SCHEMBL38141

SCHEMBL38141

O=C(CBr)c1ccccc1Cl

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ERCC5 P28715 1/20 0.58
FEN1 P39748 1/20 0.58
CES2 O00748 1/20 0.58
CES1 P23141 1/20 0.58
ALDH1A1 P00352 3/20 0.56
PTPN1 P18031 3/20 0.55
POLB P06746 1/20 0.52
GSK3B P49841 3/20 0.50
MAPT P10636 2/20 0.50
RAB9A P51151 3/20 0.47
MEN1 O00255 2/20 0.47
KMT2A Q03164 2/20 0.47
KDM4E B2RXH2 1/20 0.47
LMNA P02545 1/20 0.47
HPGD P15428 3/20 0.46
CYP1A2 P05177 2/20 0.46
CYP2C19 P33261 1/20 0.46
SMN1; SMN2 Q16637 1/20 0.45
CXCR3 P49682 1/20 0.44
HPGDS O60760 1/20 0.43

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
SCHEMBL29621373 1.00 ERCC5 (0.58) ERCC5FEN1CES2CES1ALDH1A1
Bromide SCHEMBL235266 0.98 ERCC5 (0.56) ERCC5FEN1CES2CES1ALDH1A1
SCHEMBL17376015 0.88 ERCC5 (0.56) ERCC5FEN1CES2CES1ALDH1A1
SCHEMBL9409754 0.84 PTPN1 (0.65) CES1ALDH1A1PTPN1GSK3BMAPT
SCHEMBL1199039 0.83 ERCC5 (0.61) ERCC5FEN1CES2CES1ALDH1A1
SCHEMBL30547190 0.83 ERCC5 (0.61) ERCC5FEN1CES2CES1ALDH1A1
SCHEMBL7863427 0.82 GSK3B (0.52) ERCC5FEN1CES2CES1ALDH1A1
SCHEMBL15979733 0.82 CES2 (0.62) ERCC5FEN1CES2CES1ALDH1A1
SCHEMBL29987169 0.82 ERCC5 (0.74) ERCC5FEN1CES2CES1ALDH1A1
SCHEMBL5057138 0.82 PTPN1 (0.50) ERCC5FEN1CES2CES1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118834123-A Method for preparing alpha-bromo-o-chloroacetophenone by utilizing microchannel reactor 江苏恩华药业股份有限公司 2024-10-25 CN claimed
CN-105622534-A Heterocyclic imide derivative containing bisamide structure and preparation method and application thereof HUBEI BIOPESTICIDE ENG RES CENTER 2016-06-01 CN claimed
JP-1013001-A None JP disclosed
JP-7053372-A None JP disclosed
JP-2175968-A None JP disclosed
US-12552804-B2 Tricyclic heterocycles as FGFR inhibitors INCYTE CORPORATION (US) 2026-02-17 US disclosed
US-20250388582-A1 NOVEL BICYCLIC HETEROARYL COMPOUND AND USE THEREOF ILDONG PHARMACEUTICAL CO LTD (KR) 2025-12-25 US disclosed
US-12398151-B2 Sumo inhibitor compounds and uses thereof Suvalent Therapeutics, Inc. (US) 2025-08-26 US disclosed
EP-4556476-A1 NOVEL BICYCLIC HETEROARYL COMPOUND AND USE THEREOF Ildong Pharmaceutical Co., Ltd. (KR) 2025-05-21 EP disclosed
US-20250115562-A1 METHOD FOR PREPARING ARYL 2- TETRAZOL -1 -YI KETO WITH IMPROVED SELECTIVITY SK BIOPHARMACEUTICALS CO., LTD. (KR) 2025-04-10 US disclosed
US-20250011315-A1 ARYL HYDROCARBON RECEPTOR (AHR) AGONISTS AND USES THEREOF PRISM MEDICINES, INC. 2025-01-09 US disclosed
US-4265898-A ANTICOAGULANTS BAYER AKTIENGESELLSCHAFT (DE) 1981-05-05 US disclosed
EP-0019796-A1 Propionic acid esters, preparation of these compounds, herbicides containing these compounds as active substances, and the use of such compounds and agents for combating weeds F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1980-12-10 EP disclosed
EP-0005783-A1 Imidazo (2.1-b)-(1.3.4)-thiadiazoles, process for their preparation and their use in medicaments BAYER AG (DE) 1979-12-12 EP disclosed
US-4139707-A ANTHELMINTICS AMERICAN CYANAMID COMPANY (US) 1979-02-13 US disclosed
US-4090025-A ALKOXYETHYL-PHENYL-IMIDAZOLIN-2-ONES OR 2-IMIDAZOLIDONES OR IMIDAZOLIDINE-2-THIONES AMERICAN CYANAMID COMPANY (US) 1978-05-16 US disclosed
US-4087611-A CHEMICAL INTERMEDIATES AMERICAN CYANAMID COMPANY (US) 1978-05-02 US disclosed
US-4021485-A BRONCHOSPASMOLYTICS, ANTIPRURITICS, ANTIALLERGICS BOEHRINGER INGELHEIM GMBH (DT) 1977-05-03 US disclosed
US-3965181-A Tricyclic pharmacological agents, intermediates and methods of making SYNTEX (U.S.A.) INC. (US) 1976-06-22 US disclosed
JP-S06413001-A 0001-01-01 JP 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 (5 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-20250011315-A1 ARYL HYDROCARBON RECEPTOR (AHR) AGONISTS AND USES THEREOF AHR, ARNT, HCAR1 ERCC5 3836/4885FEN1 3771/4885CES2 941/4885
US-20250115562-A1 METHOD FOR PREPARING ARYL 2- TETRAZOL -1 -YI KETO WITH IMPROVED SELECTIVITY KARS1, KMO, KYAT1 ERCC5 4695/4885FEN1 2743/4885CES2 3052/4885
US-20250388582-A1 NOVEL BICYCLIC HETEROARYL COMPOUND AND USE THEREOF GBA1, PIKFYVE, MAN2B1 ERCC5 3142/4885FEN1 3309/4885CES2 1314/4885
US-12552804-B2 Tricyclic heterocycles as FGFR inhibitors FGFR3, FGFR1, FGFR2 ERCC5 1799/4885FEN1 1802/4885CES2 1727/4885
US-12398151-B2 Sumo inhibitor compounds and uses thereof SUMO1, SUMO2, SUMO3 ERCC5 730/4885FEN1 943/4885CES2 3293/4885

“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.