SCHEMBL376231

SCHEMBL376231

O=C(Cl)c1cncc(Cl)n1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GRM5 P41594 1/20 0.47
CDK2 P24941 3/20 0.43
S1PR3 Q99500 1/20 0.40
CTSA P10619 1/20 0.38
SIRT6 Q8N6T7 1/20 0.38
HCAR2 Q8TDS4 2/20 0.33
NAPRT Q6XQN6 2/20 0.33
KDM4E B2RXH2 3/20 0.32
MEN1 O00255 1/20 0.32
ALDH1A1 P00352 1/20 0.32
CYP1A2 P05177 1/20 0.32
CYP3A4 P08684 1/20 0.32
HTR1A P08908 1/20 0.32
CYP2C9 P11712 1/20 0.32
HPGD P15428 1/20 0.32
HTR2A P28223 1/20 0.32
HTR2C P28335 1/20 0.32
CYP2C19 P33261 1/20 0.32
KMT2A Q03164 1/20 0.32
HSD17B10 Q99714 1/20 0.32

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
SCHEMBL11427001 0.85 KDM4E (0.36) GRM5SIRT6HCAR2NAPRTKDM4E
SCHEMBL27858703 0.84 GRM5 (0.49) GRM5CDK2S1PR3CTSASIRT6
SCHEMBL29913176 0.82 GRM5 (0.47) GRM5CDK2S1PR3CTSASIRT6
SCHEMBL376147 0.82 GRM5 (0.47) GRM5CDK2S1PR3CTSASIRT6
SCHEMBL12091007 0.80 GRM5 (0.46) GRM5CDK2S1PR3CTSASIRT6
SCHEMBL741061 0.80 SIRT6 (0.50) GRM5CDK2S1PR3CTSASIRT6
SCHEMBL31555012 0.80 SIRT6 (0.50) GRM5CDK2S1PR3CTSASIRT6
SCHEMBL30354632 0.80 GRM5 (0.46) GRM5CDK2S1PR3CTSASIRT6
SCHEMBL28560032 0.77 CDK2 (0.43) GRM5CDK2S1PR3CTSAKDM4E
SCHEMBL22711336 0.76 GRM5 (0.49) GRM5HCAR2KDM4EALDH1A1NPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240124431-A1 2,3-DIHYDRO-4H-BENZO[B][1,4]OXAZIN-4-YL)(5-(PHENYL)-PYRIDIN-3-YL)METHANONE DERIVATIVES AND SIMILAR COMPOUNDS AS CYP11A1 INHIBITORS FOR THE TREATMENT OF PROSTATE CANCER ORION CORPORATION (FI) 2024-04-18 US disclosed
US-11337973-B2 Substituted [1,2,4]triazolo[4,3-A]pyrazines as prolyl endopeptidase inhibitors BAYER AKTIENGESELLSCHAFT (DE) 2022-05-24 US disclosed
US-11337973-B2 Substituted [1,2,4]triazolo[4,3-A]pyrazines as prolyl endopeptidase inhibitors BAYER AKTIENGESELLSCHAFT (DE) 2022-05-24 US disclosed
EP-3707141-B1 SUBSTITUTED 2,4-DIHYDRO-3H-1,2,4-TRIAZOL-3-ONES AND USE OF SAME BAYER AG (DE) 2021-12-22 EP disclosed
EP-3707141-B1 SUBSTITUTED 2,4-DIHYDRO-3H-1,2,4-TRIAZOL-3-ONES AND USE OF SAME BAYER AG (DE) 2021-12-22 EP disclosed
US-20200375986-A1 SUBSTITUTED 2,4-DIHYDRO-3H-1,2,4-TRIAZOL-3-ONES AND USE OF SAME BAYER AKTIENGESELLSCHAFT (DE) 2020-12-03 US disclosed
US-20200375986-A1 SUBSTITUTED 2,4-DIHYDRO-3H-1,2,4-TRIAZOL-3-ONES AND USE OF SAME BAYER AKTIENGESELLSCHAFT (DE) 2020-12-03 US disclosed
EP-3707141-A1 SUBSTITUTED 2,4-DIHYDRO-3H-1,2,4-TRIAZOL-3-ONES AND USE OF SAME Bayer Aktiengesellschaft (DE) 2020-09-16 EP disclosed
US-9682995-B2 Amino-substituted isothiazoles BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2017-06-20 US disclosed
EP-2951174-B1 AMINO-SUBSTITUTED ISOTHIAZOLES Bayer Pharma AG (DE) 2017-04-26 EP disclosed
US-20110144084-A1 6 SUBSTITUTED 2- HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS PFIZER INC (US) 2011-06-16 US disclosed
US-20110144084-A1 6 SUBSTITUTED 2- HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS PFIZER INC (US) 2011-06-16 US disclosed
US-20110144084-A1 6 SUBSTITUTED 2- HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS PFIZER INC (US) 2011-06-16 US disclosed
EP-2328890-A1 6 SUBSTITUTED 2-HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS Pfizer Inc. (US) 2011-06-08 EP disclosed
CN-102015720-A Selective ligands for neuronal nicotinic receptors and uses thereof ABBOTT LAB 2011-04-13 CN disclosed
EP-2285810-A1 SELECTIVE LIGANDS FOR THE NEURONAL NICOTINIC RECEPTORS AND USES THEREOF Abbott Laboratories (US) 2011-02-23 EP disclosed
WO-2010016005-A1 6 SUBSTITUTED 2-HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS PFIZER INC. (US) 2010-02-11 WO disclosed
WO-2010016005-A1 6 SUBSTITUTED 2-HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS PFIZER INC. (US) 2010-02-11 WO disclosed
US-20090281118-A1 Selective Ligands for the Neuronal Nicotinic Receptors and Uses Thereof ABBOTT LABORATORIES (US) 2009-11-12 US disclosed
WO-2009137308-A1 SELECTIVE LIGANDS FOR THE NEURONAL NICOTINIC RECEPTORS AND USES THEREOF ABBOTT LABORATORIES (US) 2009-11-12 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-20200375986-A1 SUBSTITUTED 2,4-DIHYDRO-3H-1,2,4-TRIAZOL-3-ONES AND USE OF SAME PREP, SERPINB1, PEPD GRM5 3812/4885CDK2 1156/4885S1PR3 1337/4885
US-11337973-B2 Substituted [1,2,4]triazolo[4,3-A]pyrazines as prolyl endopeptidase inhibitors PREP, PEPD, SERPINB1 GRM5 1935/4885CDK2 819/4885S1PR3 1435/4885
US-20240124431-A1 2,3-DIHYDRO-4H-BENZO[B][1,4]OXAZIN-4-YL)(5-(PHENYL)-PYRIDIN-3-YL)METHANONE DERIVATIVES AND SIMILAR COMPOUNDS AS CYP11A1 INHIBITORS FOR THE TREATMENT OF PROSTATE CANCER CYP11B1, CYP11B2, SRD5A1 GRM5 1639/4885CDK2 447/4885S1PR3 1359/4885
US-20090281118-A1 Selective Ligands for the Neuronal Nicotinic Receptors and Uses Thereof CHRNA4, CHRNB4, CHRNA2 GRM5 64/4885CDK2 2403/4885S1PR3 688/4885
US-20110144084-A1 6 SUBSTITUTED 2- HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS CHKA, CSNK1A1, CHKB GRM5 4665/4885CDK2 157/4885S1PR3 1445/4885

“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.