SCHEMBL5246158

SCHEMBL5246158

CS(=O)(=O)OC1O[C@H](CO)[C@@H](O)[C@H]1O

nearest known ligand 0.55

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
▸ L3MBTL1 Q9Y468 1/20 0.46
▸ MAPT P10636 1/20 0.45
▸ ALDH1A1 P00352 1/20 0.43
▸ GAA P10253 1/20 0.41
▸ TYR P14679 1/20 0.41
▸ SLC28A3 Q9HAS3 2/20 0.41
▸ FGF1 P05230 1/20 0.41
▸ CA12 O43570 3/20 0.41
▸ CA1 P00915 3/20 0.41
▸ CA2 P00918 3/20 0.41
▸ CA9 Q16790 3/20 0.41
▸ POLB P06746 1/20 0.41
▸ PTPN1 P18031 1/20 0.41

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
SCHEMBL7759256 1.00 L3MBTL1 (0.46) L3MBTL1MAPTALDH1A1GAATYR
SCHEMBL27518974 1.00 L3MBTL1 (0.46) L3MBTL1MAPTALDH1A1GAATYR
SCHEMBL2244357 1.00 L3MBTL1 (0.46) L3MBTL1MAPTALDH1A1GAATYR
SCHEMBL9562278 0.98 L3MBTL1 (0.49) L3MBTL1MAPTALDH1A1GAATYR
SCHEMBL8362539 0.98 L3MBTL1 (0.49) L3MBTL1MAPTALDH1A1GAATYR
SCHEMBL8362536 0.98 L3MBTL1 (0.49) L3MBTL1MAPTALDH1A1GAATYR
SCHEMBL6517774 0.86 L3MBTL1 (0.47) L3MBTL1MAPTALDH1A1GAATYR
SCHEMBL7259429 0.86 L3MBTL1 (0.47) L3MBTL1MAPTALDH1A1GAATYR
SCHEMBL4325452 0.83 L3MBTL1 (0.47) L3MBTL1MAPTGAATYRCA12
SCHEMBL2097041 0.83 L3MBTL1 (0.47) L3MBTL1MAPTGAATYRCA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2016097989-A1 PROCESS FOR THE PREPARATION OF GEMCITABINE HYDROCHLORIDE KARIMIAN KHASHAYAR (IR) 2016-06-23 — — WO disclosed
CN-101203525-B Method for preparing alpha-anomer enriched 2-deoxy-2, 2-difluoro-D-ribofuranosyl sulfonates and use thereof for preparing beta nucleosides SCINOPHARM TAIWAN LTD 2012-06-13 — — CN disclosed
CN-101010329-B Method for the preparation of 2'-deoxy-2',2'-difluoro cytidine HANMI PHARM IND CO LTD 2011-06-08 — — CN disclosed
CN-101203525-A Method for preparing alpha-anomer enriched 2-deoxy-2, 2-difluoro-D-ribofuranosyl sulfonates and use thereof for preparing beta nucleosides SCINOPHARM TAIWAN LTD (CN) 2008-06-18 — — CN disclosed
EP-1831236-A1 METHOD FOR THE PREPARATION OF 2'-DEOXY-2',2'-DIFLUOROCYTIDINE Hanmi Pharm. Co., Ltd. (KR) 2007-09-12 — — EP disclosed
CN-101010329-A Method for the preparation of 2'-deoxy-2',2'-difluoro cytidine HANMI PHARM IND CO LTD (KR) 2007-08-01 — — CN disclosed
WO-2006071090-A1 METHOD FOR THE PREPARATION OF 2'-DEOXY-2',2'-DIFLUOROCYTIDINE HANMI PHARM. CO., LTD. (KR) 2006-07-06 — — WO disclosed
WO-2006070985-A1 METHOD FOR THE PREPARATION OF 2#-DEOXY-2#,2#-DIFLUOROCYTIDINE HANMI PHARM. CO., LTD. (KR) 2006-07-06 — — WO disclosed
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