Lomerizine dihydrochlorideProduct ingredient for Lomerizine
- Name
- Lomerizine dihydrochloride
- Drug Entry
- Lomerizine
Lomerizine is a diphenylmethylpiperazine calcium channel blocker3,4 with relatively selective central nervous system (CNS) effects.4 This drug is used to prophylactically treat migraines1,2 and is also being investigated against eye-related diseases that are associated with local circulatory disturbances, an example being normal-tension glaucoma.3
- Accession Number
- DBSALT002715
- Structure
- Synonyms
- Lomerizine HCl / Lomerizine hydrochloride
- External IDs
- KB-2796
- UNII
- 3W473D5LIY
- CAS Number
- 101477-54-7
- Weight
- Average: 541.46
Monoisotopic: 540.1758046 - Chemical Formula
- C27H32Cl2F2N2O3
- InChI Key
- LOGVKVSFYBBUAJ-UHFFFAOYSA-N
- InChI
- InChI=1S/C27H30F2N2O3.2ClH/c1-32-24-13-8-21(26(33-2)27(24)34-3)18-30-14-16-31(17-15-30)25(19-4-9-22(28)10-5-19)20-6-11-23(29)12-7-20;;/h4-13,25H,14-18H2,1-3H3;2*1H
- IUPAC Name
- 1-[bis(4-fluorophenyl)methyl]-4-[(2,3,4-trimethoxyphenyl)methyl]piperazine dihydrochloride
- SMILES
- Cl.Cl.COC1=CC=C(CN2CCN(CC2)C(C2=CC=C(F)C=C2)C2=CC=C(F)C=C2)C(OC)=C1OC
- External Links
- ChemSpider
- 108925
- ChEMBL
- CHEMBL2356978
- Predicted Properties
Property Value Source Water Solubility 0.00673 mg/mL ALOGPS logP 4.47 ALOGPS logP 5.08 Chemaxon logS -4.8 ALOGPS pKa (Strongest Basic) 6.73 Chemaxon Physiological Charge 1 Chemaxon Hydrogen Acceptor Count 5 Chemaxon Hydrogen Donor Count 0 Chemaxon Polar Surface Area 34.17 Å2 Chemaxon Rotatable Bond Count 8 Chemaxon Refractivity 129.37 m3·mol-1 Chemaxon Polarizability 49.19 Å3 Chemaxon Number of Rings 4 Chemaxon Bioavailability 0 Chemaxon Rule of Five No Chemaxon Ghose Filter No Chemaxon Veber's Rule Yes Chemaxon MDDR-like Rule Yes Chemaxon