SCHEMBL6862429

SCHEMBL6862429

COc1ccc2[nH]cc(CC(=O)NN)c2c1

nearest known ligand 0.71

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 2/20 0.71
MTNR1A P48039 11/20 0.70
MTNR1B P49286 8/20 0.70
HTR2B P41595 2/20 0.62
GPR84 Q9NQS5 1/20 0.61
CYP1A2 P05177 2/20 0.60
HTR1A P08908 2/20 0.60
CYP2D6 P10635 2/20 0.60
BLM P54132 2/20 0.60
PMP22 Q01453 2/20 0.60
MEN1 O00255 1/20 0.60
ALDH1A1 P00352 1/20 0.60
CYP1A1 P04798 1/20 0.60
MPO P05164 1/20 0.60
CYP3A4 P08684 1/20 0.60
HPGD P15428 1/20 0.60
NQO2 P16083 1/20 0.60
RAB9A P51151 1/20 0.60
KMT2A Q03164 1/20 0.60
CYP1B1 Q16678 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
SCHEMBL8252641 0.88 KDM4E (0.73) KDM4EMTNR1AMTNR1BHTR2BGPR84
SCHEMBL5239218 0.88 KDM4E (0.73) KDM4EMTNR1AMTNR1BHTR2BGPR84
SCHEMBL10670286 0.87 MTNR1A (0.71) KDM4EMTNR1AMTNR1BHTR2BCYP1A2
SCHEMBL1395687 0.85 KDM4E (0.77) KDM4EMTNR1AMTNR1BHTR2BGPR84
SCHEMBL2686551 0.85 KDM4E (0.77) KDM4EMTNR1AMTNR1BHTR2BGPR84
Hydrochloric Acid SCHEMBL5013119 0.84 KDM4E (0.75) KDM4EMTNR1AMTNR1BHTR2BGPR84
SCHEMBL674415 0.83 KDM4E (1.00) KDM4EMTNR1AMTNR1BHTR2BGPR84
SCHEMBL2633259 0.83 KDM4E (0.79) KDM4EMTNR1AMTNR1BHTR2BGPR84
SCHEMBL14664126 0.83 KDM4E (0.73) KDM4EMTNR1AMTNR1BHTR2BGPR84
SCHEMBL6945002 0.82 KDM4E (0.77) KDM4EMTNR1AMTNR1BHTR2BGPR84

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1337535-B1 BENZODIAZEPINE DERIVATIVES AS GABA A RECEPTOR MODULATORS HOFFMANN LA ROCHE (CH) 2004-06-09 EP disclosed
US-6743789-B2 SUBSTITUTED IMIDAZO (1,5-A) (1,2,4) TRIAZOLO (4,3-D) (1,4) BENZODIAZEPINE DERIVATIVES ARE USEFUL FOR TREATING ALZHEIMER'S DISEASE; REACTING A BEZODIAZEPINE DERIVATIVE WITH A HYDRAZIDE DERIVATIVE TO FORM END PRODUCT HOFFMANN-LA ROCHE INC. 2004-06-01 US disclosed
EP-1337535-A2 BENZODIAZEPINE DERIVATIVES AS GABA A RECEPTOR MODULATORS F. HOFFMANN-LA ROCHE AG (CH) 2003-08-27 EP disclosed
US-20020103371-A1 Substituted imidazo [1,5-a] [1,2,4] triazolo [4,3-d] [1,4] benzodiazepine derivatives HOFFMANN-LA ROCHE INC. 2002-08-01 US disclosed
WO-2002040487-A2 BENZODIAZEPINE DERIVATIVES AS GABA A RECEPTOR MODULATORS F. HOFFMANN-LA ROCHE AG (CH) 2002-05-23 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 (1 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-20020103371-A1 Substituted imidazo [1,5-a] [1,2,4] triazolo [4,3-d] [1,4] benzodiazepine derivatives GABRA5, GABRA1, GABRA4 KDM4E 1588/4885MTNR1A 96/4885MTNR1B 122/4885

“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.