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Erucaria microcarpa

Erucaria microcarpa - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Erucaria microcarpa - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Erucaria microcarpa - 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 UUID64401b3bbe3d2786856651
Scientific name Erucaria microcarpa
Authority Boiss.
First published in Diagn. Pl. Orient. 8: 47 (1849)

Description Top

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Synonyms Top

Scientific name Authority First published in
Reboudia microcarpa Coss. Comp. Fl. Atlant. 2: 213 (1888)
Reboudia pinnata var. liocarpa O.E.Schulz Pflanzenreich IV–105(Heft 70): 145. 1919
Erucaria microcarpa var. boissieri Täckh. 354. 354. 1956
Erucaria microcarpa var. liocarpa Täckh. 354. 354. 1956

Common names Top

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Language Common/alternative name
Hebrew בן-שלח מנוצה

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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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-0000677448
Tropicos 50213745
INPN 978606
KEW urn:lsid:ipni.org:names:283452-1
The Plant List kew-2798791
Open Tree Of Life 632830
NCBI Taxonomy 1078594
IPNI 283452-1
GBIF 5377707
EPPO EARMI

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
Active Compounds with Medicinal Potential Found in Maxillariinae Benth. (Orchidaceae Juss.) Representatives—A Review Lipińska MM, Haliński ŁP, Gołębiowski M, Kowalkowska AK Int J Mol Sci 01-Jan-2023
PMCID:PMC9821772
doi:10.3390/ijms24010739
PMID:36614181
Volatile Olfactory Profiles of Umbrian Extra Virgin Olive Oils and Their Discrimination through MOX Chemical Sensors Mariotti R, Núñez-Carmona E, Genzardi D, Pandolfi S, Sberveglieri V, Mousavi S Sensors (Basel) 21-Sep-2022
PMCID:PMC9572317
doi:10.3390/s22197164
PMID:36236259
Styrylchromones: Biological Activities and Structure-Activity Relationship Lucas M, Freitas M, Silva AM, Fernandes E, Ribeiro D Oxid Med Cell Longev 22-Dec-2021
PMCID:PMC8720608
doi:10.1155/2021/2804521
PMID:34987699
Effects of Glucosinolate-Derived Isothiocyanates on Fungi: A Comprehensive Review on Direct Effects, Mechanisms, Structure-Activity Relationship Data and Possible Agricultural Applications Plaszkó T, Szűcs Z, Vasas G, Gonda S J Fungi (Basel) 06-Jul-2021
PMCID:PMC8305656
doi:10.3390/jof7070539
PMID:34356918
Ant Abundance along a Productivity Gradient: Addressing Two Conflicting Hypotheses Segev U, Kigel J, Lubin Y, Tielbörger K PLoS One 15-Jul-2015
PMCID:PMC4503676
doi:10.1371/journal.pone.0131314
PMID:26176853
Antimicrobial components of some cruciferae plants (Diplotaxis harra Forsk. and Erucaria microcarpa Boiss.) F. A. Hashem, M. M. Saleh Wiley 02-Dec-2005
doi:10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U

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
Benzyl Isothiocyanate 2346 Click to see C1=CC=C(C=C1)CN=C=S 149.21 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
> Benzenoids / Phenol ethers / Anisoles
Anethole 637563 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
Methoxy-4-propenylbenzene 7703 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Dodecane 8182 Click to see CCCCCCCCCCCC 170.33 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
Heneicosane 12403 Click to see CCCCCCCCCCCCCCCCCCCCC 296.60 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
Hexacosane 12407 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC 366.70 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
Octacosane 12408 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC 394.80 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
Octadecane 11635 Click to see CCCCCCCCCCCCCCCCCC 254.50 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
Tetradecane 12389 Click to see CCCCCCCCCCCCCC 198.39 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid 2969 Click to see CCCCCCCCCC(=O)O 172.26 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
Lauric Acid 3893 Click to see CCCCCCCCCCCC(=O)O 200.32 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
Octanoic Acid 379 Click to see CCCCCCCC(=O)O 144.21 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
2-Cyclohexen-1-one, 5-methyl-2-(1-methylethyl)- 107372 Click to see CC1CC=C(C(=O)C1)C(C)C 152.23 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Ionone 638014 Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C 192.30 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
> Organosulfur compounds / Isothiocyanates
Butenyl isothiocyanate 6439701 Click to see CCC=CN=C=S 113.18 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U
Isopropyl Isothiocyanate 75263 Click to see CC(C)N=C=S 101.17 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<329::AID-PTR458>3.0.CO;2-U

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