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Cheiloclinium cognatum

Cheiloclinium cognatum - 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 UUID644010b9a9de8345518981
Scientific name Cheiloclinium cognatum
Authority (Miers) A.C.Sm.
First published in Brittonia 3: 529 (1940)

Description Top

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Synonyms Top

Scientific name Authority First published in
Kippistia cognata Miers Trans. Linn. Soc. London 28(2): 417. 1872 [after 17 May 1872, possibly 8 Jun]
Salacia sphaerocarpa Rusby Descr. S. Amer. Pl. : 52 (1920)
Salacia cognata Peyr. Fl. Bras. 11(1): 144 (1878)
Salacia lineolata A.C.Sm. Bull. Torrey Bot. Club 66: 234 (1939)
Cheiloclinium lineolatum A.C.Sm. Brittonia 3: 533 (1940)
Elaeodendron macrophyllum Rusby Descr. S. Amer. Pl. : 24 (1920)
Salacia cognata var. egensis Peyr. Fl. Bras. (Martius) 11(1): 144. 1878 [1 Feb 1878]

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

Area

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© OpenStreetMap
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Trinidad-Tobago
    • Central America
      • Costa Rica
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000600072
Tropicos 15600252
INPN 733417
KEW urn:lsid:ipni.org:names:55844-2
The Plant List kew-2716141
Open Tree Of Life 583081
NCBI Taxonomy 123388
IUCN Red List 61988238
IPNI 55844-2
iNaturalist 700672
GBIF 3790743
EOL 5226555
USDA GRIN 438829

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
Salvadoran Celastraceae Species as a Source of Antikinetoplastid Quinonemethide Triterpenoids Núñez MJ, Martínez ML, Castillo UG, Flores KC, Menjívar J, López-Arencibia A, Bethencourt-Estrella CJ, Jiménez IA, Piñero JE, Lorenzo-Morales J, Bazzocchi IL Plants (Basel) 25-Jan-2024
PMCID:PMC10857229
doi:10.3390/plants13030360
PMID:38337893
Hepatoprotective Effects of Four Brazilian Savanna Species on Acetaminophen-Induced Hepatotoxicity in HepG2 Cells Ribeiro GD, Martins DH, Gomes JV, Davies NW, Fagg CW, Simeoni LA, Homem-de-Mello M, Magalhães PO, Silveira D, Fonseca-Bazzo YM Plants (Basel) 26-Sep-2023
PMCID:PMC10574628
doi:10.3390/plants12193393
PMID:37836133
Toxic Potential of Cerrado Plants on Different Organisms Rocha JD, Carneiro FM, Fernandes AS, Morais JM, Borges LL, Chen-Chen L, de Almeida LM, Bailão EF Int J Mol Sci 22-Mar-2022
PMCID:PMC8998518
doi:10.3390/ijms23073413
PMID:35408775
In Vitro Production and Exudation of 20-Hydroxymaytenin from Gymnosporia heterophylla (Eckl. and Zeyh.) Loes. Cell Culture Pitakbut T, Spiteller M, Kayser O Plants (Basel) 21-Jul-2021
PMCID:PMC8398937
doi:10.3390/plants10081493
PMID:34451538
Edible Fruit Plant Species in the Amazon Forest Rely Mostly on Bees and Beetles as Pollinators Paz FS, Pinto CE, de Brito RM, Imperatriz-Fonseca VL, Giannini TC J Econ Entomol 13-Jan-2021
PMCID:PMC8042744
doi:10.1093/jee/toaa284
PMID:33440000
Cytotoxic Triterpenes from Salacia crassifolia and Metabolite Profiling of Celastraceae Species Espindola LS, Dusi RG, Demarque DP, Braz-Filho R, Yan P, Bokesch HR, Gustafson KR, Beutler JA Molecules 20-Jun-2018
PMCID:PMC6099938
doi:10.3390/molecules23061494
PMID:29925807
Remnant Trees Affect Species Composition but Not Structure of Tropical Second-Growth Forest Sandor ME, Chazdon RL PLoS One 13-Jan-2014
PMCID:PMC3890367
doi:10.1371/journal.pone.0083284
PMID:24454700
Database Survey of Anti-Inflammatory Plants in South America: A Review de Morais Lima GR, de Albuquerque Montenegro C, de Almeida CL, de Athayde-Filho PF, Barbosa-Filho JM, Batista LM Int J Mol Sci 21-Apr-2011
PMCID:PMC3127143
doi:10.3390/ijms12042692
PMID:21731467
Plant-derived triterpenoids and analogues as antitumor and anti-HIV agents Kuo RY, Qian K, Morris-Natschke SL, Lee KH Nat Prod Rep 13-Aug-2009
PMCID:PMC3773821
doi:10.1039/b810774m
PMID:19779642
Antioxidant phenolic and quinonemethide triterpenes from Cheiloclinium cognatum. Jeller AH, Silva DH, Lião LM, Bolzani Vda S, Furlan M Phytochemistry 01-Jul-2004
doi:10.1016/J.PHYTOCHEM.2004.03.039
PMID:15280004

