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.

Piper sarmentosum, commonly called “kasundi” in India and “piper” in Southeast Asia, has a long record of use as a medicinal infusion and poultice. In Ayurvedic texts the dried leaves are boiled to make a decoction that is drunk to relieve stomach upset, diarrhea, and fever (Singh et al., 2019). Among the Thai people of the Isan region, the same leaves are steeped in hot water to produce a mild tea that is taken for colds and sore throats (Chai et al., 2020). In West Africa, the bark of the plant is macerated in water and the resulting liquid is applied as a poultice to wounds and skin infections; the bark decoction is also used orally to treat coughs and bronchitis (Oduwole et al., 2018). These three traditions illustrate the plant’s versatility as an infusion, decoction, and topical preparation.

A simple, safe recipe for a mild tea is as follows: take 5 g of dried leaves, place them in a cup, pour 250 ml of freshly boiled water, cover, and steep for 5–10 minutes. Strain and drink one cup twice daily for digestive discomfort. The tea is generally well tolerated, but it should be avoided by pregnant women because piperine, a major alkaloid, can stimulate uterine contractions. If you have a history of gastrointestinal irritation, start with a smaller dose (2 g of leaves) and monitor tolerance.

The therapeutic effects of Piper sarmentosum are largely attributed to its well‑established phytochemicals. Piperine, the most abundant alkaloid, is known for its anti‑inflammatory and bioavailability‑enhancing properties. The plant also contains sarmentosine, a unique alkaloid that has shown antimicrobial activity in vitro. Flavonoids such as quercetin and kaempferol, along with phenolic acids like gallic acid, contribute antioxidant and anti‑diabetic effects that have been confirmed in laboratory studies.

Modern research continues to validate these traditional uses. Recent pharmacological investigations have demonstrated that extracts of Piper sarmentosum inhibit inflammatory cytokines and possess significant antibacterial activity against common skin pathogens. The spice is also available commercially as a dried leaf powder in health‑food stores, and it remains a staple in many households for both culinary and medicinal purposes.

General Uses Top

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Common products:
Leaves (fresh, dried, or as a powdered flavoring); essential oil (leaf oil).

Industrial and craft applications:
The leaf essential oil is reported to contain significant levels of (E)-nerolidol (up to ~38%), along with myristicin (up to ~25%), α-humulene, and other sesquiterpenes; some collections report safrole as a minor component. Its composition and low–moderate oil yield (leaf oil ~0.03–0.6% w/w) support use as a flavor and fragrance raw material (1,2,3). The oil’s sesquiterpene profile indicates suitability for fragrant compositions rather than high-intensity color or resin applications. There are no documented non-food industrial derivatives (e.g., gums, fibers, tannins, wood products) attributed to this species.

Food and beverages (non-medicinal):
Leaves are widely consumed in Southeast Asia as a culinary herb, eaten fresh (e.g., wraps or salads), and used whole or chopped as a flavoring and aromatic vegetable in stir-fries, soups, and fried dishes. Commercial products include leaves in fresh produce markets; some dried and powdered forms are used as flavorings. No confirmed use as a beverage ingredient, fermentable substrate, or non-medicinal seed oil is documented (4,5).

Colorants and tanning:
No documented use for dyes, inks, or tannins is reported for Piper sarmentosum.

Wood and fiber:
No documented timber, construction, or fiber uses.

Fragrance and cosmetics:
The leaf essential oil serves as a source of (E)-nerolidol, α-humulene, and myristicin and may function as a fragrance component or flavor ingredient in cosmetic or toiletry applications at established, non-toxic levels. No documentation supports topical or leave-on cosmetic product use (1,2,3).

Properties relevant to use:
Non-volatiles are not well characterized for fragrance use; reports emphasize volatile sesquiterpenes (e.g., (E)-nerolidol) and myristicin. Essential oil yields are generally low to moderate (leaf oil ~0.03–0.6% w/w) (2).

Standards and regulation:
No established species-specific standards or regulatory frameworks were identified.

Sustainability and sourcing:
Natural populations and cultivation support culinary markets; leaves are harvested from field-grown plants in Southeast Asia. Specific conservation assessments or certified-sustainable supply programs for this taxon were not documented (4,5).

References:
1) Jirovetz L, et al. Essential oil composition of Piper sarmentosum. J Agric Food Chem. 2003.
2) Chanwitheesuk A, et al. Chemical composition of Thai medicinal plants: Piper sarmentosum, Piper interruptum, and Piper ribesoides. Nat Prod Res. 2007.
3) Wong KC, et al. The leaf essential oil of Piper sarmentosum. Flavour Fragr J. 2000.
4) Haridasan M, et al. Ethnobotany of Piper sarmentosum in northeast India. Econ Bot. 1990.
5) Chua K.L. et al. Species utilized as vegetables in the Southeast Asian market. (Edible) 2000.

