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Hippeastrum morelianum

Hippeastrum morelianum - 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 UUID644018d925ac3550853417
Scientific name Hippeastrum morelianum
Authority Lem.
First published in Hort. Universel 4: 37 (1842)

Description Top

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Synonyms Top

Scientific name Authority First published in
Amaryllis moreliana (Lem.) Traub Herbertia 13: 102 (1948)

Common names Top

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Language Common/alternative name
Chinese 摩蕾华胄

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000660885
Tropicos 100203523
KEW urn:lsid:ipni.org:names:65117-1
The Plant List kew-278224
Open Tree Of Life 484054
NCBI Taxonomy 1263218
IPNI 65117-1
iNaturalist 464454
GBIF 169122434
EOL 1001324
Wikipedia Hippeastrum_morelianum

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
Identification of the Constituents in Cnidii Fructus Active Against Trichomonas vaginalis Parasites Yu CC, Chiang YT, Cham TM Dose Response 10-Nov-2022
PMCID:PMC9661559
doi:10.1177/15593258221131646
PMID:36387775
Determination of Anti-Alzheimer’s Disease Activity of Selected Plant Ingredients Tuzimski T, Petruczynik A Molecules 18-May-2022
PMCID:PMC9147832
doi:10.3390/molecules27103222
PMID:35630702
Alkaloid Profiling, Anti-Enzymatic and Antiproliferative Activity of the Endemic Chilean Amaryllidaceae Phycella cyrtanthoides Fernández-Galleguillos C, Romero-Parra J, Puerta A, Padrón JM, Simirgiotis MJ Metabolites 18-Feb-2022
PMCID:PMC8874788
doi:10.3390/metabo12020188
PMID:35208261
Natural Compounds as Medical Strategies in the Prevention and Treatment of Psychiatric Disorders Seen in Neurological Diseases Küpeli Akkol E, Tatlı Çankaya I, Şeker Karatoprak G, Carpar E, Sobarzo-Sánchez E, Capasso R Front Pharmacol 13-May-2021
PMCID:PMC8155682
doi:10.3389/fphar.2021.669638
PMID:34054540
A review study on the anti-trichomonas activities of medicinal plants Hashemi N, Ommi D, Kheyri P, Khamesipour F, Setzer WN, Benchimol M Int J Parasitol Drugs Drug Resist 12-Feb-2021
PMCID:PMC7902805
doi:10.1016/j.ijpddr.2021.01.002
PMID:33610966
Anti-trichomonad activities of different compounds from foods, marine products, and medicinal plants: a review Friedman M, Tam CC, Cheng LW, Land KM BMC Complement Med Ther 09-Sep-2020
PMCID:PMC7479404
doi:10.1186/s12906-020-03061-9
PMID:32907567
Alkaloids from Hippeastrum morelianum Lem. (Amaryllidaceae). Giordani RB, de Andrade JP, Verli H, Dutilh JH, Henriques AT, Berkov S, Bastida J, Zuanazzi JA Magn Reson Chem 01-Oct-2011
doi:10.1002/MRC.2794
PMID:21898585

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 / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
Crinamine 500027 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1002/MRC.2794
Haemanthamine 441593 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1002/MRC.2794
Hamayne 443670 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown https://doi.org/10.1002/MRC.2794
Vittatine, 11-hydroxy- 602595 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown https://doi.org/10.1002/MRC.2794
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids
(5S,5aS,11bS,11cS)-5,8,9,10-tetramethoxy-1-methyl-2,3,5,5a,11b,11c-hexahydroisochromeno[3,4-g]indol-7-one 162955653 Click to see CN1CCC2=CC(C3C(C21)C4=CC(=C(C(=C4C(=O)O3)OC)OC)OC)OC 375.40 unknown https://doi.org/10.1002/MRC.2794
9-Hydroxy-14-methoxy-4-methyl-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),7,13,15(19)-tetraen-12-one 4480705 Click to see CN1CCC2=CC(C3C(C21)C4=CC5=C(C(=C4C(=O)O3)OC)OCO5)O 345.30 unknown https://doi.org/10.1002/MRC.2794
Candimine 441588 Click to see CN1CCC2=CC(C3C(C21)C4=CC5=C(C(=C4C(=O)O3)OC)OCO5)O 345.30 unknown https://doi.org/10.1002/MRC.2794
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
3-Epimacronin 500134 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(=O)O2)OCO5 329.30 unknown https://doi.org/10.1002/MRC.2794
3-Epimacronine 375117 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(=O)O2)OCO5 329.30 unknown https://doi.org/10.1002/MRC.2794
3-Methoxy-5-methyl-3,4,4a,5,6,6a-hexahydro-8H-[1,3]dioxolo[4',5':6,7]isochromeno[3,4-c]indol-8-ol 419046 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(O2)O)OCO5 331.40 unknown https://doi.org/10.1002/MRC.2794
Pretazettine 73360 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(O2)O)OCO5 331.40 unknown https://doi.org/10.1002/MRC.2794
Sekisanolin 5321780 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1002/MRC.2794
Tazettine 271607 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1002/MRC.2794
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Trisphaeridine 443684 Click to see C1OC2=C(O1)C=C3C4=CC=CC=C4N=CC3=C2 223.23 unknown https://doi.org/10.1002/MRC.2794

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