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.

Anamu (Petiveria alliacea) has a broad ethnomedicinal footprint across the Neotropics. Among rural communities of northeastern Brazil, leaves are prepared as an infusion or mild decoction for fevers and colds, and as a gargle for sore throat, while rubbed leaf poultices are applied to swellings or skin lesions (de Oliveira et al., 2010). In Cuban and Puerto Rican herbal practice, aerial parts are boiled as a decoction for colds, bronchial complaints, and as a diuretic and anti-inflammatory wash (Brouwer, 2003). Amazonian curanderismo in the Peruvian and Brazilian Amazon records both internal decoctions and topical washes of leaves and stems for fevers, malaria, and female gynecologic pains (Cossio et al., 2008).

Practical preparation: mild leaf infusion. Roughly 1–2 g (1 small handful) of dried leaves or 5–10 g of fresh leaf are infused in 250 ml just-off-the-boil water for 10–15 minutes, then strained; sip 1/2–1 cup up to twice daily as needed. Traditional accounts warn against pregnancy or high-dose use; avoid in the first trimester and consult a clinician if on anticoagulants or sedatives (Brouwer, 2003).

Active constituents isolated from this species include flavonoids (e.g., quercetin- and kaempferol-3-O-rutinosides), phenolic acids (caffeic, p-coumaric), and triterpenoid saponins, which are consistent with antioxidant and anti-inflammatory actions observed in pharmacology (Barros et al., 2010). Commercial dried leaf is available in many Latin markets and is often used in home teas; modern laboratory work continues to probe its anti-inflammatory and anti-proliferative activities.

General Uses Top

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Scientific and research uses:
Petiveria alliacea serves as a subject in phytochemical and pharmacological research due to the documented presence of bioactive compounds such as saponins, flavonoids, and alkaloids. Extracts and isolated compounds are studied in laboratory settings to investigate biological activities and mechanisms. It is a model organism in these research contexts, contributing to databases and studies within the fields of ethnobotany, natural product chemistry, and related biological sciences. There are no other documented non-medicinal uses reported in reliable sources.

Synonyms Top

Scientific name	Authority	First published in
Petiveria corrientina	Rojas	Bull. Acad. Int. Géogr. Bot. 28: 163 1918
Petiveria foetida	Salisb.	Prodr. Stirp. Chap. Allerton 214. 1796 [Nov-Dec 1796]
Petiveria paraguayensis	D.Parodi	Anales Soc. Ci. Argent. 5: 160 (1878)
Petiveria ochroleuca	Moq.	Prodr. 13(2): 9 (1849)
Petiveria alliacea var. grandifolia	Moq.	Prodr. [A. P. de Candolle] 13(2): 9. 1849 [5 May 1849]
Petiveria alliacea var. octandra	(L.) Moq.	Prodr. [A. P. de Candolle] 13(2): 9. 1849 [5 May 1849]
Petiveria hexandria	Sessé & Moc.	Fl. Mexic. , ed. 2: 90 (1894)
Petiveria octandra	L.	Sp. Pl. ed. 2 : 486 (1762)
Petiveria corrientina	Rojas	Bull. Acad. Int. Géogr. Bot. 28: 163 (1918)

Common names Top

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Filter by language:

Language	Common/alternative name
English	guinea henweed
Spanish	anamu
Spanish	anamú
Spanish	muruca
Spanish	murucacaá
Persian	پتیوریا آلیاسی
gn	anamu
gn	mburika ka’a
ht	ave
ht	fèy ave
Portuguese	guiné - petiveria tetrandra
Chinese	蒜味草
Chinese	蒜香草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Petiveria alliacea var. tetrandra	(Ortega) Hauman	Anales Mus. Nac. Hist. Nat. Buenos Aires 24: 501 (1913)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Southern Africa
  - Kwazulu-Natal
- West Tropical Africa
  - Benin
- West-central Tropical Africa
  - Gulf Of Guinea Islands

Asia-tropical click to expand
- Indian Subcontinent
  - India
  - Sri Lanka
- Malesia
  - Jawa

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Gulf
  - Mexico Northeast
  - Mexico Northwest
  - Mexico Southeast
  - Mexico Southwest
- South-central U.S.A.
  - Texas
- Southeastern U.S.A.
  - Florida

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Bahamas
  - Cuba
  - Dominican Republic
  - Haiti
  - Leeward Islands
  - Puerto Rico
  - Southwest Caribbean
  - Trinidad-Tobago
  - Venezuelan Antilles
  - Windward Islands
- Central America
  - Belize
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Nicaragua
  - Panamá
- Northern South America
  - French Guiana
  - Guyana
  - Suriname
  - Venezuela
- Southern South America
  - Argentina Northeast
  - Argentina Northwest
  - Paraguay
  - Uruguay
- Western South America
  - Bolivia
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000481950
UNII	7JU9V35411
Florida Plant Atlas	2822
USDA Plants	PEAL7
Tropicos	24800061
INPN	630368
KEW	urn:lsid:ipni.org:names:323288-2
The Plant List	kew-2562647
Open Tree Of Life	883502
NCBI Taxonomy	46142
Nature Serve	2.140010
IPNI	323288-2
iNaturalist	166545
GBIF	3084012
EPPO	PEVAL
EOL	594860
USDA GRIN	431298

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

Unveiling the molecular mechanisms: dietary phytosterols as guardians against cardiovascular diseases

El Omari N, Bakrim S, Khalid A, Abdalla AN, Iesa MA, El Kadri K, Tang SY, Goh BH, Bouyahya A

Nat Prod Bioprospect

09-May-2024

PMCID:	PMC11082103
doi:	10.1007/s13659-024-00451-1
PMID:	38722432

Mitigation Potential of Herbal Extracts and Constituent Bioactive Compounds on Salmonella in Meat-Type Poultry

Orimaye OE, Ekunseitan DA, Omaliko PC, Fasina YO

Animals (Basel)

03-Apr-2024

PMCID:	PMC11011123
doi:	10.3390/ani14071087
PMID:	38612326

Plants from Arid and Semi-Arid Zones of Mexico Used to Treat Respiratory Diseases: A Review

Dávila-Rangel IE, Charles-Rodríguez AV, López-Romero JC, Flores-López ML

Plants (Basel)

11-Mar-2024

PMCID:	PMC10974781
doi:	10.3390/plants13060792
PMID:	38592789

The secretome from human-derived mesenchymal stem cells augments the activity of antitumor plant extracts in vitro

Ramirez JA, Jiménez MC, Ospina V, Rivera BS, Fiorentino S, Barreto A, Restrepo LM

Histochem Cell Biol

24-Feb-2024

PMCID:	PMC11045572
doi:	10.1007/s00418-024-02265-1
PMID:	38402366

Effect of Petiveria alliacea Extracts on Metabolism of K562 Myeloid Leukemia Cells

Rojas L, Pardo-Rodriguez D, Urueña C, Lasso P, Arévalo C, Cala MP, Fiorentino S

Int J Mol Sci

13-Dec-2023

PMCID:	PMC10743714
doi:	10.3390/ijms242417418
PMID:	38139247

Plant extracts modulate cellular stress to inhibit replication of mouse Coronavirus MHV-A59

Prieto K, Arévalo C, Lasso P, Carlosama C, Urueña C, Fiorentino S, Barreto A

Heliyon

08-Dec-2023

PMCID:	PMC10758815
doi:	10.1016/j.heliyon.2023.e23403
PMID:	38169850

Influence of Carboxymethyl Cellulose on the Green Synthesis of Gold Nanoparticles Using Gliricidia sepium and Petiveria alliacea Extracts: Surface-Enhanced Raman Scattering Effect Evaluation

Horta-Piñeres S, Cortez-Valadez M, Avila DA, Leal-Perez JE, Leyva-Porras CC, Flores-Acosta M, Torres CO

ACS Omega

29-Nov-2023

PMCID:	PMC10720281
doi:	10.1021/acsomega.3c03813
PMID:	38107913

Review green synthesis of silver nanoparticles by using plant extracts and their antimicrobial activity

Abada E, Mashraqi A, Modafer Y, Al Abboud MA, El-Shabasy A

Saudi J Biol Sci

26-Nov-2023

PMCID:	PMC10749906
doi:	10.1016/j.sjbs.2023.103877
PMID:	38148949

Natural Products Induce Different Anti-Tumor Immune Responses in Murine Models of 4T1 Mammary Carcinoma and B16-F10 Melanoma

Lasso P, Rojas L, Arévalo C, Urueña C, Murillo N, Fiorentino S

Int J Mol Sci

24-Nov-2023

PMCID:	PMC10706186
doi:	10.3390/ijms242316698
PMID:	38069022

Commodity risk assessment of Malus domestica plants from Bosnia and Herzegovina

Bragard C, Baptista P, Chatzivassiliou E, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Zappalà L, Lucchi A, Gómez P, Urek G, Bernardo U, Bubici G, Carluccio AV, Chiumenti M, Di Serio F, Fanelli E, Marzachì C, Kaczmarek A, Yuen J

EFSA J

26-Oct-2023

PMCID:	PMC10600653
doi:	10.2903/j.efsa.2023.8315
PMID:	37901690

Ethnobotanical Insights: Qualitative Analysis of Medicinal Plants in Colón Putumayo for Traditional Knowledge Preservation

Bastidas-Bacca MA, Dayve-Bacca-Descance D, Guerra-Acosta AD, Perea-Morera E, Díaz-Ariza LA, López-Álvarez D, Osorio-García AM

Plants (Basel)

26-Sep-2023

PMCID:	PMC10574470
doi:	10.3390/plants12193390
PMID:	37836130

Amazonian Plants: A Global Bibliometric Approach to Petiveria alliacea L. Pharmacological and Toxicological Properties

da Conceição BC, da Silva TA, Pantoja LV, da Luz DA, Cardoso EK, Reis LD, Raiol-da-Silva MC, Kussler MS, Maia CS, Fontes-Júnior EA

Plants (Basel)

21-Sep-2023

PMCID:	PMC10536944
doi:	10.3390/plants12183343
PMID:	37765507

Petiveria alliacea Reduces Tumor Burden and Metastasis and Regulates the Peripheral Immune Response in a Murine Myeloid Leukemia Model

Murillo N, Lasso P, Urueña C, Pardo-Rodriguez D, Ballesteros-Ramírez R, Betancourt G, Rojas L, Cala MP, Fiorentino S

Int J Mol Sci

19-Aug-2023

PMCID:	PMC10454792
doi:	10.3390/ijms241612972
PMID:	37629156

Exploring the safety and efficacy of phytomedicine Petiveria alliacea extract (Esperanza) in patients with metastatic gastrointestinal tumors and acute leukemias: study protocol for a phase Ib/randomized double blind phase II trial (PA001)

Ballesteros-Ramírez R, Pinilla P, Sanchéz J, Arévalo M, Sanchez E, Aschner P, Urueña C, Fiorentino S

BMC Complement Med Ther

10-Aug-2023

PMCID:	PMC10413616
doi:	10.1186/s12906-023-04109-2
PMID:	37563608

Plant-derived extracts and metabolic modulation in leukemia: a promising approach to overcome treatment resistance

