SCHEMBL51144

SCHEMBL51144

CC(O)=C(C#N)C(=O)Nc1cc(Br)ccc1Br

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 2/20 1.00
ALDH1A1 P00352 2/20 1.00
KMT2A Q03164 2/20 1.00
CYP1A2 P05177 1/20 1.00
CYP3A4 P08684 1/20 1.00
GAA P10253 1/20 1.00
CYP2C9 P11712 1/20 1.00
PKM P14618 1/20 1.00
ALOX15 P16050 1/20 1.00
TSHR P16473 1/20 1.00
LMNA P02545 1/20 1.00
THRB P10828 1/20 1.00
BLM P54132 1/20 1.00
BTK Q06187 1/20 1.00
NPSR1 Q6W5P4 1/20 1.00
PLK3 Q9H4B4 1/20 1.00
DHODH Q02127 18/20 0.51

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
SCHEMBL29394998 1.00 MEN1 (1.00) MEN1ALDH1A1KMT2ACYP1A2CYP3A4
SCHEMBL51142 1.00 MEN1 (1.00) MEN1ALDH1A1KMT2ACYP1A2CYP3A4
SCHEMBL51143 1.00 MEN1 (1.00) MEN1ALDH1A1KMT2ACYP1A2CYP3A4
SCHEMBL5914885 0.89 ALDH1A1 (0.80) MEN1ALDH1A1KMT2ACYP1A2CYP3A4
SCHEMBL5914888 0.89 ALDH1A1 (0.80) MEN1ALDH1A1KMT2ACYP1A2CYP3A4
SCHEMBL28057335 0.84 MEN1 (0.70) MEN1ALDH1A1KMT2ACYP1A2CYP3A4
SCHEMBL5914906 0.82 MEN1 (0.70) MEN1ALDH1A1KMT2ACYP1A2CYP3A4
SCHEMBL5914905 0.82 MEN1 (0.70) MEN1ALDH1A1KMT2ACYP1A2CYP3A4
SCHEMBL5914890 0.79 DHODH (0.70) MEN1ALDH1A1KMT2ACYP1A2CYP3A4
SCHEMBL5914891 0.79 DHODH (0.70) MEN1ALDH1A1KMT2ACYP1A2CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4531856-B1 BRUTON'S KINASE INHIBITORS FOR THE TREATMENT OF A SUDDEN ALLERGIC REACTION ALK ABELLO AS (DK) 2026-04-22 EP claimed
US-20250295655-A1 BRUTON'S KINASE INHIBITORS FOR THE TREATMENT OF A SUDDEN ALLERGIC REACTION Alk-Abelló A/S (DK) 2025-09-25 US claimed
EP-4531856-A1 BRUTON'S KINASE INHIBITORS FOR THE TREATMENT OF A SUDDEN ALLERGIC REACTION ALK-Abelló A/S (DK) 2025-04-09 EP claimed
WO-2023232958-A1 BRUTON'S KINASE INHIBITORS FOR THE TREATMENT OF A SUDDEN ALLERGIC REACTION Alk-Abelló A/S (DK) 2023-12-07 WO claimed
US-9976172-B2 Method and apparatus for measuring protein post-translational modification ICAGEN, INC. (US) 2018-05-22 US claimed
WO-2017042706-A1 PHARMACEUTICAL KIT AND USE OF ERYTHROPOIETIN AND BRUTON'S KINASE INHIBITOR UNIWERSYTET MEDYCZNY W BIAŁYMSTOKU (PL) 2017-03-16 WO claimed
US-20160251614-A1 CELL CULTURE MEDIUM AND BIOPROCESS OPTIMIZATION UNIVERSITY OF NOTRE DAME DU LAC (US) 2016-09-01 US claimed
US-20160201111-A1 Method and Apparatus for Measuring Protein Post-Translational Modification UNITED STATES GOVERNMENT 2016-07-14 US claimed
US-8129356-B2 Bmx mediated signal transduction in irradiated vascular endothelium VANDERBILT UNIVERSITY (US) 2012-03-06 US claimed
US-20090136487-A1 BMX MEDIATED SIGNAL TRANSDUCTION IN IRRADIATED VASCULAR ENDOTHELIUM VANDERBILT UNIVERSITY 2009-05-28 US claimed
US-20040127453-A1 Method for treating diseases associated with abnormal kinase activity SUPERGEN, INC. 2004-07-01 US claimed
EP-4531856-B1 BRUTON'S KINASE INHIBITORS FOR THE TREATMENT OF A SUDDEN ALLERGIC REACTION ALK ABELLO AS (DK) 2026-04-22 EP disclosed
US-12479855-B2 Morphic forms of trilaciclib and methods of manufacture thereof PHARMACOSMOS HOLDING A/S (DK) 2025-11-25 US disclosed
US-20250319091-A1 TREATMENT OF CANCERS USING PI3 KINASE ISOFORM MODULATORS INFINITY PHARMACEUTICALS INC (US) 2025-10-16 US disclosed
US-20250295655-A1 BRUTON'S KINASE INHIBITORS FOR THE TREATMENT OF A SUDDEN ALLERGIC REACTION Alk-Abelló A/S (DK) 2025-09-25 US disclosed
WO-2001041754-A2 INHIBITORS OF COLLAGEN-INDUCED PLATELET AGGREGATION PARKER HUGHES INSTITUTE (US) 2001-06-14 WO disclosed
US-6221900-B1 INHIBITORS OF BRUTON'S TYROSINE KINASE (BTK). HUGHES INSTITUTE 2001-04-24 US disclosed
EP-1071658-A2 BTK INHIBITORS AND METHODS FOR THEIR IDENTIFICATION AND USE Parker Hughes Institute (US) 2001-01-31 EP disclosed
US-6160010-A BTK inhibitors and methods for their identification and use PARKER HUGHES INSTITUTE (US) 2000-12-12 US disclosed
WO-1999054286-A2 BTK INHIBITORS AND METHODS FOR THEIR IDENTIFICATION AND USE PARKER HUGHES INSTITUTE (US) 1999-10-28 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 (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-12479855-B2 Morphic forms of trilaciclib and methods of manufacture thereof MCL1, ETV6, ALK MEN1 1647/4885ALDH1A1 1227/4885KMT2A 136/4885
US-20250319091-A1 TREATMENT OF CANCERS USING PI3 KINASE ISOFORM MODULATORS PIK3CA, MCL1, PIK3CB MEN1 1860/4885ALDH1A1 2702/4885KMT2A 985/4885
US-20250295655-A1 BRUTON'S KINASE INHIBITORS FOR THE TREATMENT OF A SUDDEN ALLERGIC REACTION BTK, SYK, ABL1 MEN1 3540/4885ALDH1A1 4690/4885KMT2A 1325/4885

“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.