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Ritlecitinib

Catalog No. T5382 CAS 1792180-81-4

Synonyms: PF-06651600

Ritlecitinib (PF-06651600) is a potent JAK3-selective inhibitor (IC50: 33.1 nM).

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Ritlecitinib, CAS 1792180-81-4

Pack Size	Availability	Price/USD
2 mg	In stock	$ 39.00
5 mg	In stock	$ 64.00
10 mg	In stock	$ 113.00
25 mg	In stock	$ 228.00
50 mg	In stock	$ 347.00
100 mg	In stock	$ 522.00
200 mg	In stock	$ 743.00
500 mg	In stock	$ 1,120.00
1 mL * 10 mM (in DMSO)	In stock	$ 70.00

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Purity: 99.92%

Purity: 99.1%

Purity: 98.92%

Purity: 98.82%

Purity: 98.81%

Biological Description

Chemical Properties

Storage & Solubility Information

Description	Ritlecitinib (PF-06651600) is a potent JAK3-selective inhibitor (IC50: 33.1 nM).
Targets&IC50	JAK3:33.1 nM (cell free)
In vitro	PF-06651600 inhibited JAK3 kinase activity with an IC50 of 33.1 nM but without activity (IC50 > 10 000 nM) against JAK1, JAK2, and TYK2. In total lymphocytes in human whole blood, PF-06651600 inhibited the phosphorylation of STAT5 elicited by IL-2, IL-4, IL-7, and IL-15 with IC50 values of 244, 340, 407, and 266 nM, respectively, and it inhibited the phosphorylation of STAT3 elicited by IL-21 with an IC50 of 355 nM [1].
In vivo	In the rat adjuvant-induced arthritis (AIA) model, PF-06651600 reduced paw swelling with an unbound EC50 of 169 nM. Similarly, PF-06651600 significantly reduced disease severity in the experimental autoimmune encephalomyelitis21,22 (EAE) mouse model when dosed either therapeutically at 30 or 100 mg/kg or prophylactically at 20 and 60 mg/kg [1].
Kinase Assay	His-tagged recombinant human TYK2 kinase domain was expressed in SF21/baculovirus and purified using a two-step affinity (Ni-NTA) and size-exclusion (SEC S200) purification method.Test compounds were solubilized in DMSO to a stock concentration of 30 mM.Compounds were diluted in DMSO to create an 11-point half log dilution series with a top concentration of 600 μM.The test compound plate also contained positive control wells containing a known inhibitor to define 100% inhibition and negative control wells containing DMSO to define no inhibition.The compound plates were diluted 1 to 60 in the assay,resulting in a final assay compound concentration range of 10 μM to 100 pM and a final assay concentration of 1.7% DMSO.Test compounds and controls solubilized in 100% DMSO were added (250 nL) to a 384 well polypropylene plate (Matrical) using a non contact acoustic dispenser.Kinase assays were carried out at room temperature in a 15 μL reaction buffer containing 20 mM HEPES,pH 7.4,10 mM magnesium chloride,0.01% bovine serum albumin (BSA),0.0005% Tween 20 and 1mM Dithiothreitol (DTT).Reaction mixtures contained 1 μM of a fluorescently labeled synthetic peptide,at a concentration less than the apparent Michaelis-Menten constant (Km) (5FAM-KKSRGDYMTMQID for JAK1 and TYK2 and FITC-KGGEEEEYFELVKK for JAK2 and JAK3).Reaction mixtures contained adenosine triphosphate (ATP) at either a level equal to the apparent Km for ATP (40 μM for JAK1,4 μM for JAK2,4 μM for JAK3 and 12 μM for TYK2) or at 1 mM ATP.Compound was added to the buffer containing ATP and substrate and immediately after this step the enzyme was added to begin the reaction.The assays were stopped with 15 μL of a buffer containing 180 mM HEPES,pH=7.4,20 mM EDTA,0.2% Coating Reagent,resulting in a final concentration of 10 mM EDTA,0.1% Coating Reagent and 100 mM HEPES,pH=7.4.
Cell Research	Human CD4+ T cells were purified from buffy coat with RosetteSep CD4+ T Cell Enrichment Cocktail and skewed for 6 days with cytokine cocktails (25 ng/mL of IL-6, 25 ng/mL of IL-23, 12.5 ng/mL of IL-1β, 25 ng/mL of IL21, 5 ng/mL of TGFβ1, 10 μg/ml of anti-CD3 antibody (pre-coated on plate surface) and 1 μg/mL of anti-CD28 antibody) in the presence of JAK inhibitors at 10 different concentrations. Supernatants were harvested and the concentrations of IL-17A were determined with MSD assay following the protocol provided by the manufacturer. To study the effect of PF-06651600 on Th17 cells post-differentiation, skewed Th17 cells were washed, rested with X-VIVO 15 medium for overnight and resuspended in medium containing the same concentrations of cytokines as during skewing but without anti-CD3 or anti-CD28 antibodies, in the presence of PF-06651600 at 10 different concentrations for 2 additional days. On Day 9, supernatant was harvested from each well and IL-17A was determined as described above [1].
Animal Research	The effect of JAK3 inhibition by PF-06651600 was evaluated in vivo using a therapeutic dosing paradigm in a rat adjuvant-induced arthritis. The efficacy of this molecule was evaluated in three separate studies using successively lower doses. Arthritis was induced by immunization of female Lewis rats (8 to 10 weeks old) via intradermal injection at the base of the tail with complete Freund's adjuvant with three 50 μL injections (15 mg/mL Mycobacterium tuberculosis) in incomplete Freund's adjuvant. Seven days after the initial immunization, the baseline hind paw volume of the immunized rats was measured via plethysmograph. The rats were monitored daily for signs of arthritis including change in body weight and hind paw volume measurement. When individual hind paw volume measurements indicated an increase of 0.2 mL (or greater) in a single hind paw, animals were randomly assigned to a treatment group. Daily treatment with PF-06651600 was administered via oral gavage. Treatment groups for Experiment 1 were: 80, 15, or 6 mg/kg or vehicle (2% Tween 80 /0.5% methylcellulose/deionized water). Treatment groups for Experiment 2 were: 30, 10, and 3 mg/kg or vehicle (0.5% methylcellulose / de-ionized water/ 1 mEQ hydrochloric acid). Treatment groups for Experiment 3 were: 10, 1, 0.3 and 0.1 mg/kg or vehicle (0.5% methylcellulose/de-ionized water/ 1 mEQ hydrochloric acid). Dosing began once individuals were enrolled into respective groups. Treatment continued for 7 days. At the conclusion of the study, whole blood was taken at 15 minutes post-dose (peak concentration in plasma) for analysis of STAT phosphorylation, and plasma was taken for exposure concentration in PF-06651600 dosed groups [1].

