SCHEMBL10272284

SCHEMBL10272284

COC(=O)c1ccc(NC(=O)c2cc(Cl)ccc2O)cc1

nearest known ligand 0.74

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.74
KMT2A Q03164 1/20 0.74
P2RX1 P51575 9/20 0.73
TMPRSS4 Q9NRS4 8/20 0.65
P2RX4 Q99571 4/20 0.62
P2RX7 Q99572 4/20 0.62
KCNMA1 Q12791 2/20 0.62
ALDH1A1 P00352 2/20 0.57
HPGD P15428 1/20 0.57
KDM4E B2RXH2 1/20 0.55

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
SCHEMBL18341044 0.86 P2RX1 (0.77) MEN1KMT2AP2RX1TMPRSS4P2RX4
SCHEMBL25349531 0.85 MEN1 (0.65) MEN1KMT2AP2RX1TMPRSS4P2RX4
SCHEMBL29454776 0.85 P2RX1 (1.00) MEN1KMT2AP2RX1TMPRSS4P2RX4
SCHEMBL2169619 0.85 P2RX1 (1.00) MEN1KMT2AP2RX1TMPRSS4P2RX4
SCHEMBL30692663 0.85 MEN1 (1.00) MEN1KMT2AKCNMA1ALDH1A1HPGD
SCHEMBL24438159 0.85 MEN1 (1.00) MEN1KMT2AKCNMA1ALDH1A1HPGD
SCHEMBL18290068 0.84 P2RX1 (0.80) MEN1KMT2AP2RX1TMPRSS4P2RX4
SCHEMBL9609313 0.84 MEN1 (0.53) MEN1KMT2AP2RX1TMPRSS4P2RX4
SCHEMBL14363286 0.84 PLAU (0.69) MEN1KMT2AP2RX1TMPRSS4ALDH1A1
SCHEMBL10272282 0.84 P2RX1 (0.79) MEN1KMT2AP2RX1TMPRSS4P2RX4

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-20230406831-A1 COMPOUNDS AND METHODS OF INHIBITING BACTERIAL CHAPERONIN SYSTEMS THE TRUSTEES OF INDIANA UNIVERSITY 2023-12-21 US disclosed
EP-4243799-A1 COMPOUNDS AND METHODS OF INHIBITING BACTERIAL CHAPERONIN SYSTEMS The Trustees of Indiana University (US) 2023-09-20 EP disclosed
WO-2022103572-A1 COMPOUNDS AND METHODS OF INHIBITING BACTERIAL CHAPERONIN SYSTEMS THE TRUSTEES OF INDIANA UNIVERSITY (US) 2022-05-19 WO disclosed
WO-2022103572-A1 COMPOUNDS AND METHODS OF INHIBITING BACTERIAL CHAPERONIN SYSTEMS THE TRUSTEES OF INDIANA UNIVERSITY (US) 2022-05-19 WO disclosed
US-8148328-B2 Salicylanilides enhance oral delivery of therapeutic peptides THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2012-04-03 US disclosed
US-20110183889-A1 SALICYLANILIDE MODIFIED PEPTIDES FOR USE AS ORAL THERAPEUTICS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2011-07-28 US disclosed
US-20090163408-A1 SALICYLANILIDES ENHANCE ORAL DELIVERY OF THERAPEUTIC PEPTIDES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2009-06-25 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 (3 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-20090163408-A1 SALICYLANILIDES ENHANCE ORAL DELIVERY OF THERAPEUTIC PEPTIDES DNPEP, NGLY1, VIP MEN1 3158/4885KMT2A 3301/4885P2RX1 3156/4885
US-20110183889-A1 SALICYLANILIDE MODIFIED PEPTIDES FOR USE AS ORAL THERAPEUTICS DNPEP, PTMS, NGLY1 MEN1 1625/4885KMT2A 2123/4885P2RX1 4373/4885
US-20230406831-A1 COMPOUNDS AND METHODS OF INHIBITING BACTERIAL CHAPERONIN SYSTEMS HSP90B1, HSPBP1, HSP90AB1 MEN1 4702/4885KMT2A 4732/4885P2RX1 4633/4885

“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.