MSC2360844

MSC2360844 Suppliers list
Company Name: WUHAN SUN-SHINE BIO-TECHNOLOGY Co., Ltd.  
Tel: 17702719238
Email: sales@sun-shinechem.com
Company Name: BOC Sciences  
Tel: 1-631-485-4226; 16314854226
Email: info@bocsci.com
Company Name: ShangHai Caerulum Pharma Discovery Co., Ltd.  
Tel: 18149758185 18149758185
Email: sales-cpd@caerulumpharma.com
Company Name: Sichuan Wei Keqi Biological Technology Co., Ltd.  
Tel: 028-81700200 18116577057
Email: 3003855609@qq.com
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 15026964105
Email: 2881489226@qq.com

MSC2360844 manufacturers

  • MSC2360844
  • MSC2360844 pictures
  • $48.00
  • 2026-07-27
  • CAS:1305267-37-1
  • Purity: 99.54%
  • Supply Ability: 10g
  • MSC2360844
  • MSC2360844 pictures
  • $48.00
  • 2026-07-27
  • CAS:1305267-37-1
  • Purity: 99.54%
  • Supply Ability: 10g
MSC2360844 Basic information
Product Name:MSC2360844
Synonyms:MSC2360844;Phosphoinositide 3-kinase,MSC 2360844,MSC2360844,cells,SLE-prone,primary,Inhibitor,functions,inhibit,PI3K,proliferation,MSC-2360844;Methanone, [6-fluoro-1,4-dihydro-1-[4-(4-morpholinylmethyl)phenyl]-5,5-dioxido[1]benzothiopyrano[4,3-c]pyrazol-3-yl]-4-morpholinyl-;(6-fluoro-1-(4-(morpholinomethyl)phenyl)-5,5-dioxido-1,4-dihydrothiochromeno[4,3-c]pyrazol-3-yl)(morpholino)methanone;MSC2360844(IOA-244 /roginolisib);MSC2360844, 10 mM in DMSO;IOA 244;IOA244
CAS:1305267-37-1
MF:C26H27FN4O5S
MW:526.58
EINECS:
Product Categories:
Mol File:1305267-37-1.mol
MSC2360844 Structure
MSC2360844 Chemical Properties
Boiling point 779.8±60.0 °C(Predicted)
density 1.50±0.1 g/cm3(Predicted)
pka6.05±0.10(Predicted)
form Solid
color White to off-white
Safety Information
MSDS Information
MSC2360844 Usage And Synthesis
UsesRoginolisib (MSC2360844; IOA-244) is a potent, orally active and selective PI3Kδ inhibitor, with an IC50 of 145 nM. Roginolisib shows highly selective against a panel of 278 additional kinases[1].
in vivo

Roginolisib (6.6-66 mg/kg; daily from week 2 to 10) ameliorates disease manifestations in a murine SLE model[1].

Animal Model:NZB/W F1 female mice[1]
Dosage:6.6, 22, or 66mg/kg
Administration:Oral; starting at week 2 post ADV-IFNα delivery, once daily at 10weeks
Result:Significantly reduced proteinuria incidence and severity in a dose-dependent manner.
IC 50PI3Kδ: 145 nM (IC50); PI3Kα: 18500 nM (IC50); PI3Kβ: 2850 nM (IC50)
References[1] Haselmayer P, et al. Characterization of Novel PI3Kδ Inhibitors as Potential Therapeutics for SLE and Lupus Nephritis in Pre-Clinical Studies. Front Immunol. 2014 May 22;5:233. DOI:10.3389/fimmu.2014.00233
MSC2360844 Preparation Products And Raw materials
Tag:MSC2360844(1305267-37-1) Related Product Information
PI-3065 LY 294002 Hydrochloride N-(2,3-Dihydro-7,8-dimethoxyimidazo[1,2-c]quinazolin-5-yl)-3-pyridinecarboxamide PI3-Kinase α Inhibitor 2 PI-103 NVP-BEZ 235