Glafenine Hydrochloride structure
|
Common Name | Glafenine Hydrochloride | ||
---|---|---|---|---|
CAS Number | 65513-72-6 | Molecular Weight | 409.26300 | |
Density | N/A | Boiling Point | 618ºC at 760 mmHg | |
Molecular Formula | C19H18Cl2N2O4 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 327.6ºC |
Use of Glafenine HydrochlorideGlafenine hydrochloride is a non-narcotic analgesic and non-steroidal anti-inflammatory drug. It is an ABCG2 inhibitor with an IC50 of 3.2 μM. |
Name | 2,3-dihydroxypropyl 2-[(7-chloroquinolin-4-yl)amino]benzoate,hydrochloride |
---|---|
Synonym | More Synonyms |
Description | Glafenine hydrochloride is a non-narcotic analgesic and non-steroidal anti-inflammatory drug. It is an ABCG2 inhibitor with an IC50 of 3.2 μM. |
---|---|
Related Catalog | |
Target |
IC50: 3.2 μM (ABCG2)[1] |
In Vitro | Glafenine increases the surface expressionof mutant CFTR in baby hamster kidney (BHK) cells to 40% of that observed for wild-type CFTR[2]. Glafenine hydrochloride inhibits the proliferation and clonogenic activity of haSMCs and ECs in a dose-dependent manner. A block in the G2/M phase and a reduction in the G1 phase occurr. The migratory ability of haSMCs is impaired in a dose-dependent manner and the extracellular matrix protein tenascin is reduced[3]. |
In Vivo | Glafenine injection (25 mg/kg i.v.) shows enhanced BLI signal in mice with an average of 2.9-fold signal enhancement over the control. Glafenine causes increases in BLI signal of up to 11.6- and 17.4-fold in two separate HEK293/ABCG2/fLuc xenografts in the same mouse compared to the signals generated by those xenografts immediately before injection[1]. Incubating polarized CFBE41o- monolayers and intestines isolated from mutant CFTR mice with glafenine increases the short-circuit current response to forskolin and genistein. Treatment with glafenine also partially restores total salivary secretion[2]. Glafenine-treated zebrafish shows evidence of endoplasmic reticulum and mitochondrial stress, with disrupted intestinal architecture and halted cell stress responses, alongside accumulation of apoptotic intestinal epithelial cells in the lumen[4]. |
Cell Assay | Glafenine hydrochloride is added to the culture medium of the smooth muscle cells at three concentrations (10 μM, 50 μM, 100 μM). After 4 days of treatment, cells are harvested and the absolute cell number is counted[3]. |
Animal Admin | Mice: HEK293/empty/fLuc and HEK293/ABCG2/fLuc cells are implanted subcutaneously into opposite flanks of female nude mice. Five mice are implanted to generate 10 ABCG2-overexpressing xenografts and five controls. Animals are imaged after D-luciferin administration, which is followed by a bolus injection of a single dose of glafenine (25 mg/kg) and continued imaging[1]. |
References |
Boiling Point | 618ºC at 760 mmHg |
---|---|
Molecular Formula | C19H18Cl2N2O4 |
Molecular Weight | 409.26300 |
Flash Point | 327.6ºC |
Exact Mass | 408.06400 |
PSA | 91.68000 |
LogP | 4.01680 |
Storage condition | 2-8℃ |
Identification of new MRP4 inhibitors from a library of FDA approved drugs using a high-throughput bioluminescence screen.
Biochem. Pharmacol. 93(3) , 380-8, (2015) Multidrug resistance protein 4 (MRP4) effluxes a wide variety of drugs and endogenous signaling molecules from cells and has been proposed as an attractive therapeutic target in several solid tumors, ... |
Glafenine hydrochloride |
Prestwick_628 |
Glafenine (hydrochloride) |