SCHEMBL394047

SCHEMBL394047

COCOc1cc(F)ccc1Br

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FFAR1 O14842 1/20 0.46
FFAR4 Q5NUL3 1/20 0.46
PKM P14618 1/20 0.40
PIK3CD O00329 1/20 0.39
ABL1 P00519 1/20 0.39
EGFR P00533 1/20 0.39
HCK P08631 1/20 0.39
SRC P12931 1/20 0.39
KDR P35968 1/20 0.39
PIK3CA P42336 1/20 0.39
PIK3CB P42338 1/20 0.39
MTOR P42345 1/20 0.39
PIK3CG P48736 1/20 0.39
EPHB4 P54760 1/20 0.39
PRKDC P78527 1/20 0.39
SCD O00767 3/20 0.35
SLC6A4 P31645 1/20 0.35
SCD5 Q86SK9 1/20 0.34
MAPT P10636 5/20 0.34
MEN1 O00255 2/20 0.34

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
SCHEMBL29385804 1.00 FFAR1 (0.46) FFAR1FFAR4PKMPIK3CDABL1
SCHEMBL29440624 0.85 PKM (0.56) PKMMAPTMEN1KMT2AALDH1A1
SCHEMBL972013 0.85 PKM (0.56) PKMMAPTMEN1KMT2AALDH1A1
SCHEMBL31314166 0.82 FFAR1 (0.43) FFAR1FFAR4PKMSCDSCD5
SCHEMBL1808652 0.81 FFAR1 (0.48) FFAR1FFAR4PKMMAPTMEN1
SCHEMBL546111 0.81 TDP1 (0.38) MEN1KMT2AALDH1A1HPGDL3MBTL1
SCHEMBL30294538 0.81 FFAR1 (0.48) FFAR1FFAR4PKMMAPTMEN1
SCHEMBL4749281 0.79 FFAR1 (0.47) FFAR1FFAR4SLC6A4GAA
SCHEMBL30755347 0.79 FFAR1 (0.47) FFAR1FFAR4SLC6A4GAA
Fluoride SCHEMBL28350549 0.79 FFAR1 (0.47) FFAR1FFAR4PKMMAPTMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025038462-A2 INHIBITORS OF RNA HELICASE DHX9 AND USES THEREOF ACCENT THERAPEUTICS, INC. (US) 2025-02-20 WO disclosed
CN-114072398-B Compounds that inhibit TDG activity 上海仕谱生物科技有限公司 2024-06-11 CN disclosed
EP-4257588-A1 SMALL MOLECULE INHIBITOR OF CATHEPSIN C AND MEDICINAL USE THEREOF Reistone Biopharma Company Limited (CN) 2023-10-11 EP disclosed
US-20220213070-A1 COMPOUNDS INHIBITING TDG ACTIVITY Epitas Biosciences (shanghai) Co., Ltd. (CN) 2022-07-07 US disclosed
WO-2022117059-A1 SMALL MOLECULE INHIBITOR OF CATHEPSIN C AND MEDICINAL USE THEREOF 瑞石生物医药有限公司 2022-06-09 WO disclosed
EP-3971180-A1 COMPOUNDS INHIBITING TDG ACTIVITY Epitas Biosciences (Shanghai) Co., Ltd. (CN) 2022-03-23 EP disclosed
CN-114072398-A Compounds that inhibit TDG activity 上海仕谱生物科技有限公司 2022-02-18 CN disclosed
WO-2020224396-A1 COMPOUNDS INHIBITING TDG ACTIVITY 上海仕谱生物科技有限公司 2020-11-12 WO disclosed
CN-111909138-A Compounds that inhibit TDG activity 上海仕谱生物科技有限公司 2020-11-10 CN disclosed
CN-101910179-B Glucocorticoid receptor modulator and use method LILLY CO ELI 2013-06-19 CN disclosed
US-7018998-B2 Glutamate receptor antagonists HOFFMANN-LA ROCHE INC. (US) 2006-03-28 US disclosed
US-6960578-B2 Glutamate receptor antagonists HOFFMANN-LA ROCHE INC. (US) 2005-11-01 US disclosed
US-20050234048-A1 Glutamate receptor antagonists ADAM GEO 2005-10-20 US disclosed
CN-1199954-C Benzodiazepine derivatives HOFFMANN LA ROCHE (CH) 2005-05-04 CN disclosed
EP-1224175-B1 BENZODIAZEPINE DERIVATIVES AS METABOTROPIC GLUTAMATE RECEPTOR ANTAGONISTS HOFFMANN LA ROCHE (CH) 2004-03-17 EP disclosed
US-20030092677-A1 Glutamate receptor antagonists ADAM GEO (DE) 2003-05-15 US disclosed
US-6509328-B1 Metabotropic glutamate receptor antagonists and accordingly are useful for the treatment of a range of neurological disorders, including psychosis, schizophrenia, Alzheimer's and others HOFFMANN-LA ROCHE INC. 2003-01-21 US disclosed
CN-1379764-A Benzodiazepine derivatives HOFFMANN LA ROCHE (CH) 2002-11-13 CN disclosed
EP-1224175-A2 BENZODIAZEPINE DERIVATIVES AS METABOTROPIC GLUTAMATE RECEPTOR ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2002-07-24 EP disclosed
WO-2001029012-A2 BENZODIAZEPINE DERIVATIVES AS METABOTROPIC GLUTAMATE RECEPTOR ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2001-04-26 WO 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 (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-20030092677-A1 Glutamate receptor antagonists GRM1, GRM3, GRM2 FFAR1 94/4885FFAR4 274/4885PKM 4579/4885
US-20050234048-A1 Glutamate receptor antagonists GRM3, GRM1, GRM2 FFAR1 168/4885FFAR4 255/4885PKM 4177/4885
US-20220213070-A1 COMPOUNDS INHIBITING TDG ACTIVITY TDO2, TFPI, PPIG FFAR1 3866/4885FFAR4 4123/4885PKM 2128/4885

“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.