SCHEMBL7182963

SCHEMBL7182963

O=[N+]([O-])c1cccc(P(=O)(c2ccc(CC=CF)cc2)c2cccc([N+](=O)[O-])c2)c1

nearest known ligand 0.40

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
▸ NPSR1 Q6W5P4 1/20 0.40
▸ TSHR P16473 4/20 0.40
▸ LMNA P02545 2/20 0.40
▸ THRA P10827 1/20 0.39
▸ ALDH1A1 P00352 4/20 0.38
▸ HPGD P15428 1/20 0.38
▸ SMN1; SMN2 Q16637 1/20 0.38
▸ MEN1 O00255 2/20 0.36
▸ KMT2A Q03164 2/20 0.36
▸ CYP1A2 P05177 1/20 0.36
▸ CYP2D6 P10635 1/20 0.36
▸ CYP2C9 P11712 1/20 0.36
▸ CYP2C19 P33261 1/20 0.36
▸ L3MBTL1 Q9Y468 2/20 0.36
▸ ACHE P22303 1/20 0.36
▸ TDP1 Q9NUW8 1/20 0.36
▸ ALOX15 P16050 1/20 0.36
▸ MAPT P10636 1/20 0.35
▸ NFE2L2 Q16236 1/20 0.35

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
SCHEMBL7170918 0.79 MAOB (0.43) NPSR1TSHRLMNAALDH1A1MEN1
SCHEMBL7180380 0.79 CYP19A1 (0.33) LMNA
SCHEMBL8408187 0.78 TSHR (0.64) NPSR1TSHRLMNAALDH1A1MEN1
SCHEMBL30764114 0.78 TSHR (0.64) NPSR1TSHRLMNAALDH1A1MEN1
SCHEMBL4323924 0.78 TSHR (0.50) NPSR1TSHRLMNAALDH1A1SMN1; SMN2
SCHEMBL29176796 0.77 TSHR (0.57) NPSR1TSHRLMNAALDH1A1SMN1; SMN2
SCHEMBL30764106 0.77 TSHR (0.57) NPSR1TSHRLMNAALDH1A1SMN1; SMN2
SCHEMBL16774768 0.77 TSHR (0.57) NPSR1TSHRLMNAALDH1A1SMN1; SMN2
SCHEMBL7620892 0.74 TSHR (0.46) NPSR1TSHRLMNAALDH1A1ACHE
SCHEMBL7186369 0.73 ALDH1A1 (0.41) NPSR1TSHRLMNATHRAALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6531633-B2 Grignard reaction of bromobenzene substituted with fluoroalkyl group and diphenylphosphinic chloride in an organic solvent and magnesium, followed by nitration in sulfuric and nitric acids and hydrogenation in presence of palladium KWANGJU INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2003-03-11 — — US disclosed
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