SCHEMBL2480472

SCHEMBL2480472

O=C(O)[C@@H]1OCCS1

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
SCHEMBL5789732 1.00
SCHEMBL9540306 1.00
Hydrochloric Acid SCHEMBL5790890 0.97
SCHEMBL11484300 0.75
SCHEMBL10077537 0.64
SCHEMBL10077535 0.64
SCHEMBL1104439 0.64
SCHEMBL23829831 0.60
SCHEMBL8807222 0.60
SCHEMBL8317048 0.60

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2014174532-A2 AN IMPROVED PROCESS FOR THE PREPARATION OF EMTRICITABINE LAURUS LABS PRIVATE LIMITED (IN) 2014-10-30 WO disclosed
EP-2542551-B1 A PROCESS FOR STEREOSELECTIVE SYNTHESIS OF 5-FLUORO-1-(2R,5S)-[2-(HYDROXYMETHYL)-1,3-OXATHIOLAN-5-YL]CYTOSINE RANBAXY LAB LTD (IN) 2014-08-27 EP disclosed
EP-2739620-A1 A STEREOSELECTIVE PROCESS FOR PREPARATION OF 1,3-OXATHIOLANE NUCLEOSIDES Lupin Limited (IN) 2014-06-11 EP disclosed
US-8748604-B2 Process for stereoselective synthesis of 5-fluoro-1-(2R,5S)-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]cytosine RANBAXY LABORATORIES LIMITED (IN) 2014-06-10 US disclosed
US-20130072681-A1 PROCESS FOR STEREOSELECTIVE SYNTHESIS OF 5-FLUORO-1-(2R,5S)-[2-(HYDROXYMETHYL)-1,3-OXATHIOLAN-5-YL]CYTOSINE RANBAXY LABORATORIES LIMITED (IN) 2013-03-21 US disclosed
WO-2013021290-A1 A STEREOSELECTIVE PROCESS FOR PREPARATION OF 1,3-OXATHIOLANE NUCLEOSIDES LUPIN LIMITED (IN) 2013-02-14 WO disclosed
EP-2542551-A1 A PROCESS FOR STEREOSELECTIVE SYNTHESIS OF 5-FLUORO-1-(2R,5S)-[2-(HYDROXYMETHYL)-1,3-OXATHIOLAN-5-YL]CYTOSINE Ranbaxy Laboratories Limited (IN) 2013-01-09 EP disclosed
WO-2011107920-A1 A PROCESS FOR STEREOSELECTIVE SYNTHESIS OF 5-FLUORO-1-(2R,5S)-[2-(HYDROXYMETHYL)-1,3-OXATHIOLAN-5-YL]CYTOSINE RANBAXY LABORATORIES LIMITED (IN) 2011-09-09 WO disclosed
CN-1109030-C Processes for preparing intermediate product used in method of diastereoselective syntheses of nucleosides IAF BIOCHEM INT (CA) 2003-05-21 CN disclosed
CN-1097049-C Processes for preparing intermediate product used in method of diastereoselective syntheses of nucleosides IAF BIOCHEM INT (CA) 2002-12-25 CN disclosed
CN-1083450-C Processes for preparing intermediate product used in method of diastereoselective syntheses of nucleosides IAF BIOCHEM INT (CA) 2002-04-24 CN disclosed
CN-1050603-C Process for the preparation of intermediates used in a process for the diastereoselective synthesis of nucleosides IAF BIOCHEM INT (CA) 2000-03-22 CN disclosed
CN-1229078-A Processes for preparing intermediate product used in method of diastereoselective syntheses of nucleosides IAF BIOCHEM INT (CA) 1999-09-22 CN disclosed
CN-1229079-A Processes for preparing intermediate product used in method of diastereoselective syntheses of nucleosides IAF BIOCHEM INT (CA) 1999-09-22 CN disclosed
CN-1229080-A Processes for preparing intermediate product used in method of diastereoselective syntheses of nucleosides IAF BIOCHEM INT (CA) 1999-09-22 CN disclosed
CN-1038591-C Process for diastereoselective synthesis of nucleosides IAF BIOCHEM INT (CA) 1998-06-03 CN disclosed
CN-1116204-A Process for diastereoselective synthesis of nucleosides IAF BIOCHEM INT (CA) 1996-02-07 CN disclosed
CN-1067654-A Process for diastereoselective synthesis of nucleosides IAF BIOCHEM INT (CA) 1993-01-06 CN disclosed