SCHEMBL102252

SCHEMBL102252

Clc1ccc2ncc(-c3ccccc3)n2n1

nearest known ligand 0.72

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
DYRK1A Q13627 9/20 0.72
DYRK2 Q92630 9/20 0.72
DYRK1B Q9Y463 8/20 0.72
CDK5 Q00535 7/20 0.72
CDK5R1 Q15078 7/20 0.72
DYRK3 O43781 7/20 0.72
CCNA2 P20248 6/20 0.72
CDK2 P24941 6/20 0.72
CCNT1 O60563 4/20 0.72
CDK9 P50750 4/20 0.72
FYN P06241 10/20 0.59
MKNK1 Q9BUB5 1/20 0.56

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
SCHEMBL28404217 0.97 DYRK1A (0.68) DYRK1ADYRK2DYRK1BCDK5CDK5R1
SCHEMBL3046666 0.87 DYRK1A (0.59) DYRK1ADYRK2DYRK1BCDK5CDK5R1
SCHEMBL15288602 0.86 DYRK1A (0.70) DYRK1ADYRK2DYRK1BCDK5CDK5R1
SCHEMBL2948779 0.85 DYRK1A (0.68) DYRK1ADYRK2DYRK1BCDK5CDK5R1
SCHEMBL477064 0.85 DYRK1A (0.70) DYRK1ADYRK2DYRK1BCDK5CDK5R1
SCHEMBL21210592 0.84 DYRK1A (0.65) DYRK1ADYRK2DYRK1BCDK5CDK5R1
SCHEMBL30027711 0.84 DYRK1A (0.65) DYRK1ADYRK2DYRK1BCDK5CDK5R1
SCHEMBL23535582 0.84 DYRK1A (1.00) DYRK1ADYRK2DYRK1BCDK5CDK5R1
SCHEMBL102942 0.84 DYRK1A (1.00) DYRK1ADYRK2DYRK1BCDK5CDK5R1
SCHEMBL102796 0.83 DYRK1A (0.71) DYRK1ADYRK2DYRK1BCDK5CDK5R1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111226956-B Application of 3, 6-disubstituted imidazo [1,2-b ] pyridazine derivative in preparation of bactericide for inhibiting plant pathogenic fungi 贵州医科大学 2021-10-26 CN claimed
CN-111226956-A Application of 3, 6-disubstituted imidazo [1,2-b ] pyridazine derivative in preparation of bactericide 贵州医科大学 2020-06-05 CN claimed
CN-120025336-A LIN28 inhibitors and methods of use thereof 加利福尼亚大学董事会 2025-05-23 CN disclosed
CN-115087657-B LIN28 inhibitors and methods of use thereof 加利福尼亚大学董事会 2025-01-21 CN disclosed
US-20230059009-A1 INHIBITORS OF LIN28 AND METHODS OF USE THEREOF THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2023-02-23 US disclosed
US-20230059009-A1 INHIBITORS OF LIN28 AND METHODS OF USE THEREOF THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2023-02-23 US disclosed
EP-4077332-A1 INHIBITORS OF LIN28 AND METHODS OF USE THEREOF The Regents of the University of California (US) 2022-10-26 EP disclosed
CN-115087657-A LIN28 inhibitor and method of use thereof 加利福尼亚大学董事会 2022-09-20 CN disclosed
CN-111226956-B Application of 3, 6-disubstituted imidazo [1,2-b ] pyridazine derivative in preparation of bactericide for inhibiting plant pathogenic fungi 贵州医科大学 2021-10-26 CN disclosed
WO-2021126779-A1 INHIBITORS OF LIN28 AND METHODS OF USE THEREOF THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2021-06-24 WO disclosed
WO-2021126779-A1 INHIBITORS OF LIN28 AND METHODS OF USE THEREOF THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2021-06-24 WO disclosed
US-7750007-B2 Imidazo[1,2-beta]pyridazine and pyrazolo[1,5-alpha]pyrimidine derivatives and their use as protein kinase inhibitors SUPERGEN, INC. (US) 2010-07-06 US disclosed
US-7750000-B2 Substituted imidazo[1,2b]pyridazines as kinase inhibitors, their preparation and use as medicaments BAYER SCHERING PHARMA AG (DE) 2010-07-06 US disclosed
EP-2176266-A2 SUBSTITUTED IMIDAZO[1,2B]PYRIDAZINES AS KINASE INHIBITORS, THE PRODUCTION THEREOF, AND USE OF THE SAME AS MEDICAMENTS Bayer Schering Pharma Aktiengesellschaft (DE) 2010-04-21 EP disclosed
US-20080261988-A1 IMIDAZO[1,2-beta]PYRIDAZINE AND PYRAZOLO[1,5-alpha]PYRIMIDINE DERIVATIVES AND THEIR USE AS PROTEIN KINASE INHIBITORS SUPERGEN, INC. (US) 2008-10-23 US disclosed
US-20070093490-A1 Substituted imidazo[1,2b]pyridazines as kinase inhibitors, their preparation and use as medicaments BAYER INTELLECTUAL PROPERTY GMBH (DE) 2007-04-26 US disclosed
US-20070093490-A1 Substituted imidazo[1,2b]pyridazines as kinase inhibitors, their preparation and use as medicaments BAYER INTELLECTUAL PROPERTY GMBH (DE) 2007-04-26 US disclosed
US-20070093490-A1 Substituted imidazo[1,2b]pyridazines as kinase inhibitors, their preparation and use as medicaments BAYER INTELLECTUAL PROPERTY GMBH (DE) 2007-04-26 US disclosed
WO-2007025540-A2 SUBSTITUTED IMIDAZO[1,2B]PYRIDAZINES AS KINASE INHIBITORS, THE PRODUCTION THEREOF, AND USE OF THE SAME AS MEDICAMENTS BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2007-03-08 WO disclosed
WO-2007025540-A2 SUBSTITUTED IMIDAZO[1,2B]PYRIDAZINES AS KINASE INHIBITORS, THE PRODUCTION THEREOF, AND USE OF THE SAME AS MEDICAMENTS BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2007-03-08 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 (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-20230059009-A1 INHIBITORS OF LIN28 AND METHODS OF USE THEREOF LIN28A, DDX21, BMI1 DYRK1A 3932/4885DYRK2 3812/4885DYRK1B 3583/4885
US-20080261988-A1 IMIDAZO[1,2-beta]PYRIDAZINE AND PYRAZOLO[1,5-alpha]PYRIMIDINE DERIVATIVES AND THEIR USE AS PROTEIN KINASE INHIBITORS PIM1, PIM2, PIM3 DYRK1A 221/4885DYRK2 229/4885DYRK1B 235/4885
US-20070093490-A1 Substituted imidazo[1,2b]pyridazines as kinase inhibitors, their preparation and use as medicaments MAP4K2, MAP3K1, MAP3K2 DYRK1A 461/4885DYRK2 336/4885DYRK1B 451/4885

“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.