Pterogyne nitens - Unknown
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Internal ID UUID643fd6d0d10e2681343187
Scientific name Pterogyne nitens
Authority Tul.
First published in Ann. Sci. Nat., Bot., sér. 2, 20: 140 (1843)

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Synonyms Top

Scientific name Authority First published in
Machaerium pseudotipe Griseb. Abh. Königl. Ges. Wiss. Göttingen24: 110 (1879)
Pterogyne nitens f. parvifolia Chodat & Hassl. Bull. Herb. Boissier, sér. 2, 4: 563 (1904)

Common names Top

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Language Common/alternative name
Spanish cocal
Spanish guiraró
Spanish tipa colorado
Spanish ybyraro
Spanish ybyraró
gn yvyra ro
Japanese アメンドイム
Lithuanian blizgioji piestoja
Portuguese amendoim-bravo

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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000170614
Tropicos 13047872
KEW urn:lsid:ipni.org:names:516619-1
The Plant List ild-1688
Open Tree Of Life 946962
NCBI Taxonomy 162890
IUCN Red List 32977
IPNI 516619-1
iNaturalist 442819
GBIF 5352650
Freebase /m/02vt55q
EPPO PTGNI
EOL 638535
USDA GRIN 30310

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
Small-molecule amines: a big role in the regulation of bone homeostasis Zhang Q, Yang J, Hu N, Liu J, Yu H, Pan H, Chen D, Ruan C Bone Res 24-Jul-2023
PMCID:PMC10363555
doi:10.1038/s41413-023-00262-z
PMID:37482549
Natural Products and Derivatives as Potential Zika virus Inhibitors: A Comprehensive Review Pereira RS, Santos FC, Campana PR, Costa VV, de Pádua RM, Souza DG, Teixeira MM, Braga FC Viruses 20-May-2023
PMCID:PMC10222392
doi:10.3390/v15051211
PMID:37243296
Antiplasmodial Activity of Hydroalcoholic Extract from Jucá (Libidibia ferrea) Pods de Assis FF, de Almeida Junior JS, Moraes TM, Varotti FD, Moraes CC, Sartoratto A, Moraes WP, Minervino AH Pharmaceutics 06-Apr-2023
PMCID:PMC10145024
doi:10.3390/pharmaceutics15041162
PMID:37111647
Natural Compounds as Non-Nucleoside Inhibitors of Zika Virus Polymerase through Integration of In Silico and In Vitro Approaches Ramos PR, Mottin M, Lima CS, Assis LR, de Oliveira KZ, Mesquita NC, Cassani NM, Santos IA, Borba JV, Fiaia Costa VA, Neves BJ, Guido RV, Oliva G, Jardim AC, Regasini LO, Andrade CH Pharmaceuticals (Basel) 30-Nov-2022
PMCID:PMC9788182
doi:10.3390/ph15121493
PMID:36558945
The impact of chromium ion stress on plant growth, developmental physiology, and molecular regulation Saud S, Wang D, Fahad S, Javed T, Jaremko M, Abdelsalam NR, Ghareeb RY Front Plant Sci 28-Oct-2022
PMCID:PMC9651928
doi:10.3389/fpls.2022.994785
PMID:36388512
Synergistic In Vitro Interaction of Isavuconazole and Isoquercitrin against Candida glabrata Schwarz PV, Nikolskiy I, Dannaoui E, Sommer F, Bange G, Schwarz P J Fungi (Basel) 20-May-2022
PMCID:PMC9147185
doi:10.3390/jof8050525
PMID:35628780
Can Nutritional Supports Beneficial in Other Viral Diseases Be Favorable for COVID-19? Zelka FZ, Kocatürk RR, Özcan ÖÖ, Karahan M Korean J Fam Med 20-Jan-2022
PMCID:PMC8820968
doi:10.4082/kjfm.20.0134
PMID:35130635
Responses of functional traits in cavity-nesting birds to logging in subtropical and temperate forests of the Americas Schaaf AA, Gomez D, Tallei E, Vivanco CG, Ruggera RA Sci Rep 21-Dec-2021
PMCID:PMC8692622
doi:10.1038/s41598-021-03756-0
PMID:34934123
Galleria mellonella: The Versatile Host for Drug Discovery, In Vivo Toxicity Testing and Characterising Host-Pathogen Interactions Piatek M, Sheehan G, Kavanagh K Antibiotics (Basel) 17-Dec-2021
PMCID:PMC8698334
doi:10.3390/antibiotics10121545
PMID:34943757
Anatomical characterization and technological properties of Pterogyne nitens wood, a very interesting species of the Brazilian Caatinga biome Pereira AK, Longue Júnior D, Carvalho AM, Mafra Neto CD Sci Rep 28-Jul-2021
PMCID:PMC8319433
doi:10.1038/s41598-021-94785-2
PMID:34321533
Antiviral activities of flavonoids Badshah SL, Faisal S, Muhammad A, Poulson BG, Emwas AH, Jaremko M Biomed Pharmacother 11-Jun-2021
PMCID:PMC8192980
doi:10.1016/j.biopha.2021.111596
PMID:34126315
Flavonoids from Pterogyne nitens as Zika virus NS2B-NS3 protease inhibitors Lima CS, Mottin M, de Assis LR, de Moraes Roso Mesquita NC, de Paula Sousa BK, Coimbra LD, dos Santos KB, Zorn KM, Guido RV, Ekins S, Marques RE, Proença-Modena JL, Oliva G, Andrade CH, Regasini LO Bioorg Chem 11-Feb-2021
PMCID:PMC8227833
doi:10.1016/j.bioorg.2021.104719
PMID:33636437
DiaNat-DB: a molecular database of antidiabetic compounds from medicinal plants Madariaga-Mazón A, Naveja JJ, Medina-Franco JL, Noriega-Colima KO, Martinez-Mayorga K RSC Adv 28-Jan-2021
PMCID:PMC8694643
doi:10.1039/d0ra10453a
PMID:35424427
Therapeutic Potential of Natural Products in Treatment of Cervical Cancer: A Review Park SH, Kim M, Lee S, Jung W, Kim B Nutrients 05-Jan-2021
PMCID:PMC7824868
doi:10.3390/nu13010154
PMID:33466408
Comprehensive Review on Current Interventions, Diagnostic, and Nanotechnology Perspectives against SARS-CoV-2 Chauhan DS, Prasad R, Srivastava R, Jaggi M, Chauhan SC, Yallapu MM Bioconjug Chem 12-Aug-2020
PMCID:PMC7425040
doi:10.1021/acs.bioconjchem.0c00323
PMID:32680422

