SCHEMBL10568929

SCHEMBL10568929

COCC(Cl)C(=O)NC(C(=O)Nc1nccs1)C(=O)c1ccc(Cl)cc1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ FFAR2 O15552 9/20 0.51
▸ LMNA P02545 2/20 0.51
▸ MEN1 O00255 3/20 0.49
▸ KMT2A Q03164 3/20 0.49
▸ GAA P10253 1/20 0.44
▸ CYP1A2 P05177 1/20 0.44
▸ CYP2D6 P10635 1/20 0.44
▸ MAPT P10636 1/20 0.44
▸ CYP2C9 P11712 1/20 0.44
▸ CYP2C19 P33261 1/20 0.44
▸ CASP3 P42574 1/20 0.44
▸ HTT P42858 1/20 0.44
▸ SMN1; SMN2 Q16637 1/20 0.44
▸ SENP8 Q96LD8 1/20 0.44
▸ SENP7 Q9BQF6 1/20 0.44
▸ SENP6 Q9GZR1 1/20 0.44
▸ KDM4E B2RXH2 1/20 0.43
▸ POLB P06746 1/20 0.43
▸ KCNMA1 Q12791 1/20 0.43
▸ NPC1 O15118 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
SCHEMBL10665904 0.76 HSPA5 (0.60) FFAR2LMNAMEN1KMT2ACYP1A2
SCHEMBL10568933 0.73 KCNMA1 (0.46) FFAR2LMNAMEN1KMT2AGAA
SCHEMBL10568923 0.72 KCNMA1 (0.48) FFAR2LMNAMEN1KMT2AGAA
SCHEMBL10660806 0.71 RECQL (0.46) FFAR2MEN1KMT2ACYP1A2CYP2D6
SCHEMBL10665055 0.69 CYP1A2 (0.46) FFAR2MEN1KMT2ACYP1A2CYP2D6
SCHEMBL10665753 0.69 HTT (0.49) FFAR2LMNAMEN1KMT2AGAA
SCHEMBL28801036 0.69 NPC1 (0.72) FFAR2LMNAMEN1KMT2ACYP1A2
SCHEMBL10946561 0.68 NPC1 (0.44) MEN1KMT2AHTTSMN1; SMN2NPC1
Bromide SCHEMBL27908399 0.68 NPC1 (0.70) FFAR2LMNAMEN1KMT2ACYP1A2
SCHEMBL10665884 0.67 SMN1; SMN2 (0.46) MEN1KMT2AHTTSMN1; SMN2NPC1

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-4845105-A 4-OH-quinoline carboxylic acid amides having analgesic and anti-inflammatory activity ROUSSEL UCLAF (FR) 1989-07-04 — — US disclosed
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