SCHEMBL4084769

SCHEMBL4084769

CCOC(=N)c1ccc2[nH]nc(-c3ccc4ccccc4c3)c2c1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TTK P33981 5/20 0.48
CDK4 P11802 1/20 0.47
CCNA2 P20248 1/20 0.47
CCND1 P24385 1/20 0.47
CDK2 P24941 1/20 0.47
CCND3 P30281 1/20 0.47
KDR P35968 1/20 0.47
MAPK8 P45983 5/20 0.45
MAPKAPK2 P49137 4/20 0.44
CSNK1D P48730 1/20 0.44
MAP2K4 P45985 7/20 0.43
MAPK1 P28482 5/20 0.43
MAPKAPK3 Q16644 4/20 0.43
MAPK6 Q16659 4/20 0.43
KDM4E B2RXH2 1/20 0.42
MAPKAPK5 Q8IW41 2/20 0.42
MAPK9 P45984 1/20 0.41
MAPK10 P53779 1/20 0.41
JAK2 O60674 1/20 0.41
JAK3 P52333 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
SCHEMBL4083929 0.89 BTK (0.43) TTKCDK4CCNA2CCND1CDK2
Hydrochloric Acid SCHEMBL4083919 0.89 MAP2K4 (0.47) TTKCDK4CCNA2CCND1CDK2
SCHEMBL4043448 0.89 BTK (0.45) TTKCDK4CCNA2CCND1CDK2
Hydrochloric Acid SCHEMBL4079950 0.88 MAP2K4 (0.42) TTKMAPK8MAPKAPK2CSNK1DMAP2K4
Hydrochloric Acid SCHEMBL5397824 0.88 BTK (0.44) TTKCDK4CCNA2CCND1CDK2
Hydrochloric Acid SCHEMBL4083323 0.88 BTK (0.44) TTKCDK4CCNA2CCND1CDK2
Hydrochloric Acid SCHEMBL4090684 0.88 MAP2K4 (0.42) TTKMAPK8MAPKAPK2MAP2K4MAPK1
SCHEMBL4050943 0.85 TTK (0.47) TTKMAPK8MAPK1
SCHEMBL4079542 0.85 TTK (0.43) TTKKDRMAPK8MAPKAPK2CSNK1D
SCHEMBL4089678 0.84 TTK (0.45) TTKMAPK8MAPKAPK2CSNK1DMAPK1

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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2065383-A1 Indazole compounds and methods of use thereof as protein kinase inhibitors Signal Pharmaceuticals, Inc. (US) 2009-06-03 EP disclosed
US-20090099178-A1 INDAZOLE COMPOUNDS AND METHODS OF USE THEREOF BHAGWAT SHRIPAD S 2009-04-16 US disclosed
EP-1692128-A1 INDAZOLE COMPOUNDS AND METHODS OF USE THEREOF AS PROTEIN KINASE INHIBITORS Signal Pharmaceuticals LLC (US) 2006-08-23 EP disclosed
US-20060004043-A1 Indazole compounds and methods of use thereof BHAGWAT SHRIPAD S 2006-01-05 US disclosed
WO-2005051942-A1 INDAZOLE COMPOUNDS AND METHODS OF USE THEREOF AS PROTEIN KINASE INHIBITORS SIGNAL PHARMACEUTICALS, LLC (US) 2005-06-09 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 (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-20090099178-A1 INDAZOLE COMPOUNDS AND METHODS OF USE THEREOF WNT3, WNT3A, WNK3 TTK 401/4885CDK4 253/4885CCNA2 2736/4885
US-20060004043-A1 Indazole compounds and methods of use thereof WNT3, WNT3A, WNK3 TTK 377/4885CDK4 215/4885CCNA2 2747/4885

“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.