SCHEMBL557285

SCHEMBL557285

O=C(C(=O)c1ccc(Br)cc1)c1ccc(Br)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CES2 O00748 6/20 1.00
CES1 P23141 6/20 1.00
CA1 P00915 2/20 0.62
CA2 P00918 2/20 0.62
GSK3B P49841 2/20 0.56
OGG1 O15527 1/20 0.54
HTT P42858 1/20 0.54
LMNA P02545 2/20 0.52
HDAC3 O15379 1/20 0.52
HDAC4 P56524 1/20 0.52
HDAC1 Q13547 1/20 0.52
HDAC7 Q8WUI4 1/20 0.52
HDAC2 Q92769 1/20 0.52
HDAC10 Q969S8 1/20 0.52
HDAC11 Q96DB2 1/20 0.52
HDAC8 Q9BY41 1/20 0.52
HDAC6 Q9UBN7 1/20 0.52
HDAC9 Q9UKV0 1/20 0.52
HDAC5 Q9UQL6 1/20 0.52
CYP2A6 P11509 1/20 0.50

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
SCHEMBL14525907 0.92 CES2 (0.84) CES2CES1CA1CA2GSK3B
SCHEMBL649996 0.89 CES2 (0.80) CES2CES1CA1CA2HPGD
SCHEMBL29825996 0.89 CES2 (0.80) CES2CES1CA1CA2GSK3B
SCHEMBL5388314 0.87 CES2 (0.76) CES2CES1CA1CA2GSK3B
SCHEMBL12204728 0.87 CES2 (0.76) CES2CES1CA1CA2GSK3B
SCHEMBL4196624 0.87 CES2 (0.76) CES2CES1CA1CA2GSK3B
SCHEMBL3500800 0.86 CES2 (0.75) CES2CES1CA1CA2GSK3B
SCHEMBL11795251 0.85 CES2 (0.73) CES2CES1CA1CA2HTT
SCHEMBL4187858 0.85 CES2 (0.73) CES2CES1CA1CA2GSK3B
SCHEMBL8387086 0.85 LMNA (0.76) CES2CES1CA1CA2GSK3B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116217500-B Cyano quinoxaline red light thermal excitation delayed fluorescent material, synthetic method and application thereof 黑龙江大学 2025-05-16 CN claimed
CN-119613746-A Directably modified hexabenzo-metal organic framework, and preparation method and application thereof 南开大学 2025-03-14 CN claimed
CN-119552352-A Triphenylamine polyamide containing quinoxaline structure, and preparation method and application thereof 黑龙江大学 2025-03-04 CN claimed
US-20250033082-A1 METHOD AND COMPOSITION FOR REDUCING SOLVENT RELEASE FROM, AND REDUCING ODOR OF, AGROCHEMICAL FORMULATIONS ADAMA MAKHTESHIM LTD. (IL) 2025-01-30 US claimed
US-12180181-B1 4-[4,5-bis(4-bromophenyl)-1-hexyl-1H-imidazol-2-yl]isoquinolin-3-ol as an antimicrobial compound King Faisal University (SA) 2024-12-31 US claimed
US-12180166-B1 6-(4,5-bis(4-bromophenyl)-2-(4-methoxyphenyl)-1H-imidazol-1-yl)hexanoic acid as an antimicrobial compound King Faisal University (SA) 2024-12-31 US claimed
US-12172967-B1 3-(4,5-bis(4-bromophenyl)-2-(4-chlorophenyl)-1H-imidazol-1-yl)propanoic acid as an antimicrobial compound King Faisal University (SA) 2024-12-24 US claimed
US-12162839-B1 4,5-bis(4-bromophenyl)-2-(4-bromophenyl)-1-hexyl-1H-imidazole as an antimicrobial compound King Faisal University (SA) 2024-12-10 US claimed
CN-117417248-B Molecular-level monolayer hydrophilic graphene quantum dot and preparation method thereof 武汉科技大学 2024-11-19 CN claimed
CN-118750912-A Delayed coking defoaming agent and preparation method thereof 江苏创新石化有限公司 2024-10-11 CN claimed
CN-113817140-A Dendritic polymer and preparation method thereof 中电科技集团重庆声光电有限公司 2021-12-21 CN claimed
CN-112939975-A Thermal activation delayed fluorescent material, preparation method and application 天津大学 2021-06-11 CN claimed
CN-112194630-A Preparation and application of organic hole transport material with imidazole derivative as core 南京林业大学 2021-01-08 CN claimed
CN-110845503-A Preparation and application of arylamine substituted benzodiindole organic hole transport material 南京林业大学 2020-02-28 CN claimed
CN-110343100-A A kind of phenothiazines is total to sensitizer and its preparation method and application 江苏理工学院 2019-10-18 CN claimed
US-7973034-B2 Ameliorating toxic effects of such as cancer therapy drugs or addictive drug overdose ST. JUDE CHILDREN'S RESEARCH HOSPITAL (US) 2011-07-05 US claimed
EP-1300132-A2 Agent for dyeing keratinous fibres Henkel Kommanditgesellschaft auf Aktien (DE) 2003-04-09 EP claimed
EP-0043480-B1 PROCESS FOR FORMING METALLIC IMAGES Hitachi, Ltd. (JP) 1985-04-03 EP claimed
US-4347304-A PHOTOSENSITIZATION WITH DISILANES OR ORGANIC COMPOUNDS HAVING COUPLED GERMANIUM OR TIN MOLECULES; PHOTORESISTS; POSITIVES; PLATING HITACHI, LTD. (JP) 1982-08-31 US claimed
EP-0043480-A2 Process for forming metallic images Hitachi, Ltd. (JP) 1982-01-13 EP claimed

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-12180181-B1 4-[4,5-bis(4-bromophenyl)-1-hexyl-1H-imidazol-2-yl]isoquinolin-3-ol as an antimicrobial compound IRF3, IFNG, TLR4 CES2 4013/4885CES1 4139/4885CA1 4871/4885
US-12172967-B1 3-(4,5-bis(4-bromophenyl)-2-(4-chlorophenyl)-1H-imidazol-1-yl)propanoic acid as an antimicrobial compound DPP4, DPP3, EBP CES2 3479/4885CES1 1745/4885CA1 4517/4885
US-12162839-B1 4,5-bis(4-bromophenyl)-2-(4-bromophenyl)-1-hexyl-1H-imidazole as an antimicrobial compound BRD4, IL4, CASP4 CES2 2907/4885CES1 4001/4885CA1 4851/4885
US-12180166-B1 6-(4,5-bis(4-bromophenyl)-2-(4-methoxyphenyl)-1H-imidazol-1-yl)hexanoic acid as an antimicrobial compound HK1, GCK, HK2 CES2 3683/4885CES1 2498/4885CA1 4655/4885

“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.