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Hofmeisteria schaffneri

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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 UUID643fd0e3f00d8929089361
Scientific name Hofmeisteria schaffneri
Authority (A.Gray) R.M.King & H.Rob.
First published in Phytologia 12: 467 (1966)

Description Top

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Synonyms Top

Scientific name Authority First published in
Fleischmannia schaffneri A.Gray Proc. Amer. Acad. Arts xvi. (1881) 101.

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Northeast
      • Mexico Southwest

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000107781
Tropicos 2714938
KEW urn:lsid:ipni.org:names:123432-2
The Plant List gcc-6620
Open Tree Of Life 481302
NCBI Taxonomy 176606
IPNI 123432-2
iNaturalist 289593
GBIF 3089456

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Plant-Based Phytochemicals as Possible Alternative to Antibiotics in Combating Bacterial Drug Resistance AlSheikh HM, Sultan I, Kumar V, Rather IA, Al-Sheikh H, Tasleem Jan A, Haq QM Antibiotics (Basel) 04-Aug-2020
PMCID:PMC7460449
doi:10.3390/antibiotics9080480
PMID:32759771
Antispasmodic Effect of Essential Oils and Their Constituents: A Review Heghes SC, Vostinaru O, Rus LM, Mogosan C, Iuga CA, Filip L Molecules 29-Apr-2019
PMCID:PMC6539827
doi:10.3390/molecules24091675
PMID:31035694
Antimicrobial Activity of Some Essential Oils—Present Status and Future Perspectives Chouhan S, Sharma K, Guleria S Medicines (Basel) 08-Aug-2017
PMCID:PMC5622393
doi:10.3390/medicines4030058
PMID:28930272
Analgesic Potential of Essential Oils Sarmento-Neto JF, do Nascimento LG, Felipe CF, de Sousa DP Molecules 23-Dec-2015
PMCID:PMC6273222
doi:10.3390/molecules21010020
PMID:26703556
Antinociceptive effect of extracts and compounds from Hofmeisteria schaffneri. Angeles-López G, Pérez-Vásquez A, Hernández-Luis F, Déciga-Campos M, Bye R, Linares E, Mata R J Ethnopharmacol 15-Sep-2010
doi:10.1016/J.JEP.2010.07.009
PMID:20633627
Phytotoxic activity and conformational analysis of thymol analogs from Hofmeisteria schaffneri. Pérez-Vásquez A, Linares E, Bye R, Cerda-García-Rojas CM, Mata R Phytochemistry 01-Apr-2008
doi:10.1016/J.PHYTOCHEM.2008.01.011
PMID:18328513
Phytotoxins from Hofmeisteria schaffneri: isolation and synthesis of 2'-(2' '-hydroxy-4' '-methylphenyl)-2'-oxoethyl acetate1. Pérez-Vásquez A, Reyes A, Linares E, Bye R, Mata R J Nat Prod 01-Jun-2005
doi:10.1021/NP0501278
PMID:15974630

