SCHEMBL400723

SCHEMBL400723

Nc1nccc2nccn12

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CLK4 Q9HAZ1 3/20 0.44
FGFR1 P11362 2/20 0.44
MAP2K2 P36507 2/20 0.44
MAPK9 P45984 2/20 0.44
NTRK1 P04629 1/20 0.44
IGF1R P08069 1/20 0.44
LTK P29376 1/20 0.44
RPS6KA3 P51812 1/20 0.44
PRKX P51817 1/20 0.44
PRKCQ Q04759 1/20 0.44
TNK2 Q07912 1/20 0.44
CDK8 P49336 3/20 0.41
ROCK1 Q13464 3/20 0.41
KDR P35968 3/20 0.41
DYRK1A Q13627 2/20 0.41
PRKACA P17612 2/20 0.41
MAP2K1 Q02750 2/20 0.41
ACVR1 Q04771 2/20 0.41
DYRK1B Q9Y463 2/20 0.41
CHEK1 O14757 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
SCHEMBL17841621 0.74 FGFR1 (0.42) CLK4FGFR1MAP2K2MAPK9NTRK1
SCHEMBL399440 0.74 CHEK1 (0.32) CDK8ROCK1KDRDYRK1APRKACA
SCHEMBL1154880 0.73 CDK8 (0.41) CLK4CDK8ROCK1KDRDYRK1A
SCHEMBL14638753 0.73 ADORA3 (0.44) CLK4CDK8ROCK1KDRDYRK1A
SCHEMBL9611703 0.73 CDK8 (0.44) CLK4CDK8ROCK1KDRDYRK1A
SCHEMBL5487082 0.71 SMPD3 (0.38) CLK4FGFR1MAP2K2MAPK9NTRK1
SCHEMBL334306 0.71 CDK8 (0.53) CLK4CDK8ROCK1KDRDYRK1A
SCHEMBL24579491 0.70 CDK8 (0.36) CLK4CDK8ROCK1KDRDYRK1A
Hydrochloric Acid SCHEMBL5442637 0.70 CDK8 (0.52) CLK4CDK8ROCK1KDRDYRK1A
SCHEMBL23979526 0.70 CDK8 (0.39) CLK4CDK8ROCK1KDRDYRK1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250179082-A1 IMIDAZO[1,2-C]PYRIMIDINE DERIVATIVES AS PRC2 INHIBITORS FOR TREATING CANCER Mirati Therapeutics, Inc. 2025-06-05 US disclosed
US-12252493-B2 Imidazo[1,2-c]pyrimidine derivatives as PRC2 inhibitors for treating cancer Mirati Therapeutics, Inc. (US) 2025-03-18 US disclosed
CN-118063491-A Imide catalyst auxiliary agent, polyimide film and preparation method 中国科学院化学研究所 2024-05-24 CN disclosed
WO-2023049723-A1 PRC2 INHIBITORS FOR USE IN TREATING BLOOD DISORDERS ORIC PHARMACEUTICALS, INC. (US) 2023-03-30 WO disclosed
US-20220274990-A1 IMIDAZO[1,2-C]PYRIMIDINE DERIVATIVES AS PRC2 INHIBITORS FOR TREATING CANCER Mirati Therapeutics, Inc. 2022-09-01 US disclosed
US-11312705-B2 Heteroaryl[4,3-C]pyrimidine-5-amine derivative, preparation method therefor, and medical uses thereof JIANGSU HENGRUI MEDICINE CO., LTD. (CN) 2022-04-26 US disclosed
EP-3980422-A1 IMIDAZO[1,2-C]PYRIMIDINE DERIVATIVES AS PRC2 INHIBITORS FOR TREATING CANCER Mirati Therapeutics, Inc. (US) 2022-04-13 EP disclosed
CN-114269748-A Imidazo [1,2-c ] pyrimidine derivatives as PRC2 inhibitors for the treatment of cancer 米拉蒂医疗股份有限公司 2022-04-01 CN disclosed
US-8735405-B2 6,6-bicyclic ring substituted heterobicyclic protein kinase inhibitors OSI Pharmaceuticals, LLC (US) 2014-05-27 US disclosed
US-8735405-B2 6,6-bicyclic ring substituted heterobicyclic protein kinase inhibitors OSI Pharmaceuticals, LLC (US) 2014-05-27 US disclosed
US-7820662-B2 6,6-bicyclic ring substituted heterobicyclic protein kinase inhibitors OSI PHARMACEUTICALS, INC. (US) 2010-10-26 US disclosed
EP-2168968-A1 6,6-bicyclic ring substituted heterobicyclic protein kinase inhibitors OSI Pharmaceuticals, Inc. (US) 2010-03-31 EP disclosed
US-20090325928-A1 6,6-Bicyclic Ring Substituted Heterobicyclic Protein Kinase Inhibitors OSI PHARMACEUTICALS, INC. 2009-12-31 US disclosed
US-20090325928-A1 6,6-Bicyclic Ring Substituted Heterobicyclic Protein Kinase Inhibitors OSI PHARMACEUTICALS, INC. 2009-12-31 US disclosed
US-20090325928-A1 6,6-Bicyclic Ring Substituted Heterobicyclic Protein Kinase Inhibitors OSI PHARMACEUTICALS, INC. 2009-12-31 US disclosed
US-7534797-B2 6,6-Bicyclic ring substituted heterobicyclic protein kinase inhibitors OSI PHARMACEUTICALS, INC. (US) 2009-05-19 US disclosed
US-7534797-B2 6,6-Bicyclic ring substituted heterobicyclic protein kinase inhibitors OSI PHARMACEUTICALS, INC. (US) 2009-05-19 US disclosed
US-7534797-B2 6,6-Bicyclic ring substituted heterobicyclic protein kinase inhibitors OSI PHARMACEUTICALS, INC. (US) 2009-05-19 US disclosed
US-20090118499-A1 6,6-Bicyclic Ring Substituted Heterobicyclic Protein Kinase Inhibitors OSI PHARMACEUTICALS, INC. 2009-05-07 US disclosed
US-20060235031-A1 6,6-Bicyclic ring substituted heterobicyclic protein kinase inhibitors ACERTA PHARMA B.V. (NL) 2006-10-19 US 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 (7 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-20090325928-A1 6,6-Bicyclic Ring Substituted Heterobicyclic Protein Kinase Inhibitors IGF1R, MAP2K7, BRCA1 CLK4 429/4885FGFR1 102/4885MAP2K2 5/4885
US-20090118499-A1 6,6-Bicyclic Ring Substituted Heterobicyclic Protein Kinase Inhibitors IGF1R, MAP2K7, BRCA1 CLK4 429/4885FGFR1 102/4885MAP2K2 5/4885
US-11312705-B2 Heteroaryl[4,3-C]pyrimidine-5-amine derivative, preparation method therefor, and medical uses thereof ADORA2A, ADORA1, ADORA3 CLK4 3725/4885FGFR1 1690/4885MAP2K2 2737/4885
US-12252493-B2 Imidazo[1,2-c]pyrimidine derivatives as PRC2 inhibitors for treating cancer BMI1, EZH2, SUZ12 CLK4 3599/4885FGFR1 1996/4885MAP2K2 2530/4885
US-20250179082-A1 IMIDAZO[1,2-C]PYRIMIDINE DERIVATIVES AS PRC2 INHIBITORS FOR TREATING CANCER BMI1, EZH2, SUZ12 CLK4 3599/4885FGFR1 1996/4885MAP2K2 2530/4885
US-20220274990-A1 IMIDAZO[1,2-C]PYRIMIDINE DERIVATIVES AS PRC2 INHIBITORS FOR TREATING CANCER BMI1, EZH2, SUZ12 CLK4 3599/4885FGFR1 1996/4885MAP2K2 2530/4885
US-20060235031-A1 6,6-Bicyclic ring substituted heterobicyclic protein kinase inhibitors IGF1R, MAP2K7, BRCA1 CLK4 429/4885FGFR1 102/4885MAP2K2 5/4885

“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.