Upadacitinib tartrateProduct ingredient for Upadacitinib

Name
Upadacitinib tartrate
Drug Entry
Upadacitinib

Upadacitinib is an oral Janus kinase (JAK)1-selective inhibitor and a disease-modifying antirheumatic drug (DMARD) used in the treatment of rheumatoid arthritis to slow down disease progression. Rheumatoid arthritis is a chronic autoimmune inflammatory disease affecting the peripheral joints. It is characterized by synovial inflammation and hyperplasia, autoantibody production, cartilage damage and bone destruction, leading to co-morbidities.4 Despite a variety of therapeutic agents available for treatment, up to 40% of the patients do not respond to current therapies, including biological therapies.6 The etiology of the disease is mostly unknown; however, the role of JAK as a driver of immune-mediated conditions was discovered, leading to the use of JAK as therapeutic targets for rheumatoid arthritis.5 To reduce dose-related toxicity (as seen with some pan-JAK inhibitors) without significantly affecting efficacy, more selective JAK1 inhibitors, upadacitinib and filgotinib, were developed.4

The FDA approved upadacitinib in August 2019 and it is used for the treatment of active rheumatoid arthritis, psoriatic arthritis, atopic dermatitis, ulcerative colitis, and ankylosing spondylitis.9 In December 2019, it was additionally approved by the European Commission and Health Canada.10,15 Upadacitinib is marketed under the brand name RINVOQ for oral administration.9

Accession Number
DBSALT002886
Structure
Synonyms
Upadacitinib tartrate
UNII
7KCW9IQM02
CAS Number
1607431-21-9
Weight
Average: 602.521
Monoisotopic: 602.215940396
Chemical Formula
C21H33F3N6O11
InChI Key
LATZVDXOTDYECD-UFTFXDLESA-N
InChI
InChI=1S/C17H19F3N6O.C4H6O6.4H2O/c1-2-10-7-25(16(27)24-9-17(18,19)20)8-11(10)13-5-22-14-6-23-15-12(26(13)14)3-4-21-15;5-1(3(7)8)2(6)4(9)10;;;;/h3-6,10-11,21H,2,7-9H2,1H3,(H,24,27);1-2,5-6H,(H,7,8)(H,9,10);4*1H2/t10-,11+;;;;;/m1...../s1
IUPAC Name
(3S,4R)-3-ethyl-4-{1,5,7,10-tetraazatricyclo[7.3.0.0^{2,6}]dodeca-2(6),3,7,9,11-pentaen-12-yl}-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide 2,3-dihydroxybutanedioic acid tetrahydrate
SMILES
O.O.O.O.OC(C(O)C(O)=O)C(O)=O.CC[C@@H]1CN(C[C@@H]1C1=CN=C2C=NC3=C(C=CN3)N12)C(=O)NCC(F)(F)F
ChEMBL
CHEMBL3707269
Predicted Properties
PropertyValueSource
Water Solubility0.0707 mg/mLALOGPS
logP2.57ALOGPS
logP0.85Chemaxon
logS-3.7ALOGPS
pKa (Strongest Acidic)13.99Chemaxon
pKa (Strongest Basic)4.11Chemaxon
Physiological Charge0Chemaxon
Hydrogen Acceptor Count3Chemaxon
Hydrogen Donor Count2Chemaxon
Polar Surface Area78.32 Å2Chemaxon
Rotatable Bond Count7Chemaxon
Refractivity93.03 m3·mol-1Chemaxon
Polarizability36.08 Å3Chemaxon
Number of Rings4Chemaxon
Bioavailability1Chemaxon
Rule of FiveNoChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleYesChemaxon