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Senna garrettiana

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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 UUID643fd9a3a0f55166834549
Scientific name Senna garrettiana
Authority (Craib) H.S.Irwin & Barneby
First published in Mem. New York Bot. Gard.35: 98 (1982)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cassia garrettiana Craib Bull. Misc. Inform. Kew1912: 151 (1912)

Common names Top

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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-0000186550
KEW urn:lsid:ipni.org:names:911339-1
The Plant List ild-33023
Open Tree Of Life 741093
NCBI Taxonomy 756587
IPNI 911339-1
GBIF 2958015
EOL 644016

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)!
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Title Authors Publication Released IDs
The Inhibitory Effect of KerraTM, KSTM, and MinozaTM on Human Papillomavirus Infection and Cervical Cancer Choowongkomon K, Choengpanya K, Pientong C, Ekalaksananan T, Talawat S, Srathong P, Chuerduangphui J Medicina (Kaunas) 14-Dec-2023
PMCID:PMC10745032
doi:10.3390/medicina59122169
PMID:38138272
Analytical determination, antioxidant and anti-inflammatory activities of Bhamrung-Lohit a traditional Thai medicine Panchakul C, Thongdeeying P, Itharat A, Pipatrattanaseree W, Kongkwamcharoen C, Davies NM Res Pharm Sci 01-Jun-2023
PMCID:PMC10443669
doi:10.4103/1735-5362.378091
PMID:37614616
Allelopathic Potential of Marsdenia tenacissima (Roxb.) Moon against Four Test Plants and the Biological Activity of Its Allelopathic Novel Compound, 8-Dehydroxy-11β-O-Acetyl-12β-O-Tigloyl-17β-Marsdenin Moh SM, Kurisawa N, Suenaga K, Kato-Noguchi H Plants (Basel) 15-Apr-2023
PMCID:PMC10142190
doi:10.3390/plants12081663
PMID:37111887
Isolation and Identification of Plant-Growth Inhibitory Constituents from Polygonum chinense Linn and Evaluation of Their Bioherbicidal Potential Lun TL, Iwasaki A, Suenaga K, Kato-Noguchi H Plants (Basel) 06-Apr-2023
PMCID:PMC10096564
doi:10.3390/plants12071577
PMID:37050203
Antiviral Potential of Plants against COVID-19 during Outbreaks—An Update Jamal QM Int J Mol Sci 05-Nov-2022
PMCID:PMC9655040
doi:10.3390/ijms232113564
PMID:36362351
Effect of Yakae-Prajamduen-Jamod Traditional Thai Remedy on Cognitive Impairment in an Ovariectomized Mouse Model and Its Mechanism of Action Daodee S, Monthakantirat O, Tantipongpiradet A, Maneenet J, Chotritthirong Y, Boonyarat C, Khamphukdee C, Kwankhao P, Pitiporn S, Awale S, Matsumoto K, Chulikhit Y Molecules 05-Jul-2022
PMCID:PMC9267962
doi:10.3390/molecules27134310
PMID:35807554
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
Drug-Herb Interactions among Thai Herbs and Anticancer Drugs: A Scoping Review Jiso A, Khemawoot P, Techapichetvanich P, Soopairin S, Phoemsap K, Damrongsakul P, Wongwiwatthananukit S, Vivithanaporn P Pharmaceuticals (Basel) 26-Jan-2022
PMCID:PMC8880589
doi:10.3390/ph15020146
PMID:35215264
Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J Int J Mol Sci 14-May-2018
