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Ibervillea sonorae

Ibervillea sonorae - 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 UUID64405c281d11f835353706
Scientific name Ibervillea sonorae
Authority (S.Watson) Greene
First published in Erythea 3: 75 (1895)

Description Top

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Synonyms Top

Scientific name Authority First published in
Maximowiczia sonorae S.Watson Proc. Amer. Acad. Arts 24: 51 (1889)
Maximowiczia insularis Brandegee Univ. Calif. Publ. Bot. 6: 361 (1916)
Ibervillea insularis (Brandegee) Wiggins Fl. Baja Calif. 391, without basionym ref. 1980
Maximowiczia sonorae var. penisularis I.M.Johnst. Proc. Calif. Acad. Sci. , ser. 4, 12: 1178 (1924)
Maximowiczia sonorae var. brevicaulis I.M.Johnst. Proc. Calif. Acad. Sci. , ser. 4, 12: 1179 (1924)
Maximowiczia sonorae var. peninsularis I.M.Johnst. Proc. Calif. Acad. Sci. , ser. 4, 12: 1178 (1924)

Common names Top

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Language Common/alternative name
Chinese 笑布袋

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Ibervillea sonorae var. peninsularis (I.M.Johnst.) Wiggins Fl. Baja Calif. 391, without basionym ref. 1980

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001301190
Tropicos 9201214
KEW urn:lsid:ipni.org:names:127278-2
The Plant List tro-9201214
Open Tree Of Life 970031
Observations.org 315325
NCBI Taxonomy 354617
IPNI 127278-2
iNaturalist 273781
GBIF 7317774
Elurikkus 587830
USDA GRIN 19654
Wikipedia Ibervillea_sonorae
CMAUP NPO17829