Synonyms	PF-06651600
Molecular Weight	285.34
Formula	C15H19N5O
CAS No.	1792180-81-4

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 130 mg/mL (455.60 mM)

References and Literature

1. Telliez JB, et al. Discovery of a JAK3-Selective Inhibitor: Functional Differentiation of JAK3-Selective Inhibition over pan-JAK or JAK1-Selective Inhibition. ACS Chem Biol. 2016 Dec 16;11(12):3442-3451. 2. Thorarensen A, et al. Design of a Janus Kinase 3 (JAK3) Specific Inhibitor 1-((2S,5R)-5-((7H-Pyrrolo[2,3-d]pyrimidin-4-yl)amino)-2-methylpiperidin-1-yl)prop-2-en-1-one (PF-06651600) Allowing for the Interrogation of JAK3 Signaling in Humans. J Med Chem. 2017 Mar 9;60(5):1971-1993.

Related compound libraries

This product is contained In the following compound libraries：

Anti-Cancer Drug Library Inhibitor Library Highly Selective Inhibitor Library Anti-Cancer Clinical Compound Library Tyrosine Kinase Inhibitor Library Drug Repurposing Compound Library EMA Approved Drug Library Clinical Compound Library Anti-Obesity Compound Library Cysteine Covalent Library

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Keywords

Ritlecitinib 1792180-81-4 Angiogenesis Chromatin/Epigenetic JAK/STAT signaling Stem Cells JAK Janus kinase Inhibitor inhibit PF06651600 PF-06651600 PF 06651600 inhibitor

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