| Cat. No. |
Product Name |
Information |
| PC-27270 |
XL20
TDP-43 inhibitor
|
XL20 is a brain-penetrant small molecule targeting the TDP-43 conserved α-helical region spanning residues 320-340 (conserved region, CR) to suppress neurotoxicity, binds to full-length TDP-43 and CR peptide with SPR KD of 10.4 uM and 7.84 uM. |
| PC-27237 |
CD73 inhibitor Compound 73
CD73 inhibitor
|
CD73 inhibitor Compound 73 (CD73-IN-5) is a potent and selective non-nucleotide small molecule inhibitor of CD73 (ecto-5′-nucleotidase, eN) with IC50 of 12 nM. |
| PC-27212 |
A2ti-2
S100A10-ANXA2 inhibitor
|
A2ti-2 (S100A10-ANXA2 heterotetramer inhibitor-2) is a specific small molecule Annexin A2 (ANXA2) inhibitor, inhibits Annexin A2-S100A10 protein interaction with IC50 of 230 nM (Annexin A2/S100A10 heterotetramer (A2t)), blocks HPV16 infection and entry into HeLa cells. |
| PC-27202 |
SGM-3
Striga germination inhibitor, ShHTL7 inhibitor
|
Striga germination modulator-3 (SGM-3) is a potent, selective germination inhibitor for Striga hermonthica, selectively binds to ShHTL7 and shows inhibitory activity against YLG hydrolysis by ShHTL7 with IC50 of 2.3 uM. |
| PC-27201 |
KK023-N1
Striga germination inhibitor, ShHTL7 inhibitor
|
KK023-N1 is a potent, specific Striga germination inhibitor, blocks the hydrolysis activity of S. hermonthica HYPO-SENSITIVE TO LIGHT 7 (ShHTL7) with IC50 of 1.78 uM, does not affect rice (Oryza sativa) SL receptor DWARF14 (OsD14). |
| PC-27135 |
Galinex
GPR17 agonist
|
Galinex is a highly potent, selective GPR17 agonist with EC50 of 0.64 nM, Emax=127.8% in [35S]GTPγS functional assays in membranes from 1321N1 cells transfected with human GPR17. |
| PC-27133 |
PT-13
Tau disaggregant
|
PT-13 is a brain-penetrant small-molecule tau disaggregant inhibiting tau seeding and disaggregating fibrils, reduces tau pathology while preserving behavioral function, proteasome capacity, and synaptic integrity in tauopathy mouse model. |
| PC-27132 |
UR214-7
Septin inhibitor
|
UR214-7 is a forchlorfenuron (FCF) analog and inhibitor of septin oligomeric assembly via preventing incorporation of SEPT2/7/9, into canonical hetero-octamers, decreases viability and proliferation in both ovarian and endometrial cancer cell lines, selectively suppress HER2 expression. |
| PC-27131 |
UR214-9
Septin inhibitor
|
UR214-9 is a forchlorfenuron (FCF) analog and inhibitor of septin oligomeric assembly via preventing incorporation of SEPT2/7/9, into canonical hetero-octamers, decreases viability and proliferation in both ovarian and endometrial cancer cell lines, selectively suppress HER2 expression. |
| PC-27105 |
A2ti-1
S100A10-ANXA2 inhibitor
|
A2ti-1 (S100A10-ANXA2 heterotetramer inhibitor-1) is a specific small molecule Annexin A2 (ANXA2) inhibitor, inhibits Annexin A2-S100A10 protein interaction with IC50 of 24 uM (Annexin A2/S100A10 heterotetramer (A2t)). |
| PC-27102 |
TRMT10C agonist TM3
TRMT10C agonist
|
TRMT10C agonist TM3 is a small molecule agonist of tRNA methyltransferase 10C (TRMT10C), exhibits direct binding with a dissociation constant (Kd) of 2.6 uM in SPR assays, promotes osteoblast differentiation and protects against osteoporosis. |
| PC-27087 |
S428-1145
PUS7 inhibitor
|
S428-1145 is a small molecule inhibitor targeting pseudouridine synthase 7 (PUS7), has anti-proliferative IC50 of 20 µM in MIA PaCa-2 cells and 20.68 µM in PANC-1 cells, respectively, significantly inhibits tumour growth. |