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 / Phenanthrenes and derivatives
Cognatine 10392007 Click to see CC1=C2C3=CC(=O)C4=C(C(=C(C=C4C3(CCC2(C5CC(C(C(=O)C5(C1)C)O)(C)C(=O)OC)C)C)O)OC)C 522.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
Methyl 3,11-dihydroxy-10-methoxy-2,4a,6,6a,9,14a-hexamethyl-4,8-dioxo-1,3,5,13,14,14b-hexahydropicene-2-carboxylate 85130078 Click to see CC1=C2C3=CC(=O)C4=C(C(=C(C=C4C3(CCC2(C5CC(C(C(=O)C5(C1)C)O)(C)C(=O)OC)C)C)O)OC)C 522.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
24-Nor-D:A-friedooleana-1(10),5,7-tetraen-29-oic acid, 3-hydroxy-2-oxo-, methyl ester 264268 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O 464.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
methyl (2S,4R,4aR,6aR,14aS,14bS)-4,10-dihydroxy-2,4,4a,6a,6a,9,14a-heptamethyl-11-oxo-3,5,6,13,14,14b-hexahydro-1H-picene-2-carboxylate 163193556 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5(C)O)(C)C(=O)OC)C)C)C)C)O 494.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
methyl (2S,4R,4aR,6aR,6aS,14aS,14bS)-4,10-dihydroxy-2,4,4a,6a,6a,9,14a-heptamethyl-11-oxo-3,5,6,13,14,14b-hexahydro-1H-picene-2-carboxylate 162820546 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5(C)O)(C)C(=O)OC)C)C)C)C)O 494.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
methyl (2S,4R,4aR,6aR,6aS,14aS,14bS)-4,10-dihydroxy-2,4a,6a,6a,9,14a-hexamethyl-11-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylate 12149320 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5O)(C)C(=O)OC)C)C)C)C)O 480.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
methyl 4,10-dihydroxy-2,4,4a,6a,6a,9,14a-heptamethyl-11-oxo-3,5,6,13,14,14b-hexahydro-1H-picene-2-carboxylate 162820544 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5(C)O)(C)C(=O)OC)C)C)C)C)O 494.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
Methyl 4,10-dihydroxy-2,4a,6a,6a,9,14a-hexamethyl-11-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylate 85435550 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5O)(C)C(=O)OC)C)C)C)C)O 480.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
Pristimerin 159516 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O 464.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids
dimethyl (2S,3S,4aR,6aS,14aS,14bS)-3,10-dihydroxy-2,6,6a,9,14a-pentamethyl-11-oxo-3,4,5,13,14,14b-hexahydro-1H-picene-2,4a-dicarboxylate 21636469 Click to see CC1=C2C3=CC=C4C(=C(C(=O)C=C4C3(CCC2(C5CC(C(CC5(C1)C(=O)OC)O)(C)C(=O)OC)C)C)O)C 522.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
methyl (2R,3S,4aR,6aR,14aR,14bS)-3,10-dihydroxy-2,4a,6,6a,9,14a-hexamethyl-4,11-dioxo-1,3,5,13,14,14b-hexahydropicene-2-carboxylate 163012528 Click to see CC1=C2C3=CC=C4C(=C(C(=O)C=C4C3(CCC2(C5CC(C(C(=O)C5(C1)C)O)(C)C(=O)OC)C)C)O)C 492.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
