Handroanthus impetiginosus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Handroanthus impetiginosus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID6440273763e3c774563087
Scientific name Handroanthus impetiginosus
Authority (Mart. ex DC.) Mattos
First published in Loefgrenia 50: 2 (1970)

Description Top

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Synonyms Top

Scientific name Authority First published in
Handroanthus avellanedae (Lorentz ex Griseb.) Mattos Loefgrenia 50: 4 (1970)
Tecoma impetiginosa Mart. Syst. Mat. Med. Bras. 54. 1843 (1843)
Tecoma impetiginosa Mart. ex DC. Prodr. 9: 218 (1845)
Tecoma integra Hassl. Addenda Pl. Hassl. 15. 1917; Chod. in Bull. Soc. Bot. Geneve, Ser. II.ix. 206 (1917), in obs.
Tabebuia impetiginosa Standl. Publ. Field Columb. Mus., Bot. Ser. 11: 176 (1936)
Tabebuia nicaraguensis S.F.Blake Contrib. Gray Herb. , n.s., 52: 95 (1917)
Tabebuia avellanedae Lorentz ex Griseb. Abh. Königl. Ges. Wiss. Göttingen 24: 258 (1879)
Tabebuia dugandii Standl. Trop. Woods 36: 17 (1933)
Tecoma adenophylla K.Schum. Fl. Bras. 8(2): 412 (1897)
Tecoma avellanedae Speg. in Speg. & Girola Cat. Descr. Maderas : 379 (1910)
Tabebuia schunkevigoi D.R.Simpson Fieldiana, Bot. 36(1): 1 (1972)
Tabebuia palmeri Rose Contr. U.S. Natl. Herb. 1: 109 (1891)
Tabebuia ipe var. integra (Sprague) Sandwith in A.C.Sm. Lloydia 2: 213 (1939)
Tecoma avellanedae var. alba Lillo Seg. Contr. Arb. Argent. : 13 (1917)
Tecoma ipe var. integra Sprague Bull. Herb. Boissier , sér. 2, 5: 86 (1905)
Tecoma ipe var. integrifolia Hassl. Revista Inst. Parag. 3: 166. 1901
Tecoma ipe f. leucotricha Hassl. Repert. Spec. Nov. Regni Veg. 9: 60. 1910 [25 Dec 1910]
Gelseminum avellanedae (Lorentz ex Griseb.) Kuntze Revis. Gen. Pl. 3(2): 245 (1898)

Common names Top

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Language Common/alternative name
English pink ipê
English pink lapacho
English pink trumpet tree
Spanish lapacho rosado
Spanish amapa
Spanish tecoma ipe
Spanish tajibo
Bulgarian розово лапачо
Catalan ipê-roxo
Estonian lapatšo-tuutupuu
Persian تابهبویا ایمپتیگینوسا
Finnish jousilieskapuu
Finnish jousisoihtupuu
Japanese パウダルコ
Japanese タヒーボ
Lithuanian penkialapis balamedis
Malayalam ഹാൻഡ്രോആന്തസ് ഇമ്പെറ്റിജിനോസസ്
Portuguese piúva
Portuguese pau d’arco
Portuguese ipê-roxo-de-bola
Portuguese ipê-roxo
Russian tabebuia ipe
Russian Муравьиное дерево
Russian Розовое ипе
Russian Айпе
Chinese 紫花风铃木
Chinese 紫花粉铃木

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 Southeast
      • Mexico Southwest
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northwest
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000778595
Tropicos 50139857
INPN 843713
KEW urn:lsid:ipni.org:names:117330-2
The Plant List kew-317146
PFAF Handroanthus impetiginosus
Open Tree Of Life 532896
Observations.org 286540
NCBI Taxonomy 429701
IUCN Red List 144297143
IPNI 117330-2
iNaturalist 281274
GBIF 7298461
Freebase /m/02r4qd7
USDA GRIN 454772
Wikipedia Handroanthus_impetiginosus
CMAUP NPO487

