SCHEMBL49654

SCHEMBL49654

N=C(N)c1cccc2ccccc12

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NR4A1 P22736 1/20 0.56
NR4A2 P43354 1/20 0.56
NR4A3 Q92570 1/20 0.56
MMP3 P08254 1/20 0.50
HDAC8 Q9BY41 1/20 0.50
PTPN1 P18031 1/20 0.48
CDC25B P30305 1/20 0.48
PLK1 P53350 1/20 0.48
PTK2B Q14289 1/20 0.47
L3MBTL1 Q9Y468 1/20 0.47
ALDH1A1 P00352 3/20 0.46
HPGD P15428 2/20 0.46
CYP1A2 P05177 2/20 0.46
CYP3A4 P08684 2/20 0.46
TSHR P16473 2/20 0.46
HSD17B10 Q99714 2/20 0.46
KEAP1 Q14145 1/20 0.46
KDM4E B2RXH2 3/20 0.45
GAA P10253 2/20 0.45
POLB P06746 1/20 0.44

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
SCHEMBL29393451 1.00 NR4A1 (0.56) NR4A1NR4A2NR4A3MMP3HDAC8
Hydrochloric Acid SCHEMBL5847290 0.98 NR4A1 (0.54) NR4A1NR4A2NR4A3MMP3HDAC8
SCHEMBL6956577 0.83 NR4A1 (0.44) NR4A1NR4A2NR4A3MMP3HDAC8
Hydrochloric Acid SCHEMBL28498400 0.81 NR4A1 (0.42) NR4A1NR4A2NR4A3MMP3HDAC8
SCHEMBL3233191 0.80 NR4A1 (0.50) NR4A1NR4A2NR4A3MMP3HDAC8
SCHEMBL23709157 0.80 NR4A1 (0.60) NR4A1NR4A2NR4A3MMP3HDAC8
SCHEMBL29381201 0.79 KDM4E (0.68) NR4A1NR4A2NR4A3MMP3HDAC8
SCHEMBL30627985 0.79 L3MBTL1 (0.55) NR4A1NR4A2NR4A3MMP3HDAC8
SCHEMBL28596381 0.79 NR4A1 (0.54) NR4A1NR4A2NR4A3MMP3HDAC8
SCHEMBL30849325 0.79 NR4A1 (0.54) NR4A1NR4A2NR4A3MMP3HDAC8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1907484-B1 NAPHTHALENE AMIDINE IMIDES BASF SE (DE) 2010-09-29 EP claimed
EP-1907484-A1 NAPHTHALENE AMIDINE IMIDES Ciba Specialty Chemicals Holding, Inc. (CH) 2008-04-09 EP claimed
CN-1972681-A Systems and methods for transdermal delivery of anticoagulants ALZA CORP (US) 2007-05-30 CN claimed
EP-1758568-A1 SYSTEM AND METHOD FOR TRANSDERMAL DELIVERY OF AN ANTICOAGULANT Alza Corporation (US) 2007-03-07 EP claimed
WO-2007012611-A1 NAPHTHALENE AMIDINE IMIDES CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2007-02-01 WO claimed
WO-2005120482-A1 SYSTEM AND METHOD FOR TRANSDERMAL DELIVERY OF AN ANTICOAGULANT ALZA CORPORATION (US) 2005-12-22 WO claimed
US-20050273047-A1 System and method for transdermal delivery of an anticoagulant ALZA CORPORATION 2005-12-08 US claimed
EP-1276722-A1 NAPHTHAMIDINE UROKINASE INHIBITORS Abbott Laboratories (US) 2003-01-22 EP claimed
WO-2001081314-A1 NAPHTHAMIDINE UROKINASE INHIBITORS ABBOTT LABORATORIES (US) 2001-11-01 WO claimed
US-20250188022-A1 PROCESS FOR THE PREPARATION OF NAFAMOSTAT, CAMOSTAT AND THEIR DERIVATIVES COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2025-06-12 US disclosed
US-20240165106-A1 POLYSUBUNIT OPIOID PRODRUGS RESISTANT TO OVERDOSE AND ABUSE ELYSIUM THERAPEUTICS, INC. 2024-05-23 US disclosed
US-11976051-B1 N′-(2-(5-(4-chlorophenyl)-1,3,4-oxadiazol-2-ylthio)acetoxy)-2-naphthimidamide as an antimicrobial compound King Faisal University (SA) 2024-05-07 US disclosed
US-11905262-B1 N′-(2-(5-(4-chlorophenyl)-1,3,4-oxadiazol-2-ylthio)acetoxy)-2-naphthimidamide as an antimicrobial compound King Faisal University (SA) 2024-02-20 US disclosed
US-20230241054-A1 POLYSUBUNIT OPIOID PRODRUGS RESISTANT TO OVERDOSE AND ABUSE ELYSIUM THERAPEUTICS, INC. 2023-08-03 US disclosed
EP-0574545-A1 PHENYL AMIDINES DERIVATIVES USEFUL AS PLATELET AGGREGATION INHIBITORS. SEARLE & CO (US) 1993-12-22 EP disclosed
WO-1992015607-A2 PHENYL AMIDINES DERIVATIVES USEFUL AS PLATELET AGGREGATION INHIBITORS G.D. SEARLE & CO. (US) 1992-09-17 WO disclosed
EP-0343893-B1 AROMATIC AND HETEROCYCLIC CARBOXAMIDE DERIVATIVES AS ANTINEOPLASTIC AGENTS PFIZER INC. (US) 1992-08-05 EP disclosed
US-4970318-A ANTICARBINOGENIC AGENTS PFIZER INC. (US) 1990-11-13 US disclosed
CN-1037898-A The preparation of aromatics and Heterocyclylcarboxamderivatives derivatives antineoplastic agent PFIZER (US) 1989-12-13 CN disclosed
EP-0343893-A1 Aromatic and heterocyclic carboxamide derivatives as antineoplastic agents PFIZER INC. (US) 1989-11-29 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 (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-20240165106-A1 POLYSUBUNIT OPIOID PRODRUGS RESISTANT TO OVERDOSE AND ABUSE OPRK1, OPRM1, CYP3A5 NR4A1 4550/4885NR4A2 4724/4885NR4A3 4539/4885
US-11905262-B1 N′-(2-(5-(4-chlorophenyl)-1,3,4-oxadiazol-2-ylthio)acetoxy)-2-naphthimidamide as an antimicrobial compound NIT2, NOC2L, B3GNT2 NR4A1 493/4885NR4A2 408/4885NR4A3 716/4885
US-20250188022-A1 PROCESS FOR THE PREPARATION OF NAFAMOSTAT, CAMOSTAT AND THEIR DERIVATIVES TPMT, ADH1C, ADH1A NR4A1 1829/4885NR4A2 2160/4885NR4A3 2374/4885
US-11976051-B1 N′-(2-(5-(4-chlorophenyl)-1,3,4-oxadiazol-2-ylthio)acetoxy)-2-naphthimidamide as an antimicrobial compound NIT2, NOC2L, B3GNT2 NR4A1 581/4885NR4A2 460/4885NR4A3 795/4885
US-20230241054-A1 POLYSUBUNIT OPIOID PRODRUGS RESISTANT TO OVERDOSE AND ABUSE OPRK1, OPRM1, CYP3A5 NR4A1 4550/4885NR4A2 4724/4885NR4A3 4539/4885

“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.