PMCID:PMC5983620
doi:10.3390/ijms19051459
PMID:29757986
Various Biological Activities of DHA Derivatives Archi Sharma Elsevier 02-Sep-2017
doi:10.1016/B978-0-08-101926-9.00005-5
Identification of a new plant extract for androgenic alopecia treatment using a non-radioactive human hair dermal papilla cell-based assay Jain R, Monthakantirat O, Tengamnuay P, De-Eknamkul W BMC Complement Altern Med 21-Jan-2016
PMCID:PMC4721057
doi:10.1186/s12906-016-1004-5
PMID:26796631
Chemical studies on the heartwood of Cassia garrettiana Craib. III. Structures of two new polyphenolic compounds. KIMIYE BABA, KAORU MAEDA, YUKO TABATA, MITSUNOBU DOI, MITSUGI KOZAWA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.36.2977
Structure of a new polyphenol from Cassia garrettiana Craib. Kimiye Baba, Yuko Tabata, Kaoru Maeda, Mitsunobu Doi, Mitsugi Kozawa Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.34.4418
Chemical studies on the heartwood of Cassia garrettiana Craib. II. Nonanthraquinonic constituents. KIYOSHI HATA, KIMIYE BABA, MITSUGI KOZAWA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.27.984
Stilbenoids from Cassia garrettiana Kimiye Baba, Tadashi Kido, Masahiko Taniguchi, Mitsugi Kozawaqa Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)89752-6

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 / Dibenzocycloheptenes
(1R,15S)-15-(3,4-dihydroxyphenyl)pentacyclo[11.8.1.03,8.09,22.016,21]docosa-3(8),4,6,9,11,13(22),16,18,20-nonaene-5,7,11,18,19-pentol 163028832 Click to see C1C(C2=CC(=C(C=C2C3CC4=C(C5=CC(=CC1=C35)O)C(=CC(=C4)O)O)O)O)C6=CC(=C(C=C6)O)O 470.50 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
(1S,15R)-15-(3,4-dihydroxyphenyl)pentacyclo[11.8.1.03,8.09,22.016,21]docosa-3(8),4,6,9,11,13(22),16,18,20-nonaene-5,7,11,18,19-pentol 163028831 Click to see C1C(C2=CC(=C(C=C2C3CC4=C(C5=CC(=CC1=C35)O)C(=CC(=C4)O)O)O)O)C6=CC(=C(C=C6)O)O 470.50 unknown https://doi.org/10.1016/0031-9422(92)83478-H
(1S,9R)-pentacyclo[7.6.6.02,7.010,15.016,21]henicosa-2(7),3,5,10(15),11,13,16,18,20-nonaene-3,5,11,13,18,19-hexol 162858154 Click to see C1C2C3=CC(=C(C=C3C(C4=C2C(=CC(=C4)O)O)C5=C1C=C(C=C5O)O)O)O 364.30 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
(2R,10S)-10-(3,4-dihydroxyphenyl)-2-[(3,5-dihydroxyphenyl)methyl]tricyclo[9.4.0.03,8]pentadeca-1(15),3(8),4,6,11,13-hexaene-4,6,13,14-tetrol 21636145 Click to see C1C(C2=CC(=C(C=C2C(C3=C1C=C(C=C3O)O)CC4=CC(=CC(=C4)O)O)O)O)C5=CC(=C(C=C5)O)O 488.50 unknown https://doi.org/10.1248/CPB.27.984
(2S,10S)-10-(3,4-dihydroxyphenyl)-2-[(3,5-dihydroxyphenyl)methyl]tricyclo[9.4.0.03,8]pentadeca-1(15),3(8),4,6,11,13-hexaene-4,6,13,14-tetrol 163042642 Click to see C1C(C2=CC(=C(C=C2C(C3=C1C=C(C=C3O)O)CC4=CC(=CC(=C4)O)O)O)O)C5=CC(=C(C=C5)O)O 488.50 unknown https://doi.org/10.1248/CPB.36.2977
https://doi.org/10.1248/CPB.34.4418
https://doi.org/10.1016/S0031-9422(00)89752-6
15-(3,4-Dihydroxyphenyl)pentacyclo[11.8.1.03,8.09,22.016,21]docosa-3(8),4,6,9,11,13(22),16,18,20-nonaene-5,7,11,18,19-pentol 163028829 Click to see C1C(C2=CC(=C(C=C2C3CC4=C(C5=CC(=CC1=C35)O)C(=CC(=C4)O)O)O)O)C6=CC(=C(C=C6)O)O 470.50 unknown https://doi.org/10.1016/0031-9422(92)83478-H
