BMS-754807

A1185-5.1 ApexBio 10 mM (in 1mL DMSO) 184.8 EUR
Description: BMS-754807 is a potent and small molecular inhibitor which targets the IGF-1R/IR family kinases with Ki <2 nmol/L[1]. The efficacy of BMS-754807 on normal tissues and tumor cell cycle is believed to be different from the effects of continuous inhibition by anti-IGF-1R antibodies.

BMS-536924

A2238-10 ApexBio 10 mg 296.4 EUR
Description: BMS-536924 is a novel inhibitor of IGF-1R with IC50 value of 100nM [1].It has been found that BMS-536924 has cell toxicity in OVCAR-3 and OVCAR-4 cell lines.

BMS-536924

A2238-5 ApexBio 5 mg 199.2 EUR
Description: BMS-536924 is a novel inhibitor of IGF-1R with IC50 value of 100nM [1].It has been found that BMS-536924 has cell toxicity in OVCAR-3 and OVCAR-4 cell lines.

BMS-536924

A2238-5.1 ApexBio 10 mM (in 1mL DMSO) 309.6 EUR
Description: BMS-536924 is a novel inhibitor of IGF-1R with IC50 value of 100nM [1].It has been found that BMS-536924 has cell toxicity in OVCAR-3 and OVCAR-4 cell lines.

BMS-536924

A2238-50 ApexBio 50 mg 1104 EUR
Description: BMS-536924 is a novel inhibitor of IGF-1R with IC50 value of 100nM [1].It has been found that BMS-536924 has cell toxicity in OVCAR-3 and OVCAR-4 cell lines.

BMS-777607

A5703-100 ApexBio 100 mg 1005.6 EUR
Description: BMS 777607 is a novel, selective and orally available ATP-competitive MET kinase inhibitor that primarily targets several MET family members, including RON, MET, Tyro-3 and AxI.

BMS-777607

A5703-25 ApexBio 25 mg 408 EUR
Description: BMS 777607 is a novel, selective and orally available ATP-competitive MET kinase inhibitor that primarily targets several MET family members, including RON, MET, Tyro-3 and AxI.

BMS-777607

A5703-5 ApexBio 5 mg 170.4 EUR
Description: BMS 777607 is a novel, selective and orally available ATP-competitive MET kinase inhibitor that primarily targets several MET family members, including RON, MET, Tyro-3 and AxI.

BMS-777607

A5703-5.1 ApexBio 10 mM (in 1mL DMSO) 177.6 EUR
Description: BMS 777607 is a novel, selective and orally available ATP-competitive MET kinase inhibitor that primarily targets several MET family members, including RON, MET, Tyro-3 and AxI.

BMS-777607

A5703-S ApexBio Evaluation Sample 97.2 EUR
Description: BMS 777607 is a novel, selective and orally available ATP-competitive MET kinase inhibitor that primarily targets several MET family members, including RON, MET, Tyro-3 and AxI.

BMS-509744

A3250-10 ApexBio 10 mg 494.4 EUR
Description: BMS-509744 is a selective inhibitor of ITK with IC50 value of 15 nM [1].ITK (IL-2-inducible T cell kinase) is an enzyme and plays an important role in T cell receptor signaling.

BMS-509744

A3250-5 ApexBio 5 mg 340.8 EUR
Description: BMS-509744 is a selective inhibitor of ITK with IC50 value of 15 nM [1].ITK (IL-2-inducible T cell kinase) is an enzyme and plays an important role in T cell receptor signaling.

BMS-509744

A3250-50 ApexBio 50 mg 2013.6 EUR
Description: BMS-509744 is a selective inhibitor of ITK with IC50 value of 15 nM [1].ITK (IL-2-inducible T cell kinase) is an enzyme and plays an important role in T cell receptor signaling.

BMS-626529

A3253-10 ApexBio 10 mg 408 EUR
Description: EC50HIV-1 attachment inhibitors represent a new class of entry inhibitors that prevent the initial interaction between virus and host cell by binding to the viral envelope protein gp120 and blocking attachment of the virus to the CD4 receptor on CD4+ T-cells.

BMS-626529

A3253-200 ApexBio 200 mg 2148 EUR
Description: EC50HIV-1 attachment inhibitors represent a new class of entry inhibitors that prevent the initial interaction between virus and host cell by binding to the viral envelope protein gp120 and blocking attachment of the virus to the CD4 receptor on CD4+ T-cells.

BMS-626529

A3253-5 ApexBio 5 mg 268.8 EUR
Description: EC50HIV-1 attachment inhibitors represent a new class of entry inhibitors that prevent the initial interaction between virus and host cell by binding to the viral envelope protein gp120 and blocking attachment of the virus to the CD4 receptor on CD4+ T-cells.

BMS-626529

A3253-50 ApexBio 50 mg 1104 EUR
Description: EC50HIV-1 attachment inhibitors represent a new class of entry inhibitors that prevent the initial interaction between virus and host cell by binding to the viral envelope protein gp120 and blocking attachment of the virus to the CD4 receptor on CD4+ T-cells.

BMS-663068

A3254-5 ApexBio 5 mg 360 EUR
Description: BMS-663068 is a small-molecule attachment inhibitor of HIV-1 gp120 with IC50 value of [1].The first step of HIV-1 virus to entry host cells is the binding of the viral gp120 envelope glycopeptide to the CD4 receptor of host cell.

BMS-663068

A3254-5.1 ApexBio 10 mM (in 1mL DMSO) 477.6 EUR
Description: BMS-663068 is a small-molecule attachment inhibitor of HIV-1 gp120 with IC50 value of [1].The first step of HIV-1 virus to entry host cells is the binding of the viral gp120 envelope glycopeptide to the CD4 receptor of host cell.

BMS-690514

A3256-10 ApexBio 10 mg 831.6 EUR
Description: BMS-690514, a potent inhibitor of human epidermal growth factor receptor (HER/EGFR).

BMS-690514

A3256-5 ApexBio 5 mg 540 EUR
Description: BMS-690514, a potent inhibitor of human epidermal growth factor receptor (HER/EGFR).

BMS-690514

A3256-5.1 ApexBio 10 mM (in 1mL DMSO) 480 EUR
Description: BMS-690514, a potent inhibitor of human epidermal growth factor receptor (HER/EGFR).

BMS-690514

A3256-50 ApexBio 50 mg 2043.6 EUR
Description: BMS-690514, a potent inhibitor of human epidermal growth factor receptor (HER/EGFR).

BMS-833923

A3258-10 ApexBio 10 mg 157.2 EUR
Description: BMS-833923 is an orally bioavailable and selective antagonist of smoothened (SMO) with IC50 value of 5.8 nM in NIH3T3 cell line [1].The Hedgehog (Hh) signaling is a critical pathway involved in embryonic development and in tissue maintenance and repair in adults.

BMS-833923

A3258-5 ApexBio 5 mg 122.4 EUR
Description: BMS-833923 is an orally bioavailable and selective antagonist of smoothened (SMO) with IC50 value of 5.8 nM in NIH3T3 cell line [1].The Hedgehog (Hh) signaling is a critical pathway involved in embryonic development and in tissue maintenance and repair in adults.

BMS-833923

A3258-5.1 ApexBio 10 mM (in 1mL DMSO) 200.4 EUR
Description: BMS-833923 is an orally bioavailable and selective antagonist of smoothened (SMO) with IC50 value of 5.8 nM in NIH3T3 cell line [1].The Hedgehog (Hh) signaling is a critical pathway involved in embryonic development and in tissue maintenance and repair in adults.

BMS-833923

A3258-50 ApexBio 50 mg 338.4 EUR
Description: BMS-833923 is an orally bioavailable and selective antagonist of smoothened (SMO) with IC50 value of 5.8 nM in NIH3T3 cell line [1].The Hedgehog (Hh) signaling is a critical pathway involved in embryonic development and in tissue maintenance and repair in adults.

BMS-927711

A3259-10 ApexBio 10 mg 753.6 EUR
Description: BMS-927711 is an orally potent CGRP receptor antagonist with IC50 of 0.14 nM. [1]Calcitonin gene-related peptide CGRP is a 37 amino acid peptide widely distributed in the nervous system, which is a highly potent vasodilator that has been directly implicated in the pathology of migraine.

BMS-927711

A3259-100 ApexBio 100 mg 4620 EUR
Description: BMS-927711 is an orally potent CGRP receptor antagonist with IC50 of 0.14 nM. [1]Calcitonin gene-related peptide CGRP is a 37 amino acid peptide widely distributed in the nervous system, which is a highly potent vasodilator that has been directly implicated in the pathology of migraine.

BMS-927711

A3259-5 ApexBio 5 mg 451.2 EUR
Description: BMS-927711 is an orally potent CGRP receptor antagonist with IC50 of 0.14 nM. [1]Calcitonin gene-related peptide CGRP is a 37 amino acid peptide widely distributed in the nervous system, which is a highly potent vasodilator that has been directly implicated in the pathology of migraine.

BMS-927711

A3259-50 ApexBio 50 mg 2666.4 EUR
Description: BMS-927711 is an orally potent CGRP receptor antagonist with IC50 of 0.14 nM. [1]Calcitonin gene-related peptide CGRP is a 37 amino acid peptide widely distributed in the nervous system, which is a highly potent vasodilator that has been directly implicated in the pathology of migraine.

BMS-707035

A4069-10 ApexBio 10 mg 234 EUR
Description: BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 value of 15 nM [1].Retroviral IN is an enzyme produced by a retrovirus (such as HIV) that enables its genetic material to be integrated into the DNA of the infected cell.

BMS-707035

A4069-100 ApexBio 100 mg 1062 EUR
Description: BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 value of 15 nM [1].Retroviral IN is an enzyme produced by a retrovirus (such as HIV) that enables its genetic material to be integrated into the DNA of the infected cell.

BMS-707035

A4069-5 ApexBio 5 mg 157.2 EUR
Description: BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 value of 15 nM [1].Retroviral IN is an enzyme produced by a retrovirus (such as HIV) that enables its genetic material to be integrated into the DNA of the infected cell.

BMS-707035

A4069-50 ApexBio 50 mg 672 EUR
Description: BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 value of 15 nM [1].Retroviral IN is an enzyme produced by a retrovirus (such as HIV) that enables its genetic material to be integrated into the DNA of the infected cell.

BMS-911543

A4152-10 ApexBio 10 mg 480 EUR
Description: BMS-911543 is a selective small-molecule inhibitor of JAK2 with IC50 value of 1.1nM [1].BMS-911543 is a reversible pyrrolopyridine ATP-competitive JAK2 inhibitor with a high selectivity.

BMS-911543

A4152-25 ApexBio 25 mg 714 EUR
Description: BMS-911543 is a selective small-molecule inhibitor of JAK2 with IC50 value of 1.1nM [1].BMS-911543 is a reversible pyrrolopyridine ATP-competitive JAK2 inhibitor with a high selectivity.

BMS-911543

A4152-5 ApexBio 5 mg 292.8 EUR
Description: BMS-911543 is a selective small-molecule inhibitor of JAK2 with IC50 value of 1.1nM [1].BMS-911543 is a reversible pyrrolopyridine ATP-competitive JAK2 inhibitor with a high selectivity.

BMS-911543

A4152-50 ApexBio 50 mg 992.4 EUR
Description: BMS-911543 is a selective small-molecule inhibitor of JAK2 with IC50 value of 1.1nM [1].BMS-911543 is a reversible pyrrolopyridine ATP-competitive JAK2 inhibitor with a high selectivity.

BMS 299897

A4400-10 ApexBio 10 mg 332.4 EUR
Description: BMS-299897 is a selective inhibitor of ?-secretase with IC50 value of 12 nM [1]. ?-secretase is an intergral membrane protein whose well-known substrate is amyloid precursor protein and involves in the process of cleaving single-pass transmembrane proteins at residues with the transmembrane domain.

BMS 299897

A4400-5.1 ApexBio 10 mM (in 1mL DMSO) 360 EUR
Description: BMS-299897 is a selective inhibitor of ?-secretase with IC50 value of 12 nM [1]. ?-secretase is an intergral membrane protein whose well-known substrate is amyloid precursor protein and involves in the process of cleaving single-pass transmembrane proteins at residues with the transmembrane domain.

BMS 299897

A4400-50 ApexBio 50 mg 831.6 EUR
Description: BMS-299897 is a selective inhibitor of ?-secretase with IC50 value of 12 nM [1]. ?-secretase is an intergral membrane protein whose well-known substrate is amyloid precursor protein and involves in the process of cleaving single-pass transmembrane proteins at residues with the transmembrane domain.

Bms 626529

20-abx182383 Abbexa
  • 2064.00 EUR
  • 744.00 EUR
  • 100 mg
  • 10 mg

BMS 753

B5438-10 ApexBio 10 mg 420 EUR
Description: Ki : 2 nM for RAR? Three retinoic acid receptors (RAR?, RAR? and RAR? and three retinoid X receptors, members of the nuclear receptor (NR) superfamily, mediate the biological effects of retinoic acids upon development, cell differentiation and proliferation, and homeostasis.

BMS 753

B5438-50 ApexBio 50 mg 1519.2 EUR
Description: Ki : 2 nM for RAR? Three retinoic acid receptors (RAR?, RAR? and RAR? and three retinoid X receptors, members of the nuclear receptor (NR) superfamily, mediate the biological effects of retinoic acids upon development, cell differentiation and proliferation, and homeostasis.

BMS-817378

B5862-10 ApexBio 10 mg 373.2 EUR
Description: Description:IC50: 1.7 nM/15 nM for Met/VEGFR2 The signaling pathway of the receptor tyrosine kinase MET and its ligand hepatocyte growth factor is important for cell growth, survival, and motility.

BMS-817378

B5862-5 ApexBio 5 mg 226.8 EUR
Description: Description:IC50: 1.7 nM/15 nM for Met/VEGFR2 The signaling pathway of the receptor tyrosine kinase MET and its ligand hepatocyte growth factor is important for cell growth, survival, and motility.

BMS-817378

B5862-50 ApexBio 50 mg 999.6 EUR
Description: Description:IC50: 1.7 nM/15 nM for Met/VEGFR2 The signaling pathway of the receptor tyrosine kinase MET and its ligand hepatocyte growth factor is important for cell growth, survival, and motility.

BMS-582949

B6187-1 ApexBio 1 mg 174 EUR
Description: IC50: 13 nMBMS-582949 is a p38 MAPK inhibitorp38R MAP kinase plays a key role in regulating the biosynthesis of various inflammatory cytokines, such as tumor necrosis factor alpha and interleukin-1?.

BMS-582949

B6187-25 ApexBio 25 mg 932.4 EUR
Description: IC50: 13 nMBMS-582949 is a p38 MAPK inhibitorp38R MAP kinase plays a key role in regulating the biosynthesis of various inflammatory cytokines, such as tumor necrosis factor alpha and interleukin-1?.

BMS-582949

B6187-5 ApexBio 5 mg 348 EUR
Description: IC50: 13 nMBMS-582949 is a p38 MAPK inhibitorp38R MAP kinase plays a key role in regulating the biosynthesis of various inflammatory cytokines, such as tumor necrosis factor alpha and interleukin-1?.

BMS-303141

B1079-10 ApexBio 10 mg 177.6 EUR
Description: BMS-303141 is a potent inhibitor of ATP-citrate lyase with IC50 value of 0.13 ?M [1]. ATP-citrate lyase (ACL) is a cytosolic enzyme that responsible for the production of cytosolic acetyl-CoA, a precursor required for de novo biosyntheses of cholesterol and fatty acids.

BMS-303141

B1079-5.1 ApexBio 10 mM (in 1mL DMSO) 160.8 EUR
Description: BMS-303141 is a potent inhibitor of ATP-citrate lyase with IC50 value of 0.13 ?M [1]. ATP-citrate lyase (ACL) is a cytosolic enzyme that responsible for the production of cytosolic acetyl-CoA, a precursor required for de novo biosyntheses of cholesterol and fatty acids.

BMS-303141

B1079-50 ApexBio 50 mg 477.6 EUR
Description: BMS-303141 is a potent inhibitor of ATP-citrate lyase with IC50 value of 0.13 ?M [1]. ATP-citrate lyase (ACL) is a cytosolic enzyme that responsible for the production of cytosolic acetyl-CoA, a precursor required for de novo biosyntheses of cholesterol and fatty acids.

BMS-794833

B1438-10 ApexBio 10 mg 303.6 EUR
Description: BMS-794833 is a potent ATP competitive, dual inhibitor of c-Met and VEGFR2 (IC50 = 1.7 nM and 15 nM, respectively). It also has inhibitory effect on Ron, Axl and Flt3 (IC50 50% TGI for at least one tumor doubling time without significant toxicity in 14 days.

BMS-794833

B1438-5 ApexBio 5 mg 196.8 EUR
Description: BMS-794833 is a potent ATP competitive, dual inhibitor of c-Met and VEGFR2 (IC50 = 1.7 nM and 15 nM, respectively). It also has inhibitory effect on Ron, Axl and Flt3 (IC50 50% TGI for at least one tumor doubling time without significant toxicity in 14 days.

