SCHEMBL9602453

SCHEMBL9602453

CC=CC(=O)Nc1ccccc1C(F)(F)F.CCC(=O)Nc1nccs1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 2/20 0.50
▸ TDP1 Q9NUW8 1/20 0.50
▸ RAB9A P51151 6/20 0.46
▸ KMT2A Q03164 4/20 0.45
▸ MEN1 O00255 2/20 0.45
▸ ADORA2A P29274 1/20 0.45
▸ NPC1 O15118 4/20 0.45
▸ SMN1; SMN2 Q16637 4/20 0.45
▸ KDM4E B2RXH2 4/20 0.45
▸ TP53 P04637 2/20 0.45
▸ NFKB1 P19838 1/20 0.45
▸ NFKB2 Q00653 1/20 0.45
▸ RELA Q04206 1/20 0.45
▸ HTT P42858 3/20 0.43
▸ LMNA P02545 1/20 0.43
▸ MAPT P10636 1/20 0.43
▸ THRB P10828 1/20 0.42
▸ HPGD P15428 1/20 0.42
▸ PKM P14618 1/20 0.42
▸ HIF1A Q16665 1/20 0.42

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
Trifluoromethylbenzene SCHEMBL10350569 0.77 MEN1 (0.65) ALDH1A1RAB9AKMT2AMEN1ADORA2A
SCHEMBL10353587 0.75 ALDH1A1 (0.51) ALDH1A1TDP1RAB9AKMT2AMEN1
SCHEMBL17844701 0.73 RAB9A (0.79) ALDH1A1TDP1RAB9AKMT2AMEN1
SCHEMBL4778269 0.73 POLB (0.65) ALDH1A1RAB9AKMT2AMEN1NPC1
SCHEMBL175217 0.73 ADORA2A (0.68) ALDH1A1RAB9AKMT2AMEN1ADORA2A
SCHEMBL10353722 0.73 ALDH1A1 (0.49) ALDH1A1TDP1RAB9AKMT2AMEN1
SCHEMBL10665049 0.73 CYP1A2 (0.46) ALDH1A1TDP1KMT2AMEN1LMNA
SCHEMBL9839292 0.72 ALDH1A1 (0.46) ALDH1A1TDP1RAB9AKMT2AMEN1
Hydrochloric Acid SCHEMBL6559022 0.72 POLB (0.63) ALDH1A1RAB9AKMT2AMEN1NPC1
Bromide SCHEMBL27891199 0.72 ADORA2A (0.67) ALDH1A1RAB9AKMT2AMEN1ADORA2A

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
EP-0214004-B1 4-OH-QUINOLINE-CARBOXYLIC-ACID DERIVATIVES SUBSTITUTED IN POSITION 2 BY A DIHYDROXY-SUBSTITUTED GROUP, POSSIBLY ETHERIFIED OR ESTERIFIED, PROCESS AND INTERMEDIATES FOR THEIR PREPARATION, THEIR USE AS MEDICAMENTS AND COMPOSITIONS CONTAINING THEM ROUSSEL-UCLAF (FR) 1993-03-31 — — EP disclosed
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