Lithium

Lithium

SCHEMBL7065338

CCOC(=O)c1sc(C(=O)OCC)c(O)c1O.[Li].[Li]

nearest known ligand 0.55

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GAA P10253 2/20 0.55
KMT2A Q03164 2/20 0.55
HSD17B10 Q99714 1/20 0.55
MAPT P10636 2/20 0.50
NPC1 O15118 1/20 0.50
RAB9A P51151 1/20 0.50
MC4R P32245 1/20 0.50
ALDH1A1 P00352 6/20 0.49
CYP1A2 P05177 1/20 0.49
HPGD P15428 3/20 0.48
SMN1; SMN2 Q16637 1/20 0.48
GSK3B P49841 1/20 0.47
MEN1 O00255 1/20 0.47
KDM4E B2RXH2 1/20 0.46
TRPM8 Q7Z2W7 2/20 0.45
CDC7 O00311 2/20 0.45
DBF4 Q9UBU7 2/20 0.45
TSHR P16473 1/20 0.45
LMNA P02545 1/20 0.45
ALOX15 P16050 1/20 0.45

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
SCHEMBL1141274 0.98 GAA (0.56) GAAKMT2AHSD17B10MAPTNPC1
Potassium SCHEMBL7063916 0.96 GAA (0.55) GAAKMT2AHSD17B10MAPTNPC1
SCHEMBL1726035 0.96 GAA (0.55) GAAKMT2AHSD17B10MAPTNPC1
SCHEMBL14650156 0.90 ALDH1A1 (0.51) GAAKMT2AHSD17B10MAPTNPC1
SCHEMBL6206616 0.90 ALDH1A1 (0.54) GAAKMT2AHSD17B10MAPTNPC1
SCHEMBL13359464 0.88 GAA (0.49) GAAKMT2AHSD17B10MAPTNPC1
SCHEMBL10925924 0.88 MAPT (0.56) GAAKMT2AHSD17B10MAPTNPC1
Protiofate SCHEMBL871311 0.81 MAPT (0.50) GAAKMT2AHSD17B10MAPTALDH1A1
SCHEMBL11099233 0.80 ALDH1A1 (0.48) GAAKMT2AHSD17B10MAPTNPC1
SCHEMBL15210472 0.80 MAPT (0.61) GAAKMT2AHSD17B10MAPTNPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6608164-B2 Diaryl carbonate reacted with dihydroxy aromatic compounds in the presence of a transesterification catalyst; furan diol derivative is dimethyl 3,4-dihydroxy-2,5-furandiacarboxylate disodium salt GENERAL ELECTRIC COMPANY 2003-08-19 US disclosed
US-20030114633-A1 Salts of heterocyclic diols as catalysts for melt polycarbonate GENERAL ELECTRIC COMPANY 2003-06-19 US disclosed