| Weight | 250.294 g/mol |
|---|---|
| Formula | C14H18O4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
Coenzyme Q1 (727-81-1)
CoQ1 · ubiquinone 5 · Ubiquinone Q1
Score:
#1152 in Biochemistry
,
#2929 in Biology
,
#3668 in Chemistry
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- Anatomic and Disease Specificity of NADH CoQ1 Reductase (Complex I) Deficiency in Parkinson's Disease (Journal of Neurochemistry, 1990)
- Expression of prokaryotic 1-deoxy-d-xylulose-5-phosphatases in Escherichia coli increases carotenoid and ubiquinone biosynthesis (FEBS Letters, 1999)
- [3] Preparation and properties of NADH: Ubiquinone oxidoreductase (complex I), EC 1.6.5.3 (Methods in Enzymology, 1978)
- [5] Preparation and properties of succinate: Ubiquinone oxidoreductase (complex II) (Methods in Enzymology, 1978)
- Effects of 3 beta-[2-(diethylamino)ethoxy]androst-5-en-17-one on the synthesis of cholesterol and ubiquinone in rat intestinal epithelial cell cultures. (Biochemistry, 1983)
- Genetic Evidence for a Multi-subunit Complex in Coenzyme Q Biosynthesis in Yeast and the Role of the Coq1 Hexaprenyl Diphosphate Synthase (Journal of Biological Chemistry, 2005)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - CoQ1
- ubiquinone 5
- Ubiquinone Q1
- coenzyme Q5
-
SMILESCC1=C(C(=O)C(=C(C1=O)OC)OC)CC=C(C)C
-
InChIKeySOECUQMRSRVZQQ-UHFFFAOYSA-N
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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Coenzyme Q1
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