SCHEMBL7182958

SCHEMBL7182958

C=CCc1cc(F)ccc1P(=O)(c1cccc([N+](=O)[O-])c1)c1cccc([N+](=O)[O-])c1

nearest known ligand 0.38

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
▸ NPSR1 Q6W5P4 2/20 0.38
▸ MAPT P10636 7/20 0.37
▸ GAA P10253 2/20 0.37
▸ LMNA P02545 2/20 0.36
▸ TSHR P16473 1/20 0.36
▸ RAB9A P51151 3/20 0.36
▸ NPC1 O15118 3/20 0.36
▸ SMN1; SMN2 Q16637 2/20 0.36
▸ MEN1 O00255 6/20 0.35
▸ KMT2A Q03164 6/20 0.35
▸ L3MBTL1 Q9Y468 2/20 0.35
▸ PDE4A P27815 1/20 0.35
▸ PDE4C Q08493 1/20 0.35
▸ PDE4D Q08499 1/20 0.35
▸ ALDH1A1 P00352 1/20 0.35
▸ KDM4E B2RXH2 1/20 0.35
▸ HTT P42858 1/20 0.35
▸ TDP1 Q9NUW8 1/20 0.35
▸ IRAK4 Q9NWZ3 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
SCHEMBL7170913 0.81 NPC1 (0.37) MAPTLMNATSHRRAB9ANPC1
SCHEMBL7180378 0.81 NPC1 (0.36) MAPTLMNARAB9ANPC1SMN1; SMN2
SCHEMBL7186373 0.80 NPSR1 (0.41) NPSR1MAPTGAALMNATSHR
SCHEMBL4323924 0.74 TSHR (0.50) NPSR1MAPTGAALMNATSHR
SCHEMBL7148168 0.72 POLB (0.42) MAPTLMNAMEN1KMT2AALDH1A1
SCHEMBL30764114 0.72 TSHR (0.64) NPSR1GAALMNATSHRMEN1
SCHEMBL8408187 0.72 TSHR (0.64) NPSR1GAALMNATSHRMEN1
SCHEMBL310240 0.70 ATM (0.53) MAPTTSHRSMN1; SMN2MEN1KMT2A
SCHEMBL16774768 0.68 TSHR (0.57) NPSR1MAPTLMNATSHRRAB9A
SCHEMBL29176796 0.68 TSHR (0.57) NPSR1MAPTLMNATSHRRAB9A

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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