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
Name Level Submitter Released Coverage Size
GCA_002762385.1 Himp0.1 Scaffold Laboratorio de Genetica & Biodiversidade, Instituto de Ciencias Biologicas,Universidade Federal de Goias 2017-11-09 91.0x 479.97 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
A novel O-methyltransferase Cp4MP-OMT catalyses the final step in the biosynthesis of the volatile 1,4-dimethoxybenzene in pumpkin (Cucurbita pepo) flowers Hoepflinger MC, Barman M, Dötterl S, Tenhaken R BMC Plant Biol 17-Apr-2024
PMCID:PMC11022444
doi:10.1186/s12870-024-04955-3
Genetic linkage mapping and quantitative trait locus (QTL) analysis of sweet basil (Ocimum basilicum L.) to identify genomic regions associated with cold tolerance and major volatiles Brindisi LJ, Mattera R III, Mudiyala S, Honig J, Simon JE PLoS One 09-Apr-2024
PMCID:PMC11003626
doi:10.1371/journal.pone.0299825
PMID:38593174
Telomerase Inhibition in the Treatment of Leukemia: A Comprehensive Review Bartoszewska E, Molik K, Woźniak M, Choromańska A Antioxidants (Basel) 30-Mar-2024
PMCID:PMC11047729
doi:10.3390/antiox13040427
PMID:38671875
The influence of exotic and native plants on illnesses with physical and spiritual causes in the semiarid region of Piauí, Northeast of Brazil da Silva PH, Ferreira Júnior WS, Zank S, do Nascimento AL, de Abreu MC J Ethnobiol Ethnomed 26-Feb-2024
PMCID:PMC10895823
doi:10.1186/s13002-024-00667-y
PMID:38409039
The Meaning of Plants' Names: A New Discovering Approach to Its Medicinal and/or Toxic Properties dos Santos Dantas Lima L, Felipe Domingues Passero L, Indriunas A, de Souza Santos I, Francisco Uchôa Coqueiro L, Alexandre Souza da Cruz K, Batista de Almeida A, Carlos Fernandes Galduróz J, Rodrigues E Evid Based Complement Alternat Med 19-Feb-2024
PMCID:PMC10896657
doi:10.1155/2024/6678557
PMID:38410808
Integrating Transcriptome and Chemical Analyses to Provide Insights into Biosynthesis of Terpenoids and Flavonoids in the Medicinal Industrial Crop Andrographis paniculate and Its Antiviral Medicinal Parts Yu K, Liang P, Yu H, Liu H, Guo J, Yan X, Li Z, Li G, Wang Y, Wang C Molecules 14-Feb-2024
PMCID:PMC10893308
doi:10.3390/molecules29040852
PMID:38398604
Hyperpolarisation of Mitochondrial Membranes Is a Critical Component of the Antifungal Mechanism of the Plant Defensin, Ppdef1 Parisi K, McKenna JA, Lowe R, Harris KS, Shafee T, Guarino R, Lee E, van der Weerden NL, Bleackley MR, Anderson MA J Fungi (Basel) 07-Jan-2024
PMCID:PMC10817573
doi:10.3390/jof10010054
PMID:38248963
Functional characterization of a manganese superoxide dismutase from Avicennia marina: insights into its role in salt, hydrogen peroxide, and heavy metal tolerance Abedi H, Shahpiri A Sci Rep 03-Jan-2024
PMCID:PMC10764323
doi:10.1038/s41598-023-50851-5
PMID:38172216
Geometric entropy of plant leaves: A measure of morphological complexity Muraleedharan V, Rajan SC, R J PLoS One 02-Jan-2024
PMCID:PMC10760904
doi:10.1371/journal.pone.0293596
PMID:38166118
Native Fauna of Tardigrades from Two Natural Areas of the Argentina Republic Ostertag BR, González-Reyes AX, Grabosky A, Meier F, Doma IL, Corronca J, Rocha AM Zool Stud 29-Dec-2023
PMCID:PMC11019430
doi:10.6620/ZS.2023.62-57
PMID:38628161
Editorial: Molecular systematics and phylogeography of tropical and subtropical biodiversity Valiati VH, Lopes F Front Genet 13-Dec-2023
PMCID:PMC10756672
doi:10.3389/fgene.2023.1345239
PMID:38162676
Effects of Natural Products on Enzymes Involved in Ferroptosis: Regulation and Implications Zuo HL, Huang HY, Lin YC, Liu KM, Lin TS, Wang YB, Huang HD Molecules 04-Dec-2023
PMCID:PMC10708253
doi:10.3390/molecules28237929
PMID:38067658
The Characterization and Study of Antibacterial, Free Radical Scavenging, and Anticancer Potential of Livistona chinensis-Mediated Silver Nanoparticles Saleem A, Ali S, Aftab MN, Shami A, Al-Saeed FA, Mustafa B, Paray BA Molecules 25-Nov-2023
PMCID:PMC10708060
doi:10.3390/molecules28237773
PMID:38067504
The Plant Defensin Ppdef1 Is a Novel Topical Treatment for Onychomycosis van der Weerden NL, Parisi K, McKenna JA, Hayes BM, Harvey PJ, Quimbar P, Wevrett SR, Veneer PK, McCorkelle O, Vasa S, Guarino R, Poon S, Gaspar YM, Baker MJ, Craik DJ, Turner RB, Brown MB, Bleackley MR, Anderson MA J Fungi (Basel) 17-Nov-2023
PMCID:PMC10672221
doi:10.3390/jof9111111
PMID:37998916
Evaluation of the hydroalcoholic extract of Clarisia racemosa as an antiparasitic agent: an in vitro approach da Cruz Filho IJ, Duarte DM, Marques DS, da Rocha JV, Diniz EG, Brayner FA, Alves LC, de Azevedo Albuquerque MC, de Lima Aires A, Nogueira F, de Lima MD 3 Biotech 09-Nov-2023
PMCID:PMC10635994
doi:10.1007/s13205-023-03799-2
PMID:37953832

