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Tovaria pendula

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ff90511a5f301413209
Scientific name Tovaria pendula
Authority Ruiz & Pav.
First published in Syst. Veg. Fl. Peruv. Chil. : 85 (1798)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Bancroftia pendula (Ruiz & Pav.) Kuntze Revis. Gen. Pl. 1: 37 (1891)

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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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 Southeast
      • Mexico Southwest
  • Southern America
    • Central America
      • Belize
      • Costa Rica
      • Guatemala
      • Honduras
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000406860
Tropicos 32300001
KEW urn:lsid:ipni.org:names:148152-1
The Plant List kew-2431268
Open Tree Of Life 125843
NCBI Taxonomy 28547
IPNI 148152-1
iNaturalist 291727
GBIF 5377847
EPPO TOVPE
USDA GRIN 36778

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
The vessel wall thickness–vessel diameter relationship across woody angiosperms Echeverría A, Petrone‐Mendoza E, Segovia‐Rivas A, Figueroa‐Abundiz VA, Olson ME Am J Bot 12-Jun-2022
PMCID:PMC9328290
doi:10.1002/ajb2.1854
PMID:35435252
Nested whole-genome duplications coincide with diversification and high morphological disparity in Brassicaceae Walden N, German DA, Wolf EM, Kiefer M, Rigault P, Huang XC, Kiefer C, Schmickl R, Franzke A, Neuffer B, Mummenhoff K, Koch MA Nat Commun 30-Jul-2020
PMCID:PMC7393125
doi:10.1038/s41467-020-17605-7
PMID:32732942
A Universal Probe Set for Targeted Sequencing of 353 Nuclear Genes from Any Flowering Plant Designed Using k-Medoids Clustering Johnson MG, Pokorny L, Dodsworth S, Botigué LR, Cowan RS, Devault A, Eiserhardt WL, Epitawalage N, Forest F, Kim JT, Leebens-Mack JH, Leitch IJ, Maurin O, Soltis DE, Soltis PS, Wong GK, Baker WJ, Wickett NJ Syst Biol 10-Dec-2018
PMCID:PMC6568016
doi:10.1093/sysbio/syy086
PMID:30535394
<sup>1</sup>-acetyl-S-indolylmethylglucosinolate in Seedlings of Tovaria pendula Ruiz et Pav. Helmut Schraudolf, Rolf Bäuerle Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1986-5-605
[Serotonin and indoleglucosinolate in Tovaria pendula]. Schraudolf H Naturwissenschaften 01-Jan-1970
doi:10.1007/BF00601073
PMID:5362720

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 / Triterpenoids
Ritterazine Q 44448219 Click to see 867.20 unknown https://doi.org/10.1515/ZNC-1986-5-605
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucosinolates / Alkylglucosinolates
[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1Z)-2-(1-methoxyindol-3-yl)-N-sulfooxyethanimidothioate 160231225 Click to see 478.50 unknown https://doi.org/10.1515/ZNC-1986-5-605
[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1Z)-2-(1H-indol-3-yl)-N-sulfooxyethanimidothioate 154496671 Click to see 448.50 unknown https://doi.org/10.1515/ZNC-1986-5-605
[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1Z)-2-(4-methoxy-1H-indol-3-yl)-N-sulfooxyethanimidothioate 158705152 Click to see COC1=CC=CC2=C1C(=CN2)CC(=NOS(=O)(=O)O)SC3C(C(C(C(O3)CO)O)O)O 478.50 unknown https://doi.org/10.1515/ZNC-1986-5-605
1-Methoxy-3-indolylmethyl glucosinolate 9576416 Click to see CON1C=C(C2=CC=CC=C21)CC(=NOS(=O)(=O)O)SC3C(C(C(C(O3)CO)O)O)O 478.50 unknown https://doi.org/10.1515/ZNC-1986-5-605
3-Indolylmethyl glucosinolate 6602378 Click to see C1=CC=C2C(=C1)C(=CN2)CC(=NOS(=O)(=O)O)SC3C(C(C(C(O3)CO)O)O)O 448.50 unknown https://doi.org/10.1515/ZNC-1986-5-605
4-Methoxy-3-indolylmethyl glucosinolate 9576738 Click to see 478.50 unknown https://doi.org/10.1515/ZNC-1986-5-605
4-Ohimg 9576741 Click to see 464.50 unknown https://doi.org/10.1515/ZNC-1986-5-605
Glucobrassicin 9601691 Click to see C1=CC=C2C(=C1)C(=CN2)CC(=NOS(=O)(=O)O)SC3C(C(C(C(O3)CO)O)O)O 448.50 unknown https://doi.org/10.1515/ZNC-1986-5-605
https://doi.org/10.1007/BF00601073
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives / Serotonins
Serotonin 5202 Click to see C1=CC2=C(C=C1O)C(=CN2)CCN 176.21 unknown https://doi.org/10.1515/ZNC-1986-5-605
https://doi.org/10.1007/BF00601073

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