SCHEMBL6841897

SCHEMBL6841897

O=Cc1ccc(Br)c(O)c1

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 1/20 0.64
PTGS2 P35354 1/20 0.64
RAB9A P51151 1/20 0.64
AKR1C3 P42330 1/20 0.58
AKR1C2 P52895 1/20 0.58
ALDH1A1 P00352 6/20 0.52
AOX1 Q06278 1/20 0.52
ALDH5A1 P51649 3/20 0.47
ABAT P80404 3/20 0.47
TRIM24 O15164 1/20 0.47
HPGD P15428 1/20 0.47
TDP1 Q9NUW8 1/20 0.47
TRIM33 Q9UPN9 1/20 0.47
ALDH1A3 P47895 2/20 0.43
TTR P02766 1/20 0.42
ERN1 O75460 1/20 0.42
XDH P47989 1/20 0.41
ALDH3A1 P30838 1/20 0.41
MAPT P10636 1/20 0.40
SNCA P37840 1/20 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
SCHEMBL190410 0.82 KDM4E (0.64) KDM4EPTGS2RAB9AALDH1A1AOX1
SCHEMBL29713168 0.82 KDM4E (0.64) KDM4EPTGS2RAB9AALDH1A1AOX1
SCHEMBL29610150 0.78 ALDH1A3 (0.52) KDM4EPTGS2RAB9AALDH1A1AOX1
SCHEMBL870202 0.78 ALDH1A3 (0.52) KDM4EPTGS2RAB9AALDH1A1AOX1
Protocatechualdehyde SCHEMBL9512877 0.78 KDM4E (1.00) KDM4EPTGS2RAB9AALDH1A1AOX1
Protocatechualdehyde SCHEMBL29349539 0.78 KDM4E (1.00) KDM4EPTGS2RAB9AALDH1A1AOX1
Protocatechualdehyde SCHEMBL36350 0.78 KDM4E (1.00) KDM4EPTGS2RAB9AALDH1A1AOX1
SCHEMBL17058724 0.78 KDM4E (0.53) KDM4EPTGS2RAB9AAKR1C3AKR1C2
SCHEMBL9305646 0.77 AKR1C3 (0.53) KDM4EPTGS2RAB9AAKR1C3AKR1C2
Protocatechualdehyde SCHEMBL4072910 0.76 KDM4E (0.95) KDM4EPTGS2RAB9AALDH1A1AOX1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0488860-B1 Method for the production of polyalkoxylated aromatic compounds RHONE POULENC CHIMIE (FR) 1995-10-11 EP claimed
EP-0423010-B1 METHOD FOR THE PRODUCTION OF ALKOXYBENZALDEHYDES RHONE-POULENC CHIMIE (FR) 1993-09-29 EP claimed
EP-4613749-A1 NLRP3 INFLAMMASOME INHIBITOR AND USE THEREOF TransThera Sciences (Nanjing), Inc. (CN) 2025-09-10 EP disclosed
US-20250177539-A1 ER DEGRADERS AND USES THEREOF ASTRAZENECA AB (SE) 2025-06-05 US disclosed
US-20250152584-A1 NLRP3 INFLAMMASOME INHIBITOR AND USES THEREOF TRANSTHERA SCIENCES (NANJING), INC. (CN) 2025-05-15 US disclosed
US-20250145566-A1 PHENETHYLAMINE DERIVATIVES, COMPOSITIONS, AND METHODS OF USE CYBIN IRL LIMITED (IE) 2025-05-08 US disclosed
CN-119798221-A NLRP3 inflammation corpuscle inhibitor and application thereof 药捷安康(南京)科技股份有限公司 2025-04-11 CN disclosed
US-20250084092-A1 ANNULATED PYRIDAZINE COMPOUND NICO THERAPEUTICS, INC. 2025-03-13 US disclosed
US-12239643-B2 Therapeutic agent for inflammatory diseases, autoimmune diseases, fibrotic diseases, and cancer diseases MEIJI SEIKA PHARMA CO., LTD. (JP) 2025-03-04 US disclosed
WO-2025036275-A1 NLRP3 INFLAMMASOME INHIBITOR AND USE THEREOF 药捷安康(南京)科技股份有限公司 2025-02-20 WO disclosed
CN-119462517-A NLRP3 inflammation corpuscle inhibitor and application thereof 药捷安康(南京)科技股份有限公司 2025-02-18 CN disclosed
WO-2017191098-A1 PYRAZOLE DERIVATIVES, COMPOSITIONS AND THERAPEUTIC USE THEREOF F. HOFFMANN-LA ROCHE AG (CH) 2017-11-09 WO disclosed
WO-2017191098-A1 PYRAZOLE DERIVATIVES, COMPOSITIONS AND THERAPEUTIC USE THEREOF F. HOFFMANN-LA ROCHE AG (CH) 2017-11-09 WO disclosed
EP-2763986-B1 FSH RECEPTOR ANTAGONISTS MERCK SHARP & DOHME (NL) 2017-06-07 EP disclosed
CN-104017008-A Boron-containing small molecules ANACOR PHARMACEUTICALS INC 2014-09-03 CN disclosed
CN-102105462-B Amidophenoxyindazoles useful as inhibitors of C-MET LILLY CO ELI 2014-07-23 CN disclosed
US-6759559-B2 HYDROGENATION CATALYST COMPLEX DEGUSSA AG (DE) 2004-07-06 US disclosed
US-20020016513-A1 Use of molecular weight-enlarged catalysts in a process for asymmetric, continous hydrogenation, novel molecular weight-enlarged ligands and catalysts DEGUSSA-HUELS AKTIENGESELLSCHAFT (DE) 2002-02-07 US disclosed
EP-1120162-A2 Use of catalysts with a higher molecular weight in an asymmetrical continous hydration reaction, ligands and catalysts Degussa AG (DE) 2001-08-01 EP disclosed
US-4394496-A POLYEPOXEDES WITH GOOD HIGH TEMPERATURE PROPERTIES THE DOW CHEMICAL COMPANY (US) 1983-07-19 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 (6 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-20020016513-A1 Use of molecular weight-enlarged catalysts in a process for asymmetric, continous hydrogenation, novel molecular weight-enlarged ligands and catalysts PCNA, DNMT1, STOM KDM4E 1445/4885PTGS2 2110/4885RAB9A 4285/4885
US-20250152584-A1 NLRP3 INFLAMMASOME INHIBITOR AND USES THEREOF NLRP3, NLRP1, PYCARD KDM4E 4454/4885PTGS2 904/4885RAB9A 3379/4885
US-20250177539-A1 ER DEGRADERS AND USES THEREOF ESR1, ESR2, ESRRA KDM4E 598/4885PTGS2 1756/4885RAB9A 2513/4885
US-20250084092-A1 ANNULATED PYRIDAZINE COMPOUND NLRP3, NLRP1, PYCARD KDM4E 2148/4885PTGS2 651/4885RAB9A 4216/4885
US-20250145566-A1 PHENETHYLAMINE DERIVATIVES, COMPOSITIONS, AND METHODS OF USE PNMT, HTR7, HTR2C KDM4E 2129/4885PTGS2 1002/4885RAB9A 1834/4885
US-12239643-B2 Therapeutic agent for inflammatory diseases, autoimmune diseases, fibrotic diseases, and cancer diseases CCR1, SSB, C5 KDM4E 2438/4885PTGS2 142/4885RAB9A 2786/4885

“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.