SCHEMBL7959032

SCHEMBL7959032

CCC(=O)c1ccccc1NN

nearest known ligand 0.45

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.45
SMN1; SMN2 Q16637 2/20 0.45
NPC1 O15118 1/20 0.45
RAB9A P51151 1/20 0.45
ELANE P08246 1/20 0.45
PRTN3 P24158 1/20 0.45
MAPT P10636 2/20 0.43
GAA P10253 2/20 0.43
KDM4E B2RXH2 2/20 0.42
LMNA P02545 1/20 0.42
HPGD P15428 1/20 0.42
CTSD P07339 1/20 0.42
L3MBTL1 Q9Y468 1/20 0.41
CLCN2 P51788 1/20 0.41
KMT2A Q03164 1/20 0.41
POLB P06746 1/20 0.40
ATM Q13315 1/20 0.40
HSP90AB1 P08238 1/20 0.40
RXFP1 Q9HBX9 1/20 0.40

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
SCHEMBL605325 0.84 KDM4E (0.58) ALDH1A1SMN1; SMN2NPC1RAB9AELANE
SCHEMBL27611476 0.83 KDM4E (0.44) ALDH1A1SMN1; SMN2NPC1RAB9AELANE
SCHEMBL4184556 0.82 KDM4E (0.46) ALDH1A1SMN1; SMN2NPC1RAB9AELANE
SCHEMBL13623623 0.82 ALDH1A1 (0.64) ALDH1A1SMN1; SMN2NPC1RAB9AMAPT
Hydrochloric Acid SCHEMBL8584876 0.82 KDM4E (0.56) ALDH1A1SMN1; SMN2NPC1RAB9AELANE
Hydrochloric Acid SCHEMBL2955045 0.81 KDM4E (0.45) ALDH1A1SMN1; SMN2NPC1RAB9AELANE
SCHEMBL6421670 0.81 CYP2C19 (0.61) ALDH1A1SMN1; SMN2NPC1RAB9AMAPT
SCHEMBL30040195 0.81 CYP2C19 (0.61) ALDH1A1SMN1; SMN2NPC1RAB9AMAPT
SCHEMBL7373425 0.80 ALDH1A1 (0.47) ALDH1A1SMN1; SMN2NPC1RAB9AELANE
SCHEMBL13990159 0.80 L3MBTL1 (0.52) ALDH1A1SMN1; SMN2MAPTL3MBTL1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6268512-B1 HEATING PROPIONYLPHENYLHYDRAZIDE IN PRESENCE OF CALCIUM OXIDE IN SOLVENT TO PRODUCE 3-METHYL-2-OXOINDOLINE MEDICAL INFORMATION SERVICES, INC. (JP) 2001-07-31 US disclosed
EP-1052251-A1 PROCESS FOR THE PREPARATION OF 3-METHYL-2-OXOINDOLINE Medical Information Services, Inc. (JP) 2000-11-15 EP disclosed
CN-1253543-A Process for producing ketoprofen and 5-benzoyl-3-methyl-2-indolinone MEDICAL INFORMATION SERVICES I (JP) 2000-05-17 CN disclosed
EP-0990637-A1 PROCESS FOR PRODUCING KETOPROFEN AND 5-BENZOYL-3-METHYL-2-INDOLINONE Medical Information Services, Inc. (JP) 2000-04-05 EP disclosed