SCHEMBL7182952

SCHEMBL7182952

C=CC(F)c1ccc(P(=O)(c2cccc([N+](=O)[O-])c2)c2cccc([N+](=O)[O-])c2)cc1

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TSHR P16473 3/20 0.40
▸ LMNA P02545 1/20 0.40
▸ ACP3 P15309 1/20 0.39
▸ NPSR1 Q6W5P4 1/20 0.38
▸ CA12 O43570 1/20 0.36
▸ CA1 P00915 1/20 0.36
▸ MMP2 P08253 1/20 0.36
▸ MEN1 O00255 2/20 0.36
▸ KMT2A Q03164 2/20 0.36
▸ ALDH1A1 P00352 3/20 0.36
▸ ACHE P22303 1/20 0.36
▸ TDP1 Q9NUW8 1/20 0.36
▸ ALOX15 P16050 1/20 0.36
▸ NFE2L2 Q16236 1/20 0.35
▸ CA2 P00918 1/20 0.35
▸ CA5A P35218 1/20 0.35
▸ HSP90AA1 P07900 1/20 0.35
▸ FBP1 P09467 1/20 0.35
▸ VCP P55072 1/20 0.35
▸ CYP19A1 P11511 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
SCHEMBL7170910 0.79 TSHR (0.40) TSHRLMNAACP3MEN1KMT2A
SCHEMBL7180372 0.79 CA1 (0.33) CA12CA1KMT2ACA2
SCHEMBL30764114 0.78 TSHR (0.64) TSHRLMNAACP3NPSR1CA12
SCHEMBL8408187 0.78 TSHR (0.64) TSHRLMNAACP3NPSR1CA12
SCHEMBL4323924 0.78 TSHR (0.50) TSHRLMNAACP3NPSR1MEN1
SCHEMBL30764106 0.77 TSHR (0.57) TSHRLMNAACP3NPSR1MEN1
SCHEMBL29176796 0.77 TSHR (0.57) TSHRLMNAACP3NPSR1MEN1
SCHEMBL16774768 0.77 TSHR (0.57) TSHRLMNAACP3NPSR1MEN1
SCHEMBL7186358 0.76 NPSR1 (0.45) TSHRLMNAACP3NPSR1MEN1
SCHEMBL28285992 0.75 ALDH1A1 (0.44) TSHRLMNACA12CA1MEN1

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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