SCHEMBL978025

SCHEMBL978025

O=C(c1ccccc1)C(Br)C(Br)c1ccccc1

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 1/20 0.57
L3MBTL1 Q9Y468 1/20 0.57
CES2 O00748 3/20 0.55
CES1 P23141 3/20 0.55
LMNA P02545 3/20 0.55
ALDH1A1 P00352 5/20 0.46
CYP3A4 P08684 1/20 0.46
CYP1A2 P05177 1/20 0.44
KMT2A Q03164 2/20 0.44
RAB9A P51151 3/20 0.43
NPC1 O15118 2/20 0.43
MDM2 Q00987 1/20 0.42
POLB P06746 1/20 0.41
MAPT P10636 1/20 0.41
MEN1 O00255 1/20 0.41
CYP2D6 P10635 1/20 0.41
SRC P12931 1/20 0.41
SMN1; SMN2 Q16637 2/20 0.41
NPSR1 Q6W5P4 1/20 0.41
DAO P14920 1/20 0.41

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
SCHEMBL28795688 0.90 MEN1 (0.50) TDP1L3MBTL1CES2CES1LMNA
SCHEMBL5873117 0.90 LMNA (0.50) TDP1L3MBTL1CES2CES1LMNA
SCHEMBL28795608 0.87 CES2 (0.48) TDP1L3MBTL1CES2CES1LMNA
SCHEMBL28795622 0.87 CES2 (0.48) TDP1L3MBTL1CES2CES1LMNA
SCHEMBL28945734 0.87 LMNA (0.46) TDP1L3MBTL1CES2CES1LMNA
SCHEMBL11056951 0.87 CES2 (0.48) TDP1L3MBTL1CES2CES1LMNA
SCHEMBL11618685 0.86 TDP1 (0.52) TDP1L3MBTL1CES2CES1LMNA
SCHEMBL5873120 0.84 ALDH1A1 (0.52) TDP1L3MBTL1CES2CES1LMNA
SCHEMBL9157900 0.84 ALDH1A1 (0.64) TDP1L3MBTL1CES2CES1LMNA
SCHEMBL9157738 0.84 TDP1 (0.56) TDP1L3MBTL1CES2CES1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5741621-A PHOTORESISTS, SOLDER MASKS, PRINTING PLATES, PROOFING FILM PRODUCTS E. I. DU PONT DE NEMOURS AND COMPANY (US) 1998-04-21 US claimed
EP-0747769-A2 Process for producing photoimageable films prepared from aqueous photoimageable liquid emulsions E.I. DU PONT DE NEMOURS AND COMPANY (US) 1996-12-11 EP claimed
CN-114805044-A Novel method for synthesizing dibromo compound 兰州大学 2022-07-29 CN disclosed
CN-103739465-A Synthesis method of 1, 3-diphenyl-2-bromo-2-propene-1-one ANHUI RUISAI BIOCHEMICAL TECHNOLOGY CO LTD 2014-04-23 CN disclosed
US-7951827-B2 Synthesis and antiprotozoal activity of dicationic 3,5-diphenylisoxazoles THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 2011-05-31 US disclosed
US-7872029-B2 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states BOWEN J PHILLIP 2011-01-18 US disclosed
US-20090018167-A1 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states Robinson, Thomas Philip (US) 2009-01-15 US disclosed
EP-1058697-B1 POLYMERIC FILMS HAVING CONTROLLED VISCOSITY RESPONSE TO TEMPERATURE AND SHEAR DU PONT (US) 2008-11-26 EP disclosed
US-7432303-B2 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states Bowen, J. Phillip (US) 2008-10-07 US disclosed
CN-100350327-C Process for continuous liquid processing of photosensitive compositions having reduced levels of residues DU PONT (US) 2007-11-21 CN disclosed
EP-1093020-B1 Wound storage roll of composite photosensitive element DU PONT (US) 2007-04-04 EP disclosed
EP-1058697-A1 POLYMERIC FILMS HAVING CONTROLLED VISCOSITY RESPONSE TO TEMPERATURE AND SHEAR E.I. DU PONT DE NEMOURS AND COMPANY (US) 2000-12-13 EP disclosed
WO-1999046644-A1 PROCESS FOR THE CONTINUOUS LIQUID PROCESSING OF PHOTOSENSITIVE COMPOSITIONS HAVING REDUCED LEVELS OF RESIDUES E.I. DU PONT DE NEMOURS AND COMPANY (US) 1999-09-16 WO disclosed
WO-1999045045-A1 POLYMERIC FILMS HAVING CONTROLLED VISCOSITY RESPONSE TO TEMPERATURE AND SHEAR E.I. DU PONT DE NEMOURS AND COMPANY (US) 1999-09-10 WO disclosed
EP-0889363-A1 Near IR sensitive photoimageable/photopolymerizable compositions, media, and associated processes E.I. DU PONT DE NEMOURS AND COMPANY (US) 1999-01-07 EP disclosed
EP-0666504-B1 Aqueous photoimageable liquid emulsion, photoimageable film and process of manufacture DU PONT (US) 1998-06-03 EP disclosed
US-5741621-A PHOTORESISTS, SOLDER MASKS, PRINTING PLATES, PROOFING FILM PRODUCTS E. I. DU PONT DE NEMOURS AND COMPANY (US) 1998-04-21 US disclosed
EP-0747769-A2 Process for producing photoimageable films prepared from aqueous photoimageable liquid emulsions E.I. DU PONT DE NEMOURS AND COMPANY (US) 1996-12-11 EP disclosed
EP-0666504-A1 Aqueous photoimageable liquid emulsion, photoimageable film and process of manufacture E.I. DU PONT DE NEMOURS AND COMPANY (US) 1995-08-09 EP disclosed
US-5407783-A Thermostability, shelf life E. I. DU PONT DE NEMOURS AND COMPANY (US) 1995-04-18 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 (1 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-20090018167-A1 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states FLT1, FLT4, VEGFA TDP1 4435/4885L3MBTL1 4205/4885CES2 3406/4885

“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.