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
Recent Advances in the Application of Cucurbitacins as Anticancer Agents Zieniuk B, Pawełkowicz M Metabolites 14-Oct-2023
PMCID:PMC10608718
doi:10.3390/metabo13101081
PMID:37887406
Agri-silvicultures of Mexican Arid America Andablo-Reyes AD, Moreno-Calles AI, Cancio-Coyac BA, Gutiérrez-Coatecatl E, Rivero-Romero AD, Hernández-Cendejas G, Casas A J Ethnobiol Ethnomed 14-Sep-2023
PMCID:PMC10503103
doi:10.1186/s13002-023-00612-5
PMID:37710240
Phenolic Compounds from Wild Plant and In Vitro Cultures of Ageratina pichichensis and Evaluation of Their Antioxidant Activity Motolinia-Alcántara EA, Franco-Vásquez AM, Nieto-Camacho A, Arreguín-Espinosa R, Rodríguez-Monroy M, Cruz-Sosa F, Román-Guerrero A Plants (Basel) 01-Mar-2023
PMCID:PMC10005229
doi:10.3390/plants12051107
PMID:36903964
Cucurbitacins as potential anticancer agents: new insights on molecular mechanisms Varela C, Melim C, Neves BG, Sharifi-Rad J, Calina D, Mamurova A, Cabral C J Transl Med 31-Dec-2022
PMCID:PMC9805216
doi:10.1186/s12967-022-03828-3
PMID:36585670
Cucurbitacins as Potent Chemo-Preventive Agents: Mechanistic Insight and Recent Trends Tuli HS, Rath P, Chauhan A, Ranjan A, Ramniwas S, Sak K, Aggarwal D, Kumar M, Dhama K, Lee EH, Yap KC, Capinpin SM, Kumar AP Biomolecules 27-Dec-2022
PMCID:PMC9855938
doi:10.3390/biom13010057
PMID:36671442
Selected Species of the Cucurbitaceae Family Used in Mexico for the Treatment of Diabetes Mellitus Huerta-Reyes M, Tavera-Hernández R, Alvarado-Sansininea JJ, Jiménez-Estrada M Molecules 26-May-2022
PMCID:PMC9182361
doi:10.3390/molecules27113440
PMID:35684376
In Vitro Antitumor Activity of Endophytic and Rhizosphere Gram-Positive Bacteria from Ibervillea sonorae (S. Watson) Greene against L5178Y-R Lymphoma Cells Romero-Arguelles R, Romo-Sáenz CI, Morán-Santibáñez K, Tamez-Guerra P, Quintanilla-Licea R, Orozco-Flores AA, Ramírez-Villalobos JM, Tamez-Guerra R, Rodríguez-Padilla C, Gomez-Flores R Int J Environ Res Public Health 14-Jan-2022
PMCID:PMC8775836
doi:10.3390/ijerph19020894
PMID:35055716
Potential antidiabetic phytochemicals in plant roots: a review of in vivo studies Ardalani H, Hejazi Amiri F, Hadipanah A, Kongstad KT J Diabetes Metab Disord 12-Jul-2021
PMCID:PMC8630315
doi:10.1007/s40200-021-00853-9
PMID:34900828
Ethnobotanical biocultural diversity by rural communities in the Cuatrociénegas Valley, Coahuila; Mexico Estrada-Castillón E, Villarreal-Quintanilla JÁ, Encina-Domínguez JA, Jurado-Ybarra E, Cuéllar-Rodríguez LG, Garza-Zambrano P, Arévalo-Sierra JR, Cantú-Ayala CM, Himmelsbach W, Salinas-Rodríguez MM, Gutiérrez-Santillán TV J Ethnobiol Ethnomed 29-Mar-2021
PMCID:PMC8008621
doi:10.1186/s13002-021-00445-0
PMID:33781298
Natural Compounds in Sex Hormone-Dependent Cancers: The Role of Triterpenes as Therapeutic Agents Şoica C, Voicu M, Ghiulai R, Dehelean C, Racoviceanu R, Trandafirescu C, Roșca OJ, Nistor G, Mioc M, Mioc A Front Endocrinol (Lausanne) 21-Jan-2021
PMCID:PMC7859451
doi:10.3389/fendo.2020.612396
PMID:33552000
Molecules Isolated from Mexican Hypoglycemic Plants: A Review Escandón-Rivera SM, Mata R, Andrade-Cetto A Molecules 10-Sep-2020
PMCID:PMC7571036
doi:10.3390/molecules25184145
PMID:32927754
Exchange of medicinal plant information in California missions McBride JR, Cavero RY, Cheshire AL, Calvo MI, McBride DL J Ethnobiol Ethnomed 15-Jun-2020
PMCID:PMC7296748
doi:10.1186/s13002-020-00388-y
PMID:32539795
Overview of the phytomedicine approaches against Helicobacter pylori Vale FF, Oleastro M World J Gastroenterol 21-May-2014
PMCID:PMC4024768
doi:10.3748/wjg.v20.i19.5594
PMID:24914319
Antiobesity and Hypoglycaemic Effects of Aqueous Extract of Ibervillea sonorae in Mice Fed a High-Fat Diet with Fructose Rivera-Ramírez F, Escalona-Cardoso GN, Garduño-Siciliano L, Galaviz-Hernández C, Paniagua-Castro N J Biomed Biotechnol 17-Nov-2011
PMCID:PMC3228589
doi:10.1155/2011/968984
PMID:22174560
Cucurbitanes and cucurbitane-type glycosides from Ibervillea sonorae Hans Achenbach, Konrad Horn, Xorge A. Dominguez, Carlos Rombold, Elda G. Gómez López Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85535-Y

