SR-717

SR-717 Suppliers list
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: Product Name:SR-717
CAS:2375421-09-1
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: InvivoChem
Tel: +1-708-310-1919 +1-13798911105
Email: sales@invivochem.cn
Products Intro: Product Name:SR-717 lithium
CAS:2375421-09-1
Purity:98% Package:5mg Remarks:V2205
Company Name: LEAP CHEM CO., LTD.
Tel: +86-852-30606658
Email: market18@leapchem.com
Products Intro: Product Name:SR-717
CAS:2375421-09-1
Package:1g; 5g; 25g; 1kg; 5kg; 25kg
Company Name: Nantong HI-FUTURE Biology Co., Ltd.
Tel: +undefined18051384581
Email: sales@chemhifuture.com
Products Intro: Product Name:SR-717
CAS:2375421-09-1
Purity:98%+ HPLC Package:100mg,500mg,1g,5g,10g
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354
Email: support@targetmol.com
Products Intro: Product Name:SR-717
CAS:2375421-09-1
Package:1 mL * 10mM (in DMSO);10 mg;100 mg;2 mg;25 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
SR-717 Basic information
Product Name:SR-717
Synonyms:SR-717;SR171;SR-717 lithium;SR 717 (lithium salt);immunity,MPYS,MITA,inhibit,ISG-THP1,Inhibitor,SR 717,mimetic,TMEM173,STING,SR717,cGAMP,THP1,antitumor,ERIS,SR-717,PD-L1,Stimulator of Interferon Genes;Lithium 2-(6-(1H-imidazol-1-yl)pyridazine-3-carboxamido)-4,5-difluorobenzoate;SR171&SR-717 lithium
CAS:2375421-09-1
MF:C15H10F2LiN5O3
MW:353.21
EINECS:
Product Categories:
Mol File:2375421-09-1.mol
SR-717 Structure
SR-717 Chemical Properties
storage temp. Inert atmosphere,Room Temperature
solubility Soluble in DMSO (>25 mg/ml)
form solid
color Off-white
Water Solubility Water: < 0.1 mg/mL (insoluble)
Stability:Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 1 month1.
Safety Information
MSDS Information
SR-717 Usage And Synthesis
DescriptionSR-717 (2375421-09-1) is a cell permeable and exceptionally selective STING agonist (IC50 = 7.8 μM).? It displayed robust antitumor activity in B16.F10 melanoma and MC38 colorectal adenocarcinoma mouse models. SR-717 promoted the activation of CD8+ T, natural killer, and dendritic cells as well as promoting antigen cross-priming. It was able to induce PD-L1 expression in THP1 cells and in primary human PBMC’s.
ReferencesChin et al. (2020), Antitumor activity of a systemic STING-activating non-nucleotide cGAMP mimetic; Science 369 993
SR-717 Preparation Products And Raw materials
Tag:SR-717(2375421-09-1) Related Product Information
2-Chloro-N-(6-methoxy-4-quinolinyl)-5-nitrobenzamide 4-Quinolinecarboxamide, N-[3-[[[2-[4-(aminosulfonyl)phenyl]ethyl]amino]carbonyl]phenyl]-1,2-dihydro-2-oxo- NA SRT3025 SR9009 SR8278 SR19881 SR-9243 SRPK inhibitor SR 1078 N-[2-[3-(1-Piperazinylmethyl)imidazo[2,1-b]thiazol-6-yl]phenyl]-2-quinoxalinecarboxamide SRI 31215 SR 0987 SR27897 SR17018 N-((4,5-difluoro-1H-benzo[d]imidazol-2-yl)methyl)-9-(3-fluorophenyl)-2-morpholino-9H-purin-6-amine SR-4835 SR18662