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
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
Anthraquinone-2-carboxylic acid 67030 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C=C3)C(=O)O 252.22 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
1-Hydroxyanthraquinone 8512 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=CC=C3)O 224.21 unknown via CMAUP database
1-Methoxy-9,10-anthracenedione 6707 Click to see COC1=CC=CC2=C1C(=O)C3=CC=CC=C3C2=O 238.24 unknown via CMAUP database
2-(Hydroxymethyl)anthraquinone 87014 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C=C3)CO 238.24 unknown via CMAUP database
2-Methylanthraquinone 6773 Click to see CC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O 222.24 unknown via CMAUP database
9,10-Dioxo-9,10-dihydroanthracene-2-carbaldehyde 344310 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C=C3)C=O 236.22 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
2-Hydroxy-3-methylanthraquinone 10889963 Click to see CC1=CC2=C(C=C1O)C(=O)C3=CC=CC=C3C2=O 238.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
(S)-6,8-Dihydroxy-3-methyl-3,4-dihydroisocoumarin 14353462 Click to see CC1CC2=C(C(=CC(=C2)O)O)C(=O)O1 194.18 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,4,5-Trimethoxybenzoic Acid 8357 Click to see COC1=CC(=CC(=C1OC)OC)C(=O)O 212.20 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 via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
[(3S,4R,5R)-3,4,5-trihydroxyoxolan-3-yl]methyl 3,4-dimethoxybenzoate 71539185 Click to see COC1=C(C=C(C=C1)C(=O)OCC2(COC(C2O)O)O)OC 314.29 unknown via CMAUP database
[(3S,4R,5R)-3,4,5-trihydroxyoxolan-3-yl]methyl 4-methoxybenzoate 71539186 Click to see COC1=CC=C(C=C1)C(=O)OCC2(COC(C2O)O)O 284.26 unknown via CMAUP database
3,4-Dimethoxybenzoic acid 7121 Click to see COC1=C(C=C(C=C1)C(=O)O)OC 182.17 unknown via CMAUP database
p-Anisic acid 7478 Click to see COC1=CC=C(C=C1)C(=O)O 152.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see C1=CC=C(C(=C1)C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
[(3S,4R,5R)-3,4,5-trihydroxyoxolan-3-yl]methyl 3,4-dihydroxybenzoate 71539188 Click to see C1C(C(C(O1)O)O)(COC(=O)C2=CC(=C(C=C2)O)O)O 286.23 unknown via CMAUP database
[(3S,4R,5R)-3,4,5-trihydroxyoxolan-3-yl]methyl 4-hydroxybenzoate 71539187 Click to see C1C(C(C(O1)O)O)(COC(=O)C2=CC=C(C=C2)O)O 270.23 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
p-Anisaldehyde 31244 Click to see COC1=CC=C(C=C1)C=O 136.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Veratraldehyde 8419 Click to see COC1=C(C=C(C=C1)C=O)OC 166.17 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Epipinoresinol 12309639 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
(-)-Pinoresinol 12309636 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
