Ritlecitinib tosylateProduct ingredient for Ritlecitinib

Name
Ritlecitinib tosylate
Drug Entry
Ritlecitinib

Ritlecitinib (PF-06651600) is a highly selective inhibitor of Janus kinase 3 (JAK3) and the tyrosine kinase expressed in hepatocellular carcinoma (TEC) kinase family. In June 2023, it was approved by the FDA for the treatment of severe alopecia areata in adults and adolescents 12 years and older.5,6 It was further approved by the EMA in September 2023.8 Ritlecitinib is administered orally and is the first member of its class.1,2

Ritlecitinib binds covalently to Cys-909 of JAK3, a site where other JAK isoforms have a serine residue. This makes ritlecitinib a highly selective and irreversible JAK3 inhibitor.1,2 Other kinases have a cysteine at a position equivalent to Cys-909 in JAK3, and several of them belong to the TEC kinase family. It has been suggested that the dual activity of ritlecitinib toward JAK3 and the TEC kinase family block cytokine signaling as well as the cytolytic activity of T cells, both implicated in the pathogenesis of alopecia areata.1

Accession Number
DBSALT003482
Structure
Synonyms
PF-06651600 TOSYLATE / RITLECITINIB TOSILATE / RITLECITINIB TOSLATE
UNII
EAG4T1459K
CAS Number
2192215-81-7
Weight
Average: 457.55
Monoisotopic: 457.178375543
Chemical Formula
C22H27N5O4S
InChI Key
YOZLVAFWYLSRRN-VZXYPILPSA-N
InChI
InChI=1S/C15H19N5O.C7H8O3S/c1-3-13(21)20-8-11(5-4-10(20)2)19-15-12-6-7-16-14(12)17-9-18-15;1-6-2-4-7(5-3-6)11(8,9)10/h3,6-7,9-11H,1,4-5,8H2,2H3,(H2,16,17,18,19);2-5H,1H3,(H,8,9,10)/t10-,11+;/m0./s1
IUPAC Name
1-[(2S,5R)-2-methyl-5-({7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)piperidin-1-yl]prop-2-en-1-one; 4-methylbenzene-1-sulfonic acid
SMILES
CC1=CC=C(C=C1)S(O)(=O)=O.C[C@H]1CC[C@H](CN1C(=O)C=C)NC1=C2C=CNC2=NC=N1
ChemSpider
81368003
Predicted Properties
PropertyValueSource
logP1.47Chemaxon
pKa (Strongest Acidic)13.59Chemaxon
pKa (Strongest Basic)7.7Chemaxon
Physiological Charge1Chemaxon
Hydrogen Acceptor Count4Chemaxon
Hydrogen Donor Count2Chemaxon
Polar Surface Area73.91 Å2Chemaxon
Rotatable Bond Count4Chemaxon
Refractivity82.84 m3·mol-1Chemaxon
Polarizability29.68 Å3Chemaxon
Number of Rings4Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterYesChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon