Details Top

Internal ID UUID644001cd341cb017418701
Scientific name Piper hispidum
Authority Sw.
First published in Prodr. Veg. Ind. Occ. : 15 (1788)

Ethnobotanical Use Top

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Important notice
  • 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.

Ethnobotanical Uses

Traditional preparations of Piper hispidum are documented in Amazonian and Andean folk medicine. Indigenous groups of Rio Negro, Brazil and adjacent Colombia use a poultice of crushed leaves or a decoction applied as a compress to reduce swelling and relieve pain in bruises or sprains (Schultes and Raffauf, 1990). In the Peruvian Amazon, herbalists prepare an infusion of fresh leaves as a fever tea and take a decoction of leaves in water to ease rheumatism and joint pain (Duke and Vásquez, 1994). Macerations of crushed leaves are traditionally applied to wounds or made into washers for skin inflammations in lowland Peru (Girault, 1984).

One practical preparation reported in Amazonian practice is a maceration of fresh leaves. Chop 25–30 g of young leaves and cover with 200 ml of warm water. Let stand 2–4 hours, then strain; apply the cooled liquid as a wash to swollen or bruised areas, 2–3 times daily. An alcohol tincture is also common: macrinate 100 g of chopped fresh leaves with 500 ml of 45% ethanol, shake daily, and strain after 2 weeks; keep 15–25 ml in 1/4 cup of water and sip 1–3 times daily for feverish discomfort. For both forms, keep a low dose and discontinue if stomach upset or skin irritation occurs; avoid during pregnancy and lactation unless guided by a practitioner.

Well-established constituents help explain these uses. The leaves contain essential oil rich in monoterpenes such as limonene and alpha-pinene, and an unsaturated amide alkaloid system featuring piperine—compounds with recognized anti-inflammatory and analgesic potential, as well as antimicrobial activity (Liang et al., 2010).

