rs 1

RS1-PDK1 inhibitor (RS 1) is a selective inhibitor of the protein kinase PDK1 that can be used to treat and prevent disease or disorders.

RS-1 is a RAD51 activator. RS-1 also increases CRISPR/Cas9-mediated knock-in efficiencies.

Ginsenoside Rs1, extracted from the root of Panax ginseng [1], is a chemical compound with potential pharmacological properties.

Ginsenoside Rs1 (Standard) is a reference standard for research and analysis in studies involving Ginsenoside Rs1. Ginsenoside Rs1, extracted from the root of Panax ginseng [1], is a chemical compound with potential pharmacological properties.

(RS)-G12Di-1 is a selective covalent inhibitor of K-Ras-G12D.

PDK1-IN-RS2 inhibits the activation of the downstream kinases S6K1 by PDK1. PDK1-IN-RS2 is a mimic of the peptide docking motif (PIFtide) and is a substrate-selective PDK1 inhibitor (Kd: 9 μM).

(1RS,2RS,5R)-Menthol-1,2,6,6-d4 is a deuterated compound of (1RS,2RS,5R)-Menthol. (1RS,2RS,5R)-Menthol has a CAS number of 1369536-10-6.

2-(1,1-Dimethylethyl)-1,2,3,4-tetrahydro-4,6,8-Isoquinolinetriol hemisulfate hydrate is an impurity of Terbutaline.

MRS 1754 is a selective antagonist radioligand for the A2B adenosine receptor, exhibiting very low affinity for A1 and A3 receptors in both humans and rats.

RS 17053 hydrochloride is a potent and selective antagonist of the α1A adrenoceptor, with a pKi value of 9.1 in native cell membranes and a pA2 value of 9.8 in functional assays.

RS 15385-198 is a less active isomer of Delequamine. Delequamine is a selective alpha2-adrenergic receptor antagonist.

MRS 1523 can exert an antihyperalgesic effect through N-type Ca channel block and action potential inhibition in isolated rat dorsal root ganglion (DRG) neurons. MRS 1523 is an effective and selective adenosine A3 receptor antagonist Ki: 18.9 nM and 113 n

antagonist for the human adenosine A3 receptor

RS 12254 is a dopamine agonist and antihypertensive agent.

RS 14203 is a selective type 4 phosphodiesterase (PDE4) inhibitor.

RS 15378 is a gonadorelin antagonist.

RS 15385-197 is a selective alpha 2-adrenoceptor antagonist.

RS 18286 is a LHRH antagonist.

RS 100329 HCl is a selective α1A-adrenoceptor antagonist (pKi = 9.6 for human cloned α1A receptors).

RS 100235 is a 5-HT4 Serotonin Receptor.

RS 116 0086 is a bioactive chemical.

RS 1893 is an orally active cardiotonic agent and its structure is different from that of cardiac glycosides and beta-stimulants.

NLRP3 modulators 1 (WO2017184746A1, compound 107) is a potent modulator of NLRP3, capable of agonizing or partially agonizing the activity of NLRP3. This compound proves valuable in investigating conditions, diseases, or disorders where a reduction in LRP3 activity plays a role in the pathology.

Protein Kinase Inhibitors 1 Hydrochloride effectively inhibits HIPK2, demonstrating high potency with IC50 values of 136 nM for HIPK1 and 74 nM for HIPK2, alongside a dissociation constant (Kd) of 9.5 nM for HIPK2.