1C(OC2=C1C=C(C=C2)C=O)C3=CC=C(C=C3)O	254.28	unknown	https://doi.org/10.1016/S0031-9422(99)00177-6
2-methoxy-4-[(2R,3R)-3-methyl-5-[(E)-prop-1-enyl]-2,3-dihydro-1-benzofuran-2-yl]phenol	14213227	Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC(=C(C=C3)O)OC	296.40	unknown	https://doi.org/10.1016/S0031-9422(99)00177-6
2-Methoxy-4-[3-methyl-5-(1-propenyl)-2-benzofuranyl]-phenol	193821	Click to see	294.30	unknown	https://doi.org/10.1248/BPB.29.2126 https://doi.org/10.1055/S-0030-1270889 https://doi.org/10.1016/S0031-9422(99)00177-6 https://doi.org/10.1055/S-2001-18838 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257596/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257403/
2'-Hydroxy-4'-methoxy-5,6-methylenedioxy-2-phenylbenzofuran	44260109	Click to see COC1=CC(=C(C=C1)C2=CC3=CC4=C(C=C3O2)OCO4)O	284.26	unknown	via CMAUP database
4-(3-Methyl-5-prop-1-enyl-2,3-dihydro-1-benzofuran-2-yl)phenol	70414118	Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC=C(C=C3)O	266.30	unknown	https://doi.org/10.1248/BPB.29.2126 https://doi.org/10.1016/S0031-9422(99)00177-6 https://doi.org/10.1055/S-2001-18838
4-[(2S,3R)-3-methyl-5-[(E)-prop-1-enyl]-2,3-dihydro-1-benzofuran-2-yl]phenol	11288585	Click to see	266.30	unknown	https://doi.org/10.1016/S0031-9422(99)00177-6
5-(3-Methyl-5-prop-1-enyl-1-benzofuran-2-yl)-1,3-benzodioxole	261729	Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC4=C(C=C3)OCO4	292.30	unknown	https://doi.org/10.1248/BPB.29.2126 https://doi.org/10.1016/S0031-9422(99)00177-6 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257596/ https://doi.org/10.1590/S0102-695X2005000300006
5-(3-Methyl-5-prop-1-enyl-2,3-dihydro-1-benzofuran-2-yl)-1,3-benzodioxole	162972184	Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC4=C(C=C3)OCO4	294.30	unknown	https://doi.org/10.1016/S0031-9422(99)00177-6
5-[(2R,3R)-3-methyl-5-[(E)-prop-1-enyl]-2,3-dihydro-1-benzofuran-2-yl]-1,3-benzodioxole	101040751	Click to see	294.30	unknown	https://doi.org/10.1016/S0031-9422(99)00177-6
5-[3-methyl-5-[(E)-prop-1-enyl]-1-benzofuran-2-yl]-1,3-benzodioxole	6051545	Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC4=C(C=C3)OCO4	292.30	unknown	https://doi.org/10.1016/S0031-9422(99)00177-6 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257596/ https://doi.org/10.1248/BPB.29.2126
Conocarpan	10999992	Click to see	266.30	unknown	https://doi.org/10.1248/BPB.29.2126 https://doi.org/10.1016/S0031-9422(99)00177-6 https://doi.org/10.1055/S-2001-18838 https://doi.org/10.1590/S0102-695X2005000300006
Eupomatenoid 5	6443783	Click to see	294.30	unknown	https://doi.org/10.1248/BPB.29.2126 https://doi.org/10.1055/S-0030-1270889 https://doi.org/10.1016/S0031-9422(99)00177-6 https://doi.org/10.1055/S-2001-18838 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257596/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257403/ https://doi.org/10.1590/S0102-695X2005000300006
Eupomatenoid 6	6261723	Click to see	264.30	unknown	https://doi.org/10.1248/BPB.29.2126 https://doi.org/10.1016/S0031-9422(99)00177-6 https://doi.org/10.1055/S-2001-18838 https://doi.org/10.1590/S0102-695X2005000300006
methyl (2R,3R)-2-(4-hydroxyphenyl)-3-methyl-2,3-dihydro-1-benzofuran-5-carboxylate	101040752	Click to see CC1C(OC2=C1C=C(C=C2)C(=O)OC)C3=CC=C(C=C3)O	284.31	unknown	https://doi.org/10.1016/S0031-9422(99)00177-6
Methyl 2-(4-hydroxyphenyl)-3-methyl-2,3-dihydro-1-benzofuran-5-carboxylate	163002179	Click to see	284.31	unknown	https://doi.org/10.1016/S0031-9422(99)00177-6
rel-(2R,3R)-2,3-Dihydro-2-(4-hydroxyphenyl)-3-methyl-5-benzofurancarboxaldehyde	101712154	Click to see	254.28	unknown	https://doi.org/10.1016/S0031-9422(99)00177-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid	2518	Click to see	180.16	unknown	via CMAUP database
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid	709	Click to see	194.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see	192.17	unknown	via CMAUP database
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S,2''S)-6-lavandulyl-5,7,2',4'-tetrahydroxylflavanone	118975901	Click to see	424.50	unknown	via CMAUP database
(2S)-2,3-Dihydro-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one	38351420	Click to see	370.40	unknown	via CMAUP database
