SCHEMBL193318

SCHEMBL193318

O=C(O)CCc1ccc(F)cc1

nearest known ligand 0.79

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
FFAR1 O14842 12/20 0.79
KEAP1 Q14145 1/20 0.64
HTT P42858 1/20 0.56
FFAR4 Q5NUL3 5/20 0.55
CA1 P00915 1/20 0.55
CA2 P00918 1/20 0.55
SLC5A1 P13866 1/20 0.53
SLC5A2 P31639 1/20 0.53
PLAAT3 P53816 1/20 0.53
PLAAT5 Q96KN8 1/20 0.53
PLAAT2 Q9NWW9 1/20 0.53
PLAAT4 Q9UL19 1/20 0.53

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
Hydrochloric Acid SCHEMBL29184696 0.98 FFAR1 (0.76) FFAR1KEAP1HTTFFAR4CA1
Hydrochloric Acid SCHEMBL28568409 0.98 FFAR1 (0.76) FFAR1KEAP1HTTFFAR4CA1
SCHEMBL1841290 0.94 FFAR1 (0.71) FFAR1KEAP1HTTFFAR4
Trifluoroacetic Acid SCHEMBL7394332 0.92 FFAR1 (0.69) FFAR1KEAP1HTTFFAR4CA1
SCHEMBL7011662 0.90 FFAR1 (0.67) FFAR1KEAP1HTTFFAR4CA1
Butyric Acid SCHEMBL30807147 0.89 FFAR1 (0.65) FFAR1KEAP1HTTFFAR4
SCHEMBL69746 0.88 FFAR1 (0.81) FFAR1KEAP1FFAR4CA1CA2
SCHEMBL10853169 0.88 FFAR1 (0.64) FFAR1KEAP1HTTFFAR4SLC5A1
SCHEMBL655425 0.87 SMN1; SMN2 (0.67) FFAR1HTT
Hydrochloric Acid SCHEMBL25264643 0.85 FFAR1 (0.77) FFAR1KEAP1FFAR4CA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122036772-A Synthesis method of beta-pinacol borate-alkyl ketone compound 陇东学院 2026-05-15 CN claimed
US-12497636-B2 Recombinant Saccharomyces cerevisiae cells for cannabinoid production NATIONAL UNIVERSITY OF SINGAPORE (SG) 2025-12-16 US claimed
CN-120137643-A Composite material, preparation method thereof, photoelectric device and display device 广东聚华新型显示研究院 2025-06-13 CN claimed
US-12304894-B2 Derivatives of adamantyl oxadiazoles and pharmaceutically acceptable solvates, hydrates and salts thereof, pharmaceutical composition comprising same, synthesis method, suitable for use as effective and selective inhibitors of the reductase activity of the enzyme 11-beta dehydrogenase type 1 (11β-HSD1) PONTIFICIA UNIVERSIDAD CATOLICA DE CHILE (CL) 2025-05-20 US claimed
CN-117143097-A Beta-carbopol compound, preparation method thereof and application of beta-carbopol compound in resisting Alzheimer disease 中国人民解放军北部战区总医院 2023-12-01 CN claimed
CN-114350062-B High-rigidity low-yield polypropylene torsion film and preparation method thereof 界首市天鸿新材料股份有限公司 2023-05-02 CN claimed
US-20220194909-A1 DERIVATIVES OF ADAMANTYL OXADIAZOLES AND PHARMACEUTICALLY ACCEPTABLE SOLVATES, HYDRATES AND SALTS THEREOF, PHARMACEUTICAL COMPOSITION COMPRISING SAME, SYNTHESIS METHOD, SUITABLE FOR USE AS EFFECTIVE AND SELECTIVE INHIBITORS OF THE REDUCTASE ACTIVITY OF THE ENZYME 11-BETA DEHYDROGENASE TYPE 1 (11B-HSD1) PONTIFICIA UNIVERSIDAD CATOLICA DE CHILE (CL) 2022-06-23 US claimed
CN-113683805-B Preparation method of cross-linked imidazole functionalized polyether sulphone anion exchange membrane containing benzimidazole structure 浙江工业大学 2022-06-21 CN claimed
CN-114350062-A High-rigidity low-yield polypropylene tangle film and preparation method thereof 界首市天鸿新材料股份有限公司 2022-04-15 CN claimed
CN-113683805-A Preparation method of cross-linked imidazole functionalized polyether sulphone anion exchange membrane containing benzimidazole structure 浙江工业大学 2021-11-23 CN claimed
CN-106748725-A A kind of preparation method of the fluorobenzene propionic acid of 4 chlorine 2 贵州大学 2017-05-31 CN claimed
CN-101268049-A Novel piperidine derivatives ASTRAZENECA AB (SE) 2008-09-17 CN claimed
EP-1620457-A2 INDUCERS OF RECOMBINANT PROTEIN EXPRESSION Immunex Corporation (US) 2006-02-01 EP claimed
US-20040265964-A1 Inducers of recombinant protein expression IMMUNEX CORPORATION 2004-12-30 US claimed
WO-2004096833-A2 INDUCERS OF RECOMBINANT PROTEIN EXPRESSION IMMUNEX CORPORATION (US) 2004-11-11 WO claimed
EP-1129076-A1 TETRAHYDROISOQUINOLINE DERIVATIVES AS LHRH ANTAGONISTS ABBOTT LABORATORIES (US) 2001-09-05 EP claimed
WO-2000029380-A1 TETRAHYDROISOQUINOLINE DERIVATIVES AS LHRH ANTAGONISTS ABBOTT LABORATORIES (US) 2000-05-25 WO claimed
US-5981521-A USEFUL FOR TREATING VARIOUS HORMONE DEPENDENT DISEASES, INCLUDING PROSTATE CANCER, ENDOMETRIOSIS, UTERINE FIBROIDS, PRECOCIOUS PUBERTY, BENIGN PROSTATE HYPERTROPY AND IN VITRO FERTILIZATION ABBOTT LABORATORIES (US) 1999-11-09 US claimed
US-5358939-A For applying to soils, seeds, plants, or for storage of cereal grains ROHM AND HAAS COMPANY (US) 1994-10-25 US claimed
EP-0576201-A2 Fungicidal 1,2,4-triazoles ROHM AND HAAS COMPANY (US) 1993-12-29 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 (3 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-20220194909-A1 DERIVATIVES OF ADAMANTYL OXADIAZOLES AND PHARMACEUTICALLY ACCEPTABLE SOLVATES, HYDRATES AND SALTS THEREOF, PHARMACEUTICAL COMPOSITION COMPRISING SAME, SYNTHESIS METHOD, SUITABLE FOR USE AS EFFECTIVE AND SELECTIVE INHIBITORS OF THE REDUCTASE ACTIVITY OF THE ENZYME 11-BETA DEHYDROGENASE TYPE 1 (11B-HSD1) HSD11B1, HSD11B2, CYP11B1 FFAR1 695/4885KEAP1 1504/4885HTT 2603/4885
US-20040265964-A1 Inducers of recombinant protein expression AADAC, CRYAA, PMAIP1 FFAR1 2596/4885KEAP1 4086/4885HTT 1033/4885
US-12304894-B2 Derivatives of adamantyl oxadiazoles and pharmaceutically acceptable solvates, hydrates and salts thereof, pharmaceutical composition comprising same, synthesis method, suitable for use as effective and selective inhibitors of the reductase activity of the enzyme 11-beta dehydrogenase type 1 (11β-HSD1) HSD11B1, HSD11B2, HSD17B1 FFAR1 623/4885KEAP1 1272/4885HTT 2435/4885

“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.