SCHEMBL870879

SCHEMBL870879

O=S(=O)(O)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)O[C@@H]1CO

nearest known ligand 0.43

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
LGALS3 P17931 1/20 0.38
CA2 P00918 4/20 0.37
CA12 O43570 3/20 0.34
CA1 P00915 3/20 0.34
CA9 Q16790 3/20 0.34
CXCL10 P02778 1/20 0.33
CXCL8 P10145 1/20 0.33
CCL2 P13500 1/20 0.33
CCL5 P13501 1/20 0.33
CXCL12 P48061 1/20 0.33
FGF1 P05230 1/20 0.33
SLC2A1 P11166 1/20 0.33
BLM P54132 1/20 0.32

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
SCHEMBL28201089 1.00 LGALS3 (0.38) LGALS3CA2CA12CA1CA9
SCHEMBL2186684 1.00 LGALS3 (0.38) LGALS3CA2CA12CA1CA9
SCHEMBL3914085 1.00 LGALS3 (0.38) LGALS3CA2CA12CA1CA9
SCHEMBL7646025 0.89 LGALS8 (0.44) LGALS3CA2CA12CA1CA9
SCHEMBL25241935 0.88 CA2 (0.47) LGALS3CA2CA12CA1CA9
SCHEMBL3653142 0.87 CA2 (0.40) LGALS3CA2CA12CA1CA9
SCHEMBL1116556 0.87 CA2 (0.40) LGALS3CA2CA12CA1CA9
SCHEMBL22121795 0.87 CA2 (0.40) LGALS3CA2CA12CA1CA9
SCHEMBL8003273 0.87 CA2 (0.40) LGALS3CA2CA12CA1CA9
SCHEMBL1116554 0.87 CA2 (0.40) LGALS3CA2CA12CA1CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026087501-A1 ANTIGEN MULTIMERS FOR DETECTION OF ANTIGEN-SPECIFIC CHIMERIC ANTIGEN RECEPTOR (CAR) T CELLS IMMUDEX APS (DK) 2026-04-30 WO disclosed
CN-118987000-A Application of kappa-carrageenan tetrasaccharide in preparation of medicines or cosmetics 集美大学 2024-11-22 CN disclosed
US-20240082276-A1 LIPID COMPOSITIONS AKER BIOMARINE HUMAN INGREDIENTS AS (NO) 2024-03-14 US disclosed
CN-115505049-B Porphyra haitanensis polysaccharide and Porphyra haitanensis polysaccharide effervescent tablet with blood lipid reducing effect and preparation method thereof 福建农林大学 2023-12-08 CN disclosed
US-11819509-B2 Lipid compositions AKER BIOMARINE ANTARCTIC AS (NO) 2023-11-21 US disclosed
EP-3090729-B1 EMULSION VITUX GROUP AS (NO) 2023-06-07 EP disclosed
EP-3008156-B1 LIPID EXTRACTION PROCESSES AKER BIOMARINE ANTARCTIC AS (NO) 2023-06-07 EP disclosed
US-11578289-B2 Lipid extraction processes AKER BIOMARINE ANTARCTIC AS (NO) 2023-02-14 US disclosed
US-20220409687-A1 GELLED OIL-IN-WATER EMULSION COMPRISING AT LEAST ONE CANNABINOID VITUX GROUP AS (NO) 2022-12-29 US disclosed
CN-115505049-A Porphyra haitanensis polysaccharide and porphyra haitanensis polysaccharide effervescent tablets with blood fat reducing effect and preparation method thereof 福建农林大学 2022-12-23 CN disclosed
EP-1115748-B1 CARRAGEENAN COMPOSITIONS, AND PROCESSES FOR THEIR PRODUCTION CP KELCO APS (DK) 2004-10-20 EP disclosed
EP-1412336-A1 PEPTOID COMPOUNDS UNIVERSITY OF WOLLONGONG (AU) 2004-04-28 EP disclosed
EP-1115850-A4 MICROBEAD IMMOBILIZATION OF ENZYMES FMC CORP (US) 2003-05-21 EP disclosed
WO-2003002545-A1 PEPTOID COMPOUNDS UNIVERSITY OF WOLLONGONG (AU) 2003-01-09 WO disclosed
US-20020068339-A1 Microbead immobilization of enzymes FMC CORPORATION 2002-06-06 US disclosed
US-6268191-B1 DEHYDRATING HYDROCOLLOID GEL BEADS HAVING A NETWORK STRUCTURE CAPABLE OF SWELLING IN AQUEOUS MEDIA, IMBIBING INTO THE GEL BEADS AN ENZYME IN AN AQEOUS SOLUTION TO FORM IMBIBED GEL BEADS, RECOVER IMBIBED BEADS WITH IMMOBILIZED ENZYME FMC CORPORATION 2001-07-31 US disclosed
EP-1115850-A1 MICROBEAD IMMOBILIZATION OF ENZYMES FMC CORPORATION (US) 2001-07-18 EP disclosed
WO-2000017333-A1 MICROBEAD IMMOBILIZATION OF ENZYMES FMC CORPORATION (US) 2000-03-30 WO disclosed
US-5658893-A Method for inhibition of rotavirus infection with carrageenan ABBOTT LABORATORIES (US) 1997-08-19 US disclosed
WO-1996030027-A1 INHIBITION OF ROTAVIRUS INFECTION WITH CARRAGEENAN OR DEXTRAN SULFATE ABBOTT LABORATORIES (US) 1996-10-03 WO disclosed