SCHEMBL93041

SCHEMBL93041

OCc1cccc(Br)c1

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
Ethylene SCHEMBL27825961 0.95 TAAR1 (0.52) —
SCHEMBL630230 0.87 PRKCI (0.58) —
SCHEMBL12715025 0.85 PRKCI (0.56) —
SCHEMBL11478458 0.82 MAOB (0.53) —
SCHEMBL31088397 0.81 — —
SCHEMBL643177 0.81 TAAR1 (0.63) —
SCHEMBL31312465 0.81 — —
SCHEMBL31088403 0.81 — —
SCHEMBL123838 0.81 TSHR (0.61) —
SCHEMBL1732196 0.79 TAAR1 (0.50) —

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 1604 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117800816-B Green synthesis method of polysubstituted benzyl ether and polysubstituted benzaldehyde 华东理工大学 2026-02-27 — — CN claimed
CN-118956043-B Light power cable for ship and processing method thereof 广州澳兴光电传输科技股份有限公司 2025-02-07 — — CN claimed
CN-118956043-A Light power cable for ship and processing method thereof 广州澳兴光电传输科技股份有限公司 2024-11-15 — — CN claimed
CN-114394922-B Preparation method of N-substituted pyrrolyl aryl propenone compound 河南农业大学 2024-06-11 — — CN claimed
CN-117800816-A Green synthesis method of polysubstituted benzyl ether and polysubstituted benzaldehyde 华东理工大学 2024-04-02 — — CN claimed
CN-114717571-B Anolyte and benzaldehyde and hydrogen coupling co-production system and application 东北师范大学 2023-11-24 — — CN claimed
CN-113121454-B Method for preparing barbituric acid alkylation derivative by using ferrous complex 上海应用技术大学 2022-10-14 — — CN claimed
CN-114717571-A Anolyte and benzaldehyde and hydrogen coupling co-production system and application 东北师范大学 2022-07-08 — — CN claimed
CN-114394922-A Preparation method of N-substituted pyrrolyl aryl propenone compound 河南农业大学 2022-04-26 — — CN claimed
CN-114213307-A Preparation method of N-alkyl substituted pyrrolidone compound 河南农业大学 2022-03-22 — — CN claimed
US-20010018446-A1 Substituted N-Aliphatic-N-Aromatictertiary-Heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity G.D. SEARLE & CO. (US) 2001-08-30 — — US claimed
EP-1115695-A1 (R)-CHIRAL HALOGENATED 1-SUBSTITUTEDAMINO-(N+1)-ALKANOLS USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY Monsanto Company (US) 2001-07-18 — — EP claimed
EP-1115693-A1 SUBSTITUTED POLYCYCLIC ARYL AND HETEROARYL $i(TERTIARY)-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY Monsanto Company (US) 2001-07-18 — — EP claimed
EP-1115694-A1 SUBSTITUTED N-ALIPHATIC-N-AROMATIC (TERTIARY)-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY Monsanto Company (US) 2001-07-18 — — EP claimed
WO-2000018724-A1 (R)-CHIRAL HALOGENATED 1-SUBSTITUTEDAMINO-(n+1)-ALKANOLS USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY MONSANTO COMPANY (US) 2000-04-06 — — WO claimed
WO-2000018723-A1 SUBSTITUTED N-ALIPHATIC-N-AROMATIC TERTIARY-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY MONSANTO COMPANY (US) 2000-04-06 — — WO claimed
WO-2000018721-A1 SUBSTITUTED POLYCYCLIC ARYL AND HETEROARYL TERTIARY-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY MONSANTO COMPANY (US) 2000-04-06 — — WO claimed
US-5972946-A NERVOUS SYSTEM DISORDERS; PSYCHOLOGICAL DISORDERS DAINIPPON PHARMACEUTICAL CO., LTD. (JP) 1999-10-26 — — US claimed
US-5021434-A Aromatase inhibitors SCHERING AKTIENGESELLSCHAFT (DE) 1991-06-04 — — US claimed
US-4916144-A ESTROGEN-CAUSE DISEASES SCHERING AKTIENGESELLSCHAFT (DE) 1990-04-10 — — US claimed
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