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Cat. No. Product Name Information
PC-49803

ClpP agonist TR-65

ClpP agonist

ClpP agonist TR-65 is a potent small molecule agonist of mitochondrial ClpP protease with KD value of 23.3 nM.
PC-49802

ClpP agonist TR-57

ClpP agonist

ClpP agonist TR-57 is a potent small molecule agonist of mitochondrial ClpP protease with KD value of 15.5 nM.
PC-49801

ClpP agonist TR-27

ClpP agonist

ClpP agonist TR-27 is a potent small molecule agonist of mitochondrial ClpP protease with KD value of 23.7 nM.
PC-49788

DHODH inhibitor M62

DHODH inhibitor

DHODH inhibitor M62 is a potent, selective dihydroorotate dehydrogenase (DHODH) inhibitor with IC50 of 6.9 nM.
PC-49783

JNJ-DHODH-IN-29

DHODH inhibitor

JNJ-DHODH-IN-29 is a potent, selective DHODH inhibitor with IC50 of 0.3 nM, inhibits MOLM-13 cell proliferation with IC50 of 0.4 nM.
PC-49782

JNJ-DHODH-IN-19

DHODH inhibitor

JNJ-DHODH-IN-19 is a potent, selective DHODH inhibitor with IC50 of 1.1 nM, inhibits MOLM-13 cell proliferation with IC50 of 2.0 nM.
PC-49779

JNJ-74856665

DHODH inhibitor

JNJ74856665 (JNJ74856665) is an orally available, potent and selective DHODH inhibitor with IC50 of 0.4 nM.
PC-49767

CNS-11g

Alpha-synuclein inhibitor

CNS-11g is a small molecules capable of disassembling preformed alpha-synuclein fibrils, may exert it's disaggregating effects on the N terminus of the fibril core.
PC-49756

NB-598 maleate

Squalene epoxidase inhibitor

NB-598 (NB598) is a potent competitive inhibitor of squalene epoxidase (SQLE, SE, squalene monooxygenase) with IC50 of 4.4 nM (rat SE), inhibits microsomal squalene epoxidase from dog liver and Hep G2 cells with IC50 of 2.0 and 0.75 nM, respectively.
PC-49755

MM0299 analog 13

Lanosterol synthase inhibitor

MM0299 analog 13 (MM 0299 derivative 13) is a potent, selective, orally bioavailable, brain-penetrant inhibitor of lanosterol synthase (LSS, competition EC50=28.7 nM) with anti-proliferative activity.
PC-49754

MM0299

Lanosterol synthase inhibitor

MM0299 (MM 0299) is a potent, selective inhibitor of lanosterol synthase (LSS, competition EC50=1.97 nM) with anti-proliferative activity, inhibits Mut6 cell growth (IC50=18.2 nM) and induces the synthesis of 24(S),25-epoxycholesterol (EPC).
PC-49751

Cl-NIO

DDAH-1 inhibitor

Cl-NIO is a potent, selective inhibitor of human dimethylarginine dimethylaminohydrolase-1 (hDDAH-1) with Ki of 1.3 uM, > 500-fold selectivity against arginase and endothelial nitric oxide synthase.

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