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Amyris texana

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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 UUID6440090061d81921941753
Scientific name Amyris texana
Authority P.Wilson
First published in Torreya 8: 139 (1908)

Description Top

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Synonyms Top

Scientific name Authority First published in
Amyris parvifolia A.Gray Proc. Amer. Acad. Arts 23: 226 (1888)
Zanthoxylum texanum Buckley Bull. Torrey Bot. Club 10: 90 (1883)

Common names Top

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Language Common/alternative name
English texas torchwood

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 Gulf
      • Mexico Northeast
    • South-central U.S.A.
      • Texas

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000532724
USDA Plants AMTE4
Tropicos 28100395
KEW urn:lsid:ipni.org:names:12195-2
The Plant List kew-2635587
Open Tree Of Life 3942533
Nature Serve 2.134712
IUCN Red List 126618470
IPNI 12195-2
iNaturalist 158324
GBIF 5421189
EOL 582198

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
New class of algicidal compounds and fungicidal activities derived from a chromene amide of Amyris texana. Meepagala KM, Schrader KK, Burandt CL, Wedge DE, Duke SO J Agric Food Chem 08-Sep-2010
doi:10.1021/JF101626G
PMID:20695429
Two New Oxazoles from Amyris texana P. Wilson Gabriel de la Fuente, Xorge A. Dom地guez, Antonio G. Gonz�ez. Mat痴 Reina, Isabel Tim溶 The Japan Institute of Heterocyclic Chemistry 23-Feb-2009
doi:10.3987/COM-87-4326
Chromene amides from Amyris texana Gabriel de la Fuente, Matias Reina, Isabel Timon Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)85122-G

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
> Organoheterocyclic compounds / Azoles / Oxazoles / Phenyl-1,3-oxazoles
5-(1,3-Benzodioxol-5-yl)-2-phenyl-1,3-oxazole 10912414 Click to see C1OC2=C(O1)C=C(C=C2)C3=CN=C(O3)C4=CC=CC=C4 265.26 unknown https://doi.org/10.3987/COM-87-4326
Pyridine, 3-[5-[4-[(3-methyl-2-butenyl)oxy]phenyl]-2-oxazolyl]- 617263 Click to see CC(=CCOC1=CC=C(C=C1)C2=CN=C(O2)C3=CN=CC=C3)C 306.40 unknown https://doi.org/10.3987/COM-87-4326
> Organoheterocyclic compounds / Benzodioxoles
Texaline 473253 Click to see C1OC2=C(O1)C=C(C=C2)C3=CN=C(O3)C4=CN=CC=C4 266.25 unknown https://doi.org/10.1016/0031-9422(91)85122-G
https://doi.org/10.3987/COM-87-4326
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
N-[2-(2,2-Dimethyl-2H-1-benzopyran-6-yl)ethyl]acetamide 15693442 Click to see CC(=O)NCCC1=CC2=C(C=C1)OC(C=C2)(C)C 245.32 unknown https://doi.org/10.1016/0031-9422(91)85122-G
N-[2-(2,2-Dimethyl-2H-1-benzopyran-6-yl)ethyl]benzamide 15693445 Click to see CC1(C=CC2=C(O1)C=CC(=C2)CCNC(=O)C3=CC=CC=C3)C 307.40 unknown https://doi.org/10.1016/0031-9422(91)85122-G
N-[2-(2,2-dimethylchromen-6-yl)ethyl]-2-methylpropanamide 14482284 Click to see CC(C)C(=O)NCCC1=CC2=C(C=C1)OC(C=C2)(C)C 273.37 unknown https://doi.org/10.1016/0031-9422(91)85122-G
N-[2-(2,2-dimethylchromen-6-yl)ethyl]-3-methylbut-2-enamide 15693444 Click to see CC(=CC(=O)NCCC1=CC2=C(C=C1)OC(C=C2)(C)C)C 285.40 unknown https://doi.org/10.1016/0031-9422(91)85122-G
N-[2-(2,2-dimethylchromen-6-yl)ethyl]-3-methylbutanamide 14482283 Click to see CC(C)CC(=O)NCCC1=CC2=C(C=C1)OC(C=C2)(C)C 287.40 unknown https://doi.org/10.1016/0031-9422(91)85122-G
N-[2-(2,2-dimethylchromen-6-yl)ethyl]-N-methylacetamide 15693447 Click to see CC(=O)N(C)CCC1=CC2=C(C=C1)OC(C=C2)(C)C 259.34 unknown https://doi.org/10.1016/0031-9422(91)85122-G
N-[2-(2,2-dimethylchromen-6-yl)ethyl]-N-methylbenzamide 15693451 Click to see CC1(C=CC2=C(O1)C=CC(=C2)CCN(C)C(=O)C3=CC=CC=C3)C 321.40 unknown https://doi.org/10.1016/0031-9422(91)85122-G
N-[2-(2,2-dimethylchromen-6-yl)ethyl]-N-methylpyridine-3-carboxamide 15693452 Click to see CC1(C=CC2=C(O1)C=CC(=C2)CCN(C)C(=O)C3=CN=CC=C3)C 322.40 unknown https://doi.org/10.1016/0031-9422(91)85122-G
N-[2-(2,2-dimethylchromen-6-yl)ethyl]-N,2-dimethylpropanamide 15693449 Click to see CC(C)C(=O)N(C)CCC1=CC2=C(C=C1)OC(C=C2)(C)C 287.40 unknown https://doi.org/10.1016/0031-9422(91)85122-G
N-[2-(2,2-dimethylchromen-6-yl)ethyl]-N,3-dimethylbut-2-enamide 15693448 Click to see CC(=CC(=O)N(C)CCC1=CC2=C(C=C1)OC(C=C2)(C)C)C 299.40 unknown https://doi.org/10.1016/0031-9422(91)85122-G
N-[2-(2,2-dimethylchromen-6-yl)ethyl]-N,3-dimethylbutanamide 15693450 Click to see CC(C)CC(=O)N(C)CCC1=CC2=C(C=C1)OC(C=C2)(C)C 301.40 unknown https://doi.org/10.1016/0031-9422(91)85122-G
https://doi.org/10.1021/JF101626G
N-[2-(2,2-dimethylchromen-6-yl)ethyl]butanamide 15693443 Click to see CCCC(=O)NCCC1=CC2=C(C=C1)OC(C=C2)(C)C 273.37 unknown https://doi.org/10.1016/0031-9422(91)85122-G
N-[2-(2,2-dimethylchromen-6-yl)ethyl]pyridine-3-carboxamide 15693446 Click to see CC1(C=CC2=C(O1)C=CC(=C2)CCNC(=O)C3=CN=CC=C3)C 308.40 unknown https://doi.org/10.1016/0031-9422(91)85122-G
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown https://doi.org/10.1016/0031-9422(91)85122-G
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1016/0031-9422(91)85122-G
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Isoimperatorin 68081 Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C 270.28 unknown https://doi.org/10.1016/0031-9422(91)85122-G
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1016/0031-9422(91)85122-G
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Seselin 68229 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC(=O)C=C3)C 228.24 unknown https://doi.org/10.1016/0031-9422(91)85122-G

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