Harpagophytum procumbens - Unknown
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Internal ID UUID64401fbe37001725925128
Scientific name Harpagophytum procumbens
Authority DC. ex Meisn.
First published in Pl. Vasc. Gen. : 206 (1840)

Description Top

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Synonyms Top

Scientific name Authority First published in
Uncaria burchellii Kuntze Revis. Gen. Pl. 2: 481. 1891 [5 Nov 1891]
Harpagophytum burchellii DC. Icon. Sel. Pl. 5: 39 (1846)
Uncaria procumbens Burch. Trav. S. Africa i. 536 (1822).

Common names Top

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Language Common/alternative name
English devil's-claw
Spanish harpagofito
Spanish harpagófito
Arabic مخلب الشيطان
Catalan harpagòfit
Catalan urpa del dimoni
Czech harpagofyt ležatý
German trampelklette
German afrikanische teufelskralle
eml grinfa dal diàvul
Esperanto diablokrifo
Esperanto harpagofito
Persian پنجه شیطان
Persian پنجهٔ شیطان
French harpagophyton
Hungarian ördögcsáklya
Italian artiglio del diavolo
Italian arpagofito
Japanese ライオンゴロシ
Latvian velna nags
Macedonian Ѓаволски канџи
Dutch harpagòfit
Chinese 爪钩草

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
  • Africa
    • South Tropical Africa
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Namibia
      • Northern Provinces
      • Swaziland

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000715793
UNII BY51E8JN4B
USDA Plants HAPR3
Tropicos 24300038
KEW urn:lsid:ipni.org:names:675824-1
Open Tree Of Life 668308
Observations.org 904923
NCBI Taxonomy 222879
IPNI 675824-1
iNaturalist 356058
iNaturalist 356056
iNaturalist 356057
GBIF 3585335
Freebase /m/04b34m
EPPO HPGPR
Elurikkus 378569
USDA GRIN 18252
CMAUP NPO5565

