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Details

Stereochemistry ACHIRAL
Molecular Formula C26H31Cl2N7O3.C2H4O2
Molecular Weight 620.527
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of INFIGRATINIB ACETATE

SMILES

CC(O)=O.CCN1CCN(CC1)C2=CC=C(NC3=CC(=NC=N3)N(C)C(=O)NC4=C(Cl)C(OC)=CC(OC)=C4Cl)C=C2

InChI

InChIKey=XHCQHOGMMJKLRU-UHFFFAOYSA-N
InChI=1S/C26H31Cl2N7O3.C2H4O2/c1-5-34-10-12-35(13-11-34)18-8-6-17(7-9-18)31-21-15-22(30-16-29-21)33(2)26(36)32-25-23(27)19(37-3)14-20(38-4)24(25)28;1-2(3)4/h6-9,14-16H,5,10-13H2,1-4H3,(H,32,36)(H,29,30,31);1H3,(H,3,4)

HIDE SMILES / InChI

Molecular Formula C26H31Cl2N7O3
Molecular Weight 560.475
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C2H4O2
Molecular Weight 60.052
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including: http://adisinsight.springer.com/drugs/ | DOI: 10.1158/2159-8290.CD-NB2014-057 | http://meetinglibrary.asco.org/content/159420-173

Infigratinib (BGJ398), a potent, orally bioavailable, small-molecule pan-FGFR kinase inhibitor. FGFR genetic alterations are the most significant predictors for BGJ398 sensitivity. It is currently in phase 2 trials for Cholangiocarcinoma, Glioblastoma and Solid tumors. Detected adverse events were hyperphosphatemia, fatigue, constipation, cough and nausea. Other adverse events were generally mild and included stomatitis, hair loss, decreased appetite, and fatigue.

Originator

Curator's Comment: # Novartis

Approval Year

TargetsConditions

Conditions

Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Biophysical characterization of drug-resistant mutants of fibroblast growth factor receptor 1.
2016 Oct
Inhibition of FGF Signalling Pathway Augments the Expression of Pluripotency and Trophoblast Lineage Marker Genes in Porcine Parthenogenetic Blastocyst.
2016 Oct
Evaluation of BGJ398, a Fibroblast Growth Factor Receptor 1-3 Kinase Inhibitor, in Patients With Advanced Solid Tumors Harboring Genetic Alterations in Fibroblast Growth Factor Receptors: Results of a Global Phase I, Dose-Escalation and Dose-Expansion Study.
2017 Jan 10
Patents

Sample Use Guides

1 x 100 mg and 1 x 25 mg capsules once daily for the first 21 days of the 28-day cycle (3 weeks on, 1 week off in a cycle).
Route of Administration: Oral
BGJ398 inhibits the proliferation of the FGFR1-, FGFR2-Q, and FGFR3-dependent BaF3 cells with IC50 of 2.9 μM, 2.0 μM and 2 μM, respectively. BGJ398 interferes with autophosphorylation on specific tyrosine residues including FGFR-WT, FGFR2-WT, FGFR3-K650E, FGFR3-S249C and FGFR4-WT with IC50 of 4.6 nM, 4.9 nM, 5 nM, 5 nM and 168 nM, respectively. BGJ398 suppresses proliferation of the cancer cells with wild-type (WT) FGFR3 overexpression such as RT112, RT4, SW780 and JMSU1 with IC50 of 5 nM, 30 nM, 32 nM and 15 nM, respectively.
Substance Class Chemical
Created
by admin
on Sat Dec 16 06:42:30 GMT 2023
Edited
by admin
on Sat Dec 16 06:42:30 GMT 2023
Record UNII
03D0789NYP
Record Status Validated (UNII)
Record Version
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Name Type Language
INFIGRATINIB ACETATE
WHO-DD  
Common Name English
Infigratinib acetate [WHO-DD]
Common Name English
BGJ-398 ACETATE
Code English
UREA, N'-(2,6-DICHLORO-3,5-DIMETHOXYPHENYL)-N-(6-((4-(4-ETHYL-1-PIPERAZINYL)PHENYL)AMINO)-4-PYRIMIDINYL)-N-METHYL-, ACETATE (1:1)
Systematic Name English
Code System Code Type Description
FDA UNII
03D0789NYP
Created by admin on Sat Dec 16 06:42:31 GMT 2023 , Edited by admin on Sat Dec 16 06:42:31 GMT 2023
PRIMARY
DRUG BANK
DBSALT002099
Created by admin on Sat Dec 16 06:42:31 GMT 2023 , Edited by admin on Sat Dec 16 06:42:31 GMT 2023
PRIMARY
PUBCHEM
91618031
Created by admin on Sat Dec 16 06:42:31 GMT 2023 , Edited by admin on Sat Dec 16 06:42:31 GMT 2023
PRIMARY
CAS
1310746-17-8
Created by admin on Sat Dec 16 06:42:31 GMT 2023 , Edited by admin on Sat Dec 16 06:42:31 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY