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Cassia leptophylla

Cassia leptophylla - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fd75206006700904208
Scientific name Cassia leptophylla
Authority Vogel
First published in Gen. Cass. Syn.: 13 (1837)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English gold medallion tree
Portuguese falso-barbatimão
Chinese 薄叶腊肠树

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000174025
USDA Plants CALE49
Tropicos 13028187
KEW urn:lsid:ipni.org:names:484754-1
The Plant List ild-20144
Missouri Botanical Garden 280438
Open Tree Of Life 3916836
NCBI Taxonomy 1933599
IUCN Red List 149205559
IPNI 484754-1
iNaturalist 335464
GBIF 5357169
EOL 640224
USDA GRIN 9354
Wikipedia Cassia_leptophylla

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
From Plant to Chemistry: Sources of Antinociceptive Non-Opioid Active Principles for Medicinal Chemistry and Drug Design Turnaturi R, Piana S, Spoto S, Costanzo G, Reina L, Pasquinucci L, Parenti C Molecules 09-Feb-2024
PMCID:PMC10892999
doi:10.3390/molecules29040815
PMID:38398566
Chemical Profiles and In Vitro Cholinesterase Inhibitory Activities of the Flower Extracts of Cassia spectabilis Suciati, Laili ER, Ekasari W, Kuatman, Nuengchamnong N, Suphrom N Adv Pharmacol Pharm Sci 28-Feb-2023
PMCID:PMC9991480
doi:10.1155/2023/6066601
PMID:36895696
Identification of the initial water-site and movement in Gleditsia sinensis seeds and its relation to seed coat structure Zhu M, Dai S, Ma Q, Li S Plant Methods 25-May-2021
PMCID:PMC8147069
doi:10.1186/s13007-021-00756-z
PMID:34034763
The Development of a Plant Risk Evaluation (PRE) Tool for Assessing the Invasive Potential of Ornamental Plants Conser C, Seebacher L, Fujino DW, Reichard S, DiTomaso JM PLoS One 24-Mar-2015
PMCID:PMC4372384
doi:10.1371/journal.pone.0121053
PMID:25803830
Thematic Review Series: Sphingolipids. Biodiversity of sphingoid bases (“sphingosines”) and related amino alcohols Pruett ST, Bushnev A, Hagedorn K, Adiga M, Haynes CA, Sullards MC, Liotta DC, Merrill AH Jr J Lipid Res 01-Aug-2008
PMCID:PMC2444003
doi:10.1194/jlr.R800012-JLR200
PMID:18499644
Further bioactive piperidine alkaloids from the flowers and green fruits of Cassia spectabilis. Viegas C Jr, da S Bolzani V, Furlan M, Barreiro EJ, Young MC, Tomazela D, Eberlin MN J Nat Prod 01-May-2004
doi:10.1021/NP0303963
PMID:15165164
Bioactive and other piperidine alkaloids from Cassia leptophylla Vanderlan da S. Bolzani, A.A. Leslie Gunatilaka, David G.I. Kingston Elsevier BV 30-Apr-2003
doi:10.1016/0040-4020(95)00254-6