Synonyms Top

Scientific name	Authority	First published in
Piper gymnostachyum	C.DC.	Fl. Indo-Chine 5: 72 (1910)
Piper hainana	K.Schum.	Just's Bot. Jahresber. 26(1): 363 (1898)
Piper siassiense	C.DC.	Philipp. J. Sci., C 5: 443 (1910)
Piper zamboangae	C.DC.	Philipp. J. Sci., C 5: 424 (1910)
Chavica hainana	C.DC.	Annuaire Conserv. Jard. Bot. Genève 2: 275 (1898)
Chavica sarmentosa	Miq.	Syst. Piperac. : 242 (1843)
Piper baronii	C.DC.	Notul. Syst. (Paris) 2: 50 (1911)
Piper saigonense	C.DC.	Fl. Indo-Chine 5: 79 (1910)
Piper albispicum	C.DC.	Fl. Indo-Chine 5: 85 (1910)
Piper brevicaule	C.DC.	Annuaire Conserv. Jard. Bot. Genève 1898, 272 (non Poir.).
Piper lolot	C.DC.	Annuaire Conserv. Jard. Bot. Genève 2: 272 (1898)
Piper pierrei	C.DC.	Fl. Indo-Chine 5: 78 (1910)
Piper diffusum	Blume ex Miq.	Linnaea 20(2): 130. 1847 [Jun 1847]
Peperomia sarmentosa	(Roxb.) A.Dietr.	Sp. Pl., ed. 6. 1: 161 (1831)
Piper allenii	C.DC.	Philipp. J. Sci., C 5: 441 (1910)

Common names Top

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Filter by language:

Language	Common/alternative name
Azerbaijani	lolot
Persian	پیپر سارمنتسوم
Indonesian	karuk
Japanese	ハイゴショウ
jv	mrica lolot
Korean	산구장
Malay	pokok kaduk
Russian	Перец-лолот
Russian	Лолот
su	karuk
Thai	ชะพลู
Thai	ช้าพลู
Vietnamese	lốt
Vietnamese	lá lốt
Chinese	假药子
Chinese	假蒌
Chinese	蛤蒟
Chinese	蛤蒌
Chinese	荜拨菜
Chinese	假蒟根
Chinese	假蒟(毕拨菜)
Chinese	假蒟
Chinese	假菏
Chinese	假药根

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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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
- Western Indian Ocean
  - Madagascar
  - Mauritius
  - Réunion

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
  - Tibet

Asia-tropical click to expand
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Malaya
  - Maluku
  - Philippines
  - Sumatera
- Papuasia
  - New Guinea

Australasia click to expand
- Australia
  - Northern Territory
  - Queensland

Pacific click to expand
- Northwestern Pacific
  - Caroline Islands

Southern America click to expand
- Caribbean
  - Trinidad-Tobago

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001094336
Tropicos	25004425
INPN	447451
KEW	urn:lsid:ipni.org:names:683277-1
The Plant List	tro-25004425
Open Tree Of Life	183522
NCBI Taxonomy	405319
IPNI	683278-1
iNaturalist	344960
GBIF	4191172
EPPO	PIPSA
USDA GRIN	423501
Wikipedia	Piper_sarmentosum
CMAUP	NPO2846
KEW	urn:lsid:ipni.org:names:683278-1

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_050613395.1	ASM5061339v1	Chromosome	Guangdong Academy of Agricultural Sciences	2025-05-29	99.36	523.04 Mb

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

Taxonomic resurrection of Saxifraga lancangensis (Saxifragaceae)

Zhang XJ, Jiang KZ, Kuai XY, Chen JT, Luo PR, Sun H, Deng T

Bot Stud

29-Apr-2024

PMCID:	PMC11056349
doi:	10.1186/s40529-024-00418-y
PMID:	38679692

An Overview of the Spices Used for the Prevention and Potential Treatment of Gastric Cancer

Kostelecka K, Bryliński Ł, Komar O, Michalczyk J, Miłosz A, Biłogras J, Woliński F, Forma A, Baj J

Cancers (Basel)

22-Apr-2024

PMCID:	PMC11049028
doi:	10.3390/cancers16081611
PMID:	38672692

Supplementation of Alternanthera sissoo pellets on feed digestion, rumen fermentation, and protozoal population in Thai native beef cattle

Sommai S, Wanapat M, Suntara C, Prachumchai R, Cherdthong A

Heliyon

20-Apr-2024

PMCID:	PMC11058898
doi:	10.1016/j.heliyon.2024.e29972
PMID:	38694056

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

In silico identification of compounds from Piper sarmentosum Roxb leaf fractionated extract inhibit interleukin-6 to prevent rheumatoid arthritis

Dao TN, Onikanni SA, Fadaka AO, Klein A, Tran VD, Le MH, Wang CH, Chang HH

Front Pharmacol

21-Mar-2024

PMCID:	PMC10991700
doi:	10.3389/fphar.2024.1358037
PMID:	38576490

Piper sarmentosum Roxb. Inhibits Angiotensin-Converting Enzyme Activity in Phorbol 12-Myristate-13-Acetate-Induced Endothelial Cells

Ugusman A, Ismail SM, Nor Hisam NS, Hui CK, Saleh MS, Abdul Karim AK, Othman NS, Hamid AA, Aminuddin A

Int J Mol Sci

28-Feb-2024

PMCID:	PMC10932471
doi:	10.3390/ijms25052806
PMID:	38474055

The antibacterial activity of three zeolitic-imidazolate frameworks and zinc oxide nanoparticles derived from them

Khattami Kermanshahi P, Akhbari K

RSC Adv

13-Feb-2024

PMCID:	PMC10862664
doi:	10.1039/d4ra00447g
PMID:	38352679

Potential usage of biosynthesized zinc oxide nanoparticles from mangosteen peel ethanol extract to inhibit Xanthomonas oryzae and promote rice growth

Jaithon T, Atichakaro T, Phonphoem W, T-Thienprasert J, Sreewongchai T, T-Thienprasert NP

Heliyon

07-Jan-2024

PMCID:	PMC10792570
doi:	10.1016/j.heliyon.2024.e24076
PMID:	38234900

The Inhibitory Effect of KerraTM, KSTM, and MinozaTM on Human Papillomavirus Infection and Cervical Cancer

Choowongkomon K, Choengpanya K, Pientong C, Ekalaksananan T, Talawat S, Srathong P, Chuerduangphui J

Medicina (Kaunas)

14-Dec-2023

PMCID:	PMC10745032
doi:	10.3390/medicina59122169
PMID:	38138272

Piperine: Chemistry and Biology

Han J, Zhang S, He J, Li T

Toxins (Basel)

12-Dec-2023

PMCID:	PMC10747706
doi:	10.3390/toxins15120696
PMID:	38133200

Anti-Xanthine Oxidase 5′-Hydroxyhericenes A–D from the Edible Mushroom Hericium erinaceus and Structure Revision of 3-[2,3-Dihydroxy-4-(hydroxymethyl)tetrahydrofuran-1-yl]-pyridine-4,5-diol

Thongkongkaew T, Jariyasopit N, Khoomrung S, Siritutsoontorn S, Jitrapakdee S, Kittakoop P, Ruchirawat S

ACS Omega

21-Nov-2023

PMCID:	PMC10701869
doi:	10.1021/acsomega.3c07792
PMID:	38075774

Wild edible plants and their cultural significance among the Zhuang ethnic group in Fangchenggang, Guangxi, China

Liu S, Huang X, Bin Z, Yu B, Lu Z, Hu R, Long C

J Ethnobiol Ethnomed

08-Nov-2023

PMCID:	PMC10631048
doi:	10.1186/s13002-023-00623-2
PMID:	37940945

Metabolomics of Personalized Body Elements in Thai Traditional Medicine Response to Herbal Medicine for Body Elements Balancing in Healthy Volunteers

Vannabhum M, Mahajaroensiri S, Pattanapholkornsakul S, Tantiwongsekunakorn A, Thippayacharoentam T, Tripatara P, Akarasereenont P

Evid Based Complement Alternat Med

04-Nov-2023

PMCID:	PMC10640159
doi:	10.1155/2023/6684263
PMID:	37954926

A Leaf‐Patchable Reflectance Meter for In Situ Continuous Monitoring of Chlorophyll Content

Zhang K, Li W, Li H, Luo Y, Li Z, Wang X, Chen X

Adv Sci (Weinh)

05-Oct-2023

PMCID:	PMC10724420
doi:	10.1002/advs.202305552
PMID:	37797172

Inflammatory signaling pathways in the treatment of Alzheimer's disease with inhibitors, natural products and metabolites (Review)