Kushenol V	10572194	Click to see	386.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R,3R)-3,5-dihydroxy-2-(7-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-8,8-dimethyl-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one	11351168	Click to see	440.50	unknown	via CMAUP database
(2R,3S)-2-(2,4-Dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-8-((R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl)chroman-4-one	102004822	Click to see	454.50	unknown	via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2,3-dihydrochromen-4-one	44563159	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O	442.50	unknown	via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	6565899	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C	424.50	unknown	via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-7-hydroxy-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	26209050	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C	438.50	unknown	via CMAUP database
(2S)-2'-methoxykurarinone	11982641	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C	452.50	unknown	via CMAUP database
(2S)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	14258999	Click to see	370.40	unknown	via CMAUP database
(2S)-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2-(2-hydroxyphenyl)-2,3-dihydrochromen-4-one	44563122	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O	426.50	unknown	via CMAUP database
(2S)-7-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	60039901	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C	452.50	unknown	via CMAUP database
(2S)-Euchrenone A7	44593508	Click to see	340.40	unknown	via CMAUP database
(2S)-Isoxanthohumol	9928523	Click to see	354.40	unknown	via CMAUP database
CID 102004745	102004745	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC(CC=C(C)C)C(=C)C)O)C	492.60	unknown	via CMAUP database
Isobavachin	193679	Click to see	324.40	unknown	via CMAUP database
Kurarinol	44563198	Click to see	456.50	unknown	via CMAUP database
Kurarinone	11982640	Click to see	438.50	unknown	via CMAUP database
Kushenol A	44563121	Click to see	408.50	unknown	via CMAUP database
Kushenol E	127234	Click to see	424.50	unknown	via CMAUP database
Kushenol H	44584091	Click to see	472.50	unknown	via CMAUP database
Kushenol I	20832634	Click to see	454.50	unknown	via CMAUP database
Kushenol L	21721878	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC=C(C)C)O)C	440.50	unknown	via CMAUP database
Kushenol M	180948	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC(CC=C(C)C)C(=C)C)O)C	508.60	unknown	via CMAUP database
Kushenol R	42607847	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=CC=C3O)C(=C)C)C	422.50	unknown	via CMAUP database
Kushenol S	10854625	Click to see	340.40	unknown	via CMAUP database
Kushenol U	42608062	Click to see	422.50	unknown	via CMAUP database
KushenolK	44428630	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O	472.50	unknown	via CMAUP database
Leachianone A	44593449	Click to see	438.50	unknown	via CMAUP database
Leachianone G	5275227	Click to see	356.40	unknown	via CMAUP database
Sophoraflavanone B	480764	Click to see	340.40	unknown	via CMAUP database
Sophoraflavanone G	72936	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C	424.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
Licoflavonol	5481964	Click to see	354.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
3-Hydroxy-2-(4-hydroxyphenyl)-5-methoxy-8,8-dimethyl-9,10-dihydropyrano[2,3-h]chromen-4-one	11451469	Click to see	368.40	unknown	via CMAUP database
5-Hydroxy-4-(4-hydroxyphenyl)-10,10,16,16-tetramethyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1,4,7,13-tetraen-6-one	11327657	Click to see	422.50	unknown	via CMAUP database
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	via CMAUP database
Isoanhydroicaritin	5322079	Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)OC)C	368.40	unknown	via CMAUP database
Kushenol C	5481237	Click to see	438.50	unknown	via CMAUP database
Kushenol G	44259516	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)O	456.50	unknown	via CMAUP database
Sophoflavescenol	9929189	Click to see CC(=CCC1=C2C(=C(C=C1O)OC)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C	368.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin	5280805	Click to see	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	13093776	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	5318902	Click to see	562.50	unknown	via CMAUP database
