SCHEMBL1210909

SCHEMBL1210909

NC(=O)c1ccn[nH]c1=O

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HCAR2 Q8TDS4 1/20 0.42
BTK Q06187 3/20 0.41
AURKA O14965 2/20 0.41
CSNK1A1 P48729 2/20 0.41
DYRK1B Q9Y463 2/20 0.41
PLK4 O00444 1/20 0.41
CHEK1 O14757 1/20 0.41
DAPK3 O43293 1/20 0.41
MAP4K4 O95819 1/20 0.41
CSF1R P07333 1/20 0.41
RET P07949 1/20 0.41
FGFR1 P11362 1/20 0.41
PDGFRA P16234 1/20 0.41
LTK P29376 1/20 0.41
KDR P35968 1/20 0.41
MAP2K2 P36507 1/20 0.41
FLT3 P36888 1/20 0.41
PRKX P51817 1/20 0.41
CDK5 Q00535 1/20 0.41
MAP2K1 Q02750 1/20 0.41

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
Pyrrole SCHEMBL2297382 0.91 BTK (0.39) HCAR2BTKAURKACSNK1A1DYRK1B
SCHEMBL2742976 0.81 HCAR2 (0.54) HCAR2TDP1KDM4CKDM4EL3MBTL1
SCHEMBL27189220 0.79 HCAR2 (0.42) HCAR2TDP1KDM4CL3MBTL1PARP1
Urea SCHEMBL11275543 0.77 MAPT (0.47) HCAR2TDP1L3MBTL1PARP1NPC1
SCHEMBL29731607 0.75 HCAR2 (0.38) HCAR2KDM4CKDM4EL3MBTL1NPC1
SCHEMBL27239649 0.73 HCAR2 (0.36) HCAR2NPC1RAB9A
SCHEMBL3344611 0.72 BTK (0.46) BTKSIRT3TDP1CDC7
SCHEMBL3342946 0.71 BTK (0.43) BTKPARP1CDC7DGAT1
SCHEMBL1504 0.71
SCHEMBL1623326 0.71 ALDH1A1 (0.51) KDM4EL3MBTL1NPC1ALDH1A1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240002362-A1 DEUTERATED 2-ARYLHETEROCYCLE-3-OXO-2,3- DIHYDROPYRIDAZINE-4-CARBOXAMIDE INHIBITOR AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOF SHANGHAI ZELGEN PHARMA.TECH CO., LTD. (CN) 2024-01-04 US claimed
EP-3843850-B1 PYRAZOLO[3,4-B]PYRIDINE COMPOUNDS AS INHIBITORS OF TAM AND MET KINASES ARRAY BIOPHARMA INC (US) 2023-11-15 EP claimed
EP-4253374-A1 DEUTERATED 2-ARYLHETEROCYCLE-3-OXO-2,3-DIHYDROPYRIDAZINE-4-CARBOXAMIDE INHIBITOR AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOF Suzhou Zelgen Biopharmaceutical Co., Ltd. (CN) 2023-10-04 EP claimed
CN-116583518-A Deuterated 2-aromatic heterocycle-3-oxo-2, 3-dihydropyridazine-4-carboxamide inhibitor as well as preparation method and application thereof 苏州泽璟生物制药股份有限公司 2023-08-11 CN claimed
CN-109863140-B 3-oxo-2, 6-diphenyl-2, 3-dihydropyridazine-4-carboxamide 拜耳医药股份有限公司 2023-02-21 CN claimed
US-20230032216-A1 INTERLEUKIN-4-INDUCED GENE 1 (IL4I1) AND RESPECTIVE METABOLITES AS BIOMARKERS FOR CANCER Deutsches Krebsforschungszentrum Stiftung des oeffentlichen Rechts Im Neuenheimer Feld 280 (DE) 2023-02-02 US claimed
EP-4076462-A1 COMBINATION OF AN AHR-INHIBITOR AND AN PD1-INHIBITOR ANTIBODY AND ITS USE IN THE TREATMENT OF CANCER Bayer Aktiengesellschaft (DE) 2022-10-26 EP claimed
US-11459312-B2 Sulphur substituted 3-oxo-2,3-dihydropyridazine-4-carboxamides BAYER AKTIENGESELLSCHAFT (DE) 2022-10-04 US claimed
CN-114901837-A Interleukin-4 inducible gene 1(IL4I1) and corresponding metabolites as biomarkers for cancer 德国癌症研究公共权益基金会 2022-08-12 CN claimed
CN-114786674-A Combination of an AHR inhibitor and a PD1 inhibitor antibody and use thereof in the treatment of cancer 拜耳公司 2022-07-22 CN claimed
CN-114539221-A Deuterated 2-heteroaromatic-3-oxo-2, 3-dihydropyridazine-4-formamide inhibitor as well as preparation method and application thereof 苏州泽璟生物制药股份有限公司 2022-05-27 CN claimed
CN-114127311-A Arene receptor (AHR) activation profile and methods for determining AHR signaling status 德国癌症研究公共权益基金会 2022-03-01 CN claimed
EP-3947734-A2 ARYL HYDROCARBON RECEPTOR (AHR) ACTIVATION SIGNATURE AND METHODS FOR DETERMINING AHR SIGNALING STATUS Deutsches Krebsforschungszentrum Stiftung des Öffentlichen Rechts (DE) 2022-02-09 EP claimed
WO-2021122434-A1 COMBINATION OF AN AHR-INHIBITOR AND AN PD1-INHIBITOR ANTIBODY AND ITS USE IN THE TREATMENT OF CANCER BAYER AKTIENGESELLSCHAFT (DE) 2021-06-24 WO claimed
WO-2021116357-A1 INTERLEUKIN-4-INDUCED GENE 1 (IL4I1) AND RESPECTIVE METABOLITES AS BIOMARKERS FOR CANCER Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts (DE) 2021-06-17 WO claimed
WO-2020201825-A2 ARYL HYDROCARBON RECEPTOR (AHR) ACTIVATION SIGNATURE AND METHODS FOR DETERMINING AHR SIGNALING STATUS DEUTSCHES KREBSFORSCHUNGSZENTRUM STIFTUNG DES OFFENTLICHEN RECHTS (DE) 2020-10-08 WO claimed
US-8946225-B2 Derivatives of 2H pyridazin-3-ones, their preparation and their use as SCD-1 inhibitors PIERRE FABRE MEDICAMENT (FR) 2015-02-03 US claimed
US-20120178678-A1 DERIVATIVES OF 2H PYRIDAZIN- 3 -ONES, THEIR PREPARATION AND THEIR USE AS SCD-1 INHIBITORS PIERRE FABRE MEDICAMENT (FR) 2012-07-12 US claimed
EP-2462121-A1 DERIVATIVES OF 2H PYRIDAZIN- 3 -ONES, THEIR PREPARATION AND THEIR USE AS SCD-1 INHIBITORS Pierre Fabre Médicament (FR) 2012-06-13 EP claimed
EP-0116494-B1 PYRIDAZINE DERIVATIVES WITH A PSYCHOTROPE ACTIVITY, PROCESS FOR THEIR PREPARATION, INTERMEDIATES AND MEDICINES CONTAINING THEM SANOFI S.A. (FR) 1988-01-27 EP claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 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-11459312-B2 Sulphur substituted 3-oxo-2,3-dihydropyridazine-4-carboxamides AHR, ARNT, MYD88 HCAR2 23/4885BTK 1924/4885AURKA 3058/4885
US-20240002362-A1 DEUTERATED 2-ARYLHETEROCYCLE-3-OXO-2,3- DIHYDROPYRIDAZINE-4-CARBOXAMIDE INHIBITOR AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOF AHR, CYP2F1, ARNT HCAR2 55/4885BTK 2907/4885AURKA 2008/4885
US-20120178678-A1 DERIVATIVES OF 2H PYRIDAZIN- 3 -ONES, THEIR PREPARATION AND THEIR USE AS SCD-1 INHIBITORS SCD, SCD5, CYP2S1 HCAR2 673/4885BTK 2370/4885AURKA 3833/4885

“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.