SCHEMBL170193

SCHEMBL170193

CCCCCNc1ncnc2ccccc12

nearest known ligand 0.97

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.97
SMN1; SMN2 Q16637 4/20 0.97
S1PR2 O95136 1/20 0.97
NPSR1 Q6W5P4 1/20 0.97
HTT P42858 5/20 0.69
KMT2A Q03164 3/20 0.69
MAPT P10636 2/20 0.69
KDM4E B2RXH2 1/20 0.69
GAA P10253 3/20 0.68
LDHA P00338 1/20 0.64
ALPG P10696 1/20 0.62
EGFR P00533 4/20 0.61
MAPK1 P28482 2/20 0.61
APP P05067 2/20 0.61
GALR3 O60755 2/20 0.56
NR2F2 P24468 2/20 0.56
RAB9A P51151 2/20 0.56
MEN1 O00255 2/20 0.55
TSHR P16473 1/20 0.55
ACP1 P24666 1/20 0.54

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
SCHEMBL31197370 0.98 LMNA (1.00) LMNASMN1; SMN2S1PR2NPSR1HTT
SCHEMBL15923566 0.98 LMNA (1.00) LMNASMN1; SMN2S1PR2NPSR1HTT
Hydrochloric Acid SCHEMBL8522254 0.98 SMN1; SMN2 (0.94) LMNASMN1; SMN2S1PR2NPSR1HTT
SCHEMBL15922842 0.98 LMNA (1.00) LMNASMN1; SMN2S1PR2NPSR1HTT
SCHEMBL11266817 0.91 LMNA (0.85) LMNASMN1; SMN2S1PR2NPSR1HTT
SCHEMBL15923281 0.91 SMN1; SMN2 (0.85) LMNASMN1; SMN2S1PR2NPSR1HTT
SCHEMBL11251521 0.91 SMN1; SMN2 (0.85) LMNASMN1; SMN2S1PR2NPSR1HTT
SCHEMBL11247766 0.91 SMN1; SMN2 (0.85) LMNASMN1; SMN2S1PR2NPSR1HTT
SCHEMBL11245701 0.91 LMNA (0.85) LMNASMN1; SMN2S1PR2NPSR1HTT
SCHEMBL15923231 0.89 SMN1; SMN2 (0.82) LMNASMN1; SMN2S1PR2NPSR1HTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8318932-B2 Process for producing 4-aminoquinazoline compound UBE INDUSTRIES, LTD. (JP) 2012-11-27 US claimed
EP-1481971-B1 PROCESS FOR PRODUCING 4-AMINOQUINAZOLINE COMPOUND UBE INDUSTRIES (JP) 2011-11-16 EP claimed
WO-2011131610-A1 HEAT TRANSFER MEDIUM BASED ON SULPHUR AND USE OF THE HEAT TRANSFER MEDIUM SIEMENS AKTIENGESELLSCHAFT (DE) 2011-10-27 WO claimed
US-20090171083-A1 PROCESS FOR PRODUCING 4-AMINOQUINAZOLINE COMPOUND UBE INDUSTRIES, LTD. (JP) 2009-07-02 US claimed
US-20050130995-A1 Chlorinating quinazolin-4-one in solvent in presence of a base; then reacting with an amine compound UBE INDUSTRIES, LTD. (JP) 2005-06-16 US claimed
EP-1481971-A1 PROCESS FOR PRODUCING 4-AMINOQUINAZOLINE COMPOUND Ube Industries, Ltd. (JP) 2004-12-01 EP claimed
EP-0954315-A2 USE OF QUINAZOLINE DERIVATIVES FOR THE MANUFACTURE OF A MEDICAMENT IN THE TREATMENT OF HYPERPROLIFERATIVE SKIN DISORDERS Sugen, Inc. (US) 1999-11-10 EP claimed
WO-1998010767-A9 USE OF QUINAZOLINE DERIVATIVES FOR THE MANUFACTURE OF A MEDICAMENT IN THE TREATMENT OF HYPERPROLIFERATIVE SKIN DISORDERS 1998-07-02 WO claimed
WO-1998010767-A2 USE OF QUINAZOLINE DERIVATIVES FOR THE MANUFACTURE OF A MEDICAMENT IN THE TREATMENT OF HYPERPROLIFERATIVE SKIN DISORDERS SUGEN, INC. (US) 1998-03-19 WO claimed
CN-111741954-B Novel benzimidazole compounds and derivatives as EGFR inhibitors 勃林格殷格翰国际有限公司 2024-04-02 CN disclosed
CN-114007698-B Macrocyclic compounds and derivatives as EGFR inhibitors 勃林格殷格翰国际有限公司 2024-01-09 CN disclosed
EP-4237423-A1 SUBSTITUTED 1H-PYRAZOLO[4,3-C]PYRIDINES AND DERIVATIVES AS EGFR INHIBITORS Boehringer Ingelheim International GmbH (DE) 2023-09-06 EP disclosed
CN-116507627-A Substituted 1H-pyrazolo [4,3-C ] pyridines and derivatives as EGFR inhibitors 勃林格殷格翰国际有限公司 2023-07-28 CN disclosed
EP-3755694-B1 NEW BENZIMIDAZOLE COMPOUNDS AND DERIVATIVES AS EGFR INHIBITORS BOEHRINGER INGELHEIM INT (DE) 2023-04-05 EP disclosed
EP-1147093-A1 SUBSTITUTED BICYCLIC DERIVATIVES USEFUL AS ANTICANCER AGENTS Pfizer Products Inc. (US) 2001-10-24 EP disclosed
US-6284764-B1 ANTIPROLIFERATIVE AGENT PFIZER INC. 2001-09-04 US disclosed
WO-2000044728-A1 SUBSTITUTED BICYCLIC DERIVATIVES USEFUL AS ANTICANCER AGENTS PFIZER PRODUCTS INC. (US) 2000-08-03 WO disclosed
EP-0954315-A2 USE OF QUINAZOLINE DERIVATIVES FOR THE MANUFACTURE OF A MEDICAMENT IN THE TREATMENT OF HYPERPROLIFERATIVE SKIN DISORDERS Sugen, Inc. (US) 1999-11-10 EP disclosed
WO-1998010767-A9 USE OF QUINAZOLINE DERIVATIVES FOR THE MANUFACTURE OF A MEDICAMENT IN THE TREATMENT OF HYPERPROLIFERATIVE SKIN DISORDERS 1998-07-02 WO disclosed
WO-1998010767-A2 USE OF QUINAZOLINE DERIVATIVES FOR THE MANUFACTURE OF A MEDICAMENT IN THE TREATMENT OF HYPERPROLIFERATIVE SKIN DISORDERS SUGEN, INC. (US) 1998-03-19 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 (2 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-20090171083-A1 PROCESS FOR PRODUCING 4-AMINOQUINAZOLINE COMPOUND HRH4, CYP3A4, HRH3 LMNA 4832/4885SMN1; SMN2 4869/4885S1PR2 4388/4885
US-20050130995-A1 Chlorinating quinazolin-4-one in solvent in presence of a base; then reacting with an amine compound HRH4, HRH3, H1-4 LMNA 4755/4885SMN1; SMN2 4852/4885S1PR2 4353/4885

“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.