7-(alpha-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one	12304095	Click to see	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain	91510	Click to see	284.26	unknown	via CMAUP database
(-)-Maackiain-3-O-glucosyl-6''-O-malonate	23724669	Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)OC5=CC6=C(C=C25)OCO6	532.40	unknown	via CMAUP database
(+)-Maackiain	161298	Click to see	284.26	unknown	via CMAUP database
(+)-Medicarpin	73067	Click to see	270.28	unknown	via CMAUP database
(1S,12S)-16-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaene	373519	Click to see	298.29	unknown	via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1S,12S)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-yl]oxy]oxane-3,4,5-triol	6326060	Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6	446.40	unknown	via CMAUP database
(6aR,11aR)-3-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-8,9-diol	361910	Click to see	286.28	unknown	via CMAUP database
(6aR,11aR)-3,9-Dimethoxy-6H-benzofuro(3,2-c)(1)benzopyran-6a(11aH)-ol	442828	Click to see	300.30	unknown	via CMAUP database
(6aR,11aR)-8-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol	21676223	Click to see COC1=C(C=C2C(=C1)C3COC4=C(C3O2)C=CC(=C4)O)O	286.28	unknown	via CMAUP database
CID 44428627	44428627	Click to see COC1=CC2=C(C=C1)C3C(CO2)(C4=C(O3)C=C(C=C4)OC)O	300.30	unknown	via CMAUP database
Pterocarpin	1715306	Click to see	298.29	unknown	via CMAUP database
Trifolirhizin	442827	Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6	446.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
3',4',7-Trihydroxyisoflavone	5284648	Click to see	270.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
(3R)-5,7-dihydroxy-3-(6-hydroxy-1,3-benzodioxol-5-yl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	101238023	Click to see CC(=CCC1=C(C2=C(C=C1O)OCC(C2=O)C3=CC4=C(C=C3O)OCO4)O)C	384.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
5,7-Dihydroxy-3-(6-hydroxy-1,3-benzodioxol-5-yl)-6-(3-methylbut-2-enyl)chromen-4-one	101238024	Click to see	382.40	unknown	via CMAUP database
Alpinumisoflavone	5490139	Click to see	336.30	unknown	via CMAUP database
Lupalbigenin	10001388	Click to see	406.50	unknown	via CMAUP database
Luteone	5281797	Click to see	354.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(1,3-benzodioxol-5-yl)-7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one	102131643	Click to see	576.50	unknown	via CMAUP database
3-(3,4-Dihydroxyphenyl)-7-(((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2h-pyran-2-yl) oxy)-4h-chromen-4-one	68607439	Click to see	432.40	unknown	via CMAUP database
3-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	73603979	Click to see	578.50	unknown	via CMAUP database
3'-Methoxy-4'-hydroxy-7-(6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranosyloxy)isoflavone	102131642	Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O	578.50	unknown	via CMAUP database
7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-3-(3-hydroxy-4-methoxyphenyl)chromen-4-one	73603978	Click to see	578.50	unknown	via CMAUP database
Calycosin 7-O-xylosylglucoside	73603980	Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O	578.50	unknown	via CMAUP database
Daidzein 7-O-apiosyl-(1->6)-glucoside	20055730	Click to see	548.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin	5280448	Click to see	284.26	unknown	via CMAUP database
Koparin	5318834	Click to see COC1=C(C(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A	5280373	Click to see	284.26	unknown	via CMAUP database
Formononetin	5280378	Click to see	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Kuraridin	44428631	Click to see	438.50	unknown	via CMAUP database
Xanthohumol	639665	Click to see CC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=C(C=C2)O)O)C	354.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
1-(3-hydroxy-4-methoxyphenyl)-2-[2-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]ethane-1,2-dione	73603972	Click to see	582.50	unknown	via CMAUP database
1-[4-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-2-hydroxyphenyl]-2-(3-hydroxy-4-methoxyphenyl)ethane-1,2-dione	73603983	Click to see COC1=C(C=C(C=C1)C(=O)C(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)O)O	582.50	unknown	via CMAUP database

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Piper regnellii

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