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Senna lindheimeriana

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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 UUID643fd7b1a8da6127237961
Scientific name Senna lindheimeriana
Authority (Scheele) H.S.Irwin & Barneby
First published in Phytologia44: 500 (1979)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cassia lindheimeriana Scheele Linnaea21: 457 (1848)
Earleocassia lindeheimeriana (Scheele) Britton N. Amer. Fl. 23(4): 249. 1930 [18 Nov 1930]
Earleocassia lindheimeriana (Scheele) Britton N.L.Britton & al. (eds.), N. Amer. Fl.23: 249 (1930)

Common names Top

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Language Common/alternative name
English velvet leaf senna
English velvet-leaved senna

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000175248
USDA Plants SELI4
Tropicos 13041362
KEW urn:lsid:ipni.org:names:518343-1
The Plant List ild-21378
Open Tree Of Life 148477
NCBI Taxonomy 162908
Nature Serve 2.157811
IPNI 234511-2
iNaturalist 168843
GBIF 2957348
EOL 641354
USDA GRIN 100046
CMAUP NPO2762
Wikipedia Senna_lindheimeriana

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
A Review of Recent Studies on the Antioxidant and Anti-Infectious Properties of Senna Plants Alshehri MM, Quispe C, Herrera-Bravo J, Sharifi-Rad J, Tutuncu S, Aydar EF, Topkaya C, Mertdinc Z, Ozcelik B, Aital M, Kumar NV, Lapava N, Rajkovic J, Ertani A, Nicola S, Semwal P, Painuli S, González-Contreras C, Martorell M, Butnariu M, Bagiu IC, Bagiu RV, Barbhai MD, Kumar M, Daştan SD, Calina D, Cho WC Oxid Med Cell Longev 04-Feb-2022
PMCID:PMC8837466
doi:10.1155/2022/6025900
PMID:35154569
Tortricid Moths Reared from the Invasive Weed Mexican Palo Verde, Parkinsonia aculeata, with Comments on their Host Specificity, Biology, Geographic Distribution, and Systematics Brown JW, Segura R, Santiago-Jiménez Q, Rota J, Heard TA J Insect Sci 24-Jan-2011
PMCID:PMC3281301
doi:10.1673/031.011.0107
PMID:21521138
Complete plastid genome sequence of the chickpea (Cicer arietinum) and the phylogenetic distribution of rps12 and clpP intron losses among legumes (Leguminosae) Jansen RK, Wojciechowski MF, Sanniyasi E, Lee SB, Daniell H Mol Phylogenet Evol 27-Jun-2008
PMCID:PMC2586962
doi:10.1016/j.ympev.2008.06.013
PMID:18638561
Anthraquinones and other constituents of two Senna species Bertha Barba, Jésus G. Díaz, Werner Herz Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80483-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 / Anthracenes / Anthraquinones
1-Hydroxy-2,6,7,8-tetramethoxy-3-methylanthracene-9,10-dione 118253906 Click to see CC1=CC2=C(C(=C1OC)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)OC)OC 358.30 unknown https://doi.org/10.1016/0031-9422(92)80483-U
1-Hydroxy-8-methoxy-3-methylanthracene-9,10-dione 11300144 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC 268.26 unknown https://doi.org/10.1016/0031-9422(92)80483-U
1,4,5-Trihydroxy-2-methoxy-7-methylanthracene-9,10-dione 12444971 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C(=C(C=C3O)OC)O 300.26 unknown https://doi.org/10.1016/0031-9422(92)80483-U
1,8-Dihydroxy-3,6-dimethylanthracene-9,10-dione 10400816 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)C 268.26 unknown https://doi.org/10.1016/0031-9422(92)80483-U
Helminthosporin 97560 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C=CC(=C3C2=O)O)O 270.24 unknown https://doi.org/10.1016/0031-9422(92)80483-U
Physcione 10639 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC 284.26 unknown https://doi.org/10.1016/0031-9422(92)80483-U
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown https://doi.org/10.1016/0031-9422(92)80483-U
Questin 160717 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC)O 284.26 unknown https://doi.org/10.1016/0031-9422(92)80483-U
> Benzenoids / Phenols / Methoxyphenols
2,4,5-Trimethoxyphenol 12445134 Click to see COC1=CC(=C(C=C1O)OC)OC 184.19 unknown https://doi.org/10.1016/0031-9422(92)80483-U
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aS,5bR,7aS,9S,11aR,11bS,13aS,13bR)-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 162955626 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/10.1016/0031-9422(92)80483-U
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/10.1016/0031-9422(92)80483-U
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/10.1016/0031-9422(92)80483-U
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(92)80483-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/10.1016/0031-9422(92)80483-U
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-Methoxy-4-(7-methoxy-3-methyl-5-prop-1-enyl-1-benzofuran-2-yl)phenol 71437692 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(=C2C)C3=CC(=C(C=C3)O)OC 324.40 unknown https://doi.org/10.1016/0031-9422(92)80483-U
Eupomatenoid-7 10314175 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(=C2C)C3=CC(=C(C=C3)O)OC 324.40 unknown https://doi.org/10.1016/0031-9422(92)80483-U
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Azaleatin 5281604 Click to see COC1=CC(=CC2=C1C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)O)O 316.26 unknown https://doi.org/10.1016/0031-9422(92)80483-U
Fisetin 5281614 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 286.24 unknown https://doi.org/10.1016/0031-9422(92)80483-U
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown https://doi.org/10.1016/0031-9422(92)80483-U
Fisetin 3-methyl ether 9839293 Click to see COC1=C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)O 300.26 unknown https://doi.org/10.1016/0031-9422(92)80483-U
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 11602329 Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC 328.27 unknown https://doi.org/10.1016/0031-9422(92)80483-U
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1016/0031-9422(92)80483-U
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1016/0031-9422(92)80483-U
> Phenylpropanoids and polyketides / Stilbenes
4-[2-(3,5-Dihydroxyphenyl)ethenyl]benzene-1,2-diol 4813 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown https://doi.org/10.1016/0031-9422(92)80483-U
Piceatannol 667639 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown https://doi.org/10.1016/0031-9422(92)80483-U

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