SCHEMBL3148490

SCHEMBL3148490

O=C1NC(=O)C(c2c[nH]c3ccccc23)=C1c1ccccc1

nearest known ligand 0.84

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PRKCB P05771 9/20 0.84
PRKCA P17252 5/20 0.84
CDK4 P11802 3/20 0.84
CCND1 P24385 3/20 0.84
CDK2 P24941 3/20 0.84
PRKCH P24723 3/20 0.84
PRKCE Q02156 3/20 0.84
PRKCQ Q04759 3/20 0.84
PRKCD Q05655 3/20 0.84
CAMK2D Q13557 2/20 0.84
ABL1 P00519 2/20 0.84
CCNE2 O96020 2/20 0.84
PRKACA P17612 2/20 0.84
PRKACG P22612 2/20 0.84
PRKACB P22694 2/20 0.84
CCNE1 P24864 2/20 0.84
SIRT2 Q8IXJ6 2/20 0.84
PRKD3 O94806 1/20 0.84
CCNB2 O95067 1/20 0.84
PRKCG P05129 1/20 0.84

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
Ro-316233 SCHEMBL29373011 0.92 PRKCB (1.00) PRKCBPRKCACDK4CCND1CDK2
Ro-316233 SCHEMBL624896 0.92 PRKCB (1.00) PRKCBPRKCACDK4CCND1CDK2
SCHEMBL8160996 0.83 PRKCB (0.67) PRKCBPRKCACDK4CCND1CDK2
SCHEMBL2013173 0.81 PRKCB (0.55) PRKCBPRKCACDK4CCND1CDK2
SCHEMBL6823304 0.81 PRKCB (0.78) PRKCBPRKCACDK4CCND1CDK2
SCHEMBL6098588 0.81 PRKCB (0.78) PRKCBPRKCACDK4CCND1CDK2
SCHEMBL5333315 0.81 PRKCB (0.78) PRKCBPRKCACDK4CCND1CDK2
SCHEMBL13917970 0.81 PRKCB (0.78) PRKCBPRKCACDK4CCND1CDK2
SCHEMBL6583607 0.81 PRKCB (0.58) PRKCBPRKCACDK4CCND1CDK2
SCHEMBL8167180 0.81 PRKCB (0.78) PRKCBPRKCACDK4CCND1CDK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090304663-A1 USE OF GSK-3 INHIBITORS FOR THE TREATMENT OF PROSTATE CANCER IMPERIAL INNOVATIONS LIMITED (GB) 2009-12-10 US claimed
EP-1786448-A1 USE OF GSK-3 INHIBITORS FOR THE TREATMENT OF PROSTATE CANCER Imperial Innovations Limited (GB) 2007-05-23 EP claimed
WO-2006018633-A1 USE OF GSK-3 INHIBITORS FOR THE TREATMENT OF PROSTATE CANCER IMPERIAL INNOVATIONS LIMITED (GB) 2006-02-23 WO claimed
US-20050075276-A1 Use of inhibitors of glycogen synthase-3 to augment CD28 dependent -T-cell responses RUDD CHRISTOPHER (US) 2005-04-07 US claimed
EP-4662319-A2 PERSONALIZED CRISPR PROFILING FOR CANCER Integrate Bioscience LLC (US) 2025-12-17 EP disclosed
WO-2024168301-A2 PERSONALIZED CRISPR PROFILING FOR CANCER FUNCTION ONCOLOGY, INC. (US) 2024-08-15 WO disclosed
EP-2125683-B1 3-BENZOFURANYL-4-INDOLYL-MALEIMIDES AS POTENT GSK-3 INHIBITORS FOR NEURODEGENERATIVE DISORDERS UNIV ILLINOIS (US) 2013-10-23 EP disclosed
US-8207216-B2 Benzofuran-3-yl(indol-3-yl) maleimides as potent GSK3 inhibitors THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) 2012-06-26 US disclosed
US-7799915-B2 Anilino-pyrimidine analogs WYETH LLC (US) 2010-09-21 US disclosed
US-20100105745-A1 Suppression of cancer and method for evaluating anticancer agent based on the effect of inhibiting gsk3 beta NATIONAL UNIVERSITY CORPORATION KANAZAWA UNIVERSITY (JP) 2010-04-29 US disclosed
US-20100004308-A1 Benzofuran-3-yl(indol-3-yl) Maleimides as Potent GSK3 Inhibitors THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS, A BODY CORPORATE AND POLITIC OF THE STATE OF ILLINOIS 2010-01-07 US disclosed
US-20090304663-A1 USE OF GSK-3 INHIBITORS FOR THE TREATMENT OF PROSTATE CANCER IMPERIAL INNOVATIONS LIMITED (GB) 2009-12-10 US disclosed
US-20020052397-A1 3-indolyl-4-phenyl-1H-pyrrole-2,5-dione derivatives as inhibitors of glycogen synthase kinase-3beta SYNTEX (U.S.A.) LLC 2002-05-02 US disclosed
US-20020052397-A1 3-indolyl-4-phenyl-1H-pyrrole-2,5-dione derivatives as inhibitors of glycogen synthase kinase-3beta SYNTEX (U.S.A.) LLC 2002-05-02 US disclosed
WO-2002010158-A2 3-INDOLYL-4-PHENYL-1H-PYRROLE-2,5-DIONE DERIVATIVES AS INHIBITORS OF GLYCOGEN SYNTHASE KINASE-3BETA F. HOFFMANN-LA ROCHE AG (CH) 2002-02-07 WO disclosed
WO-2002010158-A2 3-INDOLYL-4-PHENYL-1H-PYRROLE-2,5-DIONE DERIVATIVES AS INHIBITORS OF GLYCOGEN SYNTHASE KINASE-3BETA F. HOFFMANN-LA ROCHE AG (CH) 2002-02-07 WO disclosed
US-RE36736-E Substituted pyrroles HOFFMAN-LA ROCHE INC. (US) 2000-06-13 US disclosed
EP-0328026-B1 SUBSTITUTED PYRROLES F. HOFFMANN-LA ROCHE AG (CH) 1993-04-28 EP disclosed
US-5057614-A Antiinflammatory, immunology, bronchodilator agents, cardiovascular disorders HOFFMANN-LA ROCHE INC. (US) 1991-10-15 US disclosed
EP-0328026-A1 Substituted pyrroles F. HOFFMANN-LA ROCHE AG (CH) 1989-08-16 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 (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-20100004308-A1 Benzofuran-3-yl(indol-3-yl) Maleimides as Potent GSK3 Inhibitors GSK3B, GSK3A, GSKIP PRKCB 720/4885PRKCA 1238/4885CDK4 467/4885
US-20020052397-A1 3-indolyl-4-phenyl-1H-pyrrole-2,5-dione derivatives as inhibitors of glycogen synthase kinase-3beta GSK3B, GSK3A, PYGL PRKCB 62/4885PRKCA 61/4885CDK4 368/4885
US-20100105745-A1 Suppression of cancer and method for evaluating anticancer agent based on the effect of inhibiting gsk3 beta GSK3B, GSK3A, GSKIP PRKCB 228/4885PRKCA 356/4885CDK4 409/4885

“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.