rs 1

RS-1 是一种 RAD51 的激活剂，同时可增强 CRISPR Cas9 的活性。

RS1-PDK1 inhibitor (RS 1) 是一种选择性的蛋白激酶PDK1抑制剂，可用来治疗和预防疾病或失调。

Ginsenoside Rs1为人参根中提取的一种人参皂苷类化合物。

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 是 (1RS,2RS,5R)-Menthol 的氘代化合物。(1RS,2RS,5R)-Menthol 的 CAS 号为 1369536-10-6。

RS 15385-198 是 Delequamine 的低活性异构体。Delequamine 是一种选择性 α2-肾上腺素受体拮抗剂。

MRS 1754 是A2B 腺苷受体选择性拮抗剂，对人和大鼠的 A1和 A3受体的亲和力非常低。

RS 17053 hydrochloride 是有效的、选择性的 α1A 肾上腺素受体 (α1A adrenoceptor) 拮抗剂。RS 17053 hydrochloride 在细胞膜中测得的 pKi 值为 9.1，功能分析的 pA2 值为 9.8。

RS 15378 is a gonadorelin antagonist.

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

Protein kinase inhibitors 1 hydrochlorid (Protein kinase inhibitors 1 hydrochlorid (1365986-44-2(free base))) 是一种新型 HIPK2 抑制剂，IC50 为 74 nM，Kd 为 9.5 nM。

antagonist for the human adenosine A3 receptor

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.

ligand for the (R)-zacopride binding site

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.

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

Protein kinase inhibitors 1 是新型的 HIPK2 抑制剂，其 IC50=74 nM，Kd=9.5 nM。

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

RS 100329 hydrochloride 是α1A 肾上腺素能受体的拮抗剂。

RS 12254 is a dopamine agonist and antihypertensive agent.

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

RS 100235 is a 5-HT4 Serotonin Receptor.

RS 116 0086 is a bioactive chemical.

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