SCHEMBL2264155

SCHEMBL2264155

Cc1cc(C#N)cc(Cl)c1Oc1nc(NC2CCN(c3cccc(C(N)=O)c3)CC2)ncc1Br

nearest known ligand 0.53

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
KCNH2 Q12809 6/20 0.53
CYP2C9 P11712 2/20 0.48
CDK12 Q9NYV4 6/20 0.42
CCNK O75909 4/20 0.42
CNR1 P21554 2/20 0.39
CNR2 P34972 1/20 0.39
JAK2 O60674 4/20 0.38
JAK1 P23458 4/20 0.38
JAK3 P52333 4/20 0.38
RPS6KB1 P23443 1/20 0.37
PARP1 P09874 2/20 0.35
PARP2 Q9UGN5 2/20 0.35
MLYCD O95822 1/20 0.35
ULK1 O75385 1/20 0.35
CYP2C19 P33261 1/20 0.34

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
SCHEMBL2263186 0.95 KCNH2 (0.56) KCNH2CYP2C9CDK12CCNKCNR1
SCHEMBL2262238 0.91 KCNH2 (0.52) KCNH2CYP2C9CDK12CCNKCNR1
SCHEMBL2261142 0.91 KCNH2 (0.51) KCNH2CYP2C9CDK12CCNKCNR1
SCHEMBL2260716 0.90 KCNH2 (0.45) KCNH2CYP2C9CDK12CCNKCYP2C19
SCHEMBL2262621 0.90 KCNH2 (0.58) KCNH2CYP2C9CDK12CCNKCNR1
SCHEMBL2259775 0.88 KCNH2 (0.56) KCNH2CYP2C9CDK12CCNKJAK2
SCHEMBL2259839 0.88 KCNH2 (0.47) KCNH2CYP2C9CDK12CCNK
SCHEMBL2263209 0.88 KCNH2 (0.58) KCNH2CYP2C9CDK12CCNKCNR1
SCHEMBL2265006 0.88 KCNH2 (0.51) KCNH2CYP2C9CDK12CCNKJAK1
SCHEMBL2260973 0.87 KCNH2 (0.61) KCNH2CYP2C9CNR1CNR2JAK2

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 4033/4885CYP2C9 1382/4885CDK12 683/4885

“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.