Arévalo CM, Cruz-Rodriguez N, Quijano S, Fiorentino S

Front Mol Biosci

13-Jul-2023

PMCID:	PMC10382028
doi:	10.3389/fmolb.2023.1229760
PMID:	37520325

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
(3S,5R)-3,5-diphenyl-1,2,4-trithiolane	154497624	Click to see	276.40	unknown	https://doi.org/10.1016/S0031-9422(01)00304-1
[(Benzyltrisulfanyl)methyltrisulfanyl]methylbenzene	11079641	Click to see	388.70	unknown	https://doi.org/10.1016/S0031-9422(01)00079-6
[(S)-benzylsulfinyl]sulfanylmethylbenzene	92449246	Click to see C1=CC=C(C=C1)CSS(=O)CC2=CC=CC=C2	262.40	unknown	https://doi.org/10.1016/S0031-9422(02)00328-X
1-(1-Hydroxy-2-phenylethyl)sulfanyl-2-phenylethanol	163195816	Click to see	274.40	unknown	https://doi.org/10.1016/S0031-9422(01)00079-6
2-[(R)-benzylsulfanylsulfinyl]ethanol	163006694	Click to see C1=CC=C(C=C1)CSS(=O)CCO	216.30	unknown	https://doi.org/10.1016/S0031-9422(02)00328-X
2-[(S)-benzylsulfinyl]sulfanylethanol	163014333	Click to see	216.30	unknown	https://doi.org/10.1016/S0031-9422(02)00328-X
2-Benzylsulfanylsulfinylethanol	636831	Click to see C1=CC=C(C=C1)CSS(=O)CCO	216.30	unknown	https://doi.org/10.1016/S0031-9422(02)00328-X
2-Benzylsulfinylsulfanylethanol	11790617	Click to see C1=CC=C(C=C1)CS(=O)SCCO	216.30	unknown	https://doi.org/10.1016/S0031-9422(02)00328-X
Dibenzyl Disulfide	9012	Click to see C1=CC=C(C=C1)CSSCC2=CC=CC=C2	246.40	unknown	https://doi.org/10.1016/S0031-9422(01)00304-1 https://doi.org/10.1016/S0031-9422(01)00079-6
Dibenzyl sulfide	10867	Click to see	214.33	unknown	https://doi.org/10.1016/S0031-9422(01)00079-6
Dibenzyltetrasulfid	12416355	Click to see C1=CC=C(C=C1)CSSSSCC2=CC=CC=C2	310.50	unknown	https://doi.org/10.1016/S0031-9422(01)00079-6
Methanol, [(phenylmethyl)thio]-	259512	Click to see	154.23	unknown	https://doi.org/10.1016/S0031-9422(01)00079-6
Petivericin	10244468	Click to see	262.40	unknown	https://doi.org/10.1016/S0031-9422(02)00328-X
Sulfinylmethylbenzene	639688	Click to see	138.19	unknown	https://doi.org/10.1016/S0031-9422(02)00759-8
Trisulfide, bis(phenylmethyl)	122842	Click to see	278.50	unknown	https://doi.org/10.1002/(SICI)1096-9063(199707)50:3<228::AID-PS575>3.0.CO;2-J https://doi.org/10.1016/0031-9422(90)85294-P https://doi.org/10.1016/S0031-9422(01)00079-6 https://doi.org/10.1016/S0031-9422(01)00304-1
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Benzyl Benzoate	2345	Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2	212.24	unknown	https://doi.org/10.1016/S0031-9422(01)00304-1
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid	243	Click to see	122.12	unknown	https://doi.org/10.1016/S0031-9422(01)00304-1
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde	240	Click to see	106.12	unknown	https://doi.org/10.1016/S0031-9422(01)00304-1
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol	244	Click to see	108.14	unknown	https://doi.org/10.1016/S0031-9422(01)00304-1
> Benzenoids / Benzene and substituted derivatives / Benzyl sulfoxides / Benzyl alkyl sulfoxides
(2R)-2-amino-3-[(R)-benzylsulfinyl]propanoic acid	12991581	Click to see	227.28	unknown	https://doi.org/10.1016/S0031-9422(01)00304-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
Tetracosyl tetracosanoate	3083668	Click to see	705.30	unknown	https://doi.org/10.1016/0031-9422(90)85294-P
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Nonadecanoic Acid	12591	Click to see	298.50	unknown	https://doi.org/10.1016/0031-9422(90)85294-P
