SCHEMBL646675

SCHEMBL646675

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

nearest known ligand 0.34

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.34
MMP2 P08253 2/20 0.34
ANPEP P15144 2/20 0.34
KMT2A Q03164 1/20 0.34
POLB P06746 1/20 0.33
TP53 P04637 1/20 0.33
ALDH1A1 P00352 1/20 0.32
CYP3A4 P08684 4/20 0.31
MAPT P10636 2/20 0.31
FKBP1A P62942 1/20 0.31
KDM4E B2RXH2 1/20 0.31
SMN1; SMN2 Q16637 1/20 0.31
CYP1A2 P05177 1/20 0.31
HIF1A Q16665 1/20 0.31

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
SCHEMBL6842735 0.86 GAA (0.41) KMT2AALDH1A1CYP3A4MAPTFKBP1A
SCHEMBL8871655 0.85 TSHR (0.34) TSHRALDH1A1
SCHEMBL8871650 0.85 TSHR (0.34) TSHRALDH1A1
SCHEMBL8205840 0.85 CHRM2 (0.44) ALDH1A1FKBP1ASMN1; SMN2
SCHEMBL12328185 0.85 CHRM2 (0.44) ALDH1A1FKBP1ASMN1; SMN2
SCHEMBL5832813 0.85 CHRM2 (0.44) ALDH1A1FKBP1ASMN1; SMN2
SCHEMBL11492510 0.84 TSHR (0.41) TSHRTP53SMN1; SMN2
SCHEMBL7692263 0.79 TSHR (0.48) TSHRMMP2ANPEPKMT2APOLB
SCHEMBL12837215 0.79 ALDH1A1 (0.36) TSHRMMP2ANPEPKMT2APOLB
SCHEMBL10614925 0.77 HTR2C (0.52) TSHRPOLBALDH1A1CYP3A4MAPT

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 15 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-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
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 (5 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 TSHR 3520/4885MMP2 4073/4885ANPEP 671/4885
US-20050131019-A1 Pharmaceutical compositions as inhibitors of dipeptidyl peptidase-IV (DPP-IV) DPP4, DPP3, DPP7 TSHR 2619/4885MMP2 151/4885ANPEP 108/4885
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 TSHR 2436/4885MMP2 206/4885ANPEP 54/4885
US-20070238753-A1 Pharmaceutical Compositions as Inhibitors of Dipeptidyl Peptidase-IV (DPP-IV) DPP4, DPP3, DPP7 TSHR 3493/4885MMP2 51/4885ANPEP 47/4885
US-20040259843-A1 Pharmaceutical compositions as inhibitors of dipeptidyl peptidase-IV (DPP-IV) DPP4, DPP3, DPP7 TSHR 3464/4885MMP2 47/4885ANPEP 51/4885

“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.