Modern relevance: ongoing phytochemical studies on essential oil and amides continue, while dried leaf preparations can be found in some Amazonian plant shops and are occasionally sold by niche herbal vendors.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Piper casitense Trel. Ann. Missouri Bot. Gard. 27: 289 (1940)
Piper cerro-puntoense Trel. Ann. Missouri Bot. Gard. 27: 289 (1940)
Piper hirsutum Sw. Fl. Ind. Occid. i. 60. 1797
Piper hispidinervum C.DC. Notizbl. Königl. Bot. Gart. Berlin 6: 451. 1917
Piper asperifolium Rich. Actes Soc. Hist. Nat. Paris 1: 105 (1792)
Piper asperum Pers. Syn. Pl. 1: 33 (1805)
Piper articulosum D.Parodi Anales Soc. Ci. Argent. 6: 91 (1878)
Piper adornatispicum Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 340 (1938)
Piper angremondii C.DC. Vierteljahrsschr. Naturf. Ges. Zürich 60: 431 (1915)
Piper platannanum Trel. Repert. Spec. Nov. Regni Veg. 23: 312 (1927)
Piper pilipedunculum C.DC. Repert. Spec. Nov. Regni Veg. 15: 2 (1917)
Piper scabrum Sw. Fl. Ind. Occid. i. 59. 1797
Piper perspicuibracteum Trel. J. Washington Acad. Sci. 19: 335 (1929)
Piper patulipilum Yunck. Bol. Soc. Venez. Ci. Nat. 23: 84 (1962)
Piper williamsii Trel. Contr. U.S. Natl. Herb. 26: 32. 1927
Piper thebaudianum Trel. Repert. Spec. Nov. Regni Veg. 23: 312 (1927)
Piper fraguanum var. viride Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 346 (1938)
Piper apertum var. nodosum Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 341 (1938)
Piper scabriseptum var. reductum Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 353 (1938)
Piper hispidum var. trachydermum (Trel.) Yunck. Ann. Missouri Bot. Gard. 37: 33 (1950)
Steffensia scabra Kunth Linnaea 13: 639 (1840)
Steffensia asperifolia Kunth Linnaea 13: 644 (1840)
Artanthe aspera Miq. London J. Bot. 4: 456 (1845)
Artanthe asperifolia Miq. Syst. Piperac. : 441 (1844)
Artanthe asperifolia f. surinamensis Miq. Syst. Piperac. : 442 (1844)
Artanthe controversa Miq. Syst. Piperac. : 448 (1844)
Artanthe hirsuta Miq. Syst. Piperac. (F.A.W. Miquel) 446.
Artanthe hispida Miq. Comm. Phytogr. : 50 (1840)
Artanthe kunthiana Miq. Syst. Piperac. : 453 (1844)
Artanthe obesa Miq. Syst. Piperac. : 470 (1844)
Artanthe olfersiana Klotzsch J. Bot. (Hooker) 4: 321 (1841)
Artanthe opizii Miq. Syst. Piperac. : 440 (1844)
Artanthe scabra Miq. Syst. Piperac. : 447 (1844)
Artanthe scabra var. hirsuta (Sw.) Griseb. Fl. Brit. W. I. : 171 (1859)
Piper asperifolium Ruiz & Pav. Fl. Peruv. [Ruiz & Pavon] 1: 37, t. 56, f. b. 1798
Piper aegrum Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 132 (1936)
Piper amnigaudens Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 134 (1936)
Piper asperrimicaule Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 138 (1936)
Piper canescenticaule Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 145 (1936)
Piper canescenticaule var. expansum Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 145 (1936)
Piper cinereoramulum Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 149 (1936)
Piper glaberrimicaule Trel. in J.F.Macbr. Publ. Field Mus. Nat. Hist., Bot. Ser. 13, no. 357: 168. 1936
