Details
Stereochemistry | ACHIRAL |
Molecular Formula | C24H27F2N5O4 |
Molecular Weight | 487.4991 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCN1C(=O)N(CC2=C1C3=C(NC(CN4CCOCC4)=C3)N=C2)C5=C(F)C(OC)=CC(OC)=C5F
InChI
InChIKey=HCDMJFOHIXMBOV-UHFFFAOYSA-N
InChI=1S/C24H27F2N5O4/c1-4-30-21-14(11-27-23-16(21)9-15(28-23)13-29-5-7-35-8-6-29)12-31(24(30)32)22-19(25)17(33-2)10-18(34-3)20(22)26/h9-11H,4-8,12-13H2,1-3H3,(H,27,28)
Molecular Formula | C24H27F2N5O4 |
Molecular Weight | 487.4991 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Pemigatinib, an oral kinases inhibitor, was approved under the brand name PEMAZYRE for the treatment of adults with previously treated, unresectable locally advanced, or metastatic cholangiocarcinoma with a fibroblast growth factor receptor 2 (FGFR2) fusion. The FDA-approved indication for pemigatinib was granted under accelerated approval based on the overall response rate and duration of response in pre-marketing clinical trials. The drug inhibited FGFR1-3 phosphorylation and signaling and decreased cell viability in cancer cell lines with activating FGFR amplification and fusions that resulted in constitutive activation of FGFR signaling.
CNS Activity
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2020/213736Orig1s000MultidisciplineR.pdf
Curator's Comment: pemigatinib crossed the blood-brain barrier at low levels after IV administration.
Originator
Sources: https://pubmed.ncbi.nlm.nih.gov/32315352/
Curator's Comment: was synthesized at Incyte Corporation (Wilmington, DE).
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: P11362|||Q14307|||Q9UDF2 Gene ID: 2260.0 Gene Symbol: FGFR1 Target Organism: Homo sapiens (Human) |
0.4 nM [IC50] | ||
Target ID: P21802|||Q14301|||Q1KHY5|||Q9NZU3|||Q9UIH8 Gene ID: 2263.0 Gene Symbol: FGFR2 Target Organism: Homo sapiens (Human) |
0.5 nM [IC50] | ||
Target ID: P22607 Gene ID: 2261.0 Gene Symbol: FGFR3 Target Organism: Homo sapiens (Human) |
1.0 nM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | PEMAZYRE Approved UsePEMAZYRE is a kinase inhibitor indicated for the treatment of adults with previously treated, unresectable locally advanced or metastatic cholangiocarcinoma with a fibroblast growth factor receptor 2 (FGFR2) fusion |
Substance Class |
Chemical
Created
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admin
on
Edited
Sat Dec 16 12:06:11 GMT 2023
by
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on
Sat Dec 16 12:06:11 GMT 2023
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Record UNII |
Y6BX7BL23K
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Record Status |
Validated (UNII)
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FDA ORPHAN DRUG |
624117
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FDA ORPHAN DRUG |
696419
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NCI_THESAURUS |
C129825
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EU-Orphan Drug |
EU/3/18/2066
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NCI_THESAURUS |
C1967
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10712
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1513857-77-6
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m12200
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86705695
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100000181126
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2359268
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DB15102
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FG-16
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Pemigatinib
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C121553
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Related Record | Type | Details | ||
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EXCRETED UNCHANGED |
FECAL
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METABOLIC ENZYME -> SUBSTRATE |
MAJOR
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BINDER->LIGAND |
In vitro, pemigatinib was 90.6% bound to human plasma proteins at concentrations ranging from 1 to 10 μM.
BINDING
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TARGET -> INHIBITOR |
IC50
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TARGET -> INHIBITOR |
IC50
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EXCRETED UNCHANGED |
URINE
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TARGET -> INHIBITOR |
IC50
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IMPURITY -> PARENT |
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IMPURITY -> PARENT |
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ACTIVE MOIETY |
Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
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Biological Half-life | PHARMACOKINETIC |
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Tmax | PHARMACOKINETIC |
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Volume of Distribution | PHARMACOKINETIC |
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