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Stenocereus eruca

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64405700c3e6b363800915
Scientific name Stenocereus eruca
Authority (K.Brandegee) A.C.Gibson & K.E.Horak
First published in in Ann. Missouri Bot. Gard. 65(4): 100. 1978.

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Rathbunia eruca (K.Brandegee) P.V.Heath in Calyx 2: 102. 1992.
Cereus eruca K.Brandegee in Proc. Calif. Acad. Sci. ser. 2 2: 163. 1889.
Lemaireocereus eruca (K.Brandegee) Britton & Rose in Contr. U.S. Natl. Herb. 12(10): 425. 1909.
Machaerocereus eruca (K.Brandegee) Britton & Rose Cactaceae 2: 115–116, f. 171–172. 1920.

Common names Top

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Language Common/alternative name
Japanese クリーピング・デビル
Urdu اسٹینوسیریئس ایروکا
Chinese 入鹿

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001256510
Tropicos 50181356
KEW urn:lsid:ipni.org:names:244632-2
The Plant List tro-50181356
Open Tree Of Life 270413
NCBI Taxonomy 867530
IUCN Red List 152511
IPNI 138580-1
iNaturalist 206501
GBIF 3960636
Freebase /m/06wwkg
EOL 5184501
Wikipedia Stenocereus_eruca

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
Are 150 km of open sea enough? Gene flow and population differentiation in a bat-pollinated columnar cactus Arenas S, Búrquez A, Bustamante E, Scheinvar E, Eguiarte LE PLoS One 29-Jun-2023
PMCID:PMC10309638
doi:10.1371/journal.pone.0282932
PMID:37384637
Self-Repair in Cacti Branches: Comparative Analyses of Their Morphology, Anatomy, and Biomechanics Mylo MD, Krüger F, Speck T, Speck O Int J Mol Sci 29-Jun-2020
PMCID:PMC7370035
doi:10.3390/ijms21134630
PMID:32610697
Dynamics of distribution and performance of ramets constructing genets: a demographic–genetic study in a clonal plant, Convallaria keiskei Araki K, Shimatani K, Ohara M Ann Bot 17-Apr-2009
PMCID:PMC2706722
doi:10.1093/aob/mcp092
PMID:19376781
Structure–Function Relationships in Highly Modified Shoots of Cactaceae MAUSETH JD Ann Bot 01-Nov-2006
PMCID:PMC2803597
doi:10.1093/aob/mcl133
PMID:16820405
New Triterpenes from <i>Machaerocereus eruca</i> Yang Ye, Kaoru Kinoshita, Kiyotaka Koyama, Kunio Takahashi, Norio Kondo, Hiroshi Yuasa American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/NP970364D

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 / Triterpenoids
(1R,3aR,4S,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-4,9-dihydroxy-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 21604188 Click to see 472.70 unknown https://doi.org/10.1021/NP970364D
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-2-oxo-1-prop-1-en-2-yl-3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysene-3a-carboxylic acid 21604187 Click to see 470.70 unknown https://doi.org/10.1021/NP970364D
(1R,4R,5R,8R,10S,13R,14R,17R,18R,19R,20S)-10-hydroxy-4,5,9,9,13-pentamethyl-19-prop-1-en-2-yl-21-oxahexacyclo[18.2.1.01,18.04,17.05,14.08,13]tricosan-22-one 162980440 Click to see 454.70 unknown https://doi.org/10.1021/NP970364D
(1R,4R,5R,8S,10S,13R,14R,17R,18R,19S,20S)-10-hydroxy-19-(2-hydroxypropan-2-yl)-4,5,9,9,13-pentamethyl-21-oxahexacyclo[18.2.1.01,18.04,17.05,14.08,13]tricosan-22-one 163076374 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC56C4C(C(C5)OC6=O)C(C)(C)O)C)C)C 472.70 unknown https://doi.org/10.1021/NP970364D
(1R,4R,5R,8S,10S,13R,14R,17R,18R,19S,20S)-10-hydroxy-4,5,9,9,13,19,20-heptamethyl-21-oxahexacyclo[18.2.2.01,18.04,17.05,14.08,13]tetracosan-22-one 163102933 Click to see 456.70 unknown https://doi.org/10.1021/NP970364D
(1R,4S,5R,8R,10S,13R,14R,18S,20R,21S)-10-hydroxy-20-(hydroxymethyl)-4,5,9,9,13,20-hexamethyl-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracos-16-en-23-one 163038866 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC56C4CC(C(C5)OC6=O)(C)CO)C)C)C 470.70 unknown https://doi.org/10.1021/NP970364D
(1S,4aR,6aR,6aR,6bR,8aR,10S,12aR,14aR,14bR)-1,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-hexadecahydropicene-4a-carboxylic acid 21604186 Click to see 474.70 unknown https://doi.org/10.1021/NP970364D
(2S,3S,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-3,10-dihydroxy-2-(hydroxymethyl)-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162983877 Click to see 488.70 unknown https://doi.org/10.1021/NP970364D
(2S,4aR,6bR,10S,12aR)-10-hydroxy-2-(hydroxymethyl)-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 5320865 Click to see 472.70 unknown https://doi.org/10.1021/NP970364D
10-Hydroxy-2-(hydroxymethyl)-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 5319375 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)CO)C(=O)O)C)C)C 472.70 unknown https://doi.org/10.1021/NP970364D
10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a-tetradecahydropicene-4a-carboxylic acid 5319898 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(=O)O)C 456.70 unknown https://doi.org/10.1021/NP970364D
4,9-Dihydroxy-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 73799312 Click to see 472.70 unknown https://doi.org/10.1021/NP970364D
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1021/NP970364D
Mesembryanthemoidigenic acid 21594136 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)CO)C(=O)O)C)C)C 472.70 unknown https://doi.org/10.1021/NP970364D
Morolic Acid 489944 Click to see 456.70 unknown https://doi.org/10.1021/NP970364D
Queretaroic acid 12314864 Click to see 472.70 unknown https://doi.org/10.1021/NP970364D
Treleasegenin acid 23641097 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(C(C5)O)(C)CO)C(=O)O)C)C)C 488.70 unknown https://doi.org/10.1021/NP970364D

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