- Signalwege
- Membrane Transporter/Ion Channel
- P-glycoprotein
P-glycoprotein
P-gp; Pgp; Multidrug resistance protein 1; MDR1; ATP-binding cassette sub-family B member 1; ABCB1; Cluster of differentiation 243; CD243
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P-glycoprotein Inhibitors
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P-glycoprotein Agonists
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P-glycoprotein Antagonist
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P-glycoprotein Activators
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P-glycoprotein Modulators
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P-glycoprotein Inducer
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P-glycoprotein Controls
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P-glycoprotein Substrates
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P-glycoprotein Ligands
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P-glycoprotein Verwandte Produkte (382)
Verwandte Produkte (382)
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Antibodies (3)
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PtdIns-(4,5)-P2 (1,2-dioctanoyl)
0 ImagesArt. -Nr.: HY-149152CAS. Nr.: 204858-53-7PtdIns-(4,5)-P2 (1,2-dioctanoyl) is a phosphatidylinositol derivative that binds to ABCB5. -
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P-gp modulator-6
0 ImagesArt. -Nr.: HY-164585CAS. Nr.: 352652-36-9P-gp modulator-6 is a P-glycoprotein (P-gp) modulator. P-gp modulator-6 regulates the substrate specificity of P-gp and enhances the efflux activity of Daunorubicin (HY-13062A) and Rhodamine 123 (HY-D0816). P-gp modulator-6 can be used in the research of multidrug-resistant cancers. P-gp modulator-6 can be used in the research of multidrug-resistant pancreatic cancer and multidrug-resistant colon cancer. -
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Antitrypanosomal agent 24
0 ImagesArt. -Nr.: HY-174454Antitrypanosomal agent 24 is a benzothiazole amidoxime with strong and selective antitrypanosomal activity (IC50 = 0.92 μM). Antitrypanosomal agent 24 is a substrate of the P-glycoprotein efflux pump. Antitrypanosomal agent 24 has high membrane permeability and good metabolic stability. Antitrypanosomal agent 24 binds to DNA/RNA by intercalation. -
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Isotenulin
0 ImagesArt. -Nr.: HY-N15297CAS. Nr.: 10092-04-3Isotenulin inhibits the efflux function of P-glycoprotein by stimulation of P-glycoprotein ATPase, thereby overcoming the multidrug resistance (MDR) of cancer cells. Isotenulin exhibits cytotoxicity in multidrug-resistant cancer cell KB-vin and sensitive cancer cell HeLaS3. Isotenulin exhibits synergistic effect with Paclitaxel (HY-B0015), Vinblastine (HY-13780) and Doxorubicin (HY-15142). -
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IKK 16 (Standard)
0 ImagesIKK 16 (Standard) is the analytical standard of IKK 16. This product is intended for research and analytical applications. IKK 16 hydrochloride is an orally active IKK inhibitor. IKK 16 hydrochloride shows IC50s of 40 nM, 70 nM, 200 nM, and 50 nM for IKK2, IKK complex, IKK1, and LRRK 2, respectively. IKK 16 hydrochloride is also a pan-PKD inhibitor, inhibiting PKD1, PKD2, and PKD3 with IC50s of 153.9, 115, and 99.7 nM, respectively. IKK 16 hydrochloride is also an ABCB1 inhibitor, interfering with the binding of ABCB1 to its substrates. IKK 16 hydrochloride protects against LPS (HY-D1056)-induced multiple organ dysfunction by reducing the acute inflammatory response induced by endotoxin exposure. IKK 16 hydrochloride can restore renal function and alleviate fibrosis in acute kidney injury. IKK 16 hydrochloride attenuates cardiac dysfunction associated with polymicrobial sepsis in mice with type 2 diabetes mellitus (T2DM) by inhibiting the NF-κB pathway. -
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XR9051
0 ImagesArt. -Nr.: HY-13776CAS. Nr.: 762219-35-2XR9051 is an orally active and specific modulator of P-glycoprotein-mediated multidrug resistance (MDR). -
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Ceefourin 1 (Standard)
0 ImagesCeefourin 1 (Standard) is the analytical standard of Ceefourin 1 (HY-101453). This product is intended for research and analytical applications. Ceefourin 1 is a potent and highly selective multidrug resistance protein 4 (MRP4) inhibitor. Ceefourin 1 inhibits transport of a broad range of MRP4 substrates, yet is highly selective for MRP4 over other ABC transporters. Ceefourin 1 is a benzothiazol and primarily as a chemosensitizer for high-risk neuroblastoma. -
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Quinidine hydrochloride monohydrate (Standard)
0 ImagesQuinidine hydrochloride monohydrate (Standard) is the analytical standard of Quinidine hydrochloride monohydrate (HY-B1302). This product is intended for research and analytical applications. Quinidine hydrochloride monohydrate is an orally active antiarrhythmic agent. Quinidine hydrochloride monohydrate reduces the expression level of P-gp, inhibits P-gp-mediated efflux, increases the intracellular accumulation of P-gp substrates, induces PARP cleavage and Caspase-3 activation, and elevates the proportion of Apoptotic cells at the sub-G1 phase. Quinidine hydrochloride monohydrate exerts sustained block and open-channel block effects on IK(f). Quinidine hydrochloride monohydrate alters the urinary metabolic ratio of Amphetamine, modulates the Pentylenetetrazol-induced seizure threshold, and regulates the anticonvulsant effect of Dextromethorphan. Quinidine hydrochloride monohydrate can be used in studies related to uterine sarcoma and seizures. -