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
In vitro and in silico docking and molecular dynamic of antimicrobial activities, alpha-glucosidase, and anti-inflammatory activity of compounds from the aerial parts of Mussaenda saigonensis Ngoc Mai TT, Minh PN, Phat NT, Chi MT, Duong TH, Nhi Phan NH, Minh An TN, Dang VS, Van Hue N, Hong Anh NT, Tri MD RSC Adv 16-Apr-2024
PMCID:PMC11019407
doi:10.1039/d4ra01865f
PMID:38628478
Antiarthritic and Anti-Inflammatory Properties of Cannabis sativa Essential Oil in an Animal Model Kabdy H, Azraida H, Agouram F, Oufquir S, Laadraoui J, Baslam A, Aitbaba A, Ouazzani ME, Elyazouli L, Aboufatima R, Garzoli S, Chait A Pharmaceuticals (Basel) 22-Dec-2023
PMCID:PMC10819254
doi:10.3390/ph17010020
PMID:38256854
Potential of Selected African Medicinal Plants as Alternative Therapeutics against Multi-Drug-Resistant Bacteria Moiketsi BN, Makale KP, Rantong G, Rahube TO, Makhzoum A Biomedicines 22-Sep-2023
PMCID:PMC10604549
doi:10.3390/biomedicines11102605
PMID:37892979
Epidural Injection of Harpagoside for the Recovery of Rats with Lumbar Spinal Stenosis Hong JY, Kim H, Yeo C, Lee J, Jeon WJ, Lee YJ, Ha IH Cells 15-Sep-2023
PMCID:PMC10526993
doi:10.3390/cells12182281
PMID:37759506
Effects of blended learning training for oncology physicians to advise their patients about complementary and integrative therapies: results from the multicenter cluster-randomized KOKON-KTO trial Helmer SM, Rogge AA, King R, Canella C, Pach D, Witt CM BMC Cancer 07-Sep-2023
PMCID:PMC10483860
doi:10.1186/s12885-023-11348-6
PMID:37679678
A Pragmatic Randomized Controlled Trial on the Effectiveness and Safety of Pharmacopuncture for Chronic Lower Back Pain Park KS, Kim C, Kim JW, Kim S, Lee JY, Lee YJ, Lee J, Kim MJ, Choi YE, Yang C, Han CH, Ha IH J Pain Res 03-Aug-2023
PMCID:PMC10406108
doi:10.2147/JPR.S413512
PMID:37554434
Recent trends of machine learning applied to multi-source data of medicinal plants Zhang Y, Wang Y J Pharm Anal 25-Jul-2023
PMCID:PMC10785154
doi:10.1016/j.jpha.2023.07.012
PMID:38223450
Potential pharmacokinetic interactions with concurrent use of herbal medicines and a ritonavir-boosted COVID-19 protease inhibitor in low and middle-income countries Smith DJ, Bi H, Hamman J, Ma X, Mitchell C, Nyirenda K, Monera-Penduka T, Oketch-Rabah H, Paine MF, Pettit S, Pheiffer W, Van Breemen RB, Embry M Front Pharmacol 12-Jul-2023
PMCID:PMC10368978
doi:10.3389/fphar.2023.1210579
PMID:37502215
Seedborne mycoflora of faba bean (Vicia fabae L.) and evaluation of plant extract and Trichoderma species against mycelium growth of selected fungi Neme A, Leta A, Yones AM, Tahir M Heliyon 15-Jun-2023
PMCID:PMC10293731
doi:10.1016/j.heliyon.2023.e17291
PMID:37383212
Effects of Prolonged Fasting during Inpatient Multimodal Treatment on Pain and Functional Parameters in Knee and Hip Osteoarthritis: A Prospective Exploratory Observational Study Koppold DA, Kandil FI, Güttler O, Müller A, Steckhan N, Meiß S, Breinlinger C, Nelle E, Hartmann AM, Jeitler M, Hanslian E, Fischer JM, Michalsen A, Kessler CS Nutrients 09-Jun-2023
PMCID:PMC10301411
doi:10.3390/nu15122695
PMID:37375597
The medicinal chemistry of Urtica dioica L.: from preliminary evidence to clinical studies supporting its neuroprotective activity Semwal P, Rauf A, Olatunde A, Singh P, Zaky MY, Islam MM, Khalil AA, Aljohani AS, Al Abdulmonem W, Ribaudo G Nat Prod Bioprospect 12-May-2023
PMCID:PMC10176313
doi:10.1007/s13659-023-00380-5
PMID:37171512
Raman spectroscopy in crop quality assessment: focusing on sensing secondary metabolites: a review Park M, Somborn A, Schlehuber D, Keuter V, Deerberg G Hortic Res 19-Apr-2023
PMCID:PMC10208899
doi:10.1093/hr/uhad074
PMID:37249949
Hairy Root Cultures as a Source of Phenolic Antioxidants: Simple Phenolics, Phenolic Acids, Phenylethanoids, and Hydroxycinnamates Malarz J, Yudina YV, Stojakowska A Int J Mol Sci 07-Apr-2023
PMCID:PMC10138958
doi:10.3390/ijms24086920
PMID:37108084
Ethnobotanical survey of medicinal plants used by indigenous knowledge holders to manage healthcare needs in children Ndhlovu PT, Asong JA, Omotayo AO, Otang-Mbeng W, Aremu AO PLoS One 27-Mar-2023
PMCID:PMC10042359
doi:10.1371/journal.pone.0282113
PMID:36972257
Effect of different plant growth regulators on callus and adventitious shoots induction, polysaccharides accumulation and antioxidant activity of Rhodiola dumulosa Lu X, Fei L, Li Y, Du J, Ma W, Huang H, Wang J Chin Herb Med 15-Mar-2023
PMCID:PMC10230626
doi:10.1016/j.chmed.2022.07.005
PMID:37265763