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 / Monoterpenoids / Acyclic monoterpenoids
1,1-Bis(3,7-dimethylocta-2,6-dienyl)guanidine 85133793 Click to see CC(=CCCC(=CCN(CC=C(C)CCC=C(C)C)C(=N)N)C)C 331.50 unknown https://doi.org/10.1590/S0102-695X2010005000017
1,1-bis[(2E)-3,7-dimethylocta-2,6-dienyl]guanidine 10404473 Click to see CC(=CCCC(=CCN(CC=C(C)CCC=C(C)C)C(=N)N)C)C 331.50 unknown https://doi.org/10.1021/NP50125A006
1,2-Bis(3,7-dimethylocta-2,6-dienyl)guanidine 162820217 Click to see CC(=CCCC(=CCNC(=NCC=C(C)CCC=C(C)C)N)C)C 331.50 unknown https://doi.org/10.1590/S0102-695X2010005000017
1,3-Bis(3,7-dimethylocta-2,6-dienyl)-1,3-dimethylguanidine 85094923 Click to see CC(=CCCC(=CCN(C)C(=N)N(C)CC=C(C)CCC=C(C)C)C)C 359.60 unknown https://doi.org/10.1590/S0102-695X2010005000017
2-(3,7-Dimethylocta-2,6-dienyl)guanidine 75107490 Click to see CC(=CCCC(=CCN=C(N)N)C)C 195.30 unknown https://doi.org/10.1021/NP800612X
Nitensidine A 10246147 Click to see CC(=CCCC(=CCNC(=NCC=C(C)CCC=C(C)C)N)C)C 331.50 unknown https://doi.org/10.1021/NP50125A006
Nitensidine C 10570471 Click to see CC(=CCCC(=CCN(C)C(=N)N(C)CC=C(C)CCC=C(C)C)C)C 359.60 unknown https://doi.org/10.1021/NP50125A006
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
2,5,6,6abeta,7,10abeta-Hexahydro-4aalpha-hydroxy-1,6beta,9-trimethylnaphtho[2,1-c][1,2]dioxin-8(4aH)-one 25016669 Click to see CC1CC2(C(=C(COO2)C)C3C1CC(=O)C(=C3)C)O 264.32 unknown https://doi.org/10.1590/S0102-695X2010005000017
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
[(3S,4aR,6aR,8aR,12aR,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-yl] acetate 5458941 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.4067/S0717-97072009000300004
Taraxerol acetate 94225 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.4067/S0717-97072009000300004
Taraxeryl acetate 5205968 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.4067/S0717-97072009000300004
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,12a,14a-dodecahydro-1H-picen-3-yl] hexadec-9-enoate 163053865 Click to see CCCCCCC=CCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2C(=O)C=C4C3(CCC5(C4CC(CC5)(C)C)CO)C)C)C 693.10 unknown https://doi.org/10.1590/S0102-695X2010005000017
4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,6a,7,8,9,10,13,14,14a-dodecahydro-1H-picen-3-one 15559505 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C)C 424.70 unknown https://doi.org/10.4067/S0717-97072009000300004
> Organic nitrogen compounds / Organonitrogen compounds / Guanidines
1,2,3-Tris(3-methylbut-2-enyl)guanidine 14781546 Click to see CC(=CCNC(=NCC=C(C)C)NCC=C(C)C)C 263.42 unknown https://doi.org/10.1590/S0102-695X2010005000017
Galegine 10983 Click to see CC(=CCN=C(N)N)C 127.19 unknown https://doi.org/10.1021/NP800612X
Pterogynidine 10035557 Click to see CC(=CCNC(=NCC=C(C)C)N)C 195.30 unknown https://doi.org/10.1021/NP800612X
https://doi.org/10.1007/S13277-010-0064-2
https://doi.org/10.1590/S0102-695X2009000100014
https://doi.org/10.1021/NP50125A006
Pterogynine 45268797 Click to see CC(=CCN(CC=C(C)C)C(=N)N)C 195.30 unknown https://doi.org/10.1590/S0102-695X2009000100014
https://doi.org/10.1007/S13277-010-0064-2
https://doi.org/10.1021/NP800612X
> Organoheterocyclic compounds / Diazinanes
(6R)-6-methyl-6-[(1E)-4-methylpenta-1,3-dienyl]-4,5-dihydro-1H-pyrimidin-2-amine 162902423 Click to see CC(=CC=CC1(CCN=C(N1)N)C)C 193.29 unknown https://doi.org/10.1021/NP800612X
(6S)-6-methyl-6-[(1E)-4-methylpenta-1,3-dienyl]-4,5-dihydro-1H-pyrimidin-2-amine 162902424 Click to see CC(=CC=CC1(CCN=C(N1)N)C)C 193.29 unknown https://doi.org/10.1021/NP800612X
6-methyl-6-(4-methylpenta-1,3-dienyl)-4,5-dihydro-1H-pyrimidin-2-amine 75107221 Click to see CC(=CC=CC1(CCN=C(N1)N)C)C 193.29 unknown https://doi.org/10.1021/NP800612X
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Hydropyrimidines
nitensidine E 45267913 Click to see CC(=CC=CC1(CCN=C(N1)N)C)C 193.29 unknown https://doi.org/10.1021/NP800612X
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S,2R,3S,3'E,5R,6S,7R,8S,9R,12S)-2-hydroxy-8-methoxy-3'-(1-methoxyethylidene)-7-methyl-12-propan-2-ylspiro[4,10-dioxatetracyclo[7.2.1.02,7.03,5]dodecane-6,5'-oxolane]-2',11-dione 162948516 Click to see CC(C)C1C2C(C3(C4(CC(=C(C)OC)C(=O)O4)C5C(C3(C1C(=O)O2)O)O5)C)OC 408.40 unknown https://doi.org/10.1021/NP800612X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid 709 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1590/S0100-40422008000400018
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1590/S0100-40422008000400018