1alpha-(1,3-Benzodioxole-5-yl)-3aalpha-hydroxy-4alpha-(3-methoxy-4-hydroxyphenyl)-3aalpha,4,6,6aalpha-tetrahydro-1H,3H-furo[3,4-c]furan 102501953 Click to see COC1=C(C=CC(=C1)C2C3(COC(C3CO2)C4=CC5=C(C=C4)OCO5)O)O 372.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
4-Hydroxybenzoic acid (1S,4aalpha,7aalpha)-1beta,3alpha-dimethoxy-7alpha-hydroxy-7-methyloctahydrocyclopenta[c]pyran-5alpha-yl ester 11462293 Click to see CC1(CC(C2C1C(OC(C2)OC)OC)OC(=O)C3=CC=C(C=C3)O)O 352.40 unknown via CMAUP database
4-Hydroxybenzoic acid (1S,4aalpha,7aalpha)-1beta,3beta-dimethoxy-7alpha-hydroxy-7-methyloctahydrocyclopenta[c]pyran-5alpha-yl ester 11405465 Click to see CC1(CC(C2C1C(OC(C2)OC)OC)OC(=O)C3=CC=C(C=C3)O)O 352.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin K compounds
Deoxylapachol 97448 Click to see CC(=CCC1=CC(=O)C2=CC=CC=C2C1=O)C 226.27 unknown via CMAUP database
Lepachol acetate 276204 Click to see CC1=C(C(=O)C2=CC=CC=C2C1=O)CC=C(C)C 240.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[(1S,4aR,5R,7S,7aS)-7-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-5-yl] 4-hydroxybenzoate 14396661 Click to see CC1(CC(C2C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C4=CC=C(C=C4)O)O 468.40 unknown via CMAUP database
6-o-(4-Methoxybenzoyl)ajugol 11477204 Click to see CC1(CC(C2C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C4=CC=C(C=C4)OC)O 482.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[(3S,4R,5R)-3,4-dihydroxy-5-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy]oxolan-3-yl]methyl 4-methoxybenzoate 21579201 Click to see COC1=CC=C(C=C1)C(=O)OCC2(COC(C2O)OCC3C(C(C(C(O3)OCCC4=CC=C(C=C4)O)O)O)O)O 566.50 unknown via CMAUP database
4-Hydroxyphenethyl 6-O-[5-O-(4-hydroxybenzoyl)-D-apio-beta-D-furanosyl]-beta-D-glucopyranoside 11192111 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC=C(C=C3)O)O)O)O)O)(COC(=O)C4=CC=C(C=C4)O)O 552.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(3S,4R,5R)-3,4-dihydroxy-5-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(3,4,5-trimethoxyphenoxy)oxan-2-yl]methoxy]oxolan-3-yl]methyl 4-methoxybenzoate 21579206 Click to see COC1=CC=C(C=C1)C(=O)OCC2(COC(C2O)OCC3C(C(C(C(O3)OC4=CC(=C(C(=C4)OC)OC)OC)O)O)O)O 612.60 unknown via CMAUP database
[(3S,4R,5R)-5-[[(2R,3S,4S,5R,6S)-6-(3,4-dimethoxyphenoxy)-3,4,5-trihydroxyoxan-2-yl]methoxy]-3,4-dihydroxyoxolan-3-yl]methyl 4-hydroxybenzoate 21579205 Click to see COC1=C(C=C(C=C1)OC2C(C(C(C(O2)COC3C(C(CO3)(COC(=O)C4=CC=C(C=C4)O)O)O)O)O)O)OC 568.50 unknown via CMAUP database
[(3S,4R,5R)-5-[[(2R,3S,4S,5R,6S)-6-(3,4-dimethoxyphenoxy)-3,4,5-trihydroxyoxan-2-yl]methoxy]-3,4-dihydroxyoxolan-3-yl]methyl 4-methoxybenzoate 21579203 Click to see COC1=CC=C(C=C1)C(=O)OCC2(COC(C2O)OCC3C(C(C(C(O3)OC4=CC(=C(C=C4)OC)OC)O)O)O)O 582.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Benzofuran-6-carbaldehyde 14354086 Click to see C1=CC(=CC2=C1C=CO2)C=O 146.14 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
