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. |