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
> Alkaloids and derivatives
(-)-Spectaline 10019240 Click to see CC1C(CCC(N1)CCCCCCCCCCCCC(=O)C)O 325.50 unknown https://doi.org/10.1016/0040-4020(95)00254-6
(2R,3R,6R)-6-(11-hydroxydodecyl)-2-methylpiperidin-3-ol 12302474 Click to see CC1C(CCC(N1)CCCCCCCCCCC(C)O)O 299.50 unknown https://doi.org/10.1016/0040-4020(95)00254-6
(2R,3R,6R)-6-[(11S)-11-hydroxydodecyl]-2-methylpiperidin-3-ol 162986877 Click to see CC1C(CCC(N1)CCCCCCCCCCC(C)O)O 299.50 unknown https://doi.org/10.1016/0040-4020(95)00254-6
(2R,3R,6S)-6-(11-hydroxydodecyl)-2-methylpiperidin-3-ol 12302473 Click to see CC1C(CCC(N1)CCCCCCCCCCC(C)O)O 299.50 unknown https://doi.org/10.1016/0040-4020(95)00254-6
(2R,3R,6S)-6-[(11S)-11-hydroxydodecyl]-2-methylpiperidin-3-ol 101709556 Click to see CC1C(CCC(N1)CCCCCCCCCCC(C)O)O 299.50 unknown https://doi.org/10.1016/0040-4020(95)00254-6
(2R,3R,6S)-6-[(13S)-13-hydroxytetradecyl]-2-methylpiperidin-3-ol 162923182 Click to see CC1C(CCC(N1)CCCCCCCCCCCCC(C)O)O 327.50 unknown https://doi.org/10.1016/0040-4020(95)00254-6
(2S,3S,6R)-6-(11-hydroxydodecyl)-2-methylpiperidin-3-ol 10447484 Click to see CC1C(CCC(N1)CCCCCCCCCCC(C)O)O 299.50 unknown https://doi.org/10.1016/0040-4020(95)00254-6
(2S,3S,6R)-6-(13-hydroxytetradecyl)-2-methylpiperidin-3-ol 10314388 Click to see CC1C(CCC(N1)CCCCCCCCCCCCC(C)O)O 327.50 unknown https://doi.org/10.1016/0040-4020(95)00254-6
(2S)-12-[(2R,5S,6S)-5-hydroxy-6-methylpiperidin-2-yl]dodecane-1,2-diol 162844990 Click to see CC1C(CCC(N1)CCCCCCCCCCC(CO)O)O 315.50 unknown https://doi.org/10.1016/0040-4020(95)00254-6
[(2S,3S,6R)-6-(11,12-dihydroxydodecyl)-2-methylpiperidin-3-yl] acetate 15287169 Click to see CC1C(CCC(N1)CCCCCCCCCCC(CO)O)OC(=O)C 357.50 unknown https://doi.org/10.1016/0040-4020(95)00254-6
[6-(11,12-Dihydroxydodecyl)-2-methylpiperidin-3-yl] acetate 73190965 Click to see CC1C(CCC(N1)CCCCCCCCCCC(CO)O)OC(=O)C 357.50 unknown https://doi.org/10.1016/0040-4020(95)00254-6
12-(5-Hydroxy-6-methylpiperidin-2-yl)dodecane-1,2-diol 73190964 Click to see CC1C(CCC(N1)CCCCCCCCCCC(CO)O)O 315.50 unknown https://doi.org/10.1016/0040-4020(95)00254-6
12-[(2R,5S,6S)-5-hydroxy-6-methylpiperidin-2-yl]dodecane-1,2-diol 15287168 Click to see CC1C(CCC(N1)CCCCCCCCCCC(CO)O)O 315.50 unknown https://doi.org/10.1016/0040-4020(95)00254-6
14-(5-Hydroxy-6-methyl-2-piperidinyl)-2-tetradecanone 14312868 Click to see CC1C(CCC(N1)CCCCCCCCCCCCC(=O)C)O 325.50 unknown https://doi.org/10.1021/NP0303963
https://doi.org/10.1016/0040-4020(95)00254-6
6-(11-Hydroxydodecyl)-2-methylpiperidin-3-ol 12302472 Click to see CC1C(CCC(N1)CCCCCCCCCCC(C)O)O 299.50 unknown https://doi.org/10.1016/0040-4020(95)00254-6
6-(13-Hydroxytetradecyl)-2-methyl-3-piperidinol 73190963 Click to see CC1C(CCC(N1)CCCCCCCCCCCCC(C)O)O 327.50 unknown https://doi.org/10.1016/0040-4020(95)00254-6
Spectaline 10404073 Click to see CC1C(CCC(N1)CCCCCCCCCCCCC(=O)C)O 325.50 unknown https://doi.org/10.1016/0040-4020(95)00254-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
11-(5-Hydroxy-6-methylpiperidin-2-yl)undecanoic acid 85145794 Click to see CC1C(CCC(N1)CCCCCCCCCCC(=O)O)O 299.40 unknown https://doi.org/10.1016/0040-4020(95)00254-6
2-Piperidineundecanoicacid, 5-hydroxy-6-methyl-, (2R,5R,6R)- 10447482 Click to see CC1C(CCC(N1)CCCCCCCCCCC(=O)O)O 299.40 unknown https://doi.org/10.1016/0040-4020(95)00254-6

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