SCHEMBL144046

SCHEMBL144046

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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
SCHEMBL24599171 0.79
SCHEMBL19417378 0.76
SCHEMBL24062572 0.73 ALDH1A1 (0.30)
SCHEMBL146354 0.72
SCHEMBL18517442 0.69
SCHEMBL9301981 0.69
SCHEMBL22023931 0.68
SCHEMBL18571559 0.67
SCHEMBL19146192 0.67
SCHEMBL17053440 0.66

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3183250-B1 PROCESS FOR PREPARING CRYSTALLINE ORGANIC SEMICONDUCTOR MATERIAL CLAP CO LTD (KR) 2023-10-04 EP disclosed
EP-3183757-B1 ORGANIC SEMICONDUCTOR COMPOSITION COMPRISING LIQUID MEDIUM CLAP CO LTD (KR) 2022-05-04 EP disclosed
EP-3224246-B1 4-OXOQUINOLINE COMPOUNDS BASF SE (DE) 2022-01-12 EP disclosed
US-10454037-B2 Organic semiconductor composition comprising a liquid medium BASF SE (DE) 2019-10-22 US disclosed
EP-3274334-B1 CYANATED BENZOXANTHENE AND BENZOTHIOXANTHENE COMPOUNDS BASF SE (DE) 2019-07-10 EP disclosed
US-10224485-B2 Process for preparing a crystalline organic semiconductor material BASF SE (DE) 2019-03-05 US disclosed
US-20190010165-A1 CYANATED BENZOXANTHENE AND BENZOTHIOXANTHENE COMPOUNDS BASF SE (DE) 2019-01-10 US disclosed
US-10125143-B2 Cyanated benzoxanthene and benzothioxanthene compounds BASF SE (DE) 2018-11-13 US disclosed
US-20180065980-A1 CYANATED BENZOXANTHENE AND BENZOTHIOXANTHENE COMPOUNDS BASF SE (DE) 2018-03-08 US disclosed
EP-3274334-A1 CYANATED BENZOXANTHENE AND BENZOTHIOXANTHENE COMPOUNDS BASF SE (DE) 2018-01-31 EP disclosed
US-20090301552-A1 CHLORINATED NAPHTHALENETETRACARBOXYLIC ACID DERIVATIVES, PREPARATION THEREOF AND USE THEREOF IN ORGANIC ELECTRONICS BASF SE (DE) 2009-12-10 US disclosed
US-20090166614-A1 FLUORINATED RYLENETETRACARBOXYLIC ACID DERIVATIVES AND USE THEREOF BASF AKTIENGESELLSCHAFT (DE) 2009-07-02 US disclosed
US-20090124732-A1 Rylene Tetracarboxylic Acid Diimides Substituted By Cyclic Amino Groups BASF AKTIENGESELLSCHAFT (DE) 2009-05-14 US disclosed
US-20090030206-A1 METHOD FOR PRODUCING QUATERRYLENE-3,4:13, 14-TETRACARBOXY DIIMIDES BY DIRECT SYNTHESIS BASF AKTIENGESELLSCHAFT (DE) 2009-01-29 US disclosed
US-20080300405-A1 Naphthalenetetracarboxylic Aicd Derivatives and their Use as Semiconductors BASF SE (DE) 2008-12-04 US disclosed
US-20080287678-A1 Multiple Chromophores Based on Rylene BASF AKTIENGESELLSCHAFT (DE) 2008-11-20 US disclosed
US-20080269482-A1 Use of Rylene Derivatives as Photosensitizers in Solar Cells BASF SE (DE) 2008-10-30 US disclosed
US-20080255357-A1 Terrylene and Quaterrylene Derivatives BASF AKTIENGESELLSCHAFT (DE) 2008-10-16 US disclosed
US-20080167467-A1 Substituted Rylene Derivatives BASF AKTIENGESELLSCHAFT (DE) 2008-07-10 US disclosed
US-20080058526-A1 Halogenation of Rylen-Carboximides with Elementary Halogene in a Two-Phase Mixture Comprising an Organic Solvent and Water, Wherein Formed Halogene Hydrocide is Continously Removable from the Organic Solvent BASF AKTIENGESELLSCHAFT (DE) 2008-03-06 US disclosed