SCHEMBL7186364

SCHEMBL7186364

CC(F)CCCc1ccccc1P(=O)(c1cccc([N+](=O)[O-])c1)c1cccc([N+](=O)[O-])c1

nearest known ligand 0.40

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ NPSR1 Q6W5P4 1/20 0.39
▸ ALDH1A1 P00352 2/20 0.35
▸ HPGD P15428 2/20 0.35
▸ ACP3 P15309 1/20 0.35
▸ TSHR P16473 2/20 0.35
▸ LMNA P02545 1/20 0.35
▸ CYP1A2 P05177 1/20 0.34
▸ CYP2D6 P10635 1/20 0.34
▸ CYP2C9 P11712 1/20 0.34
▸ CYP2C19 P33261 1/20 0.34
▸ SMN1; SMN2 Q16637 1/20 0.34
▸ ACHE P22303 1/20 0.34
▸ KMT2A Q03164 2/20 0.34
▸ SIGMAR1 Q99720 1/20 0.34
▸ GRM8 O00222 1/20 0.34
▸ GRM4 Q14833 1/20 0.34
▸ MEN1 O00255 1/20 0.33
▸ POLB P06746 1/20 0.33

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
SCHEMBL7186369 0.82 ALDH1A1 (0.41) NPSR1ALDH1A1HPGDTSHRLMNA
SCHEMBL7190144 0.81 MEN1 (0.30) ALDH1A1KMT2AMEN1
SCHEMBL7186373 0.73 NPSR1 (0.41) NPSR1ALDH1A1HPGDTSHRLMNA
SCHEMBL7186358 0.70 NPSR1 (0.45) NPSR1ALDH1A1HPGDACP3TSHR
SCHEMBL8408187 0.70 TSHR (0.64) NPSR1ALDH1A1ACP3TSHRLMNA
SCHEMBL30764114 0.70 TSHR (0.64) NPSR1ALDH1A1ACP3TSHRLMNA
SCHEMBL16774768 0.69 TSHR (0.57) NPSR1ALDH1A1ACP3TSHRLMNA
SCHEMBL30764106 0.69 TSHR (0.57) NPSR1ALDH1A1ACP3TSHRLMNA
SCHEMBL29176796 0.69 TSHR (0.57) NPSR1ALDH1A1ACP3TSHRLMNA
SCHEMBL7182958 0.66 NPSR1 (0.38) NPSR1ALDH1A1TSHRLMNASMN1; SMN2

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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