Propafenone

Propafenone

SCHEMBL1651012

CCCNCC(O)COc1ccccc1C(=O)CCc1ccccc1.[Cl-].[H+]

nearest known ligand 0.96

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRB1ADRB2SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9A

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ADRB2 known ✓ P07550 1/20 0.96
▸ ADRB1 known ✓ P08588 1/20 0.96
▸ SCN5A known ✓ Q14524 1/20 0.96
▸ ABCB1 P08183 17/20 0.96
▸ LMNA P02545 2/20 0.96
▸ CYP1A2 P05177 2/20 0.96
▸ CYP2D6 P10635 2/20 0.96
▸ CYP3A4 P08684 2/20 0.96
▸ KCNH2 Q12809 2/20 0.96
▸ TSHR P16473 2/20 0.96
▸ KCNK3 O14649 1/20 0.96
▸ SLC22A1 O15245 1/20 0.96
▸ ABCC9 O60706 1/20 0.96
▸ KCNK2 O95069 1/20 0.96
▸ ABCB11 O95342 1/20 0.96
▸ ADRB3 P13945 1/20 0.96
▸ ADRA2C P18825 1/20 0.96
▸ SLC6A2 P23975 1/20 0.96
▸ HTR2A P28223 1/20 0.96
▸ HTR2C P28335 1/20 0.96

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
Propafenone SCHEMBL41413 0.98 ABCB1 (1.00) ABCB1LMNACYP1A2CYP2D6CYP3A4
Propafenone SCHEMBL27865 0.98 ABCB1 (1.00) ABCB1LMNACYP1A2CYP2D6CYP3A4
Propafenone SCHEMBL16730120 0.98 ABCB1 (1.00) ABCB1LMNACYP1A2CYP2D6CYP3A4
Propafenone SCHEMBL30416841 0.98 ABCB1 (1.00) ABCB1LMNACYP1A2CYP2D6CYP3A4
Propafenone SCHEMBL5529275 0.97 MEN1 (1.00) ABCB1LMNACYP1A2CYP2D6CYP3A4
Propafenone SCHEMBL41412 0.97 MEN1 (1.00) ABCB1LMNACYP1A2CYP2D6CYP3A4
Propafenone SCHEMBL29384899 0.97 MEN1 (1.00) ABCB1LMNACYP1A2CYP2D6CYP3A4
SCHEMBL29419081 0.92 ABCB1 (0.88) ABCB1LMNACYP1A2CYP2D6CYP3A4
Propafenone SCHEMBL15539494 0.89 ABCB1 (0.83) ABCB1LMNACYP1A2CYP2D6CYP3A4
Propafenone SCHEMBL924632 0.87 ABCB1 (0.79) ABCB1LMNACYP1A2CYP2D6CYP3A4

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 19 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4656189-A1 COMPOUND AND USE THEREOF Benethera (Shaoxing) Biotechnology Co., Ltd. (CN) 2025-12-03 — — EP disclosed
US-20210393645-A1 TREATMENT FOR PROGRESSIVE MULTIPLE SCLEROSIS UTI LIMITED PARTNERSHIP (CA) 2021-12-23 — — US disclosed
US-20190336490-A1 COMPOSITIONS AND METHODS FOR INCREASING REMYELINATION Frequency Therapeutics, Inc. 2019-11-07 — — US disclosed
US-20190262353-A1 TREATMENT FOR PROGRESSIVE MULTIPLE SCLEROSIS UTI LIMITED PARTNERSHIP (CA) 2019-08-29 — — US disclosed
EP-2576778-B1 TRANSGENIC REPORTER SYSTEM THAT REVEALS EXPRESSION PROFILES AND REGULATION MECHANISMS OF ALTERNATIVE SPLICING IN RODENTS UNIV KYOTO (JP) 2017-08-09 — — EP disclosed
US-9273364-B2 Transgenic reporter system that reveals expression profiles and regulation mechanisms of alternative splicing in mammalian organisms KYOTO UNIVERSITY (JP) 2016-03-01 — — US disclosed
US-20140221286-A1 SODIUM CHANNEL BLOCKERS REDUCE GLUCAGON SECRETION GILEAD SCIENCES, INC. 2014-08-07 — — US disclosed
EP-2758053-A1 SODIUM CHANNEL BLOCKERS REDUCE GLUCAGON SECRETION Gilead Sciences, Inc. (US) 2014-07-30 — — EP disclosed
US-20130137099-A1 TRANSGENIC REPORTER SYSTEM THAT REVEALS EXPRESSION PROFILES AND REGULATION MECHANISMS OF ALTERNATIVE SPLICING IN MAMMALIAN ORGANISMS KYOTO UNIVERSITY (JP) 2013-05-30 — — US disclosed
WO-2013043925-A1 SODIUM CHANNEL BLOCKERS REDUCE GLUCAGON SECRETION GILEAD SCIENCES, INC. (US) 2013-03-28 — — WO disclosed
US-7927613-B2 Pharmaceutical co-crystal compositions UNIVERSITY OF SOUTH FLORIDA (US) 2011-04-19 — — US disclosed
EP-1817427-B1 METHOD FOR DETERMINING GENOTOXICITY HOFFMANN LA ROCHE (CH) 2010-09-08 — — EP disclosed
US-7790905-B2 Pharmaceutical propylene glycol solvate compositions MCNEIL-PPC, INC. (US) 2010-09-07 — — US disclosed
US-7745152-B2 Method for determining genotoxicity ROCHE PALO ALTO LLC (US) 2010-06-29 — — US disclosed
EP-2021502-A1 NOVEL GENES AND MARKERS IN TYPE 2 DIABETES AND OBESITY Oy Jurilab Ltd (FI) 2009-02-11 — — EP disclosed
WO-2007128884-A1 NOVEL GENES AND MARKERS IN TYPE 2 DIABETES AND OBESITY OY JURILAB LTD (FI) 2007-11-15 — — WO disclosed
CN-101065501-A Method for determining genotoxicity HOFFMANN LA ROCHE (CH) 2007-10-31 — — CN disclosed
US-20060110768-A1 Method for determining genotoxicity ROCHE PALO ALTO LLC 2006-05-25 — — US disclosed
EP-1239280-A2 ElogDoct:A tool for lipophilicity determination in drug discovery basic and neutral compounds Pfizer Products Inc. (US) 2002-09-11 — — EP 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 (1 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-20140221286-A1 SODIUM CHANNEL BLOCKERS REDUCE GLUCAGON SECRETION IAPP, SCNN1B, GLP1R ADRB2 137/4885ADRB1 95/4885SCN5A 24/4885

“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.

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