WARNING: This product is for research use only, not for human or veterinary use.
Hodoodo CAT#: H525638
CAS#: 934017-32-0
Description: MK 0767 is a dual peroxisome proliferator-activated receptor (PPAR) alpha/gamma agonist, has been studied as a potential treatment of type 2 diabetes and dyslipidemia.
Hodoodo Cat#: H525638
Name: MK 0767
CAS#: 934017-32-0
Chemical Formula: C19H15F3N2O4S
Exact Mass: 424.07
Molecular Weight: 424.394
Elemental Analysis: C, 53.77; H, 3.56; F, 13.43; N, 6.60; O, 15.08; S, 7.55
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Synonym: MK 0767; MK-0767; MK0767
IUPAC/Chemical Name: 5-(2,4-dioxothiazolidin-5-yl)-2-methoxy-N-(4-(trifluoromethyl)benzyl)benzamide
InChi Key: PUJCSYJMQMUYPS-UHFFFAOYSA-N
InChi Code: InChI=1S/C19H15F3N2O4S/c1-28-14-7-4-11(15-17(26)24-18(27)29-15)8-13(14)16(25)23-9-10-2-5-12(6-3-10)19(20,21)22/h2-8,15H,9H2,1H3,(H,23,25)(H,24,26,27)
SMILES Code: O=C(NCC1=CC=C(C(F)(F)F)C=C1)C2=CC(C(SC(N3)=O)C3=O)=CC=C2OC
Appearance: Solid powder
Purity: >98% (or refer to the Certificate of Analysis)
Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility: Soluble in DMSO, not in water
Shelf Life: >2 years if stored properly
Drug Formulation: This drug may be formulated in DMSO
Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code: 2934.99.9001
More Info:
Biological target: | |
In vitro activity: | |
In vivo activity: |
The following data is based on the product molecular weight 424.39 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 1.15 mL | 5.76 mL | 11.51 mL |
5 mM | 0.23 mL | 1.15 mL | 2.3 mL |
10 mM | 0.12 mL | 0.58 mL | 1.15 mL |
50 mM | 0.02 mL | 0.12 mL | 0.23 mL |
Formulation protocol: | |
In vitro protocol: | |
In vivo protocol: |
1: Rippley RK, Yan KX, Matthews ND, Greenberg HE, Herman GA, Wagner JA. Human
pharmacokinetics and interconversion of enantiomers of MK-0767, a dual
PPARalpha/gamma agonist. J Clin Pharmacol. 2007 Mar;47(3):323-33. PubMed PMID:
17322144.