SCHEMBL2266935

SCHEMBL2266935

Cc1cc(C=CC#N)cc(C)c1Nc1ccnc(NC2CCN(Cc3ccc(C(N)=O)cc3Cl)CC2)n1

nearest known ligand 0.56

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CYP2C9 P11712 7/20 0.56
CYP3A4 P08684 6/20 0.56
CYP2D6 P10635 5/20 0.56
KCNH2 Q12809 5/20 0.46
CYP2C19 P33261 4/20 0.46
CYP1A2 P05177 1/20 0.46
ABCG2 Q9UNQ0 1/20 0.46
ACHE P22303 7/20 0.42
BACE1 P56817 5/20 0.42
EPHX2 P34913 1/20 0.36
HCK P08631 1/20 0.36
BTK Q06187 1/20 0.36
ABL1 P00519 1/20 0.36
BCR P11274 1/20 0.36
EPHB4 P54760 1/20 0.36

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
SCHEMBL2266932 1.00 CYP2C9 (0.56) CYP2C9CYP3A4CYP2D6KCNH2CYP2C19
SCHEMBL2260140 0.89 KCNH2 (0.53) CYP2C9CYP3A4CYP2D6KCNH2CYP2C19
SCHEMBL2266003 0.87 CYP3A4 (0.55) CYP2C9CYP3A4CYP2D6KCNH2CYP2C19
SCHEMBL2265996 0.87 CYP3A4 (0.55) CYP2C9CYP3A4CYP2D6KCNH2CYP2C19
SCHEMBL2265606 0.84 CYP3A4 (0.46) CYP2C9CYP3A4CYP2D6KCNH2CYP2C19
SCHEMBL2265610 0.84 CYP3A4 (0.46) CYP2C9CYP3A4CYP2D6KCNH2CYP2C19
SCHEMBL2260788 0.83 CYP3A4 (0.49) CYP2C9CYP3A4CYP2D6KCNH2CYP2C19
SCHEMBL2260782 0.83 CYP3A4 (0.49) CYP2C9CYP3A4CYP2D6KCNH2CYP2C19
SCHEMBL2262084 0.82 ACHE (0.47) CYP2C9KCNH2CYP2C19ACHEBACE1
SCHEMBL2260848 0.79 KCNH2 (0.45) CYP2C9KCNH2CYP2C19ACHEBACE1

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-2089384-B1 2-(PIPERIDIN-4-YL)-4-PHENOXY-OR PHENYLAMINO-PYRIMIDINE DERIVATIVES AS NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS HOFFMANN LA ROCHE (CH) 2015-08-05 EP claimed
US-7998969-B2 enzyme inhibitors such as 4-[2-(1-Benzyl-piperidin-4-ylamino)-pyrimidin-4-yloxy]-3,5-dimethyl-benzonitrile, used in combination with other viricides, for preventing and treatment of viral infections such as HIV, AIDS and AIDS related diseases ROCHE PALO ALTO LLC (US) 2011-08-16 US claimed
EP-2089384-A2 2-(PIPERIDIN-4-YL)-4-PHENOXY-OR PHENYLAMINO-PYRIMIDINE DERIVATIVES AS NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS F. Hoffmann-Roche AG (CH) 2009-08-19 EP claimed
US-20080146595-A1 Non-nucleoside reverse transcriptase inhibitors ROCHE PALO ALTO LLC 2008-06-19 US claimed
WO-2008071587-A2 2-(PIPERIDIN-4-YL)-4-PHENOXY- OR PHENYLAMINO-PYRIMIDINE DERIVATIVES AS NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2008-06-19 WO claimed

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-20080146595-A1 Non-nucleoside reverse transcriptase inhibitors NQO2, SAMHD1, POLR2A CYP2C9 1382/4885CYP3A4 832/4885CYP2D6 823/4885

“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.