[(3R)-1-[2-[1-(4-Chloro-1H-pyrazol-1-yl)cyclopropyl]-3H-imidazo[4,5-b]pyridin-5-yl]-3-piperidinyl]-1-pyrrolidinyl-methanone methanesulfonate
- Product Name
- [(3R)-1-[2-[1-(4-Chloro-1H-pyrazol-1-yl)cyclopropyl]-3H-imidazo[4,5-b]pyridin-5-yl]-3-piperidinyl]-1-pyrrolidinyl-methanone methanesulfonate
- CAS No.
- 1469284-79-4
- Chemical Name
- [(3R)-1-[2-[1-(4-Chloro-1H-pyrazol-1-yl)cyclopropyl]-3H-imidazo[4,5-b]pyridin-5-yl]-3-piperidinyl]-1-pyrrolidinyl-methanone methanesulfonate
- Synonyms
- PF-06424439;PF-06424439 ,S9921;PF-06424439【PZ0233】;PF-06424439 >=98% (HPLC);PF-06424439 methanesulfonate;PF-06424439 methanesulfonate, 10 mM in DMSO;[(3R)-1-[2-[1-(4-Chloro-1H-pyrazol-1-yl)cyclopropyl]-3H-imidazo[4,5-b]pyridin-5-yl]-3-piperidinyl]-1-pyrrolidinyl-methanone methanesulfonate;(R)-(1-(2-(1-(4-Chloro-1H-pyrazol-1-yl)cyclopropyl)-1H-imidazo[4,5-b]pyridin-5-yl)piperidin-3-yl)(pyrrolidin-1-yl)methanone methanesulfonate;acyl-CoA:cholesterol acyltransferase,Inhibitor,Acyltransferase,mono- acylglycerol acyltransferase,PF-06424439,PF 06424439 methanesulfonate,inhibit,Diacylglycerol acyltransferase,PF06424439,Diglyceride acyltransferase,PF06424439 methanesulfonate,PF 06424439
- CBNumber
- CB22750426
- Molecular Formula
- C23H30ClN7O4S
- Formula Weight
- 536.0468
- MOL File
- 1469284-79-4.mol
[(3R)-1-[2-[1-(4-Chloro-1H-pyrazol-1-yl)cyclopropyl]-3H-imidazo[4,5-b]pyridin-5-yl]-3-piperidinyl]-1-pyrrolidinyl-methanone methanesulfonate Property
- storage temp.
- room temp
- solubility
- H2O: soluble10mg/mL, clear
- form
- powder
- color
- white to light brown
- optical activity
- [α]/D +7 to +11°, c =1.0 in methanol
- Water Solubility
- H2O: 10mg/mL, clear
Safety
- WGK Germany
- 3
N-Bromosuccinimide Price
- Product number
- PZ0233
- Product name
- PF-06424439
- Purity
- ≥98% (HPLC)
- Packaging
- 5mg
- Price
- $118
- Updated
- 2024/03/01
- Product number
- PZ0233
- Product name
- PF-06424439
- Purity
- ≥98% (HPLC)
- Packaging
- 25mg
- Price
- $476
- Updated
- 2024/03/01
- Product number
- 17680
- Product name
- PF-06424439
- Purity
- ≥98%
- Packaging
- 1mg
- Price
- $44
- Updated
- 2024/03/01
- Product number
- 17680
- Product name
- PF-06424439
- Purity
- ≥98%
- Packaging
- 10mg
- Price
- $151
- Updated
- 2024/03/01
- Product number
- 17680
- Product name
- PF-06424439
- Purity
- ≥98%
- Packaging
- 25mg
- Price
- $321
- Updated
- 2024/03/01
[(3R)-1-[2-[1-(4-Chloro-1H-pyrazol-1-yl)cyclopropyl]-3H-imidazo[4,5-b]pyridin-5-yl]-3-piperidinyl]-1-pyrrolidinyl-methanone methanesulfonate Chemical Properties,Usage,Production
Description
PF-06424439 is an orally bioavailable inhibitor of diacylglycerol acyltransferase 2 (DGAT-2; IC50 = 14 nM). It is selective for DGAT-2 over the related acyltransferases DGAT-1, MGAT-2, and MGAT-3 (IC50s = >50 μM). PF-06424439 (0.1-10 mg/kg) reduces plasma triglyceride levels in sucrose-fed rats in a dose-dependent manner. It also reduces plasma levels of cholesterol and triglycerides as well as hepatic triglycerides in LDL receptor knockout mice fed a high-fat, high-cholesterol diet when administered at a dose of 60 mg/kg per day.
Uses
PF-06424439 has been used as a diacylglycerol acyltransferase 2 (DGAT2)?inhibitor:
- to study its effects on cell mortality and lipid synthesis in epithelial colon cells and colorectal cancer stem cells
- to study its effects on HeLa cells
- to study its inhibitory effects on neutral lipid synthesis in HT-1080 cells
Biochem/physiol Actions
PF-06424439 is a potent and selective inhibitor of diacylglycerol acyltransferase 2 (DGAT2).
in vivo
PF-06424439 methanesulfonate (p.o.; 60 mg/kg/day; for 3 days) reduces plasma TG and cholesterol levels and decreases nonsignificant in circulating lipids in mice (Ldlr-/-)[1].
PF-06424439 methanesulfonate (i.v.; 1 mg/kg) shows moderate clearance in rats following intravenous administration and moderate steady-state volume of distribution (Vdss) results in a short half-life[1].
| Animal Model: | Male low-density lipoprotein receptor (Ldlr) knockout mice (Ldlr-/-)[1] |
| Dosage: | 60 mg/kg |
| Administration: | P.o.; daily; for 3 days |
| Result: | Reduced plasma TG and cholesterol levels and decreased nonsignificant in circulating lipids. |
| Animal Model: | Male Wistar-Han rats[1] |
| Dosage: | 1 mg/kg |
| Administration: | I.v. |
| Result: | Showed moderate clearance and a short half-life with t1/2=1.39 h. |
storage
Desiccate at RT
References
[1] KENTARO FUTATSUGI*. Discovery and Optimization of Imidazopyridine-Based Inhibitors of Diacylglycerol Acyltransferase 2 (DGAT2)[J]. Journal of Medicinal Chemistry, 2015, 58 18: 7173-7185. DOI: 10.1021/acs.jmedchem.5b01006
[2] A. NIKOLAI VON KRUSENSTIERN. Identification of essential sites of lipid peroxidation in ferroptosis[J]. Nature chemical biology, 2023, 19 6: 719-730. DOI: 10.1038/s41589-022-01249-3
[(3R)-1-[2-[1-(4-Chloro-1H-pyrazol-1-yl)cyclopropyl]-3H-imidazo[4,5-b]pyridin-5-yl]-3-piperidinyl]-1-pyrrolidinyl-methanone methanesulfonate Preparation Products And Raw materials
Raw materials
Preparation Products
[(3R)-1-[2-[1-(4-Chloro-1H-pyrazol-1-yl)cyclopropyl]-3H-imidazo[4,5-b]pyridin-5-yl]-3-piperidinyl]-1-pyrrolidinyl-methanone methanesulfonate Suppliers
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