SCHEMBL263669

SCHEMBL263669

COc1cc(Br)ccc1Cl

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 4/20 0.47
ALDH1A1 P00352 4/20 0.47
MEN1 O00255 2/20 0.47
KMT2A Q03164 2/20 0.47
GAA P10253 3/20 0.46
POLB P06746 2/20 0.46
RECQL P46063 1/20 0.46
NPC1 O15118 1/20 0.43
DYRK1A Q13627 1/20 0.43
ACLY P53396 1/20 0.42
TSHR P16473 2/20 0.42
KDM4E B2RXH2 1/20 0.42
TDP1 Q9NUW8 1/20 0.42
USP2 O75604 1/20 0.42
CYP2C9 P11712 1/20 0.42
HPGD P15428 1/20 0.42
ALOX12 P18054 1/20 0.42
MAPK1 P28482 1/20 0.42
CYP2C19 P33261 1/20 0.42
NPSR1 Q6W5P4 1/20 0.42

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
SCHEMBL3740375 0.98 MAPT (0.46) MAPTALDH1A1MEN1KMT2AGAA
SCHEMBL858370 0.82 ALDH1A1 (0.51) MAPTALDH1A1MEN1KMT2AGAA
SCHEMBL30424732 0.82 ALDH1A1 (0.51) MAPTALDH1A1MEN1KMT2AGAA
SCHEMBL29419589 0.78 CA2 (0.56) MAPTALDH1A1POLBTSHRKDM4E
SCHEMBL20509 0.78 CA2 (0.56) MAPTALDH1A1POLBTSHRKDM4E
SCHEMBL15969085 0.78 HPGD (0.42) MAPTALDH1A1MEN1KMT2AGAA
SCHEMBL30214873 0.78 HPGD (0.42) MAPTALDH1A1MEN1KMT2AGAA
SCHEMBL1129397 0.78 MAPT (0.48) MAPTALDH1A1GAAPOLBRECQL
SCHEMBL2878953 0.77 CSNK2A1 (0.43) MAPTALDH1A1MEN1KMT2AGAA
SCHEMBL2848535 0.77 TSHR (0.47) MAPTALDH1A1MEN1KMT2AGAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116554009-A Electrophilic cross-coupling reaction method of aryl sulfone or heteroaryl sulfone and aryl bromide 南京工业大学 2023-08-08 CN claimed
CN-114685251-B Direct cross-coupling reaction method of diaryl sulfoxide and aryl bromide 南京工业大学 2022-12-27 CN claimed
CN-114685251-A Direct cross-coupling reaction method of diaryl sulfoxide and aryl bromide 南京工业大学 2022-07-01 CN claimed
CN-109180578-A A kind of preparation method of bosutinib 山东创新药物研发有限公司 2019-01-11 CN claimed
US-5502186-A Process for preparing intermediates for the synthesis of D1 antagonists SCHERING CORPORATION (US) 1996-03-26 US claimed
WO-1995009155-A2 PROCESS AND INTERMEDIATES FOR THE ENANTIOSPECIFIC SYNTHESIS OF BENZO [D]NAPHTH[2,1-B]AZEPINES SCHERING CORPORATION (US) 1995-04-06 WO claimed
JP-9003082-A None JP disclosed
US-20260124309-A1 STAT6 DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS INC (US) 2026-05-07 US disclosed
EP-4674852-A1 PREPARATION METHOD FOR AND USE OF DIHYDROTHIENOPYRIMIDINE DERIVATIVE Innovstone Therapeutics Limited (CN) 2026-01-07 EP disclosed
EP-4630403-A1 COMPOUNDS FOR THE TREATMENT OF NEUROMUSCULAR DISORDERS NMD Pharma A/S (DK) 2025-10-15 EP disclosed
US-12410212-B2 Cyclic compound having selective KRAS inhibitory effect on HRAS and NRAS CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-09-09 US disclosed
EP-4603105-A1 PHARMACEUTICAL COMPOSITION CONTAINING CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT AGAINST HRAS AND NRAS CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-08-20 EP disclosed
EP-4592308-A1 CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT ON HRAS AND NRAS CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-07-30 EP disclosed
WO-1989000561-A1 FUSED BENZAZEPINES SCHERING CORPORATION (US) 1989-01-26 WO disclosed
EP-0299101-A1 Fused benzazepines SCHERING CORPORATION (US) 1989-01-18 EP disclosed
EP-0175452-B1 1,3-DISUBSTITUTED PIPERIDINE COMPOUNDS AS NEUROLEPTIC AGENTS PFIZER INC. (US) 1988-09-21 EP disclosed
US-4623728-A NERVOUS SYSTEM DISORDERS PFIZER INC. (US) 1986-11-18 US disclosed
US-4593037-A Compound substituted with phenyl rings PFIZER INC. (US) 1986-06-03 US disclosed
EP-0175452-A1 1,3-Disubstituted piperidine compounds as neuroleptic agents PFIZER INC. (US) 1986-03-26 EP disclosed
US-4238611-A Polysubstituted derivatives of 10-piperazinodibenzo (b,f) thiepine SPOFA, UNITED PHARMACEUTICAL WORKS (CS) 1980-12-09 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 (2 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-20260124309-A1 STAT6 DEGRADERS AND USES THEREOF STAT6, NCOR2, NCOR1 MAPT 4555/4885ALDH1A1 2085/4885MEN1 4497/4885
US-12410212-B2 Cyclic compound having selective KRAS inhibitory effect on HRAS and NRAS KRAS, HRAS, NRAS MAPT 4528/4885ALDH1A1 4331/4885MEN1 1545/4885

“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.