(2R)-2,3-Dihydro-2-(1-methylethenyl)-5-hydroxynaphtho[2,3-b]furan-4,9-dione 101671142 Click to see CC(=C)C1CC2=C(O1)C(=O)C3=C(C2=O)C(=CC=C3)O 256.25 unknown via CMAUP database
(2R)-2,3-Dihydro-2-(1-methylethenyl)naphtho[2,3-b]furan-4,9-dione 101671141 Click to see CC(=C)C1CC2=C(O1)C(=O)C3=CC=CC=C3C2=O 240.25 unknown via CMAUP database
2-Acetyl-5-hydroxynaphtho[2,3-b]furan-4,9-dione 10015259 Click to see CC(=O)C1=CC2=C(O1)C(=O)C3=C(C2=O)C(=CC=C3)O 256.21 unknown via CMAUP database
5-Hydroxy-2-(1-Hydroxyethyl)Naphtho(2,3-B)Furan-4,9-Dione 147719 Click to see CC(C1=CC2=C(O1)C(=O)C3=C(C2=O)C(=CC=C3)O)O 258.23 unknown via CMAUP database
5-Hydroxy-2-(1'-hydroxyethyl)naphtho[2,3-b]furan-4,9-dione 14159819 Click to see CC(C1=CC2=C(O1)C(=O)C3=C(C2=O)C(=CC=C3)O)O 258.23 unknown via CMAUP database
5-Hydroxy-2-[(R)-1-hydroxyethyl]naphtho[2,3-b]furan-4,9-dione 14159818 Click to see CC(C1=CC2=C(O1)C(=O)C3=C(C2=O)C(=CC=C3)O)O 258.23 unknown via CMAUP database
Kigelinone 442752 Click to see CC(C1=CC2=C(O1)C(=O)C3=C(C2=O)C=CC=C3O)O 258.23 unknown via CMAUP database
Napabucasin 10331844 Click to see CC(=O)C1=CC2=C(O1)C(=O)C3=CC=CC=C3C2=O 240.21 unknown via CMAUP database
Naphtho[2,3-b]furan-4,9-dione, 2-acetyl-8-hydroxy- 9881541 Click to see CC(=O)C1=CC2=C(O1)C(=O)C3=C(C2=O)C=CC=C3O 256.21 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
alpha-Lapachone 72732 Click to see CC1(CCC2=C(O1)C(=O)C3=CC=CC=C3C2=O)C 242.27 unknown via CMAUP database
beta-Lapachone 3885 Click to see CC1(CCC2=C(O1)C3=CC=CC=C3C(=O)C2=O)C 242.27 unknown via CMAUP database
Xyloidone 72734 Click to see CC1(C=CC2=C(O1)C(=O)C3=CC=CC=C3C2=O)C 240.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(E)-3-[(2R,3S)-2-(3,4-dimethoxyphenyl)-7-hydroxy-3-(hydroxymethyl)-2,3-dihydro-1-benzofuran-5-yl]prop-2-enoic acid 71539184 Click to see COC1=C(C=C(C=C1)C2C(C3=C(O2)C(=CC(=C3)C=CC(=O)O)O)CO)OC 372.40 unknown via CMAUP database
Balanophonin 21582569 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O 356.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(1S,4aR,5R,7S,7aS)-7-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-5-yl] 3,4-dimethoxybenzoate 23900071 Click to see CC1(CC(C2C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C4=CC(=C(C=C4)OC)OC)O 512.50 unknown via CMAUP database
[(3S,4R,5R)-3,4-dihydroxy-5-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy]oxolan-3-yl]methyl 3,4-dimethoxybenzoate 21579200 Click to see COC1=C(C=C(C=C1)C(=O)OCC2(COC(C2O)OCC3C(C(C(C(O3)OCCC4=CC=C(C=C4)O)O)O)O)O)OC 596.60 unknown via CMAUP database
3,4-Dimethoxyphenyl 6-O-[5-O-(3,4-dimethoxybenzoyl)-D-apio-beta-D-furanosyl]-beta-D-glucopyranoside 21579204 Click to see COC1=C(C=C(C=C1)C(=O)OCC2(COC(C2O)OCC3C(C(C(C(O3)OC4=CC(=C(C=C4)OC)OC)O)O)O)O)OC 612.60 unknown via CMAUP database

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