SCHEMBL3677673

SCHEMBL3677673

O=C(S)SO

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
SCHEMBL735595 0.70
SCHEMBL1304594 0.70
SCHEMBL1303671 0.70
SCHEMBL5802816 0.70
SCHEMBL9846791 0.67
SCHEMBL15779512 0.67
SCHEMBL3839279 0.67
Ammonia Solution, Strong SCHEMBL10481904 0.67
SCHEMBL25876 0.65
SCHEMBL4214737 0.63

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 19 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0432416-B1 Rubber vulcanisation process using a vulcanisation system based on sulphur and dithiocarboxylic acids or salts thereof HUELS CHEMISCHE WERKE AG (DE) 1995-05-17 EP claimed
EP-0365792-B1 Process for the de-activation of radicals BUNAWERKE HUELS GMBH (DE) 1994-01-26 EP claimed
EP-0455872-A1 Vulcanisation process for unsaturated polymers dispersed in water using a vulcanisation system based on sulfur and dithiocarboxylic acids or salts thereof HÜLS AKTIENGESELLSCHAFT (DE) 1991-11-13 EP claimed
EP-0432416-A2 Rubber vulcanisation process using a vulcanisation system based on sulphur and dithiocarboxylic acids or salts thereof HÜLS AKTIENGESELLSCHAFT (DE) 1991-06-19 EP claimed
EP-0365792-A2 Process for the de-activation of radicals BUNAWERKE HÜLS GMBH (DE) 1990-05-02 EP claimed
EP-2186651-B1 Hydroxyl modified microgel lattices which can be stored safely for a long time LANXESS DEUTSCHLAND GMBH (DE) 2013-07-03 EP disclosed
EP-2186651-A1 Hydroxyl modified microgel lattices which can be stored safely for a long time Lanxess Deutschland GmbH (DE) 2010-05-19 EP disclosed
US-7585839-B2 Cyclic and linear oligopeptides; capable of increasing gap junction conductance; lack the proarrhythmic side effects; use as drug to also treat eye disorders, cancer, and gastrointestinal disorders among others ZEALAND PHARMA A/S (DK) 2009-09-08 US disclosed
US-20050113293-A1 Medical uses of intercellular communication facilitating compounds ZEALAND PHARMA A/S 2005-05-26 US disclosed
EP-1370276-A2 MEDICAL USES OF INTERCELLULAR COMMUNICATION FACILITATING COMPOUNDS Zealand Pharma A/S (DK) 2003-12-17 EP disclosed
WO-2002077017-A2 MEDICAL USES OF INTERCELLULAR COMMUNICATION FACILITATING COMPOUNDS ZEALAND PHARMA A/S (DK) 2002-10-03 WO disclosed
EP-0432416-B1 Rubber vulcanisation process using a vulcanisation system based on sulphur and dithiocarboxylic acids or salts thereof HUELS CHEMISCHE WERKE AG (DE) 1995-05-17 EP disclosed
EP-0365792-B1 Process for the de-activation of radicals BUNAWERKE HUELS GMBH (DE) 1994-01-26 EP disclosed
EP-0455872-A1 Vulcanisation process for unsaturated polymers dispersed in water using a vulcanisation system based on sulfur and dithiocarboxylic acids or salts thereof HÜLS AKTIENGESELLSCHAFT (DE) 1991-11-13 EP disclosed
EP-0455872-A1 Vulcanisation process for unsaturated polymers dispersed in water using a vulcanisation system based on sulfur and dithiocarboxylic acids or salts thereof HÜLS AKTIENGESELLSCHAFT (DE) 1991-11-13 EP disclosed
EP-0365792-A3 PROCESS FOR THE DE-ACTIVATION OF RADICALS BUNAWERKE HÜLS GMBH (DE) 1991-07-17 EP disclosed
EP-0432416-A2 Rubber vulcanisation process using a vulcanisation system based on sulphur and dithiocarboxylic acids or salts thereof HÜLS AKTIENGESELLSCHAFT (DE) 1991-06-19 EP disclosed
EP-0365792-A2 Process for the de-activation of radicals BUNAWERKE HÜLS GMBH (DE) 1990-05-02 EP disclosed
EP-0365792-A2 Process for the de-activation of radicals BUNAWERKE HÜLS GMBH (DE) 1990-05-02 EP disclosed