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Merck
CN

38775

2,3-二甲氧基-5-甲基-苯醌

≥98.0% (HPLC)

别名:

Coenzyme Q0

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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
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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

pictograms

Exclamation mark

signalword

Warning

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

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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]
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
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

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