Piper leucofustum Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 182 (1936)
Piper longegerminatum Trel. in J.F.Macbr. Publ. Field Mus. Nat. Hist., Bot. Ser. 13, no. 357: 185. 1936
Piper masiseanum Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 190 (1936)
Piper obesum Vahl Enum. Pl. 1: 321 (1804)
Piper opizii Steud. Nomencl. Bot. , ed. 2, 2: 342 (1841)
Steffensia opizii Kunth Linnaea 13: 641 (1840)
Piper paranapuranum Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 204 (1936)
Piper resatum Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 222 (1936)
Piper scabricaule Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 229 (1936)
Piper silvioberrans Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 234 (1936)
Piper tardum Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 242 (1936)
Piper virgulticola Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 251 (1936)
Piper hispidum var. ellipticifolium Yunck. Ann. Missouri Bot. Gard. 37: 34 (1950)
Piper articulosum Trel. Publ. Field Mus. Nat. Hist., Bot. Ser. 18: 332. 1937 Fl. Costa Rica
Piper hispidum var. lanceolatum (Trel. & Yunck.) Piperac. N. South Amer. vol. 1: 274. 1950
Piper hispidum var. magnifolium C.DC. Prodr. 16(1): 276 (1869)
Piper hirsutum var. magnifolium C.DC. Prodr. 16(1): 276 (1869)
Piper catucheanum Trel. & Yunck. Piperac. N. South Amer. 1: 257, fig. 219. 1950
Piper hispidum var. obliquum Trel. & Yunck. Piperac. N. South Amer. : 273 (1950)
Lindeniopiper williamsii Trel. in Standl. Publ. Field Columb. Mus., Bot. Ser. 22: 8 (1940)
Piper alluvicola C.DC. Annuaire Conserv. Jard. Bot. Genève 21: 313 (1920)
Piper bayamonanum Trel. Repert. Spec. Nov. Regni Veg. 23: 9. 1926
Piper sabanillanum Trel. Repert. Spec. Nov. Regni Veg. 23: 9. 1926
Piper sumideranum Trel. Repert. Spec. Nov. Regni Veg. 23: 9. 1926
Piper maestranum Trel. Repert. Spec. Nov. Regni Veg. 23: 10. 1926
Piper rivialbi Trel. & Yunck. Piperac. N. South Amer. 1: 265, fig. 229. 1950
Steffensia olfersiana Kunth Linnaea 13: 645 (1840)
Piper hirsutum var. fusco-punctulatum C.DC. Prodr. 16(1): 276 (1869)
Piper hirsutum var. jamaicense C.DC. Prodr. 16(1): 276 (1869)
Piper hirsutum var. olfersianum (Kunth) C.DC. Prodr. 16(1): 277 (1869)
Piper hispidum var. albescens C.DC. Symb. Antill. 3: 188 (1902)
Piper hispidum var. plurinerve C.DC. Symb. Antill. 3: 188 (1902)
Piper scabrum var. kalacroixense Trel. Repert. Spec. Nov. Regni Veg. 23: 308 (1927)
Piper fruticosum Steud. Nomencl. Bot. [Steudel], ed. 2. ii. 341.
Steffensia hirsuta Kunth Linnaea 13(6): 641. 1840 [Mar-Jun 1840]
Piper hispidum f. lanceolatum (Trel. & Yunck.) Steyerm. Fl. Venez. 2(2): 449. 1984
Piper silvivagum f. peruvianum C.DC. Notizbl. Königl. Bot. Gart. Berlin 6: 489. 1917
Piper hispidum f. patulipilum (Yunck.) Steyerm. Fl. Venez. 2(2): 451. 1984
Piper hispidum f. surinamense (Miq.) Steyerm. Fl. Venez. 2(2): 448. 1984
Piper scabrum Ruiz & Pav. Fl. Peruv. 1: 84 (1798)
Piper hispidum Kunth Nov. Gen. Sp. 1: 50 (1816)
Piper subantillanum Trel. Repert. Spec. Nov. Regni Veg. 23: 9 (1926)
Piper malanganum Trel. Candollea 8: 75 (1940)
Piper olfersianum (Kunth) Kunth ex Steud. Nomencl. Bot. , ed. 2, 2: 342 (1841)

