SCHEMBL648059

SCHEMBL648059

COC(=O)[C@@H]1CCC(=O)N1C(=O)OC

nearest known ligand 0.46

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 3/20 0.46
ACE P12821 2/20 0.39
BRD4 O60885 1/20 0.39
MMP2 P08253 1/20 0.38
ANPEP P15144 1/20 0.38
MEN1 O00255 1/20 0.37
CYP1A2 P05177 1/20 0.37
HIF1A Q16665 1/20 0.37
P2RX7 Q99572 3/20 0.36
FKBP1A P62942 1/20 0.34
TSHR P16473 2/20 0.33
HSD17B10 Q99714 1/20 0.33

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
SCHEMBL13739598 0.86 KMT2A (0.49) KMT2AACEBRD4MMP2ANPEP
SCHEMBL10410208 0.86 KMT2A (0.46) KMT2AACEBRD4MMP2ANPEP
SCHEMBL29388224 0.86 KMT2A (0.49) KMT2AACEBRD4MMP2ANPEP
SCHEMBL23201306 0.86 ACE (0.53) KMT2AACEMEN1CYP1A2HIF1A
SCHEMBL30204217 0.86 ACE (0.53) KMT2AACEMEN1CYP1A2HIF1A
SCHEMBL12306682 0.85 P2RX7 (0.38) KMT2AACEP2RX7TSHR
SCHEMBL476303 0.85 KMT2A (0.41) KMT2AACEBRD4MMP2ANPEP
SCHEMBL476304 0.85 KMT2A (0.41) KMT2AACEBRD4MMP2ANPEP
SCHEMBL540990 0.85 KMT2A (0.41) KMT2AACEBRD4MMP2ANPEP
SCHEMBL3051123 0.84 ACE (0.38) KMT2AACEP2RX7TSHRHSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20160152600-A1 SYNTHESIS OF (2S,5R)-5-ETHYNYL-1-PYRROLIDINE-2-CARBONITRILE ABBVIE INC (US) 2016-06-02 US disclosed
US-20160152600-A1 SYNTHESIS OF (2S,5R)-5-ETHYNYL-1-PYRROLIDINE-2-CARBONITRILE ABBVIE INC (US) 2016-06-02 US disclosed
US-9260411-B2 Synthesis of (2S,5R)-5-ethynyl-1-{N-(4-methyl-1-(4-carboxy-pyridin-2-yl)piperidin-4-yl)glycyl}pyrrolidine-2-carbonitrile ABBVIE INC. (US) 2016-02-16 US disclosed
US-9260411-B2 Synthesis of (2S,5R)-5-ethynyl-1-{N-(4-methyl-1-(4-carboxy-pyridin-2-yl)piperidin-4-yl)glycyl}pyrrolidine-2-carbonitrile ABBVIE INC. (US) 2016-02-16 US disclosed
US-8637546-B2 Pharmaceutical compositions as inhibitors of dipeptidyl peptidase-IV (DDP-IV) ABBVIE INC. (US) 2014-01-28 US disclosed
US-8119664-B2 Pharmaceutical compositions as inhibitors of dipeptidyl peptidase-IV (DPP-IV) ABBOTT LABORATORIES (US) 2012-02-21 US disclosed
US-8013170-B2 Substituted pyrrolo[1,2-d][1,4]-diazonines and treatment of brain damage NEUREN PHARMACEUTICALS LIMITED (AU) 2011-09-06 US disclosed
US-20110052528-A1 Neuroprotective macrocyclic compounds and methods for their use NEUREN PHARMACEUTICALS LIMITED (NZ) 2011-03-03 US disclosed
US-7485630-B2 Neuroprotective macrocyclic compounds and methods for their use NEUREN PHARMACEUTICALS LIMITED (NZ) 2009-02-03 US disclosed
US-20080058528-A1 useful in the treatment of disorders mediated by DPP-IV such as, but not limited to, diabetes, type II diabetes, hyperglycemia, Syndrome X, hyperinsulinemia and obesity ABBVIE INC. 2008-03-06 US disclosed
US-20080058528-A1 useful in the treatment of disorders mediated by DPP-IV such as, but not limited to, diabetes, type II diabetes, hyperglycemia, Syndrome X, hyperinsulinemia and obesity ABBVIE INC. 2008-03-06 US disclosed
US-20070238753-A1 Pharmaceutical Compositions as Inhibitors of Dipeptidyl Peptidase-IV (DPP-IV) MADAR DAVID J 2007-10-11 US disclosed
US-7262207-B2 Pharmaceutical compositions as inhibitors of dipeptidyl peptidase-IV (DPP-IV) ABBOTT LABORATORIES (US) 2007-08-28 US disclosed
US-7205409-B2 Pharmaceutical compositions as inhibitors of dipeptidyl peptidase-IV (DPP-IV) ABBOTT LABORATORIES (US) 2007-04-17 US disclosed
US-7205409-B2 Pharmaceutical compositions as inhibitors of dipeptidyl peptidase-IV (DPP-IV) ABBOTT LABORATORIES (US) 2007-04-17 US disclosed
US-20050131019-A1 Pharmaceutical compositions as inhibitors of dipeptidyl peptidase-IV (DPP-IV) ABBVIE INC. 2005-06-16 US disclosed
US-20050131019-A1 Pharmaceutical compositions as inhibitors of dipeptidyl peptidase-IV (DPP-IV) ABBVIE INC. 2005-06-16 US disclosed
WO-2005023762-A1 PYRROLIDINE-2-CARBONITRILE DERIVATIVES AND THEIR USE AS INHIBITORS OF DIPEPTIDYL PEPTIDASE-IV (DPP-IV) ABBOTT LABORATORIES (US) 2005-03-17 WO disclosed
US-20040259843-A1 Pharmaceutical compositions as inhibitors of dipeptidyl peptidase-IV (DPP-IV) ABBVIE INC. 2004-12-23 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 (6 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-20160152600-A1 SYNTHESIS OF (2S,5R)-5-ETHYNYL-1-PYRROLIDINE-2-CARBONITRILE PNN, PARN, AZI2 KMT2A 1672/4885ACE 3751/4885BRD4 1111/4885
US-20050131019-A1 Pharmaceutical compositions as inhibitors of dipeptidyl peptidase-IV (DPP-IV) DPP4, DPP3, DPP7 KMT2A 3899/4885ACE 29/4885BRD4 1401/4885
US-20080058528-A1 useful in the treatment of disorders mediated by DPP-IV such as, but not limited to, diabetes, type II diabetes, hyperglycemia, Syndrome X, hyperinsulinemia and obesity DPP4, DPP7, DPP3 KMT2A 1506/4885ACE 486/4885BRD4 765/4885
US-20110052528-A1 Neuroprotective macrocyclic compounds and methods for their use NLN, BAD, BDNF KMT2A 4212/4885ACE 1715/4885BRD4 1551/4885
US-20070238753-A1 Pharmaceutical Compositions as Inhibitors of Dipeptidyl Peptidase-IV (DPP-IV) DPP4, DPP3, DPP7 KMT2A 3383/4885ACE 16/4885BRD4 1565/4885
US-20040259843-A1 Pharmaceutical compositions as inhibitors of dipeptidyl peptidase-IV (DPP-IV) DPP4, DPP3, DPP7 KMT2A 3404/4885ACE 16/4885BRD4 1575/4885

“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.