General Information of Drug (ID: DMZREFQ)

Drug Name
Eslicarbazepine
Synonyms Aptiom; BIA 2-093; Exalief; SEP-0002093; Sep-93; Stedesa; Zebinix
Indication
Disease Entry ICD 11 Status REF
Seizure disorder 8A6Z Approved [1], [2]
Therapeutic Class
Neurology Agents
Drug Type
Small molecular drug
Structure
3D MOL 2D MOL
#Ro5 Violations (Lipinski): 0 Molecular Weight (mw) 254.28
Topological Polar Surface Area (xlogp) 1.4
Rotatable Bond Count (rotbonds) 0
Hydrogen Bond Donor Count (hbonddonor) 2
Hydrogen Bond Acceptor Count (hbondacc) 2
Chemical Identifiers
Formula
C15H14N2O2
IUPAC Name
(5S)-5-hydroxy-5,6-dihydrobenzo[b][1]benzazepine-11-carboxamide
Canonical SMILES
C1[C@@H](C2=CC=CC=C2N(C3=CC=CC=C31)C(=O)N)O
InChI
InChI=1S/C15H14N2O2/c16-15(19)17-12-7-3-1-5-10(12)9-14(18)11-6-2-4-8-13(11)17/h1-8,14,18H,9H2,(H2,16,19)/t14-/m0/s1
InChIKey
BMPDWHIDQYTSHX-AWEZNQCLSA-N
Cross-matching ID
PubChem CID
9881504
CAS Number
104746-04-5
DrugBank ID
DB14575
TTD ID
D04QZD
INTEDE ID
DR0624

Molecular Interaction Atlas of This Drug


Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Sodium channel unspecific (NaC) TTRK8B9 NOUNIPROTAC Blocker [3]
Voltage-gated sodium channel (Nav) TTIG65Q NOUNIPROTAC Inhibitor [4]
Voltage-gated sodium channel alpha Nav1.9 (SCN11A) TTN9VTF SCNBA_HUMAN Inhibitor [4]

Drug-Metabolizing Enzyme (DME)
DME Name DME ID UniProt ID MOA REF
UDP-glucuronosyltransferase 1A1 (UGT1A1)
Main DME
DEYGVN4 UD11_HUMAN Substrate [5]
Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This Drug

Drug-Drug Interaction (DDI) Information of This Drug

Coadministration of a Drug Treating the Disease Different from Eslicarbazepine (Comorbidity)
DDI Drug Name DDI Drug ID Severity Mechanism Comorbidity REF
Oliceridine DM6MDCF Major Increased metabolism of Eslicarbazepine caused by Oliceridine mediated induction of CYP450 enzyme. Acute pain [MG31] [36]
Ripretinib DM958QB Moderate Increased metabolism of Eslicarbazepine caused by Ripretinib mediated induction of CYP450 enzyme. Gastrointestinal stromal tumour [2B5B] [36]
Avapritinib DMK2GZX Moderate Increased metabolism of Eslicarbazepine caused by Avapritinib mediated induction of CYP450 enzyme. Gastrointestinal stromal tumour [2B5B] [37]
Pemigatinib DM819JF Moderate Increased metabolism of Eslicarbazepine caused by Pemigatinib mediated induction of CYP450 enzyme. Liver cancer [2C12] [37]
Pralsetinib DMWU0I2 Moderate Increased metabolism of Eslicarbazepine caused by Pralsetinib mediated induction of CYP450 enzyme. Lung cancer [2C25] [38]
Selpercatinib DMZR15V Moderate Increased metabolism of Eslicarbazepine caused by Selpercatinib mediated induction of CYP450 enzyme. Lung cancer [2C25] [37]
Ubrogepant DM749I3 Moderate Increased metabolism of Eslicarbazepine caused by Ubrogepant mediated induction of CYP450 enzyme. Migraine [8A80] [39]
Upadacitinib DM32B5U Moderate Increased metabolism of Eslicarbazepine caused by Upadacitinib mediated induction of CYP450 enzyme. Rheumatoid arthritis [FA20] [40]
Larotrectinib DM26CQR Moderate Increased metabolism of Eslicarbazepine caused by Larotrectinib mediated induction of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [36]
⏷ Show the Full List of 9 DDI Information of This Drug

References

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