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Cyclolepis genistoides

Cyclolepis genistoides - 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 UUID643fc91d762b6248815714
Scientific name Cyclolepis genistoides
Authority Gillies ex D.Don
First published in Philos. Mag. Ann. Chem. 11: 892. (1832)

Description Top

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Synonyms Top

Scientific name Authority First published in
Gochnatia genistoides Hook. & Arn. Companion Bot. Mag. 1: 109 (1835)

Common names Top

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Language Common/alternative name
Spanish matorro negro
Spanish palo azul
Spanish tupis
Spanish tusillo

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Argentina South
      • Paraguay

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000027853
Tropicos 2737544
KEW urn:lsid:ipni.org:names:200850-1
The Plant List gcc-126919
Open Tree Of Life 343690
NCBI Taxonomy 496609
IPNI 200850-1
iNaturalist 482060
GBIF 5386353
Freebase /m/080j27c
EOL 5112557
USDA GRIN 452880
Wikipedia Cyclolepis

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
Essential oil components of turmeric inhibit hepatic lipidification and liver fibrosis in a diet-induced NASH model rats Watanabe Y, Watanabe H, Kogure S, Tanioka Y, Yamauchi J, Furusho T Sci Rep 25-Nov-2023
PMCID:PMC10676378
doi:10.1038/s41598-023-47097-6
PMID:38007567
Medicinal plants used by rural communities in the arid zone of Viesca and Parras Coahuila in northeast Mexico Torres-León C, Rebolledo Ramírez F, Aguirre-Joya JA, Ramírez-Moreno A, Chávez-González ML, Aguillón-Gutierrez DR, Camacho-Guerra L, Ramírez-Guzmán N, Hernández Vélez S, Aguilar CN Saudi Pharm J 12-Nov-2022
PMCID:PMC9845112
doi:10.1016/j.jsps.2022.11.003
PMID:36685306
Pseudogenization of the chloroplast threonine (trnT-GGU) gene in the sunflower family (Asteraceae) Abdullah, Mehmood F, Heidari P, Rahim A, Ahmed I, Poczai P Sci Rep 26-Oct-2021
PMCID:PMC8548347
doi:10.1038/s41598-021-00510-4
PMID:34702873
Resistin: A journey from metabolism to cancer Deb A, Deshmukh B, Ramteke P, Bhati FK, Bhat MK Transl Oncol 20-Jul-2021
PMCID:PMC8319804
doi:10.1016/j.tranon.2021.101178
PMID:34293684
Arbuscular Mycorrhizal Fungal Communities in the Soils of Desert Habitats Vasar M, Davison J, Sepp SK, Öpik M, Moora M, Koorem K, Meng Y, Oja J, Akhmetzhanova AA, Al-Quraishy S, Onipchenko VG, Cantero JJ, Glassman SI, Hozzein WN, Zobel M Microorganisms 22-Jan-2021
PMCID:PMC7912695
doi:10.3390/microorganisms9020229
PMID:33499315
An Ethnobotanical Survey of Medicinal Plants Used in Papantla, Veracruz, Mexico Lara Reimers EA, C. EF, Lara Reimers DJ, Chaloupkova P, Zepeda del Valle JM, Milella L, Russo D Plants (Basel) 24-Jul-2019
PMCID:PMC6724097
doi:10.3390/plants8080246
PMID:31344952
Deacylcynaropicrin Inhibits RANKL-Induced Osteoclastogenesis by Inhibiting NF-κB and MAPK and Promoting M2 Polarization of Macrophages Li Z, Zhu X, Xu R, Wang Y, Hu R, Xu W Front Pharmacol 07-Jun-2019
PMCID:PMC6567936
doi:10.3389/fphar.2019.00599
PMID:31231214
Early evolution of the angiosperm clade Asteraceae in the Cretaceous of Antarctica Barreda VD, Palazzesi L, Tellería MC, Olivero EB, Raine JI, Forest F Proc Natl Acad Sci U S A 10-Aug-2015
PMCID:PMC4568267
doi:10.1073/pnas.1423653112
PMID:26261324
Antiprotozoal Activity against Entamoeba histolytica of Plants Used in Northeast Mexican Traditional Medicine. Bioactive Compounds from Lippia graveolens and Ruta chalepensis Quintanilla-Licea R, Mata-Cárdenas BD, Vargas-Villarreal J, Bazaldúa-Rodríguez AF, Ángeles-Hernández IK, Garza-González JN, Hernández-García ME Molecules 15-Dec-2014
PMCID:PMC6271573
doi:10.3390/molecules191221044
PMID:25517343
Movements of a juvenile Crowned Eagle (Harpyhaliaetus coronatus) tracked by satellite telemetry in central Argentina Urios V, Donat-Torres MP, Bechard M, Ferrer M J Biol Res (Thessalon) 01-Jul-2014
PMCID:PMC4389320
doi:10.1186/2241-5793-21-12
PMID:25984495
Triterpenes and sesquiterpene lactones from Cyclolepis genistoides Carola S. De Heluani, Margarita V. De Boggiato, César A.N. Catalán, Jesús G. Díaz, Thomas E. Gédris, Werner Herz Elsevier BV 04-Mar-2003
doi:10.1016/S0031-9422(97)00021-6

