38775
2,3-Dimethoxy-5-methyl-p-benzoquinone
≥98.0% (HPLC)
Synonym(s):
Coenzyme Q0
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About This Item
Empirical Formula (Hill Notation):
C9H10O4
CAS Number:
Molecular Weight:
182.17
EC Number:
210-100-8
UNSPSC Code:
41106305
MDL number:
Beilstein/REAXYS Number:
1640422
InChI
1S/C9H10O4/c1-5-4-6(10)8(12-2)9(13-3)7(5)11/h4H,1-3H3
InChI key
UIXPTCZPFCVOQF-UHFFFAOYSA-N
SMILES string
COC1=C(OC)C(=O)C(C)=CC1=O
assay
≥98.0% (HPLC)
Other Notes
Coenzyme Q
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Biochemistry, Bioenergetics and Clinical Applications of Ubiquinone,G.Lenaz ed, 517-517 (1985)
S Martinucci et al.
FEBS letters, 480(2-3), 89-94 (2000-10-18)
Ubiquinone 0 and decylubiquinone have been reported to inhibit the mitochondrial permeability transition pore (PTP) [Fontaine, E., Ichas, F. and Bernardi, P. (1998) J. Biol. Chem. 273, 25734-257401, offering a new clue to its molecular composition. In patch-clamp experiments on
Jason W Cooley et al.
Biochemistry, 43(8), 2217-2227 (2004-02-26)
We have previously reported that mutant strains of Rhodobacter capsulatus that have alanine insertions (+nAla mutants) in the hinge region of the iron sulfur (Fe-S) containing subunit of the bc(1) complex have increased redox midpoint potentials (E(m)) for their [2Fe2S]
Wei Yuan et al.
Journal of chromatography. A, 1218(18), 2561-2568 (2011-03-23)
Thiol and disulfide levels are critical to maintaining the redox potential of a cell. Perturbations of these levels are important in disease pathogenesis. To improve endogenous mammalian metabolome quantitation, thiol specific tagging, extraction and relative quantitation were undertaken. Reduced and
B K Rao et al.
Biochemistry, 39(12), 3285-3296 (2000-03-22)
The isolated cytochrome (cyt) b(6)f complex from spinach is inhibited by Cu(2+) with a K(D) of about 1 microM at pH 7.6 in the presence of 1.6 microM decyl-plastoquinol (C(10)-PQH(2)) as a substrate. Inhibition was competitive with respect to C(10)-PQH(2)
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