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aR)-6,7,10-trihydroxy-1,1,4a-trimethyl-5-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one 102184323 Click to see CC(C)C1=C2C(=CC(=C1O)O)C(=O)C(=C3C2(CCCC3(C)C)C)O 330.40 unknown https://doi.org/10.1021/NP050504G
12,13-Dihydroxy-11-isopropyl-8,11,13-podocarpatriene-7-one 11609380 Click to see CC(C)C1=C2C(=CC(=C1O)O)C(=O)CC3C2(CCCC3(C)C)C 316.40 unknown https://doi.org/10.1021/NP050504G
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1021/NP0601612
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aR,5R,7S,7aR)-7-methyl-1-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4a,5,7-triol 162989826 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.029
(1S,4aS,5R,7S,7aR)-7-methyl-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4a,5,7-triol 44438955 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown via CMAUP database
(1S,4aS,5R,7S)-7-methyl-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4a,5,7-triol 91973789 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown via CMAUP database
(1S,4aS,5S,7S,7aR)-1,4a,5,6,7,7a-Hexahydro-4a,5,7-trihydroxy-7-methylcyclopenta[c]pyran-1-yl beta-D-glucopyranoside 145706031 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown https://doi.org/10.1021/NP070204U
https://doi.org/10.1080/10826079408013512
https://doi.org/10.1248/CPB.31.2296
https://doi.org/10.1016/0378-8741(84)90071-0
(4aS,5R,7S,7aR)-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4a,5,7-triol 101286236 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown via CMAUP database
[(1R,4aR,5S,7R)-4a,5-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] (Z)-3-phenylprop-2-enoate 24085834 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=CC=C4 494.50 unknown via CMAUP database
[(1S,4aR,5R,7S,7aS)-4a-hydroxy-7-methyl-5-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] (E)-3-phenylprop-2-enoate 162922519 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C=CC5=CC=CC=C5 656.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.029
[(1S,4aR,5R,7S,7aS)-4a,5-dihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162948805 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC 540.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.029
https://doi.org/10.1021/NP0601612
[(1S,4aR,5R,7S,7aS)-4a,5-dihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] (E)-3-phenylprop-2-enoate 163030846 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O)O)O)OC(=O)C=CC5=CC=CC=C5 656.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.029
[(1S,4aR,5R,7S,7aS)-4a,5-dihydroxy-7-methyl-1-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 163082117 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=C(C=C4)O 510.50 unknown https://doi.org/10.1248/CPB.31.2296
[(1S,4aS,5R,7S,7aS)-5-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-7-yl] (E)-3-phenylprop-2-enoate 162952080 Click to see CC1(CC(C2C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)OC(=O)C=CC4=CC=CC=C4 478.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.029
[(4aS,5R,7S)-4a,5-dihydroxy-7-methyl-1-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 24893235 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC 540.50 unknown via CMAUP database
8-(4-Coumaroyl)harpagide 101416538 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=C(C=C4)O 510.50 unknown https://doi.org/10.1021/NP0601612
8-Cinnamoylmyoporoside 101402540 Click to see CC1(CC(C2C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)OC(=O)C=CC4=CC=CC=C4 478.50 unknown via CMAUP database
8-Feruloylharpagide 101416539 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC 540.50 unknown https://doi.org/10.1021/NP0601612
8-p-Coumaroylharpagide 10324058 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=C(C=C4)O 510.50 unknown https://doi.org/10.1021/NP070204U
CID 10044294 10044294 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown via CMAUP database
Harpagide 93045 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown https://doi.org/10.1080/10826079408013512
https://doi.org/10.1016/0378-8741(84)90071-0
https://doi.org/10.1248/CPB.31.2296
https://doi.org/10.1021/NP070204U
https://doi.org/10.1016/J.PHYTOCHEM.2006.05.029
