SCHEMBL7570048

SCHEMBL7570048

CC(=O)C(O)[C@@H](O)[C@@](O)(C(C)=O)[C@@](O)(C(C)=O)[C@@](O)(C=O)C(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
SCHEMBL28051640 1.00
SCHEMBL845646 1.00
SCHEMBL6568063 1.00
SCHEMBL9225223 0.84
SCHEMBL29041610 0.84
Hydrochloric Acid SCHEMBL9645090 0.79
SCHEMBL28516157 0.77
SCHEMBL28516158 0.77
SCHEMBL28557963 0.73 USP2 (0.33)
SCHEMBL29645196 0.73 USP2 (0.33)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0788504-B1 STEREODIRECTED PROCESS FOR SYNTHESIS OF ALPHA-N-ACETYLGALACTOSAMINIDES BIOMIRA INC (CA) 2002-09-04 EP disclosed
US-5837830-A CHEMICAL INTERMEDIATES OFR PREPARING OLIGOSACCHARIDES, GLYCOSYLAMINO ACIDS, GLYCOPEPTIDES WHICH ARE USEFUL IN TREATING AND DIAGNOSING CANCERS AND OTHER DISEASES BIOMIRA, INC. (CA) 1998-11-17 US disclosed
EP-0788504-A1 STEREODIRECTED PROCESS FOR SYNTHESIS OF ALPHA-N-ACETYLGALACTOSAMINIDES BIOMIRA, INC. (CA) 1997-08-13 EP disclosed
US-5527891-A REACTING N-ACETYLGALACTOSAMINE WITH DIALKYL ACETAL OF ALDEHYDE OR KETONE, PROTECTING 3-HYDROXY GROUP, INTRODUCING ANOMERIC GROUP TO FORM GLYCOSYL DONOR, REACTING WITH ALCOHOL BIOMIRA, INC. (CA) 1996-06-18 US disclosed
WO-1995024701-A1 STEREODIRECTED PROCESS FOR SYNTHESIS OF α-N-ACETYLGALACTOSAMINIDES BIOMIRA, INC. (CA) 1995-09-14 WO disclosed