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Piperin-d10
0 ImagesArt. -Nr.: HY-W654320Synonyms: Bioperine-d10; 1-Piperoylpiperidine-d10Piperin-d10 is deuterium labeled Piperine. Piperine is an alkaloid, can be isolated from pepper. Piperine can inhibit the activity of P-glycoprotein and CYP3A4. Piperine inhibits HeLa cells with an IC50 of 61.94±0.054 μg/mL. -
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Sinapine (Standard)
0 ImagesArt. -Nr.: HY-N5077RCAS. Nr.: 18696-26-9Sinapine is an alkaloid isolated from seeds of the cruciferous species. Sinapine exhibits anti-inflammatory, anti-oxidant, anti-tumor, anti-angiogenic and radio-protective effects. Sinapine is also an acetylcholinesterase (AChE) inhibitor and can be used for the research of Alzheimer’s disease, ataxia, myasthenia gravis, and Parkinson’s disease. -
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8-Prenylchrysin
0 ImagesArt. -Nr.: HY-107197CAS. Nr.: 34125-75-28-prenylchrysin is a C8-prenylated flavonoid. 8-prenylchrysin inhibits P-gp. 8-prenylchrysin can be used for tumor research. -
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Phosphatidylinositol bis-4,5-phosphate, 1,2-dioctanoyl sodium
0 ImagesArt. -Nr.: HY-165979CAS. Nr.: 1234574-20-9Phosphatidylinositol bis-4,5-phosphate, 1,2-dioctanoyl sodiumis a phosphatidylinositol derivative that binds to ABCB5. -
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Zamicastat (Standard)
0 ImagesArt. -Nr.: HY-106004RCAS. Nr.: 1080028-80-3Synonyms: BIA 5-1058 (Standard)Zamicastat (Standard) is the analytical standard of Zamicastat (HY-106004). This product is intended for research and analytical applications. Zamicastat (BIA 5-1058) is a dopamine β-hydroxylase (DBH) inhibitor and can cross the blood-brain barrier (BBB) to cause central as well as peripheral effects. Zamicastat is also a concentration-dependent dual P-gp and BCRP inhibitor with IC50 values of 73.8 μM and 17.0 μM, respectively. Zamicastat reduces high blood pressure. -
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Salviaplebeiaside
0 ImagesArt. -Nr.: HY-N11084CAS. Nr.: 1236273-88-3Salviaplebeiaside is a phenolic substance can be isolated from the aerial part of Vitex negundo var. cannabifolia. Salviaplebeiaside is an inhibitor of class I p-glycoprotein. -
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Sulfanitran (Standard)
0 ImagesSulfanitran (Standard) is the analytical standard of Sulfanitran. This product is intended for research and analytical applications. Sulfanitran is an antibacterial and anticoccidial agent used in poultry feeds. Sulfanitran also is a multidrug resistance protein 2 (MRP2) stimulator that can increase the affinity of MRP2 for estradiol-17-β-D-glucuronide (E217βG). -
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CP-724714 succinate
0 ImagesArt. -Nr.: HY-14674ACAS. Nr.: 543681-31-8CP-724714 succinate is an orally active and selective HER2 tyrosine kinase inhibitor with an IC50 of 10 nM. CP-724714 succinate inhibits HER2 receptor autophosphorylation and blocks the downstream Ras-Raf-Mek-Erk signaling pathway, thereby inducing cell cycle arrest and apoptosis in tumor cells. CP-724714 succinate exhibits antiviral activity and inhibits various porcine diarrheal coronaviruses, including SADS-CoV (IC50 of 0.91 μM). CP-724714 succinate is an inhibitor of the hepatic transport receptors OATP1B1/MDR1/BSEP, and can enter hepatocytes via active uptake and trigger the accumulation of drugs and bile acids within hepatocytes. CP-724714 succinate can be used in research related to HER2-overexpressing breast cancer and porcine diarrheal coronavirus infection. -
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Verapamil-d3
0 ImagesArt. -Nr.: HY-14275SCAS. Nr.: 152561-91-6Synonyms: (±)-Verapamil-d3; CP-16533-1-d3Verapamil-d3 ((±)-Verapamil-d3) is deuterium labeled Verapamil. Verapamil ((±)-Verapamil) is a calcium channel blocker and a potent and orally active first-generation P-glycoprotein (P-gp) inhibitor. Verapamil also inhibits CYP3A4. Verapamil has the potential for high blood pressure, heart arrhythmias and angina research. -
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P-gp inhibitor 1 (Standard)
0 ImagesP-gp inhibitor 1 (Standard) is the analytical standard of P-gp inhibitor 1 (HY-101791). This product is intended for research and analytical applications. P-gp inhibitor 1 is a novel inhibitor reversing P-glycoprotein-mediated multidrug resistance. -
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Encequidar hydrochloride
0 ImagesArt. -Nr.: HY-13646BCAS. Nr.: 849675-88-3Synonyms: HM30181 hydrochloride; HM30181A hydrochlorideEncequidar hydrochloride (HM30181 hydrochloride) is an oral P-glycoprotein (P-gp) inhibitor with the activity of enhancing the oral bioavailability of P-gp substrate drugs. Encequidar shows the highest potency among various MDR1 inhibitors, with IC50=0.63nM. Encequidar effectively blocks the transepithelial transport of paclitaxel in MDCK monolayer cells, with IC50=35.4nM. -
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α-Cryptoxanthin
0 ImagesArt. -Nr.: HY-N11697CAS. Nr.: 24480-38-4α-Cryptoxanthin is a natural carotenoid with anticancer effects. α-Cryptoxanthin inhibits multidrug resistance 1 (MDR1) mediated efflux pump. -
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