SCHEMBL6263755

SCHEMBL6263755

COC(F)(C(=O)Nc1ccc2c(c1)C(=O)NC2=O)C(F)(F)F

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 5/20 1.00
SMN1; SMN2 Q16637 1/20 1.00
HSD17B10 Q99714 1/20 1.00
KMT2A Q03164 9/20 0.54
CTDSP1 Q9GZU7 2/20 0.54
ALDH1A1 P00352 3/20 0.53
GLA P06280 1/20 0.53
MEN1 O00255 7/20 0.53
HPGD P15428 2/20 0.51
POLB P06746 3/20 0.51
RXFP1 Q9HBX9 1/20 0.51
CASP3 P42574 3/20 0.50
ALOX12 P18054 1/20 0.49
GPR55 Q9Y2T6 1/20 0.48
TDP1 Q9NUW8 1/20 0.47

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
SCHEMBL6260508 0.82 KDM4E (0.68) KDM4ESMN1; SMN2HSD17B10KMT2ACTDSP1
SCHEMBL13256671 0.74 KDM4E (0.62) KDM4ESMN1; SMN2HSD17B10KMT2ACTDSP1
SCHEMBL5838218 0.74 ALDH1A1 (0.69) KDM4ESMN1; SMN2HSD17B10KMT2ACTDSP1
SCHEMBL22079528 0.72 KMT2A (0.71) KDM4ESMN1; SMN2HSD17B10KMT2ACTDSP1
SCHEMBL4462900 0.72 KDM4E (0.66) KDM4EHSD17B10KMT2ACTDSP1ALDH1A1
SCHEMBL26695993 0.71 KDM4E (0.65) KDM4ESMN1; SMN2HSD17B10KMT2ACTDSP1
SCHEMBL6260912 0.70 KDM4E (1.00) KDM4ESMN1; SMN2HSD17B10KMT2ACTDSP1
SCHEMBL6260500 0.69 KMT2A (1.00) SMN1; SMN2KMT2ACTDSP1ALDH1A1MEN1
SCHEMBL5947099 0.69 KDM4E (0.71) KDM4ESMN1; SMN2KMT2AALDH1A1GLA
SCHEMBL195372 0.69 KDM4E (0.61) KDM4ESMN1; SMN2HSD17B10KMT2ACTDSP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20050182061-A1 Phthalimide compounds useful as protein kinase inhibitors GREEN JEREMY (US) 2005-08-18 US claimed
WO-2005039564-A1 PHTHALIMIDE COMPOUNDS USEFUL AS PROTEIN KINASE INHIBITORS VERTEX PHARMACEUTICALS INCORPORATED (US) 2005-05-06 WO claimed
US-20050182061-A1 Phthalimide compounds useful as protein kinase inhibitors GREEN JEREMY (US) 2005-08-18 US disclosed
US-20050159599-A1 Cyclic compound, process for producing the same, and pest control agent SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2005-07-21 US disclosed
WO-2005039564-A1 PHTHALIMIDE COMPOUNDS USEFUL AS PROTEIN KINASE INHIBITORS VERTEX PHARMACEUTICALS INCORPORATED (US) 2005-05-06 WO disclosed
EP-1481972-A1 CYCLIC COMPOUND, PROCESS FOR PRODUCING THE SAME, AND PEST CONTROL AGENT Sumitomo Chemical Takeda Agro Company, Limited (JP) 2004-12-01 EP 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-20050182061-A1 Phthalimide compounds useful as protein kinase inhibitors PDK1, PDPK1, MTOR KDM4E 793/4885SMN1; SMN2 969/4885HSD17B10 2659/4885
US-20050159599-A1 Cyclic compound, process for producing the same, and pest control agent CNPY2, CNPY3, HAX1 KDM4E 594/4885SMN1; SMN2 4544/4885HSD17B10 564/4885

“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.