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Ammocharis tinneana

Ammocharis tinneana - 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 UUID644025281396b276869592
Scientific name Ammocharis tinneana
Authority (Kotschy & Peyr.) Milne-Redh. & Schweick.
First published in J. Linn. Soc., Bot. 52: 177 (1939)

Description Top

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Synonyms Top

Scientific name Authority First published in
Stenolirion elliotii Baker Hooker's Icon. Pl. 25: t. 2493 (1896)
Crinum ammocharoides Baker J. Bot. 16: 195 (1878)
Crinum bainesii Baker Gard. Chron. , n.s., 16: 39 (1881)
Crinum cordofanum Kotschy & Peyr. Pl. Tinn. : 14 (1867)
Crinum lastii Baker Handb. Amaryll. : 79 (1888)
Crinum ondongense Baker Bull. Herb. Boissier , sér. 2, 3: 666 (1903)
Crinum poggei Pax Bot. Jahrb. Syst. 15: 141 (1892)
Crinum rhodanthum Baker Fl. Trop. Afr. 7: 397 (1898)
Crinum thruppii Baker ex Oliv. Unkn. Horn of Afr. , App.: 322 (1888)
Crinum tinneae Kotschy & Peyr. Flora 51: 508 (1868)
Crinum tinneanum Kotschy & Peyr. Pl. Tinn. : 44 (1867)

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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No germination or propagation data was added yet.

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
      • Ethiopia
      • Somalia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Namibia
    • West-central Tropical Africa
      • Burundi
      • Central African Republic
      • Rwanda
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000759939
USDA Plants AMTI
Tropicos 1201038
KEW urn:lsid:ipni.org:names:63101-1
The Plant List kew-299011
Open Tree Of Life 439682
NCBI Taxonomy 414783
IPNI 63101-1
iNaturalist 514219
GBIF 5325622
EPPO AORTI
EOL 1085795

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
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
Chemical Characterization and Cytotoxic and Antioxidant Activity Evaluation of the Ethanol Extract from the Bulbs of Pancratium maritimun Collected in Sicily Cicio A, Sut S, Dall’Acqua S, Bruno M, Luparello C, Serio R, Zizzo MG Molecules 09-May-2023
PMCID:PMC10222022
doi:10.3390/molecules28103986
PMID:37241726
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
Plants Used in Antivenom Therapy in Rural Kenya: Ethnobotany and Future Perspectives Omara T J Toxicol 16-Jun-2020
PMCID:PMC7315313
doi:10.1155/2020/1828521
PMID:32612650
Medicinal plants species used by herbalists in the treatment of snakebite envenomation in Uganda Okot DF, Anywar G, Namukobe J, Byamukama R Trop Med Health 05-Jun-2020
PMCID:PMC7273665
doi:10.1186/s41182-020-00229-4
PMID:32518500
Medicinal Plants for the Treatment of Local Tissue Damage Induced by Snake Venoms: An Overview from Traditional Use to Pharmacological Evidence Félix-Silva J, Silva-Junior AA, Zucolotto SM, Fernandes-Pedrosa MD Evid Based Complement Alternat Med 21-Aug-2017
PMCID:PMC5585606
doi:10.1155/2017/5748256
PMID:28904556
Kenyan medicinal plants used as antivenin: a comparison of plant usage Owuor BO, Kisangau DP J Ethnobiol Ethnomed 01-Feb-2006
PMCID:PMC1409767
doi:10.1186/1746-4269-2-7
PMID:16451723
Alkaloids from Ammocharis tinneana A MACHOCHO, S CHHABRA, F VILADOMAT, C CODINA, J BASTIDA Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00118-1

