Synonyms:
Status: Phase 3
Entry Type: Small molecule
Molecule Category: Parent
UNII: D42O649ALL

Structure

InChI Key CGDZXLJGHVKVIE-DNVCBOLYSA-N
Smile O=C(N[C@@H]1CC[C@@H](c2cccc(F)c2F)CN(CC(F)(F)F)C1=O)N1CCC(n2c(O)nc3ncccc32)CC1
InChI
InChI=1S/C26H27F5N6O3/c27-18-4-1-3-17(21(18)28)15-6-7-19(23(38)36(13-15)14-26(29,30)31)33-24(39)35-11-8-16(9-12-35)37-20-5-2-10-32-22(20)34-25(37)40/h1-5,10,15-16,19H,6-9,11-14H2,(H,33,39)(H,32,34,40)/t15-,19-/m1/s1

Physicochemical Descriptors

Property Name Value
Molecular Formula C26H27F5N6O3
Molecular Weight 566.53
AlogP 4.1
Hydrogen Bond Acceptor 6.0
Hydrogen Bond Donor 2.0
Number of Rotational Bond 4.0
Polar Surface Area 103.59
Molecular species NEUTRAL
Aromatic Rings 3.0
Heavy Atoms 40.0

Pharmacology

Action Mechanism of Action Reference
ANTAGONIST Calcitonin gene-related peptide type 1 receptor antagonist PubMed Wikipedia

Indications

Mesh Heading Maximum Phase Mesh ID Reference
Migraine Disorders 3 D008881 ClinicalTrials

Related Entries

Scaffolds

Salt

Cross References

Resources Reference
CAS NUMBER 781649-09-0
ChEMBL CHEMBL236593
DrugBank DB12228
FDA SRS D42O649ALL
Guide to Pharmacology 703
PDB N7R
PubChem 11319053
SureChEMBL SCHEMBL1198535
ZINC ZINC000028827350