SCHEMBL1305347

SCHEMBL1305347

CCCCCCOc1ccccc1Br

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR7 P34969 1/20 0.58
LMNA P02545 4/20 0.54
MAPT P10636 4/20 0.54
MEN1 O00255 3/20 0.54
KMT2A Q03164 3/20 0.54
NR1I2 O75469 1/20 0.54
CHRM2 P08172 1/20 0.54
CYP3A4 P08684 1/20 0.54
ADRA2A P08913 1/20 0.54
OPRK1 P41145 1/20 0.54
HTR2B P41595 1/20 0.54
SLC6A3 Q01959 1/20 0.54
HDAC6 Q9UBN7 1/20 0.54
CYP1A2 P05177 2/20 0.52
CYP2C9 P11712 2/20 0.52
CYP2C19 P33261 2/20 0.52
RAB9A P51151 3/20 0.51
NPC1 O15118 2/20 0.51
HPGD P15428 2/20 0.51
L3MBTL1 Q9Y468 2/20 0.51

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

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
SCHEMBL12704119 1.00 HTR7 (0.58) HTR7LMNAMAPTMEN1KMT2A
SCHEMBL4800847 1.00 HTR7 (0.58) HTR7LMNAMAPTMEN1KMT2A
SCHEMBL10429651 1.00 HTR7 (0.58) HTR7LMNAMAPTMEN1KMT2A
SCHEMBL1590919 1.00 HTR7 (0.58) HTR7LMNAMAPTMEN1KMT2A
SCHEMBL11876204 0.98 HTR7 (0.59) HTR7LMNAMAPTMEN1KMT2A
SCHEMBL4185846 0.92 HTR7 (0.61) HTR7LMNAMAPTMEN1KMT2A
SCHEMBL30883281 0.90 HTR7 (0.62) HTR7LMNAMAPTMEN1KMT2A
SCHEMBL2344935 0.88 HTR7 (0.64) HTR7LMNAMAPTMEN1KMT2A
SCHEMBL1796140 0.86 HTR7 (0.63) HTR7LMNAMAPTMEN1KMT2A
SCHEMBL2859001 0.86 LMNA (0.62) LMNAMAPTMEN1KMT2ANR1I2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117964652-A Tetradentate phenol ether ligand-metal complex derived from naphthol, preparation method and olefin polymerization method 中国科学院大连化学物理研究所 2024-05-03 CN disclosed
EP-2499181-B1 POLYMER FOR OPTOELECTRONIC DEVICE BOE TECHNOLOGY GROUP CO LTD (CN) 2020-05-13 EP disclosed
CN-107022064-B Polymer for optoelectronic devices 京东方科技集团股份有限公司 2020-05-08 CN disclosed
CN-103261191-B Naphthalene list imide derivative and in solaode and photoelectric detector as the purposes of photosensitizer 巴斯夫欧洲公司 2016-06-29 CN disclosed
EP-2373759-B1 FUNCTIONALIZED POLYFLUORENES FOR USE IN OPTOELECTRONIC DEVICES GEN ELECTRIC (US) 2015-11-11 EP disclosed
CN-102300954-B Functionalized polyfluorenes for optoelectronic devices GEN ELECTRIC 2015-04-29 CN disclosed
CN-103261191-A Naphtalene monoimide derivatives and use thereof as photosensitizers in solar cells and photodetectors BASF SE 2013-08-21 CN disclosed
US-8512879-B2 Polymer for optoelectronic device GENERAL ELECTRIC COMPANY (US) 2013-08-20 US disclosed
CN-102887880-A Dibenzofuran derivatives, and preparation method and application thereof UNIV SOUTHEAST 2013-01-23 CN disclosed
CN-102686637-A Polymer for optoelectronic devices GEN ELECTRIC 2012-09-19 CN disclosed
US-20100144992-A1 FUNCTIONALIZED POLYFLUORENES FOR USE IN OPTOELECTRONIC DEVICES GENERAL ELECTRIC COMPANY (US) 2010-06-10 US disclosed
CN-101595153-A Be used to prepare method that aromatic(based)polymer wherein is attached to the structure on the base material, contain the structure of the aromatic(based)polymer chain that is attached on the conductive base and contain the electron device of this structure SUMITOMO CHEMICAL CO (JP) 2009-12-02 CN disclosed
WO-2009079039-A1 EMISSIVE POLYMERIC MATERIALS FOR OPTOELECTRONIC DEVICES GENERAL ELECTRIC COMPANY (US) 2009-06-25 WO disclosed
US-20090156783-A1 EMISSIVE POLYMERIC MATERIALS FOR OPTOELECTRONIC DEVICES GENERAL ELECTRIC COMPANY (US) 2009-06-18 US disclosed
CN-101405347-A Organic compound, and semiconductor thin-film electrode, photoelectric conversion element, and photoelectrochemical solar cell using same NAT INST OF ADVANCED IND SCIEN (JP) 2009-04-08 CN disclosed
US-5872148-A BRONCHODILATOR AGENTS AND ANALGESICS UNIVERSITY OF CONNECTICUT (US) 1999-02-16 US disclosed
US-5440052-A Compositions useful as a cannabinoid receptor probe UNIVERSITY OF CONNECTICUT (US) 1995-08-08 US disclosed
WO-1995019336-A1 PHENYL ETHANOL AMINE ETHERS AND USES THEREOF AS β-ADRENO-RECEPTOR AGONISTS IOVIS BIOMEDICAL AND PHARMACEUTICAL CONSULTANTS (NL) 1995-07-20 WO disclosed
CN-1022919-C Process for preparing pyrazole oxime derivatives NIHON NOHYAKU CO LTD (JP) 1993-12-01 CN disclosed
CN-86108691-A Pyrazole oxime derivatives, process for their preparation and their use NIHON NOHYAKU CO LTD (JP) 1988-01-20 CN disclosed