Company Name: |
ChemCell Biomedicine Co.,Ltd.
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Tel: |
020-13556033878 2965585218 13556033878 |
Email: |
chemcell@hotmail.com |
Products Intro: |
Product Name:AZD4604 CAS:2241039-81-4 Purity:98% Package:5mg;10mg;20mg;50mg;100mg;250mg;500mg;1g;5g;10g;25g;100g
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JAK1-IN-7 manufacturers
- Londamocitinib
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- $189.00 / 1mg
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2025-07-29
- CAS:2241039-81-4
- Min. Order:
- Purity: 99.56%
- Supply Ability: 10g
- Londamocitinib
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- $189.00 / 1mg
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2025-07-14
- CAS:2241039-81-4
- Min. Order:
- Purity: 99.56%
- Supply Ability: 10g
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| JAK1-IN-7 Basic information |
Product Name: | JAK1-IN-7 | Synonyms: | JAK1-IN-7;AZD4604;JAK1IN7,JAK-1-IN-7,JAK1 IN 7;1-Piperazineacetamide, N-[3-[5-fluoro-2-[[2-fluoro-3-(methylsulfonyl)phenyl]amino]-4-pyrimidinyl]-1H-indol-7-yl]-α-(methoxymethyl)-4-methyl-, (αR)-;AZD4604,
JAK1-IN-7;Londamocitinib/AZD4604/JAK1-IN-7;Londamocitinib;(R)-N-(3-(5-Fluoro-2-((2-fluoro-3-(methylsulfonyl)phenyl)amino)pyrimidin-4-yl)-1H-indol-7-yl)-3-methoxy-2-(4-methylpiperazin-1-yl)propanamide | CAS: | 2241039-81-4 | MF: | C28H31F2N7O4S | MW: | 599.66 | EINECS: | | Product Categories: | | Mol File: | 2241039-81-4.mol |  |
| JAK1-IN-7 Chemical Properties |
density | 1.411±0.06 g/cm3(Predicted) | storage temp. | Store at -20°C | solubility | Soluble in DMSO | form | Solid | pka | 13.90±0.30(Predicted) | color | White to off-white |
| JAK1-IN-7 Usage And Synthesis |
Uses | Londamocitinib (AZD4604) is a potent and selective JAK1 inhibitor with IC50 at 0.54 nM. Londamocitinib has anti-inflammatory activity[1][2][3]. | in vivo | Londamocitinib (1 mg/kg, intravenous injection, single dose) can reduce the phosphorylation of STAT3 and STAT5 in the lung of obumin-induced asthmatic rats, inhibit pulmonary eosinophilia, and reduce advanced asthma response in the same model[3].
Animal Model: | OVA-Induced Rat Model of Asthma[3] | Dosage: | 1 mg/kg | Administration: | i.v. | Result: | Reduced the proportion of phosphorylated STAT3-positive cell nuclei. |
| IC 50 | JAK1: 0.54 nM (IC50) | References | [1] NILSSON, Karl, Magnus, et al. Jak1 selective inhibitors. WO2018134213A1. [2] Nilsson M, et al. Discovery of the Potent and Selective Inhaled Janus Kinase 1 Inhibitor AZD4604 and Its Preclinical Characterization. J Med Chem. 2023 Oct 12;66(19):13400-13415. DOI:10.1021/acs.jmedchem.3c00554 [3] Nilsson M, et al. Characterization of Selective and Potent JAK1 Inhibitors Intended for the Inhaled Treatment of Asthma. Drug Des Devel Ther. 2022 Aug 31;16:2901-2917. DOI:10.2147/DDDT.S354291 |
| JAK1-IN-7 Preparation Products And Raw materials |
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