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Habranthus brachyandrus

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Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
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Details Top

Internal ID UUID644016e064361566478315
Scientific name Habranthus brachyandrus
Authority (Baker) Sealy
First published in J. Roy. Hort. Soc. 62: 208 (1937)

Description Top

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Synonyms Top

Scientific name Authority First published in
Hippeastrum brachyandrum Baker Handb. Amaryll. : 42 (1888)
Zephyranthes porphyrospila E.Holmb. Anales Mus. Nac. Buenos Aires , ser. 3, 5: 65 (1905)
Zephyranthes brachyandra (Baker) Backer & Beknopte Fl. Java 11(228): 11 (1951)

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000645851
Tropicos 1202206
KEW urn:lsid:ipni.org:names:116707-2
The Plant List kew-276653
Open Tree Of Life 539720
NCBI Taxonomy 146427
IPNI 116707-2
iNaturalist 482877
GBIF 2853489
EOL 991810
USDA GRIN 18140

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
Studies on the Nonalkaloidal Secondary Metabolites of Hippeastrum vittatum (L’Her.) Herb. Bulbs Khalifa MF, Fahim JR, Allam AE, Shoman ME, El Zawily A, Kamel MS, Shimizu K, Attia EZ ACS Omega 23-Jul-2023
PMCID:PMC10398848
doi:10.1021/acsomega.2c07886
PMID:37546665
Wild Argentinian Amaryllidaceae, a New Renewable Source of the Acetylcholinesterase Inhibitor Galanthamine and Other Alkaloids Ortiz JE, Berkov S, Pigni NB, Theoduloz C, Roitman G, Tapia A, Bastida J, Feresin GE Molecules 13-Nov-2012
PMCID:PMC6268904
doi:10.3390/molecules171113473
PMID:23149565
Chemical constituents of the bulbs of Habranthus brachyandrus and their cytotoxic activities. Jitsuno M, Yokosuka A, Sakagami H, Mimaki Y Chem Pharm Bull (Tokyo) 01-Oct-2009
doi:10.1248/CPB.57.1153
PMID:19801880
Alkaloide aus <i>Hippeastrum brachyandrum</i> und <i>Hippeastrum rutilum</i> Hans‐G. Boit, Werner Döpke Wiley 02-Jun-2007
doi:10.1002/CBER.19590921029

