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Acourtia carpholepis

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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 UUID643fc6916b817066892847
Scientific name Acourtia carpholepis
Authority (A.Gray) Reveal & R.M.King
First published in Phytologia 27: 229 (1973)

Description Top

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Synonyms Top

Scientific name Authority First published in
Perezia carpholepis A.Gray Proc. Amer. Acad. Arts 19: 60 (1883)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southeast
      • Mexico Southwest

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000006373
Tropicos 2726370
KEW urn:lsid:ipni.org:names:3461-2
The Plant List gcc-106142
Open Tree Of Life 7624049
IPNI 3461-2
iNaturalist 279810
GBIF 5388109
EOL 6236684

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
Antidiabetic and Antihyperalgesic Effects of a Decoction and Compounds from Acourtia thurberi. Martínez AL, Madariaga-Mazón A, Rivero-Cruz I, Bye R, Mata R Planta Med 01-Apr-2017
doi:10.1055/S-0042-119652
PMID:27824405
<sup>-13</sup>C-nmr Studies of Curcumenes P. Joseph-Nathan, R. Tovar-Miranda, E. Martínez, R. L. Santillan American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50060A012
Sesquiterpenes from Perezia carpholepis P. Joseph-Nathan, J.D. Hernández, L.U. Román, G. E. García, V. Mendoza Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(82)83162-2

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 / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(10R)-3,6,10-trimethyl-5,8,9,10-tetrahydrobenzo[8]annulen-2-ol 182352 Click to see CC1CCC=C(CC2=C1C=C(C(=C2)C)O)C 216.32 unknown https://doi.org/10.1016/0031-9422(82)83162-2
(6Z,10R)-3,6,10-trimethyl-5,8,9,10-tetrahydrobenzo[8]annulen-2-ol 6442684 Click to see CC1CCC=C(CC2=C1C=C(C(=C2)C)O)C 216.32 unknown https://doi.org/10.1016/0031-9422(82)83162-2
(6Z,10S)-3,6,10-trimethyl-5,8,9,10-tetrahydrobenzo[8]annulen-2-ol 13996861 Click to see CC1CCC=C(CC2=C1C=C(C(=C2)C)O)C 216.32 unknown https://doi.org/10.1016/0031-9422(82)83162-2
3,6,10-Trimethyl-5,8,9,10-tetrahydrobenzo[8]annulen-2-ol 78410270 Click to see CC1CCC=C(CC2=C1C=C(C(=C2)C)O)C 216.32 unknown https://doi.org/10.1016/0031-9422(82)83162-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Curcumene 442360 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1021/NP50060A012
(-)-Cyperene 12308843 Click to see CC1CCC2CC3=C(CCC13C2(C)C)C 204.35 unknown https://doi.org/10.1016/0031-9422(82)83162-2
[4-Hydroxy-5-methyl-2-(6-methylhept-5-en-2-yl)phenyl] 3-methylbutanoate 162852152 Click to see CC1=CC(=C(C=C1O)C(C)CCC=C(C)C)OC(=O)CC(C)C 318.40 unknown https://doi.org/10.1016/0031-9422(82)83162-2
[4-hydroxy-5-methyl-2-[(2R)-6-methylhept-5-en-2-yl]phenyl] 3-methylbutanoate 162852153 Click to see CC1=CC(=C(C=C1O)C(C)CCC=C(C)C)OC(=O)CC(C)C 318.40 unknown https://doi.org/10.1016/0031-9422(82)83162-2
2-(1,5-Dimethyl-4-hexenyl)-3-hydroxy-5-methylbenzo-1,4-quinone 339385 Click to see CC1=CC(=O)C(=C(C1=O)O)C(C)CCC=C(C)C 248.32 unknown https://doi.org/10.1016/0031-9422(82)83162-2
3H-3a,7-Methanoazulene, 2,4,5,6,7,8-hexahydro-1,4,9,9-tetramethyl-, [3aR-(3aalpha,4beta,7alpha)]- 99856 Click to see CC1CCC2CC3=C(CCC13C2(C)C)C 204.35 unknown https://doi.org/10.1016/0031-9422(82)83162-2
4,10,11,11-Tetramethyltricyclo[5.3.1.0^{1,5}]undec-4-en-3-one 12308614 Click to see CC1CCC2CC3=C(C(=O)CC13C2(C)C)C 218.33 unknown https://doi.org/10.1016/0031-9422(82)83162-2
alpha-Curcumene 92139 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1021/NP50060A012
Cyperotundone 12308615 Click to see CC1CCC2CC3=C(C(=O)CC13C2(C)C)C 218.33 unknown https://doi.org/10.1016/0031-9422(82)83162-2
Perezone 92964 Click to see CC1=CC(=O)C(=C(C1=O)O)C(C)CCC=C(C)C 248.32 unknown https://doi.org/10.1016/0031-9422(82)83162-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(1R,2R,5S,7R)-9-Hydroxy-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-ene-10,11-dione 12314345 Click to see CC1CCC2C13C(=O)C(C2(C)C)C(=C(C3=O)O)C 248.32 unknown https://doi.org/10.1016/0031-9422(82)83162-2
(1S,2R,5S,7S)-9-hydroxy-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-ene-10,11-dione 162923014 Click to see CC1CCC2C13C(=O)C(C2(C)C)C(=C(C3=O)O)C 248.32 unknown https://doi.org/10.1016/0031-9422(82)83162-2
9-Hydroxycedr-8-ene-10,11-dione 12314344 Click to see CC1CCC2C13C(=O)C(C2(C)C)C(=C(C3=O)O)C 248.32 unknown https://doi.org/10.1055/S-0042-119652
https://doi.org/10.1016/0031-9422(82)83162-2
beta-Pipitzol 12314346 Click to see CC1CCC2C13C(=O)C(C2(C)C)C(=C(C3=O)O)C 248.32 unknown https://doi.org/10.1016/0031-9422(82)83162-2

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