brepocitinib

brepocitinib Struktur
1883299-62-4
CAS-Nr.
1883299-62-4
Englisch Name:
brepocitinib
Synonyma:
PF841;PF 841;PF-841;CS-2861;PF6700841;PF 6700841;PF-6700841;PF-06700841-00;PF-06700841 tosylate;Brepocitinib (PF-06700841)
CBNumber:
CB94674167
Summenformel:
C18H21F2N7O
Molgewicht:
389.4
MOL-Datei:
1883299-62-4.mol

brepocitinib Eigenschaften

Siedepunkt:
637.1±65.0 °C(Predicted)
Dichte
1.63±0.1 g/cm3(Predicted)
storage temp. 
room temp
Löslichkeit
DMSO: 78 mg/mL (200.31 mM);Ethanol: 78 mg/mL (200.31 mM)
pka
7.28±0.10(Predicted)
Aggregatzustand
powder
Farbe
white to beige
Wasserlöslichkeit
Water: Insoluble
InChIKey
BUWBRTXGQRBBHG-RUXDESIVSA-N
SMILES
C([C@@H]1CC1(F)F)(N1C2CCC1CN(C1C=CN=C(NC3=CN(C)N=C3)N=1)C2)=O

Sicherheit

WGK Germany  WGK 3
Speicherklasse 11 - Combustible Solids

brepocitinib Chemische Eigenschaften,Einsatz,Produktion Methoden

Charakteristisch

Class: non-receptor tyrosine kinase
Treatment: immunological disorders
Other name: PF-06700841; Brepocitinib
Elimination half-life = 3.8–7.5 h
Protein binding = 39%

Verwenden

PF-06700841 tosylate salt has been used as an inhibitor of Janus kinase1 (JAK1) to study its therapeutic effect on the adjuvant induced arthritis (AIA) rat model. It has also been used as an inhibitor of interferon-α/β receptor alpha chain (IFNAR1) signaling adaptor tyrosine kinase (2TYK2) in mice.

Biochem/physiol Actions

PF-06700841 prevents IL-23 (interleukin 23) signaling through TYK2 (Tyrosine-protein kinase 2)/JAK1 (Janus kinase 1) inhibition.

Sicherheit(Safety)

Brepocitinib(PF-06700841) was generally effective and well tolerated in patients with moderate-to-severe plaque psoriasis.

Synthese

Brepocitinib(PF06700841) can be synthesized as follows : Add 4-((1R,5S)-3,8-diazabicyclo[3.2.1]octan-3-yl)-N-(1-methyl-1H-pyrazol-4-yl)pyrimidin-2-amine hydrochloride (700 mg), HATU (1.02 g, 2.61 mmol) and DIPEA (0.76 mL, 4.34 mmol) to a solution of (S)-2,2-difluorocyclopropane-1-carboxylic acid (318 mg) in DCM (20 mL); Stir the reaction at room temperature for 18 hours; Dilute the reaction with DCM and saturated aqueous ammonium chloride solution; Separate the organic layer; Wash the organic layer with ammonium chloride solution; Concentrate the organic layer in vacuo; Purify the residue using silica gel column chromatography eluting with 0-12% MeOH and 1% NH4OH in DCM; Dissolve the residue in DCM; Wash the residue with saturated aqueous ammonium chloride solution three times; Collect the organic layer; Concentrate the organic layer in vacuo; Dry the organic layer.

brepocitinib Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


brepocitinib Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 91)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795
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Jinan Carbotang Biotech Co.,Ltd.
+8615866703830
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contact@trustwe.com China 5742 58
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+8618530059196
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laboratory@coreychem.com China 30227 58
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+8615990591583 15990591583
CHINA 2029 58
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86-571-88216897,88216896 13588875226
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InvivoChem
+1-708-310-1919 +1-13798911105
sales@invivochem.cn United States 6391 58
HANGZHOU LEAP CHEM CO., LTD.
+86-571-87711850
market18@leapchem.com China 24597 58

  • PF-06700841 tosylate
  • ((S)-2,2-difluorocyclopropyl)(3-(2-((1-methyl-1H-pyrazol-4-yl)amino)pyrimidin-4-yl)-3,8-diazabicyclo[3.2.1]octan-8-yl)methanone
  • PF 6700841
  • PF-06700841; PF 06700841; PF06700841; PF-6700841; PF 6700841; PF6700841; PF-06700841 TOSYLATE SALT
  • PF6700841
  • PF-6700841
  • CS-2861
  • ((S)-2,2-difluorocyclopropyl)((1R,5S)-3-(2-((1-methyl-1H-pyrazol-4-yl)amino)pyrimidin-4-yl)-3,8-diazabicyclo[3.2.1]octan-8-yl)methanone
  • Methanone, [(1S)-2,2-difluorocyclopropyl][3-[2-[(1-methyl-1H-pyrazol-4-yl)amino]-4-pyrimidinyl]-3,8-diazabicyclo[3.2.1]oct-8-yl]-
  • Brepocitinib (PF-06700841)
  • inhibit,Janus kinase,PF06700841,JAK,Brepocitinib,Inhibitor,PF 06700841
  • PF 841
  • PF841
  • PF-841
  • Brepocitinib, 10 mM in DMSO
  • PF-06700841-00
  • PF-06700841 (Brepocitinib) free base
  • Brepocitinib (PF-06700841) ,S8804
  • (Brepocitinib)((S)-2,2-difluorocyclopropyl)((1R,5S)-3-(2-((1-methyl-1H-pyrazol-4-yl)amino)pyrimidin-4-yl)-3,8-diazabicyclo[3.2.1]octan-8-yl)methanone
  • 1883299-62-4
  • C18H21F2N7O
  • api
  • APIS
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