SCHEMBL51143

SCHEMBL51143

C/C(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
SCHEMBL51144 1.00 MEN1 (1.00) MEN1ALDH1A1KMT2ACYP1A2CYP3A4
SCHEMBL29394998 1.00 MEN1 (1.00) MEN1ALDH1A1KMT2ACYP1A2CYP3A4
SCHEMBL51142 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 366 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9820987-B2 Modulator compounds of drug resistance in epithelial tumor cells BIONSIL S.R.L. IN LIQUIDAZIONE (IT) 2017-11-21 US claimed
US-20160251614-A1 CELL CULTURE MEDIUM AND BIOPROCESS OPTIMIZATION UNIVERSITY OF NOTRE DAME DU LAC (US) 2016-09-01 US claimed
US-20150111953-A1 Modulator Compounds of Drug Resistance in Epithelial Tumor Cells BIONSIL S.R.L. IN LIQUIDAZIONE (IT) 2015-04-23 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-3645001-B1 MORPHIC FORMS OF GIT38 AND METHODS OF MANUFACTURE THEREOF G1 THERAPEUTICS INC (US) 2024-07-03 EP disclosed
US-20240199581-A1 THERAPEUTICS FOR THE DEGRADATION OF MUTANT BRAF C4 THERAPEUTICS, INC. (US) 2024-06-20 US disclosed
EP-4384162-A1 COMPOSITIONS AND METHODS FOR EXTENDED RELEASE CROMAKALIM THERAPY Qlaris Bio, Inc. (US) 2024-06-19 EP disclosed
US-11992531-B2 C3-carbon linked glutarimide degronimers for target protein degradation C4 THERAPEUTICS, INC. (US) 2024-05-28 US disclosed
US-20240158418-A1 EGFR Degraders to Treat Cancer Metastasis to the Brain or CNS C4 THERAPEUTICS, INC. (US) 2024-05-16 US disclosed
WO-2024097980-A1 RET-LDD PROTEIN INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2024-05-10 WO disclosed
WO-2024097989-A1 RET-LDD PROTEIN DEGRADERS BRISTOL-MYERS SQUIBB COMPANY (US) 2024-05-10 WO disclosed
US-6294575-B1 FOR THERAPY OF ALLERGY BY ADMINISTERING INHIBITORS OF BRUTON'S TYROSINE KINASE (BTK) PARKER HUGHES INSTITUTE 2001-09-25 US disclosed
US-6248790-B1 Treatment of inflammation with 2,4,6-trihydroxy-alpha-rho-methoxyphenylacetophenone, or its pharmaceutically acceptable derivatives PARKER HUGHES INSTITUTE 2001-06-19 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 (4 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-20240199581-A1 THERAPEUTICS FOR THE DEGRADATION OF MUTANT BRAF BRAF, NRAS, KRAS MEN1 594/4885ALDH1A1 1471/4885KMT2A 1520/4885
US-20240158418-A1 EGFR Degraders to Treat Cancer Metastasis to the Brain or CNS EGFR, ERBB2, ERBB3 MEN1 1683/4885ALDH1A1 3277/4885KMT2A 738/4885
US-20150111953-A1 Modulator Compounds of Drug Resistance in Epithelial Tumor Cells BTK, PRKDC, PCLAF MEN1 3314/4885ALDH1A1 4313/4885KMT2A 1708/4885
US-11992531-B2 C3-carbon linked glutarimide degronimers for target protein degradation STUB1, UBE3C, UBE3A MEN1 1031/4885ALDH1A1 2819/4885KMT2A 2966/4885

“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.