Hoslundia opposita - Unknown
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Details Top

Internal ID UUID643fdf4293008305584739
Scientific name Hoslundia opposita
Authority Vahl
First published in Enum. Pl. Obs. 1: 212 (1804)

Description Top

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Synonyms Top

Scientific name Authority First published in
Hoslundia decumbens Benth. Prodr. 12: 54 (1848)
Hoslundia oppositifolia P.Beauv. Fl. Oware 1: 53 (1806)
Hoslundia verticillata Vahl Enum. Pl. Obs. 1: 213 (1804)
Micranthes menthoides Bertol. Mem. Acc. Sc. Bolog. ix. (1858) 172; (Misc. Bot. xix. 8. t. 4).
Orthosiphon physocalycinus A.Rich. Tent. Fl. Abyss. 2: 180 (1850)
Premna longipes Baker Fl. Trop. Afr. 5: 288 (1900)
Clerodendrum micranthum Gilli Ann. Naturhist. Mus. Wien 77: 29 (1973)
Hoslundia opposita var. verticillata (Vahl) Baker Fl. Trop. Afr. 5: 377. 1900
Hoslundia opposita var. decumbens (Benth.) Baker Fl. Trop. Afr. 5: 377. 1900

Common names Top

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Language Common/alternative name
Bambara sukolan
Sango nzôlogê

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Caprivi Strip
      • Kwazulu-Natal
      • Namibia
      • Northern Provinces
      • Swaziland
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Niger
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Madagascar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000215083
Tropicos 17602845
KEW urn:lsid:ipni.org:names:447886-1
The Plant List kew-100248
Open Tree Of Life 707364
NCBI Taxonomy 204228
IPNI 447886-1
iNaturalist 340372
GBIF 3884477
EPPO HSLOP
EOL 5380680
USDA GRIN 407622

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
Medicinal plants used for cutaneous wound healing in Uganda; ethnomedicinal reports and pharmacological evidences Gang R, Okello D, Kang Y Heliyon 16-Apr-2024
PMCID:PMC11058731
doi:10.1016/j.heliyon.2024.e29717
PMID:38694090
Evaluation of packaging, labels, and some physicochemical properties of herbal antimalarial products on the Ghanaian market Amekyeh H, Kumadoh D, Adongo DW, Orman E, Abubakar S, Dwamena A, Aggrey MO Heliyon 28-Feb-2024
PMCID:PMC10920373
doi:10.1016/j.heliyon.2024.e27032
PMID:38463810
Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review Islam Shawon S, Nargis Reyda R, Qais N Heliyon 01-Feb-2024
PMCID:PMC10864916
doi:10.1016/j.heliyon.2024.e25340
PMID:38356556
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
Lived experiences and drivers of induced abortion among women in central Uganda Kibira SP, Stillman M, Makumbi FE, Giorgio M, Nabukeera S, Nalwoga GK, Sully EA PLOS Glob Public Health 06-Dec-2023
PMCID:PMC10699625
doi:10.1371/journal.pgph.0002236
PMID:38055682
Ethnobotanical, Phytochemical, and Pharmacological Properties of the Subfamily Nepetoideae (Lamiaceae) in Inflammatory Diseases Ortiz-Mendoza N, Martínez-Gordillo MJ, Martínez-Ambriz E, Basurto-Peña FA, González-Trujano ME, Aguirre-Hernández E Plants (Basel) 02-Nov-2023
PMCID:PMC10648697
doi:10.3390/plants12213752
PMID:37960108
Medicinal plants of the upper Aswa River catchment of northern Uganda - a cultural crossroads Masters ET J Ethnobiol Ethnomed 27-Oct-2023
PMCID:PMC10605377
doi:10.1186/s13002-023-00620-5
PMID:37884931
Potential of medicinal plants as antimalarial agents: a review of work done at Kenya Medical Research Institute Irungu B, Okari E, Nyangi M, Njeru S, Koech L Front Pharmacol 20-Oct-2023
PMCID:PMC10623325
doi:10.3389/fphar.2023.1268924
PMID:37927601
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
Ethnobotanical study of nutraceutical plants used to manage opportunistic infections associated with HIV/AIDS in Acholi sub-region, Northern Uganda Ikinyom N, Lamwaka AV, Malagala AT, Ndyomugyenyi EK Trop Med Health 01-Sep-2023
PMCID:PMC10472741
doi:10.1186/s41182-023-00540-w
PMID:37658427
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
Ocular complications and associated factors among traditional eye medicines users attending the eye clinic at Mulago national referral hospital, Uganda Msonge F, Clare LR, Musika AA, Atukunda I, Otike C, Paul J, Nagawa E, Headcraph E, Nakiyingi L, Yancey CM, John A, Otiti-Sengeri J Afr Health Sci 01-Jun-2023
PMCID:PMC10782305
doi:10.4314/ahs.v23i2.53
PMID:38223586
A review of efficacy and safety of Ugandan anti-malarial plants with application of RITAM score Angupale JR, Tusiimire J, Ngwuluka NC Malar J 17-Mar-2023
PMCID:PMC10021060
doi:10.1186/s12936-023-04486-6
PMID:36932389
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
Potentially harmful medication use and the associated factors among pregnant women visiting antenatal care clinics in Mbarara Regional Referral Hospital, Southwestern Uganda Isiiko J, Kiptoo J, Yadesa TM, Mwandah DC, Alinaiswe R, Ngonzi J, Alele PE J Clin Transl Res 28-Dec-2022
PMCID:PMC9844225
doi:10.18053/jctres.09.202301.004
PMID:36687297

