SCHEMBL2265006

SCHEMBL2265006

CNC(=O)c1cccc(N2CCC(Nc3ncc(Br)c(Oc4c(C)cc(C#N)cc4C)n3)CC2)c1

nearest known ligand 0.51

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
KCNH2 Q12809 4/20 0.51
ULK1 O75385 2/20 0.44
CYP2C9 P11712 2/20 0.44
SCN9A Q15858 7/20 0.40
CCNK O75909 1/20 0.39
CDK12 Q9NYV4 1/20 0.39
PTK2 Q05397 2/20 0.37
CYP2C19 P33261 1/20 0.37
ADRA2A P08913 1/20 0.36
ADRA1A P35348 1/20 0.36
HRH1 P35367 1/20 0.36
HTR2B P41595 1/20 0.36
MCHR1 Q99705 1/20 0.36
JAK1 P23458 1/20 0.36
MLYCD O95822 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
SCHEMBL2260779 0.93 KCNH2 (0.48) KCNH2ULK1CYP2C9CCNKCDK12
SCHEMBL2263186 0.92 KCNH2 (0.56) KCNH2CYP2C9CCNKCDK12PTK2
SCHEMBL2261965 0.91 KCNH2 (0.49) KCNH2ULK1CYP2C9CCNKCDK12
SCHEMBL2261270 0.89 KCNH2 (0.46) KCNH2CYP2C9CCNKCDK12PTK2
SCHEMBL2262338 0.88 KCNH2 (0.47) KCNH2CYP2C9CYP2C19ADRA2A
SCHEMBL2262238 0.88 KCNH2 (0.52) KCNH2CYP2C9CCNKCDK12PTK2
SCHEMBL2264155 0.88 KCNH2 (0.53) KCNH2ULK1CYP2C9CCNKCDK12
SCHEMBL2261142 0.87 KCNH2 (0.51) KCNH2ULK1CYP2C9CCNKCDK12
SCHEMBL2259518 0.87 KCNH2 (0.47) KCNH2CYP2C9CYP2C19ADRA2A
SCHEMBL2262939 0.86 KCNH2 (0.48) KCNH2ULK1CYP2C9CYP2C19ADRA2A

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 KCNH2 4033/4885ULK1 4538/4885CYP2C9 1382/4885

“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.