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Cat. No. Product Name Information
PC-72918

G6PDi-1

G6PD inhibitor

G6PDi-1 is a non-steroidal, potent cell active small molecule inhibitor of glucose-6-phosphate dehydrogenase (G6PD) with IC50 of 70 nM (hG6PD).
PC-72917

IMT1B

POLRMT inhibitor

IMT1B (LDC203974) a first-in-class specific inhibitor of mitochondrial transcription that target the human mitochondrial RNA polymerase (POLRMT)..
PC-72916

IMT1

POLRMT inhibitor

IMT1 (LDC195943) is a first-in-class specific inhibitor of mitochondrial transcription that target the human mitochondrial RNA polymerase (POLRMT).
PC-72915

ABA Antagonist AA1

ABA antagonist

ABA Antagonist AA1 is a small molecule that inhibits ABA signaling with IC50 of 2.5 uM, targets all ABA receptors.
PC-72907

YB-0158

Sam68 inhibitor

YB-0158 (YB0158) is a β-turn peptidomimetic small molecule altering key hallmarks of human colorectal tumorigenesis, with high predicted affinity for Sam68.
PC-72902

LY 3372689

O-GlcNAcase inhibitor

LY 3372689 is an oral, small molecule O-GlcNAcase (OGA) enzyme inhibitor for the treatment of Alzeimer's disease.
PC-72901

LP0200

IL17 modulator

LP0200 (LP 0200) is a small-molecule modulator of IL-17 under development for psoriasis.
PC-72887

FECH inhibitor 4e

Ferrochelatase inhibitor

FECH inhibitor 4e (FECH-IN-4e) is a potent, specifc, competitive inhibitor of ferrochelatase (FECH) with IC50 in the high-nanomolar range.
PC-72885

LCS3

GSR inhibitor

LCS3 is a small molecule that selectively impairs the growth of human lung adenocarcinoma (LUAD) cells, induces oxidative stress, inhibits glutathione disulfide reductase (GSR) and thioredoxin reductase 1 (TXNRD1) with IC50 of 3.3 and 3.8 uM, respectively.
PC-72877

CW5107

HSD17B7 inhibitor

CW5107 (CW 5107) is a small molecule HSD17B7 inhibitor that enhances oligodendrocyte formation.
PC-72876

CW4142

SC4MOL inhibitor

CW4142 (CW 4142) is a small molecule SC4MOL inhibitor that enhances oligodendrocyte formation.
PC-72871

NERx 329

RPA inhibitor

NERx 329 (RPAi 329, NERx329) is a novel potent, specific inhibitor of replication protein A (RPA), demonstrated potent RPA inhibitory activity in vitro, in vivo, and in cellular assays.

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