| Cat. No. |
Product Name |
Information |
| PC-72976 |
FOXM1 inhibitor RCM-1
FOXM1 inhibitor
|
FOXM1 inhibitor RCM-1 (Robert Costa Memorial drug-1, RCM-1) is a small molecule potent inhibitor of FOXM1 transcription factor. |
| PC-72968 |
SOD3 inducer BNTA
SOD3 inducer
|
SOD3 inducer BNTA (BNTA) is a small molecule with ECM modulatory properties with target of Superoxide dismutase 3 (SOD3), a strong chondrogenic inducer that increased anabolism of chondrocytes in vitro. |
| PC-72962 |
TASIN-1
EBP inhibitor
|
TASIN-1 (Truncated APC selective inhibitor-1) is a small molecule that specifically kills cells with APC truncations but spares normal and cancer cells with wild-type APC, inhibits emopamil-binding protein (EBP). |
| PC-72961 |
CW3388
EBP inhibitor
|
CW3388 (CW-3388, CW3388) is a potent, cell-active Δ8,7-sterol isomerase (EBP) inhibitor, shows near-maximal effects on oligodendrocyte formation at 110 nM. |
| PC-72959 |
Etavopivat
PKR activator
|
Etavopivat (FT-4202) is a novel oral activator of PKR that decreases 2,3-DPG levels and hence would increase the HbS O2 affinity to reduce sickling. |
| PC-72948 |
CMP05-7
Endosomolytic compound
|
CMP05-7 (Endosomolytic compound CMP05-7) is a novel endosomolytic small-molecule compound that exhibits higher transfection efficiency/ability to induce endosomal escape of oligonucleotides (ONs) than current compounds such as chloroquine. |
| PC-72947 |
UNC2383
Endosomolytic compound
|
UNC2383 (UNC-2383) is a small molecule that enhances the intracellular delivery and pharmacological effectiveness of antisense oligonucleotides (ONs) and splice switching oligonucleotides (SSOs). |
| PC-72946 |
CMP05
Endosomolytic compound
|
CMP05 (Endosomolytic compound CMP05) is a novel endosomolytic small-molecule compound that exhibits higher transfection efficiency/ability to induce endosomal escape of oligonucleotides (ONs) than current compounds such as chloroquine. |
| PC-72941 |
SN-401
SWELL1 inhibitor
|
SN-401 (DCPIB) is a SWELL1 channel inhibitor that bind the SWELL1-LRRC8 channel complexes (IC50=3.9 uM). |
| PC-72934 |
CELF1-IN-841
CELF1 inhibitor
|
CELF1-IN-841 is a selective CUGBP Elav-like family member 1 (CELF1) inhibitor that disrupted CELF1-RNA binding, targets RRM1/2 of CELF1. |
| PC-72933 |
CELF1-IN-27
CELF1 inhibitor
|
CELF1-IN-27 is a selective CUGBP Elav-like family member 1 (CELF1) inhibitor that disrupted CELF1-RNA binding with IC50 of 23 uM, targets RRM1/2 of CELF1. |
| PC-72921 |
Diethyl-pythiDC
P4HA1 inhibitor
|
Diethyl-pythiDC (diethyl pythiDC) is a selective, small molecule inhibitor of P4HA1, inhibits collagen biosynthesis in breast cancer cells. |
