ChemicalBook > CAS DataBase List > Fenofibrate-d6

Fenofibrate-d6

Product Name
Fenofibrate-d6
CAS No.
1092484-56-4
Chemical Name
Fenofibrate-d6
Synonyms
Lipsin-d6; LF 178-d6;Lipirex-d6;Liposit-d6;Nolipax-d6;Lipofene-d6;Lipoclar-d6;Lipantil-d6;MeltDose-d6;Lipanthyl-d6
CBNumber
CB11176332
Molecular Formula
C20H21ClO4
Formula Weight
360.83
MOL File
1092484-56-4.mol
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Fenofibrate-d6 Property

Melting point:
70-720C
storage temp. 
-20°C Freezer
solubility 
Chloroform (Slightly), Methanol (Sightly)
form 
Solid
color 
White to Off-White
CAS DataBase Reference
1092484-56-4
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
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N-Bromosuccinimide Price

Cayman Chemical
Product number
25710
Product name
Fenofibrate-d6
Purity
≥99% deuterated forms (d1-d6)
Packaging
500μg
Price
$93
Updated
2024/03/01
Cayman Chemical
Product number
25710
Product name
Fenofibrate-d6
Purity
≥99% deuterated forms (d1-d6)
Packaging
1mg
Price
$166
Updated
2024/03/01
Cayman Chemical
Product number
25710
Product name
Fenofibrate-d6
Purity
≥99% deuterated forms (d1-d6)
Packaging
5mg
Price
$684
Updated
2024/03/01
TRC
Product number
F248642
Product name
Fenofibrate-d6
Packaging
1mg
Price
$175
Updated
2021/12/16
Usbiological
Product number
011976
Product name
Fenofibrate-d6
Packaging
1mg
Price
$446
Updated
2021/12/16
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Fenofibrate-d6 Chemical Properties,Usage,Production

Description

Fenofibrate-d6 is intended for use as an internal standard for the quantification of fenofibrate by GC- or LC-MS. Fenofibrate is an agonist of peroxisome proliferator-activated receptor α (PPARα) with EC50 values of 18 and 30 μM for mouse and human receptors, respectively, in a transactivation assay. It is selective for PPARα over PPARγ (EC50s = 300 and 200 μM for mouse and human receptors, respectively) and lacks activity at mouse and human PPARδ at a concentration of 100 μM. In vivo, fenofibrate (50-100 mg/kg) reduces plasma levels of triglycerides, C-reactive protein, and malondialdehyde (MDA) in mice with fructose-induced hypertriglycemia in a dose-dependent manner. It decreases glomerular and tubular atrophy and necrosis induced by cisplatin in rat kidney when administered at a dose of 100 mg/kg. Fenofibrate also reduces the number of pulmonary lesions induced by 4-nitroquinoline 1-oxide (4-NQO) in lung of Tsumura Suzuki obese diabetic (TSOD) mice.

Chemical Properties

White Solid

Uses

Antilipemic. It is a lipid regulating drug. Increases high density lipoprotein levels by reducing cholesteryl ester transfer protein expresion.

Fenofibrate-d6 Preparation Products And Raw materials

Raw materials

Preparation Products

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Fenofibrate-d6 Suppliers

SIMSON PHARMA LIMITED
Tel
+91-8291074273
Email
k.das@simsonpharma.com
Country
India
ProdList
228
Advantage
58
Pharma Affiliates
Tel
--
Fax
--
Email
@pharmaffiliates.com
Country
India
ProdList
6754
Advantage
58
SynZeal Research Pvt Ltd
Tel
--
Fax
--
Email
standards@synzeal.com
Country
India
ProdList
6514
Advantage
58
Pharmaffiliates Analytics and Synthetics P. Ltd
Tel
--
Fax
--
Email
mktg@pharmaffiliates.com
Country
India
ProdList
6739
Advantage
58

1092484-56-4, Fenofibrate-d6Related Search:


  • LF 178-d6
  • 2-[4-(4-Chlorobenzoyl)phenoxy]-2-methyl-propanoic Acid-d6 1-Methylethyl Ester
  • Fenofibrate-d6
  • Lipanthyl-d6
  • Lipantil-d6
  • Lipidil Supra-d6
  • Lipirex-d6
  • Lipoclar-d6
  • Lipofene-d6
  • Liposit-d6
  • Lipsin-d6
  • MeltDose-d6
  • Nolipax-d6
  • NSC 281319-d6
  • YMTINGFKWWXKFG-LIJFRPJRSA-N
  • 1092484-56-4
  • Intermediates & Fine Chemicals
  • Isotope Labeled Compounds
  • Pharmaceuticals
  • Isotope Labelled Compounds