SCHEMBL7522263

SCHEMBL7522263

O=C1O[C@@H](COCc2ccccc2)[C@@H](OCc2ccccc2)[C@@H]1OCc1ccccc1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
BCHE P06276 2/20 0.54
ACHE P22303 2/20 0.54
LMNA P02545 1/20 0.45
HTR1A P08908 1/20 0.42
TACR2 P21452 3/20 0.42
NT5E P21589 1/20 0.42
PDPK1 O15530 1/20 0.40
MTOR P42345 1/20 0.40
CA1 P00915 1/20 0.40
CA2 P00918 1/20 0.40
CA9 Q16790 1/20 0.40
CTRB1 P17538 1/20 0.40
PSEN1 P49768 1/20 0.40
PSEN2 P49810 1/20 0.40
APH1B Q8WW43 1/20 0.40
NCSTN Q92542 1/20 0.40
APH1A Q96BI3 1/20 0.40
PSENEN Q9NZ42 1/20 0.40
FASN P49327 1/20 0.39
TSHR P16473 1/20 0.39

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
SCHEMBL7525585 1.00 BCHE (0.54) BCHEACHELMNAHTR1ATACR2
SCHEMBL14571363 1.00 BCHE (0.54) BCHEACHELMNAHTR1ATACR2
SCHEMBL13591463 1.00 BCHE (0.54) BCHEACHELMNAHTR1ATACR2
SCHEMBL30801101 1.00 BCHE (0.54) BCHEACHELMNAHTR1ATACR2
SCHEMBL3304205 1.00 BCHE (0.54) BCHEACHELMNAHTR1ATACR2
SCHEMBL18497676 1.00 BCHE (0.54) BCHEACHELMNAHTR1ATACR2
SCHEMBL18852561 1.00 BCHE (0.54) BCHEACHELMNAHTR1ATACR2
SCHEMBL12896359 1.00 BCHE (0.54) BCHEACHELMNAHTR1ATACR2
SCHEMBL22796970 1.00 BCHE (0.54) BCHEACHELMNAHTR1ATACR2
SCHEMBL1087871 0.96 BCHE (0.56) BCHEACHELMNAHTR1ATACR2

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-6448415-B1 Chirality conversion method in lactone sugar compounds HANCHEM CO., LTD. (KR) 2002-09-10 US disclosed
US-20020028955-A1 Chirality conversion method in lactone sugar compounds HANCHEM CO., LTD. (KR) 2002-03-07 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 (1 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-20020028955-A1 Chirality conversion method in lactone sugar compounds TREH, FUT6, TALDO1 BCHE 798/4885ACHE 507/4885LMNA 1562/4885

“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.