APD668
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MedKoo CAT#: 510309

CAS#: 832714-46-2

Description: APD668, also known as JNJ-28630368, is a potent GPR119 agonist with EC50 of 2.7 nM and 33 nM for hGPR119 and ratGPR119 respectively. Receptor GPR119 is a target that has been of significant recent interest in the field of metabolism. ADP668 showed activity to reduce blood glucose and glycated hemoglobin (HbA1c) levels in Zucker Diabetic Fatty (ZDF) rats over several weeks of dosing. ADP668 is currently under clinical trial for diabetes.


Chemical Structure

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APD668
CAS# 832714-46-2

Theoretical Analysis

MedKoo Cat#: 510309
Name: APD668
CAS#: 832714-46-2
Chemical Formula: C21H24FN5O5S
Exact Mass: 477.15
Molecular Weight: 477.510
Elemental Analysis: C, 52.82; H, 5.07; F, 3.98; N, 14.67; O, 16.75; S, 6.72

Price and Availability

Size Price Availability Quantity
100mg USD 950
200mg USD 1650
500mg USD 2750
1g USD 3450
2g USD 4950
5g USD 7950
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Synonym: APD668; APD-668; APD 668; JNJ28630368; JNJ-28630368; JNJ 28630368.

IUPAC/Chemical Name: isopropyl 4-((1-(2-fluoro-4-(methylsulfonyl)phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)oxy)piperidine-1-carboxylate .

InChi Key: XTRUQJBVQBUKSQ-UHFFFAOYSA-N

InChi Code: InChI=1S/C21H24FN5O5S/c1-13(2)31-21(28)26-8-6-14(7-9-26)32-20-16-11-25-27(19(16)23-12-24-20)18-5-4-15(10-17(18)22)33(3,29)30/h4-5,10-14H,6-9H2,1-3H3

SMILES Code: O=C(N1CCC(OC2=C3C(N(C4=CC=C(S(=O)(C)=O)C=C4F)N=C3)=NC=N2)CC1)OC(C)C

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:          

Product Data:
Biological target: APD668 is an agonist of G-protein coupled receptor GPR119, with EC50s of 2.7 nM and 33 nM for hGPR119 and rGPR119, respectively.
In vitro activity: Thus, 3k (APD668) was shown to increase adenylate cyclase activation in HEK293 cells transfected with human GPR119 (but not in non-transfected cells) in a concentration-dependent manner with an EC50 of 23 nM. Compound 3k also enhanced insulin release from both rat and human isolated pancreatic islets in a glucose-dependent manner as previously observed for 1a.1 In a standard panel of around 80 known receptors and ion channels, 3k did not show any binding in excess of 50% of control to any other proteins at concentrations up to 10 μM. Reference: Bioorg Med Chem Lett. 2011 May 15;21(10):3134-41. https://pubmed.ncbi.nlm.nih.gov/21444206/
In vivo activity: To investigate the effect of APD668 on intestinal lipid absorption, this study conducted an oral fat tolerance test in normal mice. As shown in Fig. 1A, olive oil administration elevated plasma triglyceride levels in vehicle treated mice. Treatment with APD668 (30 mg/kg, p.o.) reduced the elevated plasma triglyceride levels at 2 h as compared to vehicle treated mice (P<0.001). Next, this study calculated area under curve and APD668 significantly inhibited the lipid excursion by approximately 42% in mice (Fig. 1A and B). Reference: Eur J Pharmacol. 2017 Apr 15;801:35-45. https://pubmed.ncbi.nlm.nih.gov/28274625/

Solubility Data

Solvent Max Conc. mg/mL Max Conc. mM
Solubility
DMSO 49.8 104.25
DMF 25.0 52.35
DMF:PBS (pH 7.2) (1:8) 0.1 0.21
Ethanol 2.0 4.19

Preparing Stock Solutions

The following data is based on the product molecular weight 477.51 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. Bahirat UA, Shenoy RR, Goel RN, Nemmani KV. APD668, a G protein-coupled receptor 119 agonist improves fat tolerance and attenuates fatty liver in high-trans fat diet induced steatohepatitis model in C57BL/6 mice. Eur J Pharmacol. 2017 Apr 15;801:35-45. doi: 10.1016/j.ejphar.2017.02.043. Epub 2017 Mar 6. PMID: 28274625. 2. Semple G, Ren A, Fioravanti B, Pereira G, Calderon I, Choi K, Xiong Y, Shin YJ, Gharbaoui T, Sage CR, Morgan M, Xing C, Chu ZL, Leonard JN, Grottick AJ, Al-Shamma H, Liang Y, Demarest KT, Jones RM. Discovery of fused bicyclic agonists of the orphan G-protein coupled receptor GPR119 with in vivo activity in rodent models of glucose control. Bioorg Med Chem Lett. 2011 May 15;21(10):3134-41. doi: 10.1016/j.bmcl.2011.03.007. Epub 2011 Mar 13. PMID: 21444206.
In vitro protocol: 1. Semple G, Ren A, Fioravanti B, Pereira G, Calderon I, Choi K, Xiong Y, Shin YJ, Gharbaoui T, Sage CR, Morgan M, Xing C, Chu ZL, Leonard JN, Grottick AJ, Al-Shamma H, Liang Y, Demarest KT, Jones RM. Discovery of fused bicyclic agonists of the orphan G-protein coupled receptor GPR119 with in vivo activity in rodent models of glucose control. Bioorg Med Chem Lett. 2011 May 15;21(10):3134-41. doi: 10.1016/j.bmcl.2011.03.007. Epub 2011 Mar 13. PMID: 21444206.
In vivo protocol: 1. Bahirat UA, Shenoy RR, Goel RN, Nemmani KV. APD668, a G protein-coupled receptor 119 agonist improves fat tolerance and attenuates fatty liver in high-trans fat diet induced steatohepatitis model in C57BL/6 mice. Eur J Pharmacol. 2017 Apr 15;801:35-45. doi: 10.1016/j.ejphar.2017.02.043. Epub 2017 Mar 6. PMID: 28274625. 2. Semple G, Ren A, Fioravanti B, Pereira G, Calderon I, Choi K, Xiong Y, Shin YJ, Gharbaoui T, Sage CR, Morgan M, Xing C, Chu ZL, Leonard JN, Grottick AJ, Al-Shamma H, Liang Y, Demarest KT, Jones RM. Discovery of fused bicyclic agonists of the orphan G-protein coupled receptor GPR119 with in vivo activity in rodent models of glucose control. Bioorg Med Chem Lett. 2011 May 15;21(10):3134-41. doi: 10.1016/j.bmcl.2011.03.007. Epub 2011 Mar 13. PMID: 21444206.

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1: Semple G, Ren A, Fioravanti B, Pereira G, Calderon I, Choi K, Xiong Y, Shin YJ, Gharbaoui T, Sage CR, Morgan M, Xing C, Chu ZL, Leonard JN, Grottick AJ, Al-Shamma H, Liang Y, Demarest KT, Jones RM. Discovery of fused bicyclic agonists of the orphan G-protein coupled receptor GPR119 with in vivo activity in rodent models of glucose control. Bioorg Med Chem Lett. 2011 May 15;21(10):3134-41. doi:  10.1016/j.bmcl.2011.03.007. Epub 2011 Mar 13. PubMed PMID: 21444206.