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Cat. No. Product Name Information
PC-20313

SJ572946

BAK activator

SJ572946 is a small molecule BAK activator, binds to the activation groove of BAK and selectively triggers BAK activation over that of BAX in liposome and mitochondrial permeabilization assays.
PC-20306

ELOVL6 inhibitor Compound B

ELOVL6 inhibitor

ELOVL6 inhibitor Compound B is a potent and selective ELOVL6 inhibitor with IC50 of 85 and 38 nM for human and mouse ELOVL6, respectively.
PC-20305

ELOVL6 inhibitor 37

ELOVL6 inhibitor

ELOVL6 inhibitor 37 (ELOVL6-IN-2) is a potent, selective inhibitor of elongase of long-chain fatty acids family 6 (ELOVL6) with IC50 of 8.9 and 31 nM for human and mouse ELOVL6, respectively.
PC-20304

ELOVL6 inhibitor Compound A

ELOVL6 inhibitor

ELOVL6 inhibitor Compound-A is a potent, selective inhibitor of elongase of long-chain fatty acids family 6 (ELOVL6) with IC50 of 169 and 350 nM for human and mouse ELOVL6, respectively.
PC-20302

HTS13286

AQP9 inhibitor

HTS13286 is a selective Aquaporin 9 (AQP9) inhibitor with IC50 of 1.5 uM (inhibition of CHO-AQP9 cell water permeability).
PC-20301

RF03176

AQP9 inhibitor

RF03176 is a selective Aquaporin 9 (AQP9) inhibitor with IC50 of 1.3 uM (inhibition of CHO-AQP9 cell water permeability).
PC-20300

TGN-020

AQP4 inhibitor

TGN-020 (TGN020) is a potent, selective aquaporin 4 (AQP4) inhibitor with IC50 of 3 uM.
PC-20274

SPT inhibitor compound-2

SPT inhibitor

SPT inhibitor compound-2 is a potent, orally active serine palmitoyltransferase (SPT) inhibitor with IXC50 of 0.51 nM in cell-free assays.
PC-20264

Indoluidin E

DHODH inhibitor

Indoluidin E is an indoluidin D derivative, and potent selective dihydroorotate dehydrogenase (DHODH) inhibitor, suppresses cancer cell growth.
PC-20263

Indoluidin D

DHODH inhibitor

Indoluidin D is a potent selective dihydroorotate dehydrogenase (DHODH) inhibitor, promotes myeloid differentiation and inhibits the proliferation of acute promyelocytic leukemia HL-60 cells.
PC-20258

Dichloroallyl lawsone

DHODH inhibitor

Dichloroallyl lawsone (Dichlorolapachol, DCL, NSC-126771) is a synthetic analogue of the antimalarial lapachol, inhibits mitochondrial dihydroorotate dehydrogenase (DHODH) with antineoplastic activity.
PC-20224

Compound 30666

IgH gene enhancer inhibitor

Compound 30666 is a specific small molecule inhibitor of IgH enhancer transcriptional activity with IC50 of 2.1 uM, inhibits immunoglobulin production by MM cells.

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