Vixotrigine

Vixotrigine

SCHEMBL311438

NC(=O)[C@@H]1CCC(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 1.00
KCNH2 Q12809 18/20 1.00
SCN3A Q9NY46 10/20 1.00
SCN1A P35498 1/20 1.00
SCN4A P35499 1/20 1.00
SCN7A Q01118 1/20 1.00
SCN5A Q14524 1/20 1.00
SCN2A Q99250 1/20 1.00
SCN8A Q9UQD0 1/20 1.00
SCN10A Q9Y5Y9 1/20 1.00
CYP1A2 P05177 1/20 0.98
CYP2B6 P20813 1/20 0.98
MAOB P27338 1/20 0.98
CYP2C19 P33261 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 SCHEMBL311437 1.00 KCNH2 (1.00) KCNH2SCN3ASCN1ASCN4ASCN7A
Vixotrigine SCHEMBL310473 1.00 KCNH2 (1.00) KCNH2SCN3ASCN1ASCN4ASCN7A
Vixotrigine SCHEMBL862301 1.00 KCNH2 (1.00) KCNH2SCN3ASCN1ASCN4ASCN7A
Vixotrigine SCHEMBL29385387 1.00 KCNH2 (1.00) KCNH2SCN3ASCN1ASCN4ASCN7A
Vixotrigine SCHEMBL840590 1.00 KCNH2 (1.00) KCNH2SCN3ASCN1ASCN4ASCN7A
Vixotrigine SCHEMBL2831660 1.00 KCNH2 (1.00) KCNH2SCN3ASCN1ASCN4ASCN7A
Vixotrigine SCHEMBL862457 1.00 KCNH2 (1.00) KCNH2SCN3ASCN1ASCN4ASCN7A
Vixotrigine SCHEMBL840179 0.99 KCNH2 (1.00) KCNH2SCN3ASCN1ASCN4ASCN7A
Vixotrigine SCHEMBL20562288 0.99 KCNH2 (1.00) KCNH2SCN3ASCN1ASCN4ASCN7A
Vixotrigine SCHEMBL4446697 0.99 KCNH2 (1.00) KCNH2SCN3ASCN1ASCN4ASCN7A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3781157-A1 METHODS OF TREATING NEUROPATHIC PAIN Biogen MA Inc. (US) 2021-02-24 EP claimed
WO-2019204136-A1 METHODS OF TREATING NEUROPATHIC PAIN BIOGEN MA INC. (US) 2019-10-24 WO claimed
EP-1934177-B8 PROLINAMIDE DERIVATIVES AS SODIUM CHANNEL MODULATORS CONVERGENCE PHARMACEUTICALS (GB) 2012-09-05 EP claimed
EP-1934177-B1 PROLINAMIDE DERIVATIVES AS SODIUM CHANNEL MODULATORS GLAXO GROUP LTD (GB) 2012-05-02 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
US-11192856-B2 Process for preparing alpha-carboxamide pyrrolidine derivatives BIOGEN INC. (US) 2021-12-07 US disclosed
EP-3781157-A1 METHODS OF TREATING NEUROPATHIC PAIN Biogen MA Inc. (US) 2021-02-24 EP disclosed
US-20200270206-A1 PROCESS FOR PREPARING ALPHA-CARBOXAMIDE PYRROLIDINE DERIVATIVES BIOGEN INC. 2020-08-27 US disclosed
US-20200147041-A1 PAROXYSMAL EXTREME PAIN DISORDER TREATMENT Convergence Pharmaceuticals Limited (GB) 2020-05-14 US disclosed
US-20200147041-A1 PAROXYSMAL EXTREME PAIN DISORDER TREATMENT Convergence Pharmaceuticals Limited (GB) 2020-05-14 US disclosed
EP-3634400-A1 NOVEL CRYSTALLINE FORMS Biogen MA Inc. (US) 2020-04-15 EP disclosed
US-20200062705-A1 NOVEL CRYSTALLINE FORMS BIOGEN INC. 2020-02-27 US disclosed
EP-2117538-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING 2-METHOXY-5- (5-TRIFLUOROMETHYL-TETRAZOL-I-YL-BENZYL) - (2S-PHENYL-PIPERIDIN-3S-YL-) Glaxo Group Limited (GB) 2009-11-18 EP disclosed
US-20080280969-A1 Novel Compounds GLAXO GROUP LIMITED 2008-11-13 US disclosed
WO-2008090116-A1 NOVEL PHARMACEUTICAL COMPOSITIONS GLAXO GROUP LIMITED (GB) 2008-07-31 WO disclosed
WO-2008090117-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING 3, 5-DIAMIN0-6- (2, 3-DICHL0PHENYL) -L, 2, 4-TRIAZINE OR R (-) -2, 4-DIAMINO-5- (2, 3-DICHLOROPHENYL) -6-FLUOROMETHYL PYRIMIDINE AND AN NK1 GLAXO GROUP LIMITED (GB) 2008-07-31 WO disclosed
WO-2008090114-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING 2-METHOXY-5- (5-TRIFLUOROMETHYL-TETRAZOL-I-YL-BENZYL) - (2S-PHENYL-PIPERIDIN-3S-YL-) GLAXO GROUP LIMITED (GB) 2008-07-31 WO disclosed
EP-1934177-A1 PROLINAMIDE DERIVATIVES AS SODIUM CHANNEL MODULATORS GLAXO GROUP LIMITED (GB) 2008-06-25 EP disclosed
WO-2007042239-A1 PROLINAMIDE DERIVATIVES AS SODIUM CHANNEL MODULATORS GLAXO GROUP LIMITED (GB) 2007-04-19 WO disclosed

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

For each of this compound's patents that has machine-readable text (5 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-20200270206-A1 PROCESS FOR PREPARING ALPHA-CARBOXAMIDE PYRROLIDINE DERIVATIVES CPS1, ALDH18A1, PCCA SCN9A 2462/4885KCNH2 896/4885SCN3A 2812/4885
US-11192856-B2 Process for preparing alpha-carboxamide pyrrolidine derivatives CPS1, ALDH18A1, PCCA SCN9A 2462/4885KCNH2 896/4885SCN3A 2812/4885
US-20200062705-A1 NOVEL CRYSTALLINE FORMS SCN5A, KCNQ5, HCN4 SCN9A 11/4885KCNH2 23/4885SCN3A 5/4885
US-20080280969-A1 Novel Compounds CYP11B2, CYP46A1, SLC10A1 SCN9A 1889/4885KCNH2 1998/4885SCN3A 2634/4885
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.