SCHEMBL7186358

SCHEMBL7186358

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

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ NPSR1 Q6W5P4 2/20 0.45
▸ GAA P10253 2/20 0.40
▸ MAPT P10636 1/20 0.40
▸ L3MBTL1 Q9Y468 1/20 0.40
▸ TDP1 Q9NUW8 1/20 0.39
▸ GRM8 O00222 3/20 0.38
▸ GRM4 Q14833 3/20 0.38
▸ MEN1 O00255 2/20 0.36
▸ KMT2A Q03164 2/20 0.36
▸ POLB P06746 1/20 0.36
▸ TSHR P16473 2/20 0.36
▸ ACP3 P15309 1/20 0.36
▸ LMNA P02545 1/20 0.36
▸ CYP1A2 P05177 2/20 0.36
▸ CYP2C9 P11712 2/20 0.36
▸ CYP2C19 P33261 2/20 0.36
▸ ALDH1A1 P00352 2/20 0.36
▸ SMN1; SMN2 Q16637 2/20 0.36
▸ AKR1C3 P42330 1/20 0.36
▸ AKR1C2 P52895 1/20 0.36

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
SCHEMBL7190141 0.81 TSHR (0.34) GAAMAPTMEN1KMT2ATSHR
SCHEMBL7186369 0.77 ALDH1A1 (0.41) NPSR1TDP1MEN1KMT2ATSHR
SCHEMBL7182952 0.76 TSHR (0.40) NPSR1TDP1MEN1KMT2ATSHR
SCHEMBL30764114 0.75 TSHR (0.64) NPSR1GAATDP1MEN1KMT2A
SCHEMBL8408187 0.75 TSHR (0.64) NPSR1GAATDP1MEN1KMT2A
SCHEMBL4323924 0.74 TSHR (0.50) NPSR1GAAMAPTTDP1MEN1
SCHEMBL16774768 0.73 TSHR (0.57) NPSR1MAPTTDP1MEN1KMT2A
SCHEMBL30764106 0.73 TSHR (0.57) NPSR1MAPTTDP1MEN1KMT2A
SCHEMBL29176796 0.73 TSHR (0.57) NPSR1MAPTTDP1MEN1KMT2A
SCHEMBL7620892 0.71 TSHR (0.46) NPSR1MAPTTDP1TSHRLMNA

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 claimed
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