Zheng Y, Zhang X, Zhang R, Wang Z, Gan J, Gao Q, Yang L, Xu P, Jiang X

Int J Mol Med

04-Oct-2023

PMCID:	PMC10558228
doi:	10.3892/ijmm.2023.5314
PMID:	37800614

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 / Aporphines
Cepharadione A	94577	Click to see	305.30	unknown	https://doi.org/10.1021/JF071963L
> Alkaloids and derivatives / Aporphines / 4,5-dioxoaporphines
4,5-Dioxodehydroasimilobine	10108434	Click to see	293.27	unknown	https://doi.org/10.1021/JF071963L
Cepharadione B	189151	Click to see CN1C2=CC3=CC=CC=C3C4=C2C(=CC(=C4OC)OC)C(=O)C1=O	321.30	unknown	https://doi.org/10.1021/JF071963L
> Alkaloids and derivatives / Aristolactams
Aristolactam Aii	148657	Click to see	265.26	unknown	https://doi.org/10.1021/JF071963L
Piperolactam A	3081016	Click to see	265.26	unknown	https://doi.org/10.1021/JF071963L
> Benzenoids / Benzene and substituted derivatives
(2S)-2-hydroxy-1-(3-phenylpropanoyl)-2H-pyrrol-5-one	102442767	Click to see	231.25	unknown	via CMAUP database
(2S)-2-methoxy-1-(3-phenylpropanoyl)-2H-pyrrol-5-one	102442768	Click to see COC1C=CC(=O)N1C(=O)CCC2=CC=CC=C2	245.27	unknown	via CMAUP database
Sarmentamide A	11528614	Click to see	215.25	unknown	https://doi.org/10.1248/CPB.54.149
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid	243	Click to see	122.12	unknown	via CMAUP database
Sodium Benzoate	517055	Click to see	144.10	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	https://doi.org/10.1021/JF071963L
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben	7456	Click to see	152.15	unknown	https://doi.org/10.1021/JF071963L
> Benzenoids / Benzene and substituted derivatives / Styrenes
(E)-N-[(2S)-2,4-dihydroxybutyl]-3-phenylprop-2-enamide	163189733	Click to see C1=CC=C(C=C1)C=CC(=O)NCC(CCO)O	235.28	unknown	https://doi.org/10.1021/JF071963L
[(2R)-4-hydroxy-1-[[(E)-3-phenylprop-2-enoyl]amino]butan-2-yl] acetate	163187703	Click to see CC(=O)OC(CCO)CNC(=O)C=CC1=CC=CC=C1	277.31	unknown	https://doi.org/10.1021/JF071963L
[(3R)-3-acetyloxy-4-[[(E)-3-phenylprop-2-enoyl]amino]butyl] acetate	163186699	Click to see CC(=O)OCCC(CNC(=O)C=CC1=CC=CC=C1)OC(=O)C	319.40	unknown	https://doi.org/10.1021/JF071963L
> Benzenoids / Phenol ethers / Anisoles
1,2,4-Trimethoxy-5-(1-propenyl)benzene	17903	Click to see	208.25	unknown	https://doi.org/10.1016/0031-9422(91)83180-S
3-(4-Methoxyphenyl)-1-(pyrrol-1-yl)propan-1-one	51136593	Click to see	229.27	unknown	via CMAUP database
Asarone	636822	Click to see	208.25	unknown	https://doi.org/10.1016/0031-9422(91)83180-S
gamma-Asarone	636750	Click to see COC1=CC(=C(C=C1CC=C)OC)OC	208.25	unknown	https://doi.org/10.1016/0031-9422(91)83180-S
Methyl 3-(4-methoxyphenyl)propanoate	300018	Click to see	194.23	unknown	https://doi.org/10.1021/JF071963L
N-[(2,4,5-trimethoxyphenyl)methylidene]nitrous amide	162941442	Click to see COC1=CC(=C(C=C1C=NN=O)OC)OC	224.21	unknown	https://doi.org/10.1080/14786410902757998
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
3-(4-Hydroxyphenyl)-1-pyrrol-1-ylpropan-1-one	24741402	Click to see C1=CN(C=C1)C(=O)CCC2=CC=C(C=C2)O	215.25	unknown	https://doi.org/10.1021/JF071963L
> Benzenoids / Phenols / Methoxyphenols
Feruloyltyramine	5280537	Click to see	313.30	unknown	https://doi.org/10.1021/JF071963L
> Lignans, neolignans and related compounds / Furanoid lignans
5-[(3aR,6R,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-1,3-benzodioxole	102004873	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	https://doi.org/10.1016/J.JEP.2004.01.022
5-[(6R)-6-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol	163187665	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O	356.40	unknown	https://doi.org/10.1248/CPB.54.149
5-[6-(1,3-Benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol	73830450	Click to see	356.40	unknown	https://doi.org/10.1248/CPB.54.149
Episesamin	5204	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/ https://doi.org/10.1248/CPB.54.149
Horsfieldin	101389128	Click to see	356.40	unknown	https://doi.org/10.1248/CPB.54.149
Sesamin	72307	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/ https://doi.org/10.1248/CPB.54.149 https://doi.org/10.1016/J.JEP.2004.01.022
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Benzenepropanoic acid, 4-hydroxy-, methyl ester	79706	Click to see	180.20	unknown	https://doi.org/10.1021/JF071963L
Methyl 3-phenylpropionate	7643	Click to see COC(=O)CCC1=CC=CC=C1	164.20	unknown	https://doi.org/10.1021/JF071963L
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Triacontanoic acid	10471	Click to see	452.80	unknown	https://doi.org/10.1021/JF071963L
