SCHEMBL9782

SCHEMBL9782

Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(-c2cccnc2)n1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDGFRA P16234 14/20 1.00
ABL1 P00519 13/20 1.00
BCR P11274 9/20 1.00
PDGFRB P09619 8/20 1.00
PRKCA P17252 4/20 1.00
EGFR P00533 1/20 1.00
KIT P10721 4/20 0.80
KDR P35968 1/20 0.75
ABL2 P42684 1/20 0.75
PRKD3 O94806 1/20 0.74
PRKCG P05129 1/20 0.74
PRKCB P05771 1/20 0.74
SRC P12931 1/20 0.74
PRKCH P24723 1/20 0.74
PRKCI P41743 1/20 0.74
PRKCE Q02156 1/20 0.74
PRKCQ Q04759 1/20 0.74
PRKCZ Q05513 1/20 0.74
PRKCD Q05655 1/20 0.74
PRKD1 Q15139 1/20 0.74

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
SCHEMBL29498750 1.00 PDGFRA (1.00) PDGFRAABL1BCRPDGFRBPRKCA
Methane SCHEMBL5972158 0.99 PDGFRA (0.98) PDGFRAABL1BCRPDGFRBPRKCA
SCHEMBL2004455 0.95 PDGFRA (0.91) PDGFRAABL1BCRPDGFRBPRKCA
SCHEMBL3055349 0.94 PDGFRA (0.89) PDGFRAABL1BCRPDGFRBPRKCA
SCHEMBL9820 0.93 PDGFRA (1.00) PDGFRAABL1BCRPDGFRBPRKCA
SCHEMBL13498211 0.92 PDGFRA (0.88) PDGFRAABL1BCRPDGFRBPRKCA
SCHEMBL30197820 0.92 PDGFRA (0.85) PDGFRAABL1BCRPDGFRBPRKCA
SCHEMBL9677 0.92 PDGFRA (1.00) PDGFRAABL1BCRPDGFRBPRKCA
SCHEMBL11927842 0.92 ABL1 (1.00) PDGFRAABL1BCRPDGFRBPRKCA
SCHEMBL11932096 0.92 PDGFRA (0.86) PDGFRAABL1BCRPDGFRBPRKCA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2023104155-A1 LIGAND COMPOUNDS FOR E3 UBIQUITIN LIGASE, PROTEIN DEGRADERS DEVELOPED ON BASIS OF LIGAND COMPOUNDS, AND USES THEREOF 标新生物医药科技(上海)有限公司 2023-06-15 WO claimed
CN-116239566-A E3 ubiquitin ligase ligand compound, protein degradation agent developed based on ligand compound and application thereof 标新生物医药科技(上海)有限公司 2023-06-09 CN claimed
US-20220347108-A1 PROCESS FOR PRODUCING A PHARMACEUTICAL FORMULATION COMPRISING CRYSTALLINE AND AMORPHOUS FRACTIONS OF AN ACTIVE SUBSTANCE BAYER AKTIENGESELLSCHAFT (DE) 2022-11-03 US claimed
CN-114514019-A Method for producing pharmaceutical preparations containing crystalline and amorphous fractions of active substances 拜耳股份有限公司 2022-05-17 CN claimed
WO-2021069349-A1 PROCESS FOR PRODUCING A PHARMACEUTICAL FORMULATION COMPRISING CRYSTALLINE AND AMORPHOUS FRACTIONS OF AN ACTIVE SUBSTANCE BAYER AKTIENGESELLSCHAFT (DE) 2021-04-15 WO claimed
EP-3804701-A1 METHOD FOR PREPARING A PHARMACEUTICAL FORMULATION COMPRISING CRYSTALLINE AND AMORPHOUS PORTIONS OF AN ACTIVE SUBSTANCE Bayer AG (DE) 2021-04-14 EP claimed
EP-3804702-A1 METHOD FOR PREPARING A PHARMACEUTICAL FORMULATION COMPRISING ACTIVE AGENT, POLYMER AND SURFACTANT Bayer AG (DE) 2021-04-14 EP claimed
CN-112110906-A Novel use of conjugates 中山万汉制药有限公司 2020-12-22 CN claimed
CN-112079821-A Conjugate formed by orlistat and phenylaminopyrimidine compound and preparation method and application thereof 中山万汉制药有限公司 2020-12-15 CN claimed
CN-112043708-A Anti-hepatitis B use of conjugates 中山万汉制药有限公司 2020-12-08 CN claimed
CN-102372690-A Intermediate for synthesizing imatinib and application of intermediate in imatinib synthesis CHENGDU DIAO PHARMACEUTICAL GROUP CO LTD 2012-03-14 CN claimed
EP-1940894-B1 TRIFLUSAL-CONTAINING POLYMERS FOR STENT COATING PALAU PHARMA SA (ES) 2011-06-08 EP claimed
EP-1721609-A2 Pyridylpyrimidine derivatives as effective compounds against prion infections and prion diseases GPC Biotech AG (DE) 2006-11-15 EP claimed
US-20060217404-A1 Pyridylpyrimidine derivatives as effective compounds against prion infections and prion diseases GPC BIOTECH FORSCHUNGSGESELLSCHAFT MBH (DE) 2006-09-28 US claimed
EP-1395261-B1 PYRIDYLPYRIMIDINE DERIVATIVES AS EFFECTIVE COMPOUNDS AGAINST PRION DISEASES GPC BIOTECH AG (DE) 2006-06-28 EP claimed
WO-2005065074-A2 PROTECTION OF TISSUES AND CELLS FROM CYTOTOXIC EFFECTS OF IONIZING RADIATION BY ABL INHIBITORS TEMPLE UNIVERSITY OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2005-07-21 WO claimed
US-20030176443-A1 Pyridylpyrimidine derivatives as effective compounds against prion diseases GPC BIOTECH FORSCHUNGSGESELLSCHAFT MBH (DE) 2003-09-18 US claimed
EP-0564409-B1 Pyrimidin derivatives and process for their preparation NOVARTIS AG (CH) 2000-01-19 EP claimed
US-5521184-A ANTITUMOR AGENTS; imatinib mesylate CIBA-GEIGY CORPORATION (US) 1996-05-28 US claimed
EP-0564409-A1 Pyrimidin derivatives and process for their preparation CIBA-GEIGY AG (CH) 1993-10-06 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 (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-20030176443-A1 Pyridylpyrimidine derivatives as effective compounds against prion diseases PRNP, PPM1D, PPM1F PDGFRA 2586/4885ABL1 901/4885BCR 1338/4885
US-20060217404-A1 Pyridylpyrimidine derivatives as effective compounds against prion infections and prion diseases PRNP, PPM1D, PPM1F PDGFRA 2913/4885ABL1 904/4885BCR 1230/4885

“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.