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
> Alkaloids and derivatives / Amaryllidaceae alkaloids
5-Methoxy-9-azatetracyclo[7.6.1.02,7.012,16]hexadeca-2,4,6-triene-4,15-diol 162945003 Click to see COC1=C(C=C2C3C(CCC4C3N(CC4)CC2=C1)O)O 275.34 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(1R,13R,15R,16S,18R,19S)-9,15-dimethoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-trien-19-ol 162985204 Click to see COC1CC2C3(C(CN2CC4=C(C5=C(C=C43)OCO5)OC)O)C6C1O6 347.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
(1S,11R,13R,15R,16S,18R)-9-methoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-triene-11,15-diol 101036743 Click to see COC1=C2C(N3CCC4(C3CC(C5C4O5)O)C2=CC6=C1OCO6)O 333.30 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
(1S,13R,15R,16S,18R,19R)-9,15-dimethoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-trien-19-ol 5281171 Click to see COC1CC2C3(C(CN2CC4=C(C5=C(C=C43)OCO5)OC)O)C6C1O6 347.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
(3R)-7-Methoxy-1,2-didehydrocrinan-3-ol 627287 Click to see COC1=C2CN3CCC4(C3CC(C=C4)O)C2=CC5=C1OCO5 301.34 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
(9,15-Dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-yl) acetate 78180690 Click to see CC(=O)OC1CN2CC3=C(C4=C(C=C3C15C2CC(C=C5)OC)OCO4)OC 373.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
(9,15-Dimethoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-trien-19-yl) acetate 78180691 Click to see CC(=O)OC1CN2CC3=C(C4=C(C=C3C15C2CC(C6C5O6)OC)OCO4)OC 389.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
[(1R,13R,15R,18R)-9,15-dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-yl] acetate 101682301 Click to see CC(=O)OC1CN2CC3=C(C4=C(C=C3C15C2CC(C=C5)OC)OCO4)OC 373.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
[(1S,13R,15R,16S,18R,19R)-9,15-dimethoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-trien-19-yl] acetate 162845168 Click to see CC(=O)OC1CN2CC3=C(C4=C(C=C3C15C2CC(C6C5O6)OC)OCO4)OC 389.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
1,2-Didehydrocrinan-3-ol 101727 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
6-Hydroxyundulatine 545030 Click to see COC1CC2C3(CCN2C(C4=C(C5=C(C=C43)OCO5)OC)O)C6C1O6 347.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
6Alpha-Hydroxyundulatine 15479738 Click to see COC1CC2C3(CCN2C(C4=C(C5=C(C=C43)OCO5)OC)O)C6C1O6 347.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
9-Methoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-trien-15-ol 625708 Click to see COC1=C2CN3CCC4(C3CC(C5C4O5)O)C2=CC6=C1OCO6 317.34 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
9-Methoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-triene-11,15-diol 78180692 Click to see COC1=C2C(N3CCC4(C3CC(C5C4O5)O)C2=CC6=C1OCO6)O 333.30 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
9,15-Dimethoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-trien-19-ol 4480708 Click to see COC1CC2C3(C(CN2CC4=C(C5=C(C=C43)OCO5)OC)O)C6C1O6 347.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
9,15-Dimethoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-triene 271606 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C6C1O6 331.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Ambelline 25092366 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 331.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Amberline 494154 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 331.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Bulphanidine 407581 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C=C1 315.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Buphanidrine 338023 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C=C1 315.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Buphanisin 625225 Click to see COC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 285.34 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Buphanisine 12302149 Click to see COC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 285.34 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Crinamidine 399204 Click to see COC1=C2CN3CCC4(C3CC(C5C4O5)O)C2=CC6=C1OCO6 317.34 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Crinan-12-ol, 1,2-didehydro-3alpha,7-dimethoxy- 441585 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 331.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Crinan, 3alpha-methoxy- 625509 Click to see COC1CCC23CCN(C2C1)CC4=CC5=C(C=C34)OCO5 287.35 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Crinan,3,7-dimethoxy-,(3alpha- 629061 Click to see COC1CCC23CCN(C2C1)CC4=C(C5=C(C=C34)OCO5)OC 317.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Crinine 398937 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Flexinine 398936 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C6C5O6)O)OCO4 287.31 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Powelline 443669 Click to see COC1=C2CN3CCC4(C3CC(C=C4)O)C2=CC5=C1OCO5 301.34 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Powelline, 1,2-dihydro- 627523 Click to see COC1=C2CN3CCC4(C3CC(CC4)O)C2=CC5=C1OCO5 303.35 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Undulatin 3083985 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C6C1O6 331.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Lycorine 72378 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(4E,7E,10R)-5,9,9-trimethyl-11-oxabicyclo[8.2.1]trideca-1(13),4,7-triene-6,12-dione 92977572 Click to see CC1=CCCC2=CC(C(C=CC1=O)(C)C)OC2=O 246.30 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(5,14-Dihydroxy-4-methoxy-9-azatetracyclo[7.6.1.02,7.012,16]hexadeca-2,4,6,12-tetraen-15-yl) acetate 78172915 Click to see CC(=O)OC1C(C=C2CCN3C2C1C4=CC(=C(C=C4C3)O)OC)O 331.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Norpluviine 12313583 Click to see COC1=C(C=C2CN3CCC4=CCC(C(C43)C2=C1)O)O 273.33 unknown https://doi.org/10.1016/S0031-9422(99)00118-1
Sternbergine 178814 Click to see CC(=O)OC1C(C=C2CCN3C2C1C4=CC(=C(C=C4C3)O)OC)O 331.40 unknown https://doi.org/10.1016/S0031-9422(99)00118-1

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