SCHEMBL4939489

SCHEMBL4939489

CC(C)Oc1nc(S(C)(=O)=O)nc(Cl)c1-c1c(F)cc(F)cc1F

nearest known ligand 0.33

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 2/20 0.33
▸ SMN1; SMN2 Q16637 2/20 0.33
▸ MAPK8 P45983 1/20 0.31
▸ MAPK9 P45984 1/20 0.31
▸ MAPK10 P53779 1/20 0.31
▸ KDM4E B2RXH2 1/20 0.30
▸ MITF O75030 1/20 0.30
▸ ALDH1A1 P00352 1/20 0.30
▸ STAT3 P40763 1/20 0.30
▸ STAT1 P42224 1/20 0.30
▸ RAB9A P51151 1/20 0.30
▸ NPSR1 Q6W5P4 1/20 0.30
▸ TLR9 Q9NR96 1/20 0.30
▸ PTGS1 P23219 1/20 0.30
▸ PTGS2 P35354 1/20 0.30
▸ MEN1 O00255 1/20 0.30
▸ KMT2A Q03164 1/20 0.30

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
SCHEMBL4826868 0.77 GLP1R (0.42) LMNASMN1; SMN2KDM4EMITFALDH1A1
SCHEMBL4935623 0.76 LMNA (0.42) LMNASMN1; SMN2KDM4EALDH1A1MEN1
SCHEMBL4938646 0.75 CNR1 (0.33) LMNAMAPK8MAPK9
SCHEMBL2833122 0.73 KDM4E (0.33) LMNASMN1; SMN2KDM4EMITFALDH1A1
SCHEMBL2833125 0.73 KDM4E (0.33) LMNASMN1; SMN2KDM4EMITFALDH1A1
SCHEMBL5164507 0.72 NPC1 (0.34) SMN1; SMN2RAB9A
SCHEMBL5167350 0.72 — —
SCHEMBL4932061 0.71 MAPT (0.41) LMNASMN1; SMN2KDM4EALDH1A1NPSR1
SCHEMBL6079376 0.70 TLR8 (0.43) PTGS1PTGS2
SCHEMBL4937597 0.69 LMNA (0.31) LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20080132522-A1 2-Substituted Pyrimidines, Method for Their Production and Their Use for Controlling Pathogenic Fungi BASF AKTIENGESELLSCHAFT (DE) 2008-06-05 — — US disclosed
EP-1768972-A1 2-SUBSTITUTED PYRIMIDINES, METHOD FOR THEIR PRODUCTION AND THEIR USE FOR CONTROLLING PATHOGENIC FUNGI BASF AKTIENGESELLSCHAFT (DE) 2007-04-04 — — EP disclosed
WO-2006005571-A1 2-SUBSTITUTED PYRIMIDINES, METHOD FOR THEIR PRODUCTION AND THEIR USE FOR CONTROLLING PATHOGENIC FUNGI BASF AKTIENGESELLSCHAFT (DE) 2006-01-19 — — 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 (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-20080132522-A1 2-Substituted Pyrimidines, Method for Their Production and Their Use for Controlling Pathogenic Fungi TYMS, TYMP, PNPO LMNA 2500/4885SMN1; SMN2 1907/4885MAPK8 4542/4885

“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.

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