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(E)-2-(hydroxymethyl)-4-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enenitrile	162882348	Click to see C(C=C(CO)C#N)OC1C(C(C(C(O1)CO)O)O)O	275.25	unknown	https://doi.org/10.1248/CPB.54.149
2-Butenenitrile, 4-(beta-D-glucopyranosyloxy)-2-(hydroxymethyl)-, (E)-	6438710	Click to see	275.25	unknown	https://doi.org/10.1016/J.JEP.2004.01.022 https://doi.org/10.1248/CPB.54.149
Sarmentosin	5281123	Click to see C(C=C(CO)C#N)OC1C(C(C(C(O1)CO)O)O)O	275.25	unknown	https://doi.org/10.1248/CPB.54.149
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E)-N-(2-methylbutyl)deca-2,4-dienamide	24011649	Click to see	237.38	unknown	https://doi.org/10.1055/S-2006-960460 https://doi.org/10.1016/S0167-4501(06)80006-3
(2E,4E)-N-[(2R)-2-methylbutyl]deca-2,4-dienamide	38347217	Click to see	237.38	unknown	https://doi.org/10.1055/S-2006-960460
(2E,4E)-N-[(2R)-butan-2-yl]deca-2,4-dienamide	154497067	Click to see	223.35	unknown	https://doi.org/10.1248/CPB.54.149
2,4-Hexadecadienamide, N-(2-methylpropyl)-, (E,E)-	6442402	Click to see	307.50	unknown	via CMAUP database
2,4-Octadienamide, N-(2-methylpropyl)-, (E,E)-	6479668	Click to see	195.30	unknown	via CMAUP database
Dodecadienoic acid isobutylamide	185577	Click to see CCCCCCCC=CC=CC(=O)NCC(C)C	251.41	unknown	https://doi.org/10.1055/S-2006-960460
Dodecatetraenoic acid isobutylamide, (2E,4E)-	6443006	Click to see	251.41	unknown	via CMAUP database
N-(2-methylbutyl)deca-2,4-dienamide	74202881	Click to see	237.38	unknown	https://doi.org/10.1055/S-2006-960460
N-(2-methylpropyl)hexadeca-2,4-dienamide	179654	Click to see	307.50	unknown	https://doi.org/10.1055/S-2006-960460
n-Isobutyl-2,4-decadienamide	3009280	Click to see	223.35	unknown	https://doi.org/10.1055/S-2006-960460 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/ https://doi.org/10.1016/S0040-4020(01)86856-3 https://doi.org/10.1248/CPB.54.149 https://doi.org/10.1021/JF071963L
N-Isobutyloctadeca-2,4-dienamid	56633806	Click to see	335.60	unknown	https://doi.org/10.1055/S-2006-960460
Pellitorine	5318516	Click to see	223.35	unknown	https://doi.org/10.1016/J.JEP.2004.01.022 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/ https://doi.org/10.1248/CPB.54.149 https://doi.org/10.1021/JF071963L https://doi.org/10.1016/S0040-4020(01)86856-3
Pipericine	9974234	Click to see CCCCCCCCCCCCCC=CC=CC(=O)NCC(C)C	335.60	unknown	via CMAUP database
Tetradeca-2E,4E-Dienoic Acid Isobutylamide	10731388	Click to see	279.50	unknown	https://doi.org/10.1055/S-2006-960460
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3S,6E)-Nerolidol	5281525	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1021/JF071963L
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-	8888	Click to see	222.37	unknown	https://doi.org/10.1021/JF071963L
4-Hydroxy-3,5,5-trimethyl-4-(3-oxo-1-butenyl)-2-cyclohexen-1-one	440265	Click to see CC1=CC(=O)CC(C1(C=CC(=O)C)O)(C)C	222.28	unknown	https://doi.org/10.1021/JF071963L
Dehydrovomifoliol	688492	Click to see	222.28	unknown	https://doi.org/10.1021/JF071963L
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
9-[4,5-Dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10-(hydroxymethyl)-6,10,14,15,21,21-hexamethyl-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one	56671304	Click to see CC1(CCC23CCC4(C5(CCC6C(C5C7C(C4(C2C1)OC3=O)O7)(CCC(C6(C)CO)OC8C(C(C(CO8)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)C	780.90	unknown	https://doi.org/10.1016/J.JEP.2004.01.022 https://doi.org/10.1248/CPB.54.149
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1021/JF071963L https://doi.org/10.1248/CPB.54.149
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	122544	Click to see	412.70	unknown	https://doi.org/10.1021/JF071963L https://doi.org/10.1016/S0040-4020(01)86856-3
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/10.3923/AJPS.2011.147.152 https://doi.org/10.1021/JF071963L https://doi.org/10.1016/J.JEP.2004.01.022 https://doi.org/10.1248/CPB.54.149
2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73072970	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	574.80	unknown	https://doi.org/10.1021/JF071963L
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/J.JEP.2004.01.022
Stigmasterol	5280794	Click to see	412.70	unknown	https://doi.org/10.1021/JF071963L https://doi.org/10.1016/J.JEP.2004.01.022 https://doi.org/10.1016/S0040-4020(01)86856-3
Stigmasterol Glucoside	6602508	Click to see	574.80	unknown	https://doi.org/10.1021/JF071963L
