SCHEMBL6277950

SCHEMBL6277950

[NH]C(=O)CCC[C]=O

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL9835411 0.92
SCHEMBL300224 0.82
SCHEMBL7771422 0.76
SCHEMBL1170826 0.76
SCHEMBL8011163 0.74
SCHEMBL5341058 0.74
SCHEMBL563582 0.74
SCHEMBL116689 0.72
SCHEMBL9643826 0.72
SCHEMBL4968791 0.72

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0275901-B1 USE OF GAMMA-GLUTAMYL-TRANSPEPTIDASE HOECHST AKTIENGESELLSCHAFT (DE) 1993-06-09 EP claimed
US-4990444-A Fermentation of bacteria; used for hydrolysis of (adipinyl-or glutaryl)-7-aminocephalosporanic acid HOECHST AKTIENGESELLSCHAFT (DE) 1991-02-05 US claimed
EP-1322751-B1 GLUTARYL CEPHALOSPORIN AMIDASE FROM PSEUDOMONAS DIMINUTA BS-203 BRISTOL MYERS SQUIBB CO (US) 2005-11-23 EP disclosed
US-6942990-B2 Glutaryl cephalosporin amidase from Pseudomonas diminuta BS-203 BRISTOL MYERS SQUIBB COMPANY (US) 2005-09-13 US disclosed
US-20030143715-A1 Glutaryl cephalosporin amidase from pseudomonas diminuta BS-203 BINDER ROSS (US) 2003-07-31 US disclosed
EP-1322751-A2 GLUTARYL CEPHALOSPORIN AMIDASE FROM PSEUDOMONAS DIMINUTA BS-203 Bristol-Myers Squibb Company (US) 2003-07-02 EP disclosed
US-6528300-B2 For use in obtaining 7-aminocephalosporanic acid (7-ACA) from 7- beta -(4-carboxybutanamido)cephalosporanic acid (glutaryl 7-ACA) by enzymatic hydrolysis BRISTOL-MYERS SQUIBB CO. 2003-03-04 US disclosed
US-20020160500-A1 Glutaryl cephalosporin amidase from pseudomonas diminuta BS-203 BRISTOL-MEYERS SQUIBB COMPANY 2002-10-31 US disclosed
WO-2002024879-A2 GLUTARYL CEPHALOSPORIN AMIDASE FROM PSEUDOMONAS DIMINUTA BS-203 BRISTOL-MYERS SQUIBB COMPANY (US) 2002-03-28 WO disclosed
EP-0720611-A1 GLUTARYL 7-ACA DERIVATIVES AND PROCESSES FOR OBTAINING THEM ANTIBIOTICOS S.P.A. (IT) 1996-07-10 EP disclosed
WO-1995035020-A2 GLUTARYL 7-ACA DERIVATIVES AND PROCESSES FOR OBTAINING THEM ANTIBIOTICOS S.P.A. (IT) 1995-12-28 WO disclosed
EP-0605589-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING NATRIURETIC PEPTIDES OR NEUTRAL ENDOPEPTIDASE INHIBITORS FOR TREATING OR PREVENTING MYOINTIMAL PROLIFERATION SCHERING CORPORATION (US) 1994-07-13 EP disclosed
WO-1993010773-A1 USE OF NEUTRAL ENDOPEPTIDASE INHIBITORS IN THE TREATMENT OF LEFT VENTRICULAR HYPERTROPHY SCHERING-PLOUGH S.P.A. (IT) 1993-06-10 WO disclosed
WO-1993005809-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING NATRIURETIC PEPTIDES OR NEUTRAL ENDOPEPTIDASE INHIBITORS FOR TREATING OR PREVENTING MYOINTIMAL PROLIFERATION SCHERING CORPORATION (US) 1993-04-01 WO disclosed
EP-0533084-A1 Pharmaceutical compositions comprising natriuretic peptides or neutral endopeptidase inhibitors for treating and preventing myointimal proliferation SCHERING CORPORATION (US) 1993-03-24 EP disclosed
WO-1992018159-A1 USE OF NEUTRAL ENDOPEPTIDASE INHIBITORS IN THE TREATMENT OF NEPHROTOXICITY SCHERING CORPORATION (US) 1992-10-29 WO disclosed
EP-0509442-A1 Use of neutral endopeptidase inhibitors in the treatment of nephrotoxicity SCHERING CORPORATION (US) 1992-10-21 EP disclosed
US-4990444-A Fermentation of bacteria; used for hydrolysis of (adipinyl-or glutaryl)-7-aminocephalosporanic acid HOECHST AKTIENGESELLSCHAFT (DE) 1991-02-05 US disclosed
US-4990444-A Fermentation of bacteria; used for hydrolysis of (adipinyl-or glutaryl)-7-aminocephalosporanic acid HOECHST AKTIENGESELLSCHAFT (DE) 1991-02-05 US disclosed
EP-0275901-A2 Use of gamma-glutamyl-transpeptidase HOECHST AKTIENGESELLSCHAFT (DE) 1988-07-27 EP disclosed