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Gonzalezia hypargyrea

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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 UUID64405e94b6a61673751366
Scientific name Gonzalezia hypargyrea
Authority (Greenm.) E.E.Schill. & Panero
First published in Bot. J. Linn. Soc. 167(3):327 (2011)

Description Top

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Synonyms Top

Scientific name Authority First published in
Viguiera hypargyrea Greenm. Proc. Amer. Acad. Arts 39: 105 (1903)

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

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- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001332084
Tropicos 100382308
KEW urn:lsid:ipni.org:names:77115784-1
IPNI 77115784-1
iNaturalist 937155
GBIF 9022510

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
Notes: External Flavonoids of Three Species of Viguiera, Section Hypargyrea (Asteraceae) Eckhard Wollenweber, Marion Dörr, James N. Roitman, Edward Schilling Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1995-7-819
Sesquiterpene lactones from Viguiera hypargyrea L Alvarez Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80616-0
Sesquiterpene lactones from Viguiera hypargyrea Laura Alvarez, Rachel Mata, Guillermo Delgado, Alfonso Romo de Vivar Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(85)80038-8
Antispasmodic and antimicrobial diterpenic acids from Viguiera hypargyrea roots. Zamilpa A, Tortoriello J, Navarro V, Delgado G, Alvarez L Planta Med 01-Mar-2002
doi:10.1055/S-2002-23146
PMID:11914972

