SCHEMBL9407441

SCHEMBL9407441

CCCCCCCCOc1ccc(N=Nc2ccccc2)cc1

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LTA4H P09960 2/20 0.64
CHRNA7 P36544 1/20 0.60
CHRNA10 Q9GZZ6 1/20 0.60
CHRNA9 Q9UGM1 1/20 0.60
PPARA Q07869 1/20 0.56
NR5A1 Q13285 1/20 0.56
TP53 P04637 2/20 0.54
TSHR P16473 1/20 0.54
PLA2G4B P0C869 1/20 0.53
MLNR O43193 1/20 0.51
NR1I2 O75469 1/20 0.51
ESR1 P03372 1/20 0.51
NR3C1 P04150 1/20 0.51
PGR P06401 1/20 0.51
ADRB2 P07550 1/20 0.51
CHRM2 P08172 1/20 0.51
ADRB1 P08588 1/20 0.51
HTR1A P08908 1/20 0.51
ADRA2A P08913 1/20 0.51
ADORA3 P0DMS8 1/20 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
SCHEMBL28700494 1.00 LTA4H (0.64) LTA4HCHRNA7CHRNA10CHRNA9PPARA
SCHEMBL1986653 1.00 LTA4H (0.64) LTA4HCHRNA7CHRNA10CHRNA9PPARA
SCHEMBL28474484 1.00 LTA4H (0.64) LTA4HCHRNA7CHRNA10CHRNA9PPARA
SCHEMBL1984435 1.00 LTA4H (0.64) LTA4HCHRNA7CHRNA10CHRNA9PPARA
SCHEMBL13417485 1.00 LTA4H (0.64) LTA4HCHRNA7CHRNA10CHRNA9PPARA
SCHEMBL19281444 1.00 LTA4H (0.64) LTA4HCHRNA7CHRNA10CHRNA9PPARA
SCHEMBL28678951 1.00 LTA4H (0.64) LTA4HCHRNA7CHRNA10CHRNA9PPARA
SCHEMBL11836150 1.00 LTA4H (0.64) LTA4HCHRNA7CHRNA10CHRNA9PPARA
SCHEMBL4942746 1.00 LTA4H (0.64) LTA4HCHRNA7CHRNA10CHRNA9PPARA
SCHEMBL28940534 1.00 LTA4H (0.64) LTA4HCHRNA7CHRNA10CHRNA9PPARA

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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111748323-A Preparation method and application of optical energy storage phase change material based on azobenzene 江南大学 2020-10-09 CN disclosed
US-5314997-A Optically active azo compound, producing method thereof, and liquid crystal composition containing said compound RICOH COMPANY, LTD. (JP) 1994-05-24 US disclosed
EP-0260077-B1 PHENYL PYRIMIDINE COMPOUND AND LIQUID CRYSTALLINE COMPOSITION AJINOMOTO CO., INC. (JP) 1993-05-26 EP disclosed
US-4892676-A FERROELECTRIC, HIGH SPEED RESPONSE AJINOMOTO CO., INC. (JP) 1990-01-09 US disclosed
EP-0260077-A1 Phenyl pyrimidine compound and liquid crystalline composition AJINOMOTO CO., INC. (JP) 1988-03-16 EP disclosed