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Fridericia triplinervia

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440279a270ba340187099
Scientific name Fridericia triplinervia
Authority (Mart. ex DC.) L.G.Lohmann
First published in Ann. Missouri Bot. Gard. 99: 446 (2014)

Description Top

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Synonyms Top

Scientific name Authority First published in
Arrabidaea triplinervia var. brachycalix Hassl. Bull. Herb. Boissier 6(App. 1): 26 (1898)
Petastoma triplinerve Miers Proc. Roy. Hort. Soc. iii. (1863) 195.
Saritaea triplinervia (Mart. ex DC.) Dugand Caldasia 3: 266 (1945)
Arrabidaea ateramnantha Bureau & K.Schum. Fl. Bras. 8(2): 68 (1896)
Arrabidaea triplinervia Baill. Hist. Pl. 10: 28 (1888)
Bignonia triplinervia Mart. ex DC. Prodr. 9: 153 (1845)

Common names Top

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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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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
      • Paraguay
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000782570
Tropicos 100193272
INPN 886187
KEW urn:lsid:ipni.org:names:77142081-1
The Plant List kew-321054
Open Tree Of Life 946244
NCBI Taxonomy 353957
IPNI 77142081-1
iNaturalist 909530
GBIF 7418332
CMAUP NPO17822

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
A Review of the Phytochemistry and Pharmacological Properties of the Genus Arrabidaea do Nascimento JR, de Jesus Alves Miranda A, Vieira FC, Rodrigues CD, Vasconcelos LN, Filho JL, Lopes AC, Tangerina MM, Vilegas W, da Rocha CQ Pharmaceuticals (Basel) 25-May-2022
PMCID:PMC9227117
doi:10.3390/ph15060658
PMID:35745577
Trichome structure and evolution in Neotropical lianas Nogueira A, El Ottra JH, Guimarães E, Machado SR, Lohmann LG Ann Bot 29-Sep-2013
PMCID:PMC3806532
doi:10.1093/aob/mct201
PMID:24081281
Current and developing therapeutic agents in the treatment of Chagas disease Apt W Drug Des Devel Ther 24-Sep-2010
PMCID:PMC2948934
doi:10.2147/dddt.s8338
PMID:20957215
Trypanocidal activity of triterpenes from Arrabidaea triplinervia and derivatives. Leite JP, Oliveira AB, Lombardi JA, Filho JD, Chiari E Biol Pharm Bull 01-Nov-2006
doi:10.1248/BPB.29.2307
PMID:17077535
Secretory Trichomes, a Substitutive Floral Nectar Source in Lundia A. DC. (Bignoniaceae), a Genus Lacking a Functional Disc LOPES AV, VOGEL S, MACHADO IC Ann Bot 01-Aug-2002
PMCID:PMC4240414
doi:10.1093/aob/mcf169
PMID:12197514

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
> Benzenoids / Anthracenes
(10S)-10-[(9R)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-1,3,8-trihydroxy-6-methyl-10H-anthracen-9-one 44567184 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C5=C(C(=CC(=C5)C)O)C(=O)C6=C4C=C(C=C6O)O)C=CC=C3O 494.50 unknown via CMAUP database
(inverted exclamation markA)-Emodin bianthrone 12096290 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C5=C(C(=CC(=C5)C)O)C(=O)C6=C4C=C(C=C6O)O)C=C(C=C3O)O 510.50 unknown via CMAUP database
Chrysophanol-9-anthrone 68111 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2)C=CC=C3O 240.25 unknown via CMAUP database
Emodin anthrone 122635 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2)C=C(C=C3O)O 256.25 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
Aloe emodin 10207 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)CO 270.24 unknown via CMAUP database
Chrysophanic acid 10208 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 254.24 unknown via CMAUP database
Physcione 10639 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC 284.26 unknown via CMAUP database
Rheochrysin 168938 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)OC 446.40 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1248/BPB.29.2307
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1248/BPB.29.2307
CID 3838010 3838010 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown https://doi.org/10.1248/BPB.29.2307
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1248/BPB.29.2307
Pomolic acid 382831 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown https://doi.org/10.1248/BPB.29.2307
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1248/BPB.29.2307
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Cascaroside A 442727 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2C5C(C(C(C(O5)CO)O)O)O)C=C(C=C4O)CO 580.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
7-Hydroxy-5-methoxy-2-phenylchroman-4-one 4053302 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1248/BPB.29.2307
Alpinetin 154279 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1248/BPB.29.2307

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