Harpagoside 5281542 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=CC=C4 494.50 unknown https://doi.org/10.1016/J.PHYMED.2004.02.003
https://doi.org/10.1007/978-3-642-85436-1_9
https://doi.org/10.1021/NP070204U
https://doi.org/10.1016/S0031-9422(00)81833-6
https://doi.org/10.1007/978-3-540-71095-0_4593
https://doi.org/10.1002/BIP.20158
https://doi.org/10.1078/0944-7113-00140
https://doi.org/10.1016/S0944-7113(00)80076-8
https://doi.org/10.1248/CPB.31.2296
https://doi.org/10.1016/0378-8741(85)90006-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8R,8aR,9S,10R,11R,12aR,14bS)-8,10,11-trihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 102005082 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 666.80 unknown via CMAUP database
chebuloside II 44567150 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 666.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Maytenone 44558957 Click to see CC(C)C1(C2C3C4(CCC5C(CCCC5(C4=CC(=O)C3(C(C)C)O)C)(C)C)C(C1=O)C6=C2CCC7C6(CCCC7(C)C)C)O 604.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Maytenoquinone 45109910 Click to see CC(C)C1=C(C(=O)C=C2C1=CC(=O)C3C2(CCCC3(C)C)C)O 314.40 unknown https://doi.org/10.1021/NP0601612
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4R,5S,6S)-2-(hydroxymethyl)-6-[[(1S,2S,4R,5S,6S,8R,10S)-10-hydroxy-4-methyl-3,7,11-trioxatetracyclo[6.2.1.02,4.05,10]undecan-6-yl]oxy]oxane-3,4,5-triol 154497277 Click to see CC12C3C(OC4CC3(C(C1O2)O4)O)OC5C(C(C(C(O5)CO)O)O)O 362.33 unknown https://doi.org/10.1248/CPB.31.2296
(2S,3R,4S,5R,6R)-2-[[(1S,2R,4S,5S,6R,10S)-5,6-dihydroxy-2-methyl-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154497276 Click to see CC12C3C(OC=CC3(C(C1O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 362.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.029
2-(Hydroxymethyl)-6-[(10-hydroxy-4-methyl-3,7,11-trioxatetracyclo[6.2.1.02,4.05,10]undecan-6-yl)oxy]oxane-3,4,5-triol 163004743 Click to see CC12C3C(OC4CC3(C(C1O2)O4)O)OC5C(C(C(C(O5)CO)O)O)O 362.33 unknown https://doi.org/10.1248/CPB.31.2296
Procumbide 21604824 Click to see CC12C3C(OC=CC3(C(C1O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 362.33 unknown https://doi.org/10.1016/S0031-9422(00)81833-6
https://doi.org/10.1007/978-3-540-71095-0_4593
https://doi.org/10.1248/CPB.31.2296
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1021/NP0601612
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1021/NP0601612
cis-Cinnamic acid 5372954 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 / Coumaric acids and derivatives
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 73323377 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(00)81833-6
https://doi.org/10.1021/NP0601612
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP070204U
https://doi.org/10.1016/S0031-9422(00)81833-6
https://doi.org/10.1021/NP050504G
https://doi.org/10.1021/NP0601612
https://doi.org/10.1016/S0031-9422(02)00700-8
2-Acetylacteoside 21629996 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C)OCCC3=CC(=C(C=C3)O)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O 666.60 unknown via CMAUP database
Ethyl caffeate 5317238 Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O 208.21 unknown https://doi.org/10.1016/J.JPBA.2011.02.029
Isoacteoside 6476333 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP070204U
https://doi.org/10.1016/S0031-9422(00)81833-6
https://doi.org/10.1021/NP050504G
https://doi.org/10.1021/NP0601612
https://doi.org/10.1016/S0031-9422(02)00700-8
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(2R,3S,4R,5S,6S)-6-[[(1S,2R,4S,5S,6R,10S)-5,6-dihydroxy-2-methyl-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 162990975 Click to see CC12C3C(OC=CC3(C(C1O2)O)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O 508.50 unknown https://doi.org/10.1248/CPB.31.2296
[(2R,3S,4S,5R,6S)-6-[[(1S,2R,4S,5S,6R,10S)-5,6-dihydroxy-2-methyl-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (Z)-3-(4-hydroxyphenyl)prop-2-enoate 162990977 Click to see CC12C3C(OC=CC3(C(C1O2)O)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O 508.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.029
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
cis-Caffeic acid 1549111 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database

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