Standard InChI: InChI=1S/C18H18FN5O2/c1-10-8-20-18(25)14-9-21-24-6-5-16(23-17(14)24)22-11(2)13-7-12(19)3-4-15(13)26-10/h3-7,9-11H,8H2,1-2H3,(H,20,25)(H,22,23)/t10-,11+/m0/s1 (Source: PubChem)

IUPAC Name: (3R,11S)-6-fluoro-3,11-dimethyl-10-oxa-2,13,17,18,21-pentazatetracyclo[13.5.2.04,9.018,22]docosa-1(21),4(9),5,7,15(22),16,19-heptaen-14-one (Source: PubChem)

PubChem CID: 135565923 (Source: PubChem)

SMILES String: C[C@H]1CNC(=O)C2=C3N=C(C=CN3N=C2)N[C@@H](C4=C(O1)C=CC(=C4)F)C (Source: PubChem)

Connectivity SMILES string: CC1CNC(=O)C2=C3N=C(C=CN3N=C2)NC(C4=C(O1)C=CC(=C4)F)C (Source: PubChem)

Standard InChIKey: FIKPXCOQUIZNHB-WDEREUQCSA-N (Source: PubChem)

CAS Registry Number: 1802220-02-5 (Source: PubChem)

ChEBI ID: CHEBI:229220 (Source: PubChem)

ChEMBL ID: CHEMBL4298138 (Source: PubChem)

CompTox Dashboard Substance ID: DTXSID001358953 (Source: PubChem)

WHO ATC Classification Drug Code: L01EX28 (Source: ChEMBL)

WHO ATC Classification Drug Name: Repotrectinib (Source: ChEMBL)

Connectivity SMILES string: C[C@H]1CNC(=O)c2cnn3ccc(nc23)N[C@H](C)c2cc(F)ccc2O1 (Source: ChEMBL)

International Nonproprietary Name: Repotrectinib (Source: ChEMBL)

Preferred Name: REPOTRECTINIB (Source: ChEMBL)

Standard InChI: InChI=1S/C18H18FN5O2/c1-10-8-20-18(25)14-9-21-24-6-5-16(23-17(14)24)22-11(2)13-7-12(19)3-4-15(13)26-10/h3-7,9-11H,8H2,1-2H3,(H,20,25)(H,22,23)/t10-,11+/m0/s1 (Source: ChEMBL)

Standard InChIKey: FIKPXCOQUIZNHB-WDEREUQCSA-N (Source: ChEMBL)

US Adopted Name: Repotrectinib (Source: ChEMBL)

Mass parameters: 355.144453 (Source: PubChem)

Surface parameters: 80.6 (Source: PubChem)

Thermodynamic parameters: 2.1 (Source: PubChem)

Molecule statistics: 2 (Source: PubChem)

Molecule statistics: 6 (Source: PubChem)

Surface parameters: 26 (Source: PubChem)

Molecule statistics: 0 (Source: PubChem)

Stuctural analysis: 524 (Source: PubChem)

Molecule statistics: 2 (Source: PubChem)

Molecule statistics: 0 (Source: PubChem)

Thermodynamic parameters: 2.1 (Source: PubChem)

Molecule statistics: 1 (Source: PubChem)

Molecule statistics: 2 (Source: PubChem)

Molecule statistics: 0 (Source: PubChem)

Mass parameters: 355.14445300 Da (Source: PubChem)

Molecule statistics: 26 (Source: PubChem)

Molecule statistics: 6 (Source: PubChem)

Molecule statistics: 2 (Source: PubChem)

Molecule statistics: 0 (Source: PubChem)

Surface parameters: 0 (Source: PubChem)

Stuctural analysis: 524 (Source: PubChem)

Stuctural analysis: 265.4 (Source: PubChem)

Mass parameters: 355.4 g/mol (Source: PubChem)

Mass parameters: 355.14445300 Da (Source: PubChem)

Molecule statistics: 0 (Source: PubChem)

Surface parameters: 80.6 Ų (Source: PubChem)

Molecule statistics: 0 (Source: PubChem)

Molecule statistics: 0 (Source: PubChem)

Thermodynamic parameters: 3 (Source: ChEMBL)

Thermodynamic parameters: 2.55 (Source: ChEMBL)

Molecule statistics: 26 (Source: ChEMBL)

Molecule statistics: 6 (Source: ChEMBL)

Molecule statistics: 2 (Source: ChEMBL)

Mass parameters: 355.37 g/mol (Source: ChEMBL)

Mass parameters: 355.37 g/mol (Source: ChEMBL)

Molecule statistics: -0.53 (Source: ChEMBL)

Molecule statistics: 80.55 (Source: ChEMBL)

Molecule statistics: 0.65 (Source: ChEMBL)

Chemical formula: C18H18FN5O2 (Source: PubChem)

Chirality: 1 (Source: ChEMBL)

Chemical formula: C18H18FN5O2 (Source: ChEMBL)

Molecule type: Small molecule (Source: ChEMBL)

Passes the rule of three : N (Source: ChEMBL)

USAN STEM Defintion: tyrosine kinase inhibitors: tropomyosin receptor kinase (TRK) inhibitors (Source: ChEMBL)

USAN STEM: -tinib (Source: ChEMBL)