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Cat. No. Product Name Information
PC-62073

Surfen hydrate

Heparan sulfate antagonist

Surfen hydrate is a small molecule antagonist of heparan sulfate, binds to heparin, low molecular weight heparins, and to HS and other GAGs.
PC-62072

Surfen

Heparan sulfate antagonist

Surfen is a small molecule antagonist of heparan sulfate, binds to heparin, low molecular weight heparins, and to HS and other GAGs.
PC-62062

CMA-008

NAADP inhibitor

CMA-008 is a cell-permeable, small molecule modulator of NAADP-mediated Ca2+ release, competes with NAADP binding, inhibits Ca2+ release via the NAADP receptor (IC50=15 uM-1 mM).
PC-62061

BZ194

NAADP inhibitor

BZ194 (BZ-194) is a small molecule inhibitor of NAADP action that inhibit NAADP-mediated Ca2+ signaling in T cells, neither interferes with Ca2+ mobilization by IP3 or cyclic ADP-ribose nor with capacitative Ca2+ entry.
PC-62059

FSC231

PICK1 inhibitor

FSC231 (FSC-231) is the first, cell-permeable small-molecule inhibitor of PICK1 PDZ domain with Kd of 10.1 uM.
PC-62048

MitoBloCK 6

Erv1 oxidase inhibitor

MitoBloCK 6 is a small molecule mitochondrial protein import blocker that inhibits Erv1 oxidase activity.
PC-62047

MitoBloCK 1

TIM22 inhibitor

MitoBloCK 1 is a small molecule inhibitor that blocks the import of substrates that use the TIM22 import pathway, but not TIM23 or the Mia40/Erv1 translocation pathways.
PC-62043

DM-PIT-1

PIP3 antagonist

DM-PIT-1 is a specific PIP3 antagonist that disrupts PIP3/Akt PH domain, PIP3/PDK1 PH domain, and PIP3/GRP1 PH domain with IC50 of 27.1 uM, 80.5 uM, and 35.5 uM, respectively.
PC-62042

PIT-1

PIP3 antagonist

PIT-1 is a specific PIP3 antagonist that disrupts PIP3/Akt PH domain binding with IC50 of 30 uM, Kd of 43.2 uM.
PC-62033

LCS-1.34

SOD1 inhibitor

LCS-1.34 is a small molecule that inhibits growth of human lung adenocarcinoma cells harboring mutations in EGFR or KRAS with IC50 of 0.1-1.1 uM.
PC-62032

LCS-1.28

SOD1 inhibitor

LCS-1.28 is a small molecule that inhibits growth of human lung adenocarcinoma cells harboring mutations in EGFR or KRAS with IC50 of 0.05-1.6 uM.
PC-62031

LCS-1

SOD1 inhibitor

LCS-1 is a small molecule that inhibits growth of human lung adenocarcinoma cells harboring mutations in EGFR or KRAS with IC50 of 0.1-1.5 uM.

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