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 / Diterpenoids
(1,1-dimethyl-5,6-dioxo-7-propan-2-yl-3,10a-dihydro-2H-phenanthren-2-yl) benzoate 162897787 Click to see CC(C)C1=CC2=C(C3=CCC(C(C3C=C2)(C)C)OC(=O)C4=CC=CC=C4)C(=O)C1=O 402.50 unknown https://doi.org/10.1016/S0031-9422(00)97526-5
(5-hydroxy-1,1,4a-trimethyl-6-oxo-7-propan-2-yl-3,4-dihydro-2H-phenanthren-2-yl) 3-phenylprop-2-enoate 85103381 Click to see CC(C)C1=CC2=CC=C3C(C(CCC3(C2=C(C1=O)O)C)OC(=O)C=CC4=CC=CC=C4)(C)C 444.60 unknown https://doi.org/10.1016/S0031-9422(00)97526-5
(5-hydroxy-1,1,4a-trimethyl-6-oxo-7-propan-2-yl-3,4-dihydro-2H-phenanthren-2-yl) benzoate 85153781 Click to see CC(C)C1=CC2=CC=C3C(C(CCC3(C2=C(C1=O)O)C)OC(=O)C4=CC=CC=C4)(C)C 418.50 unknown https://doi.org/10.1016/S0031-9422(00)97526-5
(6-Hydroxy-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-2-yl) benzoate 163003722 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)C)OC(=O)C4=CC=CC=C4)C)O 406.60 unknown https://doi.org/10.1016/S0031-9422(00)97526-5
[(2S,10aR)-1,1-dimethyl-5,6-dioxo-7-propan-2-yl-3,10a-dihydro-2H-phenanthren-2-yl] benzoate 162897788 Click to see CC(C)C1=CC2=C(C3=CCC(C(C3C=C2)(C)C)OC(=O)C4=CC=CC=C4)C(=O)C1=O 402.50 unknown https://doi.org/10.1016/S0031-9422(00)97526-5
[(2S,4aS,10aR)-6-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-2-yl] benzoate 101635422 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)C)OC(=O)C4=CC=CC=C4)C)O 406.60 unknown https://doi.org/10.1016/S0031-9422(00)97526-5
[(2S,4aS)-5-hydroxy-1,1,4a-trimethyl-6-oxo-7-propan-2-yl-3,4-dihydro-2H-phenanthren-2-yl] (E)-3-phenylprop-2-enoate 10049125 Click to see CC(C)C1=CC2=CC=C3C(C(CCC3(C2=C(C1=O)O)C)OC(=O)C=CC4=CC=CC=C4)(C)C 444.60 unknown https://doi.org/10.1016/S0031-9422(00)97526-5
[(2S,4aS)-5-hydroxy-1,1,4a-trimethyl-6-oxo-7-propan-2-yl-3,4-dihydro-2H-phenanthren-2-yl] benzoate 10477133 Click to see CC(C)C1=CC2=CC=C3C(C(CCC3(C2=C(C1=O)O)C)OC(=O)C4=CC=CC=C4)(C)C 418.50 unknown https://doi.org/10.1016/S0031-9422(00)97526-5
> 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/10.1055/S-2006-962206
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1055/S-2006-962206
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-962206
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-962206
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
2-Epitormentic acid 490364 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1021/NP50115A014
2alpha,3alpha,19 alpha-Trihydroxyurs-12-en-28-oic acid 73645 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1021/NP50115A014
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)95112-4
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)95112-4
Euscaphic Acid 471426 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1021/NP50115A014
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1021/NP50115A014
