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Glaucium oxylobum

Glaucium oxylobum - Unknown
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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 UUID64401e0f208b1617446598
Scientific name Glaucium oxylobum
Authority Boiss. & Buhse
First published in Nouv. Mém. Soc. Imp. Naturalistes Moscou 12: 12 (1860)

Description Top

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Synonyms Top

Scientific name Authority First published in
Glaucium golestanicum A.Gran & Sharifnia Iran. J. Bot. 14: 26 (2008)
Glaucium elegantissimum Mobayen Iran. J. Bot. 2: 163 (1984)
Glaucium oxylobum var. paucilobatum (Freyn) Parsa Fl. Iran 2: 444 (1986)
Glaucium paucilobatum Freyn Bull. Herb. Boissier , sér. 2, 3: 566 (1903)
Glaucium pulchrum Stapf Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 51: 27 (1886)
Glaucium oxylobum subsp. rechingeri Mory Feddes Repert. 89: 566 (1978 publ. 1979)

Common names Top

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Language Common/alternative name
Arabic ماميثا حادة الفصوص

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.
Requires Darkness: These seeds need to be covered with soil or otherwise kept in the dark to germinate properly. Light inhibits their germination process.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Middle Asia
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Iran

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000703607
Tropicos 24000593
KEW urn:lsid:ipni.org:names:673184-1
The Plant List kew-2826391
Open Tree Of Life 5727867
Observations.org 137102
IPNI 673184-1
GBIF 7315004
Elurikkus 587439
USDA GRIN 17620
Wikipedia Glaucium_oxylobum
CMAUP NPO15612

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

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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 / Aporphines
Oxoglaucine 97662 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC(=C(C=C42)OC)OC)OC 351.40 unknown via CMAUP database
> Alkaloids and derivatives / Plumeran-type alkaloids
Methyl 11-ethyl-5-methoxy-15-oxo-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5,9,13-pentaene-10-carboxylate 5320331 Click to see CCC1C2C=CC(=O)N3C2C4(CC3)C5=C(C=C(C=C5)OC)NC4=C1C(=O)OC 380.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Cyclohexylphenols
Secoabietane dialdehyde 15404650 Click to see CC(C)C1=C(C=C(C(=C1)C=O)C2(CCCC(C2C=O)(C)C)C)O 316.40 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Catechols
3-(3-Hydroxypropyl)benzene-1,2-diol 18982198 Click to see C1=CC(=C(C(=C1)O)O)CCCO 168.19 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,4S,6S)-6-[[(4bS,8aS)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-yl]oxy]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol 11553935 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)OC4CC5CC(C4(C5(C)C)C)O 438.70 unknown via CMAUP database
(4bS,8aS,10S)-10-[[4-(2-hydroxypropan-2-yl)phenyl]methyl]-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol 66555987 Click to see CC(C)C1=C(C=C2C(=C1)C(CC3C2(CCCC3(C)C)C)CC4=CC=C(C=C4)C(C)(C)O)O 434.70 unknown via CMAUP database
6,7-Dehydroferruginol 10978982 Click to see CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)O 284.40 unknown via CMAUP database
6alpha-(Abieta-6,8,11,13-tetraene-12-yloxy)-7alpha,12-diacetoxyabieta-8,11,13-triene 11650468 Click to see CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)OC4C(C5=CC(=C(C=C5C6(C4C(CCC6)(C)C)C)OC(=O)C)C(C)C)OC(=O)C 668.90 unknown via CMAUP database
6alpha-(Abieta-6,8,11,13-tetraene-12-yloxy)abieta-8,11,13-triene-7alpha,12-diol 11635634 Click to see CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)OC4C(C5=CC(=C(C=C5C6(C4C(CCC6)(C)C)C)O)C(C)C)O 584.90 unknown via CMAUP database
Calocedimers B 11677578 Click to see CC1=CC2C(CCC(C2CC1)(C)OC3=C(C=C4CCC5C(CCCC5(C4=C3)C)(C)C)C(C)C)C(C)C 490.80 unknown via CMAUP database
Ferrugicadinol 11562492 Click to see CC(C)C1CCC(C2C1C=C(CC2)CC3CC4C(CCCC4(C5=CC(=C(C=C35)C(C)C)O)C)(C)C)(C)O 506.80 unknown via CMAUP database
Ferrugieudesmol 11994700 Click to see CC(C)C1=C(C=C2C(=C1)C(CC3C2(CCCC3(C)C)C)C4CCC(=C)C5C4(CCC(C5)C(C)(C)O)C)O 506.80 unknown via CMAUP database
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown via CMAUP database
Formosadimer A 11563385 Click to see CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)OC4C(C5=CC(=C(C=C5C6(C4C(CCC6)(C)C)C)OC)C(C)C)O 598.90 unknown via CMAUP database
Formosadimer B 11498485 Click to see CCCCOCCOC1C(C2C(CCCC2(C3=CC(=C(C=C13)C(C)C)O)C)(C)C)OC4=C(C=C5C=CC6C(CCCC6(C5=C4)C)(C)C)C(C)C 685.00 unknown via CMAUP database
Formosadimer C 11686328 Click to see CCCCOCCOC1C(C2C(CCCC2(C3=CC(=C(C=C13)C(C)C)OC(=O)C)C)(C)C)OC4=C(C=C5C=CC6C(CCCC6(C5=C4)C)(C)C)C(C)C 727.10 unknown via CMAUP database
Sugikurojin B 23250764 Click to see CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)OC4C(C5=CC(=C(C=C5C6(C4C(CCC6)(C)C)C)O)C(C)C)OC 598.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Isonerylgeraniol-18-oic acid 11232455 Click to see CC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C(=O)O)C 320.50 unknown via CMAUP database
Nerylgeraniol-18-oic acid 11186287 Click to see CC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C(=O)O)C 320.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1S,4aR,5S,8aR)-5-[2-[(2S)-2-methoxy-5-oxo-2H-furan-4-yl]ethyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 93476678 Click to see CC12CCCC(C1CCC(=C)C2CCC3=CC(OC3=O)OC)(C)C(=O)O 362.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,8aalpha)-1,4abeta-Dimethyl-5beta-[[(1R)-2-methyl-5alpha,6beta-[3-butene-1,3-diyl[(1S)-3,3-dimethylcyclobutane-1alpha,2beta-diyl]ethylene]-6-(hydroxycarbonyl)-2-cyclohexene-1alpha-yl]methyl]-6-methylenedecahydronaphthalene-1beta-carboxylic acid 51039134 Click to see CC1=CCC2CCC(=C)C3CC(C3CCC2(C1CC4C(=C)CCC5C4(CCCC5(C)C(=O)O)C)C(=O)O)(C)C 536.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Obtusadione 21577111 Click to see CC(C)C1=CC2(CC1=O)C(=O)CCC3C2(CCCC3(C)C)C 302.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Taiwaniaflavone 44456685 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown via CMAUP database

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