Common names Top

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Language Common/alternative name
English jamaican pepper

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southwest
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Paraguay
    • Western South America
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000478980
USDA Plants PIHI2
Tropicos 25001135
KEW urn:lsid:ipni.org:names:681674-1
The Plant List kew-2558107
Open Tree Of Life 1081775
NCBI Taxonomy 130401
IUCN Red List 150117584
IPNI 681674-1
iNaturalist 292150
GBIF 3086355
EPPO PIPHI
USDA GRIN 417544
IPNI 1002992-1
GBIF 4186223

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
Essential oil of Piper hispidum (Piperaceae) has efficacy against monogeneans, and effects on hematology and gill histology of Colossoma macropomum Alves CM, Baia RR, Farias VA, Farias MA, de Souza FL, Videira MN, Chagas FC, Yoshioka ET, Tavares-Dias M Rev Bras Parasitol Vet 11-Dec-2023
PMCID:PMC10782507
doi:10.1590/S1984-29612024001
PMID:38088653
Discovering Potential Compounds for Venous Disease Treatment through Virtual Screening and Network Pharmacology Approach Barrera-Vázquez OS, Escobar-Ramírez JL, Santiago-Mejía J, Carrasco-Ortega OF, Magos-Guerrero GA Molecules 05-Dec-2023
PMCID:PMC10745828
doi:10.3390/molecules28247937
PMID:38138427
Enzymatic potential of endophytic fungi: xylanase production by Colletotrichum boninense from sugarcane biomass Flores AC, Kimiko Kadowaki M, da Conceição Silva JL, de Andrade Bianchini I, de Almeida Felipe MD, Sene L Braz J Microbiol 22-Sep-2023
PMCID:PMC10689674
doi:10.1007/s42770-023-01131-x
PMID:37735300
Antitumor and antibacterial activity of metabolites of endophytic Colletotrichum siamense isolated from coffee (Coffea arabica L. cv IAPAR-59) do Espírito Santo BC, Oliveira JA, Ribeiro MA, Schoffen RP, Polli AD, Polonio JC, da Silva AA, de Abreu Filho BA, Heck MC, Meurer EC, Constantin PP, Pileggi M, Vicentini VE, Golias HC, Pamphile JA Braz J Microbiol 29-Aug-2023
PMCID:PMC10689633
doi:10.1007/s42770-023-01104-0
PMID:37642890
Differences in the Production of Extracellular Polymeric Substances (EPS) and Other Metabolites of Plenodomus (Leptosphaeria) Infecting Winter Oilseed Rape (Brassica napus L.) Nowak A, Kutyła M, Kaczmarek J, Jaroszuk-Ściseł J, Jędryczka M Metabolites 17-Jun-2023
PMCID:PMC10302272
doi:10.3390/metabo13060759
PMID:37367918
Endophytic fungi mediates production of bioactive secondary metabolites via modulation of genes involved in key metabolic pathways and their contribution in different biotechnological sector Toppo P, Kagatay LL, Gurung A, Singla P, Chakraborty R, Roy S, Mathur P 3 Biotech 14-May-2023
PMCID:PMC10183385
doi:10.1007/s13205-023-03605-z
PMID:37197561
Ethnobotanical inventory of medicinal plants used by Cashinahua (Huni Kuin) herbalists in Purus Province, Peruvian Amazon Horackova J, Chuspe Zans ME, Kokoska L, Sulaiman N, Clavo Peralta ZM, Bortl L, Polesny Z J Ethnobiol Ethnomed 12-May-2023
PMCID:PMC10176740
doi:10.1186/s13002-023-00586-4
PMID:37170108
Phenolic Compounds in Bacterial Inactivation: A Perspective from Brazil Kauffmann AC, Castro VS Antibiotics (Basel) 24-Mar-2023
PMCID:PMC10135396
doi:10.3390/antibiotics12040645
PMID:37107007
Effects of Microencapsulated Essential Oils on Equine Health: Nutrition, Metabolism and Methane Emission Elghandour MM, Maggiolino A, García EI, Sánchez-Aparicio P, De Palo P, Ponce-Covarrubias JL, Pliego AB, Salem AZ Life (Basel) 06-Feb-2023
PMCID:PMC9963397
doi:10.3390/life13020455
PMID:36836812
Physical, chemical, and biological control of black rot of brassicaceae vegetables: A review Liu Z, Wang H, Wang J, Lv J, Xie B, Luo S, Wang S, Zhang B, Li Z, Yue Z, Yu J Front Microbiol 23-Nov-2022
PMCID:PMC9726911
doi:10.3389/fmicb.2022.1023826
PMID:36504826
Endophytic Fungi as a Source of Antibacterial Compounds—A Focus on Gram-Negative Bacteria Silva DP, Cardoso MS, Macedo AJ Antibiotics (Basel) 29-Oct-2022
PMCID:PMC9687006
doi:10.3390/antibiotics11111509
PMID:36358164
Chalcone: A Promising Bioactive Scaffold in Medicinal Chemistry Rajendran G, Bhanu D, Aruchamy B, Ramani P, Pandurangan N, Bobba KN, Oh EJ, Chung HY, Gangadaran P, Ahn BC Pharmaceuticals (Basel) 11-Oct-2022
PMCID:PMC9607481
doi:10.3390/ph15101250
PMID:36297362
A Review of Bioactive Compounds and Antioxidant Activity Properties of Piper Species Carsono N, Tumilaar SG, Kurnia D, Latipudin D, Satari MH Molecules 10-Oct-2022
PMCID:PMC9573611
doi:10.3390/molecules27196774
PMID:36235309
The anti‐Trypanosoma activities of medicinal plants: A systematic review of the literature Nekoei S, Khamesipour F, Habtemariam S, de Souza W, Mohammadi Pour P, Hosseini SR Vet Med Sci 29-Aug-2022
PMCID:PMC9677405
doi:10.1002/vms3.912
PMID:36037401
Study of the dermal anti-inflammatory, antioxidant, and analgesic activity of pinostrobin González AS, Soto Tellini VH, Benjumea Gutiérrez DM Heliyon 27-Aug-2022
PMCID:PMC9463643
doi:10.1016/j.heliyon.2022.e10413
PMID:36097473

