Drug Information
Drug (ID: DG02021) and It's Reported Resistant Information
| Name |
PF-06424439
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| Synonyms |
PF-06424439|1469284-78-3|[(3R)-1-[2-[1-(4-chloropyrazol-1-yl)cyclopropyl]-1H-imidazo[4,5-b]pyridin-5-yl]piperidin-3-yl]-pyrrolidin-1-ylmethanone|CHEMBL4098964|SCHEMBL15322997|PZHNKPBYOPQTRG-OAHLLOKOSA-N|BDBM215552|EX-A5493|AKOS040734393|NCGC00485074-01|DA-56731|HY-108341|CS-0028405|US9296745, 109-A|US9296745, 109-B|US9296745, 190|(3R)-1-{2-[1-(4-chloropyrazol-1-yl)cyclopropyl]-1H-imidazo[4,5-b]pyridin-5-yl}-3-(pyrrolidine-1-carbonyl)piperidine|(R)-(1-(2-(1-(4-chloro-1H-pyrazol-1-yl)cyclopropyl)-3H-imidazo[4,5-b]pyridin-5-yl)piperidin-3-yl)(pyrrolidin-1-yl)methanone|[(3r)-1-[2-[1-(4-chloro-1h-pyrazol-1-yl)cyclopropyl]-3h-imidazo[4,5-b]pyridin-5-yl]-3-piperidinyl]-1-pyrrolidinyl-methanone
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| Indication |
In total 1 Indication(s)
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| Structure |
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| Click to Show/Hide the Molecular Information and External Link(s) of This Drug | |||||
| Formula |
C22H26ClN7O
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| IsoSMILES |
C1CCN(C1)C(=O)[C@@H]2CCCN(C2)C3=NC4=C(C=C3)NC(=N4)C5(CC5)N6C=C(C=N6)Cl
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| InChI |
InChI=1S/C22H26ClN7O/c23-16-12-24-30(14-16)22(7-8-22)21-25-17-5-6-18(26-19(17)27-21)29-11-3-4-15(13-29)20(31)28-9-1-2-10-28/h5-6,12,14-15H,1-4,7-11,13H2,(H,25,26,27)/t15-/m1/s1
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| InChIKey |
PZHNKPBYOPQTRG-OAHLLOKOSA-N
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| PubChem CID | |||||
Type(s) of Resistant Mechanism of This Drug
Drug Resistance Data Categorized by Their Corresponding Diseases
ICD-02: Benign/in-situ/malignant neoplasm
| Drug Sensitivity Data Categorized by Their Corresponding Mechanisms | ||||
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| Key Molecule: Neurofibromin 1 (NF1) | [1] | |||
| Metabolic Type | Lipid metabolism | |||
| Sensitive Disease | ER+ breast adenocarcinoma [ICD-11: 2C61.1] | |||
| Molecule Alteration | Mutation | . |
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| Experimental Note | Revealed Based on the Cell Line Data | |||
| In Vivo Model | Rat, with ER + MCF7 cell lines | Rats | ||
| Experiment for Molecule Alteration |
LC-MS | |||
| Experiment for Drug Resistance |
Incucyte proliferation assay | |||
| Mechanism Description | Lastly,NF1deficiency alters the synergy between metabolic inhibitors and traditional targeted inhibitors. This includes increased synergy with inhibitors targeting glycolysis, glutamine metabolism, mitochondrial fatty acid transport, and TG synthesis. | |||
References
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