BMS-794833

B1438-5.1 ApexBio 10 mM (in 1mL DMSO) 212.4 EUR
Description: BMS-794833 is a potent ATP competitive, dual inhibitor of c-Met and VEGFR2 (IC50 = 1.7 nM and 15 nM, respectively). It also has inhibitory effect on Ron, Axl and Flt3 (IC50 50% TGI for at least one tumor doubling time without significant toxicity in 14 days.

BMS-794833

B1438-50 ApexBio 50 mg 999.6 EUR
Description: BMS-794833 is a potent ATP competitive, dual inhibitor of c-Met and VEGFR2 (IC50 = 1.7 nM and 15 nM, respectively). It also has inhibitory effect on Ron, Axl and Flt3 (IC50 50% TGI for at least one tumor doubling time without significant toxicity in 14 days.

BMS-794833

B1438-S ApexBio Evaluation Sample 97.2 EUR
Description: BMS-794833 is a potent ATP competitive, dual inhibitor of c-Met and VEGFR2 (IC50 = 1.7 nM and 15 nM, respectively). It also has inhibitory effect on Ron, Axl and Flt3 (IC50 50% TGI for at least one tumor doubling time without significant toxicity in 14 days.

BMS-378806

B1533-10 ApexBio 10 mg 366 EUR
Description: BMS-378806 is a novel attachment inhibitor of HIV with EC50 values of 2.68±1.64nM, 26.5±3.5nM.

BMS-378806

B1533-100 ApexBio 100 mg 1423.2 EUR
Description: BMS-378806 is a novel attachment inhibitor of HIV with EC50 values of 2.68±1.64nM, 26.5±3.5nM.

BMS-378806

B1533-5.1 ApexBio 10 mM (in 1mL DMSO) 282 EUR
Description: BMS-378806 is a novel attachment inhibitor of HIV with EC50 values of 2.68±1.64nM, 26.5±3.5nM.

BMS-378806

B1533-50 ApexBio 50 mg 1005.6 EUR
Description: BMS-378806 is a novel attachment inhibitor of HIV with EC50 values of 2.68±1.64nM, 26.5±3.5nM.

BMS 193885

B7327-10 ApexBio 10 mg 544.8 EUR
Description: BMS-193885 is a potent and selective neuropeptide Y1 receptor antagonist with IC50 of 5.9nM.Neuropeptide Y receptor 1 is G-protein coupled receptors and implicated in the modulation of food intake and energy homeostasis.

BMS 193885

B7327-50 ApexBio 50 mg 2056.8 EUR
Description: BMS-193885 is a potent and selective neuropeptide Y1 receptor antagonist with IC50 of 5.9nM.Neuropeptide Y receptor 1 is G-protein coupled receptors and implicated in the modulation of food intake and energy homeostasis.

BMS 453

B7396-10 ApexBio 10 mg 324 EUR
Description: BMS 453 is a synthetic RAR (retinoic acid receptor) antagonist [1]. The retinoic acid receptors (RAR?, RAR?, RAR?) belong to steroid nuclear receptor superfamily and the expressions of retinoid receptor RAR? and RAR? are correlated with the antiproliferative effects of retinoids.

BMS 453

B7396-25 ApexBio 25 mg 644.4 EUR
Description: BMS 453 is a synthetic RAR (retinoic acid receptor) antagonist [1]. The retinoic acid receptors (RAR?, RAR?, RAR?) belong to steroid nuclear receptor superfamily and the expressions of retinoid receptor RAR? and RAR? are correlated with the antiproliferative effects of retinoids.

BMS 453

B7396-5 ApexBio 5 mg 205.2 EUR
Description: BMS 453 is a synthetic RAR (retinoic acid receptor) antagonist [1]. The retinoic acid receptors (RAR?, RAR?, RAR?) belong to steroid nuclear receptor superfamily and the expressions of retinoid receptor RAR? and RAR? are correlated with the antiproliferative effects of retinoids.

BMS 961

B7397-10 ApexBio 10 mg 439.2 EUR
Description: BMS961 is a potent and selective retinoic acid receptor gamma (RAR?) agonist with IC50 values of 30 nM.RAR? belongs to the family of nuclear receptors which regulates transcription.

BMS 961

B7397-50 ApexBio 50 mg 1616.4 EUR
Description: BMS961 is a potent and selective retinoic acid receptor gamma (RAR?) agonist with IC50 values of 30 nM.RAR? belongs to the family of nuclear receptors which regulates transcription.

BMS 493

B7415-10 ApexBio 10 mg 351.6 EUR
Description: BMS493 is an inverse agonist of pan-retinoic acid receptors (pan-RARs). This compound has been shown to increase nuclear corepressor (NCoR) interaction with RARs.