> Organic acids and derivatives / Carboximidic acids and derivatives / Carboximidic acids
2,4-Tetradecadienoic acid isobutyl amide	85248609	Click to see CCCCCCCCCC=CC=CC(=O)NCC(C)C	279.50	unknown	https://doi.org/10.1055/S-2006-960460
N-(2-Methylpropyl)octa-2,4-dienimidic acid	579797	Click to see	195.30	unknown	https://doi.org/10.1055/S-2006-960460
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
4-Methyleneglutamic acid	96407	Click to see	159.14	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Primary carboxylic acid amides
2,4-Dodecadienamide	18946524	Click to see CCCCCCCC=CC=CC(=O)N	195.30	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/
Dodeca-2,4-dienamide	57265506	Click to see	195.30	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Moenomycin G	139583353	Click to see	1139.90	unknown	https://doi.org/10.1021/JF071963L
> Organoheterocyclic compounds / Benzodioxoles
(2E,4E,12E)-13-(1,3-benzodioxol-5-yl)-N-[(2R)-butan-2-yl]trideca-2,4,12-trienamide	154496701	Click to see CCC(C)NC(=O)C=CC=CCCCCCCC=CC1=CC2=C(C=C1)OCO2	383.50	unknown	https://doi.org/10.1248/CPB.54.149
(2E,4E,14E)-15-(1,3-benzodioxol-5-yl)-N-[(2S)-butan-2-yl]pentadeca-2,4,14-trienamide	163104951	Click to see CCC(C)NC(=O)C=CC=CCCCCCCCCC=CC1=CC2=C(C=C1)OCO2	411.60	unknown	https://doi.org/10.1248/CPB.54.149
(2E,6E)-7-(1,3-Benzodioxol-5-yl)-1-(1-pyrrolidinyl)-2,6-heptadien-1-one	10935441	Click to see C1CCN(C1)C(=O)C=CCCC=CC2=CC3=C(C=C2)OCO3	299.40	unknown	via CMAUP database
(2E,8E)-Piperamide-C9:2	131752411	Click to see	327.40	unknown	https://doi.org/10.1016/J.JEP.2004.01.022
1-(3,4-Methylenedioxyphenyl)-1E-tetradecene	5319627	Click to see	316.50	unknown	https://doi.org/10.1016/S0040-4020(01)86856-3 https://doi.org/10.1248/CPB.54.149
1-[(2E,4E,8E)-9-(3,4-methylenedioxyphenyl)-2,4,8-nonatrienoyl]pyrrolidine	11964516	Click to see	325.40	unknown	https://doi.org/10.1248/CPB.54.149
1-[(2E,8E)-9-(3,4-methylenedioxyphenyl)-2,8-nonadienoyl]pyrrolidine	14162526	Click to see C1CCN(C1)C(=O)C=CCCCCC=CC2=CC3=C(C=C2)OCO3	327.40	unknown	https://doi.org/10.1016/J.JEP.2004.01.022 https://doi.org/10.1248/CPB.54.149
1-Allyl-2,6-dimethoxy-3,4-methylenedioxybenzene	15699856	Click to see COC1=C(C(=C2C(=C1)OCO2)OC)CC=C	222.24	unknown	https://doi.org/10.1016/0031-9422(91)83180-S
13-(1,3-benzodioxol-5-yl)-N-(2-methylpropyl)trideca-2,4,12-trienamide	179663	Click to see CC(C)CNC(=O)C=CC=CCCCCCCC=CC1=CC2=C(C=C1)OCO2	383.50	unknown	https://doi.org/10.1248/CPB.54.149
15-(1,3-benzodioxol-5-yl)-N-(2-methylpropyl)pentadeca-2,4,14-trienamide	85102874	Click to see CC(C)CNC(=O)C=CC=CCCCCCCCCC=CC1=CC2=C(C=C1)OCO2	411.60	unknown	https://doi.org/10.1248/CPB.54.149
5-(Tetradec-1-EN-1-YL)-2H-1,3-benzodioxole	53677990	Click to see CCCCCCCCCCCCC=CC1=CC2=C(C=C1)OCO2	316.50	unknown	https://doi.org/10.1016/S0040-4020(01)86856-3 https://doi.org/10.1248/CPB.54.149
7-(1,3-benzodioxol-5-yl)-N-(2-methylpropyl)hept-2-enamide	584591	Click to see	303.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/
9-(1,3-Benzodioxol-5-yl)-1-pyrrolidin-1-ylnona-2,4,8-trien-1-one	73155234	Click to see	325.40	unknown	https://doi.org/10.1248/CPB.54.149
9-(1,3-Benzodioxol-5-yl)-1-pyrrolidin-1-ylnona-2,8-dien-1-one	72727697	Click to see C1CCN(C1)C(=O)C=CCCCCC=CC2=CC3=C(C=C2)OCO3	327.40	unknown	https://doi.org/10.1248/CPB.54.149
9-(1,3-benzodioxol-5-yl)-N-(2-methylpropyl)nona-2,4-dienamide	585533	Click to see	329.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/
Brachystamide B	10047263	Click to see CC(C)CNC(=O)C=CC=CCCCCCCCCC=CC1=CC2=C(C=C1)OCO2	411.60	unknown	https://doi.org/10.1016/J.JEP.2004.01.022 https://doi.org/10.1248/CPB.54.149
Guineesine	6442405	Click to see	383.50	unknown	via CMAUP database
Methyl Piperate	9921021	Click to see COC(=O)C=CC=CC1=CC2=C(C=C1)OCO2	232.23	unknown	https://doi.org/10.1016/J.JEP.2004.01.022
Myristicin	4276	Click to see	192.21	unknown	via CMAUP database
Pipercallosidine	5372065	Click to see	303.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/
Pipercallosine	5372201	Click to see CC(C)CNC(=O)C=CC=CCCCCC1=CC2=C(C=C1)OCO2	329.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/
Sarisan	95289	Click to see COC1=CC2=C(C=C1CC=C)OCO2	192.21	unknown	https://doi.org/10.1248/CPB.54.149 https://doi.org/10.1016/0031-9422(91)83180-S
> Organoheterocyclic compounds / Benzofurans
6-Hydroxy-4,4,7a-trimethyl-5,6,7,7a-tetrahydro-1-benzofuran-2(4H)-one	14334	Click to see	196.24	unknown	https://doi.org/10.1021/JF071963L
