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Escontria chiotilla

Escontria chiotilla - 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 UUID64401baaf0c55691294928
Scientific name Escontria chiotilla
Authority (F.A.C.Weber ex K.Schum.) Rose
First published in in Contr. U.S. Natl. Herb. 10: 126, pl. 43. 1906.

Description Top

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Synonyms Top

Scientific name Authority First published in
Cereus chiotilla F.A.C.Weber ex K.Schum. Gesamtbeschr. Kakt.: 83. 1897.
Myrtillocactus chiotilla (F.A.C.Weber ex K.Schum.) P.V.Heath in Calyx 2(3): 105. 1992.
Myrtillocactus chiotilla f. spiralis P.V.Heath in Calyx 2: 105. 1992.

Common names Top

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Language Common/alternative name
English chiotilla
English jiotilla
Spanish chiotillo
Spanish chitillilla
German chiotilla
Swedish chiotillakaktus
Chinese 白焰柱

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000680760
Tropicos 50004437
KEW urn:lsid:ipni.org:names:97551-2
The Plant List kew-2802296
Open Tree Of Life 295076
NCBI Taxonomy 153861
IUCN Red List 152145
IPNI 97551-2
iNaturalist 274225
GBIF 3941495
Freebase /m/07y3c3
EPPO ESNCH
EOL 5182031
USDA GRIN 448395
CMAUP NPO23750

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
Green Solvents for Extraction of Natural Food Colorants from Plants: Selectivity and Stability Issues Tzanova MT, Yaneva Z, Ivanova D, Toneva M, Grozeva N, Memdueva N Foods 16-Feb-2024
PMCID:PMC10887973
doi:10.3390/foods13040605
PMID:38397582
Measuring the shape of mortality across animals and plants: Alternatives to H entropy metrics reveal hidden type IV survivorship curves and associations with parental care at macro‐ecological scales Healy K, Kelly R, Carnevale A, Buckley YM Ecol Evol 17-May-2023
PMCID:PMC10191775
doi:10.1002/ece3.10076
PMID:37206684
Evaluation of three methods for betanin quantification in fruits from cacti Sandate-Flores L, Rodríguez-Hernández DV, Rostro-Alanis M, Melchor-Martínez EM, Brambila-Paz C, Sosa-Hernández JE, Parra-Saldívar R, Rodríguez-Rodríguez J, Iqbal HM MethodsX 29-May-2022
PMCID:PMC9189195
doi:10.1016/j.mex.2022.101746
PMID:35707638
Traditional Fermented Beverages of Mexico: A Biocultural Unseen Foodscape Ojeda-Linares C, Álvarez-Ríos GD, Figueredo-Urbina CJ, Islas LA, Lappe-Oliveras P, Nabhan GP, Torres-García I, Vallejo M, Casas A Foods 09-Oct-2021
PMCID:PMC8535898
doi:10.3390/foods10102390
PMID:34681439
Comparative effects of pollen limitation, floral traits and pollinators on reproductive success of Hedysarum scoparium Fisch. et Mey. in different habitats Chen M, Zhao XY, Zuo XA, Wang SK, Qu H, Ping Y, Ma XJ, Liu LX BMC Plant Biol 18-Sep-2021
PMCID:PMC8449482
doi:10.1186/s12870-021-03211-2
PMID:34537013
Validation of aqueous two-phase extraction method Sandate-Flores L, Rodríguez-Rodríguez J, Rostro-Alanis M, Urbina JA, Mayolo-Deloisa K, Melchor-Martínez EM, Sosa-Hernández JE, Parra-Saldívar R, Iqbal HM MethodsX 18-Jun-2021
PMCID:PMC8374489
doi:10.1016/j.mex.2021.101421
PMID:34430316
Nephroprotective Effect Assessment From Arid Lands Fruits Extracts in an Experimental Model With Cisplatine-Induced Nephrotoxicity Guerrero AR, Rodríguez YR, González VR, Silva DT Curr Dev Nutr 07-Jun-2021
PMCID:PMC8181607
doi:10.1093/cdn/nzab037_073
Functional Attributes and Anticancer Potentialities of Chico (Pachycereus Weberi) and Jiotilla (Escontria Chiotilla) Fruits Extract Sandate-Flores L, Romero-Esquivel E, Rodríguez-Rodríguez J, Rostro-Alanis M, Melchor-Martínez EM, Castillo-Zacarías C, Ontiveros PR, Celaya MF, Chen WN, Iqbal HM, Parra-Saldívar R Plants (Basel) 22-Nov-2020
PMCID:PMC7700655
doi:10.3390/plants9111623
PMID:33266445
Traditional management of microorganisms in fermented beverages from cactus fruits in Mexico: an ethnobiological approach Ojeda-Linares CI, Vallejo M, Lappe-Oliveras P, Casas A J Ethnobiol Ethnomed 10-Jan-2020
PMCID:PMC6954596
doi:10.1186/s13002-019-0351-y
PMID:31924218
Stabilization of betalains by encapsulation—a review Castro-Enríquez DD, Montaño-Leyva B, Del Toro-Sánchez CL, Juaréz-Onofre JE, Carvajal-Millan E, Burruel-Ibarra SE, Tapia-Hernández JA, Barreras-Urbina CG, Rodríguez-Félix F J Food Sci Technol 10-Oct-2019
PMCID:PMC7171008
doi:10.1007/s13197-019-04120-x
PMID:32327769
Species delimitation in the Stenocereus griseus (Cactaceae) species complex reveals a new species, S. huastecorum Alvarado-Sizzo H, Casas A, Parra F, Arreola-Nava HJ, Terrazas T, Sánchez C PLoS One 17-Jan-2018
PMCID:PMC5771577
doi:10.1371/journal.pone.0190385
PMID:29342184
High tolerance to high-light conditions for the protected species Ariocarpus kotschoubeyanus (Cactaceae) Arroyo-Pérez E, Flores J, González-Salvatierra C, Matías-Palafox ML, Jiménez-Sierra C Conserv Physiol 17-Jul-2017
PMCID:PMC5511894
doi:10.1093/conphys/cox042
PMID:28729902
TEK and biodiversity management in agroforestry systems of different socio-ecological contexts of the Tehuacán Valley Vallejo-Ramos M, Moreno-Calles AI, Casas A J Ethnobiol Ethnomed 22-Jul-2016
PMCID:PMC4957363
doi:10.1186/s13002-016-0102-2
PMID:27449507
Ixcatec ethnoecology: plant management and biocultural heritage in Oaxaca, Mexico Rangel-Landa S, Casas A, Rivera-Lozoya E, Torres-García I, Vallejo-Ramos M J Ethnobiol Ethnomed 20-Jul-2016
PMCID:PMC4955254
doi:10.1186/s13002-016-0101-3
PMID:27439512
Effects of natural and artificial selection on survival of columnar cacti seedlings: the role of adaptation to xeric and mesic environments Guillén S, Terrazas T, Casas A Ecol Evol 25-Mar-2015
PMCID:PMC4485958
doi:10.1002/ece3.1478
PMID:26140193

