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Pancratium biflorum

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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 UUID64402170a96e4154444637
Scientific name Pancratium biflorum
Authority Roxb.
First published in Fl. Ind. ed. 1832 , 2: 125 (1832)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 全能花

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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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-0000728348
Tropicos 1202486
KEW urn:lsid:ipni.org:names:66401-1
The Plant List kew-285900
Open Tree Of Life 3994692
IPNI 66401-1
iNaturalist 841748
GBIF 2853264
EOL 1081632

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)!
Title Authors Publication Released IDs
Free and glucosyloxy acetophenones from Pancratium biflorum Shibnath Ghosal, Peeyush Mittal, Yatendra Kumar, Sushil K. Singh Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80305-X
Biflorin, a chromone-C-glucoside from Pancratium biflorum Shibnath Ghosal, Yatendra Kumar, Shripati Singh, Kamal Ahad Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(83)80172-1
Three chromones from bulbs of Pancratium biflorum Shibnath Ghosal, Shripati Singh, Mahendra P. Bhagat, Yatendra Kumar Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)85074-6
Glucosyloxy alkaloids from Pancratium biflorum Shibnath Ghosal, Yatendra Kumar, Shripati Singh Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82631-X
Parasitism of imperata cylindrica on pancratium biflorum and the concomitant chemical changes in the host species Shibnath Ghosal, Yatendra Kumar, Dilip K. Chakrabarti, Jawahar Lal, Sushil K. Singh Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81561-7

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 / Lycorine-type amaryllidaceae alkaloids
(2R,3S,4R,5S,6R)-2-[[(1R,17S,18S,19R)-17-hydroxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,15-tetraen-18-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162932793 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5OC6C(C(C(C(O6)CO)O)O)O)O)OCO4 449.40 unknown https://doi.org/10.1016/S0031-9422(00)82631-X
2-[(17-Hydroxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,15-tetraen-18-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 76469086 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5OC6C(C(C(C(O6)CO)O)O)O)O)OCO4 449.40 unknown https://doi.org/10.1016/S0031-9422(00)82631-X
Lycorine 72378 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown https://doi.org/10.1016/S0031-9422(00)82631-X
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
(1S,13S,16R,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-13-ol 11873227 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1016/S0031-9422(00)82631-X
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/10.1016/S0031-9422(00)82631-X
Pretazettine 73360 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(O2)O)OCO5 331.40 unknown https://doi.org/10.1016/S0031-9422(00)82631-X
Sekisanin 443682 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1016/S0031-9422(00)82631-X
Sekisanolin 5321780 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1016/S0031-9422(00)82631-X
Tazettine 271607 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1016/S0031-9422(00)82631-X
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Hordenine 68313 Click to see CN(C)CCC1=CC=C(C=C1)O 165.23 unknown https://doi.org/10.1016/S0031-9422(00)82631-X
Phenethylamine 1001 Click to see C1=CC=C(C=C1)CCN 121.18 unknown https://doi.org/10.1016/S0031-9422(00)82631-X
Tyramine 5610 Click to see C1=CC(=CC=C1CCN)O 137.18 unknown https://doi.org/10.1016/S0031-9422(00)82631-X
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
1-Phenylethylamine 7408 Click to see CC(C1=CC=CC=C1)N 121.18 unknown https://doi.org/10.1016/S0031-9422(00)82631-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-[4-[2-(dimethylamino)ethyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 132572340 Click to see CN(C)CCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 327.37 unknown https://doi.org/10.1016/S0031-9422(00)82631-X
1-[2,4-dimethoxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethanone 14427352 Click to see CC(=O)C1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)OC)OC 358.34 unknown https://doi.org/10.1016/0031-9422(89)80305-X
1-[2,4-Dimethoxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethanone 14427351 Click to see CC(=O)C1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)OC)OC 358.34 unknown https://doi.org/10.1016/0031-9422(89)80305-X
1-[2,6-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethanone 14427354 Click to see CC(=O)C1=C(C=C(C=C1OC)OC2C(C(C(C(O2)CO)O)O)O)OC 358.34 unknown https://doi.org/10.1016/0031-9422(89)80305-X
1-[2,6-Dimethoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethanone 14427353 Click to see CC(=O)C1=C(C=C(C=C1OC)OC2C(C(C(C(O2)CO)O)O)O)OC 358.34 unknown https://doi.org/10.1016/0031-9422(89)80305-X
1,5-Anhydro-1-(5,7-dihydroxy-2-methyl-4-oxo-4H-1-benzopyran-6-yl)hexitol 5087647 Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O 354.31 unknown https://doi.org/10.1016/0031-9422(83)80172-1
2-[4-[2-(Dimethylamino)ethyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162890878 Click to see CN(C)CCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 327.37 unknown https://doi.org/10.1016/S0031-9422(00)82631-X
5-Hydroxy-2-methyl-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 73241921 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)OC3C(C(C(C(O3)CO)O)O)O)O 354.31 unknown https://doi.org/10.1016/0031-9422(83)80172-1
https://doi.org/10.1016/0031-9422(80)85074-6
Biflorin 441959 Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O 354.31 unknown https://doi.org/10.1016/0031-9422(83)80172-1
Undulatoside A 5321494 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)OC3C(C(C(C(O3)CO)O)O)O)O 354.31 unknown https://doi.org/10.1016/0031-9422(80)85074-6
https://doi.org/10.1016/0031-9422(83)80172-1
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
2',4',6'-Trimethoxyacetophenone 123089 Click to see CC(=O)C1=C(C=C(C=C1OC)OC)OC 210.23 unknown https://doi.org/10.1016/0031-9422(89)80305-X
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,6-Dihydroxy-7-methoxy-2-methyl-4H-1-benzopyran-4-one 52918156 Click to see CC1=CC(=O)C2=C(C(=C(C=C2O1)OC)O)O 222.19 unknown https://doi.org/10.1016/0031-9422(80)85074-6
Noreugenin 5375252 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)O 192.17 unknown https://doi.org/10.1016/0031-9422(80)85074-6
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(2R,3S,4S,5R,6S)-2-[[(1R,14S,15S,16S)-4,14-dihydroxy-5-methoxy-9-azatetracyclo[7.6.1.02,7.012,16]hexadeca-2,4,6,12-tetraen-15-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163106298 Click to see COC1=C(C=C2C3C(C(C=C4C3N(CC4)CC2=C1)O)OC5C(C(C(C(O5)CO)O)O)O)O 451.50 unknown https://doi.org/10.1016/S0031-9422(00)82631-X
Pseudolycorine 443689 Click to see COC1=C(C=C2C3C(C(C=C4C3N(CC4)CC2=C1)O)O)O 289.33 unknown https://doi.org/10.1016/S0031-9422(00)82631-X
Ungeremine 159646 Click to see C1C[N+]2=CC3=CC4=C(C=C3C5=CC(=CC1=C52)O)OCO4 266.27 unknown https://doi.org/10.1016/S0031-9422(00)81561-7

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