27597

Coenzyme Q₉

≥96.0% (HPLC)

• Synonim(y): Q-9, Ubiquinone-45, Ubiquinone-9
• Wzór empiryczny (zapis Hilla): C₅₄H₈₂O₄
• Numer CAS: 303-97-9
• Masa cząsteczkowa: 795.23
• UNSPSC Code: 12352204
• NACRES: NA.51
• PubChem Substance ID: 57648260
• MDL number: MFCD00056635
• Beilstein/REAXYS Number: 1900081

Właściwości

• Quality Segment: 100
• assay: ≥96.0% (HPLC)
• form: powder
• application(s): cell analysis
• storage temp.: −20°C
• SMILES string: COC1=C(OC)C(=O)C(C\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(\C)C)=C(C)C1=O
• InChI: 1S/C54H82O4/c1-40(2)22-14-23-41(3)24-15-25-42(4)26-16-27-43(5)28-17-29-44(6)30-18-31-45(7)32-19-33-46(8)34-20-35-47(9)36-21-37-48(10)38-39-50-49(11)51(55)53(57-12)54(58-13)52(50)56/h22,24,26,28,30,32,34,36,38H,14-21,23,25,27,29,31,33,35,37,39H2,1-13H3/b41-24+,42-26+,43-28+,44-30+,45-32+,46-34+,47-36+,48-38+
• InChI key: UUGXJSBPSRROMU-WJNLUYJISA-N

Opis

General description

Coenzyme Q9 (Ubiquinone-9; Ubi-9) is a 9 isoprenyl group member of a family of ubiquinones that share a quinine chemical group but differ in the number of isoprenyl chemical subunits in their tail. The CoQ compounds are lipid soluble components of cell membranes.[1]

Application

Coenzyme Q9 (Ubiquinone-9; Ubi-9) may be used in the study of ubiquinones in vivo and in vitro. Coenzyme Q9 may be used as a reference compound in analytic procedures that monitor specific ubiquinone levels under various physiological and pathological conditions and in food-stocks.[2]

Coenzyme Q₉ has been used to investigate its interference in the detection of coenzyme Q₁₀ (CoQ₁₀) by fluorescent spectrophotometer (FS-ECA). It has also been used as an analyte in chromatographic analysis of different biological samples that correspond to different genetic conditions.

Biochem/physiol Actions

The coenzyme Q (CoQ) can perform multiple functions such as electron and proton transport.[1] CoQ₉ performs similar functions to CoQ₁₀ as the native CoQ in Caenorhabditis elegans. CoQ₉ as well as other CoQ molecules may have an impact on cell life-span and these molecules are seeing increase usage in such studies.[3]

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

An efficient electron and proton translocator in liposome systems; Prevents the appearance of adriamycin^®-associated cardiotoxic phenomena in mice and rabbits.[4]

Legal Information

Adriamycin is a registered trademark of RDF Pharmacia & Upjohn S.P.A.

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Informacja o środkach bezpieczeństwa

• Klasa składowania: 11 - Combustible Solids
• wgk: WGK 2
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)