Ruxolitinib

Ruxolitinib Struktur
941678-49-5
CAS-Nr.
941678-49-5
Englisch Name:
Ruxolitinib
Synonyma:
Jakafi;Roxolitinib;(R)-3-(4-(7H-Pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl)-3-cyclopentylpropanenitrile;(R)-Ruxolitinib;CS-163;Pridazole;Rusotinib;Russolinib;Benzalolin;Ruxolitinib
CBNumber:
CB02499581
Summenformel:
C17H18N6
Molgewicht:
306.37
MOL-Datei:
941678-49-5.mol

Ruxolitinib Eigenschaften

Schmelzpunkt:
84-89°C
Dichte
1.40
storage temp. 
-20°
Löslichkeit
Soluble in DMSO (up to 28 mg/ml) or in Ethanol (up to 15 mg/ml with warming).
Aggregatzustand
White powder.
pka
11.63±0.50(Predicted)
Farbe
White
Stabilität:
Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 3 months.
InChI
InChI=1/C17H18N6/c18-7-5-15(12-3-1-2-4-12)23-10-13(9-22-23)16-14-6-8-19-17(14)21-11-20-16/h6,8-12,15H,1-5H2,(H,19,20,21)/t15-/s3
InChIKey
HFNKQEVNSGCOJV-UJHUVDBMNA-N
SMILES
[C@@H](C1CCCC1)(N1N=CC(C2N=CN=C3NC=CC=23)=C1)CC#N |&1:0,r|
CAS Datenbank
941678-49-5
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
HS Code  29335990
Giftige Stoffe Daten 941678-49-5(Hazardous Substances Data)
Bildanzeige (GHS) GHS hazard pictogramsGHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitsschädlich bei Verschlucken. Akute Toxizität oral Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P270, P301+P312, P330, P501
Sicherheit
P202 Vor Gebrauch alle Sicherheitshinweise lesen und verstehen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.

Ruxolitinib Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

In November 2011, the U.S. FDA approved ruxolitinib (INCB018424) for the treatment of patients with intermediate or high-risk myelofibrosis. Ruxolitinib is an ATP-competitive inhibitor of JAK1 and JAK2 (IC50's of 3.3±1.2 nM and 2.8±1.2 nM, respectively) and inhibition occurs regardless of the JAK2V617F mutational status. Ruxolitinib is a moderately potent inhibitor of the related JAK, TYK2 (IC50=19±3.2 nM) but is selective versus JAK3 (IC50=428±243 nM). It was also selective versus a panel of 26 other kinases at concentrations approximately 100-fold the IC50 of JAK1 and JAK2. Inhibition of JAK1 and JAK2 downregulates the JAK-signal transducer and activator of transcription (STAT) pathway, inhibiting myeloproliferation, inducing apoptosis, and reducing numerous cytokine plasma levels.

Charakteristisch

Class: non-receptor tyrosine kinase
Treatment: MF, PV, cGVHD
Oral bioavailability >95%
Elimination half-life = 3 h
Protein binding = 97%

Verwenden

Ruxolitinib is a selective Janus tyrosine kinase (JAK1 and JAK2) inhibitor used in the treatment of myeloproliferative neoplasms and psoriasis.

Indications

The JAK family includes four isoforms, JAK1, JAK2, JAK3, and tyrosine kinase (TYK2). Ruxolitinib (Jakafi(R), Incyte Corp.) was the first approved JAK inhibitor, which inhibits both JAK1 and JAK2, used for the treatment of different types of myelofibrosis. Tofacitinib (Xeljanz(R), Pfizer) was approved by FDA as a JAK3-selective inhibitor for the treatment of rheumatoid arthritis and is one of the only two FDA-approved kinase inhibitors for non-oncological indications.

Definition

ChEBI: A pyrazole substituted at position 1 by a 2-cyano-1-cyclopentylethyl group and at position 3 by a pyrrolo[2,3-d]pyrimidin-4-yl group. Used as the phosphate salt for the treatment of patients with intermediate or high-risk myelofibrosis, includ ng primary myelofibrosis, post-polycythemia vera myelofibrosis and post-essential thrombocythemia myelofibrosis.

Ruxolitinib Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Ruxolitinib Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 395)Lieferanten
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Zhengzhou Anhuida Chemical Co., Ltd
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941678-49-5()Verwandte Suche:


  • (betaR)-beta-Cyclopentyl-4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazole-1-propanenitrile
  • (3R)-3-(4-(7H-pyrrolo[2,3-d]pyriMidin-4-yl)-1H-pyrazol-1-yl)-3-cyclopentylpropanenitrile
  • (3R)-3-cyclopentyl-3-(4-{7H-pyrrolo[2,3-d]pyriMidin-4-yl}-1H-pyrazol-1-yl)propanenitrile
  • INCB018424 (Ruxolitinib)
  • β-Cyclopentyl-4-(7H-pyrrolo[2,3-d]pyriMidin-4-yl)-(βR)-1H-pyrazole-1-propanenitrile
  • (βR)-β-Cyclopentyl-4-(7H-pyrrolo[2,3-d]pyriMidin-4-yl)-1H-pyrazole-1-propanenitrile
  • Ruxolitinib(INCB-018424)
  • 1H-Pyrazole-1-propanenitrile,.beta.-cyclopentyl-4-(7H-pyrrolo[2,3-d]pyriMidin-4-yl)-,(.beta.R)-
  • Ruxolitinib
  • Ruxolitinib INCB018424 Jakafi
  • Jakafi Ruxolitinib (INCB018424)
  • (R)-Ruxolitinib (>90%)
  • (betaR)-beta-Cyclopentyl-4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazole-1-propanenitrile Ruxolitinib(INCB018424)
  • R-Ruxolitinib (R-INCB018424)
  • Ruxolitinib, >=98%
  • Ruxolitinib free base
  • 3-Cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrazol-1-yl]-propionitrile
  • (R)-Ruxolitinib (INCB018424)
  • Russolinib
  • CS-163
  • BETAR-?CYCLOPENTYL-?4-?(7H-?PYRROLO[2,?3-?D]PYRIMIDIN-?4-?YL)-?1H-?PYRAZOLE-?1-?PROPANENITRILE
  • RUXOLITINIB (INCB18424)
  • (R)-Ruxolitinib (>
  • 1H-Pyrazole-1-propanenitrile, β-cyclopentyl-4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-, (βR)-
  • Ruxolitinib ISO 9001:2015 REACH
  • β-Cyclopentyl-4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-(βR)-1H-pyrazole-1-propanenitrile
  • Benzalolin
  • Pridazole
  • (R)-3-(4-(7H-Pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl)-3-cyclopentylpropanenitrile
  • Jakafi
  • Roxolitinib
  • (R)-Ruxolitinib
  • Ruxolitinib(Jakafi)
  • JAK,INCB 18424,inhibit,Mitochondrial Autophagy,Mitophagy,INCB18424,Janus kinase,Autophagy,Apoptosis,INCB-18424,Ruxolitinib,Inhibitor
  • INCB018424(Ruxolitinib)/Ruxolitinib
  • (βR)-β-Cyclopentyl-4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazole-1-propanenitrile
  • 2H9]-Rac-Ruxolitinib
  • Rusotinib
  • 941678-49-5
  • 971648-49-5
  • 52606144-44-7
  • JAK
  • STAT
  • Inhibitors
  • Anti-cancer&immunity
  • Inhibitor
  • APIs
  • Aromatics
  • Chiral Reagents
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Tyrosine Kinase Inhibitors
  • Antineoplastic
  • API
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