Oleic Acid	445639	Click to see	282.50	unknown	https://doi.org/10.1016/0031-9422(90)85294-P
Palmitic Acid	985	Click to see	256.42	unknown	https://doi.org/10.1016/0031-9422(90)85294-P
Stearic Acid	5281	Click to see	284.50	unknown	https://doi.org/10.1016/0031-9422(90)85294-P
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Lignoceric Acid	11197	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O	368.60	unknown	https://doi.org/10.1016/0031-9422(90)85294-P
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Tetracosanol	10472	Click to see	354.70	unknown	https://doi.org/10.1016/0031-9422(90)85294-P
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see	280.40	unknown	https://doi.org/10.1016/0031-9422(90)85294-P
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4S,5R,6R)-5-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18S)-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-4-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]methoxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162847591	Click to see	1357.50	unknown	https://doi.org/10.1016/S0031-9422(01)00304-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1016/0031-9422(90)85294-P
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/0031-9422(90)85294-P
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
2-Amino-3-(2-hydroxyethylsulfinyl)propanoic acid	74324904	Click to see	181.21	unknown	https://doi.org/10.1016/S0031-9422(02)00328-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2R)-2-azaniumyl-3-[(S)-2-hydroxyethylsulfinyl]propanoate	26087987	Click to see	181.21	unknown	https://doi.org/10.1016/S0031-9422(02)00328-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
(2R,4S)-4-methoxy-1-methylpyrrolidine-2-carboxylic acid	638217	Click to see	159.18	unknown	https://doi.org/10.1016/0031-9422(90)85294-P
(2S,4R)-4-Methoxy-1-methylpyrrolidine-2-carboxylic acid	14704645	Click to see	159.18	unknown	https://doi.org/10.1016/0031-9422(90)85294-P
4-Methoxy-1-methylpyrrolidine-2-carboxylic acid	14704644	Click to see CN1CC(CC1C(=O)O)OC	159.18	unknown	https://doi.org/10.1016/0031-9422(90)85294-P
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Cysteine and derivatives
2-Amino-3-(2-hydroxy-ethylsulfanyl)-propionic acid	4610750	Click to see C(CSCC(C(=O)O)N)O	165.21	unknown	https://doi.org/10.1016/S0031-9422(02)00328-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Cysteine and derivatives / L-cysteine-S-conjugates
S-(2-hydroxyethyl)cysteine	119224	Click to see	165.21	unknown	https://doi.org/10.1016/S0031-9422(02)00328-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Dipeptides
(2S)-2-amino-5-[[(1R)-2-[(R)-benzylsulfinyl]-1-carboxyethyl]amino]-5-oxopentanoic acid	21574471	Click to see C1=CC=C(C=C1)CS(=O)CC(C(=O)O)NC(=O)CCC(C(=O)O)N	356.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.06.029
(2S)-2-amino-5-[[(1R)-2-benzylsulfanyl-1-carboxyethyl]amino]-5-oxopentanoic acid	21574469	Click to see	340.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.06.029
2-Amino-5-[(2-benzylsulfanyl-1-carboxyethyl)amino]-5-oxopentanoic acid	73797110	Click to see C1=CC=C(C=C1)CSCC(C(=O)O)NC(=O)CCC(C(=O)O)N	340.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.06.029
