SCHEMBL434434

SCHEMBL434434

[CH2]C(C)N1CC1C

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
SCHEMBL19997520 0.73
SCHEMBL10213112 0.73
SCHEMBL23114277 0.71 L3MBTL1 (0.33)
SCHEMBL24536431 0.71 L3MBTL1 (0.33)
SCHEMBL2758654 0.71 L3MBTL1 (0.33)
SCHEMBL3319142 0.69 KDM4E (0.40)
SCHEMBL18154861 0.69
SCHEMBL9559860 0.67 SMN1; SMN2 (0.33)
SCHEMBL32677710 0.65
SCHEMBL11058420 0.63 SMN1; SMN2 (0.31)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3297434-A1 NON-AQUEOUS ORGANO LIQUID DELIVERY SYSTEMS CONTAINING DISPERSED POLY (ORGANIC ACIDS) THAT IMPROVE AVAILABILITY OF MACRO&amp;MICRO-NUTRIENTS TO PLANTS Mcknight, Gary, David (US) 2018-03-28 EP claimed
WO-2016183511-A1 NON-AQUEOUS ORGANO LIQUID DELIVERY SYSTEMS CONTAINING DISPERSED POLY (ORGANIC ACIDS) THAT IMPROVE AVAILABILITY OF MACRO &amp; MICRO-NUTRIENTS TO PLANTS MCKNIGHT GARY DAVID (US) 2016-11-17 WO claimed
US-8940929-B2 Preparation method of high-optical purity N2-[1 -(S)-ethoxycarbonyl-3-phenylpropyl]-N6-trifluoroacetyl-L-lysine ABA CHEMICALS CORPORATION (CN) 2015-01-27 US claimed
US-20130178651-A1 PREPARATION METHOD OF HIGH-OPTICAL PURITY N2-[1-(S)-ETHOXYCARBONYL-3-PHENYLPROPYL]-N6-TRIFLUOROACETYL-L-LYSINE ABA CHEMICALS CORPORATION (CN) 2013-07-11 US claimed
US-11351518-B2 Cesium adsorbent and method of preparing the same KOREA INSTITUTE OF CIVIL ENGINEERING AND BUILDING TECHNOLOGY (KR) 2022-06-07 US disclosed
US-20200061577-A1 CESIUM ADSORBENT AND METHOD OF PREPARING THE SAME KOREA INSTITUTE OF CIVIL ENGINEERING AND BUILDING TECHNOLOGY (KR) 2020-02-27 US disclosed
EP-3613502-A1 CESIUM ADSORBENT AND METHOD OF PREPARING THE SAME Korea Institute Of Civil Engineering And Building Technology (KR) 2020-02-26 EP disclosed
EP-2621463-A2 STRUCTURED ACRYLATE COPOLYMER FOR USE IN MULTI-PHASE SYSTEMS Lubrizol Advanced Materials, Inc. (US) 2013-08-07 EP disclosed
EP-2596159-A1 BONDED MINERAL FIBRE PRODUCT HAVING HIGH FIRE AND PUNKING RESISTANCE Rockwool International A/S (DK) 2013-05-29 EP disclosed
WO-2012044929-A2 STRUCTURED ACRYLATE COPOLYMER FOR USE IN MULTI-PHASE SYSTEMS LUBRIZOL ADVANCED MATERIALS, INC. (US) 2012-04-05 WO disclosed
WO-2012010694-A1 BONDED MINERAL FIBRE PRODUCT HAVING HIGH FIRE AND PUNKING RESISTANCE ROCKWOOL INTERNATIONAL A/S (DK) 2012-01-26 WO disclosed
US-7648838-B2 Cell lysis method by immobilized metal-ligand complex SAMSUNG ELECTRONICS CO., LTD. (KR) 2010-01-19 US disclosed
US-20060099711-A1 Cell lysis method by immobilized metal-ligand complex SAMSUNG ELECTRONICS CO., LTD. (KR) 2006-05-11 US disclosed
EP-1549295-A2 COHESIVE COPRECIPITATES OF SULFATED POLYSACCHARIDE AND FIBRILLAR PROTEIN AND USE THEREOF NVR Labs, Ltd., Neural &amp; Vascular Reconstruction (IL) 2005-07-06 EP disclosed
US-20050064037-A1 Transdermal delivery of oxybutynin in gel formulations ORIENT EUROPHARMA CO., LTD. (TW) 2005-03-24 US disclosed
WO-2004029095-A2 COHESIVE COPRECIPITATES OF SULFATED POLYSACCHARIDE AND FIBRILLAR PROTEIN AND USE THEREOF NVR LABS, LTD. (IL) 2004-04-08 WO disclosed
WO-2001009231-A9 CURED COATINGS HAVING IMPROVED SCRATCH RESISTANCE, COATED SUBSTRATES AND METHODS RELATED THERETO PPG IND OHIO INC (US) 2002-09-06 WO disclosed
EP-1204865-A1 USE OF STABILISED SYNTHETIC COMPOUNDS IN IMMUNOASSAY Bio-Rad Pasteur (FR) 2002-05-15 EP disclosed
US-6267939-B1 FOR THE PURIFICATION OF ANY GAS WHICH CONTAINS CARBON DIOXIDE AND/OR ACIDIC SULFIDES SUCH AS HYDROGEN SULFIDE, CARBON OXYSULFIDE AS COMPONENTS TO BE REMOVED; EXAMPLES OF SUCH GASES ARE NATURAL GAS, SYNTHESIS GAS, VARIOUS BIOGASES HUNTSMAN CORPORATION HUNGARY VEGYIPARI TERMELO-FEJLESZTO RESZVENYTARSASAG (HU) 2001-07-31 US disclosed
WO-2001013114-A1 USE OF STABILISED SYNTHETIC COMPOUNDS IN IMMUNOASSAY BIO-RAD PASTEUR (FR) 2001-02-22 WO disclosed