SCHEMBL7049331

SCHEMBL7049331

Cc1ccccc1CC1CO1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.48
GLA P06280 1/20 0.48
TAAR1 Q96RJ0 1/20 0.43
CYP2A13 Q16696 1/20 0.43
KMT2A Q03164 2/20 0.42
MEN1 O00255 1/20 0.42
GAA P10253 1/20 0.42
ACHE P22303 2/20 0.42
TDP1 Q9NUW8 1/20 0.39
CES2 O00748 1/20 0.38
LMNA P02545 1/20 0.38
CTSB P07858 1/20 0.38
CYP2D6 P10635 1/20 0.38
SLC6A2 P23975 1/20 0.38
SLC6A4 P31645 1/20 0.38
DRD4 P21917 1/20 0.38
ADRA2A P08913 1/20 0.38
ADRA2B P18089 1/20 0.38
ADRA2C P18825 1/20 0.38
TSHR P16473 1/20 0.38

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
SCHEMBL31438264 1.00 ALDH1A1 (0.48) ALDH1A1GLATAAR1CYP2A13KMT2A
SCHEMBL29826970 0.86 TDP1 (0.45) ALDH1A1GLATAAR1KMT2AMEN1
SCHEMBL6480647 0.86 TDP1 (0.45) ALDH1A1GLATAAR1KMT2AMEN1
SCHEMBL11864659 0.85 CHRM2 (0.42) ALDH1A1GLATAAR1CYP2A13KMT2A
SCHEMBL14248992 0.83 ALDH1A1 (0.42) ALDH1A1GLACYP2A13GAATDP1
SCHEMBL3117388 0.82 ALDH1A1 (0.41) ALDH1A1GLATAAR1CYP2A13KMT2A
SCHEMBL8976185 0.80 ALDH1A1 (0.46) ALDH1A1GLATSHRDRD2DRD1
SCHEMBL30607492 0.80 TDP1 (0.41) ALDH1A1GLATAAR1KMT2AMEN1
SCHEMBL28454337 0.80 TDP1 (0.41) ALDH1A1GLATAAR1KMT2AMEN1
SCHEMBL2675606 0.80 TDP1 (0.41) ALDH1A1GLATAAR1KMT2AMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110564755-B Method for preparing (S) -3-phenyl-1, 2-epoxypropane and derivatives thereof by using biological enzyme catalysis 河南农业大学 2021-01-12 CN disclosed
CN-110564755-A Method for preparing (S) -3-phenyl-1, 2-epoxypropane and derivatives thereof by using biological enzyme catalysis 河南农业大学 2019-12-13 CN disclosed
CN-110226120-A Sealing agent for liquid crystal display element, vertical conduction material, and liquid crystal display element 积水化学工业株式会社 2019-09-10 CN disclosed
CN-110168442-A Sealing agent for liquid crystal display element, vertical conduction material, and liquid crystal display element 积水化学工业株式会社 2019-08-23 CN disclosed
CN-105579558-B Quaternary ammonium compounds as fuel or lubricant additives 因诺斯佩克有限公司 2018-02-27 CN disclosed
CN-107735859-A Semiconductor device and semiconductor element protection material 积水化学工业株式会社 2018-02-23 CN disclosed
CN-103992464-B Epoxy resin composition for carbon-fiber-reinforced composite material, prepreg and fiber-reinforced composite material board 东丽株式会社 2017-07-21 CN disclosed
CN-103402975-B beta-hydroxyalkylamide and resin composition 东洋油墨SC控股株式会社 2016-08-17 CN disclosed
CN-102736414-B Dyeing composition and color filter using same TOYO INK SC KK 2015-01-28 CN disclosed
CN-103857750-A Resin composition, coating film, and insulating film for touch panel TOYO INK SC HOLDINGS CO LTD 2014-06-11 CN disclosed
CN-101666975-A Coloring radiation sensitive composition, color filter and color liquid crystal display elements JSR CORP 2010-03-10 CN disclosed
CN-1312189-C Epoxy resin with three functional groups and its derivatives, their preparation method and use CHINESE ACAD INST CHEMISTRY (CN) 2007-04-25 CN disclosed
CN-1287222-C Photosensitive composition SUMITOMO CHEMICAL CO (JP) 2006-11-29 CN disclosed
CN-1670053-A Epoxy resin with three functional groups and its derivatives, their preparation method and use CHINESE ACAD INST CHEMISTRY (CN) 2005-09-21 CN disclosed
CN-1424624-A Photosensitive composition SUMITOMO CHEMICAL CO (JP) 2003-06-18 CN disclosed
EP-0611826-B1 Processes for production of optically active epoxides DAICEL CHEM (JP) 2003-05-02 EP disclosed
US-5672504-A TREATING MIXED EPOXIDE ENANTIOMORPHS WITH MICROORGANISMS TO INCREASE CONCENTRATION OF OPTICALLY PURE S-ENANTIOMORPHS DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1997-09-30 US disclosed
EP-0611826-A2 Processes for production of optically active epoxides DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1994-08-24 EP disclosed
US-4143206-A COPOLYMERS OF ACRYLIC AMIDES CIBA-GEIGY CORPORATION (US) 1979-03-06 US disclosed
US-4066597-A METHOD OF FINISHING SYNTHETIC ORGANIC FIBROUS MATERIAL, IN PARTICULAR OF PROVIDING IT WITH AN ANTISTATIC FINISH CIBA-GEIGY CORPORATION (US) 1978-01-03 US disclosed