SCHEMBL2264867

SCHEMBL2264867

Cc1cc(C#N)cc(Cl)c1Oc1ccnc(NC2CCN(Cc3ccc(S(C)(=O)=O)cc3Cl)CC2)n1

nearest known ligand 0.47

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
KCNH2 Q12809 7/20 0.47
CYP2C9 P11712 5/20 0.41
CYP3A4 P08684 4/20 0.41
CYP2C19 P33261 3/20 0.41
CYP2D6 P10635 3/20 0.39
ACHE P22303 6/20 0.39
BACE1 P56817 4/20 0.39
CCNA2 P20248 1/20 0.35
CDK2 P24941 1/20 0.35
MCHR1 Q99705 1/20 0.35
SCN1A P35498 1/20 0.35
SCN8A Q9UQD0 1/20 0.35
IKBKB O14920 2/20 0.35

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
SCHEMBL2265539 0.97 KCNH2 (0.49) KCNH2CYP2C9CYP3A4CYP2C19CYP2D6
SCHEMBL2263684 0.94 KCNH2 (0.53) KCNH2CYP2C9CYP3A4CYP2C19CYP2D6
SCHEMBL2260711 0.91 KCNH2 (0.56) KCNH2CYP2C9CYP3A4CYP2C19CYP2D6
SCHEMBL2261425 0.89 KCNH2 (0.49) KCNH2CYP2C9CYP3A4CYP2C19CYP2D6
SCHEMBL2265614 0.87 KCNH2 (0.52) KCNH2CYP2C9CYP3A4CYP2C19CYP2D6
SCHEMBL2263785 0.87 KCNH2 (0.58) KCNH2CYP2C9CYP3A4CYP2C19CYP2D6
SCHEMBL2261187 0.86 KCNH2 (0.57) KCNH2CYP2C9CYP3A4CYP2C19CYP2D6
SCHEMBL2259928 0.86 ACHE (0.45) KCNH2CYP2C9CYP3A4CYP2C19CYP2D6
SCHEMBL2263109 0.85 KCNH2 (0.41) KCNH2CYP2C9CYP3A4CYP2C19CYP2D6
SCHEMBL2261325 0.85 KCNH2 (0.56) KCNH2CYP2C9CYP3A4CYP2C19CYP2D6

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-20080146595-A1 Non-nucleoside reverse transcriptase inhibitors ROCHE PALO ALTO LLC 2008-06-19 US claimed
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 disclosed
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 disclosed
US-20080146595-A1 Non-nucleoside reverse transcriptase inhibitors ROCHE PALO ALTO LLC 2008-06-19 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-20080146595-A1 Non-nucleoside reverse transcriptase inhibitors NQO2, SAMHD1, POLR2A KCNH2 4033/4885CYP2C9 1382/4885CYP3A4 832/4885

“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.