SCHEMBL5025486

SCHEMBL5025486

O=C(O)Cc1csc(-c2ccc(C(F)(F)F)cc2)n1

nearest known ligand 0.72

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
LMNA P02545 5/20 0.72
HTT P42858 1/20 0.66
KDM4E B2RXH2 5/20 0.63
ALDH1A1 P00352 2/20 0.63
HPGD P15428 2/20 0.63
SMN1; SMN2 Q16637 2/20 0.59
TP53 P04637 7/20 0.58
GAA P10253 2/20 0.56
MAPT P10636 2/20 0.56
SHMT2 P34897 1/20 0.54
POLB P06746 1/20 0.54
RHOC P08134 1/20 0.51
RHOA P61586 1/20 0.51

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
SCHEMBL20255532 0.86 SHMT2 (0.74) LMNAHTTKDM4EALDH1A1HPGD
SCHEMBL627651 0.86 LMNA (0.59) LMNAHTTKDM4EALDH1A1HPGD
SCHEMBL5017463 0.84 LMNA (0.61) LMNAHTTKDM4EALDH1A1HPGD
SCHEMBL9555570 0.84 LMNA (1.00) LMNAKDM4EALDH1A1HPGDSMN1; SMN2
SCHEMBL5461325 0.83 LMNA (0.72) LMNAHTTKDM4EALDH1A1HPGD
SCHEMBL5437975 0.82 ALOX5 (0.56) LMNAHTTKDM4EALDH1A1TP53
SCHEMBL2088799 0.82 LMNA (0.54) LMNAHTTKDM4ESMN1; SMN2TP53
SCHEMBL12151145 0.82 POLB (0.55) LMNAHTTKDM4ESMN1; SMN2TP53
SCHEMBL4905943 0.82 POLB (0.62) LMNAHTTKDM4ESMN1; SMN2TP53
SCHEMBL1422234 0.82 LMNA (0.74) LMNAHTTKDM4EALDH1A1HPGD

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-1644368-B1 INDOLYL DERIVATIVES SUBSTITUTED WITH A THIAZOLE RING AND THEIR USE AS PPAR MODULATORS HOFFMANN LA ROCHE (CH) 2008-08-27 EP disclosed
US-7235572-B2 Thiazolyl-indole derivatives, their manufacture and use as pharmaceutical agents HOFFMAN-LA ROCHE INC. (US) 2007-06-26 US disclosed
EP-1644368-A1 INDOLYL DERIVATIVES SUBSTITUTED WITH A THIAZOLE RING AND THEIR USE AS PPAR MODULATORS F. HOFFMANN-LA ROCHE AG (CH) 2006-04-12 EP disclosed
WO-2005005423-A1 INDOLYL DERIVATIVES SUBSTITUTED WITH A THIAZOLE RING AND THEIR USE AS PPAR MODULATORS F. HOFFMANN-LA ROCHE AG (CH) 2005-01-20 WO disclosed
US-20050004187-A1 Thiazolyl-indole derivatives, their manufacture and use as pharmaceutical agents HOFFMANN-LA ROCHE INC. 2005-01-06 US 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-20050004187-A1 Thiazolyl-indole derivatives, their manufacture and use as pharmaceutical agents PPARD, PPARA, PPARG LMNA 3202/4885HTT 989/4885KDM4E 1998/4885

“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.