SCHEMBL198765

SCHEMBL198765

[CH2]C(O)SC(C)C

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
Hydrochloric Acid SCHEMBL28062402 0.71
SCHEMBL2976798 0.69
SCHEMBL8438420 0.69
SCHEMBL5170346 0.69
Hydrochloric Acid SCHEMBL28391738 0.68
SCHEMBL265333 0.66
SCHEMBL210425 0.66
SCHEMBL15676 0.66
SCHEMBL2069043 0.66
SCHEMBL212534 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 49 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-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
US-10230023-B2 Color converter BASF SE (DE) 2019-03-12 US disclosed
US-10224485-B2 Process for preparing a crystalline organic semiconductor material BASF SE (DE) 2019-03-05 US disclosed
US-20170327465-A1 4-HYDROXYQUINOLINE COMPOUNDS BASF SE (DE) 2017-11-16 US disclosed
US-20170331049-A1 4-OXOQUINOLINE COMPOUNDS BASF SE (DE) 2017-11-16 US disclosed
EP-3224247-A1 4-HYDROXYQUINOLINE COMPOUNDS BASF SE (DE) 2017-10-04 EP disclosed
EP-3224246-A1 4-OXOQUINOLINE COMPOUNDS BASF SE (DE) 2017-10-04 EP disclosed
US-20170250347-A1 ORGANIC SEMICONDUCTOR COMPOSITION COMPRISING A LIQUID MEDIUM BASF SE (DE) 2017-08-31 US disclosed
US-20100317876-A1 TERRYLENE AND QUATERRYLENE DERIVATIVES BASF AKTIENGESELLSCHAFT (DE) 2010-12-16 US disclosed
US-7795431-B2 such as N-(2,6-Diisopropylphenyl)-1,6,9,14-tetra[4-(1,1,3,3-tetramethylbutyl)phenoxy]terrylene-3, 4:11,12-tetracarboxylic monoimide monoanhydride, used as dyes, as infrared absorbers, as semiconductors in organic electronics, emitters in electro- and chemiluminescence applications and in photovoltaics BASF AKTIENGESELLSCHAFT (DE) 2010-09-14 US disclosed
US-20100048904-A1 DIBENZORYLENETETRACARBOXIMIDES AS INFRARED ABSORBERS BASF AKTIENGESELLSCHAFT (DE) 2010-02-25 US disclosed
WO-2010010198-A2 NEW AZIDE SUBSTITUTED NAPHTHYLENE OR RYLENE IMIDE DERIVATIVES AND THEIR USE AS REAGENTS IN CLICK-REACTIONS BASF SE (DE) 2010-01-28 WO disclosed
EP-2022105-A1 METHOD FOR PRODUCING ORGANIC FIELD-EFFECT TRANSISTORS BASF SE (DE) 2009-02-11 EP disclosed
US-20080255357-A1 Terrylene and Quaterrylene Derivatives BASF AKTIENGESELLSCHAFT (DE) 2008-10-16 US disclosed
US-20080090325-A1 METHOD FOR PRODUCING ORGANIC FIELD-EFFECT TRANSISTORS BASF AKTIENGESELLSCHAFT (DE) 2008-04-17 US disclosed
US-20080017850-A1 applying n-type organic semiconducting compound 1,6,7,12-Tetrachloro-N,N'-benzyl-perylene-3,9; 11,12-tetracarboxylic diimide or 1,6,7,12-tetrachloroperylen-3,9; 9,10-tetracarboxylic dianhydride; charge transfer compounds for electronics, optoelectronics and photonic applications; chemical intermediates BASF AKTIENGESELLSCHAFT (DE) 2008-01-24 US disclosed
WO-2007128774-A1 METHOD FOR PRODUCING ORGANIC FIELD-EFFECT TRANSISTORS BASF SE (DE) 2007-11-15 WO disclosed
US-20070259475-A1 METHOD FOR PRODUCING ORGANIC FIELD-EFFECT TRANSISTORS BASF AKTIENGESELLSCHAFT (DE) 2007-11-08 US disclosed