a 22 hydrochloride

MreB Perturbing Compound A22 hydrochloride is an effective inhibitor of MreB, a bacterial actin-like protein. It disrupts cell wall assembly and causes morphological changes, used for bacterial morphogenesis and antibiotic research.

GW-311616 hydrochloride is a long duration, orally bioavailable, and selective human neutrophil elastase (HNE) inhibitor (IC50: 22 nM; Ki: 0.31 nM).

Regorafenib Hydrochloride (BAY73-4506 hydrochloride) is a new oral multikinase inhibitor of angiogenic, stromal and oncogenic receptor tyrosine kinases with potent preclinical antitumor activity

1H-imidazol-2-ylmethanol hydrochloride ,with CAS No. 116177-22-1, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 1H-imidazol-2-ylmethanol hydrochloride provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

2,3,4,5-Tetrahydro-1H-2-benzazepine Hydrochloride, with CAS No. 7216-22-0, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 2,3,4,5-Tetrahydro-1H-2-benzazepine Hydrochloride provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

Ilginatinib hydrochloride (NS-018 hydrochloride) is a highly active, orally bioavailable JAK2 inhibitor.

Aramisulpride (hydrochloride) is a 5-HT7 receptor antagonist with a Ki value of 22 nM. It also acts as a D2/D3 receptor antagonist, exhibiting a Ki value of 140 nM for D2 receptors and 13.9 nM for D3 receptors. This compound is utilized in the study of psychiatric disorders.

PKI-179 hydrochloride is a potent and orally available dual PI3K/mTOR inhibitor. Its IC₅₀ values against PI3K-α, PI3K-β, PI3K-γ, PI3K-δ and mTOR are 8 nM, 24 nM, 74 nM, 77 nM and 0.42 nM respectively. It also exerts inhibitory activity against E545K and H1047R mutants with IC₅₀ values of 14 nM and 11 nM, and exhibits significant antitumor effects in in vivo models.

CCR4 antagonist 3 hydrochloride is an orally active, potent and selective CCR4 antagonist. CCR4 antagonist 3, featuring a novel piperidinyl-azetidine motif, has IC 50 s of 22 nM and 50 nM in the calcium flux and CTX assay. CCR4 antagonist 3 has antitumor activity.

Liproxstatin-1 hydrochloride is a high-potency ferroptosis inhibitor capable of effectively preventing ferroptotic cell death, with an IC50 value of 22 nM [1].

Pacritinib hydrochloride is a potent inhibitor of wild-type JAK2 (IC50: 23 nM) and the JAK2V617F mutant (IC50: 19 nM), and can be used in the study of acute myeloid leukaemia (AML) and myelofibrosis (MF).

Methyl-D3-amine hydrochloride is a useful organic compound for research related to life sciences. The catalog number is T64497 and the CAS number is 7436-22-8.

(S)-tert-Butyl 2-amino-6-(((benzyloxy)carbonyl)amino)hexanoate hydrochloride is a useful organic compound for research related to life sciences. The catalog number is T65633 and the CAS number is 5978-22-3.

(R)-2-((4-Aminophenethyl)amino)-1-phenylethanol hydrochloride is a useful organic compound for research related to life sciences. The catalog number is T66549 and the CAS number is 521284-22-0.

4-Perhydroazepinone hydrochloride is a useful organic compound for research related to life sciences. The catalog number is T66790 and the CAS number is 50492-22-3.

1-Naphthyl PP1 hydrochloride (1-NA-PP 1 hydrochloride) is a selective inhibitor of Src family kinases v-Src.

EST64454 hydrochloride (EST64454) is a highly soluble σ1 receptor antagonist (Ki : 22 nM),has the potential for Pain Management.

Propafenone-D5 hydrochloride is a deuterated compound of Propafenone Hydrochloride (T6955). Propafenone hydrochloride has a CAS number of 34183-22-7. Propafenone hydrochloride is a classic anti-arrhythmic medication, which treats illnesses associated with rapid heartbeats such as atrial and ventricular arrhythmias.