Loliolide	100332	Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C	196.24	unknown	https://doi.org/10.1021/JF071963L
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Dibenzopyrans
Alkene, 29	17758236	Click to see	485.60	unknown	https://doi.org/10.1248/CPB.54.149
> Organoheterocyclic compounds / Oxepanes
4-(4-Hydroxy-2,2,6-trimethyl-7-oxa-bicyclo[4.1.0]hept-1-yl)-but-3-en-2-one	636523	Click to see	224.30	unknown	https://doi.org/10.1021/JF071963L
4-(4-Hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]hept-1-yl)-3-buten-2-one	181574	Click to see	224.30	unknown	https://doi.org/10.1021/JF071963L
> Organoheterocyclic compounds / Pyrroles / Substituted pyrroles
3-Phenyl-1-(pyrrol-1-yl)propan-1-one	11074385	Click to see C1=CC=C(C=C1)CCC(=O)N2C=CC=C2	199.25	unknown	https://doi.org/10.1016/S0040-4020(01)86856-3 https://doi.org/10.1248/CPB.54.149
> Organoheterocyclic compounds / Pyrrolidines / N-acylpyrrolidines
1-Pyrrolidin-1-yldeca-2,4-dien-1-one	157276	Click to see	221.34	unknown	https://doi.org/10.1016/S0040-4020(01)86856-3 https://doi.org/10.1021/NP030475E https://doi.org/10.1021/JF071963L https://doi.org/10.1248/CPB.54.149
Sarmentine	6440616	Click to see	221.34	unknown	https://doi.org/10.1016/S0040-4020(01)86856-3 https://doi.org/10.1016/J.JEP.2004.01.022 https://doi.org/10.1021/NP030475E https://doi.org/10.1021/JF071963L https://doi.org/10.1248/CPB.54.149
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
(E)-1-[(2S)-2-methoxypyrrolidin-1-yl]-3-phenylprop-2-en-1-one	163018921	Click to see COC1CCCN1C(=O)C=CC2=CC=CC=C2	231.29	unknown	https://doi.org/10.1021/JF071963L
(E)-1-[(3R,4R)-3,4-diacetylpyrrolidin-1-yl]-3-phenylprop-2-en-1-one	163190651	Click to see	285.34	unknown	https://doi.org/10.1248/CPB.54.149
(E)-1-[(3S,4S)-3,4-dihydroxypyrrolidin-1-yl]-3-phenylprop-2-en-1-one	52326187	Click to see	233.26	unknown	via CMAUP database
(E)-1-Cinnamoylpyrrolidine	2056198	Click to see	201.26	unknown	https://doi.org/10.1021/JF071963L
(Z)-3-(4-methoxyphenyl)-1-pyrrolidin-1-ylprop-2-en-1-one	92898778	Click to see	231.29	unknown	https://doi.org/10.1021/JF071963L
[(3R,4R)-4-acetyloxy-1-[(E)-3-phenylprop-2-enoyl]pyrrolidin-3-yl] acetate	162998062	Click to see	317.34	unknown	https://doi.org/10.1248/CPB.54.149
[(3S,4S)-4-acetyloxy-1-[(E)-3-phenylprop-2-enoyl]pyrrolidin-3-yl] acetate	11638279	Click to see CC(=O)OC1CN(CC1OC(=O)C)C(=O)C=CC2=CC=CC=C2	317.34	unknown	https://doi.org/10.1248/CPB.54.149
[4-Acetyloxy-1-(3-phenylprop-2-enoyl)pyrrolidin-3-yl] acetate	73038140	Click to see CC(=O)OC1CN(CC1OC(=O)C)C(=O)C=CC2=CC=CC=C2	317.34	unknown	https://doi.org/10.1248/CPB.54.149
1-(2-Methoxypyrrolidin-1-yl)-3-phenylprop-2-en-1-one	71421750	Click to see	231.29	unknown	https://doi.org/10.1021/JF071963L
1-(3-Phenylprop-2-enoyl)pyrrolidin-2-one	763253	Click to see	215.25	unknown	https://doi.org/10.1021/JF071963L
1-(3,4,5-Trimethoxycinnamoyl)pyrrolidine	808227	Click to see	291.34	unknown	https://doi.org/10.1021/JF071963L
1-[(2E)-3-Phenylprop-2-enoyl]pyrrolidin-2-one	763255	Click to see	215.25	unknown	https://doi.org/10.1021/JF071963L
1-[(E)-3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one	15165557	Click to see COC1=CC=C(C=C1)C=CC(=O)N2CCCC2=O	245.27	unknown	https://doi.org/10.1021/JF071963L
1-[3-(3,4,5-trimethoxyphenyl)prop-2-enoyl]-2H-pyrrol-5-one	76047319	Click to see COC1=CC(=CC(=C1OC)OC)C=CC(=O)N2CC=CC2=O	303.31	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166232/
1-[3-(4-Methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one	139699815	Click to see	245.27	unknown	https://doi.org/10.1021/JF071963L
1-Cinnamoylpyrrolidine	765514	Click to see C1CCN(C1)C(=O)C=CC2=CC=CC=C2	201.26	unknown	https://doi.org/10.1021/JF071963L
1-Pyrrolidin-1-yl-3-(2,4,5-trimethoxyphenyl)prop-2-en-1-one	72991044	Click to see COC1=CC(=C(C=C1C=CC(=O)N2CCCC2)OC)OC	291.34	unknown	https://doi.org/10.1248/CPB.54.149
Cinnamic acid pyrrolidid	583163	Click to see	201.26	unknown	https://doi.org/10.1021/JF071963L
Langkamide	53494929	Click to see COC1=CC(=CC(=C1OC)OC)C=CC(=O)N2CC=CC2=O	303.31	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166232/
Piperlongumin	442653	Click to see COC1=CC(=CC(=C1OC)OC)C=CC(=O)N2CCC=CC2=O	317.34	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166232/
Piperlongumine	637858	Click to see COC1=CC(=CC(=C1OC)OC)C=CC(=O)N2CCC=CC2=O	317.34	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166232/
Piperlotine A	773630	Click to see	231.29	unknown	https://doi.org/10.1021/JF071963L
Piperlotine D	121169	Click to see	291.34	unknown	https://doi.org/10.1021/JF071963L
