SCHEMBL7186369

SCHEMBL7186369

CC(F)CCCc1ccc(P(=O)(c2cccc([N+](=O)[O-])c2)c2cccc([N+](=O)[O-])c2)cc1

nearest known ligand 0.42

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 3/20 0.41
▸ HPGD P15428 2/20 0.41
▸ NPSR1 Q6W5P4 1/20 0.40
▸ SIGMAR1 Q99720 1/20 0.40
▸ SMN1; SMN2 Q16637 1/20 0.38
▸ KMT2A Q03164 2/20 0.37
▸ MEN1 O00255 1/20 0.37
▸ NPC1 O15118 1/20 0.37
▸ RAB9A P51151 1/20 0.37
▸ TSHR P16473 3/20 0.36
▸ LMNA P02545 1/20 0.36
▸ THRA P10827 1/20 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
▸ KDM4E B2RXH2 1/20 0.36
▸ TDP1 Q9NUW8 1/20 0.36
▸ ACHE P22303 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
SCHEMBL7186364 0.82 NPSR1 (0.39) ALDH1A1HPGDNPSR1SIGMAR1SMN1; SMN2
SCHEMBL7190146 0.81 CYP19A1 (0.36) SIGMAR1
SCHEMBL7186358 0.77 NPSR1 (0.45) ALDH1A1HPGDNPSR1SMN1; SMN2KMT2A
SCHEMBL30764114 0.75 TSHR (0.64) ALDH1A1NPSR1KMT2AMEN1TSHR
SCHEMBL8408187 0.75 TSHR (0.64) ALDH1A1NPSR1KMT2AMEN1TSHR
SCHEMBL4323924 0.74 TSHR (0.50) ALDH1A1NPSR1SMN1; SMN2KMT2AMEN1
SCHEMBL30764106 0.73 TSHR (0.57) ALDH1A1NPSR1SMN1; SMN2KMT2AMEN1
SCHEMBL29176796 0.73 TSHR (0.57) ALDH1A1NPSR1SMN1; SMN2KMT2AMEN1
SCHEMBL16774768 0.73 TSHR (0.57) ALDH1A1NPSR1SMN1; SMN2KMT2AMEN1
SCHEMBL7182963 0.73 NPSR1 (0.40) ALDH1A1HPGDNPSR1SMN1; SMN2KMT2A

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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