SCHEMBL4332813

SCHEMBL4332813

COc1ccccc1C(O)(c1ccccc1OC)[C@H](NC(=O)C(=O)N[C@H](c1ccccc1)C(O)(c1ccccc1OC)c1ccccc1OC)c1ccccc1

nearest known ligand 0.46

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.46
HPGD P15428 1/20 0.46
GAA P10253 3/20 0.44
KMT2A Q03164 9/20 0.43
MEN1 O00255 7/20 0.43
HTT P42858 3/20 0.42
L3MBTL1 Q9Y468 1/20 0.41
RXFP1 Q9HBX9 1/20 0.41
RCE1 Q9Y256 1/20 0.40
ATM Q13315 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
SCHEMBL4339894 0.89 ALDH1A1 (0.44) ALDH1A1HPGDGAAKMT2AMEN1
SCHEMBL4337750 0.88 ALDH1A1 (0.45) ALDH1A1HPGDGAAKMT2AMEN1
SCHEMBL4348990 0.84 MMP9 (0.49) ALDH1A1GAAKMT2AMEN1
SCHEMBL1153344 0.84 ALDH1A1 (0.40) ALDH1A1HPGDGAAKMT2AMEN1
SCHEMBL1153692 0.82 HTT (0.39) ALDH1A1HPGDGAAKMT2AMEN1
SCHEMBL1152551 0.82 L3MBTL1 (0.41) ALDH1A1HPGDGAAKMT2AMEN1
SCHEMBL1153308 0.81 L3MBTL1 (0.40) ALDH1A1HPGDGAAKMT2AMEN1
SCHEMBL4350908 0.81 GAA (0.47) ALDH1A1HPGDGAAKMT2AMEN1
SCHEMBL4337462 0.79 MEN1 (0.49) ALDH1A1GAAKMT2AMEN1L3MBTL1
SCHEMBL4339805 0.78 GAA (0.45) ALDH1A1HPGDGAAKMT2AMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7612236-B2 Method for producing optically active bisamidoalcohol compound SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2009-11-03 US disclosed
US-20070100163-A1 Reacting an optically active aminoalcohol compound with a diester compound in the presence of a lithium compound wherein the lithium compound is selected from lithium hydroxide, a lithium alkoxide and a lithium halide; product can be efficiently and inexpensively produced SUMITOMO CHEMICAL COMPANY, LIMITED 2007-05-03 US disclosed
EP-1698616-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE BISAMIDO ALCOHOL COMPOUND Sumitomo Chemical Company, Limited (JP) 2006-09-06 EP 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-20070100163-A1 Reacting an optically active aminoalcohol compound with a diester compound in the presence of a lithium compound wherein the lithium compound is selected from lithium hydroxide, a lithium alkoxide and a lithium halide; product can be efficiently and inexpensively produced CCNL2, ARL1, ACSL3 ALDH1A1 1303/4885HPGD 4281/4885GAA 2869/4885

“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.