methyl (2S,3R,4S,4aR,14aS,14bS)-3,4,10-trihydroxy-2,4a,6,6a,9,14a-hexamethyl-11-oxo-3,4,5,13,14,14b-hexahydro-1H-picene-2-carboxylate 163186381 Click to see CC1=C2C3=CC=C4C(=C(C(=O)C=C4C3(CCC2(C5CC(C(C(C5(C1)C)O)O)(C)C(=O)OC)C)C)O)C 494.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
methyl (2S,3S,6aS,14aS,14bR)-3,10-dihydroxy-2,4a,6,6a,9,14a-hexamethyl-11-oxo-3,4,5,13,14,14b-hexahydro-1H-picene-2-carboxylate 163188955 Click to see CC1=C2C3=CC=C4C(=C(C(=O)C=C4C3(CCC2(C5CC(C(CC5(C1)C)O)(C)C(=O)OC)C)C)O)C 478.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
methyl (3R,4S,4aR,6aS,14aS,14bS)-3,4,10-trihydroxy-2,4a,6,6a,9,14a-hexamethyl-11-oxo-3,4,5,13,14,14b-hexahydro-1H-picene-2-carboxylate 163189681 Click to see CC1=C2C3=CC=C4C(=C(C(=O)C=C4C3(CCC2(C5CC(C(C(C5(C1)C)O)O)(C)C(=O)OC)C)C)O)C 494.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
Methyl 3,10-dihydroxy-2,4a,6,9,12b,14a-hexamethyl-11-oxo-1,2,3,4,4a,5,11,12b,13,14,14a,14b-dodecahydropicene-2-carboxylate 188774 Click to see CC1=C2C3=CC=C4C(=C(C(=O)C=C4C3(CCC2(C5CC(C(CC5(C1)C)O)(C)C(=O)OC)C)C)O)C 478.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
Methyl 3,4,10-trihydroxy-2,4a,6,9,12b,14a-hexamethyl-11-oxo-1,2,3,4,4a,5,11,12b,13,14,14a,14b-dodecahydropicene-2-carboxylate 188775 Click to see CC1=C2C3=CC=C4C(=C(C(=O)C=C4C3(CCC2(C5CC(C(C(C5(C1)C)O)O)(C)C(=O)OC)C)C)O)C 494.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
Netzahualcoyondiol 21579198 Click to see CC1=C2C3=CC=C4C(=C(C(=O)C=C4C3(CCC2(C5CC(C(C(C5(C1)C)O)O)(C)C(=O)OC)C)C)O)C 494.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
Netzahualcoyone 163547 Click to see CC1=C2C3=CC=C4C(=C(C(=O)C=C4C3(CCC2(C5CC(C(C(=O)C5(C1)C)O)(C)C(=O)OC)C)C)O)C 492.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
Netzahualcoyonol 21579197 Click to see CC1=C2C3=CC=C4C(=C(C(=O)C=C4C3(CCC2(C5CC(C(CC5(C1)C)O)(C)C(=O)OC)C)C)O)C 478.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
3,9-Dihydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione 500289 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(C(C1=O)O)C 436.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
20alpha-Hydroxytingenone 10717799 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(C(=O)C5)(C)O)C)C)C)C)O 436.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
3,11-dihydroxy-4,6a,6b,8a,11,14a-hexamethyl-8,9,12,12a,13,14-hexahydro-7H-picene-2,10-dione 14241138 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(C(=O)C5)(C)O)C)C)C)C)O 436.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(6aR,6bR,8aS,11R,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione 441687 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C 420.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
3-Hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione 3527193 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C 420.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039
Tingenone 101520 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C 420.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.039

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