Umbralisib tosylateProduct ingredient for Umbralisib

Name
Umbralisib tosylate
Drug Entry
Umbralisib

Marginal zone lymphoma is a rare, slowly progressing type of non-Hodgkin lymphoma initially treated with rituximab (an anti-CD20 drug), either alone or in combination with chemotherapy. Unfortunately, many patients experience a relapse or develop resistance to these drugs. Treatment options then become limited, and alternate treatments for the lymphoma are required to control disease progression.1 Follicular lymphoma is also treated with rituximab and other chemotherapeutic agents, but may show similar progression.5

On February 5, 2021, the Food and Drug Administration granted accelerated approval to umbralisib, a kinase inhibitor for PI3K-delta and casein kinase CK1-epsilon, based on promising results from clinical trials. It was marketed as Ukoniq by TG Therapeutics and has been approved for the treatment of relapsing and refractory marginal cell lymphoma and follicular lymphoma in adults.6 Umbralisib inhibits casein kinase, a primary regulator of protein translation, kinase-1ε, distinguishing it from other lymphoma treatments. While it initially offered a promising therapy for patients experiencing relapsing or refractory disease,1 umbralisib was withdrawn from the market due to safety concerns as the drug was associated with a possible increased risk of death outweighing the benefits.10

Accession Number
DBSALT003156
Structure
Synonyms
Umbralisib tosylate
External IDs
RP-5307
UNII
FU8XW5V3FS
CAS Number
1532533-72-4
Weight
Average: 743.76
Monoisotopic: 743.202539433
Chemical Formula
C38H32F3N5O6S
InChI Key
KYJWUPZPSXZEPG-NTISSMGPSA-N
InChI
InChI=1S/C31H24F3N5O3.C7H8O3S/c1-15(2)41-24-9-7-18(12-22(24)34)27-26-30(35)36-14-37-31(26)39(38-27)16(3)29-25(17-5-4-6-19(32)11-17)28(40)21-13-20(33)8-10-23(21)42-29;1-6-2-4-7(5-3-6)11(8,9)10/h4-16H,1-3H3,(H2,35,36,37);2-5H,1H3,(H,8,9,10)/t16-;/m0./s1
IUPAC Name
2-[(1S)-1-{4-amino-3-[3-fluoro-4-(propan-2-yloxy)phenyl]-1H-pyrazolo[3,4-d]pyrimidin-1-yl}ethyl]-6-fluoro-3-(3-fluorophenyl)-4H-chromen-4-one; 4-methylbenzene-1-sulfonic acid
SMILES
CC1=CC=C(C=C1)S(O)(=O)=O.[H][C@@](C)(N1N=C(C2=C1N=CN=C2N)C1=CC=C(OC(C)C)C(F)=C1)C1=C(C2=CC=CC(F)=C2)C(=O)C2=C(O1)C=CC(F)=C2
ChemSpider
58790036
ChEMBL
CHEMBL3989869
Predicted Properties
PropertyValueSource
logP6.13Chemaxon
pKa (Strongest Acidic)19.68Chemaxon
pKa (Strongest Basic)4.01Chemaxon
Physiological Charge0Chemaxon
Hydrogen Acceptor Count7Chemaxon
Hydrogen Donor Count1Chemaxon
Polar Surface Area105.15 Å2Chemaxon
Rotatable Bond Count7Chemaxon
Refractivity163.22 m3·mol-1Chemaxon
Polarizability56.31 Å3Chemaxon
Number of Rings7Chemaxon
Bioavailability0Chemaxon
Rule of FiveNoChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleYesChemaxon