| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
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. |
Products are for research use only; We do not sell to patients
Copyright 2020 InvivoChem LLC | All Rights Reserved
