Cat. No. | Product name | CAS No. |
DCC1148 |
bsc4090
Fluorescent probe in vitro and in vivo aiming at a tau-based diagnosis of Alzheimer's disease |
1154426-01-3 |
DCC1149 |
bsc4704
Fluorescent probe, binding to neurofibrillary tangles with high contrast and selectivity over amyloid |
25470-94-4 |
DCC1150 |
Bsc4750
Fluorescent probe visualizing neurofibrillary tangles in Alzheimer's disease |
25850-25-3 |
DCC1151 |
Bsh-in-7
Novel potent covalent inhibitor of gut bacterial bile salt hydrolases (BSH) |
|
DCC1152 |
Bss-730a
Novel potent inhibitor of both HIV-1 and HIV-2 replication, being also active against the erythrocytic stages of P. falciparum |
|
DCC1153 |
Bta9881
Novel respiratory syncytial virus (RSV) fusion inhibitor |
1646857-24-0 |
DCC1154 |
btb02467
Novel cell-permeable modulator of cellular morphogenesis in yeast and mammalian cells; Inhibitor of SARS-CoV Mpro activity via intensive H-bond network and hydrophobic interactions |
217490-08-9 |
DCC1155 |
btb03156
Novel cell-permeable modulator of cellular morphogenesis in yeast and mammalian cells |
218287-44-6 |
DCC1156 |
btb03195
Novel activator of PC1/3 and inhibitor of PC2 |
218287-68-4 |
DCC1157 |
Btgh84 Activator I
Novel activator of BtGH84, the first experimentally discovered small molecule activator of a glycoside hydrolase |
16347-96-9 |
DCC1158 |
Bti-a-404
Novel selective and potent competitive inverse agonist of human GPR43 |
537679-57-5 |
DCC1159 |
Btk-in-27
Novel potent and selective covalent inhibitor of Bruton’s tyrosine kinase (BTK), targeting a noncatalytic cysteine residue (Cys481) for covalent bond formation |
|
DCC1160 |
Btk-in-3
Novel potent inhibitor of Bruton’s tyrosine kinase (BTK) |
|
DCC1161 |
B-tpmf
The first small-molecule inhibitor with significant selectivity among the KCa2 channel subtypes |
477865-65-9 |
DCC1162 |
Btt-3035
Novel inhibitor of alpha2beta1 integrin, decreasing average platelet adhesion in individuals with the C/T807T genotype but not in those harboring C807C |
|
DCC1163 |
Btx-yne
Novel unique Na V modulator, acting as a conspicuous outlier, eliminating fast but not slow inactivation |
|
DCC1164 |
Btz-n3
Novel effective reversible and noncovalent inhibitor of DprE1. |
1839081-05-8 |
DCC1165 |
Btzo-4
Negative control for BTZO-1 |
|
DCC1166 |
Bu99008
Ligand of the Imidazoline(2) binding site (I 2 BS), showing very good affinity for the I 2 BS (K i of 1.4 nM; K d = 1.3 nM), good selectivity compared with the α 2 -adrenoceptor (909-fold) |
108796-88-9 |
DCC1167 |
Bucinnazine
Potent and selective agonist of μ-opioid receptor (MOR) with relatively low affinity for the δ-opioid receptor and the κ-opioid receptor |
17719-89-0 |
DCC1168 |
Budralazine
Direct-acting vasodilator with anti-tachycardiac effect |
36798-79-5 |
DCC1169 |
Bulgecin A
Featured
Bulgecin A is an inhibitor of binuclear metallo-beta-lactamases and Lytic transglycosolase. |
92953-54-3 |