| RH131569 |
Z-VEID-FMK |
Z-VEID-FMK (Z-VE(OMe)ID(OMe)-FMK) is a selective and irreversible caspase-6
|
| RH131570 |
CA-074(OH) |
CA-074 is a potent inhibitor of cathepsin B with a Ki of 2 to 5 nM.
|
| RH131571 |
PD-1-IN-17 |
PD-1-IN-17 is a programmed cell death-1 (PD-1) inhibitor extracted from patent W
|
| RH131572 |
Z-FG-NHO-BzOMe |
Z-FG-NHO-BzOME is a cysteine protease inhibitor that selectively inhibits cathep
|
| RH131573 |
PSB-1115 |
PSB-1115 is a selective A2B Adenosine Receptor antagonist. PSB-1115 inhibits the
|
| RH131574 |
VK-2019 |
VK-2019 is an oral active, selective EBNA1((Epstein-Barr Nuclear Antigen 1) inhi
|
| RH131575 |
BSJ-03-204 |
BSJ-03-204 is a PROTAC connected by ligands for Cereblon and CDK. BSJ-03-204 is
|
| RH131576 |
SRX3177 |
SRX3177 is a triple inhibitor of CDK4/6, PI3K, and BRD4, with IC50s of 33 nM (BR
|
| RH131578 |
PE154 |
PE154 (Compound 13) is a potent fluorescent inhibitor of human acetylcholinester
|
| RH131579 |
IT1t dihydrochloride |
IT1t dihydrochloride is a potent CXCR4 antagonist; inhibits CXCL12/CXCR4 interac
|
| RH131580 |
Lobeglitazone sulfate |
Lobeglitazone sulfate is a new type of thiazolidinedione. Lobeglitazone sulfate
|
| RH131581 |
NecroX-7 |
NecroX-7 is a potent free radical scavenger and a HMGB1 (high-mobility group box
|
| RH131582 |
EGFR-IN-99 |
EGFR-IN-99 (compound 1a) is a potent EGFR and HER2 Exon 20 insertion mutant inhi
|
| RH131583 |
UNC8153 TFA |
UNC8153 TFA is a potent and selective nuclear receptor-binding SET domain-contai
|
| RH131586 |
Ansornitinib(ANG-3070) |
Ansornitinib is an orally active dual kinase inhibitor that inhibits platelet-de
|
| RH131587 |
DPBQ |
DPBQ (ZINC1620467) is a p53 activator. DPBQ could activate p53 and trigger apopt
|
| R11111890 |
CL 316243 |
CL316243 is a highly potent selective agonist of β3-adrenoceptor, with a EC50 of
|
| RH131589 |
Sisunatovir(RV521) |
Sisunatovir (RV521), an orally available inhibitor of the RSV protein, exhibits
|
| RH131590 |
Sirpiglenastat (DRP-104) |
Sirpiglenastat (DRP-104) is a glutamine antagonist, a prodrug of DON, with antit
|
| RH131591 |
glucosamine |
Glucosamine (D-Glucosamine) is an amino sugar and a prominent precursor in the b
|
| RH131592 |
3-[[(1S)-1,3-dicarboxypropyl]carbamoyl]-3-hydroxy-pentanedioic acid |
β-Citryl-L-glutamic acid (β-Citrylglutamic acid) is a citrylglutamic acid, that
|
| Bucindolol |
Bucindolol |
Bucindolol is a β1-adrenergic receptor blocker, with intrinsic sympathomimetic a
|
| RH131594 |
CP-320626 |
CP320626 is a potent inhibitor of human liver glycogen phosphorylase (IC50=205 n
|
| RH131598 |
Cholanic acid |
5β-Cholanic acid can be used for 5β-Cholanic acid derivatives synthesis.
|
| RH131595 |
Propiomazine |
Propiomazine is an orally active antihistamine agent with sedative effects. Prop
|