Psacalium decompositum - Unknown
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Internal ID UUID643fce53428bf463742484
Scientific name Psacalium decompositum
Authority (A.Gray) H.Rob. & Brettell
First published in Phytologia 27: 260 (1973)

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Synonyms Top

Scientific name Authority First published in
Senecio grayanus Hemsl. Biol. Cent.-Amer., Bot. 2: 241 (1881)
Odontotrichum decompositum Rydb. Bull. Torrey Bot. Club 51: 414 (1924)
Mesadenia decomposita Standl. Contr. U.S. Natl. Herb. 19: 749 (1915)
Cacalia decomposita A.Gray Smithsonian Contr. Knowl. 5(6): 99. 1853 [1 Feb 1853] ; Plantae Wrightianae

Common names Top

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Language Common/alternative name
English desert indianbush

Subspecies (abbr. subsp./ssp.) 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 Northeast
      • Mexico Northwest
    • South-central U.S.A.
      • New Mexico
    • Southwestern U.S.A.
      • Arizona

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000080406
UNII EG29W26I8Z
USDA Plants PSDE2
Tropicos 50080092
KEW urn:lsid:ipni.org:names:210972-2
The Plant List gcc-36976
Open Tree Of Life 4727347
Nature Serve 2.139401
IPNI 210972-2
iNaturalist 156514
GBIF 3097629
EOL 509697
USDA GRIN 430220

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
Furanoeremophilane-type sesquiterpenes from Cacalia adenostyloides. MASANORI KUROYANAGI, HIROSHI NAITO, TAKATAKA NORO, AKIRA UENO, SEIGO FUKUSHIMA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.33.4792
THE SESQUITERPENES OF CACALIA SPECIES. II. THE STRUCTURE OF CACALAL AND THE INTERCONVERSIONS OF THE CONSTITUENTS Keizo Naya, Kunihiro Takai, Mikihiko Nakanishi, Kanji Omura Oxford University Press (OUP) 25-Jul-2006
doi:10.1246/CL.1977.1179
Anti-inflammatory activity of cacalol and cacalone sesquiterpenes isolated from Psacalium decompositum. Jimenez-Estrada M, Chilpa RR, Apan TR, Lledias F, Hansberg W, Arrieta D, Aguilar FJ J Ethnopharmacol 21-Apr-2006
doi:10.1016/J.JEP.2005.09.039
PMID:16307855
A novel cacalolide from Psacalium decompositum. Reyes-Chilpa R, Jiménez-Estrada M, Godínez MV, Hernández-Ortega S, Campos M, Béjar E Nat Prod Lett 01-Aug-2002
doi:10.1080/10575630290020532
PMID:12168758
The constituents of cacalia decomposita a. gray. structures of maturin, maturinin, maturone and maturinone J. Correa, J. Romo Elsevier BV 25-Jul-2002
doi:10.1016/0040-4020(66)80038-8
Antihyperglycemic sesquiterpenes from Psacalium decompositum. Inman WD, Luo J, Jolad SD, King SR, Cooper R J Nat Prod 01-Aug-1999
doi:10.1021/NP990023V
PMID:10479309
Hydroperoxycacalone: a new furanoeremophilane from Psacalium decompositum. Jiménez-Estrada M, Navarro-Ocaña A, Villanueva E, Paredes-González B, Reyes-Chilpa R, Román-Ramos R, Alarcón F Planta Med 01-Aug-1997
doi:10.1055/S-2006-957717
PMID:17252402
Phytotoxicity of cacalol and some derivatives obtained from the roots ofPsacalium decompositum (A. Gray) H. Rob. & Brettell (Asteraceae), matarique or maturin. Anaya AL, Hernández-Bautista BE, Torres-Barragán A, León-Cantero J, Jiménez-Estrada M J Chem Ecol 01-Mar-1996
doi:10.1007/BF02033643
PMID:24227480