Sinapic acid 10743 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown https://doi.org/10.1590/S0100-40422008000400018
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown https://doi.org/10.1590/S0100-40422008000400018
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
[(2R,3R)-5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-8-[(2R,3R,4S)-3,5,7-triacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] 4-acetyloxybenzoate 162974965 Click to see CC(=O)OC1C(C2=C(C=C(C=C2OC(=O)C)OC(=O)C)OC1C3=CC(=C(C(=C3)OC(=O)C)OC(=O)C)OC(=O)C)C4=C(C=C(C5=C4OC(C(C5)OC(=O)C6=CC=C(C=C6)OC(=O)C)C7=CC(=C(C(=C7)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 1235.10 unknown https://doi.org/10.1590/S0102-695X2010005000017
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(-)-Egc-4'-O-ME 53463000 Click to see COC1=C(C=C(C=C1O)C2C(CC3=C(C=C(C=C3O2)O)O)O)O 320.29 unknown https://doi.org/10.1590/S0100-40422008000400018
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1021/NP50125A006
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.006
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.006
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-methoxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 73981696 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 478.40 unknown https://doi.org/10.1248/CPB.56.723
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-methoxy-6-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 74343445 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=C4C(=C3O)C(=O)C=C(O4)C5=CC(=C(C=C5)O)O)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1248/CPB.56.723
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxy-6-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one 52946745 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1248/CPB.56.723
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74977855 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1248/CPB.56.723
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxy-6-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 74343444 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=C4C(=C3O)C(=O)C=C(O4)C5=CC=C(C=C5)O)OC)O)O)O)O)O)O 608.50 unknown https://doi.org/10.1248/CPB.56.723
Nitensoside A 24881306 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=C4C(=C3O)C(=O)C=C(O4)C5=CC=C(C=C5)O)OC)O)O)O)O)O)O 608.50 unknown https://doi.org/10.1248/CPB.56.723
Nitensoside B 24881307 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=C4C(=C3O)C(=O)C=C(O4)C5=CC(=C(C=C5)O)O)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1248/CPB.56.723
Pedaliin 5320439 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 478.40 unknown https://doi.org/10.1248/CPB.56.723
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[2-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl] 3,5-dihydroxy-4-methoxybenzoate 74343916 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)OC(=O)C5=CC(=C(C(=C5)O)OC)O)O 598.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.006
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.006
3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 42613954 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1590/S0100-40422008000400018
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 14185727 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1590/S0100-40422008000400018
Afzelin 5316673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.006
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.006
Kaempferol-3-O-rhamnoside 5835713 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.006
Pterogynoside 24882501 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)OC(=O)C5=CC(=C(C(=C5)O)OC)O)O 598.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.006
Quosp 5282166 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1590/S0100-40422008000400018
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.006
Vitamin P 5293655 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.006
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Lespedin 5486199 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.006
Lespedin;Lespenephryl 12305415 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.006
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Pedalitin 31161 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)O 316.26 unknown https://doi.org/10.1248/CPB.56.723
Sorbifolin 3084390 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)O 300.26 unknown https://doi.org/10.1248/CPB.56.723

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