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
> Benzenoids / Phenol esters
[2-[(2R)-2-(acetyloxymethyl)oxiran-2-yl]-5-methylphenyl] (Z)-2-methylbut-2-enoate 163190303 Click to see CC=C(C)C(=O)OC1=C(C=CC(=C1)C)C2(CO2)COC(=O)C 304.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
[2-[(2S)-2-(hydroxymethyl)oxiran-2-yl]-5-methylphenyl] (Z)-2-methylbut-2-enoate 163187515 Click to see CC=C(C)C(=O)OC1=C(C=CC(=C1)C)C2(CO2)CO 262.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
[2-[(2S)-2-acetyloxiran-2-yl]-5-methylphenyl] (Z)-2-methylbut-2-enoate 163187268 Click to see CC=C(C)C(=O)OC1=C(C=CC(=C1)C)C2(CO2)C(=O)C 274.31 unknown https://doi.org/10.1016/J.JEP.2010.07.009
[2-[(2S)-2-acetyloxiran-2-yl]-5-methylphenyl] 2-methylbut-2-enoate 162868188 Click to see CC=C(C)C(=O)OC1=C(C=CC(=C1)C)C2(CO2)C(=O)C 274.31 unknown https://doi.org/10.1016/J.JEP.2010.07.009
[2-[2-(Acetyloxymethyl)oxiran-2-yl]-5-methylphenyl] 2-methylbut-2-enoate 595607 Click to see CC=C(C)C(=O)OC1=C(C=CC(=C1)C)C2(CO2)COC(=O)C 304.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
[2-[2-(hydroxymethyl)oxiran-2-yl]-5-methylphenyl] (Z)-2-methylbut-2-enoate 21592274 Click to see CC=C(C)C(=O)OC1=C(C=CC(=C1)C)C2(CO2)CO 262.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
[2-[2-(Hydroxymethyl)oxiran-2-yl]-5-methylphenyl] 2-methylbut-2-enoate 73196965 Click to see CC=C(C)C(=O)OC1=C(C=CC(=C1)C)C2(CO2)CO 262.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
10-Acetoxy-8,9-epoxythymol 3-angelate 5373805 Click to see CC=C(C)C(=O)OC1=C(C=CC(=C1)C)C2(CO2)COC(=O)C 304.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
> Benzenoids / Phenols / Cresols / Meta cresols
[(2R)-2,3-dihydroxy-2-(2-hydroxy-4-methylphenyl)propyl] (Z)-2-methylbut-2-enoate 163187252 Click to see CC=C(C)C(=O)OCC(CO)(C1=C(C=C(C=C1)C)O)O 280.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
[(2R)-3-acetyloxy-2-hydroxy-2-(2-hydroxy-4-methylphenyl)propyl] (Z)-2-methylbut-2-enoate 162939748 Click to see CC=C(C)C(=O)OCC(COC(=O)C)(C1=C(C=C(C=C1)C)O)O 322.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
[2-Hydroxy-2-(2-hydroxy-4-methylphenyl)-3-(2-methylbut-2-enoyloxy)propyl] 2-methylbut-2-enoate 91213125 Click to see CC=C(C)C(=O)OCC(COC(=O)C(=CC)C)(C1=C(C=C(C=C1)C)O)O 362.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
[2-hydroxy-2-(2-hydroxy-4-methylphenyl)-3-[(Z)-2-methylbut-2-enoyl]oxypropyl] (Z)-2-methylbut-2-enoate 101854609 Click to see CC=C(C)C(=O)OCC(COC(=O)C(=CC)C)(C1=C(C=C(C=C1)C)O)O 362.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
[2,3-dihydroxy-2-(2-hydroxy-4-methylphenyl)propyl] (Z)-2-methylbut-2-enoate 21630998 Click to see CC=C(C)C(=O)OCC(CO)(C1=C(C=C(C=C1)C)O)O 280.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
[2,3-Dihydroxy-2-(2-hydroxy-4-methylphenyl)propyl] 2-methylbut-2-enoate 73815066 Click to see CC=C(C)C(=O)OCC(CO)(C1=C(C=C(C=C1)C)O)O 280.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
[3-Acetyloxy-2-hydroxy-2-(2-hydroxy-4-methylphenyl)propyl] 2-methylbut-2-enoate 85402240 Click to see CC=C(C)C(=O)OCC(COC(=O)C)(C1=C(C=C(C=C1)C)O)O 322.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
10-acetoxy-8-hydroxy-9-O-angeloylthmol 11110063 Click to see CC=C(C)C(=O)OCC(COC(=O)C)(C1=C(C=C(C=C1)C)O)O 322.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
4-Ethenyl-5-methyl-2-methylidenehex-5-ene-1,3-diol 14705672 Click to see CC(=C)C(C=C)C(C(=C)CO)O 168.23 unknown https://doi.org/10.1016/J.JEP.2010.07.009
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(5-Methyl-2-propan-2-ylphenyl) 2-methylbut-2-enoate 74336961 Click to see CC=C(C)C(=O)OC1=C(C=CC(=C1)C)C(C)C 232.32 unknown https://doi.org/10.1016/J.JEP.2010.07.009
https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1016/J.JEP.2010.07.009
https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
Thymol angelate 24862589 Click to see CC=C(C)C(=O)OC1=C(C=CC(=C1)C)C(C)C 232.32 unknown https://doi.org/10.1016/J.JEP.2010.07.009
https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohexene 152743364 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C 536.90 unknown https://doi.org/10.1021/NP0501278
Beta-Carotene 5280489 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C 536.90 unknown https://doi.org/10.1021/NP0501278
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acid esters
methyl (3aR,6R,6aS)-6-[(S)-[(1S)-cyclohex-2-en-1-yl]-hydroxymethyl]-6a-methyl-4-oxo-2,3,3a,5-tetrahydrofuro[2,3-c]pyrrole-6-carboxylate 11301327 Click to see CC12C(CCO1)C(=O)NC2(C(C3CCCC=C3)O)C(=O)OC 309.36 unknown https://doi.org/10.1016/J.JEP.2010.07.009
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(2-Methoxy-4-methylphenyl)ethanone 9167405 Click to see CC1=CC(=C(C=C1)C(=O)C)OC 164.20 unknown https://doi.org/10.1021/NP0501278
Hofmeisterin 11148458 Click to see CC1=CC(=C(C=C1)C(=O)COC(=O)C)O 208.21 unknown https://doi.org/10.1021/NP0501278
Hofmeisterin II 14107494 Click to see CC1=CC(=C(C=C1)C(=O)CCC(=O)C2=C(C=C(C=C2)C)O)O 298.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
> Organoheterocyclic compounds / Benzofurans
Euparin 119039 Click to see CC(=C)C1=CC2=CC(=C(C=C2O1)O)C(=O)C 216.23 unknown https://doi.org/10.1021/NP0501278
> Organoheterocyclic compounds / Furopyrans
(2R,3R,4'aS)-2,6,7'-trimethylspiro[2H-1-benzofuran-3,2'-4,9a-dihydro-3H-pyrano[2,3-b][1]benzofuran]-4'a-ol 162868457 Click to see CC1C2(CCC3(C(O2)OC4=C3C=CC(=C4)C)O)C5=C(O1)C=C(C=C5)C 338.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.011
(2S,3S,4'aR,9'aS)-6,8'-dimethylspiro[2H-1-benzofuran-3,2'-4,9a-dihydro-3H-pyrano[2,3-b][1]benzofuran]-2,4'a-diol 162952737 Click to see CC1=CC2=C(C=C1)C3(CCC4(C(O3)OC5=C(C=CC=C54)C)O)C(O2)O 340.40 unknown https://doi.org/10.1021/NP0501278
3',4',4a',9a'-tetrahydro-6,7'-dimethylspiro[benzofuran-3(2H),2'-pyrano[2,3-b]benzofuran]-2,4a'-diol 44559245 Click to see CC1=CC2=C(C=C1)C3(CCC4(C(O3)OC5=C4C=CC(=C5)C)O)C(O2)O 340.40 unknown https://doi.org/10.1021/NP0501278
6,7'-dimethylspiro[2H-1-benzofuran-3,2'-4,9a-dihydro-3H-pyrano[2,3-b][1]benzofuran]-2,4'a-diol 15406570 Click to see CC1=CC2=C(C=C1)C3(CCC4(C(O3)OC5=C4C=CC(=C5)C)O)C(O2)O 340.40 unknown https://doi.org/10.1021/NP0501278

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