SCHEMBL7170913

SCHEMBL7170913

C=CCc1cc(F)ccc1P(=O)(c1ccccc1)c1ccccc1

nearest known ligand 0.41

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ NPC1 O15118 1/20 0.37
▸ RAB9A P51151 1/20 0.37
▸ ALDH1A1 P00352 2/20 0.36
▸ HTT P42858 2/20 0.36
▸ POLB P06746 1/20 0.36
▸ KCNN4 O15554 1/20 0.34
▸ KCNA5 P22460 1/20 0.34
▸ PDE4B Q07343 1/20 0.34
▸ LMNA P02545 2/20 0.34
▸ ALOX15 P16050 1/20 0.34
▸ TSHR P16473 1/20 0.34
▸ SMN1; SMN2 Q16637 2/20 0.34
▸ PKM P14618 1/20 0.34
▸ TOP1 P11387 1/20 0.34
▸ L3MBTL1 Q9Y468 2/20 0.33
▸ MAPT P10636 2/20 0.33
▸ KDM4E B2RXH2 1/20 0.33
▸ KMT2A Q03164 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
SCHEMBL7180378 0.85 NPC1 (0.36) NPC1RAB9AALDH1A1HTTLMNA
SCHEMBL7182958 0.81 NPSR1 (0.38) NPC1RAB9AALDH1A1HTTLMNA
SCHEMBL5827068 0.74 TOP1 (0.42) NPC1RAB9AALDH1A1HTTPOLB
SCHEMBL3266859 0.72 GABRA1 (0.40) NPC1RAB9AALDH1A1HTTPOLB
SCHEMBL26090846 0.71 POLB (0.46) NPC1RAB9AALDH1A1HTTPOLB
SCHEMBL26454100 0.71 POLB (0.38) NPC1RAB9AALDH1A1HTTPOLB
SCHEMBL26088780 0.71 KMT2A (0.50) NPC1RAB9AALDH1A1HTTPOLB
SCHEMBL28483999 0.71 TOP1 (0.45) NPC1RAB9AALDH1A1HTTPOLB
SCHEMBL11870406 0.70 GABRA1 (0.42) ALDH1A1HTTPOLBMAPTKDM4E
SCHEMBL7372058 0.69 ALDH1A1 (0.38) ALDH1A1HTTPOLBKCNA5LMNA

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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