https://doi.org/10.1016/S0031-9422(00)89752-6
Cassigarol A 129314 Click to see C1C(C2=CC(=C(C=C2C(C3=C1C=C(C=C3O)O)CC4=CC(=CC(=C4)O)O)O)O)C5=CC(=C(C=C5)O)O 488.50 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
https://doi.org/10.1016/0031-9422(92)83478-H
https://doi.org/10.1248/CPB.34.4418
https://doi.org/10.1248/CPB.36.2977
https://doi.org/10.1016/0006-2952(92)90034-G
Pentacyclo[7.6.6.02,7.010,15.016,21]henicosa-2(7),3,5,10,12,14,16(21),17,19-nonaene-3,5,12,13,17,19-hexol 101631690 Click to see C1C2C3=CC(=C(C=C3C(C4=C1C=C(C=C4O)O)C5=C2C=C(C=C5O)O)O)O 364.30 unknown https://doi.org/10.1248/CPB.36.2977
https://doi.org/10.1016/0031-9422(92)83478-H
Pentacyclo[7.6.6.02,7.010,15.016,21]henicosa-2(7),3,5,10(15),11,13,16,18,20-nonaene-3,5,11,13,18,19-hexol 14188663 Click to see C1C2C3=CC(=C(C=C3C(C4=C2C(=CC(=C4)O)O)C5=C1C=C(C=C5O)O)O)O 364.30 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
9,10-Dihydro-2,3,5,7-Phenanthrenetetrol 22753774 Click to see C1CC2=C(C3=CC(=C(C=C31)O)O)C(=CC(=C2)O)O 244.24 unknown https://doi.org/10.1248/CPB.27.984
> Lignans, neolignans and related compounds / Stilbenolignans
[2-acetyloxy-4-[(2R,3R)-2-(3,5-diacetyloxyphenyl)-6-[(E)-2-(3,5-diacetyloxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-3-yl]phenyl] acetate 46226511 Click to see CC(=O)OC1=C(C=C(C=C1)C2C(OC3=C(O2)C=C(C=C3)C=CC4=CC(=CC(=C4)OC(=O)C)OC(=O)C)C5=CC(=CC(=C5)OC(=O)C)OC(=O)C)OC(=O)C 738.70 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
[2-Acetyloxy-4-[2-(3,5-diacetyloxyphenyl)-6-[2-(3,5-diacetyloxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-3-yl]phenyl] acetate 75178414 Click to see CC(=O)OC1=C(C=C(C=C1)C2C(OC3=C(O2)C=C(C=C3)C=CC4=CC(=CC(=C4)OC(=O)C)OC(=O)C)C5=CC(=CC(=C5)OC(=O)C)OC(=O)C)OC(=O)C 738.70 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
[3-acetyloxy-5-[(E)-2-[(8bS,14aS)-2,4,6,7-tetraacetyloxy-8b,14a-dihydrophenanthro[9,10-b][1,4]benzodioxin-11-yl]ethenyl]phenyl] acetate 163185658 Click to see CC(=O)OC1=CC(=CC(=C1)C=CC2=CC3=C(C=C2)OC4C(O3)C5=CC(=C(C=C5C6=C4C=C(C=C6OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 736.70 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
[3-Acetyloxy-5-[2-(2,4,6,7-tetraacetyloxy-8b,14a-dihydrophenanthro[9,10-b][1,4]benzodioxin-11-yl)ethenyl]phenyl] acetate 163018903 Click to see CC(=O)OC1=CC(=CC(=C1)C=CC2=CC3=C(C=C2)OC4C(O3)C5=CC(=C(C=C5C6=C4C=C(C=C6OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 736.70 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
4-[(2R,3R)-2-(3,5-dihydroxyphenyl)-6-[(Z)-2-(3,5-dihydroxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-3-yl]benzene-1,2-diol 5315730 Click to see C1=CC2=C(C=C1C=CC3=CC(=CC(=C3)O)O)OC(C(O2)C4=CC(=CC(=C4)O)O)C5=CC(=C(C=C5)O)O 486.50 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
cassigarol E 5315729 Click to see C1=CC2=C(C=C1C=CC3=CC(=CC(=C3)O)O)OC(C(O2)C4=CC(=CC(=C4)O)O)C5=CC(=C(C=C5)O)O 486.50 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