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> Benzenoids / Tetralins
(4S)-10-Nor-calamenen-10-one 73350586 Click to see CC1=CC2=C(C=C1)C(=O)CCC2C(C)C 202.29 unknown via CMAUP database
Oxyphyllenotriol A 51041015 Click to see CC(C)C1=C2C(C(CCC2=C(C=C1)O)(C)O)O 236.31 unknown via CMAUP database
Oxyphyllone G 51041016 Click to see CC1=C(C2=C(C=C1)C(=O)CCC2C(C)C)O 218.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Tetracosanoic acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Labda-8(17),12-diene-15,16-dial 11077520 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1r,2r)-p-Menth-3-en-1,2-diol 71423340 Click to see CC(C)C1=CC(C(CC1)(C)O)O 170.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2R,3R,6S,7S)-1-hydroxy-3,7-dimethyl-10-propan-2-yl-11-oxatricyclo[5.3.1.02,6]undec-9-en-8-one 76285513 Click to see CC1CCC2C1C3(C(=CC(=O)C2(O3)C)C(C)C)O 250.33 unknown via CMAUP database
Oxyphyllanene D 57396910 Click to see CC(=C)C1(CCC2(CCC(=O)C3(C2(C1)O3)C)C)O 250.33 unknown via CMAUP database
Oxyphyllol E 51041018 Click to see CC(=C)C1(CCC2(CCC(=O)C3(C2(C1)O3)C)C)O 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(11S)-Nootkatone-11,12-diol 15601439 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(C)(CO)O)C 252.35 unknown via CMAUP database
(1S)-1,2,3,4,4a,5,6,7-Octahydro-4beta,4abeta-dimethyl-6alpha-(1-methylethenyl)naphthalene-1beta-ol 44576208 Click to see CC1CCC(C2=CCC(CC12C)C(=C)C)O 220.35 unknown via CMAUP database
(3S,4aS,5R)-4a,5-dimethyl-3-prop-1-en-2-yl-3,4,5,6-tetrahydro-2H-naphthalene-1,7-dione 72715093 Click to see CC1CC(=O)C=C2C1(CC(CC2=O)C(=C)C)C 232.32 unknown via CMAUP database
(4R,4aR)-6-acetyl-4,4a-dimethyl-3,4,7,8-tetrahydronaphthalen-2-one 117654813 Click to see CC1CC(=O)C=C2C1(C=C(CC2)C(=O)C)C 218.29 unknown via CMAUP database
(4R,4aS,6R)-6-(2-hydroxypropan-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one 89960876 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(C)(C)O)C 236.35 unknown via CMAUP database
(4R,4aS,6R)-6-(3-hydroxyprop-1-en-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one 53249021 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)CO)C 234.33 unknown via CMAUP database
(4R)-4beta,4abeta-Dimethyl-6alpha-isopropenyl-8alpha-hydroxy-2,3,4,4a,5,6,7,8-octahydronaphthalene-2-one 11651584 Click to see CC1CC(=O)C=C2C1(CC(CC2O)C(=C)C)C 234.33 unknown via CMAUP database
Nootkatene 25200342 Click to see CC1CC=CC2=CCC(CC12C)C(=C)C 202.33 unknown via CMAUP database
Nootkatol 182645 Click to see CC1CC(C=C2C1(CC(CC2)C(=C)C)C)O 220.35 unknown via CMAUP database
Nootkatone 1268142 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)C)C 218.33 unknown via CMAUP database
oxyphyllol C 10857540 Click to see CC1CCC(C2(C1(CC(CC2)C(=C)C)C)O)O 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,4aR,7R,8aS)-1,4a-dimethyl-7-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol 15560338 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 222.37 unknown via CMAUP database
(2R,4aS,7R,8aR)-4a-Methyl-1-methylidene-7-(prop-1-en-2-yl)decahydronaphthalen-2-ol 14076604 Click to see CC(=C)C1CCC2(CCC(C(=C)C2C1)O)C 220.35 unknown via CMAUP database
(4aS,7S,8R)-8-hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one 57393410 Click to see CC1=C2C(C(CCC2(CCC1=O)C)C(=C)C)O 234.33 unknown via CMAUP database
(4aS,7S)-7-hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-4,5,6,8-tetrahydro-3H-naphthalen-2-one 57335617 Click to see CC1=C2CC(CCC2(CCC1=O)C)(C(=C)C)O 234.33 unknown via CMAUP database
7-Epi-Teucrenone B 57393409 Click to see CC1=CC(=O)CC2(C1CC(CC2)(C(=C)C)O)C 234.33 unknown via CMAUP database
