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Ungernia vvedenskyi

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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 UUID644026bbf25dc633902588
Scientific name Ungernia vvedenskyi
Authority Khamidch.
First published in Dokl. Akad. Nauk Tadzhiksk. S.S.R. 5: 54 (1979)

Description Top

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Synonyms Top

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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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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-0000771593
Tropicos 100271505
KEW urn:lsid:ipni.org:names:77176753-1
The Plant List kew-310258
Open Tree Of Life 3994619
Observations.org 150380
IPNI 77176753-1
iNaturalist 896328
GBIF 2858135
EOL 1089225
Elurikkus 318823

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
Alkaloids ofUngernia vvedenskyi Kh. A. Kadyrov, S. A. Khamidkhodzhaev Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00566110
Ungvedine — A new alkaloid fromUngernia vvedenskyi Kh. A. Kadyrov, A. Abdusamatov, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00565070

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
(1S,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 154496716 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1007/BF00566110
> 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/10.1007/BF00565070
Zephyranthine 193339 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1CC(C5O)O)OCO4 289.33 unknown https://doi.org/10.1007/BF00566110
> 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/10.1007/BF00565070
(1S,13S,16S,18R)-13,18-dimethoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9-triene 163033418 Click to see CN1CC2(C3(C1CC(CC3)OC)C4=CC5=C(C=C4CO2)OCO5)OC 347.40 unknown https://doi.org/10.1007/BF00565070
https://doi.org/10.1007/BF00566110
13,18-Dimethoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9-triene 74039739 Click to see CN1CC2(C3(C1CC(CC3)OC)C4=CC5=C(C=C4CO2)OCO5)OC 347.40 unknown https://doi.org/10.1007/BF00565070
Sekisanin 443682 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1007/BF00565070
Sekisanolin 5321780 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1007/BF00566110
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Ungiminorine 10425948 Click to see COC1C(C2C3C(=CCN3CC4=CC5=C(C=C24)OCO5)C1O)O 317.34 unknown https://doi.org/10.1007/BF00566110

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