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1021/NP50115A014
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/S0031-9422(00)95112-4
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/S0031-9422(00)95112-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,5S,9S,10S,13R,17R)-17-[(2R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol 91746710 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C 416.70 unknown https://doi.org/10.1016/S0031-9422(00)95112-4
(3S,6R)-6-[(8R,9S,10S,13R,14S,17R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-3-propan-2-ylheptan-1-ol 56924079 Click to see CC(C)C(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCCC4)C)C)CCO 416.70 unknown https://doi.org/10.1016/S0031-9422(00)95112-4
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/10.1016/S0031-9422(00)95112-4
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)95112-4
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/S0031-9422(00)95112-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
6-(4,5-Dihydroxy-6-methyloxan-2-yl)-5-hydroxy-7-methoxy-2-phenylchromen-4-one 74977419 Click to see CC1C(C(CC(O1)C2=C(C=C3C(=C2O)C(=O)C=C(O3)C4=CC=CC=C4)OC)O)O 398.40 unknown https://doi.org/10.1016/S0040-4020(01)80869-3
6-[(2R,4S,5S,6R)-4,5-dihydroxy-6-methyloxan-2-yl]-5-hydroxy-7-methoxy-2-phenylchromen-4-one 15726098 Click to see CC1C(C(CC(O1)C2=C(C=C3C(=C2O)C(=O)C=C(O3)C4=CC=CC=C4)OC)O)O 398.40 unknown https://doi.org/10.1016/S0040-4020(01)80869-3
Hoslunddiol 44257619 Click to see CC1C(C(CC(O1)C2=C(C=C3C(=C2O)C(=O)C=C(O3)C4=CC=CC=C4)OC)O)O 398.40 unknown https://doi.org/10.1016/S0031-9422(00)95112-4
https://doi.org/10.1016/S0040-4020(01)80869-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-O-Methylhoslundin 15726099 Click to see CC1=C(C(=O)C(=CO1)C2=C(C=C3C(=C2OC)C(=O)C=C(O3)C4=CC=CC=C4)OC)OC 420.40 unknown https://doi.org/10.1021/NP50115A014
https://doi.org/10.1016/S0031-9422(00)95112-4
Hosloppin 44257646 Click to see CC1=C(C(=O)C(=CO1)C2=C(C=C3C(=C2O)C(=O)C=C(O3)C4=CC=CC=C4)OC)O 392.40 unknown https://doi.org/10.1021/NP50115A014
Hoslundal 15726097 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O)CC=O 310.30 unknown https://doi.org/10.1016/S0040-4020(01)80869-3
Hoslundin 15726096 Click to see CC1=C(C(=O)C(=CO1)C2=C(C=C3C(=C2O)C(=O)C=C(O3)C4=CC=CC=C4)OC)OC 406.40 unknown https://doi.org/10.1021/NP50115A014
https://doi.org/10.1016/S0031-9422(00)95112-4
https://doi.org/10.1016/S0040-4020(01)80869-3
Oppositin 10477206 Click to see CC1=C(C(=O)C=C(O1)C2=C(C=C3C(=C2OC)C(=O)C=C(O3)C4=CC=CC=C4)OC)OC 420.40 unknown https://doi.org/10.1016/S0031-9422(00)95112-4
Tectochrysin 5281954 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O 268.26 unknown https://doi.org/10.1016/S0031-9422(00)95112-4

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