SCHEMBL13347237

SCHEMBL13347237

O=C([C@@H]1CN(S(=O)(=O)c2ccc(F)cc2F)CCN1)N1CCC[C@H]1B(O)O

nearest known ligand 0.50

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
DPP4 P27487 9/20 0.50
DPP9 Q86TI2 6/20 0.48
DPP7 Q9UHL4 6/20 0.48
FAP Q12884 5/20 0.48
DPP8 Q6V1X1 5/20 0.48
AKR1C3 P42330 1/20 0.39
PREP P48147 2/20 0.38
PITRM1 Q5JRX3 3/20 0.38
PKM P14618 2/20 0.38
SMN1; SMN2 Q16637 2/20 0.37
HTR6 P50406 1/20 0.36
TDO2 P48775 1/20 0.35
MAPT P10636 2/20 0.35
PKLR P30613 1/20 0.35
ALDH1A1 P00352 1/20 0.35
KCNH2 Q12809 1/20 0.35

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
SCHEMBL8214179 0.82 PREP (0.39) DPP4DPP9DPP7FAPDPP8
SCHEMBL8288249 0.82 ALDH1A1 (0.41) DPP4DPP9DPP7FAPDPP8
SCHEMBL13372095 0.82 PREP (0.37) DPP4DPP9DPP7FAPDPP8
SCHEMBL8288240 0.81 DPP4 (0.55) DPP4DPP9DPP7FAPDPP8
SCHEMBL13347238 0.80 DPP4 (0.49) DPP4DPP9DPP7FAPDPP8
SCHEMBL13347236 0.79 DPP4 (0.53) DPP4DPP9DPP7FAPDPP8
SCHEMBL13347239 0.79 DPP4 (0.50) DPP4DPP9DPP7FAPDPP8
SCHEMBL13347235 0.77 DPP4 (0.64) DPP4DPP9DPP7FAPDPP8
SCHEMBL8288248 0.77 MEN1 (0.48) DPP4DPP9DPP7FAPDPP8
SCHEMBL8214993 0.71 PREP (0.39) DPP4DPP9DPP7FAPDPP8

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-8415295-B2 Heterocyclic boronic acid compounds PHENOMIX CORPORATION (US) 2013-04-09 US disclosed
US-20100120661-A1 HETEROCYCLIC BORONIC ACID COMPOUNDS PHENOMIX CORPORATION (US) 2010-05-13 US disclosed
US-7674913-B2 Heterocyclic boronic acid compounds PHENOMIX CORPORATION (US) 2010-03-09 US disclosed
EP-1997533-A1 Heterocyclic boronic acid compounds, dipeptidyl peptidase IV inhibitors Phenomix Corporation (US) 2008-12-03 EP disclosed
US-20070185061-A1 (2R)-1-{2-[(3R)-pyrrolidin-3-ylamino]-acetyl}-pyrrolidine-2-boronic acid; Dipeptidyl peptidase IV (DPP-IV) inhibitors; diabetes, hyperglycemia, Syndrome X, hyperinsulinemia, obesity, atherosclerosis PHENOMIX CORPORATION 2007-08-09 US disclosed
US-20070060547-A1 (2R)-1-{2-[(3R)-pyrrolidin-3-ylamino]-acetyl}-pyrrolidine-2-boronic acid; Dipeptidyl peptidase IV (DPP-IV) inhibitors; diabetes, hyperglycemia, Syndrome X, hyperinsulinemia, obesity, atherosclerosis PHENOMIX CORPORATION 2007-03-15 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-20070060547-A1 (2R)-1-{2-[(3R)-pyrrolidin-3-ylamino]-acetyl}-pyrrolidine-2-boronic acid; Dipeptidyl peptidase IV (DPP-IV) inhibitors; diabetes, hyperglycemia, Syndrome X, hyperinsulinemia, obesity, atherosclerosis DPP4, DPP7, DPP3 DPP4 1/4885DPP9 6/4885DPP7 2/4885
US-20070185061-A1 (2R)-1-{2-[(3R)-pyrrolidin-3-ylamino]-acetyl}-pyrrolidine-2-boronic acid; Dipeptidyl peptidase IV (DPP-IV) inhibitors; diabetes, hyperglycemia, Syndrome X, hyperinsulinemia, obesity, atherosclerosis DPP4, DPP7, DPP3 DPP4 1/4885DPP9 5/4885DPP7 2/4885
US-20100120661-A1 HETEROCYCLIC BORONIC ACID COMPOUNDS DPP4, DPP7, DPP3 DPP4 1/4885DPP9 7/4885DPP7 2/4885

“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.