SCHEMBL590353

SCHEMBL590353

O=C(O)c1cc(F)c(Br)cc1F

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AKR1C4 P17516 2/20 0.47
AKR1C3 P42330 2/20 0.47
AKR1C2 P52895 2/20 0.47
AKR1C1 Q04828 2/20 0.47
KDM4E B2RXH2 1/20 0.44
ASPH Q12797 1/20 0.44
KDM8 Q8N371 1/20 0.44
KEAP1 Q14145 1/20 0.44
NFE2L2 Q16236 1/20 0.44
PTPN1 P18031 3/20 0.42
GPR27 Q9NS67 1/20 0.42
TTR P02766 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.40
CES2 O00748 1/20 0.40
CES1 P23141 1/20 0.40
LCK P06239 1/20 0.39
FYN P06241 1/20 0.39
DGAT1 O75907 1/20 0.39
KCNK2 O95069 1/20 0.39
KCNK10 P57789 1/20 0.39

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
SCHEMBL29851193 1.00 AKR1C4 (0.47) AKR1C4AKR1C3AKR1C2AKR1C1KDM4E
SCHEMBL366568 0.91 AKR1C4 (0.47) AKR1C4AKR1C3AKR1C2AKR1C1KDM4E
SCHEMBL29705176 0.91 AKR1C4 (0.47) AKR1C4AKR1C3AKR1C2AKR1C1KDM4E
SCHEMBL24697741 0.88 KEAP1 (0.45) AKR1C4AKR1C3AKR1C2AKR1C1KDM4E
SCHEMBL2371182 0.86 LCK (0.48) AKR1C4AKR1C3AKR1C2AKR1C1KDM4E
SCHEMBL31430795 0.86 SMN1; SMN2 (0.48) AKR1C4AKR1C3AKR1C2AKR1C1KDM4E
SCHEMBL6860298 0.86 SMN1; SMN2 (0.48) AKR1C4AKR1C3AKR1C2AKR1C1KDM4E
SCHEMBL27575950 0.86 CA12 (0.52) AKR1C4AKR1C3AKR1C2AKR1C1KDM4E
SCHEMBL1713733 0.85 KDM4E (0.54) AKR1C4AKR1C3AKR1C2AKR1C1KDM4E
SCHEMBL500029 0.84 SMN1; SMN2 (0.50) AKR1C4AKR1C3AKR1C2AKR1C1KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250228848-A1 PROCESS FOR MAKING A KRAS G12C INHIBITOR ELI LILLY AND COMPANY 2025-07-17 US claimed
EP-4504710-A1 PROCESS FOR MAKING A KRAS G12C INHIBITOR Eli Lilly and Company (US) 2025-02-12 EP claimed
CN-119343334-A Methods of making KRAS G12C inhibitors 伊莱利利公司 2025-01-21 CN claimed
WO-2023196959-A1 PROCESS FOR MAKING A KRAS G12C INHIBITOR ELI LILLY AND COMPANY (US) 2023-10-12 WO claimed
CN-122029168-A Methods for preparing KRAS G12C inhibitors 伊莱利利公司 2026-05-12 CN disclosed
EP-4716531-A2 HETEROCYCLIC COMPOUNDS AS NRAS INHIBITORS Board of Regents, The University of Texas System (US) 2026-04-01 EP disclosed
US-20260070925-A1 HETEROCYCLIC COMPOUNDS AS NRAS INHIBITORS UNIV TEXAS (US) 2026-03-12 US disclosed
US-20260062420-A1 NOVEL DPP1 INHIBITORS AND USES THEREOF INSMED INC (US) 2026-03-05 US disclosed
EP-4696692-A1 CRYSTAL OF NITROGEN-CONTAINING HETEROCYCLIC COMPOUND HAVING NRF2 ACTIVATION EFFECT CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2026-02-18 EP disclosed
US-12441735-B2 Nitrogen-containing heterocyclic compound having NRF2 activation effect CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-10-14 US disclosed
US-12410187-B2 Fused tricyclic compounds useful as anticancer agents ASTRAZENECA AB (SE) 2025-09-09 US disclosed
US-20250249019-A1 METHOD OF TREATMENT INCLUDING KRAS G12C INHIBITORS AND AURORA A INHIBITORS LOXO ONCOLOGY, INC. 2025-08-07 US disclosed
US-5081254-A Antibacterial agents WARNER-LAMBERT COMPANY (US) 1992-01-14 US disclosed
US-5075319-A Bactericides STERLING DRUG INC. (US) 1991-12-24 US disclosed
EP-0417669-A2 Pyridinyl-quinolone compounds, their preparation and use STERLING WINTHROP INC. (US) 1991-03-20 EP disclosed
US-4996355-A Novel intermediates for the production of 2,4,5-trifluorobenzoyl fluoride MALLINCKRODT, INC. (US) 1991-02-26 US disclosed
WO-1990012780-A1 INTERMEDIATES FOR THE PRODUCTION OF 2,4,5-TRIFLUORBENZOYL FLUORIDE MALLINCKRODT, INC. (US) 1990-11-01 WO disclosed
US-4929613-A Antibacterial agents WARNER-LAMBERT COMPANY (US) 1990-05-29 US disclosed
EP-0309789-A1 4-Oxo-3-quinolinecarboxylic acids useful as antibacterial agents and preparation thereof STERLING WINTHROP INC. (US) 1989-04-05 EP disclosed
EP-0306764-A2 4-Quinolone-3-carboxylic-acid derivatives and their use as antibacterial agents WARNER-LAMBERT COMPANY (US) 1989-03-15 EP 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-12410187-B2 Fused tricyclic compounds useful as anticancer agents MCL1, TP53, CCNA2 AKR1C4 575/4885AKR1C3 638/4885AKR1C2 584/4885
US-20260070925-A1 HETEROCYCLIC COMPOUNDS AS NRAS INHIBITORS NRAS, KRAS, HRAS AKR1C4 2690/4885AKR1C3 1551/4885AKR1C2 2056/4885
US-20250228848-A1 PROCESS FOR MAKING A KRAS G12C INHIBITOR KRAS, NRAS, HRAS AKR1C4 918/4885AKR1C3 670/4885AKR1C2 550/4885
US-20250249019-A1 METHOD OF TREATMENT INCLUDING KRAS G12C INHIBITORS AND AURORA A INHIBITORS KRAS, AURKC, NRAS AKR1C4 1309/4885AKR1C3 1212/4885AKR1C2 901/4885
US-12441735-B2 Nitrogen-containing heterocyclic compound having NRF2 activation effect KEAP1, NFE2L2, BACH1 AKR1C4 283/4885AKR1C3 165/4885AKR1C2 343/4885
US-20260062420-A1 NOVEL DPP1 INHIBITORS AND USES THEREOF DPP4, DPP3, DPP7 AKR1C4 2439/4885AKR1C3 2097/4885AKR1C2 2684/4885

“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.