Back
Product details:
CAS
142715-48-8
Purity
95%
CP-100356 hydrochloride is an orally active dual MDR1 (P-gp)/BCRP inhibitor.
Properties
Name
CP-100356 hydrochloride
Smiles
Cl.COC=1C=CC(CCNC=2N=C(N3CCC=4C=C(OC)C(OC)=CC4C3)C=5C=C(OC)C(OC)=CC5N2)=CC1OC
Targets
Please log in to see this information
Sold for research purposes under agreement from Pfizer Inc.
CP-100356 hydrochloride, also known as cp-100356 and PF-01731298, is a selective inhibitor widely used in pharmacological research focused on drug transport and multidrug resistance mechanisms. Identified under CAS 142715-48-8, this compound is recognized for its ability to modulate P-glycoprotein activity, making it relevant in studies of drug absorption and distribution. CP-100356 hydrochloride Pfizer development programs contributed to its use as a reference tool in transporter-related research.
Researchers often review CP-100356 hydrochloride chemical structure to better understand its interaction with efflux transporters and membrane proteins. In addition, CP-100356 hydrochloride molecular weight is an important parameter in experimental planning, supporting accurate preparation of solutions and consistency across assays.
Application CP-100356 hydrochloride is primarily associated with studies of P-glycoprotein inhibition and drug transport across biological membranes. It is frequently used in research where understanding compound permeability and resistance mechanisms is essential.
Its selectivity makes cp-100356 a useful tool in screening workflows and in studies aimed at improving pharmacokinetic profiles of candidate molecules.
In vitro, CP-100356 hydrochloride is commonly applied in cell-based assays to assess transporter inhibition and intracellular accumulation of compounds. It enables researchers to measure changes in drug retention within cells and to evaluate the role of efflux pumps in limiting compound efficacy.
These assays are particularly valuable in oncology and central nervous system research, where transporter activity significantly influences therapeutic outcomes.
In vivo studies of CP-100356 hydrochloride focus on its ability to enhance drug penetration by inhibiting transporter-mediated efflux. It has been used in animal models to examine how modulation of P-glycoprotein affects tissue distribution, especially in the brain.
Such studies support translational research by providing insights into how transporter inhibition can improve drug exposure in target tissues.
The primary biochemical action of CP-100356 hydrochloride involves inhibition of P-glycoprotein, a key transporter responsible for limiting intracellular accumulation of many compounds. By blocking this efflux mechanism, CP-100356 hydrochloride allows increased retention of substrates within cells.
Physiologically, this effect is important in understanding drug resistance and distribution, particularly in tissues protected by biological barriers such as the blood-brain barrier.
CP-100356 hydrochloride provides a well-characterized approach to studying transporter-related processes, making it valuable for both basic and applied research. When sourced as EBC-497105, it is supported by quality control and analytical validation.
As part of a broader portfolio of bioactive compounds, CP-100356 hydrochloride supports efficient investigation of drug transport pathways, helping researchers refine experimental strategies and improve understanding of compound behavior in biological systems.
SDS
CP-100356 | CP-100356 monohydrochloride
No data available
The compound has purity validated by NMR and/or LCMS methods.
1 mg
$85
2 mg
$85
5 mg
$120
10 mg
$208
15 mg
$252
20 mg
$296
25 mg
$359
30 mg
$423
35 mg
$487
40 mg
$551
45 mg
$591
50 mg
$630
75 mg
$838
100 mg
$POA
Quantity
1
Total amount
$ 120
CP-100356 | CP-100356 monohydrochloride
No data available
The compound has purity validated by NMR and/or LCMS methods.
Target activity features
It should be emphasized that the product may be active against a larger number of targets than shown on the card. The information represented here refers to the targets with the largest value of pX or the targets with ΔpX less than 1.5 from the largest pX value.