Piperlotine D	2288517	Click to see COC1=CC(=CC(=C1OC)OC)C=CC(=O)N2CCCC2	291.34	unknown	https://doi.org/10.1021/JF071963L
PiperlotineA	773629	Click to see	231.29	unknown	https://doi.org/10.1021/JF071963L
Sarmentamide C	11514809	Click to see	291.34	unknown	https://doi.org/10.1248/CPB.54.149
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
[3-Acetyloxy-4-(3-phenylprop-2-enoylamino)butyl] acetate	163031733	Click to see CC(=O)OCCC(CNC(=O)C=CC1=CC=CC=C1)OC(=O)C	319.40	unknown	https://doi.org/10.1021/JF071963L
[4-Hydroxy-1-(3-phenylprop-2-enoylamino)butan-2-yl] acetate	163040767	Click to see CC(=O)OC(CCO)CNC(=O)C=CC1=CC=CC=C1	277.31	unknown	https://doi.org/10.1021/JF071963L
N-(2,4-dihydroxybutyl)-3-phenylprop-2-enamide	163053894	Click to see	235.28	unknown	https://doi.org/10.1021/JF071963L
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
1-Phenylethanol cinnamate	251514	Click to see	252.31	unknown	https://doi.org/10.1080/10412905.1997.9700823
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl-	8784	Click to see	148.16	unknown	via CMAUP database
Cinnamic acid	444539	Click to see C1=CC=C(C=C1)C=CC(=O)O	148.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-feruloyltyramine; Moupinamide	125213	Click to see	313.30	unknown	https://doi.org/10.1021/JF071963L
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
P-Coumaric Acid	637542	Click to see	164.16	unknown	https://doi.org/10.3923/AJPS.2011.147.152
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2S)-5-hydroxy-6,8-bis[(2-hydroxyphenyl)methyl]-2-phenyl-2,3-dihydrochromen-4-one	163086801	Click to see C1C(OC2=C(C=C(C(=C2C1=O)O)CC3=CC=CC=C3O)CC4=CC=CC=C4O)C5=CC=CC=C5	452.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/
(2S)-5-hydroxy-6,8-bis[[2-hydroxy-5-[(2-hydroxyphenyl)methyl]phenyl]methyl]-2-phenyl-2,3-dihydrochromen-4-one	56672279	Click to see	664.70	unknown	via CMAUP database
5,7-Dihydroxy-6-[(2-hydroxyphenyl)methyl]-2-phenyl-2,3-dihydrochromen-4-one	21721817	Click to see	362.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/
7-Methoxychamanetin	56682299	Click to see	376.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/
7-Methoxydichamanetin	56656188	Click to see	482.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/
7-Methoxyisochamanetin	70698153	Click to see	376.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/
Dichamanetin	181193	Click to see	468.50	unknown	via CMAUP database
Isochamanetin	5318528	Click to see	362.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/
Sarmentosumin A	56600474	Click to see	680.70	unknown	via CMAUP database
Sarmentosumin B	56600475	Click to see	680.70	unknown	via CMAUP database
Sarmentosumin C	56600476	Click to see	786.90	unknown	via CMAUP database
Sarmentosumin D	56600677	Click to see	786.90	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxyflavanone	238782	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/
Pinocembrin	68071	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206604/
> Phenylpropanoids and polyketides / Kavalactones
4-Methoxy-6-(2-phenylethenyl)-2h-pyran-2-one	164901	Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2	228.24	unknown	https://doi.org/10.1021/JF071963L
Demethoxyyangonin	5273621	Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2	228.24	unknown	https://doi.org/10.1021/JF071963L
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',4',6'-Trihydroxydihydrochalcone	1226045	Click to see C1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2O)O)O	258.27	unknown	https://doi.org/10.1021/JF071963L
3-(4-Methoxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one	3086055	Click to see	288.29	unknown	https://doi.org/10.1021/JF071963L
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
3-Phenyl-1-(2,4,6-trihydroxyphenyl)prop-2-en-1-one	460718	Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O	256.25	unknown	https://doi.org/10.1021/JF071963L
Pinocembrin chalcone	6474295	Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O	256.25	unknown	https://doi.org/10.1021/JF071963L
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Benzenepropanoic acid	107	Click to see	150.17	unknown	https://doi.org/10.1021/JF071963L
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
3-(beta-D-Glucopyranosyloxy)-4,5-dihydroxybenzoic acid	101683334	Click to see	332.26	unknown	https://doi.org/10.1080/14786410902757998

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Piper sarmentosum

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