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Moquiniastrum polymorphum subsp. polymorphum

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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
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Details Top

Internal ID UUID6440697a2492b501661830
Scientific name Moquiniastrum polymorphum subsp. polymorphum
First published in Unknown

Description Top

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Common names Top

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Varieties (abbr. var.) 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

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-0001425631
KEW urn:lsid:ipni.org:names:77180744-1
GBIF 9500313

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
Constituents of Mochinea polymorpha Antonio C. Monteiro de Farias, Antonio Jorge R. da Silva, Therezinha C. B. Tomassini American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50032A021
Ent-kaurene diterpenes from Gochnatia polymorpha var. polymorpha Ana C.B.C. Sacilotto, Walter Vichnewski, Werner Herz Elsevier BV 13-May-2003
doi:10.1016/S0031-9422(96)00601-2
Coumarins and a kaurane from Gochnatia polymorpha ssp. polymorpha from Paraguay C.A.N Catalan, M.I Vega, M.E Lopez, M del R. Cuenca, T.E Gedris, W Herz Elsevier BV 17-Feb-2003
doi:10.1016/S0305-1978(02)00163-1
Dimeric guaianolides and other constituents from Gochnatia species Ferdinand Bohlmann, Christa Zdero, Guillermo Schmeda-Hirschmann, Jasmin Jakupovic, Xorge A. Dominguez, Robert M. King, Harold Robinson Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81575-7
Antiinflammatory activity of extracts and fractions from the leaves of Gochnatia polymorpha. Moreira AS, Spitzer V, Schapoval EE, Schenkel EP Phytother Res 01-Dec-2000
doi:10.1002/1099-1573(200012)14:8<638::AID-PTR681>3.0.CO;2-Q
PMID:11114003

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
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
(1R,2S,3'aS,6S,6'aR,9'aR,9'bS,12R,13S)-13-hydroxy-3',5,6',15-tetramethylidenespiro[3-oxatetracyclo[7.6.1.02,6.013,16]hexadec-9(16)-ene-12,9'-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan]-2',4,8',14-tetrone 162996499 Click to see C=C1CCC2C(C3C1CC(=O)C34CCC5=C6C4(C(=O)C(=C)C6C7C(CC5)C(=C)C(=O)O7)O)OC(=O)C2=C 502.60 unknown https://doi.org/10.1016/S0031-9422(00)81575-7
13-hydroxy-3',5,6',15-tetramethylidenespiro[3-oxatetracyclo[7.6.1.02,6.013,16]hexadec-9(16)-ene-12,9'-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan]-2',4,8',14-tetrone 162996498 Click to see C=C1CCC2C(C3C1CC(=O)C34CCC5=C6C4(C(=O)C(=C)C6C7C(CC5)C(=C)C(=O)O7)O)OC(=O)C2=C 502.60 unknown https://doi.org/10.1016/S0031-9422(00)81575-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Nuciferal 10900058 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C=O 216.32 unknown https://doi.org/10.1016/S0031-9422(00)81575-7
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Epitaraxerol 344467 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(96)00601-2
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(96)00601-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,5aS,6S,9aR,9bR)-6-hydroxy-5a,9-dimethyl-3-methylidene-4,5,6,7,9a,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one 124708200 Click to see CC1=CCC(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(96)00601-2
Santamarine 188297 Click to see CC1=CCC(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(96)00601-2
Sesquiterpene lactone CP-1 331391 Click to see CC1=CCC(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(96)00601-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aS,6E,11aR)-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 133640194 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1016/S0031-9422(00)81575-7
Costunolide 5281437 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1016/S0031-9422(00)81575-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Dehydrocostus lactone, (-)- 73174 Click to see C=C1CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1021/NP50032A021
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0305-1978(02)00163-1
Bauerenyl acetate 177801 Click to see CC1CCC2(CCC3(C4=CCC5C(C(CCC5(C4CCC3(C2C1C)C)C)OC(=O)C)(C)C)C)C 468.80 unknown https://doi.org/10.1021/NP50032A021
CID 5256173 5256173 Click to see CC1CCC2(CCC3(C4=CCC5C(C(CCC5(C4CCC3(C2C1C)C)C)OC(=O)C)(C)C)C)C 468.80 unknown https://doi.org/10.1021/NP50032A021
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0305-1978(02)00163-1
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0305-1978(02)00163-1
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
4-Hydroxy-methylprolin 11499239 Click to see CN1CC(CC1C(=O)O)O 145.16 unknown https://doi.org/10.1002/1099-1573(200012)14:8<638::AID-PTR681>3.0.CO;2-Q
Proline 145742 Click to see C1CC(NC1)C(=O)O 115.13 unknown https://doi.org/10.1002/1099-1573(200012)14:8<638::AID-PTR681>3.0.CO;2-Q
> Organoheterocyclic compounds / Benzofurans
Loliolide 100332 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1016/S0305-1978(02)00163-1
> Phenylpropanoids and polyketides / Coumarins and derivatives / p-Dioxolo[2,3-h]coumarins
2-(2-Hydroxypropan-2-yl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 11507587 Click to see CC(C)(C1COC2=C(C=C3C=CC(=O)OC3=C2O1)OC)O 292.28 unknown https://doi.org/10.1016/S0305-1978(02)00163-1
6-Hydroxy-2-(2-hydroxypropan-2-yl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 15287104 Click to see CC(C)(C1COC2=C(C(=C3C=CC(=O)OC3=C2O1)O)OC)O 308.28 unknown https://doi.org/10.1016/S0305-1978(02)00163-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Desmethoxycentaureidin 5469524 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown https://doi.org/10.1016/S0031-9422(96)00601-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1016/S0031-9422(96)00601-2

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