2-Amino-5-[(2-benzylsulfinyl-1-carboxyethyl)amino]-5-oxopentanoic acid	73797111	Click to see C1=CC=C(C=C1)CS(=O)CC(C(=O)O)NC(=O)CCC(C(=O)O)N	356.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.06.029
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
6-Methoxycyclohexane-1,2,3,4,5-pentol	230881	Click to see COC1C(C(C(C(C1O)O)O)O)O	194.18	unknown	https://doi.org/10.1016/0031-9422(90)85294-P
> Organoheterocyclic compounds / Azoles / Imidazoles
Allantoin	204	Click to see C1(C(=O)NC(=O)N1)NC(=O)N	158.12	unknown	https://doi.org/10.1016/0031-9422(90)85294-P
> Organosulfur compounds / Organic disulfides / Dialkyldisulfides
Dipropyl disulfide	12377	Click to see	150.30	unknown	https://doi.org/10.1016/S0031-9422(01)00079-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2R,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one	122173240	Click to see	434.40	unknown	https://doi.org/10.1016/0031-9422(92)83304-H
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-oxa N-2-YL)oxy-chroman-4-one	316844	Click to see	450.40	unknown	https://doi.org/10.1016/0031-9422(92)83304-H
5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxy-2-(3,4,5-Trihydroxyphenyl)Chromen-4-One	5352000	Click to see	464.40	unknown	https://doi.org/10.1016/0031-9422(92)83304-H
Astilbin	119258	Click to see	450.40	unknown	https://doi.org/10.1016/0031-9422(92)83304-H
Myricitrin	5281673	Click to see	464.40	unknown	https://doi.org/10.1016/0031-9422(92)83304-H
Neoisoastilbin	10114809	Click to see	450.40	unknown	https://doi.org/10.1016/0031-9422(92)83304-H
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(+)-(r)-5-Hydroxy-6-hydroxymethyl-7-methoxy-8-methylflavanone	15896345	Click to see	314.30	unknown	https://doi.org/10.1016/0031-9422(92)83304-H
(2R)-5-hydroxy-7-methoxy-8-methyl-4-oxo-2-phenyl-2,3-dihydrochromene-6-carbaldehyde	154496887	Click to see CC1=C2C(=C(C(=C1OC)C=O)O)C(=O)CC(O2)C3=CC=CC=C3	312.30	unknown	https://doi.org/10.1016/0031-9422(92)83304-H
(2R)-6-(hydroxymethyl)-5,7-dimethoxy-8-methyl-2-phenyl-2,3-dihydrochromen-4-one	162924883	Click to see CC1=C2C(=C(C(=C1OC)CO)OC)C(=O)CC(O2)C3=CC=CC=C3	328.40	unknown	https://doi.org/10.1016/0031-9422(92)83304-H
(2S)-5-hydroxy-6-(hydroxymethyl)-7-methoxy-8-methyl-2-phenyl-2,3-dihydrochromen-4-one	101630662	Click to see	314.30	unknown	https://doi.org/10.1016/0031-9422(92)83304-H
(2S)-6-(hydroxymethyl)-5,7-dimethoxy-8-methyl-2-phenyl-2,3-dihydrochromen-4-one	101630663	Click to see CC1=C2C(=C(C(=C1OC)CO)OC)C(=O)CC(O2)C3=CC=CC=C3	328.40	unknown	https://doi.org/10.1016/0031-9422(92)83304-H
(2S)-6-formyl-8-methyl-7-O-methylpinocembrin	52945746	Click to see	312.30	unknown	https://doi.org/10.1016/0031-9422(92)83304-H
5-O-Methylleridol	42607881	Click to see CC1=C2C(=C(C(=C1OC)CO)OC)C(=O)CC(O2)C3=CC=CC=C3	328.40	unknown	https://doi.org/10.1016/0031-9422(92)83304-H
Leridal	42607880	Click to see	312.30	unknown	https://doi.org/10.1016/0031-9422(92)83304-H
Leridol	10495449	Click to see	314.30	unknown	https://doi.org/10.1016/0031-9422(92)83304-H
> Phenylpropanoids and polyketides / Stilbenes
Stilbene	11502	Click to see C1=CC=C(C=C1)C=CC2=CC=CC=C2	180.24	unknown	https://doi.org/10.1039/C39740000906
trans-Stilbene	638088	Click to see C1=CC=C(C=C1)C=CC2=CC=CC=C2	180.24	unknown	https://doi.org/10.1039/C39740000906 https://doi.org/10.1016/S0031-9422(01)00304-1

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Petiveria alliacea

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