SCHEMBL2392

SCHEMBL2392

Cc1ccc(N)cc1Nc1nccc(-c2cccnc2)n1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
ABL1 P00519 14/20 1.00
BCR P11274 12/20 1.00
PRKCA P17252 3/20 0.73
PDGFRA P16234 7/20 0.68
PDGFRB P09619 6/20 0.68
EGFR P00533 5/20 0.67
SRC P12931 1/20 0.67
PRKACA P17612 1/20 0.67
PRKACG P22612 1/20 0.67
PRKACB P22694 1/20 0.67
JAK3 P52333 1/20 0.63
BTK Q06187 1/20 0.63
ITK Q08881 1/20 0.63
KIT P10721 2/20 0.61

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
SCHEMBL29555505 1.00 ABL1 (1.00) ABL1BCRPRKCAPDGFRAPDGFRB
SCHEMBL29366999 1.00 ABL1 (1.00) ABL1BCRPRKCAPDGFRAPDGFRB
Ammonia Solution, Strong SCHEMBL4749564 0.99 ABL1 (0.98) ABL1BCRPRKCAPDGFRAPDGFRB
Hydrochloric Acid SCHEMBL2419016 0.99 ABL1 (0.98) ABL1BCRPRKCAPDGFRAPDGFRB
SCHEMBL14938216 0.92 ABL1 (0.85) ABL1BCRPRKCAPDGFRAPDGFRB
SCHEMBL3860532 0.91 ABL1 (0.83) ABL1BCRPRKCAPDGFRAPDGFRB
SCHEMBL2575958 0.88 ABL1 (0.78) ABL1BCRPRKCAPDGFRAPDGFRB
SCHEMBL12320924 0.88 ABL1 (0.78) ABL1BCRPRKCAPDGFRAPDGFRB
SCHEMBL7601457 0.88 ABL1 (0.78) ABL1BCRPRKCAPDGFRAPDGFRB
SCHEMBL14041906 0.87 ABL1 (0.78) ABL1BCRPRKCAPDGFRAPDGFRB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112125882-B Method for synthesizing imatinib free base 山东汇海医药化工有限公司 2023-04-11 CN claimed
CN-111440147-B Synthesis method of N- (2-methyl-5-aminophenyl) -4- (3-pyridyl) -2-pyrimidinamine 苏州卫生职业技术学院 2023-03-07 CN claimed
CN-114685428-A Preparation method of imatinib mesylate 重庆圣华曦药业股份有限公司 2022-07-01 CN claimed
CN-110078706-B Imatinib derivative and preparation method and application thereof 浙江师范大学 2022-02-01 CN claimed
CN-112125882-A Method for synthesizing imatinib free base 山东汇海医药化工有限公司 2020-12-25 CN claimed
CN-111440147-A Synthesis method of N- (2-methyl-5-aminophenyl) -4- (3-pyridyl) -2-pyrimidinamine 苏州卫生职业技术学院 2020-07-24 CN claimed
CN-107089969-B Method for synthesizing imatinib intermediate 黑龙江鑫创生物科技开发有限公司 2020-04-24 CN claimed
CN-111039921-A Synthesis process of imatinib and imatinib mesylate 杭州沧海帆医药科技有限公司 2020-04-21 CN claimed
WO-2018204829-A1 METHODS FOR PREVENTING NEURAL TUBE DEFECTS IN DIABETIC PREGNANCY UNIVERSITY OF MARYLAND, BALTIMORE (US) 2018-11-08 WO claimed
EP-2608791-B1 A PROCESS FOR THE PREPARATION OF IMATINIB BASE MUSTAFA NEVZAT ILAC SANAYII A S (TR) 2016-05-18 EP claimed
WO-2007067629-A1 BRADYKININ 1 RECEPTOR ANTAGONISTS AMGEN INC. (US) 2007-06-14 WO 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
WO-2006071130-A2 A PROCESS FOR PREPARATION OF IMATINIB BASE INSTYTUT FARMACEUTYCZNY (PL) 2006-07-06 WO claimed
US-20060149061-A1 Novel process for preparing Imatinib PERRIGO API LTD. (IL) 2006-07-06 US claimed
EP-1395261-B1 PYRIDYLPYRIMIDINE DERIVATIVES AS EFFECTIVE COMPOUNDS AGAINST PRION DISEASES GPC BIOTECH AG (DE) 2006-06-28 EP claimed
WO-2004108699-A1 PROCESS FOR THE PREPARATION OF THE ANTI-CANCER DRUG IMATINIB AND ITS ANALOGUES NATCO PHARMA LIMITED (IN) 2004-12-16 WO claimed
EP-1395261-A2 PYRIDYLPYRIMIDINE DERIVATIVES AS EFFECTIVE COMPOUNDS AGAINST PRION DISEASES Axxima Pharmaceuticals Aktiengesellschaft (DE) 2004-03-10 EP claimed
US-20030176443-A1 Pyridylpyrimidine derivatives as effective compounds against prion diseases GPC BIOTECH FORSCHUNGSGESELLSCHAFT MBH (DE) 2003-09-18 US claimed
WO-2002093164-A2 PYRIDYLPYRIMIDINE DERIVATIVES AS EFFECTIVE COMPOUNDS AGAINST PRION DISEASES AXXIMA PHARMACEUTICALS AG (DE) 2002-11-21 WO 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-20030176443-A1 Pyridylpyrimidine derivatives as effective compounds against prion diseases PRNP, PPM1D, PPM1F ABL1 901/4885BCR 1338/4885PRKCA 138/4885
US-20060217404-A1 Pyridylpyrimidine derivatives as effective compounds against prion infections and prion diseases PRNP, PPM1D, PPM1F ABL1 904/4885BCR 1230/4885PRKCA 121/4885
US-20060149061-A1 Novel process for preparing Imatinib ABL1, ABL2, PDGFRA ABL1 1/4885BCR 22/4885PRKCA 140/4885

“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.