SCHEMBL348190

SCHEMBL348190

COC(=O)c1ccc2[nH]ncc2c1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 5/20 0.58
RAB9A P51151 5/20 0.58
CTNNB1 P35222 3/20 0.57
WNT3A P56704 3/20 0.57
MAOB P27338 8/20 0.55
MAOA P21397 2/20 0.55
ROCK2 O75116 3/20 0.55
ROCK1 Q13464 3/20 0.55
PRKD3 O94806 1/20 0.51
MAP4K4 O95819 1/20 0.51
RPS6KB1 P23443 1/20 0.51
CLK2 P49760 1/20 0.51
DYRK1A Q13627 1/20 0.51
PRKG1 Q13976 1/20 0.51
PRKD2 Q9BZL6 1/20 0.51
CLK4 Q9HAZ1 1/20 0.51
SGK2 Q9HBY8 1/20 0.51
STK17A Q9UEE5 1/20 0.51
MEN1 O00255 1/20 0.51
KMT2A Q03164 1/20 0.51

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
SCHEMBL29643714 1.00 NPC1 (0.58) NPC1RAB9ACTNNB1WNT3AMAOB
SCHEMBL23063836 0.88 GSK3B (0.56) NPC1RAB9ACTNNB1WNT3AMAOB
SCHEMBL29643878 0.87 MAOB (0.55) NPC1RAB9AMAOBMAP4K4CLK2
SCHEMBL347171 0.87 MAOB (0.55) NPC1RAB9AMAOBMAP4K4CLK2
SCHEMBL28887308 0.86 MAOB (0.50) NPC1RAB9ACTNNB1WNT3AMAOB
SCHEMBL30074092 0.83 CTNNB1 (0.53) NPC1RAB9ACTNNB1WNT3AMAOB
SCHEMBL27836079 0.83 MAOB (0.58) NPC1RAB9ACTNNB1WNT3AMAOB
SCHEMBL145658 0.83 CTNNB1 (0.60) NPC1RAB9ACTNNB1WNT3AMEN1
SCHEMBL29925697 0.83 CTNNB1 (0.60) NPC1RAB9ACTNNB1WNT3AMEN1
SCHEMBL27836080 0.83 CTNNB1 (0.53) NPC1RAB9ACTNNB1WNT3AMAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112573978-B High-efficiency halogenation synthesis method of aryl halide 北京大学 2022-05-13 CN claimed
CN-112573978-A High-efficiency halogenation synthesis method of aryl halide 北京大学 2021-03-30 CN claimed
EP-1628972-B1 INDAZOLE-DERIVATIVES AS FACTOR Xa INHIBITORS SANOFI AVENTIS DEUTSCHLAND (DE) 2009-04-22 EP claimed
US-12612412-B2 Antiviral heterocyclic compounds ENANTA PHARMACEUTICALS, INC. (US) 2026-04-28 US disclosed
US-12606533-B2 3-phenylpropylamine derivative DAIICHI SANKYO COMPANY, LIMITED (JP) 2026-04-21 US disclosed
WO-2025262295-A1 PROTAC DEGRADERS OF MLLT1 AND/OR MLLT3 DARK BLUE THERAPEUTICS LTD (GB) 2025-12-26 WO disclosed
EP-4667466-A1 PROTAC DEGRADERS OF MLLT1 AND/OR MLLT3 Dark Blue Therapeutics Ltd (GB) 2025-12-24 EP disclosed
US-12485109-B2 Pyrrolo 12.3-dipyrimidine compounds and analogues thereof BIOCRYST PHARMACEUTICALS, INC. (US) 2025-12-02 US disclosed
US-20250353824-A1 3-PHENYLPROPYLAMINE DERIVATIVE DAIICHI SANKYO COMPANY, LIMITED (JP) 2025-11-20 US disclosed
US-20250346600-A1 TRICYCLIC DERIVATIVES AND RELATED USES MOMA THERAPEUTICS, INC. 2025-11-13 US disclosed
EP-4610260-A1 ARYL HETEROCYCLIC KV1.3 INHIBITOR, PREPARATION METHOD THEREFOR, AND USE THEREOF Shanghai Shenshi Wise Technology Co., Ltd. (CN) 2025-09-03 EP disclosed
WO-2004101556-A1 INDAZOLE-DERIVATIVES AS FACTOR Xa INHIBITORS SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2004-11-25 WO disclosed
EP-1479675-A1 Indazole-derivatives as factor Xa inhibitors Aventis Pharma Deutschland GmbH (DE) 2004-11-24 EP disclosed
EP-1438308-A1 N-AZABICYCLO-SUBSTITUTED HETERO-BICYCLIC CARBOXAMIDES AS NACHR AGONISTS PHARMACIA & UPJOHN COMPANY (US) 2004-07-21 EP disclosed
US-20040138286-A1 Rho kinase inhibitors DAINIPPON SUMITOMO PHARMA CO., LTD. (JP) 2004-07-15 US disclosed
US-20040127538-A1 Novel 1h-indazole compound EISAI R&D MANAGEMENT CO., LTD. (JP) 2004-07-01 US disclosed
EP-1403255-A1 Rho KINASE INHIBITORS SUMITOMO PHARMACEUTICALS COMPANY, LIMITED (JP) 2004-03-31 EP disclosed
EP-1380576-A1 NOVEL 1H-INDAZOLE COMPOUND Eisai Co., Ltd. (JP) 2004-01-14 EP disclosed
US-20030176702-A1 N-(azabicyclo moieties)-substituted hetero-bicyclic aromatic compounds for the treatment of disease PHARMACIA & UPJOHN COMPANY 2003-09-18 US disclosed
WO-2003037896-A1 N-AZABICYCLO-SUBSTITUTED HETERO-BICYCLIC CARBOXAMIDES AS NACHR AGONISTS PHARMACIA & UPJOHN COMPANY (US) 2003-05-08 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 (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-12485109-B2 Pyrrolo 12.3-dipyrimidine compounds and analogues thereof C5, DPYD, C9 NPC1 2033/4885RAB9A 3313/4885CTNNB1 4466/4885
US-20250353824-A1 3-PHENYLPROPYLAMINE DERIVATIVE SF1, SF3A1, SFXN1 NPC1 2279/4885RAB9A 4417/4885CTNNB1 1727/4885
US-20030176702-A1 N-(azabicyclo moieties)-substituted hetero-bicyclic aromatic compounds for the treatment of disease CYP1B1, ABCB1, NAT1 NPC1 220/4885RAB9A 1422/4885CTNNB1 819/4885
US-20040127538-A1 Novel 1h-indazole compound MAPK1, MAPK14, MAPK3 NPC1 1171/4885RAB9A 2697/4885CTNNB1 425/4885
US-20040138286-A1 Rho kinase inhibitors ROCK1, ROCK2, ARHGDIA NPC1 837/4885RAB9A 85/4885CTNNB1 2647/4885
US-12612412-B2 Antiviral heterocyclic compounds ZC3HAV1, NHERF1, HM13 NPC1 792/4885RAB9A 352/4885CTNNB1 442/4885
US-12606533-B2 3-phenylpropylamine derivative SF3A1, SF1, HTR1D NPC1 1729/4885RAB9A 4351/4885CTNNB1 789/4885
US-20250346600-A1 TRICYCLIC DERIVATIVES AND RELATED USES WRN, RECQL, BLM NPC1 2175/4885RAB9A 2157/4885CTNNB1 3556/4885

“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.