38775
2,3-二甲氧基-5-甲基-对苯醌
≥98.0% (HPLC)
别名:
Coenzyme Q0
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关于此项目
经验公式（希尔记法）:
C9H10O4
化学文摘社编号:
分子量:
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
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Biochemistry, Bioenergetics and Clinical Applications of Ubiquinone,G.Lenaz ed, 517-517 (1985)
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]
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
Andreas Bock et al.
European journal of biochemistry, 269(14), 3479-3484 (2002-07-24)
The purified soluble forms of the histidine kinases BvgS and EvgS of Bordetella pertussis and Escherichia coli, respectively, are shown to be responsive to oxidized ubiquinone-0 (Q-0) in vitro. The oxidized ubiquinone is a strong inhibitor of kinase activity of
Wen-Wu Li et al.
Journal of the American Chemical Society, 127(17), 6140-6141 (2005-04-28)
Ubiquinone-0, menaquinone-0, and 2,3,5-trimethyl-1,4-benzoquinone were site-specifically bound to free cysteine of proteins (yeast iso-1 cytochrome c as a model protein) through thioether bond formation. Model thioether quinone conjugates showed unexpected reactivity to cysteine of proteins as their parent quinones by
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