SCHEMBL7656556

SCHEMBL7656556

O=C(Nc1ccccc1)c1ncccc1CCc1cccc(Cl)c1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GRM4 Q14833 2/20 0.55
BACE1 P56817 1/20 0.53
HDAC6 Q9UBN7 1/20 0.51
KDM4E B2RXH2 3/20 0.51
MAPT P10636 3/20 0.51
GAA P10253 1/20 0.51
ALDH1A1 P00352 3/20 0.49
ADRB2 P07550 1/20 0.49
SGMS2 Q8NHU3 1/20 0.47
KDR P35968 1/20 0.47
EGFR P00533 1/20 0.47
PPIA P62937 1/20 0.47
CNR2 P34972 1/20 0.46
ATR Q13535 1/20 0.46
NPC1 O15118 2/20 0.45
RAB9A P51151 2/20 0.45
MEN1 O00255 3/20 0.45
KMT2A Q03164 3/20 0.45
LMNA P02545 1/20 0.45
GLA P06280 1/20 0.45

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
SCHEMBL6948731 0.93 BACE1 (0.53) GRM4BACE1HDAC6KDM4EMAPT
SCHEMBL14012061 0.84 BACE1 (0.56) GRM4BACE1HDAC6KDM4EMAPT
SCHEMBL4452291 0.84 BACE1 (0.62) GRM4BACE1KDM4EMAPTGAA
Hydrochloric Acid SCHEMBL4603331 0.83 BACE1 (0.60) GRM4BACE1KDM4EMAPTGAA
SCHEMBL4606123 0.81 BACE1 (0.53) GRM4BACE1HDAC6KDM4EMAPT
SCHEMBL13962883 0.81 BACE1 (0.62) GRM4BACE1HDAC6GAAALDH1A1
SCHEMBL4558113 0.80 BACE1 (0.64) GRM4BACE1HDAC6KDM4EGAA
SCHEMBL13962869 0.80 BACE1 (0.60) GRM4BACE1HDAC6KDM4EMAPT
SCHEMBL5743593 0.73 BACE1 (0.58) BACE1MAPTGAAALDH1A1PPIA
SCHEMBL19539578 0.73 ALDH1A1 (0.47) HDAC6KDM4EMAPTALDH1A1ADRB2

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
US-6495689-B2 DEHYDRATING COMPOUND COMPRISING 2-AMIDO ARYL OR HETEROARYL-3-ETHYLPHENYL-PYRIDINE COMPOUND TO FORM IMINE DERIVATIVE; HYDROLYSIS TO FORM (SUBSTITUTED) 5,6-DIHYDRO-11HBENZO(5,6)CYCLOHEPTA(1,2B)PYRID-11-ONE COMPOUND SCHERING CORPORATION 2002-12-17 US disclosed
US-20020077331-A1 Synthesis of intermediates useful in preparing tricyclic compounds MERCK SHARP & DOHME CORP. 2002-06-20 US disclosed
US-6372909-B1 REACTING 3-PHENYLETHYL-2-PYRIDINECARBOXAMIDE WITH DEHYDRATING AGENT TO CYCLIZE AND FORM TRICYCLIC IMINE, HYDROLYZING TO FORM TRICYCLIC KETONE SCHERING CORPORATION 2002-04-16 US disclosed
EP-1131296-A2 SYNTHESIS OF INTERMEDIATES USEFUL IN PREPARING TRICYCLIC COMPOUNDS SCHERING CORPORATION (US) 2001-09-12 EP disclosed
WO-2000030589-A2 SYNTHESIS OF INTERMEDIATES USEFUL IN PREPARING TRICYCLIC COMPOUNDS SCHERING CORPORATION (US) 2000-06-02 WO disclosed
US-4873335-A 3-phenethyl-2-benzene-amides or aza-derivatives thereof SCHERING CORPORATION (US) 1989-10-10 US disclosed
US-4731447-A Process for preparing piperidylidene dihydro-dibenzo(a,d)-cycloheptenes or aza-derivatives thereof SCHERING CORPORATION (US) 1988-03-15 US 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-20020077331-A1 Synthesis of intermediates useful in preparing tricyclic compounds CBR1, CYP2F1, REV1 GRM4 2273/4885BACE1 2672/4885HDAC6 2104/4885

“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.