SCHEMBL9938111

SCHEMBL9938111

O=Cc1cc(Cl)ncc1Br

nearest known ligand 0.41

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
ERN1 O75460 7/20 0.41
LMNA P02545 1/20 0.39
PRKDC P78527 1/20 0.38
TRIM24 O15164 1/20 0.35
TRIM33 Q9UPN9 1/20 0.35
TDP1 Q9NUW8 1/20 0.33
CSNK2A1 P68400 1/20 0.32
CYP1A2 P05177 1/20 0.31
CYP3A4 P08684 1/20 0.31
CYP2D6 P10635 1/20 0.31
CYP2C19 P33261 1/20 0.31

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
SCHEMBL30054303 1.00 ERN1 (0.41) ERN1LMNAPRKDCTRIM24TRIM33
SCHEMBL15332623 0.83 ERN1 (0.41) ERN1LMNAPRKDCTRIM24TRIM33
SCHEMBL31252016 0.79 ALDH1A1 (0.31)
SCHEMBL1533918 0.78 TDP1 (0.40) ERN1TDP1CYP1A2CYP3A4CYP2D6
SCHEMBL29411231 0.78 LMNA (0.41) ERN1LMNAPRKDCTRIM24TRIM33
SCHEMBL30589401 0.78 TDP1 (0.40) ERN1TDP1CYP1A2CYP3A4CYP2D6
SCHEMBL19794988 0.78 LMNA (0.41) ERN1LMNAPRKDCTRIM24TRIM33
SCHEMBL24458114 0.75 ERN1 (0.35) ERN1TDP1CYP1A2CYP3A4CYP2D6
SCHEMBL6856975 0.75 ERN1 (0.34) ERN1TDP1CYP1A2CYP3A4CYP2D6
SCHEMBL1389512 0.75 ERN1 (0.48) ERN1LMNATRIM24TRIM33TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025237891-A1 QUINOLINE-2-CARBOXAMIDE DERIVATIVES AS RAD51 INHIBITORS FOR THE TREATMENT OF CANCER NERVIANO MEDICAL SCIENCES S.R.L. (IT) 2025-11-20 WO disclosed
US-20250163043-A1 CDK9 INHIBITOR AND USE THEREOF TRANSTHERA SCIENCES (NANJING), INC. (CN) 2025-05-22 US disclosed
EP-4217356-B1 CYCLIN-DEPENDENT KINASE 7 (CDK7) NON-COVALENT INHIBITORS JANSSEN PHARMACEUTICA NV (BE) 2025-05-14 EP disclosed
US-20240376058-A1 GCN2 AND PERK KINASE INHIBITORS AND METHODS OF USE THEREOF DECIPHERA PHARMACEUTICALS, LLC 2024-11-14 US disclosed
EP-4450501-A1 CDK9 INHIBITOR AND USE THEREOF TransThera Sciences (Nanjing), Inc. (CN) 2024-10-23 EP disclosed
US-20240262822-A1 WDR5 INHIBITORS AND MODULATORS NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2024-08-08 US disclosed
WO-2024118460-A1 ADENOSINE A2A AND A2B RECEPTOR ANTAGONISTS, PHARMACEUTICAL COMPOSITIONS AND USE THEREOF MERCK SHARP & DOHME LLC (US) 2024-06-06 WO disclosed
US-20240158415-A1 AMINOPYRIDINE DERIVATIVES AS PHOSPHATIDYLINOSITOL PHOSPHATE KINASE INHIBITORS HIBERCELL INC (US) 2024-05-16 US disclosed
WO-2024097953-A1 NAPHTHYRIDINE COMPOUNDS FOR INHIBITION OF RAF KINASES ENLIVEN INC. (US) 2024-05-10 WO disclosed
US-20240101554-A1 CYCLIN-DEPENDENT KINASE 7 (CDK7) NON-COVALENT INHIBITORS JANSSEN PHARMACEUTICA NV (BE) 2024-03-28 US disclosed
