SCHEMBL4922997

SCHEMBL4922997

C[C@H](c1ccccc1)N1CCC(CO)C1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.55
SMN1; SMN2 Q16637 1/20 0.55
HTT P42858 1/20 0.54
CYP2D6 P10635 2/20 0.53
MAPT P10636 2/20 0.53
ALDH1A1 P00352 2/20 0.53
DUSP3 P51452 1/20 0.53
PTPN5 P54829 1/20 0.53
PTPN11 Q06124 1/20 0.53
KDM4E B2RXH2 1/20 0.51
MC4R P32245 1/20 0.47
OPRK1 P41145 2/20 0.44
OPRM1 P35372 1/20 0.44
OPRD1 P41143 1/20 0.44
OPRL1 P41146 1/20 0.44
CCR5 P51681 1/20 0.44
CHRM4 P08173 1/20 0.42
GRIN2B Q13224 5/20 0.42
ADRA2A P08913 4/20 0.42
HTR2A P28223 4/20 0.42

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
SCHEMBL7291562 1.00 LMNA (0.55) LMNASMN1; SMN2HTTCYP2D6MAPT
SCHEMBL28463472 1.00 LMNA (0.55) LMNASMN1; SMN2HTTCYP2D6MAPT
SCHEMBL27626473 1.00 LMNA (0.55) LMNASMN1; SMN2HTTCYP2D6MAPT
SCHEMBL7459001 1.00 LMNA (0.55) LMNASMN1; SMN2HTTCYP2D6MAPT
SCHEMBL5453145 1.00 LMNA (0.55) LMNASMN1; SMN2HTTCYP2D6MAPT
SCHEMBL879237 1.00 LMNA (0.55) LMNASMN1; SMN2HTTCYP2D6MAPT
SCHEMBL1713427 1.00 LMNA (0.55) LMNASMN1; SMN2HTTCYP2D6MAPT
SCHEMBL6773183 0.90 CYP2D6 (0.61) LMNASMN1; SMN2HTTCYP2D6MAPT
SCHEMBL9683895 0.87 CYP2D6 (0.55) LMNASMN1; SMN2HTTCYP2D6MAPT
SCHEMBL14026665 0.86 CYP2D6 (0.55) LMNASMN1; SMN2HTTCYP2D6MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111808007-B Preparation method of chiral 3-substituted pyrrolidine derivative 青岛贞开生物医药技术有限公司 2023-04-21 CN disclosed
CN-111808007-A Preparation method of chiral 3-substituted pyrrolidine derivative 青岛贞开生物医药技术有限公司 2020-10-23 CN disclosed
EP-2928888-A1 SUBSTITUTED PYRIDOPYRAZINES AS SYK INHIBITORS Hutchison Medipharma Limited (CN) 2015-10-14 EP disclosed
WO-2014086316-A1 SUBSTITUTED PYRIDOPYRAZINES AS SYK INHIBITORS HUTCHISON MEDIPHARMA LIMITED (CN) 2014-06-12 WO disclosed
EP-2463274-A1 Tri-or tetra-substituted-3-aminopyrrolidine deritatives DAIICHI SANKYO COMPANY, LIMITED (JP) 2012-06-13 EP disclosed
US-20080262075-A1 Pyrrolidine Derivatives as Muscarinic Receptor Antagonists RANBAXY LABORATORIES LIMITED (IN) 2008-10-23 US disclosed
EP-1781607-A2 PYRROLIDINE DERIVATIVES AS MUSCARINIC RECEPTOR ANTAGONISTS Ranbaxy Laboratories Limited (IN) 2007-05-09 EP disclosed
WO-2006018708-A2 PYRROLIDINE DERIVATIVES AS MUSCARINIC RECEPTOR ANTAGONISTS RANBAXY LABORATORIES LIMITED (IN) 2006-02-23 WO disclosed
EP-0928793-B1 Thiazole derivatives HOFFMANN LA ROCHE (CH) 2002-05-15 EP disclosed
US-6001855-A REACTING A THIAZOLE DERIVATIVE AND A CYCLIC AMINE DERIVATIVE; INHIBITS BINDING OF ADHESIVE PROTEINS TO THE SURFACE OF DIFFERENT TYPES OF CELL AND ACCORDINGLY INFLUENCE CELL-CELL AND CELL-MATRIX INTERACTIONS HOFFMAN-LA ROCHE INC. (US) 1999-12-14 US disclosed
EP-0928793-A1 Thiazole derivatives F. HOFFMANN-LA ROCHE AG (CH) 1999-07-14 EP disclosed
US-5726182-A TREATMENT OF BACTERIAL INFECTIONS ABBOTT LABORATORIES (US) 1998-03-10 US disclosed
US-5599816-A BACTERICIDE ABBOTT LABORATORIES (US) 1997-02-04 US disclosed
WO-1996039407-A1 QUINOLIZINONE TYPE COMPOUNDS ABBOTT LABORATORIES (US) 1996-12-12 WO 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-20080262075-A1 Pyrrolidine Derivatives as Muscarinic Receptor Antagonists CHRM3, CHRM2, CHRM5 LMNA 4322/4885SMN1; SMN2 3750/4885HTT 2838/4885

“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.