Cassia abbreviata - Unknown
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Internal ID UUID643fdf35c5cdb225519376
Scientific name Cassia abbreviata
Authority Oliv.
First published in Fl. Trop. Afr.2: 271 (1871)

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English long-pod-cassia
Afrikaans sambokpeul

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Cassia abbreviata subsp. abbreviata Oliv. Unknown
Cassia abbreviata subsp. beareana (Holmes) Brenan Kew Bull.13: 232 (1958)
Cassia abbreviata subsp. kassneri (Baker f.) Brenan Kew Bull.13: 234 (1958)

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
    • Northeast Tropical Africa
      • Somalia
    • South Tropical Africa
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Caprivi Strip
      • Namibia
      • Northern Provinces
      • Swaziland
    • West-central Tropical Africa
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000214576
USDA Plants CAAB13
Tropicos 13027825
KEW urn:lsid:ipni.org:names:484036-1
The Plant List ild-972
Open Tree Of Life 499473
NCBI Taxonomy 992663
IUCN Red List 158023
IPNI 484036-1
iNaturalist 147000
GBIF 5357073
Freebase /m/0bh8z94
EOL 703799
USDA GRIN 300111
Wikipedia Cassia_abbreviata

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 comprehensive review of antimalarial medicinal plants used by Tanzanians Kacholi DS Pharm Biol 25-Jan-2024
PMCID:PMC10812860
doi:10.1080/13880209.2024.2305453
PMID:38270178
Pharmacology of bioactive compounds from plant extracts for improving non-alcoholic fatty liver disease through endoplasmic reticulum stress modulation: A comprehensive review Huang L, Tan L, Lv Z, Chen W, Wu J Heliyon 23-Jan-2024
PMCID:PMC10844061
doi:10.1016/j.heliyon.2024.e25053
PMID:38322838
Screening of the key response component groups and mechanism verification of Huangqi-Guizhi-Wuwu-Decoction in treating rheumatoid arthritis based on a novel computational pharmacological model Liu Q, Luo Q, Fan Q, Li Y, Lu A, Guan D BMC Complement Med Ther 02-Jan-2024
PMCID:PMC10759359
doi:10.1186/s12906-023-04315-y
PMID:38166916
Medicinal plants for treatment of diarrhoeal diseases among under-five children: experience from traditional healers in North-eastern Tanzania Liheluka E, Gibore NS, Lusingu JP, Gesase S, Minja DT, Lamshöft M, Dekker D, Bali T BMC Complement Med Ther 25-Oct-2023
PMCID:PMC10601235
doi:10.1186/s12906-023-04216-0
PMID:37880735
Potential of Selected African Medicinal Plants as Alternative Therapeutics against Multi-Drug-Resistant Bacteria Moiketsi BN, Makale KP, Rantong G, Rahube TO, Makhzoum A Biomedicines 22-Sep-2023
PMCID:PMC10604549
doi:10.3390/biomedicines11102605
PMID:37892979
Medicinal Plants Used in the Management of Sexual Dysfunction, Infertility and Improving Virility in the East African Community: A Systematic Review Kyarimpa C, Nagawa CB, Omara T, Odongo S, Ssebugere P, Lugasi SO, Gumula I Evid Based Complement Alternat Med 12-Aug-2023
PMCID:PMC10439835
doi:10.1155/2023/6878852
PMID:37600549
Dracocephalum jacutense Peschkova from Yakutia: Extraction and Mass Spectrometric Characterization of 128 Chemical Compounds Okhlopkova ZM, Razgonova MP, Rozhina ZG, Egorova PS, Golokhvast KS Molecules 28-May-2023
PMCID:PMC10254129
doi:10.3390/molecules28114402
PMID:37298879
An insight into novel therapeutic potentials of taxifolin Liu Y, Shi X, Tian Y, Zhai S, Liu Y, Xiong Z, Chu S Front Pharmacol 12-May-2023
PMCID:PMC10227600
doi:10.3389/fphar.2023.1173855
PMID:37261284
A clinical experience-based Chinese herbal formula improves ethanol-induced drunken behavior and hepatic steatohepatitis in mice models Gao H, Li Z, Liu Y, Zhao YK, Cheng C, Qiu F, Gao Y, Lu YW, Song XH, Wang JB, Ma ZT Chin Med 01-May-2023
PMCID:PMC10150545
doi:10.1186/s13020-023-00753-5
PMID:37127639
Medicinal Uses of the Fabaceae Family in Zimbabwe: A Review Maroyi A Plants (Basel) 10-Mar-2023
PMCID:PMC10051751
doi:10.3390/plants12061255
PMID:36986943
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Smallholders’ knowledge about healing goat gastrointestinal parasite infections with wild plants in southern DR Congo Mavungu GN, Mutombo CS, Numbi DM, Nsenga SN, Muyumba WN, Pongombo CS, Bakari SA, Nachtergael A, Vandenput S, Okombe VE, Duez P Front Pharmacol 01-Mar-2023
PMCID:PMC10016610
doi:10.3389/fphar.2023.1124267
PMID:36937835
Effects of Vegetal Extracts and Metabolites against Oxidative Stress and Associated Diseases: Studies in Caenorhabditis elegans Hernández-Cruz EY, Eugenio-Pérez D, Ramírez-Magaña KJ, Pedraza-Chaverri J ACS Omega 27-Feb-2023
PMCID:PMC10018526
doi:10.1021/acsomega.2c07025
PMID:36936291
A systematic analysis of anti-diabetic medicinal plants from cells to clinical trials Omale S, Amagon KI, Johnson TO, Bremner SK, Gould GW PeerJ 05-Jan-2023
PMCID:PMC9826616
doi:10.7717/peerj.14639
PMID:36627919
An Inventory of South African Medicinal Plants Used in the Management of Sexually Transmitted and Related Opportunistic Infections: An Appraisal and Some Scientific Evidence (1990–2020) Mongalo NI, Raletsena MV Plants (Basel) 25-Nov-2022
PMCID:PMC9738887
doi:10.3390/plants11233241
PMID:36501281