US-20140088076-A1 SUBSTITUTED 6,6-FUSED NITROGENOUS HETEROCYCLIC COMPOUNDS AND USES THEREOF GENENTECH, INC. (US) 2014-03-27 US disclosed
US-20140088076-A1 SUBSTITUTED 6,6-FUSED NITROGENOUS HETEROCYCLIC COMPOUNDS AND USES THEREOF GENENTECH, INC. (US) 2014-03-27 US disclosed
US-8623889-B2 Substituted 6,6-fused nitrogenous heterocyclic compounds and uses thereof GENENTECH, INC. (US) 2014-01-07 US disclosed
US-8623889-B2 Substituted 6,6-fused nitrogenous heterocyclic compounds and uses thereof GENENTECH, INC. (US) 2014-01-07 US disclosed
US-8623889-B2 Substituted 6,6-fused nitrogenous heterocyclic compounds and uses thereof GENENTECH, INC. (US) 2014-01-07 US disclosed
EP-2651899-A2 SUBSTITUTED 6,6-FUSED NITROGENOUS HETEROCYCLIC COMPOUNDS AND USES THEREOF F.HOFFMANN-LA ROCHE AG (CH) 2013-10-23 EP disclosed
US-20120322785-A1 SUBSTITUTED 6,6-FUSED NITROGENOUS HETEROCYCLIC COMPOUNDS AND USES THEREOF GENENTECH, INC. (US) 2012-12-20 US disclosed
US-20120322785-A1 SUBSTITUTED 6,6-FUSED NITROGENOUS HETEROCYCLIC COMPOUNDS AND USES THEREOF GENENTECH, INC. (US) 2012-12-20 US disclosed
US-20120322785-A1 SUBSTITUTED 6,6-FUSED NITROGENOUS HETEROCYCLIC COMPOUNDS AND USES THEREOF GENENTECH, INC. (US) 2012-12-20 US disclosed
WO-2012080284-A2 SUBSTITUTED 6,6-FUSED NITROGENOUS HETEROCYCLIC COMPOUNDS AND USES THEREOF F. HOFFMANN-LA ROCHE AG (CH) 2012-06-21 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 (7 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-20240262822-A1 WDR5 INHIBITORS AND MODULATORS WDR5, WDR1, WDR3 ERN1 1405/4885LMNA 3249/4885PRKDC 2946/4885
US-20240158415-A1 AMINOPYRIDINE DERIVATIVES AS PHOSPHATIDYLINOSITOL PHOSPHATE KINASE INHIBITORS PIP5K1B, PIP5K1A, PIP5K1C ERN1 831/4885LMNA 4267/4885PRKDC 832/4885
US-20120322785-A1 SUBSTITUTED 6,6-FUSED NITROGENOUS HETEROCYCLIC COMPOUNDS AND USES THEREOF XDH, CYP2B6, COX6B1 ERN1 2368/4885LMNA 1213/4885PRKDC 4759/4885
US-20240376058-A1 GCN2 AND PERK KINASE INHIBITORS AND METHODS OF USE THEREOF EIF2AK4, GCN1, EEF2K ERN1 9/4885LMNA 992/4885PRKDC 183/4885
US-20240101554-A1 CYCLIN-DEPENDENT KINASE 7 (CDK7) NON-COVALENT INHIBITORS CDK7, CDK9, CDK1 ERN1 879/4885LMNA 1570/4885PRKDC 402/4885
US-20140088076-A1 SUBSTITUTED 6,6-FUSED NITROGENOUS HETEROCYCLIC COMPOUNDS AND USES THEREOF XDH, CYP2B6, COX6B1 ERN1 2368/4885LMNA 1213/4885PRKDC 4759/4885
US-20250163043-A1 CDK9 INHIBITOR AND USE THEREOF CDK9, CDK19, CDKL1 ERN1 1194/4885LMNA 224/4885PRKDC 865/4885

“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.