JTP 103237
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    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 585073

CAS#: 1883864-16-1

Description: JTP 103237 is a potent and selective monoacyglycerol acyltransferase 2 (MOGAT2) inhibitor.


Chemical Structure

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JTP 103237
CAS# 1883864-16-1

Theoretical Analysis

MedKoo Cat#: 585073
Name: JTP 103237
CAS#: 1883864-16-1
Chemical Formula: C24H29F3N6O
Exact Mass: 474.24
Molecular Weight: 474.532
Elemental Analysis: C, 60.75; H, 6.16; F, 12.01; N, 17.71; O, 3.37

Price and Availability

Size Price Availability Quantity
10mg USD 450 2 Weeks
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Synonym: JTP 103237; JTP103237; JTP-103237

IUPAC/Chemical Name: 7-[4,6-Bis(1,1-dimethylethyl)-2-pyrimidinyl]-5,6,7,8-tetrahydro-3-[4-(trifluoromethoxy)phenyl]-1,2,4-triazolo[4,3-a]pyrazine

InChi Key: KELNXHBJTXCXSN-UHFFFAOYSA-N

InChi Code: InChI=1S/C24H29F3N6O/c1-22(2,3)17-13-18(23(4,5)6)29-21(28-17)32-11-12-33-19(14-32)30-31-20(33)15-7-9-16(10-8-15)34-24(25,26)27/h7-10,13H,11-12,14H2,1-6H3

SMILES Code: FC(F)(F)OC1=CC=C(C2=NN=C3CN(C4=NC(C(C)(C)C)=CC(C(C)(C)C)=N4)CCN32)C=C1

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

Shelf Life: >3 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:

Product Data:
Biological target: Potent and selective monoacyglycerol acyltransferase 2 (MOGAT2) inhibitor.
In vitro activity: TBD
In vivo activity: In the present study, JTP-103237 prevented carbohydrate-induced fatty liver and suppressed both TG synthesis and de novo lipogenesis, suggesting MGAT inhibitor may prevent carbohydrate-induced metabolic disorders, including NAFLD, obesity and diabetes. The results showed that JTP-103237 significantly decreased hepatic triglyceride (45.0 ± 5.5 mg/g liver in vehicle group and 27.1 ± 7.3 mg/g liver, respectively. P < 0.01 in Student's t-test) in mice. Reference: J Pharmacol Sci. 2015 Jul;128(3):150-7. https://pubmed.ncbi.nlm.nih.gov/26215699/

Solubility Data

Solvent Max Conc. mg/mL Max Conc. mM
Solubility
DMSO 9.5 20.00
Ethanol 47.5 100.00

Preparing Stock Solutions

The following data is based on the product molecular weight 474.53 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.

Recalculate based on batch purity %
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: 1. Okuma C, Ohta T, Tadaki H, Ishigure T, Sakata S, Taniuchi H, Sano R, Hamada H, Kume S, Nishiu J, Kakutani M. JTP-103237, a monoacylglycerol acyltransferase inhibitor, prevents fatty liver and suppresses both triglyceride synthesis and de novo lipogenesis. J Pharmacol Sci. 2015 Jul;128(3):150-7. doi: 10.1016/j.jphs.2015.06.007. Epub 2015 Jul 2. PMID: 26215699.
In vitro protocol: TBD
In vivo protocol: 1. Okuma C, Ohta T, Tadaki H, Ishigure T, Sakata S, Taniuchi H, Sano R, Hamada H, Kume S, Nishiu J, Kakutani M. JTP-103237, a monoacylglycerol acyltransferase inhibitor, prevents fatty liver and suppresses both triglyceride synthesis and de novo lipogenesis. J Pharmacol Sci. 2015 Jul;128(3):150-7. doi: 10.1016/j.jphs.2015.06.007. Epub 2015 Jul 2. PMID: 26215699.

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Okuma et al (2015) JTP-103237, a novel monoacylglycerol acyltransferase inhibitor, modulates fat absorption and prevents diet-induced obesity. Eur.J.Pharmacol. 758 72 PMID: 25857225

Okuma et al (2015) JTP-103237, a monoacylglycerol acyltransferase inhibitor, prevents fatty liver and suppresses both triglyceride synthesis and de novo lipogenesis. J.Pharmacol.Sci. 128 150 PMID: 26215699