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
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3R)-8-[(2R,3S,4R)-3,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 14353356 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 546.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
(2R,3R)-8-[(2R,3S,4R)-3,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 15297954 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC=C(C=C5)O)O)O)O)C6=CC=C(C=C6)O)O 530.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
(2R,3R)-8-[(2S,3R,4R)-3,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 14353357 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 546.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
(2R,3S)-6-[(2R,3S,4S)-3,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 15297961 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C3C=CC(=C4)O)C5=CC=C(C=C5)O)O)O)C6=CC=C(C=C6)O)O 530.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
(2R,3S)-8-[(2R,3S,4R)-3,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 15297952 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC=C(C=C5)O)O)O)O)C6=CC=C(C=C6)O)O 530.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
(2R,3S)-8-[(2R,3S,4S)-3,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 14353355 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 546.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
(2R,3S)-8-[(2R,3S,4S)-3,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 15297951 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC=C(C=C5)O)O)O)O)C6=CC=C(C=C6)O)O 530.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
6-[3,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 163043538 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C3C=CC(=C4)O)C5=CC=C(C=C5)O)O)O)C6=CC=C(C=C6)O)O 530.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
8-[3,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 14353358 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 546.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
8-[3,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 162848705 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC=C(C=C5)O)O)O)O)C6=CC=C(C=C6)O)O 530.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
Guibourtinidol-(4a inverted question mark8)-epiafzelechin 15297953 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC=C(C=C5)O)O)O)O)C6=CC=C(C=C6)O)O 530.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
(2R,4R)-2-(4-hydroxyphenyl)-4-methoxy-3,4-dihydro-2H-chromen-7-ol 163023528 Click to see COC1CC(OC2=C1C=CC(=C2)O)C3=CC=C(C=C3)O 272.29 unknown https://doi.org/10.1016/S0031-9422(98)00218-0
(2S,4R)-2-(4-hydroxyphenyl)-4-methoxy-3,4-dihydro-2H-chromen-7-ol 100929631 Click to see COC1CC(OC2=C1C=CC(=C2)O)C3=CC=C(C=C3)O 272.29 unknown https://doi.org/10.1016/S0031-9422(98)00218-0
7,4'-Dihydroxy-4-methoxyflavan 129710702 Click to see COC1CC(OC2=C1C=CC(=C2)O)C3=CC=C(C=C3)O 272.29 unknown https://doi.org/10.1016/S0031-9422(98)00218-0

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