SCHEMBL7543450

SCHEMBL7543450

CN1C(=N)N[C@](C)(c2cccc(C#N)c2)[C@@H](c2ccc(C3CCC3)cc2)C1=O

nearest known ligand 0.38

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
DRD3 P35462 6/20 0.38
DRD2 P14416 5/20 0.38
CYP2D6 P10635 1/20 0.36
TSHR P16473 1/20 0.36
NFKB1 P19838 1/20 0.36
CASP1 P29466 1/20 0.36
BACE1 P56817 4/20 0.36
BACE2 Q9Y5Z0 1/20 0.36
NPSR1 Q6W5P4 1/20 0.35
TNKS O95271 3/20 0.34
NSD2 O96028 1/20 0.33
CHRM3 P20309 1/20 0.33

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
SCHEMBL13054364 1.00 DRD3 (0.38) DRD3DRD2CYP2D6TSHRNFKB1
SCHEMBL7549001 0.96 BACE1 (0.37) DRD3DRD2CYP2D6TSHRNFKB1
SCHEMBL7575500 0.96 BACE1 (0.37) DRD3DRD2CYP2D6TSHRNFKB1
SCHEMBL12174164 0.91 BACE1 (0.44) BACE1BACE2
SCHEMBL7559867 0.91 BACE1 (0.44) BACE1BACE2
SCHEMBL13054227 0.91 BACE1 (0.44) BACE1BACE2
SCHEMBL13054721 0.90 BACE1 (0.39) BACE1BACE2TNKSNSD2CHRM3
SCHEMBL7574530 0.90 BACE1 (0.39) BACE1BACE2TNKSNSD2CHRM3
SCHEMBL7580426 0.88 BACE1 (0.35) DRD3DRD2BACE1BACE2NSD2
SCHEMBL8414498 0.87 BACE1 (0.37) BACE1BACE2TNKSNSD2CHRM3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2097387-B1 HETEROCYCLIC ASPARTYL PROTEASE INHIBITORS MERCK SHARP & DOHME (US) 2016-05-04 EP disclosed
US-8829036-B2 Heterocyclic aspartyl protease inhibitors MERCK SHARP & DOHME CORP. (US) 2014-09-09 US disclosed
US-20120276118-A1 HETEROCYCLIC ASPARTYL PROTEASE INHIBITORS PHARMACOPEIA INC. (US) 2012-11-01 US disclosed
US-20120276118-A1 HETEROCYCLIC ASPARTYL PROTEASE INHIBITORS PHARMACOPEIA INC. (US) 2012-11-01 US disclosed
US-20120231018-A1 HETEROCYCLIC ASPARTYL PROTEASE INHIBITORS PHARMACOPEIA INC. (US) 2012-09-13 US disclosed
US-20120231017-A1 HETEROCYCLIC ASPARTYL PROTEASE INHIBITORS PHARMACOPEIA INC. (US) 2012-09-13 US disclosed
US-20120231017-A1 HETEROCYCLIC ASPARTYL PROTEASE INHIBITORS PHARMACOPEIA INC. (US) 2012-09-13 US disclosed
US-8183252-B2 Heterocyclic aspartyl protease inhibitors SCHERING CORPORATION (US) 2012-05-22 US disclosed
US-8183252-B2 Heterocyclic aspartyl protease inhibitors SCHERING CORPORATION (US) 2012-05-22 US disclosed
US-20100292203-A1 HETEROCYCLIC ASPARTYL PROTEASE INHIBITORS SCHERING CORPORATION 2010-11-18 US disclosed
US-20100292203-A1 HETEROCYCLIC ASPARTYL PROTEASE INHIBITORS SCHERING CORPORATION 2010-11-18 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 (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-20100292203-A1 HETEROCYCLIC ASPARTYL PROTEASE INHIBITORS CHRM1, CHRM2, PRSS1 DRD3 350/4885DRD2 440/4885CYP2D6 959/4885
US-20120276118-A1 HETEROCYCLIC ASPARTYL PROTEASE INHIBITORS BACE1, PRSS1, TMPRSS11D DRD3 760/4885DRD2 971/4885CYP2D6 1323/4885
US-20120231018-A1 HETEROCYCLIC ASPARTYL PROTEASE INHIBITORS BACE1, PRSS1, TMPRSS11D DRD3 760/4885DRD2 971/4885CYP2D6 1323/4885
US-20120231017-A1 HETEROCYCLIC ASPARTYL PROTEASE INHIBITORS BACE1, PRSS1, TMPRSS11D DRD3 760/4885DRD2 971/4885CYP2D6 1323/4885

“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.