You Searched For: Cyclohexyl+phenyl+ketone

Catalog Number: (CAAA16797-51)

Supplier: Thermo Scientific Chemicals

Description: NMR solvent

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Supplier: Thermo Scientific Chemicals

Description: 2,6-Dimethyl-4-heptanone ≥90%

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Supplier: Thermo Scientific Chemicals

Description: 4,4'-Dibromobenzophenone 98+%

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Supplier: MilliporeSigma

Description: Cas Number 119-61-9, Cas Number 119-61-9,For Synthesis

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Supplier: Burdick & Jackson

Description: For HPLC, liquid and gas chromatography, pesticide residue analysis, spectophotometry, organic synthesis and combinatorial chemistry.

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Supplier: TCI America

Description: CAS Number: 71119-22-7
MDL Number: MFCD00064350
Molecular Formula: C7H15NO4S
Molecular Weight: 231.24
Purity/Analysis Method: >98.0% (T)
Form: Crystal

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Supplier: Thermo Scientific Chemicals

Description: MDL: MFCD00000353 Beilstein Registry No.: 516231

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Supplier: Brandtech

Description: Polyoxymethylene (POM) forceps with rounded ends.

Catalog Number: (10407-240)

Supplier: Bioss

Description: This gene encodes a member of the short-chain dehydrogenase/reductase gene family. The encoded protein forms a homotetrameric lipid-requiring enzyme of the mitochondrial membrane and has a specific requirement for phosphatidylcholine for optimal enzymatic activity. The encoded protein catalyzes the interconversion of acetoacetate and (R)-3-hydroxybutyrate, the two major ketone bodies produced during fatty acid catabolism. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008].

Catalog Number: (TCM0737-025G)

Supplier: TCI America

Description: CAS Number: 71119-23-8
MDL Number: MFCD00065473
Molecular Formula: C6H13NO4S
Molecular Weight: 217.21
Purity/Analysis Method: >97.0% (N)
Form: Crystal

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Supplier: Thermo Scientific Chemicals

Description: Packaged under Argon in resealable ChemSeal™ bottles Uses: reducing agent of olefinic groups and ketones

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Catalog Number: (10408-234)

Supplier: Bioss

Description: Key enzyme for ketone body catabolism. Transfers the CoA moiety from succinate to acetoacetate. Formation of the enzyme-CoA intermediate proceeds via an unstable anhydride species formed between the carboxylate groups of the enzyme and substrate.

Catalog Number: (76079-696)

Supplier: Bioss

Description: Key enzyme for ketone body catabolism. Transfers the CoA moiety from succinate to acetoacetate. Formation of the enzyme-CoA intermediate proceeds via an unstable anhydride species formed between the carboxylate groups of the enzyme and substrate.

Supplier: MilliporeSigma

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Catalog Number: (CAAA42263-SA)

Supplier: Thermo Scientific Chemicals

Description: MDL: MFCD00044635 Notes: Minimum isotopic purity 99.96%

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Catalog Number: (10430-698)

Supplier: Bioss

Description: Acts as an electrogenic sodium (Na(+)) and chloride (Cl-)-dependent sodium-coupled solute transporter, including transport of monocarboxylates (short-chain fatty acids including L-lactate, D-lactate, pyruvate, acetate, propionate, valerate and butyrate), lactate, mocarboxylate drugs (nicotinate, benzoate, salicylate and 5-aminosalicylate) and ketone bodies (beta-D-hydroxybutyrate, acetoacetate and alpha-ketoisocaproate), with a Na(+):substrate stoichiometry of between 4:1 and 2:1. Catalyzes passive carrier mediated diffusion of iodide. Mediates iodide transport from the thyrocyte into the colloid lumen through the apical membrane. May be responsible for the absorption of D-lactate and monocarboxylate drugs from the intestinal tract. Acts as a tumor suppressor, suppressing colony formation in colon cancer, prostate cancer and glioma cell lines. May play a critical role in the entry of L-lactate and ketone bodies into neurons by a process driven by an electrochemical Na(+) gradient and hence contribute to the maintenance of the energy status and function of neurons.