SCHEMBL14536556

SCHEMBL14536556

B[C@@H]1O[C@H](CO)[C@H](OCC)C1O

nearest known ligand 0.38

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
▸ MAPK1 P28482 1/20 0.34
▸ LGALS8 O00214 3/20 0.33
▸ LGALS3 P17931 1/20 0.33
▸ LGALS4 P56470 1/20 0.33
▸ L3MBTL1 Q9Y468 1/20 0.33
▸ GJB2 P29033 1/20 0.32
▸ CA1 P00915 1/20 0.32
▸ CA2 P00918 1/20 0.32
▸ CA9 Q16790 1/20 0.32
▸ GAA P10253 1/20 0.32
▸ MAPT P10636 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
SCHEMBL15304344 1.00 MAPK1 (0.34) MAPK1LGALS8LGALS3LGALS4L3MBTL1
SCHEMBL9971203 1.00 MAPK1 (0.34) MAPK1LGALS8LGALS3LGALS4L3MBTL1
SCHEMBL25597683 0.86 GJB2 (0.38) MAPK1LGALS8LGALS3LGALS4GJB2
SCHEMBL15935858 0.85 LGALS8 (0.41) MAPK1LGALS8LGALS3L3MBTL1CA1
SCHEMBL13073700 0.81 LGALS8 (0.44) MAPK1LGALS8LGALS3LGALS4L3MBTL1
SCHEMBL10820762 0.81 SLC2A1 (0.37) LGALS8LGALS3LGALS4GAA
SCHEMBL26262226 0.81 LGALS3 (0.40) MAPK1LGALS8LGALS3LGALS4L3MBTL1
SCHEMBL9968286 0.81 LGALS8 (0.31) MAPK1LGALS8LGALS3LGALS4L3MBTL1
SCHEMBL14511583 0.81 L3MBTL1 (0.36) LGALS8LGALS3LGALS4L3MBTL1MAPT
SCHEMBL13241371 0.81 LGALS8 (0.31) MAPK1LGALS8LGALS3LGALS4L3MBTL1

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-20070100138-A1 Monomer compositions for the synthesis of polynucleotides, methods of synthesis, and methods of deprotection THE REGENTS OF THE UNIVERSITY OF COLORADO 2007-05-03 — — US disclosed
US-20070100137-A1 Solutions, methods, and processes for deprotection of polynucleotides THE REGENTS OF THE UNIVERSITY OF COLORADO 2007-05-03 — — US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20070100138-A1 Monomer compositions for the synthesis of polynucleotides, methods of synthesis, and methods of deprotection POLN, NT5C3B, PCNA MAPK1 3279/4885LGALS8 2402/4885LGALS3 3294/4885
US-20070100137-A1 Solutions, methods, and processes for deprotection of polynucleotides POLN, POLRMT, POLM MAPK1 4161/4885LGALS8 1120/4885LGALS3 1778/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.

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