|
V56743
|
RIG012
|
2642218-43-5 |
RIG012 is a potent RIG-I inhibitor (antagonist) with IC50 of 0.71 μM when measured using NADH-coupled ATPase. |
|
V56813
|
Ritlecitinib tosylate
|
2192215-81-7 |
Ritlecitinib, also known as PF-06651600, is a potent and specific JAK3 inhibitor. |
|
V56804
|
Ro60-0175 free base
|
169675-08-5 |
Ro60-0175 is a potent and specific SR-2 agonist. |
|
V56659
|
ROS-IN-1
|
298193-11-0 |
ROS-IN-1 is a mitochondrial ROS inhibitor. |
|
V56719
|
RS 100329 HCl
|
215654-26-4 |
RS 100329 is a subtype-selective α1A-adrenergic receptor antagonist (pKi = 9.6 for human cloned α1A receptor). |
|
V56788
|
RTC13
|
313530-30-2 |
RTC13, also known as WAY301503, is a premature stop codon (PTC) readthrough inducer that restores dystrophin expression and improves muscle function in the mdx mouse model of Duchenne muscular dystrophy. |
|
V56710
|
RWJ-54428
|
189448-35-9 |
RWJ-54428 is a novel cephalosporin effective against Gram-positive (Gram+) bacteria such as methicillin-resistant Staphylococcus aureus (MRSA). |
|
V56726
|
S-(3-Carboxypropyl)-L-cysteine
|
30845-11-5 |
S-(3-Carboxypropyl)-L-cysteine is the thioether analogue of L-cysteine. |
|
V56718
|
S1R agonist 2
|
150085-21-5 |
S1R agonist 2 (Compound 8b) is a selective S1R agonist with Ki of 1.1 nM and 88 nM for S1R and S2R, respectively. |
|
V56806
|
sEH inhibitor-14
|
2890221-26-6 |
sEH inhibitor-14 (compound 33) is a benzoxazolone-5-urea analog. |
|
V56754
|
SEP-0371845
|
1516896-06-2 |
SEP-0371845 is a biochemical drug |
|
V56692
|
Sevelamer carbonate
|
845273-93-0 |
Sevelamer carbonate is a phosphate-conjugated polymeric amine used to treat hyperphosphatemia in patients with renal disease. |
|
V56760
|
SJ6986
|
2765625-93-0 |
SJ6986 is a potent, selective, orally bioavailable GSPT1/2 degrader with DC50 of 2.1 nM (Dmax 99%) for GSPT1. |
|
V56753
|
SKF-38393 HBr
|
20012-10-6 |
SKF-38393, also known as (+/-)-SKF-38393, is a synthetic compound of the benzazepine chemical class that works as a selective D1/D5 receptor partial agonist. |
|
V56770
|
SKF89976A HCl
|
85375-85-5 |
SKF89976A is a potent GABA uptake inhibitor selective for GAT-1 (IC50s for hGAT-1, rGAT-2, hGAT-3, and hBGT-1 are 0.13, 550, 944, and 7210 μM, respectively). |
|
V56811
|
Skp2 inhibitor 1
|
2760612-63-1 |
Skp2 inhibitor 1(compound 14i) is a Skp2 inhibitor that interferes with the Skp2-Cks1 interaction with IC50 of 2.8 μM. |
|
V56698
|
SLU-PP-332
|
303760-60-3 |
SLU-PP-332 is an ERR pan-agonist/activator with the highest affinity for ERRα and has been shown to cause increases in mitochondrial function and cellular respiration in specific skeletal muscle cell lines. |
|
V56694
|
sMpa
|
1821155-77-4 |
seMpai is a novel AkaLumine analogue as a near-infrared emitting fluorescein with enhanced water solubility. |
|
V56776
|
SNIPER(CRABP)-11
|
1384275-50-6 |
SNIPER(CRABP)-11, also known as PROTAC cIAP1 degrader-4, is a potent protein degrader. |
|
V56611
|
SOD1-Derlin-1 inhibitor 56-59
|
2170170-27-9 |
SOD1-Derlin-1 inhibitor-2 (compound 56-59) is an inhibitor (blocker/antagonist) of SOD1-Derlin-1 interaction. |