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 / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,4S,5R,9R,10R,13R,15S)-10-hydroxy-5,9-dimethyl-15-[(E)-2-methylbut-2-enoyl]oxy-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 101618870 Click to see CC=C(C)C(=O)OC1C(=C)C2CCC3(C1(C2)CCC4C3(CCCC4(C)C(=O)O)C)O 416.50 unknown https://doi.org/10.1016/0031-9422(85)80038-8
(5R,9S,13S)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 49775756 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1055/S-2002-23146
https://doi.org/10.1016/S0031-9422(00)80616-0
10-Hydroxy-5,9-dimethyl-15-(2-methylbut-2-enoyloxy)-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 74146145 Click to see CC=C(C)C(=O)OC1C(=C)C2CCC3(C1(C2)CCC4C3(CCCC4(C)C(=O)O)C)O 416.50 unknown https://doi.org/10.1016/0031-9422(85)80038-8
CID 433869 433869 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/0031-9422(85)80038-8
Kaurenoic Acid 73062 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/S0031-9422(00)80616-0
https://doi.org/10.1016/0031-9422(85)80038-8
https://doi.org/10.1055/S-2002-23146
methyl (1S,4S,5R,9R,10R,13R,15S)-10-hydroxy-5,9-dimethyl-15-[(Z)-2-methylbut-2-enoyl]oxy-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 101596879 Click to see CC=C(C)C(=O)OC1C(=C)C2CCC3(C1(C2)CCC4C3(CCCC4(C)C(=O)OC)C)O 430.60 unknown https://doi.org/10.1016/0031-9422(85)80038-8
Methyl 10-hydroxy-5,9-dimethyl-15-(2-methylbut-2-enoyloxy)-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 162904649 Click to see CC=C(C)C(=O)OC1C(=C)C2CCC3(C1(C2)CCC4C3(CCCC4(C)C(=O)OC)C)O 430.60 unknown https://doi.org/10.1016/0031-9422(85)80038-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Clovandiol 76319362 Click to see CC1(CC(C23C1CCC(C2)(C(CC3)O)C)O)C 238.37 unknown https://doi.org/10.1016/S0031-9422(00)80616-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aR,11aR)-4-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 137706071 Click to see CC1=CC2C(C(CC(=CCC1)C)O)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/S0031-9422(00)80616-0
(3aR,4S,6E,10Z,11aR)-4-hydroxy-6-(hydroxymethyl)-10-methyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 101306906 Click to see CC1=CC2C(C(CC(=CCC1)CO)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1016/S0031-9422(00)80616-0
(3aS,6E,9R,10E,11aR)-9-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 12443214 Click to see CC1=CCC(C(=CC2C(CC1)C(=C)C(=O)O2)C)O 248.32 unknown https://doi.org/10.1016/0031-9422(85)80038-8
(3aS,6Z,9S,10Z,11aR)-9-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 101316778 Click to see CC1=CCC(C(=CC2C(CC1)C(=C)C(=O)O2)C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)80616-0
[(1R,2R,4S,6R,9E,11R)-4-(acetyloxymethyl)-9-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] (2S,3R)-2,3-dimethyloxirane-2-carboxylate 162961085 Click to see CC1C(O1)(C)C(=O)OC2CC3(C(O3)CCC(=CC4C2C(=C)C(=O)O4)C)COC(=O)C 420.50 unknown https://doi.org/10.1016/0031-9422(85)80038-8
[(1R,2R,4S,6R,9E,11R)-4-(hydroxymethyl)-9-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] (2S,3R)-2,3-dimethyloxirane-2-carboxylate 162946480 Click to see CC1C(O1)(C)C(=O)OC2CC3(C(O3)CCC(=CC4C2C(=C)C(=O)O4)C)CO 378.40 unknown https://doi.org/10.1016/0031-9422(85)80038-8
[(3aR,4R,6Z,10E,11aR)-6-(acetyloxymethyl)-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (2S,3R)-2,3-dimethyloxirane-2-carboxylate 162989533 Click to see CC1C(O1)(C)C(=O)OC2CC(=CCCC(=CC3C2C(=C)C(=O)O3)C)COC(=O)C 404.50 unknown https://doi.org/10.1016/0031-9422(85)80038-8
[4-(Acetyloxymethyl)-9-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] 2,3-dimethyloxirane-2-carboxylate 162961077 Click to see CC1C(O1)(C)C(=O)OC2CC3(C(O3)CCC(=CC4C2C(=C)C(=O)O4)C)COC(=O)C 420.50 unknown https://doi.org/10.1016/0031-9422(85)80038-8
[4-(Hydroxymethyl)-9-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] 2,3-dimethyloxirane-2-carboxylate 162946479 Click to see CC1C(O1)(C)C(=O)OC2CC3(C(O3)CCC(=CC4C2C(=C)C(=O)O4)C)CO 378.40 unknown https://doi.org/10.1016/0031-9422(85)80038-8
[6-(Acetyloxymethyl)-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2,3-dimethyloxirane-2-carboxylate 162989531 Click to see CC1C(O1)(C)C(=O)OC2CC(=CCCC(=CC3C2C(=C)C(=O)O3)C)COC(=O)C 404.50 unknown https://doi.org/10.1016/0031-9422(85)80038-8
4-Hydroxy-6-(hydroxymethyl)-10-methyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 72656715 Click to see CC1=CC2C(C(CC(=CCC1)CO)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1016/0031-9422(85)80038-8
4-Hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 98949 Click to see CC1=CC2C(C(CC(=CCC1)C)O)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/0031-9422(85)80038-8
9-Hydroxy-6,10-dimethyl-3-methylene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2(3H)-one 5377194 Click to see CC1=CCC(C(=CC2C(CC1)C(=C)C(=O)O2)C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)80616-0
9-Hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 281981 Click to see CC1=CCC(C(=CC2C(CC1)C(=C)C(=O)O2)C)O 248.32 unknown https://doi.org/10.1016/0031-9422(85)80038-8
Deacetylovatifolin 11108215 Click to see CC1=CC2C(C(CC(=CCC1)CO)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1016/0031-9422(85)80038-8
Eupatolide 5281460 Click to see CC1=CC2C(C(CC(=CCC1)C)O)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/0031-9422(85)80038-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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/10.1055/S-2002-23146
> Lipids and lipid-like molecules / Saccharolipids
Methyl 4-[2-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-methyl-4-oxobutanoate 78407186 Click to see CC(CC(=O)OC)C(=O)C1=C(C(=CC=C1)OC2C(C(C(C(O2)CO)O)O)O)O 400.40 unknown https://doi.org/10.1016/S0031-9422(00)80616-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(85)80038-8
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(85)80038-8
https://doi.org/10.1016/S0031-9422(00)80616-0
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1515/ZNC-1995-7-819
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1515/ZNC-1995-7-819
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1515/ZNC-1995-7-819

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