Ruxolitinib

Ruxolitinib Struktur
941678-49-5
CAS-Nr.
941678-49-5
Englisch Name:
Ruxolitinib
Synonyma:
Jakafi;(R)-3-(4-(7H-Pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl)-3-cyclopentylpropanenitrile;Roxolitinib;(R)-Ruxolitinib;Ruxolitinib free base;(betaR)-beta-Cyclopentyl-4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazole-1-propanenitrile;CS-163;Pridazole;Rusotinib;Russolinib
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) Exclamation Mark (GHS07)Health Hazard (GHS08)
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitsschädlich bei Verschlucken. Akute Toxizität oral Kategorie 4 Warnung 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.

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.

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.

Ruxolitinib Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Ruxolitinib Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 469)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Cangzhou Nianke Pharmaceutical Technology Co., Ltd. 18958645613 15076704415
3190065639@qq.com China 678 58
Chongqing Meixing Pharmaceutical Technology Co., Ltd. 15023715366
henry124604479@163.com China 233 58
Changzhou Yongfeng Biomedicine Co. Ltd. 15006117673
2973592490@qq.com China 268 58
Yunfei Pharmaceutical(Shenzhen) Co., Ltd. 0755-61160828 15994832653;
hulixiu@yunfeipharma.com China 257 58
Wuhan Juchengyuan Biotechnology Co., Ltd 400-027-6007 18062142210
804180422@qq.com China 145 58
Cangzhou Kangrui Medical Technology Co., LTD 18632776803
cangzhoukangrui@126.com;355803330@qq.com China 676 58
Changzhou Borl Biotechnology Co.,LTD 13656121842
luyan0021@163.com China 265 58
Hubei widely chemical technology Co., Ltd. 186-02735115 18602735115
18602735115@163.com China 1896 64
Shanghai Boyle Chemical Co., Ltd.
sales@boylechem.com China 2915 55
J & K SCIENTIFIC LTD. 18210857532 18210857532
jkinfo@jkchemical.com China 96815 76

941678-49-5()Verwandte Suche:


  • (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)
  • Roxolitinib
  • 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%
  • 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
  • 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
  • Ruxolitinib, ATP-competitive JAK1/2 inhibitor
  • Ruxolitinib, 10 mM in DMSO
  • D9-Rac-Ruxolitinib
  • (betaR)-beta-Cyclopentyl-4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazole-1-propanenitrile
  • (R)-Ruxolitinib
  • (R)-3-(4-(7H-Pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl)-3-cyclopentylpropanenitrile
  • Jakafi
  • Ruxolitinib free base
  • Ruxolitinib R-isomer
  • 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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