pnu-282987 s enantiomer

PNU-282987 S enantiomer free base 是 PNU-282987 的 S 型对映体，是 α7 烟碱乙酰胆碱受体的激动剂。

(S)-PNU-282987 is the absolute stereochemistry form of PNU-282987. PNU 282987, a potent agonist of α7-containing neuronal nicotinic acetylcholine receptors (nAChRs) with Ki of 26 nM for the rat receptor, has negligible activity against α1β1γδ and α3β4 nAC

Cipropride S enantiomer 是止吐药环普必利的S 对映体。

GSK2850163 (S enantiomer) 是 GSK2850163 的无活性对映体。GSK2850163 是一种新型的肌醇需求酶-1α (IRE1a) 抑制剂。

PNU 282987 是一种选择性 α7 烟碱型乙酰胆碱受体 (α7 nAChR) 激动剂，Ki 为 26 nM。

Tipifarnib S enantiomer ((S)-(-)-R-115777) 是Tipifarnib 的 S 型对映体，它比 Tipifarnib 特性低。其中 Tipifarnib 是farnesyltransferase 高效特异性抑制剂，IC50=0.6 nM。

MK-7246 S enantiomer is a potent and selective CRTH2 antagonist.

LY 344864 S-enantiomer, the S-enantiomer of LY344864, serves as a 5-HT1F receptor agonist.

Firsocostat S enantiomer is the less active S enantiomer of Firsocostat.

Necrostatin 2 S enantiomer is the S enantiomer of Necrostatin 2

Elacestrant S enantiomer is a selective and orally available estrogen receptor (ERR) degrader with IC50 values of 48 and 870 nM for ERα and ERβ, respectively.

Veledimex S enantiomer is the S enantiomer of veledimex. Veledimex is an oral activator ligand for a proprietary gene therapy promoter system and CYP3A4 5 inhibitor.

Gepotidacin S enantiomer is the S enantiomer of gepotidacin.

BET-BAY 002 S enantiomer为BET-BAY 002的S型对映异构体，属于BET小分子抑制剂。

GDC-0834, the S-enantiomer, is a potent and selective inhibitor of Bruton's tyrosine kinase (BTK).

Firsocostat S enantiomer (ND-630 S enantiomer) 是 Firsocostat 的低活性的 S 型异构体。Firsocostat 是乙酰辅酶 A 羧化酶抑制剂。

Nazartinib is an EGFR inhibitor. Nazartinib S-enantiomer is the less active S-enantiomer of Nazartinib.

Atuveciclib S-Enantiomer (BAY-1143572 S-Enantiomer) 是 BAY-1143572的 S-对映异构体 ，是一种有效的选择性 CDK9抑制剂，抑制 CDK9 CycT1，IC50为 16 nM。

Elacestrant (RAD1901) dihydrochloride is a selective and orally available estrogen receptor (ERR) degrader with IC50 values of 48 and 870 nM for ERα and ERβ, respectively. Elacestrant S enantiomer dihydrochloride is an low activity enantiomer of elacestrant dihydrochloride.

PNU-282987 free base 是一种具有选择性和高效性的 α7 烟碱乙酰胆碱受体 (nAChR) 激动剂 ， 也是5-HT3受体的拮抗剂，具有抗炎活性，对脓毒症诱导的小鼠急性肺损伤有保护作用，可减弱 ILC2s 活化和链格孢菌诱导的气道炎症。PNU-282987 free base 可用于研究神经系统疾病。

Fulvestrant S enantiomer is the less active S enantiomer of Fulvestrant. Fulvestrant is a potent estrogen receptor antagonist with an IC50 of 9.4 nM.

AMG 487 S-enantiomer is the S enantiomer of AMG 487. AMG 487 is an CXCR3 antagonist.

Selisistat S-enantiomer (EX-527 S-enantiomer) 是一种选择性的SIRT1抑制剂，IC50值为 98 nM。

IACS-8968 S-enantiomer is the S-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).

Ruxolitinib S enantiomer (INCB18424) 是 Ruxolitinib 的 S 型对映体，是一种JAK 抑制剂。