Necrosis Inhibitor

Necrosis Inhibitor, Necrox-2

2228-5
EUR 615

Necrosis Inhibitor, Necrox-5

2229-1
EUR 191

Necrosis Inhibitor, Necrox-5

2229-5
EUR 615

Ribunuclease Inhibitor / RNase Inhibitor

105-310 2000 u
EUR 76

Ribunuclease Inhibitor / RNase Inhibitor

105-350 10000 u
EUR 237

Tumor necrosis factor antibody

70R-15095 100 ug
EUR 327
Description: Rabbit polyclonal Tumor necrosis factor antibody

Necrosis vs Apoptosis Kits

KF17371 50-100 Tests
EUR 435

Necrosis vs Apoptosis Kits

KF17372 100-200 Tests
EUR 768

MAPKII Kinase Inhibitor (Hsp25 Kinase Inhibitor)

SIH-120A 1 mg
EUR 179
  • The MAPK (mitogen activated protein kinase) comprises a family of ubiquitous praline-directed, protein serine/threonine kinases which signal transduction pathways that control intracellular events including acute responses to hormones and major devel
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Description: The substance MAPKII Kinase Inhibitor is a hsp25 kinase inhibitor. It is synthetically produced and has a purity of >95%. The pure substance is white solid which is soluble in DMSO or H20.

Renin Inhibitor

2084-25
EUR 838

Renin Inhibitor

2084-5
EUR 262

Apoptosis inhibitor

2783-25
EUR 457

Apoptosis inhibitor

2783-5
EUR 153

Papain Inhibitor

A1035-25 25 mg
EUR 90
Description: Papain Inhibitor peptide,(C19H29N7O6),a peptide with the sequence H-Gly-Gly-Tyr-Arg-OH,MW= 451.4,this peptide Inhibits the peptidase activity of Papain.

Chk2 Inhibitor

1702-1
EUR 180

SCD1 Inhibitor

1716-1
EUR 218

SCD1 Inhibitor

1716-5
EUR 577

ACC2 Inhibitor

1717-1
EUR 218

ACC2 Inhibitor

1717-5
EUR 686

SIRT2 Inhibitor

1857-25
EUR 436

SIRT2 Inhibitor

1857-5
EUR 147

Elastase Inhibitor

1922-5
EUR 262

Myeloperoxidase Inhibitor

1977-100
EUR 115

Myeloperoxidase Inhibitor

1977-500
EUR 240

Syk Inhibitor

1983-1
EUR 126

Syk Inhibitor

1983-5
EUR 283

Kallikrein Inhibitor

5-01416 4 x 5mg Ask for price

Papain Inhibitor

5-01715 10mg Ask for price

Endotoxin Inhibitor

5-01105 4 x 1mg Ask for price

Trypsin inhibitor

44R-1107 50 gram
EUR 3589
Description: Trypsin inhibitor enzyme

PI3K-? Inhibitor

B1869-25
EUR 675

PI3K-? Inhibitor

B1869-5
EUR 207

PKM2 Inhibitor

B2593-25
EUR 631

PKM2 Inhibitor

B2593-5
EUR 196

CDK4 inhibitor

B1233-10 10 mg
EUR 469
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family.

CDK4 inhibitor

B1233-100 100 mg
EUR 1592
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family.

CDK4 inhibitor

B1233-25 25 mg
EUR 656
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family.

CDK4 inhibitor

B1233-5 5 mg
EUR 325
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family.

CDK4 inhibitor

B1233-50 50 mg
EUR 1041
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family.

Trypsin inhibitor

AT160 1mg
EUR 1368

Stat5 Inhibitor

9484-1
EUR 120

Stat5 Inhibitor

9484-5
EUR 327

Rinbonuclease Inhibitor

abx098030-10kU 10 kU
EUR 537
  • Shipped within 5-10 working days.

Rinbonuclease Inhibitor

abx098030-2kU 2 kU
EUR 425
  • Shipped within 5-10 working days.

