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MF 438

Product Name
MF 438
CAS No.
921605-87-0
Chemical Name
MF 438
Synonyms
MF 438;MF-438, 10 mM in DMSO;Stearoyl-CoA Desaturase (SCD),inhibit,MF438,MF 438,MF-438,Inhibitor;3-(5-Methyl-1,3,4-thiadiazol-2-yl)-6-[4-[2-(trifluoromethyl)phenoxy]-1-piperidinyl]pyridazine;2-methyl-5-[6-[4-[2-(trifluoromethyl)phenoxy]piperidin-1-yl]pyridazin-3-yl]-1,3,4-thiadiazole;Pyridazine, 3-(5-methyl-1,3,4-thiadiazol-2-yl)-6-[4-[2-(trifluoromethyl)phenoxy]-1-piperidinyl]-;3-(5-Methyl-1,3,4-thiadiazol-2-yl)-6-[4-[2-(trifluoromethyl)phenoxy]-1-piperidinyl]pyridazine(MF-438)
CBNumber
CB52716285
Molecular Formula
C19H18F3N5OS
Formula Weight
421.44
MOL File
921605-87-0.mol
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MF 438 Property

Boiling point:
614.5±65.0 °C(Predicted)
Density 
1.365±0.06 g/cm3(Predicted)
storage temp. 
-20°
solubility 
Soluble in DMSO (up to 5 mg/ml) or in Ethanol (up to 2 mg/ml with warming).
form 
solid
pka
2.29±0.10(Predicted)
color 
Off-white
Stability:
Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 1 month.
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

ChemScene
Product number
CS-0009306
Product name
MF-438
Purity
99.92%
Packaging
5mg
Price
$250
Updated
2021/12/16
ChemScene
Product number
CS-0009306
Product name
MF-438
Purity
99.92%
Packaging
10mg
Price
$380
Updated
2021/12/16
ChemScene
Product number
CS-0009306
Product name
MF-438
Purity
99.92%
Packaging
50mg
Price
$1150
Updated
2021/12/16
ChemScene
Product number
CS-0009306
Product name
MF-438
Purity
99.92%
Packaging
100mg
Price
$1650
Updated
2021/12/16
Ambeed
Product number
A1148548
Product name
2-Methyl-5-(6-(4-(2-(trifluoromethyl)phenoxy)piperidin-1-yl)pyridazin-3-yl)-1,3,4-thiadiazole
Purity
95+%
Packaging
1mg
Price
$130
Updated
2021/12/16
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MF 438 Chemical Properties,Usage,Production

Description

MF-438 (921605-87-0) is a potent inhibitor of stearoyl-CoA desaturase 1 (SCD1) – IC50?= 2.3 nM.1?MF-438 was potent in an?in vivo?mouse liver PD assay (ED50?between 1 and 3 mg/kg).1?Cancer initiating cells (CSC-like) were shown to be much more sensitive to MF-438 inhibition of SCD1 than progenitor and terminally differentiated cancer cells in a lung cancer model.2?MF-438 showed good oral bioavailability and metabolic stability making it an excellent tool for studying the effects of SCD1 in various disease models.

Uses

MF-438 is a potent and orally bioavailable stearoyl-CoA desaturase 1 (SCD1) inhibitor with an IC50 of 2.3 nM for rSCD1[1].

in vivo

MF-438 exhibits an ED50 between 1 and 3 mg/kg in a mouse model[1].

References

[1] SERGE LÉGER. Synthesis and biological activity of a potent and orally bioavailable SCD inhibitor (MF-438)[J]. Bioorganic & Medicinal Chemistry Letters, 2010, 20 2: Pages 499-502. DOI:10.1016/j.bmcl.2009.11.111
[2] A NOTO. Stearoyl-CoA desaturase-1 is a key factor for lung cancer-initiating cells[J]. Cell Death & Disease, 2013, 4 12: e947-e947. DOI:10.1038/cddis.2013.444
[3] N. RODRIGUEZ-PEREZ. Altered fatty acid metabolism and reduced stearoyl-coenzyme a desaturase activity in asthma[J]. Allergy, 2017, 72 11: 1744-1752. DOI:10.1111/all.13180

MF 438 Preparation Products And Raw materials

Raw materials

Preparation Products

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921605-87-0, MF 438Related Search:


  • MF 438
  • 2-methyl-5-[6-[4-[2-(trifluoromethyl)phenoxy]piperidin-1-yl]pyridazin-3-yl]-1,3,4-thiadiazole
  • 3-(5-Methyl-1,3,4-thiadiazol-2-yl)-6-[4-[2-(trifluoromethyl)phenoxy]-1-piperidinyl]pyridazine
  • Pyridazine, 3-(5-methyl-1,3,4-thiadiazol-2-yl)-6-[4-[2-(trifluoromethyl)phenoxy]-1-piperidinyl]-
  • 3-(5-Methyl-1,3,4-thiadiazol-2-yl)-6-[4-[2-(trifluoromethyl)phenoxy]-1-piperidinyl]pyridazine(MF-438)
  • Stearoyl-CoA Desaturase (SCD),inhibit,MF438,MF 438,MF-438,Inhibitor
  • MF-438, 10 mM in DMSO
  • 921605-87-0