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxy-3-(3-methylbut-2-en-1-yl)benzoic acid 443852 Click to see 206.24 unknown https://doi.org/10.1002/CHIN.200541203
Nervogenic acid 5320129 Click to see 274.35 unknown https://doi.org/10.1002/CHIN.200541203
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3,5-Bis(3-hydroxy-3-methylbut-1-enyl)-4-methoxybenzoic acid 68843065 Click to see 320.40 unknown https://doi.org/10.1002/CHIN.200541203
3,5-bis[(E)-3-hydroxy-3-methylbut-1-enyl]-4-methoxybenzoic acid 11151359 Click to see CC(C)(C=CC1=CC(=CC(=C1OC)C=CC(C)(C)O)C(=O)O)O 320.40 unknown https://doi.org/10.1002/CHIN.200541203
4-Methoxy-3,5-bis(3-methylbut-2-enyl)benzoic acid 185077 Click to see 288.40 unknown https://doi.org/10.1002/CHIN.200541203
https://doi.org/10.1016/S0031-9422(00)81303-5
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylamides
2-hydroxy-N-methyl-N-[2-(3,4,5-trimethoxyphenyl)ethyl]benzamide 162886604 Click to see 345.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.001
> Benzenoids / Benzene and substituted derivatives / Phenylmethylamines / Phenylbenzamines
Bamipine 72075 Click to see 280.40 unknown https://doi.org/10.1016/S0031-9422(00)00226-0
> Benzenoids / Phenols / Methoxyphenols
Feruloyltyramine 5280537 Click to see 313.30 unknown https://doi.org/10.1002/CHIN.200541203
> Organoheterocyclic compounds / Benzodioxoles
(2E)-Piperamide-C5:1 12073743 Click to see C1CCN(C1)C(=O)C=CCCC2=CC3=C(C=C2)OCO3 273.33 unknown https://doi.org/10.1021/NP9703656
https://doi.org/10.1016/S0031-9422(00)00226-0
https://doi.org/10.1021/NP030475E
(2Z,4Z)-7-(1,3-benzodioxol-5-yl)-1-pyrrolidin-1-ylhepta-2,4-dien-1-one 11779500 Click to see 299.40 unknown https://doi.org/10.1021/NP9703656
1,3-Benzodioxole-5-carboxaldehyde, 6,7-dimethoxy- 185549 Click to see 210.18 unknown https://doi.org/10.1002/CHIN.200541203
1,3-Benzodioxole, 4,5-dimethoxy-7-(2-propenyl)- 12558252 Click to see 222.24 unknown https://doi.org/10.1016/S0031-9422(00)81303-5
3-(6-Methoxy-1,3-benzodioxol-5-yl)-1-pyrrolidin-1-ylprop-2-en-1-one 162908861 Click to see 275.30 unknown https://doi.org/10.1021/NP9703656
https://doi.org/10.1016/S0031-9422(00)00226-0
5-(1,3-Benzodioxol-5-yl)-1-pyrrolidin-1-ylpent-2-en-1-one 85433734 Click to see 273.33 unknown https://doi.org/10.1016/S0031-9422(00)00226-0
https://doi.org/10.1016/S0031-9422(01)00431-9
https://doi.org/10.1021/NP9703656
https://doi.org/10.1021/NP030475E
7-(1,3-Benzodioxol-5-yl)-1-pyrrolidin-1-ylhepta-2,4-dien-1-one 73097841 Click to see C1CCN(C1)C(=O)C=CC=CCCC2=CC3=C(C=C2)OCO3 299.40 unknown https://doi.org/10.1021/NP100606U
https://doi.org/10.1021/NP9703656
7-(1,3-benzodioxol-5-yl)-N-(2-methylpropyl)hepta-2,4-dienamide 78200770 Click to see 301.40 unknown https://doi.org/10.1021/NP100606U
https://doi.org/10.1016/S0031-9422(00)00226-0
7-Benzo[1,3]dioxol-5-yl-hepta-2,4-dienoic acid isobutyl-amide 643765 Click to see CC(C)CNC(=O)C=CC=CCCC1=CC2=C(C=C1)OCO2 301.40 unknown https://doi.org/10.1016/S0031-9422(00)00226-0
omega-Hydroxyisodillapiole 6241978 Click to see COC1=C(C2=C(C=C1C=CCO)OCO2)OC 238.24 unknown https://doi.org/10.1002/CHIN.200541203
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
2,2-Dimethyl-8-prenylchromene 6-carboxylic acid 441962 Click to see CC(=CCC1=CC(=CC2=C1OC(C=C2)(C)C)C(=O)O)C 272.34 unknown https://doi.org/10.1002/CHIN.200541203
> Organoheterocyclic compounds / Coumarans