XL647Kinase Inhibitor

E1KS1083 5 mg
EUR 873

PKR Inhibitor

C4439-10 10 mg
EUR 206
Description: IC50: 186-210 nMPKR Inhibitor is a double-stranded RNA-activated protein kinase (PKR) inhibitor. Initiation of protein synthesis is reported to be regulated by kinase-dependent phosphorylation reactions.

PKR Inhibitor

C4439-25 25 mg
EUR 398
Description: IC50: 186-210 nMPKR Inhibitor is a double-stranded RNA-activated protein kinase (PKR) inhibitor. Initiation of protein synthesis is reported to be regulated by kinase-dependent phosphorylation reactions.

PKR Inhibitor

C4439-5 5 mg
EUR 137
Description: IC50: 186-210 nMPKR Inhibitor is a double-stranded RNA-activated protein kinase (PKR) inhibitor. Initiation of protein synthesis is reported to be regulated by kinase-dependent phosphorylation reactions.

EGFR Inhibitor

C3327-1 1 mg
EUR 154
Description: EGFR inhibitor is a cell permeable, pyrimidine compound that selectively inhibits the EGFR kinase with IC50 value of 21 nM [1]. EGFR is a transmembrane protein, and is a receptor for members of epidermal growth factor family.

EGFR Inhibitor

C3327-25 25 mg
EUR 1146
Description: EGFR inhibitor is a cell permeable, pyrimidine compound that selectively inhibits the EGFR kinase with IC50 value of 21 nM [1]. EGFR is a transmembrane protein, and is a receptor for members of epidermal growth factor family.

EGFR Inhibitor

C3327-5 5 mg
EUR 363
Description: EGFR inhibitor is a cell permeable, pyrimidine compound that selectively inhibits the EGFR kinase with IC50 value of 21 nM [1]. EGFR is a transmembrane protein, and is a receptor for members of epidermal growth factor family.

CBF? Inhibitor

C3398-10 10 mg
EUR 203
Description: CBF? inhibitor is a small molecule which binds to CBF? and inhibits its association with Runx1 [1].Core binding factors (CBFs) are heterodimeric transcription factors containing a DNA-binding CBF? component (a RUNX protein) and an enhancer of binding, CBF?.

CBF? Inhibitor

C3398-25 25 mg
EUR 393
Description: CBF? inhibitor is a small molecule which binds to CBF? and inhibits its association with Runx1 [1].Core binding factors (CBFs) are heterodimeric transcription factors containing a DNA-binding CBF? component (a RUNX protein) and an enhancer of binding, CBF?.

CBF? Inhibitor

C3398-5 5 mg
EUR 131
Description: CBF? inhibitor is a small molecule which binds to CBF? and inhibits its association with Runx1 [1].Core binding factors (CBFs) are heterodimeric transcription factors containing a DNA-binding CBF? component (a RUNX protein) and an enhancer of binding, CBF?.

STAT5 Inhibitor

C4105-10 10 mg
EUR 196
Description: STAT5 Inhibitor is a cell-permeable inhibitor of STAT5 with IC50 value of 47 ?M against STAT5? SH2 domain EPO peptide binding activity [1].

STAT5 Inhibitor

C4105-25 25 mg
EUR 376
Description: STAT5 Inhibitor is a cell-permeable inhibitor of STAT5 with IC50 value of 47 ?M against STAT5? SH2 domain EPO peptide binding activity [1].

STAT5 Inhibitor

C4105-5 5 mg
EUR 126
Description: STAT5 Inhibitor is a cell-permeable inhibitor of STAT5 with IC50 value of 47 ?M against STAT5? SH2 domain EPO peptide binding activity [1].

Trypsin inhibitor

AG160 1 mg
EUR 523

BRAF inhibitor

A3263-10 10 mg
EUR 383
Description: BRAF inhibitor is a potent BRAF inhibitor.

BRAF inhibitor

A3263-5.1 10 mM (in 1mL DMSO)
EUR 448
Description: BRAF inhibitor is a potent BRAF inhibitor.

BRAF inhibitor

A3263-50 50 mg
EUR 985
Description: BRAF inhibitor is a potent BRAF inhibitor.

CDK9 inhibitor

A3294-10 10 mg
EUR 328
Description: CDK9 inhibitor is a small-molecule selective inhibitor of CDK9 (cyclin dependent kinase 9) with IC50 value of 39 nM [1].CDKs are a group of serine/threonine kinases and are widely spread in all known eukaryotes.

CDK9 inhibitor

A3294-100 100 mg
EUR 1497
Description: CDK9 inhibitor is a small-molecule selective inhibitor of CDK9 (cyclin dependent kinase 9) with IC50 value of 39 nM [1].CDKs are a group of serine/threonine kinases and are widely spread in all known eukaryotes.

CDK9 inhibitor

A3294-5 5 mg
EUR 197
Description: CDK9 inhibitor is a small-molecule selective inhibitor of CDK9 (cyclin dependent kinase 9) with IC50 value of 39 nM [1].CDKs are a group of serine/threonine kinases and are widely spread in all known eukaryotes.

CDK9 inhibitor

A3294-5.1 10 mM (in 1mL DMSO)
EUR 212
Description: CDK9 inhibitor is a small-molecule selective inhibitor of CDK9 (cyclin dependent kinase 9) with IC50 value of 39 nM [1].CDKs are a group of serine/threonine kinases and are widely spread in all known eukaryotes.

CDK9 inhibitor

A3294-50 50 mg
EUR 846
Description: CDK9 inhibitor is a small-molecule selective inhibitor of CDK9 (cyclin dependent kinase 9) with IC50 value of 39 nM [1].CDKs are a group of serine/threonine kinases and are widely spread in all known eukaryotes.

ITK inhibitor

A3509-10 10 mg
EUR 773
Description: Interleukin-2-inducible T cell kinase (ITK) is a non-receptor tyrosine kinase expressed in T cells, NKT cells and mast cells which plays a crucial role in regulating the T cell receptor (TCR), CD28, CD2, chemokine receptor CXCR4, and FcepsilonR-mediated signaling pathways.

ITK inhibitor

A3509-50 50 mg
EUR 2040
Description: Interleukin-2-inducible T cell kinase (ITK) is a non-receptor tyrosine kinase expressed in T cells, NKT cells and mast cells which plays a crucial role in regulating the T cell receptor (TCR), CD28, CD2, chemokine receptor CXCR4, and FcepsilonR-mediated signaling pathways.

Lck Inhibitor

A3539-1 1 mg
EUR 154
Description: Lck Inhibitor is a small-molecule inhibitor of with IC50 value of 7 nM [1].The lymphocyte specific kinase which expressed in NK cells and T-cells is a member of the Src kinase family.

Lck Inhibitor

A3539-5 5 mg
EUR 222
Description: Lck Inhibitor is a small-molecule inhibitor of with IC50 value of 7 nM [1].The lymphocyte specific kinase which expressed in NK cells and T-cells is a member of the Src kinase family.

MEK inhibitor

A3594-10 10 mg
EUR 746
Description: A potent MEK inhibitor, Antitumor agent.

MEK inhibitor

A3594-5 5 mg
EUR 547
Description: A potent MEK inhibitor, Antitumor agent.

MEK inhibitor

A3594-5.1 10 mM (in 1mL DMSO)
EUR 598
Description: A potent MEK inhibitor, Antitumor agent.

PDK1 inhibitor

A3706-10 10 mg
EUR 495
Description: PDK1 inhibitor is an potent and selective inhibitor of PDK1 with potential as anticancer agent. GSK 2334470,a inhibitor of PDK1, has IC50 value of 0.00251µM and CHEMBL1172241 with IC50 value of 0.085µM.

PDK1 inhibitor

A3706-100 100 mg
EUR 2583
Description: PDK1 inhibitor is an potent and selective inhibitor of PDK1 with potential as anticancer agent. GSK 2334470,a inhibitor of PDK1, has IC50 value of 0.00251µM and CHEMBL1172241 with IC50 value of 0.085µM.

PDK1 inhibitor

A3706-5 5 mg
EUR 290
Description: PDK1 inhibitor is an potent and selective inhibitor of PDK1 with potential as anticancer agent. GSK 2334470,a inhibitor of PDK1, has IC50 value of 0.00251µM and CHEMBL1172241 with IC50 value of 0.085µM.

PDK1 inhibitor

A3706-50 50 mg
EUR 1723
Description: PDK1 inhibitor is an potent and selective inhibitor of PDK1 with potential as anticancer agent. GSK 2334470,a inhibitor of PDK1, has IC50 value of 0.00251µM and CHEMBL1172241 with IC50 value of 0.085µM.

Apoptosis Inhibitor

A1930-10 10 mg
EUR 142
Description: M50054, 2,2'-methylenebis (1,3-cyclohexanedione), is a novel inhibitor of apoptosis. [1] In human Fas-expressing WC8 cells, M50054 inhibited apoptosis by soluble human Fas ligand in vitro cell death assay.

Apoptosis Inhibitor

A1930-100 100 mg
EUR 456
Description: M50054, 2,2'-methylenebis (1,3-cyclohexanedione), is a novel inhibitor of apoptosis. [1] In human Fas-expressing WC8 cells, M50054 inhibited apoptosis by soluble human Fas ligand in vitro cell death assay.

Apoptosis Inhibitor

A1930-25 25 mg
EUR 235
Description: M50054, 2,2'-methylenebis (1,3-cyclohexanedione), is a novel inhibitor of apoptosis. [1] In human Fas-expressing WC8 cells, M50054 inhibited apoptosis by soluble human Fas ligand in vitro cell death assay.

Apoptosis Inhibitor

A1930-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: M50054, 2,2'-methylenebis (1,3-cyclohexanedione), is a novel inhibitor of apoptosis. [1] In human Fas-expressing WC8 cells, M50054 inhibited apoptosis by soluble human Fas ligand in vitro cell death assay.

Apoptosis Inhibitor

A1930-S Evaluation Sample
EUR 81
Description: M50054, 2,2'-methylenebis (1,3-cyclohexanedione), is a novel inhibitor of apoptosis. [1] In human Fas-expressing WC8 cells, M50054 inhibited apoptosis by soluble human Fas ligand in vitro cell death assay.

Elastase Inhibitor

A2579-5 5 mg
EUR 166
Description: A potent, irreversible inhibitor of human neutrophil elastase (HNE). The structure of the enzyme-inhibitor complex reveals crosslinking of the catalytic residues His-57 and Ser-195 by the peptidyl chloromethylketone.

NFAT Inhibitor

A4539-1 1 mg
EUR 138
Description: Selective inhibitor of calcineurin-mediated dephosphorylation of nuclear factor of activated T cells (NFAT). Does not disrupt other calcineurin-dependent pathways. Inhibits NFAT activation and NFAT-dependent expression of endogenous cytokine genes in T cells.

NFAT Inhibitor

A4539-10 10 mg
EUR 763
Description: Selective inhibitor of calcineurin-mediated dephosphorylation of nuclear factor of activated T cells (NFAT). Does not disrupt other calcineurin-dependent pathways. Inhibits NFAT activation and NFAT-dependent expression of endogenous cytokine genes in T cells.

NFAT Inhibitor

A4539-5 5 mg
EUR 450
Description: Selective inhibitor of calcineurin-mediated dephosphorylation of nuclear factor of activated T cells (NFAT). Does not disrupt other calcineurin-dependent pathways. Inhibits NFAT activation and NFAT-dependent expression of endogenous cytokine genes in T cells.

Neurotoxin Inhibitor

HY-112722 10mM/1mL
EUR 744

Lck Inhibitor

HY-12072 100mg
EUR 2019

MEK inhibitor

HY-12202 5mg
EUR 429

Nav1.7 inhibitor

HY-13985 10mM/1mL
EUR 580

PLpro inhibitor

HY-17542 5mg
EUR 533

CPA inhibitor

HY-70005 50mg
EUR 1297

NFAT Inhibitor

HY-P1026 5mg
EUR 436

BRAF inhibitor

HY-10247 10mM/1mL
EUR 354

Endotoxin Inhibitor

H-1382.0001 1.0mg
EUR 113
Description: Sum Formula: C55H97N15O12S2; CAS# [147396-10-9]

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