SCHEMBL7529153

SCHEMBL7529153

CC(=O)C(Cl)NC(=O)c1ccccc1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 6/20 0.56
HPGD P15428 2/20 0.56
ALDH1A1 P00352 7/20 0.53
SMN1; SMN2 Q16637 4/20 0.53
TP53 P04637 1/20 0.49
CTRB1 P17538 2/20 0.47
RAB9A P51151 1/20 0.47
SLC1A2 P43004 1/20 0.47
HDAC3 O15379 1/20 0.47
CA12 O43570 1/20 0.47
CA1 P00915 1/20 0.47
IDO1 P14902 1/20 0.47
ALOX15 P16050 1/20 0.47
HDAC1 Q13547 1/20 0.47
CA9 Q16790 1/20 0.47
HDAC7 Q8WUI4 1/20 0.47
HDAC2 Q92769 1/20 0.47
HSD17B10 Q99714 1/20 0.47
HDAC8 Q9BY41 1/20 0.47
HDAC6 Q9UBN7 1/20 0.47

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
SCHEMBL10589495 0.84 LMNA (0.59) LMNAHPGDALDH1A1SMN1; SMN2TP53
SCHEMBL27244159 0.82 LMNA (0.58) LMNAHPGDALDH1A1SMN1; SMN2TP53
SCHEMBL28274372 0.82 LMNA (0.58) LMNAHPGDALDH1A1SMN1; SMN2TP53
SCHEMBL9815318 0.82 LMNA (0.61) LMNAHPGDALDH1A1SMN1; SMN2TP53
SCHEMBL8234446 0.81 GAA (0.56) LMNAHPGDALDH1A1SMN1; SMN2TP53
SCHEMBL28033840 0.79 LMNA (0.63) LMNAHPGDALDH1A1SMN1; SMN2TP53
SCHEMBL28641833 0.79 HDAC3 (0.58) LMNAHPGDALDH1A1SMN1; SMN2TP53
SCHEMBL12561786 0.78 ALDH1A1 (0.49) LMNAHPGDALDH1A1SMN1; SMN2CTRB1
SCHEMBL28458590 0.77 SLC1A2 (0.51) LMNAHPGDALDH1A1SMN1; SMN2CTRB1
SCHEMBL7371458 0.77 PDE4A (0.50) LMNAHPGDALDH1A1SMN1; SMN2RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0816328-B1 Process for the manufacture of acetonylbenzamides DOW AGROSCIENCES LLC (US) 2002-03-27 EP disclosed
US-5969200-A CHLORINATING PARA-TOLUOYL CHLORIDE IN PRESENCE OF CHLORINE GAS AND ALUMINUM CHLORIDE OR ANTIMONY CHLORIDE CATALYST, DISTILLING MIXTURE PRODUCED TO RECOVER 3,5-DICHLORO-4-METHYLBENZOYL CHLORIDE ROHM AND HAAS COMPANY (US) 1999-10-19 US disclosed
US-5945565-A SYNTHESIS OF 4-AMINO-3-CHLORO-5-(METHOXYIMINOMETHYL)BENZOYL CHLORIDE STARTING WITH THE CONVERSION OF 5-METHYL-4-NITRO-BENZOIC ACID TO 4-NITRO-5-(METHOXYIMINOMETHYL)-BENZOIC ACID, METHYL ESTER ROHM AND HAAS COMPANY (US) 1999-08-31 US disclosed
US-5874466-A REACTING AMINE AND ACYL CHLORIDE, HYDROGENOLYSIS ROHM AND HAAS COMPANY (US) 1999-02-23 US disclosed
US-5859063-A Use of certain N-acetonylbenzamides as fungicides ROHM AND HAAS COMPANY (US) 1999-01-12 US disclosed
EP-0816328-A2 Process for the manufacture of acetonylbenzamides ROHM AND HAAS COMPANY (US) 1998-01-07 EP disclosed
US-5629346-A LOW TOXICITY ROHM AND HAAS COMPANY (US) 1997-05-13 US disclosed
US-4822902-A LOW PHYTOTOXICITY ROHM AND HAAS COMPANY (US) 1989-04-18 US disclosed
EP-0173453-B1 SUBSTITUTED N-ACETONYLBENZAMIDES AND THEIR USE AS FUNGICIDES ROHM AND HAAS COMPANY (US) 1988-07-13 EP disclosed
EP-0173453-A1 Substituted N-acetonylbenzamides and their use as fungicides ROHM AND HAAS COMPANY (US) 1986-03-05 EP disclosed