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
(1R,11S,13S,15S,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 163195046 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1248/CPB.57.1153
(1R,13S,15R,18S)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-15,18-diol 162950865 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown https://doi.org/10.1248/CPB.57.1153
(1R,13S,15S,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 162954179 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1248/CPB.57.1153
(1S,11R,13S,15S,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 49799009 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1248/CPB.57.1153
(1S,13S,15S,18S)-15-Methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 5282090 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1248/CPB.57.1153
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/10.1002/CBER.19590921029
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/10.1002/CBER.19590921029
Crinamidine 399204 Click to see COC1=C2CN3CCC4(C3CC(C5C4O5)O)C2=CC6=C1OCO6 317.34 unknown https://doi.org/10.1002/CBER.19590921029
Crinamine 500027 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1248/CPB.57.1153
Haemanthamine 441593 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1248/CPB.57.1153
Haemanthidine 544807 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1248/CPB.57.1153
Undulatine 3083985 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C6C1O6 331.40 unknown https://doi.org/10.1002/CBER.19590921029
Vittatine, 11-hydroxy- 602595 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown https://doi.org/10.1248/CPB.57.1153
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
1,2,3,4,7-pentahydroxy-2,3,4,4a,5,11b-hexahydro-1H-[1,3]dioxolo[4,5-j]phenanthridin-6-one 609635 Click to see C1OC2=C(O1)C(=C3C(=C2)C4C(C(C(C(C4O)O)O)O)NC3=O)O 325.27 unknown https://doi.org/10.1248/CPB.57.1153
Pancratistatin 441597 Click to see C1OC2=C(O1)C(=C3C(=C2)C4C(C(C(C(C4O)O)O)O)NC3=O)O 325.27 unknown https://doi.org/10.1248/CPB.57.1153
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
methyl (3S)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutanoate 44475663 Click to see CC(CC(=O)OC)OC1C(C(C(C(O1)CO)O)O)O 280.27 unknown https://doi.org/10.1248/CPB.57.1153
Methyl 3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutanoate 75031902 Click to see CC(CC(=O)OC)OC1C(C(C(C(O1)CO)O)O)O 280.27 unknown https://doi.org/10.1248/CPB.57.1153
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Xanthoxylin 66654 Click to see CC(=O)C1=C(C=C(C=C1OC)OC)O 196.20 unknown https://doi.org/10.1248/CPB.57.1153
> Organic oxygen compounds / Organooxygen compounds / Ethers / Alkyl aryl ethers
Dehydroconiferyl alcohol 129638468 Click to see COC1=C(C#CC(=C1)C=CCO)O 178.18 unknown https://doi.org/10.1248/CPB.57.1153
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
6-Hydroxy-7,8-dimethoxy-2-(2-oxopropyl)-2,3,3a,9b-tetrahydrofuro[3,2-c]isochromen-5-one 71436822 Click to see CC(=O)CC1CC2C(O1)C3=CC(=C(C(=C3C(=O)O2)O)OC)OC 322.31 unknown https://doi.org/10.1248/CPB.57.1153
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1R,14R,15R,16R)-4,5,14-trimethoxy-9-azatetracyclo[7.6.1.02,7.012,16]hexadeca-2,4,6,12-tetraen-15-ol 133564758 Click to see COC1C=C2CCN3C2C(C1O)C4=CC(=C(C=C4C3)OC)OC 317.40 unknown https://doi.org/10.1248/CPB.57.1153
3,12-Didehydro-2beta,9,10-trimethoxygalanthan-1alpha-ol 97315 Click to see COC1C=C2CCN3C2C(C1O)C4=CC(=C(C=C4C3)OC)OC 317.40 unknown https://doi.org/10.1248/CPB.57.1153
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+)-Dehydrodiconiferyl alcohol 11824478 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO 358.40 unknown https://doi.org/10.1248/CPB.57.1153
5-O-Methylhierochin D 188976 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO 358.40 unknown https://doi.org/10.1248/CPB.57.1153
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
(2R,3R)-2-(1,3-benzodioxol-5-yl)-3,4-dihydro-2H-chromene-3,7-diol 44475662 Click to see C1C(C(OC2=C1C=CC(=C2)O)C3=CC4=C(C=C3)OCO4)O 286.28 unknown https://doi.org/10.1248/CPB.57.1153
(2R,3R)-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromene-3,7-diol 15515919 Click to see C1C(C(OC2=C1C=CC(=C2)O)C3=CC=C(C=C3)O)O 258.27 unknown https://doi.org/10.1248/CPB.57.1153
(2R,3R)-2-phenyl-3,4-dihydro-2H-chromene-3,7-diol 44475661 Click to see C1C(C(OC2=C1C=CC(=C2)O)C3=CC=CC=C3)O 242.27 unknown https://doi.org/10.1248/CPB.57.1153
2-(1,3-benzodioxol-5-yl)-3,4-dihydro-2H-chromene-3,7-diol 75031904 Click to see C1C(C(OC2=C1C=CC(=C2)O)C3=CC4=C(C=C3)OCO4)O 286.28 unknown https://doi.org/10.1248/CPB.57.1153
2-phenyl-3,4-dihydro-2H-chromene-3,7-diol 75031903 Click to see C1C(C(OC2=C1C=CC(=C2)O)C3=CC=CC=C3)O 242.27 unknown https://doi.org/10.1248/CPB.57.1153
4',7-Dihydroxyflavanol 71308214 Click to see C1C(C(OC2=C1C=CC(=C2)O)C3=CC=C(C=C3)O)O 258.27 unknown https://doi.org/10.1248/CPB.57.1153
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
2-Phenylchroman-7-ol 3512638 Click to see C1CC2=C(C=C(C=C2)O)OC1C3=CC=CC=C3 226.27 unknown https://doi.org/10.1248/CPB.57.1153
2H-1-Benzopyran-7-ol, 2-(1,3-benzodioxol-5-yl)-3,4-dihydro-, (S)- 12052874 Click to see C1CC2=C(C=C(C=C2)O)OC1C3=CC4=C(C=C3)OCO4 270.28 unknown https://doi.org/10.1248/CPB.57.1153
3,4-Dihydro-2-(4-hydroxyphenyl)-2H-1-benzopyran-7-ol 3500616 Click to see C1CC2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O 242.27 unknown https://doi.org/10.1248/CPB.57.1153
7-Hydroxy-3',4'-methylenedioxyflavan 466078 Click to see C1CC2=C(C=C(C=C2)O)OC1C3=CC4=C(C=C3)OCO4 270.28 unknown https://doi.org/10.1248/CPB.57.1153
7-Hydroxyflavan 442413 Click to see C1CC2=C(C=C(C=C2)O)OC1C3=CC=CC=C3 226.27 unknown https://doi.org/10.1248/CPB.57.1153
7,4'-Dihydroxyflavan 158280 Click to see C1CC2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O 242.27 unknown https://doi.org/10.1248/CPB.57.1153
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
(S)-2-(3-Hydroxy-4-methoxyphenyl)chroman-7-ol 44257179 Click to see COC1=C(C=C(C=C1)C2CCC3=C(O2)C=C(C=C3)O)O 272.29 unknown https://doi.org/10.1248/CPB.57.1153
2-(3-hydroxy-4-methoxyphenyl)-3,4-dihydro-2H-chromen-7-ol 11196546 Click to see COC1=C(C=C(C=C1)C2CCC3=C(O2)C=C(C=C3)O)O 272.29 unknown https://doi.org/10.1248/CPB.57.1153
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R,3R)-2-(4-hydroxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-3-ol 44475659 Click to see COC1=CC2=C(CC(C(O2)C3=CC=C(C=C3)O)O)C=C1 272.29 unknown https://doi.org/10.1248/CPB.57.1153
2-(4-hydroxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-3-ol 54481478 Click to see COC1=CC2=C(CC(C(O2)C3=CC=C(C=C3)O)O)C=C1 272.29 unknown https://doi.org/10.1248/CPB.57.1153
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retro-dihydrochalcones
2,4,4'-Trihydroxydihydrochalcone 10801179 Click to see C1=CC(=CC=C1C(=O)CCC2=C(C=C(C=C2)O)O)O 258.27 unknown https://doi.org/10.1248/CPB.57.1153

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