SCHEMBL5696563

SCHEMBL5696563

CCCCCC(=O)NC(=O)c1ccccc1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
POLB P06746 1/20 0.61
NAAA Q02083 1/20 0.58
CES2 O00748 2/20 0.57
CES1 P23141 2/20 0.57
ALDH1A1 P00352 3/20 0.57
PKM P14618 1/20 0.57
EPHX2 P34913 1/20 0.55
MEN1 O00255 1/20 0.54
KMT2A Q03164 1/20 0.54
HDAC1 Q13547 3/20 0.52
HDAC8 Q9BY41 3/20 0.52
HDAC3 O15379 1/20 0.52
HDAC4 P56524 1/20 0.52
HDAC2 Q92769 1/20 0.52
HDAC10 Q969S8 1/20 0.52
HDAC11 Q96DB2 1/20 0.52
HDAC6 Q9UBN7 1/20 0.52
HDAC9 Q9UKV0 1/20 0.52
HDAC5 Q9UQL6 1/20 0.52
GAA P10253 1/20 0.51

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
SCHEMBL1343140 0.98 NAAA (0.61) POLBNAAACES2CES1ALDH1A1
SCHEMBL3947433 0.98 NAAA (0.61) POLBNAAACES2CES1ALDH1A1
SCHEMBL21615871 0.98 NAAA (0.61) POLBNAAACES2CES1ALDH1A1
SCHEMBL7697401 0.95 ALDH1A1 (0.62) POLBNAAACES2CES1ALDH1A1
SCHEMBL27989558 0.90 SOAT2 (0.67) POLBNAAAEPHX2MEN1KMT2A
SCHEMBL8154519 0.90 SOAT2 (0.67) POLBNAAAEPHX2MEN1KMT2A
SCHEMBL3364793 0.87 ALDH1A1 (0.58) NAAACES2CES1ALDH1A1PKM
SCHEMBL29779165 0.87 SMN1; SMN2 (0.57) POLBCES2CES1ALDH1A1PKM
SCHEMBL28929265 0.85 ALDH1A1 (0.67) POLBALDH1A1MEN1KMT2AHDAC1
SCHEMBL27581307 0.84 HDAC1 (0.59) HDAC1HDAC8HDAC3HDAC4HDAC2

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 9 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115557849-A Method for synthesizing imide compound under induction of NBS and water by visible light 西南大学 2023-01-03 CN disclosed
EP-1118644-B1 Hot melt printing ink SIEGWERK DRUCKFARBEN AG (DE) 2006-06-14 EP disclosed
EP-1118644-A2 Hot melt printing ink Siegwerk Druckfarben GmbH & Co. KG (DE) 2001-07-25 EP disclosed
EP-0719250-B1 SYNTHESIS OF AMIDO ACIDS FROM CARBOXYLIC ACIDS AND LACTAMS PROCTER & GAMBLE (US) 1999-04-14 EP disclosed
EP-0884306-A2 Synthesis of amido acids from Carboxylic acids and lactams THE PROCTER & GAMBLE COMPANY (US) 1998-12-16 EP disclosed
US-5534642-A FOLLOWED BY CONVERSION TO PHENYL ESTER SULFONATES, SIMPLE, LOW COST, BLEACH ACTIVATORS FOR DETERGENTS THE PROCTER & GAMBLE COMPANY (US) 1996-07-09 US disclosed
EP-0719250-A1 SYNTHESIS OF AMIDO ACIDS FROM CARBOXYLIC ACIDS AND LACTAMS THE PROCTER & GAMBLE COMPANY (US) 1996-07-03 EP disclosed
US-5414099-A Acid catalyst; also making phenyl esters by reacting the amido acids either with phenol in presence of acid catalyst and boric acid or with phenol ester of lower molecular weight carboxylic acid in presence of basic catalyst THE PROCTER & GAMBLE COMPANY (US) 1995-05-09 US disclosed
WO-1995007883-A1 SYNTHESIS OF AMIDO ACIDS FROM CARBOXYLIC ACIDS AND LACTAMS THE PROCTER & GAMBLE COMPANY (US) 1995-03-23 WO disclosed