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 / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(4R,5S)-4-hydroperoxy-3,4,5-trimethyl-5,6,7,8-tetrahydrobenzo[f][1]benzofuran-9-one 101715635 Click to see CC1CCCC2=C1C(C3=C(C2=O)OC=C3C)(C)OO 262.30 unknown https://doi.org/10.1055/S-2006-957717
(4R,5S)-4-hydroxy-3,4,5-trimethyl-5,6,7,8-tetrahydronaphtho[2,3-b]furan-9(4H)-one 642921 Click to see CC1CCCC2=C1C(C3=C(C2=O)OC=C3C)(C)O 246.30 unknown https://doi.org/10.1248/CPB.33.4792
https://doi.org/10.1055/S-2006-957717
https://doi.org/10.1016/J.JEP.2005.09.039
https://doi.org/10.1021/NP990023V
(5-Methyl-4,9-dioxobenzo[f][1]benzofuran-3-yl)methyl formate 163192691 Click to see CC1=C2C(=CC=C1)C(=O)C3=C(C2=O)C(=CO3)COC=O 270.24 unknown https://doi.org/10.1080/10575630290020532
4-Hydroperoxy-3,4,5-trimethyl-5,6,7,8-tetrahydrobenzo[f][1]benzofuran-9-one 163040470 Click to see CC1CCCC2=C1C(C3=C(C2=O)OC=C3C)(C)OO 262.30 unknown https://doi.org/10.1055/S-2006-957717
Bohlmann 183 330226 Click to see CC1CCCC2=C1C(=C3C(=COC3=C2O)C)C 230.30 unknown https://doi.org/10.1021/NP990023V
Cacalol 181105 Click to see CC1CCCC2=C1C(=C3C(=COC3=C2O)C)C 230.30 unknown https://doi.org/10.1007/BF02033643
https://doi.org/10.1246/CL.1977.1179
https://doi.org/10.1016/J.JEP.2005.09.039
https://doi.org/10.1021/NP990023V
Cacalone 73817341 Click to see CC1CCCC2=C1C(C3=C(C2=O)OC=C3C)(C)O 246.30 unknown https://doi.org/10.1021/NP990023V
https://doi.org/10.1055/S-2006-957717
Epicacalone 21635815 Click to see CC1CCCC2=C1C(C3=C(C2=O)OC=C3C)(C)O 246.30 unknown https://doi.org/10.1021/NP990023V
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3R,5S)-3,9-dihydroxy-3,4,5-trimethyl-5,6,7,8-tetrahydrobenzo[f][1]benzofuran-2-one 9871485 Click to see CC1CCCC2=C(C3=C(C(=C12)C)C(C(=O)O3)(C)O)O 262.30 unknown https://doi.org/10.1021/NP990023V
(3S,5R)-3,9-dihydroxy-3,4,5-trimethyl-5,6,7,8-tetrahydrobenzo[f][1]benzofuran-2-one 162905965 Click to see CC1CCCC2=C(C3=C(C(=C12)C)C(C(=O)O3)(C)O)O 262.30 unknown https://doi.org/10.1021/NP990023V
(3S,5S)-3,9-dihydroxy-3,4,5-trimethyl-5,6,7,8-tetrahydrobenzo[f][1]benzofuran-2-one 9871484 Click to see CC1CCCC2=C(C3=C(C(=C12)C)C(C(=O)O3)(C)O)O 262.30 unknown https://doi.org/10.1021/NP990023V
3,9-Dihydroxy-3,4,5-trimethyl-5,6,7,8-tetrahydrobenzo[f][1]benzofuran-2-one 78422559 Click to see CC1CCCC2=C(C3=C(C(=C12)C)C(C(=O)O3)(C)O)O 262.30 unknown https://doi.org/10.1021/NP990023V
> Organoheterocyclic compounds / Naphthofurans
3-(Hydroxymethyl)-8-methylbenzo[f][1]benzofuran-4,9-dione 11085934 Click to see CC1=C2C(=CC=C1)C(=O)C3=C(C2=O)OC=C3CO 242.23 unknown https://doi.org/10.1016/0040-4020(66)80038-8
3-(Hydroxymethyl)-9-methoxy-8-methylbenzo[f][1]benzofuran-4-carbaldehyde 15560151 Click to see CC1=C2C(=CC=C1)C(=C3C(=COC3=C2OC)CO)C=O 270.28 unknown https://doi.org/10.1016/0040-4020(66)80038-8
3,8-Dimethylbenzo[f][1]benzofuran-4,9-dione 85860360 Click to see CC1=C2C(=CC=C1)C(=O)C3=C(C2=O)OC=C3C 226.23 unknown https://doi.org/10.1016/0040-4020(66)80038-8
9-Methoxy-3,8-dimethylbenzo[f][1]benzofuran-4-carbaldehyde 15560152 Click to see CC1=C2C(=CC=C1)C(=C3C(=COC3=C2OC)C)C=O 254.28 unknown https://doi.org/10.1016/0040-4020(66)80038-8
> Organoheterocyclic compounds / Naphthopyrans
(15S)-8,15-dimethoxy-6-methyl-10,14-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-1(16),2,4,6,8,11-hexaene 163049365 Click to see CC1=C2C(=CC=C1)C3=C4C(=COC4=C2OC)COC3OC 284.31 unknown https://doi.org/10.1016/0040-4020(66)80038-8
8,15-Dimethoxy-6-methyl-10,14-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-1(16),2,4,6,8,11-hexaene 163049364 Click to see CC1=C2C(=CC=C1)C3=C4C(=COC4=C2OC)COC3OC 284.31 unknown https://doi.org/10.1016/0040-4020(66)80038-8
9-methoxy-3-[[(15S)-8-methoxy-6-methyl-10,14-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-1(16),2,4,6,8,11-hexaen-15-yl]oxymethyl]-8-methylbenzo[f][1]benzofuran-4-carbaldehyde 162921126 Click to see CC1=C2C(=CC=C1)C(=C3C(=COC3=C2OC)COC4C5=C6C(=COC6=C(C7=C(C=CC=C57)C)OC)CO4)C=O 522.50 unknown https://doi.org/10.1016/0040-4020(66)80038-8
Naphtho[2,3-b]furan-4-carboxaldehyde, 9-methoxy-3-[[(6-methoxy-7-methyl-1H,3H-benzo[h]furo[4,3,2-de]-2-benzopyran-1-yl)oxy]methyl]-8-methyl- 162921125 Click to see CC1=C2C(=CC=C1)C(=C3C(=COC3=C2OC)COC4C5=C6C(=COC6=C(C7=C(C=CC=C57)C)OC)CO4)C=O 522.50 unknown https://doi.org/10.1016/0040-4020(66)80038-8

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