(2R,3R)-3-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-carboxylic acid 162986130 Click to see 238.24 unknown https://doi.org/10.1002/CHIN.200541203
3-Hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-carboxylic acid 68842885 Click to see 238.24 unknown https://doi.org/10.1002/CHIN.200541203
methyl (2R,3R)-3-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-carboxylate 102150110 Click to see 252.26 unknown https://doi.org/10.1002/CHIN.200541203
Methyl 3-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-carboxylate 68844368 Click to see 252.26 unknown https://doi.org/10.1002/CHIN.200541203
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-(6,7-Dimethoxy-1,3-benzodioxol-5-yl)prop-2-enal 340064 Click to see COC1=C(C2=C(C=C1C=CC=O)OCO2)OC 236.22 unknown https://doi.org/10.1002/CHIN.200541203
Dillapional 5458880 Click to see 236.22 unknown https://doi.org/10.1002/CHIN.200541203
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
(Z)-3-(6-methoxy-1,3-benzodioxol-5-yl)-1-pyrrolidin-1-ylprop-2-en-1-one 92020008 Click to see COC1=CC2=C(C=C1C=CC(=O)N3CCCC3)OCO2 275.30 unknown https://doi.org/10.1021/NP9703656
https://doi.org/10.1016/S0031-9422(00)00226-0
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-feruloyltyramine; Moupinamide 125213 Click to see 313.30 unknown https://doi.org/10.1002/CHIN.200541203
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3-(6,7-Dimethoxy-1,3-benzodioxol-5-yl)prop-2-en-1-ol 286711 Click to see 238.24 unknown https://doi.org/10.1002/CHIN.200541203
> 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://doi.org/10.1016/J.PHYTOL.2011.08.001
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.001
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(-)-Pinostrobin 73201 Click to see 270.28 unknown https://doi.org/10.1016/S0031-9422(00)81303-5
(2R)-6-hydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydrochromen-4-one 163071725 Click to see 300.30 unknown https://doi.org/10.1055/S-2008-1074918
(2R)-8-hydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydrochromen-4-one 154496083 Click to see 300.30 unknown https://doi.org/10.1055/S-2008-1074918
Npc235117 4101463 Click to see 270.28 unknown https://doi.org/10.1016/S0031-9422(00)81303-5
Pinostrobin 6950539 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/S0031-9422(00)81303-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2R)-5,7,8-trimethoxy-2-phenyl-2,3-dihydrochromen-4-one 154496040 Click to see 314.30 unknown https://doi.org/10.1055/S-2008-1074918
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',6'-Dihydroxy-4'-methoxydihydrochalcone 169676 Click to see 272.29 unknown https://doi.org/10.1016/S0031-9422(00)81303-5
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxy-6-methoxyphenyl)-3-phenylprop-2-en-1-one 154102 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.001
2-Propen-1-one,1-(2-hydroxy-3,4,6-trimethoxyphenyl)-3-phenyl- 227450 Click to see 314.30 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.001
2'-Hydroxy-3',4',6'-trimethoxychalcone 5354780 Click to see 314.30 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.001
https://doi.org/10.1055/S-2008-1074918
2',3'-Dihydroxy-4',6'-dimethoxychalcone 14159747 Click to see COC1=CC(=C(C(=C1C(=O)C=CC2=CC=CC=C2)O)O)OC 300.30 unknown https://doi.org/10.1055/S-2008-1074918
Cardamonin 641785 Click to see 270.28 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.001

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