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 / Diterpenoids / Tigliane and ingenane diterpenoids
[(1R,2R,6S,10R,11R,13S,14R,15R)-13-acetyloxy-8-formyl-1-hydroxy-4,12,12,15-tetramethyl-5-oxo-14-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] 2-(methylamino)benzoate 162901456 Click to see CC1C(C2(C(C2(C)C)C3C1(C4C=C(C(=O)C4CC(=C3)C=O)C)O)OC(=O)C)OC(=O)C5=CC=CC=C5NC 521.60 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(4-acetyloxy-3-methyl-6,9-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-8-yl) acetate 162949307 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)OC(=O)C)OC(=O)C 348.40 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
(4-Hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-8-yl) acetate 85127064 Click to see CC(=O)OC1CC2C(C1=C)C3C(C(CC2=C)O)C(=C)C(=O)O3 304.34 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
[(3aR,4S,6aR,8S,9aR,9bR)-4-hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-8-yl] acetate 101036702 Click to see CC(=O)OC1CC2C(C1=C)C3C(C(CC2=C)O)C(=C)C(=O)O3 304.34 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
[(3S,3aR,4S,6aR,8S,9aR,9bR)-4-acetyloxy-3-methyl-6,9-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-8-yl] acetate 101707498 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)OC(=O)C)OC(=O)C 348.40 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
11,13-Dihydrodesacylcynaropicrin 12047617 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)O 264.32 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
4,8-dihydroxy-3-methyl-6,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 15628151 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)O 264.32 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
4,8-Dihydroxy-3,9-dimethyl-6-methylidene-3,3a,4,5,6a,7,8,9,9a,9b-decahydroazuleno[4,5-b]furan-2-one 14589527 Click to see CC1C(CC2C1C3C(C(C(=O)O3)C)C(CC2=C)O)O 266.33 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
Deacylcynaropicrin 71586749 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)O 262.30 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
Deacylcynaropicrin 3084544 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)O 262.30 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
Desacylcynaropicrin 13943205 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)O 262.30 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
Isolipidiol 14589530 Click to see CC1C(CC2C1C3C(C(C(=O)O3)C)C(CC2=C)O)O 266.33 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-methyl 9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysene-3a-carboxylate 134688158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)OC 470.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
(1R,3S,5R,6R,9S,11R,14R,15S,18S,23R)-9-hydroxy-6,10,10,14,15,21,21-heptamethyl-2-oxahexacyclo[13.8.0.01,3.05,14.06,11.018,23]tricosane-18-carboxylic acid 101707497 Click to see CC1(CCC2(CCC3(C4(CCC5C(C(CCC5(C4CC6C3(C2C1)O6)C)O)(C)C)C)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
(1R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14aR,14bS)-10-hydroxy-1,6a,6b,9,9,12a-hexamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-hexadecahydropicene-4a-carboxylic acid 162898119 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C(=O)O)C)C)(C)C)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
(2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14aR,14bR)-10-hydroxy-2,6a,6b,9,9,12a-hexamethyl-1-methylidene-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-hexadecahydropicene-4a-carboxylic acid 162897633 Click to see CC1CCC2(CCC3(C(C2C1=C)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
(3S,4aR,6aR,6aR,6bR,8aR,12aS,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol 40557055 Click to see CC1(CCC2(CCC3(C(C2C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 428.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
(6aR,6bR,8aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol 145706026 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
1-(3-Hydroxyprop-1-en-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 14108935 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
10-Hydroxy-1,6a,6b,9,9,12a-hexamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-hexadecahydropicene-4a-carboxylic acid 162898118 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C(=O)O)C)C)(C)C)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
10-Hydroxy-2,6a,6b,9,9,12a-hexamethyl-1-methylidene-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-hexadecahydropicene-4a-carboxylic acid 162897632 Click to see CC1CCC2(CCC3(C(C2C1=C)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
10,16-Dihydroxy-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-23-one 53744937 Click to see CC1(CCC23CCC4(C5(CCC6C(C(CCC6(C5CC(C4(C2C1)OC3=O)O)C)O)(C)C)C)C)C 472.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
2-[(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-9-hydroxy-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-1-yl]prop-2-enal 70696539 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)C=O)CO)C)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
2-[9-Hydroxy-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-1-yl]prop-2-enal 72670381 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)C=O)CO)C)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
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/10.1016/S0031-9422(97)00021-6
3-Oxo-olean-12-en-28-oic acid 12313702 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C(=O)O)C 454.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
4,4,6a,6b,8a,11,11,14b-Octamethyl-docosahydropicen-3-ol 605867 Click to see CC1(CCC2(CCC3(C(C2C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 428.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
4,4,6a,6b,8a,12,14b-Heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol 610148 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
9-Hydroxy-6,10,10,14,15,21,21-heptamethyl-2-oxahexacyclo[13.8.0.01,3.05,14.06,11.018,23]tricosane-18-carboxylic acid 78384885 Click to see CC1(CCC2(CCC3(C4(CCC5C(C(CCC5(C4CC6C3(C2C1)O6)C)O)(C)C)C)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
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/10.1016/S0031-9422(97)00021-6
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
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/10.1016/S0031-9422(97)00021-6
Hennadiol 489919 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
Lup-20(29)-ene-3beta,28-diol 221023 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
Methyl betulate 423298 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)OC 470.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
Methyl betulinate 73493 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)OC 470.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
Oleanderolide 11113483 Click to see CC1(CCC23CCC4(C5(CCC6C(C(CCC6(C5CC(C4(C2C1)OC3=O)O)C)O)(C)C)C)C)C 472.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
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/10.1016/S0031-9422(97)00021-6
Oleanonic acid 12313704 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C(=O)O)C 454.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
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/10.1016/S0031-9422(97)00021-6
Taraxasterol 115250 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00021-6
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/10.1016/S0031-9422(97)00021-6

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