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 / Steroids and steroid derivatives / Cucurbitacins
(3R,8S,9R,10R,13R,14S,16R,17R)-17-[(2R)-2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl]-3,16-dihydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 162888986 Click to see CC1(C(CCC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(=O)CCC(C)(C)O)O)O)C)C)C)O)C 504.70 unknown https://doi.org/10.1016/0031-9422(93)85535-Y
(3R,8S,9R,10R,13R,14S,16R,17R)-3,16-dihydroxy-4,4,9,13,14-pentamethyl-17-[(E,2R,3S)-2,3,6-trihydroxy-6-methylhept-4-en-2-yl]-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 162974639 Click to see CC1(C(CCC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(C=CC(C)(C)O)O)O)O)C)C)C)O)C 504.70 unknown https://doi.org/10.1016/0031-9422(93)85535-Y
17-(2,6-Dihydroxy-6-methyl-3-oxoheptan-2-yl)-3,16-dihydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 162888985 Click to see CC1(C(CCC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(=O)CCC(C)(C)O)O)O)C)C)C)O)C 504.70 unknown https://doi.org/10.1016/0031-9422(93)85535-Y
3,16-Dihydroxy-4,4,9,13,14-pentamethyl-17-(2,3,6-trihydroxy-6-methylhept-4-en-2-yl)-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 162974638 Click to see CC1(C(CCC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(C=CC(C)(C)O)O)O)O)C)C)C)O)C 504.70 unknown https://doi.org/10.1016/0031-9422(93)85535-Y
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
(3R,8S,9R,10R,13R,14S,16R,17R)-17-acetyl-3,16-dihydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 162866873 Click to see CC(=O)C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CCC(C4(C)C)O)C)C)C)O 388.50 unknown https://doi.org/10.1016/0031-9422(93)85535-Y
17-Acetyl-3,16-dihydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 162866871 Click to see CC(=O)C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CCC(C4(C)C)O)C)C)C)O 388.50 unknown https://doi.org/10.1016/0031-9422(93)85535-Y
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(3R,8S,9R,10R,13R,14S,16R,17R)-16-hydroxy-4,4,9,13,14-pentamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-[(E,2R,3S)-2,3,6-trihydroxy-6-methylhept-4-en-2-yl]-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 163048765 Click to see CC1(C(CCC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(C=CC(C)(C)O)O)O)O)C)C)C)OC5C(C(C(C(O5)CO)O)O)O)C 666.80 unknown https://doi.org/10.1016/0031-9422(93)85535-Y
(3R,8S,9R,10R,13R,14S,16R,17R)-3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-16-hydroxy-4,4,9,13,14-pentamethyl-17-[(E,2R,3S)-2,3,6-trihydroxy-6-methylhept-4-en-2-yl]-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 163186510 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4C(=CCC5C4(C(=O)CC6(C5(CC(C6C(C)(C(C=CC(C)(C)O)O)O)O)C)C)C)C3(C)C)CO)O)O)O)O)O 813.00 unknown https://doi.org/10.1016/0031-9422(93)85535-Y
(3R,8S,9R,10R,13R,14S,16R,17R)-3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-17-[(2R)-2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl]-16-hydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 162854977 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4C(=CCC5C4(C(=O)CC6(C5(CC(C6C(C)(C(=O)CCC(C)(C)O)O)O)C)C)C)C3(C)C)CO)O)O)O)O)O 813.00 unknown https://doi.org/10.1016/0031-9422(93)85535-Y
16-Hydroxy-4,4,9,13,14-pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-(2,3,6-trihydroxy-6-methylhept-4-en-2-yl)-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 163048763 Click to see CC1(C(CCC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(C=CC(C)(C)O)O)O)O)C)C)C)OC5C(C(C(C(O5)CO)O)O)O)C 666.80 unknown https://doi.org/10.1016/0031-9422(93)85535-Y
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-16-hydroxy-4,4,9,13,14-pentamethyl-17-(2,3,6-trihydroxy-6-methylhept-4-en-2-yl)-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 162910285 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4C(=CCC5C4(C(=O)CC6(C5(CC(C6C(C)(C(C=CC(C)(C)O)O)O)O)C)C)C)C3(C)C)CO)O)O)O)O)O 813.00 unknown https://doi.org/10.1016/0031-9422(93)85535-Y
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-17-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-16-hydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 162854975 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4C(=CCC5C4(C(=O)CC6(C5(CC(C6C(C)(C(=O)CCC(C)(C)O)O)O)C)C)C)C3(C)C)CO)O)O)O)O)O 813.00 unknown https://doi.org/10.1016/0031-9422(93)85535-Y
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Eupatin 5317287 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O)O 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11968829 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 494.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-4-oxochromen-3-yl] sulfate 21676165 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OS(=O)(=O)[O-])C3=CC(=C(C=C3)O)O)O 411.30 unknown via CMAUP database
Centaureidin 5315773 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown via CMAUP database
Desmethoxycentaureidin 5469524 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown via CMAUP database
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown via CMAUP database
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown via CMAUP database
Salvigenin 161271 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown via CMAUP database

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