SCHEMBL4611078

SCHEMBL4611078

CC(=O)O[C@@H](C)Br

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
SCHEMBL4611710 1.00
SCHEMBL230054 1.00
SCHEMBL29034781 0.97
SCHEMBL31065523 0.80
SCHEMBL18074210 0.78 TSHR (0.53)
SCHEMBL341632 0.78
SCHEMBL11182956 0.78
SCHEMBL291550 0.78 TSHR (0.38)
SCHEMBL7752345 0.77
SCHEMBL790192 0.77

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 25 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1409492-B1 AN IMPROVED METHOD FOR PREPARATION OF CEFUROXIME AXETIL LUPIN LTD (IN) 2008-10-15 EP claimed
US-7064198-B2 Method for preparation of cefuroxime axetil LUPIN LIMITED (IN) 2006-06-20 US claimed
US-6833452-B2 Reacting an amine salt of cefuroxime with an esterifying agent RANBAXY LABORATORIES LIMITED (IN) 2004-12-21 US claimed
US-20040077850-A1 Method for preparation of cefuroxime axetil LUPIN LIMITED (IN) 2004-04-22 US claimed
EP-1303523-A1 PROCESS FOR THE PREPARATION OF THE HIGHLY PURE CRYSTALLINE (R, S) - CEFUROXIME AXETIL RANBAXY LABORATORIES, LTD. (IN) 2003-04-23 EP claimed
US-20020016456-A1 Process for the preparation of highly pure crystalline (R,S) - cefuroxime axetil RANBAXY LABORATORIES LIMITED (IN) 2002-02-07 US claimed
WO-2002006289-A1 PROCESS FOR THE PREPARATION OF HIGHLY PURE CRYSTALLINE (R,S) - CEFUROXIME AXETIL RANBAXY LABORATORIES LIMITED (IN) 2002-01-24 WO claimed
EP-1409492-B1 AN IMPROVED METHOD FOR PREPARATION OF CEFUROXIME AXETIL LUPIN LTD (IN) 2008-10-15 EP disclosed
US-7064198-B2 Method for preparation of cefuroxime axetil LUPIN LIMITED (IN) 2006-06-20 US disclosed
US-7064198-B2 Method for preparation of cefuroxime axetil LUPIN LIMITED (IN) 2006-06-20 US disclosed
US-6833452-B2 Reacting an amine salt of cefuroxime with an esterifying agent RANBAXY LABORATORIES LIMITED (IN) 2004-12-21 US disclosed
US-20040077850-A1 Method for preparation of cefuroxime axetil LUPIN LIMITED (IN) 2004-04-22 US disclosed
EP-1409492-A1 AN IMPROVED METHOD FOR PREPARATION OF CEFUROXIME AXETIL Lupin Limited (IN) 2004-04-21 EP disclosed
US-5677443-A HEATING IN WATER OR WATER MISCIBLE SOLVENT; COOLING; SEPARATION ACS DOBFAR S.P.A. (IT) 1997-10-14 US disclosed
EP-0757991-A1 Bioavailable crystalline form of cefuroxime axetil ACS DOBFAR S.p.A. (IT) 1997-02-12 EP disclosed
EP-0338824-A2 Esters of 6-beta-(alpha-oxyimino)-acylamino-penicillanic acid derivatives BEECHAM GROUP PLC (GB) 1989-10-25 EP disclosed
US-4816452-A ANTIBIOTICS BEECHAM GROUP P.L.C. (GB) 1989-03-28 US disclosed
US-4385054-A 1-Acetoxyethyl-3-(2-chloroethylcarbamoyloxymethyl)-7-[2-(fur-2-yl)-2-methoxyiminoacetamido]ceph-3-em-4-carboxylate GLAXO GROUP LIMITED (GB) 1983-05-24 US disclosed
US-4284766-A Process for the preparation of cephalosporin compounds GLAXO GROUP LIMITED (GB) 1981-08-18 US disclosed
US-4258183-A Process for the preparation of cephalosporin compounds GLAXO GROUP LIMITED (GB) 1981-03-24 US disclosed