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Cat. No. Product Name Information
PC-72687

Ethanimidothioic acid

Scramblase inhibitor

Ethanimidothioic acid (R5421) is an inhibitor of platelet scramblase activity.
PC-72667

UNC10245131

CIB1 inhibitor

UNC10245131 (UNC 10245131) is a potent, selective cyclic peptide inhibitor of calcium and integrin binding protein 1 (CIB1) with ITC Kd of 6.17 nM.
PC-72664

DS96432529

Bone anabolic agent

DS96432529 (DS 96432529) is a potent and orally active bone anabolic agent with EC200 value of 0.024 ug/mL.
PC-72661

Vanin-1 inhibitor 2

Vanin-1 inhibitor

Vanin-1 inhibitor 2 is a potent, selective, oral Vanin-1 inhibitor with IC50 of 3.4 and 1.5 nM for human and mouse Vanin-1, respectively.
PC-72660

PFI-653

Vanin-1 inhibitor

PFI-653 (Vanin-1-IN-1) is a highly potent vanin-1 inhibitor with IC50 of 6.8 nM (human Vanin-1).
PC-72652

JNJ-40929837

LTA4H inhibitor

JNJ-40929837 (JNJ40929837) is a potent, highly selective, oral leukotriene A4 hydrolase (LTA4H) inhibitor with IC50 of 1.9 nM, demonstrates high potency (IC50=48 nM) in human whole blood ionophore-stimulated LTB4 release assay.
PC-72651

LYS-006

LTA4H inhibitor

LYS-006 (LYS006) is a potent, highly selective leukotriene A4 hydrolase (LTA4H) inhibitor with biochemical IC50 <3 nM.
PC-72648

ASC inhibitor MM01

ASC inhibitor

ASC inhibitor MM01 (MM01) is a first-in-class, specific small-molecule inhibitor of ASC protein that interferes with ASC speck formation, inhibited ASC-mediated pro-Casp-1 activation with IC50 of 0.5 uM.
PC-72643

TRC102

BER inhibitor

TRC102 (Methoxyamine HCl, TRC-102) is a small-molecule base-excision repair (BER) inhibitor, potentiates the cytotoxicity of pemetrexed and reverses resistance by binding to chemotherapy-induced abasic sites in DNA.
PC-72641

STI1

SQOR inhibitor

STI1 (SQOR inhibitor STI1) is a potent, specific, competitive inhibitor of human sulfide:quinone oxidoreductase (SQOR) with IC50 of 29 nM.
PC-72638

AG-270

MAT2A inhibitor

AG-270 (AG270) is a highly potent, selective, orally bioavailable MAT2A inhibitor with IC50 of 14 nM.
PC-72631

AK-3280

Antifibrotic agent

AK-3280 (AK 3280, GDC 3280, RG 6069) is an orally available, potential novel anti-fibrotic small molecule under investigation for the treatment of interstitial lung diseases.

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