Ligucyperonol 14681770 Click to see CC1=C2CC(CCC2(C(CC1=O)O)C)C(=C)C 234.33 unknown via CMAUP database
Oxyphyllol A 637451 Click to see CC(=C)C1CCC2(CCCC(C2=C1)(C)O)C 220.35 unknown via CMAUP database
Rel-Oxyphyllanene E 57400339 Click to see CC(=C)C1(CCC2(CCC(C(=C)C2C1)O)C)O 236.35 unknown via CMAUP database
Teucrenone 10105443 Click to see CC1=CC(=O)CC2(C1CC(CC2)(C(=C)C)O)C 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(4aS,8aR,9aR)-3,5,8a-trimethyl-4a,8,9,9a-tetrahydro-4H-benzo[f][1]benzofuran-2,7-dione 71681246 Click to see CC1=CC(=O)CC2(C1CC3=C(C(=O)OC3C2)C)C 246.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Sitosteryl palmitate 9852570 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 653.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Pubescone 102054514 Click to see CC(C)C1C2C(C2CCC(=O)C)CCC1=O 222.32 unknown via CMAUP database
Spiro[4.4]nonan-2-one 549163 Click to see C1CCC2(C1)CCC(=O)C2 138.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(4aR,6S,8aS)-6-acetyl-4a-hydroxy-4,8a-dimethyl-5,6,7,8-tetrahydro-1H-naphthalen-2-one 71681103 Click to see CC1=CC(=O)CC2(C1(CC(CC2)C(=O)C)O)C 236.31 unknown via CMAUP database
(4aR)-7-acetyl-1,4a-dimethyl-3,4,5,6-tetrahydronaphthalen-2-one 71681245 Click to see CC1=C2C=C(CCC2(CCC1=O)C)C(=O)C 218.29 unknown via CMAUP database
4-Hydroxy-11,12,13-trinor-5-eudesmen-7-one 15153217 Click to see CC12CCCC(C1=CC(=O)CC2)(C)O 194.27 unknown via CMAUP database
OxyphyllaneneA 122402647 Click to see CC1=CC(=O)CC2(C1CC(=O)CC2)C 192.25 unknown via CMAUP database
Oxyphyllenodiol A 10082923 Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O 238.32 unknown via CMAUP database
Oxyphyllenodiol B 5279294 Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O 238.32 unknown via CMAUP database
Oxyphyllenone A 10262534 Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O 210.27 unknown via CMAUP database
Oxyphyllenone B 44310512 Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O 210.27 unknown via CMAUP database
Oxyphyllone C 44255203 Click to see CC(C)C1CCC(=O)C2=C1C3C(O3)(CC2)C 220.31 unknown via CMAUP database
Teuhetenone A 15153216 Click to see CC12CCCC(C1=CC(=O)CC2)(C)O 194.27 unknown via CMAUP database
> Organoheterocyclic compounds / Epoxides
(1S,4S,6S,8E,12S)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.04,6]tridec-8-ene 12014673 Click to see CC1(CC2C(O2)(CCC3C(O3)(CC=C1)C)C)C 236.35 unknown via CMAUP database
> Organoheterocyclic compounds / Oxepanes
Oxyphyllanene C 57335616 Click to see CC1=C2C3C(O3)(CCC2(CCC1=O)C)C(=O)C 234.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E)-1-(4-Hydroxy-3-methoxyphenyl)-7-phenyl-1-hepten-3-one 6440365 Click to see COC1=C(C=CC(=C1)C=CC(=O)CCCCC2=CC=CC=C2)O 310.40 unknown via CMAUP database
1-(2,4-Dihydroxy-3-methoxyphenyl)-7-(4-methoxyphenyl)heptan-3-one 72708396 Click to see COC1=CC=C(C=C1)CCCCC(=O)CCC2=C(C(=C(C=C2)O)OC)O 358.40 unknown via CMAUP database
1-(3,5-Dihydroxy-4-methoxyphenyl)-7-phenylheptan-3-one 72708395 Click to see COC1=C(C=C(C=C1O)CCC(=O)CCCCC2=CC=CC=C2)O 328.40 unknown via CMAUP database
Yakuchinone-A 133145 Click to see COC1=C(C=CC(=C1)CCC(=O)CCCCC2=CC=CC=C2)O 312.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5-Dihydroxy-7-methoxy-2-(4-methoxyphenyl)-4H-chromen-4-one 5378823 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)O 314.29 unknown via CMAUP database
Izalpinin 5318691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O 284.26 unknown via CMAUP database
Kaempferide 5281666 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin 5281954 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O 268.26 unknown via CMAUP database

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