Centromadia fitchii - Unknown
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Internal ID UUID643fcaf329107109155788
Scientific name Centromadia fitchii
Authority Greene
First published in Man. Bot. San Francisco : 197 (1894)

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Synonyms Top

Scientific name Authority First published in
Hemizonia fitchii A.Gray Pacif. Railr. Rep. Parke, Bot. iv. 109

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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
    • Northwestern U.S.A.
      • Oregon
    • Southwestern U.S.A.
      • California

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000042487
Tropicos 50159526
KEW urn:lsid:ipni.org:names:51449-2
The Plant List gcc-141100
Open Tree Of Life 3899669
NCBI Taxonomy 2894882
IPNI 51449-2
iNaturalist 58804
GBIF 3141050
Freebase /m/013c9l9q
EOL 844841
Calflora (Californian flora) 10809
USDA GRIN 452938
Wikipedia Centromadia_fitchii

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 CentralĀ®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
A parasitic plant increases native and exotic plant species richness in vernal pools Graffis AM, Kneitel JM AoB Plants 22-Aug-2015
PMCID:PMC4612139
doi:10.1093/aobpla/plv100
PMID:26307042
Foliar flavonoid exudates and sectional taxonomy of Hemizonia Barry D. Tanowitz, Gerhard Leeder, Patrick N. Ross, Peter Proksch Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(87)90101-3
Labdane derivatives from hemizonia species Ferdinand Bohlmann, Jasmin Jakupovic, Maniruddin Ahmed, Michael Wallmeyer, Harold Robinsont, Robert M. King Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82671-0
Insecticidal chromenes from the volatile oil ofHemizonia fitchii. Klocke JA, Balandrin MF, Adams RP, Kingsford E J Chem Ecol 01-Jun-1985
doi:10.1007/BF00988299
PMID:24310216

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 / Naphthalenes
Naphthalene 931 Click to see C1=CC=C2C=CC=CC2=C1 128.17 unknown https://doi.org/10.1007/BF00988299
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptacosane 11636 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC 380.70 unknown https://doi.org/10.1007/BF00988299
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1007/BF00988299
Pentacosane 12406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC 352.70 unknown https://doi.org/10.1007/BF00988299
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
2-Methylbutanoic acid 8314 Click to see CCC(C)C(=O)O 102.13 unknown https://doi.org/10.1007/BF00988299
Isovaleric acid 10430 Click to see CC(C)CC(=O)O 102.13 unknown https://doi.org/10.1007/BF00988299
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1007/BF00988299
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1007/BF00988299
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown https://doi.org/10.1007/BF00988299
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1007/BF00988299
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1007/BF00988299
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1007/BF00988299
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3R,6E)-nerolidol 11241545 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1007/BF00988299
(E,Z)-farnesol 1549109 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.1007/BF00988299
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1007/BF00988299
Farnesol 3327 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.1007/BF00988299
Nerolidol 8888 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1007/BF00988299
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Isobutyric acid 6590 Click to see CC(C)C(=O)O 88.11 unknown https://doi.org/10.1007/BF00988299
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(1S)-1-(7-methoxy-2,2-dimethylchromen-6-yl)ethanol 162955950 Click to see CC(C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC)O 234.29 unknown https://doi.org/10.1016/S0031-9422(00)82671-0
[(1R)-1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl] (2R)-2-methylbutanoate 163049360 Click to see CCC(C)C(=O)OC(C)C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC 318.40 unknown https://doi.org/10.1016/S0031-9422(00)82671-0
[(1S)-1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl] 3-methylbutanoate 162909598 Click to see CC(C)CC(=O)OC(C)C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC 318.40 unknown https://doi.org/10.1016/S0031-9422(00)82671-0
1-(2,2-Dimethylchromen-6-yl)ethanone 177040 Click to see CC(=O)C1=CC2=C(C=C1)OC(C=C2)(C)C 202.25 unknown https://doi.org/10.1007/BF00988299
1-(7-Methoxy-2,2-dimethylchromen-6-yl)ethyl 2-methylbutanoate 163049359 Click to see CCC(C)C(=O)OC(C)C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC 318.40 unknown https://doi.org/10.1016/S0031-9422(00)82671-0
1-(7-Methoxy-2,2-dimethylchromen-6-yl)ethyl 3-methylbutanoate 162909597 Click to see CC(C)CC(=O)OC(C)C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC 318.40 unknown https://doi.org/10.1016/S0031-9422(00)82671-0
Encecalin 114703 Click to see CC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC 232.27 unknown https://doi.org/10.1016/S0031-9422(00)82671-0
https://doi.org/10.1007/BF00988299
Eupatoriochromene 100768 Click to see CC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)C)O 218.25 unknown https://doi.org/10.1007/BF00988299
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
(Z)-3-[4-[(3-Methyl-2-butenyl)oxy]phenyl]-2-propenoic acid methyl ester 163184441 Click to see CC(=CCOC1=CC=C(C=C1)C=CC(=O)OC)C 246.30 unknown https://doi.org/10.1016/S0031-9422(00)82671-0
Methyl 3-[4-(3-methylbut-2-enoxy)phenyl]prop-2-enoate 72731127 Click to see CC(=CCOC1=CC=C(C=C1)C=CC(=O)OC)C 246.30 unknown https://doi.org/10.1016/S0031-9422(00)82671-0
> 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/10.1016/0305-1978(87)90101-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferide 5281666 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/0305-1978(87)90101-3

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