| R21122085 |
CCT077791 |
CCT077791 is a p300 and PCAF histone acetyltransferase activity inhibitor.
|
| R21122086 |
BMS-195614 |
BMS 195614 is a neutral RAR α-selective antagonist (Ki = 2.5 nM) and exhibits no
|
| R21122087 |
A-196 |
A-196 is a potent and selective inhibitor of SUV420H1 and SUV420H2 with IC50 val
|
| R21122088 |
DDD85646 Hydrochloride |
DDD 85646 is a potent and specific double NMT1/NMT2 inhibitor with IC50 of 17 nM
|
| R21122089 |
UNC-4219 TFA |
UNC4219 is a negative control compound for UNC3866, a potent antagonist of the m
|
| R21122090 |
SB674042 |
SB-674042 is a potent and selective non-peptide orexin OX1 receptor antagonist (
|
| R21122091 |
BRD4884 |
BRD4884 is a selective inhibitor of HDAC2 that acts by enhancing the learning an
|
| R21122092 |
GSK2193874 |
GSK2193874 is an orally active, potent, and selective TRPV4 antagonist with IC50
|
| R21122093 |
PF-794 |
Pf-06279794, also known as PF-794, is a potent, selective and ATP-competitive TN
|
| R21122094 |
MRT68921 |
MRT68921 is a potent inhibitor of ULK1 and ULK2, with IC50 values of 2.9 nM and
|
| R21122095 |
Diethyl-pythiDC |
Diethyl-pythiDC is an inhibitor of collagen prolyl 4-hydroxylases (CP4Hs).
|
| R21122096 |
UNC4219 |
|
| R21122097 |
GSK1059865 |
GSK1059865 is a potent orexin 1 receptor antagonist.
|
| R21122098 |
MS-444 |
MS-444 inhibits the activity of purified smooth muscle myosin light chain kinase
|
| R21122099 |
SR 11302 |
SR 11302 is an activator protein-1 (AP-1) transcription factor inhibitor. SR 113
|
| R21122100 |
NAI-N3 |
NAI-N3 is a RNA acylation reagent that enables RNA purification. NAI-N3 is a dua
|
| R21122101 |
NVS-CECR2-1 |
NVS-CECR2-1, a non-BET family Bromodomain (BRD) inhibitor, is a potent and selec
|
| R21122102 |
AM6545 |
CB1 selective neutral antagonist
|
| R21122103 |
NBD-Pen |
Nbd-pen high sensitivity, specific lipid free radical fluorescent probe. NBD-Pe
|
| R21122104 |
APS-2-79 |
APS-2-79 hydrochloride is a KSR-dependent MEK antagonist. APS-2-79 inhibits ATPb
|
| R21122105 |
CS-2100 |
S1P1 agonist
|
| R21122106 |
DL5H3 |
DL5H3 is a biochemical.
|
| R21122107 |
CVT-11127 |
CVT-11127 is an StearoylCoA Desaturase-1 (SCD1) inhibitor.
|
| R21122108 |
TM2-115 |
Inhibition of histone methyltransferase biX-01294 derivatives of malaria parasit
|
| R21122109 |
HyT36 |
Hydrophobic inducers degrade stable proteins and HaloTag2 fusion proteins
|