SCHEMBL3322903

SCHEMBL3322903

CCOC(=O)c1c(C)nc2ccc(Cl)cc2c1-c1ccccc1

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FABP4 P15090 4/20 0.73
FABP3 P05413 3/20 0.73
SMN1; SMN2 Q16637 4/20 0.72
LMNA P02545 2/20 0.72
MEN1 O00255 1/20 0.72
KMT2A Q03164 1/20 0.72
ALDH1A1 P00352 4/20 0.66
KDM4E B2RXH2 3/20 0.66
MAPT P10636 3/20 0.66
HPGD P15428 2/20 0.66
NPC1 O15118 1/20 0.66
GAA P10253 1/20 0.66
RAB9A P51151 1/20 0.66
NPSR1 Q6W5P4 1/20 0.66
PLA2G2A P14555 1/20 0.64
CSF1R P07333 1/20 0.62
FABP5 Q01469 3/20 0.62
CYP1A2 P05177 2/20 0.60
XBP1 P17861 1/20 0.60
CYP2C19 P33261 1/20 0.60

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
Diethylamine SCHEMBL8121508 0.94 FABP4 (0.66) FABP4FABP3SMN1; SMN2LMNAMEN1
SCHEMBL14916920 0.91 FABP4 (0.62) FABP4FABP3SMN1; SMN2LMNAMEN1
Diethylamine SCHEMBL8131909 0.89 FABP3 (0.58) FABP4FABP3SMN1; SMN2LMNAMEN1
SCHEMBL3346637 0.88 FABP4 (0.66) FABP4FABP3SMN1; SMN2LMNAMEN1
SCHEMBL3321046 0.87 FABP3 (0.56) FABP4FABP3SMN1; SMN2LMNAMEN1
SCHEMBL3318169 0.87 KDM4E (0.77) FABP4FABP3SMN1; SMN2LMNAMEN1
SCHEMBL3319814 0.87 FABP4 (0.65) FABP4FABP3SMN1; SMN2LMNAMEN1
SCHEMBL31442597 0.87 SMN1; SMN2 (0.81) FABP4FABP3SMN1; SMN2LMNAMEN1
SCHEMBL14917264 0.86 FABP4 (0.73) FABP4FABP3SMN1; SMN2LMNAMEN1
SCHEMBL12498023 0.86 SMN1; SMN2 (0.72) FABP4FABP3SMN1; SMN2LMNAMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240325340-A1 ISOFORM SPECIFIC AGONISTS TARGETING AKT KINASE LANDAUER, STEPHEN PAUL 2024-10-03 US claimed
WO-2023009629-A1 ISOFORM SPECIFIC AGONISTS TARGETING AKT KINASE THOMAS JEFFERSON UNIVERSITY (US) 2023-02-02 WO claimed
US-8865739-B2 Substituted heterocyclic compounds as ion channel modulators GILEAD SCIENCES, INC. (US) 2014-10-21 US claimed
US-20140107155-A1 SUBSTITUTED HETEROCYCLIC COMPOUNDS AS ION CHANNEL MODULATORS GILEAD SCIENCES, INC. (US) 2014-04-17 US claimed
US-8664399-B2 Substituted heterocyclic compounds as ion channel modulators GILEAD SCIENCES, INC. (US) 2014-03-04 US claimed
US-20130102632-A1 SUBSTITUTED HETEROCYCLIC COMPOUNDS AS ION CHANNEL MODULATORS GILEAD SCIENCES, INC. (US) 2013-04-25 US claimed
US-20100125091-A1 SUBSTITUTED HETEROCYCLIC COMPOUNDS AS ION CHANNEL MODULATORS GILEAD PALO ALTO, INC. (US) 2010-05-20 US claimed
WO-2010056865-A1 QUINOLINE DERIVATIVES AS ION CHANNEL MODULATORS GILEAD PALO ALTO, INC. (US) 2010-05-20 WO claimed
US-20240325340-A1 ISOFORM SPECIFIC AGONISTS TARGETING AKT KINASE LANDAUER, STEPHEN PAUL 2024-10-03 US disclosed
WO-2023009629-A1 ISOFORM SPECIFIC AGONISTS TARGETING AKT KINASE THOMAS JEFFERSON UNIVERSITY (US) 2023-02-02 WO disclosed
US-8865739-B2 Substituted heterocyclic compounds as ion channel modulators GILEAD SCIENCES, INC. (US) 2014-10-21 US disclosed
US-20140107155-A1 SUBSTITUTED HETEROCYCLIC COMPOUNDS AS ION CHANNEL MODULATORS GILEAD SCIENCES, INC. (US) 2014-04-17 US disclosed
US-8664399-B2 Substituted heterocyclic compounds as ion channel modulators GILEAD SCIENCES, INC. (US) 2014-03-04 US disclosed
US-20130102632-A1 SUBSTITUTED HETEROCYCLIC COMPOUNDS AS ION CHANNEL MODULATORS GILEAD SCIENCES, INC. (US) 2013-04-25 US disclosed
US-20100125091-A1 SUBSTITUTED HETEROCYCLIC COMPOUNDS AS ION CHANNEL MODULATORS GILEAD PALO ALTO, INC. (US) 2010-05-20 US disclosed
WO-2010056865-A1 QUINOLINE DERIVATIVES AS ION CHANNEL MODULATORS GILEAD PALO ALTO, INC. (US) 2010-05-20 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20140107155-A1 SUBSTITUTED HETEROCYCLIC COMPOUNDS AS ION CHANNEL MODULATORS KCNH2, KCNJ2, CACNA1E FABP4 3868/4885FABP3 1216/4885SMN1; SMN2 2201/4885
US-20100125091-A1 SUBSTITUTED HETEROCYCLIC COMPOUNDS AS ION CHANNEL MODULATORS KCNH2, KCNJ2, CACNA1E FABP4 3868/4885FABP3 1216/4885SMN1; SMN2 2201/4885
US-20240325340-A1 ISOFORM SPECIFIC AGONISTS TARGETING AKT KINASE AKT3, AKT1, AKT2 FABP4 1907/4885FABP3 969/4885SMN1; SMN2 1012/4885
US-20130102632-A1 SUBSTITUTED HETEROCYCLIC COMPOUNDS AS ION CHANNEL MODULATORS KCNH2, KCNJ2, CACNA1E FABP4 3868/4885FABP3 1216/4885SMN1; SMN2 2201/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.