SCHEMBL15939671

SCHEMBL15939671

COc1ccc(F)cc1-c1ccc(CC(CC(=O)O)NC(=O)c2n[nH]c(=O)o2)cc1

nearest known ligand 0.69

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
▸ MMEL1 Q495T6 8/20 0.69
▸ MME P08473 5/20 0.50
▸ ITGB1 P05556 2/20 0.45
▸ ITGA4 P13612 1/20 0.45
▸ CTSA P10619 7/20 0.42
▸ FFAR4 Q5NUL3 1/20 0.41
▸ ITGB3 P05106 1/20 0.41
▸ ITGAV P06756 1/20 0.41
▸ ITGA5 P08648 1/20 0.41

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
SCHEMBL15940117 1.00 MMEL1 (0.69) MMEL1MMEITGB1ITGA4CTSA
SCHEMBL15947115 0.94 MMEL1 (0.61) MMEL1MMEITGB1ITGA4CTSA
SCHEMBL15947116 0.94 MMEL1 (0.61) MMEL1MMEITGB1ITGA4CTSA
SCHEMBL15947120 0.93 MMEL1 (0.60) MMEL1MMEITGB1ITGA4CTSA
SCHEMBL15948921 0.91 MMEL1 (0.57) MMEL1MMEITGB1ITGA4CTSA
SCHEMBL15947127 0.90 MMEL1 (0.57) MMEL1MMEITGB1ITGA4CTSA
SCHEMBL15940111 0.84 MMEL1 (0.60) MMEL1MMEITGB1ITGA4CTSA
SCHEMBL15940304 0.84 MMEL1 (0.60) MMEL1MMEITGB1ITGA4CTSA
SCHEMBL15940159 0.82 MMEL1 (0.52) MMEL1MMEITGB1ITGA4CTSA
SCHEMBL15940160 0.82 MMEL1 (0.52) MMEL1MMEITGB1ITGA4CTSA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2956445-A1 SUBSTITUTED BISPHENYL BUTANOIC ACID DERIVATIVES AS NEP INHIBITORS WITH IMPROVED IN VIVO EFFICACY Novartis AG (CH) 2015-12-23 — — EP disclosed
US-9102635-B2 Substituted bisphenyl butanoic acid derivatives as NEP inhibitors with improved in vivo efficacy NOVARTIS AG (CH) 2015-08-11 — — US disclosed
WO-2014126972-A1 SUBSTITUTED BISPHENYL BUTANOIC ACID DERIVATIVES AS NEP INHIBITORS WITH IMPROVED IN VIVO EFFICACY NOVARTIS AG (CH) 2014-08-21 — — WO disclosed
US-20140228415-A1 Substituted bisphenyl butanoic acid derivatives as NEP inhibitors with improved in vivo Efficacy NOVARTIS AG (CH) 2014-08-14 — — 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-20140228415-A1 Substituted bisphenyl butanoic acid derivatives as NEP inhibitors with improved in vivo Efficacy MME, REN, ACE MMEL1 424/4885MME 1/4885ITGB1 4823/4885

“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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