SCHEMBL430890

SCHEMBL430890

N#Cc1cnc2ccc(Cl)nn12

nearest known ligand 0.49

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
TNF P01375 1/20 0.49
DYRK1A Q13627 5/20 0.45
DYRK2 Q92630 5/20 0.45
DYRK3 O43781 4/20 0.45
CCNA2 P20248 4/20 0.45
CDK2 P24941 4/20 0.45
CDK5 Q00535 4/20 0.45
CDK5R1 Q15078 4/20 0.45
DYRK1B Q9Y463 4/20 0.45
CCNT1 O60563 2/20 0.45
CDK9 P50750 2/20 0.45
TGFBR1 P36897 13/20 0.44
TGFBR2 P37173 4/20 0.44
KDM4E B2RXH2 1/20 0.43
ALDH1A1 P00352 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43

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
SCHEMBL16620325 0.82 TNF (0.49) TNFDYRK1ADYRK2DYRK3CCNA2
SCHEMBL15674118 0.79 TNF (0.46) TNFDYRK1ADYRK2DYRK3CCNA2
SCHEMBL16620555 0.79 DYRK1A (0.47) TNFDYRK1ADYRK2DYRK3CCNA2
SCHEMBL15638125 0.79 TGFBR1 (0.45) TGFBR1TGFBR2
SCHEMBL7889752 0.79 TGFBR1 (0.51) TGFBR1TGFBR2KDM4E
SCHEMBL31691002 0.79 TGFBR1 (0.45) TGFBR1TGFBR2
SCHEMBL16620406 0.77 TNF (0.44) TNFDYRK1ADYRK2DYRK3CCNA2
SCHEMBL16620525 0.75 RET (0.43) TNFDYRK1ADYRK2DYRK3CCNA2
SCHEMBL3452842 0.75 TNF (0.56) TNFDYRK1ADYRK2DYRK3CCNA2
SCHEMBL13080170 0.75 TGFBR1 (0.46) TGFBR1TGFBR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117417340-A Preparation method of 6-chloroimidazo [1,2-b ] pyridazine-3-carbonitrile 山东省科学院菏泽分院 2024-01-19 CN claimed
CN-112321592-B Synthesis method of 6-chloroimidazo [1,2-b ] pyridazine-3-carbonitrile 山东省科学院菏泽分院 2022-03-04 CN claimed
CN-112321592-A Synthesis method of 6-chloroimidazo [1,2-b ] pyridazine-3-carbonitrile 山东省科学院菏泽分院 2021-02-05 CN claimed
CN-117417340-B Preparation method of 6-chloroimidazo [1,2-b ] pyridazine-3-carbonitrile 山东省科学院菏泽分院 2025-08-26 CN disclosed
CN-117417340-B Preparation method of 6-chloroimidazo [1,2-b ] pyridazine-3-carbonitrile 山东省科学院菏泽分院 2025-08-26 CN disclosed
US-12110294-B2 CD73 compounds GILEAD SCIENCES, INC. (US) 2024-10-08 US disclosed
CN-114989173-B Imidazole compound, pharmaceutical composition and application thereof 广州市恒诺康医药科技有限公司 2024-03-19 CN disclosed
US-20240043427-A1 CD73 COMPOUNDS GILEAD SCIENCES, INC. 2024-02-08 US disclosed
CN-117417340-A Preparation method of 6-chloroimidazo [1,2-b ] pyridazine-3-carbonitrile 山东省科学院菏泽分院 2024-01-19 CN disclosed
CN-117417340-A Preparation method of 6-chloroimidazo [1,2-b ] pyridazine-3-carbonitrile 山东省科学院菏泽分院 2024-01-19 CN disclosed
CN-117417340-A Preparation method of 6-chloroimidazo [1,2-b ] pyridazine-3-carbonitrile 山东省科学院菏泽分院 2024-01-19 CN disclosed
EP-2614062-A1 IMIDAZO [1, 2]PYRIDAZIN COMPOUNDS AND COMPOSITIONS AS TRK INHIBITORS IRM LLC (BM) 2013-07-17 EP disclosed
US-20120065184-A1 COMPOUNDS AND COMPOSITIONS AS TRK INHIBITORS IRM LLC (BM) 2012-03-15 US disclosed
US-20120065184-A1 COMPOUNDS AND COMPOSITIONS AS TRK INHIBITORS IRM LLC (BM) 2012-03-15 US disclosed
US-20120065184-A1 COMPOUNDS AND COMPOSITIONS AS TRK INHIBITORS IRM LLC (BM) 2012-03-15 US disclosed
WO-2012034091-A1 IMIDAZO [1, 2] PYRIDAZIN COMPOUNDS AND COMPOSITIONS AS TRK INHIBITORS IRM LLC (BM) 2012-03-15 WO disclosed
WO-2012034091-A1 IMIDAZO [1, 2] PYRIDAZIN COMPOUNDS AND COMPOSITIONS AS TRK INHIBITORS IRM LLC (BM) 2012-03-15 WO disclosed
US-20110046127-A1 Imidazopyridazines for Use as Protein Kinase Inhibitors CENTRO NACIONAL DE INVESTIGACIONES ONCOLOGICAS (CNIO) (ES) 2011-02-24 US disclosed
EP-2217601-A1 IMIDAZOPYRIDAZINES FOR USE AS PROTEIN KINASE INHIBITORS Centro Nacional de Investigaciones Oncológicas (CNIO) (ES) 2010-08-18 EP disclosed
WO-2009060197-A1 IMIDAZOPYRIDAZINES FOR USE AS PROTEIN KINASE INHIBITORS CENTRO NACIONAL DE INVESTIGACIONES ONCOLOGICAS (CNIO) (ES) 2009-05-14 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 (4 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-20240043427-A1 CD73 COMPOUNDS ENTPD5, ENTPD1, NT5E TNF 2852/4885DYRK1A 2886/4885DYRK2 2847/4885
US-12110294-B2 CD73 compounds ENTPD5, ENTPD1, NT5E TNF 2894/4885DYRK1A 3442/4885DYRK2 3401/4885
US-20120065184-A1 COMPOUNDS AND COMPOSITIONS AS TRK INHIBITORS TNK2, CNKSR1, BMP2K TNF 2369/4885DYRK1A 1516/4885DYRK2 1560/4885
US-20110046127-A1 Imidazopyridazines for Use as Protein Kinase Inhibitors PIM1, PIM3, PIM2 TNF 4372/4885DYRK1A 588/4885DYRK2 737/4885

“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.