SCHEMBL2919088

SCHEMBL2919088

COc1ccc(OC)c(C(=O)Nc2n[nH]c3c2CN(C(C)=O)C3)c1

nearest known ligand 0.72

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
CCNA2 P20248 11/20 0.72
CDK2 P24941 11/20 0.72
CCNA1 P78396 11/20 0.72
AURKA O14965 9/20 0.72
EP300 Q09472 7/20 0.53
CREBBP Q92793 7/20 0.53
BRD4 O60885 2/20 0.47
NAMPT P43490 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
SCHEMBL2918214 0.91 CCNA2 (0.59) CCNA2CDK2CCNA1AURKAEP300
SCHEMBL2919793 0.88 CCNA2 (0.56) CCNA2CDK2CCNA1AURKAEP300
SCHEMBL2916155 0.87 CCNA2 (0.56) CCNA2CDK2CCNA1AURKAEP300
SCHEMBL2918881 0.86 CDK2 (0.69) CCNA2CDK2CCNA1AURKAEP300
SCHEMBL2921951 0.85 AURKA (0.58) CCNA2CDK2CCNA1AURKAEP300
SCHEMBL2917938 0.84 CCNA2 (0.51) CCNA2CDK2CCNA1AURKAEP300
SCHEMBL2918082 0.84 CCNA2 (0.51) CCNA2CDK2CCNA1AURKAEP300
SCHEMBL2915176 0.84 AURKA (1.00) CCNA2CDK2CCNA1AURKAEP300
SCHEMBL2923243 0.84 CCNA2 (0.52) CCNA2CDK2CCNA1AURKAEP300
SCHEMBL2922678 0.83 AURKA (0.75) CCNA2CDK2CCNA1AURKAEP300

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1320531-B1 BICYCLO-PYRAZOLES ACTIVE AS KINASE INHIBITORS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEM PFIZER ITALIA SRL (IT) 2010-09-08 EP claimed
US-7541354-B2 Bicyclo-pyrazoles PFIZER ITALIA S.R.L. (IT) 2009-06-02 US claimed
US-20030171357-A1 Bicyclo-pyrazoles active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them NERVIANO MEDICAL SCIENCES S.R.L (IT) 2003-09-11 US claimed
EP-0533047-B1 Preparation of a cephalosporin antibiotic using the synisomer of a thiazolyl intermediate BRISTOL MYERS SQUIBB CO (US) 2003-05-07 EP claimed
EP-1084130-B1 SUBSTITUTED FIVE MEMBERED HETEROCYCLIC COMPOUNDS, FUNGICIDAL COMPOSITIONS CONTAINING THEM AND METHODS OF MANUFACTURE THEREOF MONSANTO TECHNOLOGY LLC (US) 2002-09-04 EP claimed
EP-0585165-B1 Process for the preparation of acyl isocyanates POUDRES & EXPLOSIFS STE NALE (FR) 1997-06-04 EP claimed
WO-2023213445-A1 METHOD FOR PREPARING 4-[5-[BIS(2-CHLOROETHYL)AMINO]-1-METHYL-1H-BENZO[D]IMIDAZOL-2-YL]BUTYRIC ACID ALKYL ESTERS AND FORMYLATED DERIVATIVES Heraeus Deutschland GmbH & Co. KG (DE) 2023-11-09 WO disclosed
EP-2766450-B1 SUBSTITUTED AMINO ALCOHOLS AS CHIRAL DOPANTS FRAUNHOFER GES FORSCHUNG (DE) 2018-12-12 EP disclosed
EP-2802627-B1 PARTICULATE SOLID, PROCESS FOR THE PRODUCTION THEREOF, USE AS FILLER AND ASSOCIATED ARTICLES EVONIK DEGUSSA GMBH (DE) 2018-05-23 EP disclosed
EP-2802627-A1 PARTICULATE SOLID, PROCESS FOR THE PRODUCTION THEREOF, USE AS FILLER AND ASSOCIATED ARTICLES Evonik Industries AG (DE) 2014-11-19 EP disclosed
EP-2766450-A1 SUBSTITUTED AMINO ALCOHOLS AS CHIRAL DOPANTS FRAUNHOFER-GESELLSCHAFT zur Förderung der angewandten Forschung e.V. (DE) 2014-08-20 EP disclosed
WO-2013104497-A1 PARTICULATE SOLID, PROCESS FOR THE PRODUCTION THEREOF, USE AS FILLER AND ASSOCIATED ARTICLES EVONIK INDUSTRIES AG (DE) 2013-07-18 WO disclosed
WO-2013053752-A1 SUBSTITUTED AMINO ALCOHOLS AS CHIRAL DOPANTS Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. (DE) 2013-04-18 WO disclosed
EP-0360163-A2 Aromatic carboxylic-acid derivatives and their use in combating the growth of undesirable plants BASF Aktiengesellschaft (DE) 1990-03-28 EP disclosed
EP-0346789-A2 Salicylic-acid derivatives and their sulfur analogues BASF Aktiengesellschaft (DE) 1989-12-20 EP disclosed
EP-0302491-A1 5-Formyl-isoxazoles BASF Aktiengesellschaft (DE) 1989-02-08 EP disclosed
EP-0044442-B1 N-(4-PHENYL-2-THIAZOLYL)-OXAMIDIC-ACID-2-ETHOXYETHYLESTER, PROCESS FOR ITS PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THIS COMPOUND BASF Aktiengesellschaft (DE) 1984-02-15 EP disclosed
EP-0044442-A1 N-(4-Phenyl-2-thiazolyl)-oxamidic-acid-2-ethoxyethylester, process for its preparation and pharmaceutical compositions containing this compound BASF Aktiengesellschaft (DE) 1982-01-27 EP disclosed
EP-0009658-B1 PROCESS FOR THE PREPARATION OF OXALYL CHLORIDE BAYER AG (DE) 1981-08-26 EP disclosed
EP-0009658-A1 Process for the preparation of oxalyl chloride BAYER AG (DE) 1980-04-16 EP 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 (1 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-20030171357-A1 Bicyclo-pyrazoles active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them MAP3K20, MAP3K19, MAP3K1 CCNA2 848/4885CDK2 43/4885CCNA1 793/4885

“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.