SCHEMBL249482

SCHEMBL249482

C=CCc1ccsc1Br

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
SCHEMBL2486256 0.78
SCHEMBL6036916 0.78
SCHEMBL4591842 0.77 GABRA1 (0.38)
SCHEMBL1164626 0.76 GABRA1 (0.36)
SCHEMBL8508207 0.75 SLC6A4 (0.36)
SCHEMBL13572315 0.74
SCHEMBL29259237 0.74
SCHEMBL4677442 0.74
SCHEMBL2882496 0.74
SCHEMBL5455704 0.74

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11773074-B2 Method for aerobic oxidative coupling of thiophenes with a ligand-supported palladium catalyst WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2023-10-03 US disclosed
US-20210047285-A1 Method for Aerobic Oxidative Coupling of Thiophenes with a Ligand-Supported Palladium Catalyst WISCONSIN ALUMNI RESEARCH FOUNDATION 2021-02-18 US disclosed
US-10858334-B2 Method for aerobic oxidative coupling of thiophenes with a ligand-supported palladium catalyst WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2020-12-08 US disclosed
US-20190210993-A1 Method for Aerobic Oxidative Coupling of Thiophenes with a Ligand-Supported Palladium Catalyst NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2019-07-11 US disclosed
EP-2626375-B1 Semiconductor materials prepared from dithienylvinylene copolymers BASF SE (DE) 2017-11-22 EP disclosed
EP-3037836-B1 ULTRASENSITIVE MAGNETIC SENSOR BASED ON GIANT FARADAY ROTATION TOYOTA MOTOR CO LTD (JP) 2017-09-13 EP disclosed
US-9650461-B2 Semiconductor materials prepared from dithienylvinylene copolymers BASF SE (DE) 2017-05-16 US disclosed
US-9494809-B2 Ultrasensitive magnetic sensor with magneto-optically active material with high verdet constant TOYOTA JIDOSHA KABUSHIKI KAISHA (JP) 2016-11-15 US disclosed
EP-3037836-A1 ULTRASENSITIVE MAGNETIC SENSOR BASED ON GIANT FARADAY ROTATION Toyota Jidosha Kabushiki Kaisha (JP) 2016-06-29 EP disclosed
US-20160075808-A1 SEMICONDUCTOR MATERIALS PREPARED FROM DITHIENYLVINYLENE COPOLYMERS USINVEST LLC 2016-03-17 US disclosed
EP-1475401-A2 Mono-, oligo- and polymers comprising fluorene and aryl groups MERCK PATENT GmbH (DE) 2004-11-10 EP disclosed
US-20040176560-A1 Mono-, Oligo-and polymers comprising fluorene and aryl groups MERCK PATENT GMBH (DE) 2004-09-09 US disclosed
US-20030164495-A1 Polythiophenes and devices thereof XEROX CORPORATION 2003-09-04 US disclosed
US-20030166829-A1 Polythiophenes and devices thereof XEROX CORPORATION 2003-09-04 US disclosed
US-20030160234-A1 Polythiophenes and devices thereof XEROX CORPORATION 2003-08-28 US disclosed
EP-1327647-A1 Polythiophenes and devices thereof Xerox Corporation (US) 2003-07-16 EP disclosed
EP-1327646-A1 Polythiophenes and devices thereof Xerox Corporation (US) 2003-07-16 EP disclosed
US-6166172-A Method of forming poly-(3-substituted) thiophenes CARNEGIE MELLON UNIVERSITY (US) 2000-12-26 US disclosed
EP-1028136-A2 A method of forming poly-(3-substituted) thiophenes CARNEGIE-MELLON UNIVERSITY (US) 2000-08-16 EP disclosed
WO-1994002530-A1 NOVEL PROCESSABLE THIOPHENE BASED POLYMERS AND COPOLYMERS AND THERMALLY STABLE ELECTRICALLY CONDUCTING COMPOSITIONS THEREOF NESTE OY (FI) 1994-02-03 WO disclosed