Cassigarol G 10005549 Click to see C1=CC2=C(C=C1C=CC3=CC(=CC(=C3)O)O)OC4C(O2)C5=C(C6=CC(=C(C=C46)O)O)C(=CC(=C5)O)O 484.50 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
[(2S,3S,5R,7S,8R,9R)-2-[(1R,3R,4R,5S,6S,7E,9Z,11E,13E)-14-cyano-3,5-dihydroxy-1-methoxy-4,6,8,9,13-pentamethyltetradeca-7,9,11,13-tetraenyl]-9-[(E)-3-[2-[(2R,4S)-4-[[(2R,3R,4R)-4-(dimethylamino)-2,3-dihydroxy-5-methoxypentanoyl]amino]pentan-2-yl]-1,3-oxazol-4-yl]prop-2-enyl]-7-hydroxy-4,4,8-trimethyl-1,10-dioxaspiro[4.5]decan-3-yl] dihydrogen phosphate 21726439 Click to see CC1C(CC2(C(C(C(O2)C(CC(C(C)C(C(C)C=C(C)C(=CC=CC(=CC#N)C)C)O)O)OC)OP(=O)(O)O)(C)C)OC1CC=CC3=COC(=N3)C(C)CC(C)NC(=O)C(C(C(COC)N(C)C)O)O)O 1023.20 unknown https://doi.org/10.1248/CPB.27.984
> Organoheterocyclic compounds / Naphthofurans
Arbusclin D 3035762 Click to see CC12CCCC(C1C3C(=C(C(=O)O3)CO)CC2)(C)O 266.33 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R,3R)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2,3-dihydronaphtho[2,1-e][1]benzofuran-7,8,10-triol 101631691 Click to see C1=CC(=C(C=C1C2C(C3=C(O2)C=C(C4=C3C=CC5=CC(=C(C=C54)O)O)O)C6=CC(=CC(=C6)O)O)O)O 484.50 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
https://doi.org/10.1016/0031-9422(92)83478-H
[2-acetyloxy-4-[(E)-2-[(2S,3S)-6-acetyloxy-2-(3,4-diacetyloxyphenyl)-3-(3,5-diacetyloxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]ethenyl]phenyl] acetate 21770601 Click to see CC(=O)OC1=C(C=C(C=C1)C=CC2=C3C(C(OC3=CC(=C2)OC(=O)C)C4=CC(=C(C=C4)OC(=O)C)OC(=O)C)C5=CC(=CC(=C5)OC(=O)C)OC(=O)C)OC(=O)C 780.70 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
2-(3,4-Dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2,3-dihydronaphtho[2,1-e][1]benzofuran-7,8,10-triol 162898483 Click to see C1=CC(=C(C=C1C2C(C3=C(O2)C=C(C4=C3C=CC5=CC(=C(C=C54)O)O)O)C6=CC(=CC(=C6)O)O)O)O 484.50 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
https://doi.org/10.1016/0031-9422(92)83478-H
Scirpusin B 5458999 Click to see C1=CC(=C(C=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O)O 486.50 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
> Phenylpropanoids and polyketides / Stilbenes
1,2-Bis(3-hydroxyphenyl)ethane 4535180 Click to see C1=CC(=CC(=C1)O)CCC2=CC(=CC=C2)O 214.26 unknown https://doi.org/10.1248/CPB.27.984
3,3',4-Trihydroxybibenzyl 85975989 Click to see C1=CC(=CC(=C1)O)CCC2=CC(=C(C=C2)O)O 230.26 unknown https://doi.org/10.1248/CPB.27.984
3,3',4,5'-Tetrahydroxybibenzyl 152444 Click to see C1=CC(=C(C=C1CCC2=CC(=CC(=C2)O)O)O)O 246.26 unknown https://doi.org/10.1248/CPB.27.984
https://doi.org/10.1248/CPB.39.3353
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/10.1248/CPB.39.3353
Piceatannol 667639 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown https://doi.org/10.1248/YAKUSHI1947.104.7_819
https://doi.org/10.1016/0006-2952(92)90096-2
https://doi.org/10.1016/B978-0-08-101926-9.00005-5
https://doi.org/10.1248/CPB.27.984
https://doi.org/10.1248/CPB.39.3353
https://doi.org/10.1248/CPB.32.213

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