SCHEMBL4350865

SCHEMBL4350865

C=CC(=O)OCCOc1ccc(C(=O)Oc2ccc(-c3ccc(C#N)cc3)cc2)cc1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
THRB P10828 1/20 0.51
MAPT P10636 4/20 0.50
ALDH1A1 P00352 2/20 0.50
MMP2 P08253 7/20 0.49
MMP3 P08254 5/20 0.46
MMP1 P03956 1/20 0.46
MMP9 P14780 1/20 0.46
MMP13 P45452 1/20 0.46
HDAC1 Q13547 1/20 0.44
HDAC2 Q92769 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.41
LMNA P02545 1/20 0.41
TP53 P04637 1/20 0.41
CYP1A2 P05177 1/20 0.41
CYP2D6 P10635 1/20 0.41
HIF1A Q16665 1/20 0.41
HRH2 P25021 1/20 0.40
HRH1 P35367 1/20 0.40
HRH3 Q9Y5N1 1/20 0.40
POLB P06746 1/20 0.40

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
SCHEMBL14379724 1.00 THRB (0.51) THRBMAPTALDH1A1MMP2MMP3
SCHEMBL21500157 0.97 THRB (0.48) THRBMAPTALDH1A1MMP2MMP3
SCHEMBL8461569 0.96 THRB (0.55) THRBMAPTALDH1A1MMP2MMP3
SCHEMBL24599323 0.94 MMP3 (0.49) THRBMAPTALDH1A1MMP2MMP3
SCHEMBL13871163 0.94 MMP2 (0.48) THRBMAPTALDH1A1MMP2MMP3
SCHEMBL14130800 0.94 MMP3 (0.49) THRBMAPTALDH1A1MMP2MMP3
SCHEMBL16425790 0.94 MMP3 (0.49) THRBMAPTALDH1A1MMP2MMP3
SCHEMBL12676172 0.93 HDAC1 (0.50) THRBMAPTALDH1A1MMP2MMP3
SCHEMBL12723887 0.93 THRB (0.51) THRBMAPTALDH1A1MMP2MMP3
SCHEMBL11917944 0.91 ALDH1A1 (0.49) THRBMAPTALDH1A1MMP2MMP3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11332670-B2 Side-chain liquid crystal polymer, liquid crystal composition, retardation film, method for producing retardation film, transfer laminate, optical member, method for producing optical member, and display device DAI NIPPON PRINTING CO., LTD. (JP) 2022-05-17 US disclosed
US-20210189239-A1 LIQUID CRYSTAL COMPOSITION, RETARDATION FILM, METHOD FOR PRODUCING RETARDATION FILM, TRANSFER LAMINATE, OPTICAL MEMBER, METHOD FOR PRODUCING OPTICAL MEMBER, AND DISPLAY DEVICE DAI NIPPON PRINTING CO., LTD. (JP) 2021-06-24 US disclosed
US-20190136134-A1 SIDE-CHAIN LIQUID CRYSTAL POLYMER, LIQUID CRYSTAL COMPOSITION, RETARDATION FILM, METHOD FOR PRODUCING RETARDATION FILM, TRANSFER LAMINATE, OPTICAL MEMBER, METHOD FOR PRODUCING OPTICAL MEMBER, AND DISPLAY DEVICE DAI NIPPON PRINTING CO., LTD. (JP) 2019-05-09 US disclosed
EP-1803773-B1 POLYMERIZABLE LIQUID-CRYSTAL COMPOSITION AND LIQUID-CRYSTAL FILM MADE FROM THE COMPOSITION NIPPON OIL CORP (JP) 2013-02-27 EP disclosed
EP-1428065-B1 CHOLESTERIC LIQUID CRYSTAL OPTICAL BODIES AND METHODS OF MANUFACTURE AND USE 3M INNOVATIVE PROPERTIES CO (US) 2012-09-19 EP disclosed
EP-1990339-B1 DIOXETANE COMPOUND, CATIONICALLY POLYMERIZABLE COMPOSITION, OPTICAL FILM AND LIQUID CRYSTAL DISPLAY UNIT NIPPON OIL CORP (JP) 2012-05-02 EP disclosed
US-7998543-B2 Dioxetane compound, cationically polymerizable composition, optical film, and liquid crystal display device NIPPON OIL CORPORATION (JP) 2011-08-16 US disclosed
US-7982952-B2 Polarization component, polarization light source and image display apparatus using the same NITTO DENKO CORPORATION (JP) 2011-07-19 US disclosed
US-7982952-B2 Polarization component, polarization light source and image display apparatus using the same NITTO DENKO CORPORATION (JP) 2011-07-19 US disclosed
US-7841730-B2 Light source device and crystal display device NITTO DENKO CORPORATION (JP) 2010-11-30 US disclosed
US-7029729-B2 liquid crystal polymer and a non-liquid crystalline additive; optical displays that include the composition as a reflective polarizer, preferably haing no more than 10% absorption for transmission polarization over the wavelength desired 3M INNOVATIVE PROPERTIES COMPANY (US) 2006-04-18 US disclosed
EP-1601742-A1 CHOLESTERIC LIQUID CRYSTAL ADDITIVES 3M Innovative Properties Company (US) 2005-12-07 EP disclosed
EP-1597337-A1 CHOLESTERIC LIQUID CRYSTAL DRYING PROCESS AND SOLVENT 3M Innovative Properties Company (US) 2005-11-23 EP disclosed
US-6913708-B2 Cholesteric liquid crystal drying process and solvent 3M INNOVATIVE PROPERTIES COMPANY (US) 2005-07-05 US disclosed
WO-2005023964-A2 CHOLESTERIC LIQUID CRYSTAL COPOLYMERS AND ADDITIVES 3M INNOVATIVE PROPERTIES COMPANY (US) 2005-03-17 WO disclosed
US-20050045854-A1 Cholesteric liquid crystal copolymers and additives 3M INNOVATIVE PROPERTIES COMPANY 2005-03-03 US disclosed
WO-2004076589-A1 CHOLESTERIC LIQUID CRYSTAL ADDITIVES 3M INNOVATIVE PROPERTIES COMPANY (US) 2004-09-10 WO disclosed
WO-2004076588-A1 CHOLESTERIC LIQUID CRYSTAL DRYING PROCESS AND SOLVENT 3M INNOVATIVE PROPERTIES COMPANY (US) 2004-09-10 WO disclosed
US-20040164275-A1 Cholesteric liquid crystal additives 3M INNOVATIVE PROPERTIES COMPANY 2004-08-26 US disclosed
US-20040164274-A1 Cholesteric liquid crystal drying process and solvent 3M INNOVATIVE PROPERTIES COMPANY 2004-08-26 US disclosed