Vixotrigine

Vixotrigine

SCHEMBL312349

Cl.NC(=O)[C@@H]1CC[C@H](c2ccc(OCc3ccccc3F)cc2)N1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SCN9A

The experimentally established mechanism targets of Vixotrigine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
SCN9A known ✓ Q15858 1/20 0.98
KCNH2 Q12809 18/20 1.00
SCN3A Q9NY46 10/20 1.00
CYP1A2 P05177 1/20 1.00
CYP2B6 P20813 1/20 1.00
MAOB P27338 1/20 1.00
CYP2C19 P33261 1/20 1.00
SCN1A P35498 1/20 0.98
SCN4A P35499 1/20 0.98
SCN7A Q01118 1/20 0.98
SCN5A Q14524 1/20 0.98
SCN2A Q99250 1/20 0.98
SCN8A Q9UQD0 1/20 0.98
SCN10A Q9Y5Y9 1/20 0.98

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Vixotrigine SCHEMBL840484 1.00 KCNH2 (1.00) KCNH2SCN3ACYP1A2CYP2B6MAOB
Vixotrigine SCHEMBL841096 1.00 KCNH2 (1.00) KCNH2SCN3ACYP1A2CYP2B6MAOB
Vixotrigine SCHEMBL20562288 1.00 KCNH2 (1.00) KCNH2SCN3ACYP1A2CYP2B6MAOB
Vixotrigine SCHEMBL29388010 1.00 KCNH2 (1.00) KCNH2SCN3ACYP1A2CYP2B6MAOB
Vixotrigine SCHEMBL840179 1.00 KCNH2 (1.00) KCNH2SCN3ACYP1A2CYP2B6MAOB
Vixotrigine SCHEMBL4446697 1.00 KCNH2 (1.00) KCNH2SCN3ACYP1A2CYP2B6MAOB
Vixotrigine SCHEMBL2831660 0.99 KCNH2 (1.00) KCNH2SCN3ACYP1A2CYP2B6MAOB
Vixotrigine SCHEMBL862301 0.99 KCNH2 (1.00) KCNH2SCN3ACYP1A2CYP2B6MAOB
Vixotrigine SCHEMBL311438 0.99 KCNH2 (1.00) KCNH2SCN3ACYP1A2CYP2B6MAOB
Vixotrigine SCHEMBL311437 0.99 KCNH2 (1.00) KCNH2SCN3ACYP1A2CYP2B6MAOB

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 90 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112812048-B Preparation method of sodium ion channel retarder CNV1014802 hydrochloride form 北京蓝博特科技有限公司 2022-08-26 CN claimed
US-20220098150-A1 Novel Crystalline Forms BIOGEN MA INC. 2022-03-31 US claimed
US-20200147041-A1 PAROXYSMAL EXTREME PAIN DISORDER TREATMENT Convergence Pharmaceuticals Limited (GB) 2020-05-14 US claimed
CN-110913852-A Novel crystalline forms 生物基因麻省公司 2020-03-24 CN claimed
US-20200062705-A1 NOVEL CRYSTALLINE FORMS BIOGEN INC. 2020-02-27 US claimed
EP-3200783-B1 ERYTHROMELALGIA TREATMENT CONVERGENCE PHARMACEUTICALS (GB) 2019-07-31 EP claimed
EP-3200785-B1 PAROXYSMAL EXTREME PAIN DISORDER TREATMENT CONVERGENCE PHARMACEUTICALS (GB) 2019-07-31 EP claimed
EP-3200784-B1 SMALL FIBRE NEUROPATHY TREATMENT CONVERGENCE PHARMACEUTICALS (GB) 2019-07-31 EP claimed
US-20170304264-A1 Novel Erythromelalgia Treatment Convergence Pharmaceuticals Limited (GB) 2017-10-26 US claimed
US-20170304265-A1 Paroxysmal Extreme Pain Disorder Treatment Convergence Pharmaceuticals Limited (GB) 2017-10-26 US claimed
US-8153681-B2 Method of treating epilepsy by administering 5-(4{[(2-fluorophenyl)methyl]oxy}phenyl)prolinamide Convergence Pharmaceuticals Limited (GB) 2012-04-10 US claimed
US-8143306-B2 Methods of treating bipolar disorders Convergence Pharmaceuticals Limited (GB) 2012-03-27 US claimed
US-20110098335-A1 NOVEL COMPOUNDS Convergence Pharmaceuticals Limited (GB) 2011-04-28 US claimed
US-20100105754-A1 5-(4PHENYL)PROLINAMIDE FOR TREATMENT OF EPILEPSY GLAXO GROUP LIMITED (GB) 2010-04-29 US claimed
US-7655693-B2 Compounds GLAXO GROUP LIMITED (GB) 2010-02-02 US claimed
US-20080280969-A1 Novel Compounds GLAXO GROUP LIMITED 2008-11-13 US claimed
EP-1943216-A1 PROLINAMIDE DERIVATIVES AS SODIUM CHANNEL MODULATORS GLAXO GROUP LIMITED (GB) 2008-07-16 EP claimed
EP-1934177-A1 PROLINAMIDE DERIVATIVES AS SODIUM CHANNEL MODULATORS GLAXO GROUP LIMITED (GB) 2008-06-25 EP claimed
WO-2007042239-A1 PROLINAMIDE DERIVATIVES AS SODIUM CHANNEL MODULATORS GLAXO GROUP LIMITED (GB) 2007-04-19 WO claimed
WO-2007042250-A1 PROLINAMIDE DERIVATIVES AS SODIUM CHANNEL MODULATORS GLAXO GROUP LIMITED (GB) 2007-04-19 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (8 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20220098150-A1 Novel Crystalline Forms SCN5A, HCN4, SCN4A SCN9A 11/4885KCNH2 20/4885SCN3A 7/4885
US-20110098335-A1 NOVEL COMPOUNDS SCN1A, SCN1B, SCNN1B SCN9A 35/4885KCNH2 65/4885SCN3A 8/4885
US-20200062705-A1 NOVEL CRYSTALLINE FORMS SCN5A, KCNQ5, HCN4 SCN9A 11/4885KCNH2 23/4885SCN3A 5/4885
US-20170304265-A1 Paroxysmal Extreme Pain Disorder Treatment PEPD, FAP, PREP SCN9A 75/4885KCNH2 348/4885SCN3A 17/4885
US-20080280969-A1 Novel Compounds CYP11B2, CYP46A1, SLC10A1 SCN9A 1889/4885KCNH2 1998/4885SCN3A 2634/4885
US-20100105754-A1 5-(4PHENYL)PROLINAMIDE FOR TREATMENT OF EPILEPSY SCN5A, SCN1A, SCN7A SCN9A 14/4885KCNH2 58/4885SCN3A 6/4885
US-20170304264-A1 Novel Erythromelalgia Treatment TYR, PAH, EGLN3 SCN9A 1753/4885KCNH2 3226/4885SCN3A 1019/4885
US-20200147041-A1 PAROXYSMAL EXTREME PAIN DISORDER TREATMENT PEPD, FAP, PREP SCN9A 75/4885KCNH2 348/4885SCN3A 17/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.