SCHEMBL12807117

SCHEMBL12807117

C=CC(=O)Nc1cccc(-c2ccncn2)c1

nearest known ligand 0.59

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
▸ JAK3 P52333 8/20 0.59
▸ JAK1 P23458 4/20 0.56
▸ JAK2 O60674 4/20 0.53
▸ EGFR P00533 1/20 0.53
▸ PLCG1 P19174 4/20 0.53
▸ BTK Q06187 4/20 0.52
▸ ITK Q08881 2/20 0.51
▸ TYK2 P29597 1/20 0.50
▸ TGM2 P21980 1/20 0.50
▸ MAP2K7 O14733 1/20 0.50
▸ AURKA O14965 1/20 0.50

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
SCHEMBL17939611 0.83 PLCG1 (0.77) PLCG1BTKITK
SCHEMBL1444775 0.82 FYN (0.56) JAK3
SCHEMBL28144707 0.76 CYP17A1 (0.59) —
SCHEMBL24150634 0.75 JAK3 (0.68) JAK3JAK1JAK2EGFRPLCG1
SCHEMBL30190947 0.75 JAK3 (0.68) JAK3JAK1JAK2EGFRPLCG1
SCHEMBL30190528 0.75 JAK3 (0.58) JAK3JAK1PLCG1BTKITK
SCHEMBL24151660 0.75 JAK3 (0.58) JAK3JAK1PLCG1BTKITK
SCHEMBL30191150 0.75 JAK3 (0.74) JAK3JAK1JAK2EGFRPLCG1
SCHEMBL24151517 0.75 JAK3 (0.74) JAK3JAK1JAK2EGFRPLCG1
SCHEMBL24150540 0.75 JAK3 (0.60) JAK3JAK1EGFRPLCG1BTK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12286422-B2 Methods and compositions of 4-substituted benzoylpiperazine-1-substituted carbonyls as β-catenin/B-cell lymphoma 9 inhibitors UNIVERSITY OF UTAH RESEARCH FOUNDATION (US) 2025-04-29 — — US disclosed
US-20230122912-A1 Methods and Compositions of 4-Substituted Benzoylpiperazine-1-Substituted Carbonyls as Beta-Catenin/B-Cell Lymphoma 9 Imhibitors UNIVERSITY OF UTAH RESEARCH FOUNDATION 2023-04-20 — — US disclosed
US-11542254-B2 Methods and composition of 4-substituted benzoylpiperazine-1-substituted carbonyls as beta-catenin/B-cell lymphoma 9 inhibitors UNIVERSISITY OF UTAH RESEARCH FOUNDATION (US) 2023-01-03 — — US disclosed
US-20210171502-A1 METHODS AND COMPOSITION OF 4-SUBSTITUTED BENZOYLPIPERAZINE-1-SUBSTITUTED CARBONYLS AS BETA-CATENIN/B-CELL LYMPHOMA 9 INHIBITORS UNITED STATES GOVERNMENT 2021-06-10 — — US disclosed
EP-3680238-A1 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS University of Utah Research Foundation (US) 2020-07-15 — — EP disclosed
EP-2903971-B1 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS UNIV UTAH RES FOUND (US) 2019-06-12 — — EP disclosed
US-20180134719-A1 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS UNIVERSITY OF UTAH RESEARCH FOUNDATION 2018-05-17 — — US disclosed
US-20180134719-A1 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS UNIVERSITY OF UTAH RESEARCH FOUNDATION 2018-05-17 — — US disclosed
EP-2694486-B1 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS UNIV UTAH RES FOUND (US) 2018-01-10 — — EP disclosed
US-9828376-B2 Substituted N-(3-pyrimidin-4-yl)phenyl)acrylamide analogs as tyrosine receptor kinase BTK inhibitors UNIVERSITY OF UTAH RESEARCH FOUNDATION (US) 2017-11-28 — — US disclosed
WO-2014055928-A2 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS UNIVERSITY OF UTAH RESEARCH FOUNDATION (US) 2014-04-10 — — WO disclosed
WO-2014055934-A2 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS UNIVERSITY OF UTAH RESEARCH FOUNDATION (US) 2014-04-10 — — WO disclosed
WO-2014055934-A2 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS UNIVERSITY OF UTAH RESEARCH FOUNDATION (US) 2014-04-10 — — WO disclosed
WO-2014055928-A2 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS UNIVERSITY OF UTAH RESEARCH FOUNDATION (US) 2014-04-10 — — WO disclosed
EP-2694486-A1 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS University of Utah Research Foundation (US) 2014-02-12 — — EP disclosed
EP-2694486-A1 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS University of Utah Research Foundation (US) 2014-02-12 — — EP disclosed
US-20130059847-A1 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS UNIVERSITY OF UTAH 2013-03-07 — — US disclosed
US-20130059847-A1 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS UNIVERSITY OF UTAH 2013-03-07 — — US disclosed
WO-2012135801-A1 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS UNIVERSITY OF UTAH RESEARCH FOUNDATION (US) 2012-10-04 — — WO disclosed
WO-2012135801-A1 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS UNIVERSITY OF UTAH RESEARCH FOUNDATION (US) 2012-10-04 — — 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 (6 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-20210171502-A1 METHODS AND COMPOSITION OF 4-SUBSTITUTED BENZOYLPIPERAZINE-1-SUBSTITUTED CARBONYLS AS BETA-CATENIN/B-CELL LYMPHOMA 9 INHIBITORS BCL9, BCL9L, BCL3 JAK3 3056/4885JAK1 3373/4885JAK2 1442/4885
US-11542254-B2 Methods and composition of 4-substituted benzoylpiperazine-1-substituted carbonyls as beta-catenin/B-cell lymphoma 9 inhibitors BCL9, BCL9L, BCL3 JAK3 3203/4885JAK1 3236/4885JAK2 1436/4885
US-12286422-B2 Methods and compositions of 4-substituted benzoylpiperazine-1-substituted carbonyls as β-catenin/B-cell lymphoma 9 inhibitors BCL9, BCL9L, BCL3 JAK3 3051/4885JAK1 3044/4885JAK2 1170/4885
US-20130059847-A1 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS BTK, SYK, LYN JAK3 58/4885JAK1 42/4885JAK2 20/4885
US-20230122912-A1 Methods and Compositions of 4-Substituted Benzoylpiperazine-1-Substituted Carbonyls as Beta-Catenin/B-Cell Lymphoma 9 Imhibitors BCL9, BCL9L, BCL3 JAK3 3373/4885JAK1 3264/4885JAK2 1338/4885
US-20180134719-A1 SUBSTITUTED N-(3-(PYRIMIDIN-4-YL)PHENYL)ACRYLAMIDE ANALOGS AS TYROSINE RECEPTOR KINASE BTK INHIBITORS BTK, SYK, LYN JAK3 58/4885JAK1 42/4885JAK2 20/4885

“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.

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