SCHEMBL5483695

SCHEMBL5483695

Oc1cc(C(F)(F)F)nc(-c2ncccn2)n1

nearest known ligand 0.42

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 4/20 0.42
CYP2C9 P11712 2/20 0.42
CYP2D6 P10635 1/20 0.42
GAA P10253 2/20 0.41
KDM4E B2RXH2 1/20 0.41
MDM2 Q00987 1/20 0.41
LMNA P02545 2/20 0.41
POLB P06746 1/20 0.41
KMT2A Q03164 3/20 0.39
BLM P54132 2/20 0.39
ALDH1A1 P00352 4/20 0.38
MEN1 O00255 2/20 0.38
MAPT P10636 1/20 0.38
ATM Q13315 1/20 0.38
NPSR1 Q6W5P4 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.38
SMN1; SMN2 Q16637 2/20 0.36
IGF1R P08069 1/20 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
SCHEMBL5479409 0.82 CYP1A2 (0.64) CYP1A2CYP2C9CYP2D6GAAKDM4E
SCHEMBL602293 0.78 LMNA (0.64) CYP1A2CYP2C9CYP2D6KDM4ELMNA
SCHEMBL5475997 0.78 HIF1A (0.42) CYP1A2CYP2C9CYP2D6GAAKDM4E
SCHEMBL5475318 0.75 CYP1A2 (0.41) CYP1A2CYP2C9CYP2D6GAAKDM4E
SCHEMBL5483659 0.74 PIK3CA (0.43)
SCHEMBL5482562 0.73 LMNA (0.40) KDM4ELMNAPOLBKMT2AALDH1A1
SCHEMBL6494121 0.71 ALDH1A1 (0.51) CYP1A2CYP2C9KDM4ELMNAPOLB
SCHEMBL1258669 0.71 HSP90AA1 (0.38) CYP2D6GAAKDM4ELMNAPOLB
SCHEMBL601042 0.70 HSP90AA1 (0.36) CYP2D6GAAKDM4ELMNAPOLB
SCHEMBL1483169 0.69 HIF1A (0.42) CYP1A2CYP2C9CYP2D6GAAKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7226927-B2 Substituted 2-aryl-4-arylaminopyrimidines and analogs as activators of caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. (US) 2007-06-05 US disclosed
EP-1351691-A4 SUBSTITUTED 2-ARYL-4-ARYLAMINOPYRIMIDINES AND ANALOGS AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS AND THE USE THEREOF CYTOVIA INC (US) 2005-06-22 EP disclosed
US-20040097503-A1 Substituted 2-aryl-4-arylaminopyrimidines and analogs as activators of caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. 2004-05-20 US disclosed
US-6716851-B2 ANTICANCER AGENTS CYTOVIA, INC. 2004-04-06 US disclosed
EP-1351691-A1 SUBSTITUTED 2-ARYL-4-ARYLAMINOPYRIMIDINES AND ANALOGS AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS AND THE USE THEREOF Cytovia, Inc. (US) 2003-10-15 EP disclosed
US-20030069239-A1 Substituted 2-aryl-4-arylaminopyrimidines and analogs as activators or caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. 2003-04-10 US disclosed
WO-2002047690-A1 SUBSTITUTED 2-ARYL-4-ARYLAMINOPYRIMIDINES AND ANALOGS AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS AND THE USE THEREOF CYTOVIA, INC. (US) 2002-06-20 WO 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 (2 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-20030069239-A1 Substituted 2-aryl-4-arylaminopyrimidines and analogs as activators or caspases and inducers of apoptosis and the use thereof API5, CASP2, APAF1 CYP1A2 300/4885CYP2C9 2141/4885CYP2D6 475/4885
US-20040097503-A1 Substituted 2-aryl-4-arylaminopyrimidines and analogs as activators of caspases and inducers of apoptosis and the use thereof API5, CASP2, APAF1 CYP1A2 294/4885CYP2C9 2086/4885CYP2D6 468/4885

“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.