BMS 493

B7415-25 ApexBio 25 mg 717.6 EUR
Description: BMS493 is an inverse agonist of pan-retinoic acid receptors (pan-RARs). This compound has been shown to increase nuclear corepressor (NCoR) interaction with RARs.

BMS 493

B7415-5 ApexBio 5 mg 235.2 EUR
Description: BMS493 is an inverse agonist of pan-retinoic acid receptors (pan-RARs). This compound has been shown to increase nuclear corepressor (NCoR) interaction with RARs.

BMS 195614

B7459-10 ApexBio 10 mg 373.2 EUR
Description: BMS 195614 is a selective RAR? antagonist [1]. It can bind to the RAR? subunit [5].

BMS 195614

B7459-5 ApexBio 5 mg 236.4 EUR
Description: BMS 195614 is a selective RAR? antagonist [1]. It can bind to the RAR? subunit [5].

BMS 195614

B7459-50 ApexBio 50 mg 1417.2 EUR
Description: BMS 195614 is a selective RAR? antagonist [1]. It can bind to the RAR? subunit [5].

BMS 309403

B7794-10 ApexBio 10 mg 226.8 EUR
Description: BMS309403 is specifically designed to target FABP4 with a Ki value less than 2 nM. It is a potent and selective FABP4 inhibitor.

BMS 309403

B7794-25 ApexBio 25 mg 421.2 EUR
Description: BMS309403 is specifically designed to target FABP4 with a Ki value less than 2 nM. It is a potent and selective FABP4 inhibitor.

BMS 309403

B7794-5 ApexBio 5 mg 157.2 EUR
Description: BMS309403 is specifically designed to target FABP4 with a Ki value less than 2 nM. It is a potent and selective FABP4 inhibitor.

BMS 309403

B7794-5.1 ApexBio 10 mM (in 1mL DMSO) 254.4 EUR
Description: BMS309403 is specifically designed to target FABP4 with a Ki value less than 2 nM. It is a potent and selective FABP4 inhibitor.

BMS 191011

B7146-10 ApexBio 10 mg 278.4 EUR
Description: BMS 191011 is a maxi-K channel opener [1].Maxi-K channels consist of a pore-forming ? subunit and a regulatory ? subunit. Maxi-K channels are of a high Ca2+ sensitivity [2].Bath application of BMS-191011 at a concentration of 20 ?M strongly reduced the calcium transients.

BMS 191011

B7146-25 ApexBio 25 mg 579.6 EUR
Description: BMS 191011 is a maxi-K channel opener [1].Maxi-K channels consist of a pore-forming ? subunit and a regulatory ? subunit. Maxi-K channels are of a high Ca2+ sensitivity [2].Bath application of BMS-191011 at a concentration of 20 ?M strongly reduced the calcium transients.

BMS 191011

B7146-5 ApexBio 5 mg 174 EUR
Description: BMS 191011 is a maxi-K channel opener [1].Maxi-K channels consist of a pore-forming ? subunit and a regulatory ? subunit. Maxi-K channels are of a high Ca2+ sensitivity [2].Bath application of BMS-191011 at a concentration of 20 ?M strongly reduced the calcium transients.

BMS 191011

B7146-50 ApexBio 50 mg 981.6 EUR
Description: BMS 191011 is a maxi-K channel opener [1].Maxi-K channels consist of a pore-forming ? subunit and a regulatory ? subunit. Maxi-K channels are of a high Ca2+ sensitivity [2].Bath application of BMS-191011 at a concentration of 20 ?M strongly reduced the calcium transients.

BMS 687453

C3544-10 ApexBio 10 mg 393.6 EUR
Description: IC50: 10 nM for human PPAR?BMS 687453 is a PPAR? agonist.

BMS 687453

C3544-25 ApexBio 25 mg 790.8 EUR
Description: IC50: 10 nM for human PPAR?BMS 687453 is a PPAR? agonist.

BMS 687453

C3544-5 ApexBio 5 mg 247.2 EUR
Description: IC50: 10 nM for human PPAR?BMS 687453 is a PPAR? agonist.

BMS-833923

HY-13809 MedChemExpress 100mg 687.6 EUR

BMS-378806

HY-14134 MedChemExpress 50mg 1424.4 EUR

BMS-191095

HY-14256 MedChemExpress 50mg 2704.8 EUR