SCHEMBL8366567

SCHEMBL8366567

CCOC(=O)CC(=O)Cc1c[nH]c2ccccc12

nearest known ligand 0.80

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
PKM P14618 1/20 0.80
SMN1; SMN2 Q16637 4/20 0.64
CYP1A2 P05177 2/20 0.64
CYP3A4 P08684 2/20 0.64
CYP2C19 P33261 2/20 0.64
CYP2D6 P10635 1/20 0.64
CYP2C9 P11712 1/20 0.64
MAPT P10636 5/20 0.62
ALDH1A1 P00352 4/20 0.62
MEN1 O00255 4/20 0.62
KMT2A Q03164 4/20 0.62
LMNA P02545 1/20 0.62
KDM4E B2RXH2 2/20 0.62
TDP1 Q9NUW8 1/20 0.54
HPGD P15428 1/20 0.54
SLC6A2 P23975 1/20 0.51
FNTA P49354 1/20 0.51
FNTB P49356 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
SCHEMBL30419025 0.89 PKM (1.00) PKMSMN1; SMN2CYP1A2CYP3A4CYP2C19
SCHEMBL361312 0.89 PKM (1.00) PKMSMN1; SMN2CYP1A2CYP3A4CYP2C19
SCHEMBL8978266 0.85 SMN1; SMN2 (0.81) PKMSMN1; SMN2CYP1A2CYP3A4CYP2C19
Indole-3-Acetic Acid SCHEMBL7048296 0.84 PKM (0.89) PKMSMN1; SMN2CYP1A2CYP3A4CYP2C19
SCHEMBL9967917 0.81 PKM (0.66) PKMSMN1; SMN2CYP1A2CYP3A4CYP2C19
SCHEMBL30354024 0.81 PKM (0.66) PKMSMN1; SMN2CYP1A2CYP3A4CYP2C19
SCHEMBL29407882 0.81 MAPT (0.72) PKMSMN1; SMN2CYP1A2CYP3A4CYP2C19
SCHEMBL21479833 0.81 MAPT (0.72) PKMSMN1; SMN2CYP1A2CYP3A4CYP2C19
SCHEMBL3845771 0.81 PKM (0.74) PKMSMN1; SMN2CYP1A2CYP3A4CYP2C19
SCHEMBL392573 0.81 SMN1; SMN2 (0.85) PKMSMN1; SMN2CYP1A2CYP3A4CYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-4299987-A None JP disclosed
US-5929067-A N-ACYLATING AMINE DERIVATIVE OF CAPROLACTAM COMPOUND WITH A CARBOXYLIC ACID OR DERIVATIVES TO FORM AMIDE DERIVATIVE OF CAPROLACTAM COMPOUND NOVARTIS AG (CH) 1999-07-27 US disclosed
EP-0810991-B1 1-ARYL-2-ACYLAMINO-ETHANE COMPOUNDS AND THEIR USE AS NEUROKININ ESPECIALLY NEUROKININ 1 ANTAGONISTS NOVARTIS AG (CH) 1999-04-14 EP disclosed
EP-0810991-A1 1-ARYL-2-ACYLAMINO-ETHANE COMPOUNDS AND THEIR USE AS NEUROKININ ESPECIALLY NEUROKININ 1 ANTAGONISTS Novartis AG (CH) 1997-12-10 EP disclosed
WO-1996026183-A1 1-ARYL-2-ACYLAMINO-ETHANE COMPOUNDS AND THEIR USE AS NEUROKININ ESPECIALLY NEUROKININ 1 ANTAGONISTS NOVARTIS AG (CH) 1996-08-29 WO disclosed
US-5484940-A ULTRAVIOLET RADIATION ABSORBERS FOR PLASTICS, AMYLOID PEPTIDE INHIBITORS, ALZHEIMER*S DISEASE ATHENA NEUROSCIENCES, INC. 1996-01-16 US disclosed
JP-H04299987-A PRODUCTION OF OPTICALLY ACTIVE INDOLE HYDROXY ACIDS KAWAKEN FINE CHEM CO LTD 1992-10-23 JP disclosed