SCHEMBL4293263

SCHEMBL4293263

CC=CCOCCCC

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
SCHEMBL8064977 1.00
SCHEMBL5683264 1.00
SCHEMBL135519 0.93 HTT (0.41)
SCHEMBL7936971 0.93 HTT (0.41)
SCHEMBL14939100 0.91 HTT (0.45)
SCHEMBL9146283 0.91 HTT (0.45)
SCHEMBL14939101 0.91 HTT (0.45)
SCHEMBL9050529 0.91 HTT (0.45)
SCHEMBL9148832 0.91 HTT (0.45)
SCHEMBL14938976 0.91 HTT (0.45)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105446080-B A kind of coating composition, its application and the substrate using it 深圳市容大感光科技股份有限公司 2019-11-08 CN claimed
CN-102936264-A Synthetic method of aromatic base chiral oxazoline phosphine ligand BEIJING J & K SCIENT LTD 2013-02-20 CN claimed
EP-0906299-B1 PROCESS FOR PREPARING TETRAHYDROFURAN FROM DIALKOXYBUTENES BASF AG (DE) 2004-08-04 EP claimed
US-6245948-B1 REACTING 2-BUTENOL ETHERS IN PRESENCE OF METATHESIS CATALYST TO GIVE BUTENE AND CORRESPONDING 1,4-BUTENEDIOL DIETHERS BASF AKTIENGESELLSCHAFT (DE) 2001-06-12 US claimed
US-6169189-B1 REACTING DIALKOXYBUTENES WITH WATER AND HYDROGEN IN PRESENCE OF CATALYSTS OR CATALYST COMBINATIONS WHICH ARE BOTH CAPABLE OF HYDROGENATION AND HAVE ACIDIC OR BASIC CENTERS BASF AKTIENGESELLSCHAFT (DE) 2001-01-02 US claimed
EP-0983986-A1 Process for separating 1,3-butadiene and water from mixtures containing them and 1-n-butoxy-2-butene, 3-n-butoxy-1-butene, n-butanol and di-n-butyl ether BASF AKTIENGESELLSCHAFT (DE) 2000-03-08 EP claimed
EP-0906299-A1 PROCESS FOR PREPARING TETRAHYDROFURAN FROM DIALKOXYBUTENES BASF AKTIENGESELLSCHAFT (DE) 1999-04-07 EP claimed
CN-1210526-A Process for preparing tetrahydrofuran from dialkoxybutenes BASF AG (DE) 1999-03-10 CN claimed
EP-0847380-A1 MIXTURE OF ESTERS AND USE THEREOF BP Chemicals Limited (GB) 1998-06-17 EP claimed
WO-1998000387-A1 MIXTURE OF ESTERS AND USE THEREOF BP CHEMICALS LIMITED (GB) 1998-01-08 WO claimed
WO-1997046546-A1 PROCESS FOR PREPARING TETRAHYDROFURAN FROM DIALKOXYBUTENES BASF AKTIENGESELLSCHAFT (DE) 1997-12-11 WO claimed
US-12410333-B2 Inkjet ink NORITAKE CO., LIMITED (JP) 2025-09-09 US disclosed
US-12370135-B2 Anhydrous composition for caring for and/or making up keratin materials L'OREAL (FR) 2025-07-29 US disclosed
US-12163038-B2 Inkjet ink NORITAKE CO., LIMITED (JP) 2024-12-10 US disclosed
US-12162299-B2 Inkjet ink NORITAKE CO., LIMITED (JP) 2024-12-10 US disclosed
EP-0739332-A1 PROCESS FOR PRODUCING n-BUTYRALDEHYDE AND/OR n-BUTANOL BASF AKTIENGESELLSCHAFT (DE) 1996-10-30 EP disclosed
WO-1996029300-A1 METHOD OF PRODUCING 3-PENTENIC ACID ESTERS BY CARBONYLATION OF ALKOXYBUTENES BASF AKTIENGESELLSCHAFT (DE) 1996-09-26 WO disclosed
EP-0668259-A1 A method for the preparation of optically active 2-aryl alkyl aldehydes and formation of 2-aryl-alkanoic acids therefrom MEDICEChem.-Pharm. Fabrik Pütter GmbH & Co. KG (DE) 1995-08-23 EP disclosed
WO-1995019334-A1 PROCESS FOR PRODUCING n-BUTYRALDEHYDE AND/OR n-BUTANOL BASF AKTIENGESELLSCHAFT (DE) 1995-07-20 WO disclosed
US-5434302-A Method for the preparation of optically active 2-aryl alkyl aldehydes and formation of 2-aryl-alkanoic acids therefrom PARADIES H HENRICH (DE) 1995-07-18 US disclosed