1 INN Class Route (list ) PK parameters= Cmax; Tmax; F: bioavailability; t1/2: half-life; VD: volume of distribution; Cl: clearance; PPB: plasma protein binding;(EQN means that value was calculated using VD=(Cl*t1/2)/0.693) Primary Target and PDB code of Protein-Drug complex Targets from DrugCentral Links
M RIPRETINIB (is an active metabolite )
RIPRETINIB ATC L01EX19
ANTINEOPLASTIC KIT PROTO-ONCOGENE RECEPTOR TYROSINE KINASE INHIBITOR PLATELET DERIVED GROWTH FACTOR RECEPTOR A (PDGFRA) INHIBITOR TREATMENT OF ADVANCED GASTROINTESTINAL STROMAL TUMOR (GIST) INHIBITS PDGFRB, TIE2, VEGFR2, AND BRAF
- Cmax 1.62 MICROMOLAR
Tmax 15.6 HOUR
VD 507 LITER
PPB 99.8 PERCENT
Cl 17.5 LITER / HOUR
HT 17.8 HOUR
PROTO-ONCOGENE RECEPTOR TYROSINE KINASE (KIT)
Mast,stem cell growth factor receptor Kit UNIPROT P10721 KIT -- Platelet-derived growth factor receptor alpha UNIPROT P16234 PDGFRA more at DrugCentral
EMA ANSM (in French)
Inxight Drugs Dailymed Drugs.com
SIDER side effects
Chemical Probes Portal
ChEMBL BindingDB DrugBank
2 INN Class Route (list ) PK parameters= Cmax; Tmax; F: bioavailability; t1/2: half-life; VD: volume of distribution; Cl: clearance; PPB: plasma protein binding;(EQN means that value was calculated using VD=(Cl*t1/2)/0.693) Primary Target and PDB code of Protein-Drug complex Targets from DrugCentral Links
RIPRETINIB (has an active metabolite )
RIPRETINIB ATC L01EX19
ANTINEOPLASTIC KIT PROTO-ONCOGENE RECEPTOR TYROSINE KINASE INHIBITOR PLATELET DERIVED GROWTH FACTOR RECEPTOR A (PDGFRA) INHIBITOR TREATMENT OF ADVANCED GASTROINTESTINAL STROMAL TUMOR (GIST) INHIBITS PDGFRB, TIE2, VEGFR2, AND BRAF
ORAL Cmax 1.49 MICROMOLAR
Tmax 4 HOUR
VD 307 LITER
PPB 99.8 PERCENT
Cl 15.3 LITER / HOUR
HT 14.8 HOUR
SOLUBILITY PRACTICALLY INSOLUBLE IN WATER
PROTO-ONCOGENE RECEPTOR TYROSINE KINASE (KIT)
Mast,stem cell growth factor receptor Kit UNIPROT P10721 KIT -- Platelet-derived growth factor receptor alpha UNIPROT P16234 PDGFRA more at DrugCentral
EMA ANSM (in French)
Inxight Drugs Dailymed Drugs.com
SIDER side effects
Chemical Probes Portal
ChEMBL BindingDB DrugBank