ML329 is a small molecule inhibitor of MITF which inhibits TRPM-1 promoter activity with an IC50 of 1.2 μM.

ML329 is a small molecule inhibitor of MITF which inhibits TRPM-1 promoter activity with an IC50 of 1.2 μM.

ML329 is a small molecule inhibitor of MITF which inhibits TRPM-1 promoter activity with an IC50 of 1.2 μM.

ML329 is a small molecule inhibitor of MITF which inhibits TRPM-1 promoter activity with an IC50 of 1.2 μM.

ML346 is an activator of Hsp70 with EC50 of 4600 nM in HeLa cell toxicity assay.

ML346 is an activator of Hsp70 with EC50 of 4600 nM in HeLa cell toxicity assay.

ML346 is an activator of Hsp70 with EC50 of 4600 nM in HeLa cell toxicity assay.

ML346 is an activator of Hsp70 with EC50 of 4600 nM in HeLa cell toxicity assay.

ML346 is an activator of Hsp70 with EC50 of 4600 nM in HeLa cell toxicity assay.

ML346 is an activator of Hsp70 with EC50 of 4600 nM in HeLa cell toxicity assay.

ML352 is a novel and noncompetitive inhibitor of the presynaptic choline transporter, with Ki of 92 nM.

ML406 is a small molecule probe with anti-tubercular activity via MtbbioA (DAPA synthase) enzyme inhibition with IC50 of 30 nM. It can inhibit biotin biosynthesis in mycobacterium tuberculosis.

ML406 is a small molecule probe with anti-tubercular activity via MtbbioA (DAPA synthase) enzyme inhibition with IC50 of 30 nM. It can inhibit biotin biosynthesis in mycobacterium tuberculosis.

ML406 is a small molecule probe with anti-tubercular activity via MtbbioA (DAPA synthase) enzyme inhibition with IC50 of 30 nM. It can inhibit biotin biosynthesis in mycobacterium tuberculosis.

ML406 is a small molecule probe with anti-tubercular activity via MtbbioA (DAPA synthase) enzyme inhibition with IC50 of 30 nM. It can inhibit biotin biosynthesis in mycobacterium tuberculosis.

ML406 is a small molecule probe with anti-tubercular activity via MtbbioA (DAPA synthase) enzyme inhibition with IC50 of 30 nM. It can inhibit biotin biosynthesis in mycobacterium tuberculosis.

ML406 is a small molecule probe with anti-tubercular activity via MtbbioA (DAPA synthase) enzyme inhibition with IC50 of 30 nM. It can inhibit biotin biosynthesis in mycobacterium tuberculosis.

ML418 is the first potent, selective and CNS penetrating blocker of Kir7.1 potassium channel (IC50, 310 nM), which also potently inhibits Kir6.2/SUR1, and exhibits superior selectivity over other Kir channels.

ML418 is the first potent, selective and CNS penetrating blocker of Kir7.1 potassium channel (IC50, 310 nM), which also potently inhibits Kir6.2/SUR1, and exhibits superior selectivity over other Kir channels.

ML418 is the first potent, selective and CNS penetrating blocker of Kir7.1 potassium channel (IC50, 310 nM), which also potently inhibits Kir6.2/SUR1, and exhibits superior selectivity over other Kir channels.

ML418 is the first potent, selective and CNS penetrating blocker of Kir7.1 potassium channel (IC50, 310 nM), which also potently inhibits Kir6.2/SUR1, and exhibits superior selectivity over other Kir channels.

ML418 is the first potent, selective and CNS penetrating blocker of Kir7.1 potassium channel (IC50, 310 nM), which also potently inhibits Kir6.2/SUR1, and exhibits superior selectivity over other Kir channels.

MLR-1023 is a chemical compound which inhibits acid secretion in animal models and also acts as a bronchodilator in histamine-challenged animals.

MLR-1023 is a chemical compound which inhibits acid secretion in animal models and also acts as a bronchodilator in histamine-challenged animals.

MLS000532223 is a high affinity, selective inhibitor of Rho family GTPases, with EC50 ranging from 16 μM to 120 μM. Small GTPases are key regulators of cellular activity .

MLS000532223 is a high affinity, selective inhibitor of Rho family GTPases, with EC50 ranging from 16 μM to 120 μM. Small GTPases are key regulators of cellular activity .

MLS000532223 is a high affinity, selective inhibitor of Rho family GTPases, with EC50 ranging from 16 μM to 120 μM. Small GTPases are key regulators of cellular activity .

MMAF HCl is an antitubulin agent that inhibit cell division. It inhibits H3397 cell growth with an IC50 of 105 nM.

MMAF HCl is an antitubulin agent that inhibit cell division. It inhibits H3397 cell growth with an IC50 of 105 nM.

MMAF HCl is an antitubulin agent that inhibit cell division. It inhibits H3397 cell growth with an IC50 of 105 nM.

mMelin is a natural product isolated and purified from the herbs of Micromelum integerrimum with antitumor activity and cytotoxicity against cholangiocarcinoma cell line, KKU-100.

MMPX is a specific inhibitor of calmodulin-sensitive cyclic GMP phosphodiesterase 1 with IC50 of 5.2 μM.

MMPX is a specific inhibitor of calmodulin-sensitive cyclic GMP phosphodiesterase 1 with IC50 of 5.2 μM.

MMPX is a specific inhibitor of calmodulin-sensitive cyclic GMP phosphodiesterase 1 with IC50 of 5.2 μM.

MMPX is a specific inhibitor of calmodulin-sensitive cyclic GMP phosphodiesterase 1 with IC50 of 5.2 μM.

MMPX is a specific inhibitor of calmodulin-sensitive cyclic GMP phosphodiesterase 1 with IC50 of 5.2 μM.