Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C18H19FN2O2.ClH |
Molecular Weight | 350.815 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.NC(=O)[C@@H]1CC[C@@H](N1)C2=CC=C(OCC3=CC=CC=C3F)C=C2
InChI
InChIKey=HEPUBAGOKRIZEO-PPPUBMIESA-N
InChI=1S/C18H19FN2O2.ClH/c19-15-4-2-1-3-13(15)11-23-14-7-5-12(6-8-14)16-9-10-17(21-16)18(20)22;/h1-8,16-17,21H,9-11H2,(H2,20,22);1H/t16-,17+;/m1./s1
Raxatrigine also known as GSK1014802 and CNV-1014802, is a novel analgesic under development by Convergence Pharmaceuticals for the treatment of lumbosacral radiculopathy (sciatica) and trigeminal neuralgia (TGN). It is a novel state dependent small molecule sodium channel blocker that preferentially inhibits the Nav 1.7 ion channel, a therapeutic target implicated by genetics in human pain conditions. Raxatrigine is thought to penetrate the central nervous system and block Nav channels in a novel manner. CNV1014802 was granted orphan drug designation in 2013 by the US Food and Drug Administration (FDA) for the treatment of trigeminal neuralgia.
CNS Activity
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: CHEMBL4296 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26646477 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Palliative | Unknown Approved UseUnknown |
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Palliative | Unknown Approved UseUnknown |
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Palliative | Unknown Approved UseUnknown |
Cmax
Value | Dose | Co-administered | Analyte | Population |
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4410 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/30144099 |
400 mg 2 times / day steady-state, oral dose: 400 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
RAXATRIGINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
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3780 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/30144099 |
400 mg single, oral dose: 400 mg route of administration: Oral experiment type: SINGLE co-administered: |
RAXATRIGINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: FASTED |
AUC
Value | Dose | Co-administered | Analyte | Population |
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60100 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/30144099 |
400 mg 2 times / day steady-state, oral dose: 400 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
RAXATRIGINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
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38700 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/30144099 |
400 mg single, oral dose: 400 mg route of administration: Oral experiment type: SINGLE co-administered: |
RAXATRIGINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: FASTED |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
8.91 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/30144099 |
400 mg single, oral dose: 400 mg route of administration: Oral experiment type: SINGLE co-administered: |
RAXATRIGINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: FASTED |
Overview
CYP3A4 | CYP2C9 | CYP2D6 | hERG |
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OverviewOther
Other Inhibitor | Other Substrate | Other Inducer |
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Drug as perpetrator
Target | Modality | Activity | Metabolite | Clinical evidence |
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no [IC50 >100 uM] | ||||
no [IC50 >100 uM] | ||||
no [IC50 >100 uM] | ||||
no [IC50 >100 uM] | ||||
no [IC50 >100 uM] | ||||
no [Inhibition 100 uM] | ||||
no | ||||
no | ||||
no | ||||
no | ||||
no | ||||
weak [IC50 79 uM] | ||||
yes [IC50 13 uM] | ||||
yes [IC50 31 uM] |
Drug as victim
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
major | yes (co-administration study) Comment: Carbamazepine decreased AUCtau and Cmax by 31.6% and 26.3%. |
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minor | ||||
minor | (co-administration study) Sources: https://pubmed.ncbi.nlm.nih.gov/32564301/ |
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yes | ||||
yes | yes (co-administration study) Comment: Carbamazepine decreased AUCtau and Cmax by 31.6% and 26.3%. Sources: https://pubmed.ncbi.nlm.nih.gov/31650711/ |
Tox targets
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C241
Created by
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FDA ORPHAN DRUG |
401613
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admin on Fri Dec 15 18:07:40 GMT 2023 , Edited by admin on Fri Dec 15 18:07:40 GMT 2023
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FDA ORPHAN DRUG |
553016
Created by
admin on Fri Dec 15 18:07:40 GMT 2023 , Edited by admin on Fri Dec 15 18:07:40 GMT 2023
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Code System | Code | Type | Description | ||
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CHEMBL3544913
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16046067
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DBSALT002054
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300000042438
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934240-31-0
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7L3OLR4M8T
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C152900
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CD-37
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ACTIVE MOIETY
SUBSTANCE RECORD