SCHEMBL899479

SCHEMBL899479

O=C(O)c1cc(Br)c(Br)s1

nearest known ligand 0.61

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
GSK3B P49841 2/20 0.61
MEN1 O00255 4/20 0.50
KMT2A Q03164 4/20 0.50
DAO P14920 5/20 0.46
GPR35 Q9HC97 3/20 0.46
ALDH1A1 P00352 3/20 0.46
MAPT P10636 3/20 0.46
KDM4E B2RXH2 2/20 0.46
LMNA P02545 1/20 0.46
POLB P06746 1/20 0.46
HTT P42858 1/20 0.46
L3MBTL1 Q9Y468 1/20 0.46
BCL2L1 Q07817 1/20 0.41
PTPN2 P17706 2/20 0.40

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
Bromide SCHEMBL8935164 0.98 GSK3B (0.59) GSK3BMEN1KMT2ADAOGPR35
Hydrochloric Acid SCHEMBL8935203 0.98 GSK3B (0.59) GSK3BMEN1KMT2ADAOGPR35
4-Bromoaniline SCHEMBL9422575 0.84 MEN1 (0.54) GSK3BMEN1KMT2ADAOGPR35
SCHEMBL7043189 0.82 GSK3B (0.57) GSK3BMEN1KMT2ADAOALDH1A1
SCHEMBL8651250 0.81 GSK3B (0.61) GSK3BMEN1KMT2AALDH1A1MAPT
SCHEMBL7892619 0.79 GSK3B (0.62) GSK3BMEN1KMT2AALDH1A1MAPT
SCHEMBL2043829 0.79 GSK3B (0.59) GSK3BMEN1KMT2AALDH1A1MAPT
SCHEMBL5010509 0.79 GSK3B (0.59) GSK3BMEN1KMT2AALDH1A1MAPT
SCHEMBL17201685 0.79 DAO (0.45) GSK3BMEN1KMT2ADAOGPR35
SCHEMBL30020630 0.79 GPR35 (0.48) GSK3BMEN1KMT2ADAOGPR35

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108350034-B Antimicrobial polymyxin derived compounds 莫纳什大学 2022-03-11 CN claimed
EP-1863766-B1 CERTAIN SUBSTITUTED AMIDES, METHOD OF MAKING, AND METHOD OF USE THEREOF GILEAD CONNECTICUT INC (US) 2015-05-20 EP claimed
EP-1863766-A2 CERTAIN SUBSTITUTED AMIDES, METHOD OF MAKING, AND METHOD OF USE THEREOF CGI Pharmaceuticals, Inc. (US) 2007-12-12 EP claimed
US-20060229337-A1 Certain substituted amides, method of making, and method of use thereof GILEAD CONNECTICUT, INC. 2006-10-12 US claimed
WO-2006099075-A2 CERTAIN SUBSTITUTED AMIDES, METHOD OF MAKING, AND METHOD OF USE THEREOF CGI PHARMACEUTICALS, INC. (US) 2006-09-21 WO claimed
US-20050256104-A1 substituted 1,1,4-1l6-trioxo[1,2]thiazepan-4-ylamide-derived protease inhibitors which inhibit the likes of cathepsin K; treating osteoporosis, osteo- and rheumatoid arthritis and periodontal disease; inhibiting excessive cartilage or matrix degradation SMITHKLINE BEECHAM CORPORATION 2005-11-17 US claimed
EP-1377589-B1 OXAZOLYL-PYRAZOLE DERIVATIVES AS KINASE INHIBITORS PHARMACIA ITALIA SPA (IT) 2005-09-07 EP claimed
EP-1384713-A1 4-amino-azepan-3-one derivatives as protease inhibitors SmithKline Beecham Corporation (US) 2004-01-28 EP claimed
US-20040002487-A1 Protease inhibitors MARQUIS ROBERT WELLS (US) 2004-01-01 US claimed
US-20030225061-A1 Protease inhibitors MARQUIS ROBERT WELLS (US) 2003-12-04 US claimed
US-20030144175-A1 Protease inhibitors SMITHKLINE BEECHAM CORPORATION 2003-07-31 US claimed
US-20030044399-A1 Method of treatment SMITHKLINE BEECHAM CORPORATION 2003-03-06 US claimed
US-20020147188-A1 Protease inhibitors SMITHKLINE BEECHAM CORPORATION 2002-10-10 US claimed
EP-1158986-A4 PROTEASE INHIBITORS SMITHKLINE BEECHAM CORP (US) 2002-03-27 EP claimed
EP-1158986-A1 PROTEASE INHIBITORS SmithKline Beecham Corporation (US) 2001-12-05 EP claimed
WO-2000038687-A1 PROTEASE INHIBITORS SMITHKLINE BEECHAM CORPORATION (US) 2000-07-06 WO claimed
EP-4132508-B1 NOVEL INHIBITORS OF HISTONE ACETYLTRANSFERASE P300/CBP FOR CANCER THERAPY BAYLOR COLLEGE MEDICINE (US) 2025-11-12 EP disclosed
US-20250296926-A1 SELECTIVE LIGANDS FOR MODULATION OF GIRK CHANNELS INDIANA UNIVERSITY RESEARCH AND TECHNOLOGY CORPORATION 2025-09-25 US disclosed
EP-0379003-A1 Thiophene-2-carboxylic-acid derivatives, process for their preparation and their use in combating undesired plant growth BASF Aktiengesellschaft (DE) 1990-07-25 EP disclosed
US-3887354-A Method for facilitating the harvest of fruit MONSANTO CO 1975-06-03 US 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 (8 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-20030225061-A1 Protease inhibitors CTSK, MMP13, CTSZ GSK3B 308/4885MEN1 2054/4885KMT2A 2920/4885
US-20030044399-A1 Method of treatment DNPEP, PEPD, ANPEP GSK3B 4021/4885MEN1 3024/4885KMT2A 1833/4885
US-20060229337-A1 Certain substituted amides, method of making, and method of use thereof BTK, SYK, MYD88 GSK3B 938/4885MEN1 3962/4885KMT2A 618/4885
US-20250296926-A1 SELECTIVE LIGANDS FOR MODULATION OF GIRK CHANNELS GRIK4, GRIK2, GRIK1 GSK3B 1751/4885MEN1 3693/4885KMT2A 2424/4885
US-20050256104-A1 substituted 1,1,4-1l6-trioxo[1,2]thiazepan-4-ylamide-derived protease inhibitors which inhibit the likes of cathepsin K; treating osteoporosis, osteo- and rheumatoid arthritis and periodontal disease; inhibiting excessive cartilage or matrix degradation CTSK, CTSZ, CTSE GSK3B 474/4885MEN1 3396/4885KMT2A 2410/4885
US-20020147188-A1 Protease inhibitors CTSK, MMP13, CTSZ GSK3B 308/4885MEN1 2054/4885KMT2A 2920/4885
US-20040002487-A1 Protease inhibitors CTSK, MMP13, CTSZ GSK3B 308/4885MEN1 2054/4885KMT2A 2920/4885
US-20030144175-A1 Protease inhibitors CTSK, MMP13, CTSZ GSK3B 308/4885MEN1 2054/4885KMT2A 2920/4885

“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.