SCHEMBL5193894

SCHEMBL5193894

O=C(Cl)c1ccc(-c2ccc(Cl)cc2Cl)o1

nearest known ligand 0.77

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 9/20 0.60
MAPT P10636 7/20 0.60
NPC1 O15118 6/20 0.60
SMN1; SMN2 Q16637 6/20 0.60
RAB9A P51151 5/20 0.60
HTT P42858 4/20 0.60
POLB P06746 3/20 0.60
MEN1 O00255 2/20 0.60
KMT2A Q03164 2/20 0.60
PKM P14618 1/20 0.58
LMNA P02545 2/20 0.58
NPSR1 Q6W5P4 2/20 0.58
S1PR2 O95136 1/20 0.58
S1PR4 O95977 1/20 0.58
S1PR3 Q99500 1/20 0.58
S1PR5 Q9H228 1/20 0.58
HPGD P15428 6/20 0.57
TDP1 Q9NUW8 1/20 0.57
KDM4E B2RXH2 4/20 0.56
HSD11B1 P28845 1/20 0.56

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
SCHEMBL30775594 0.87 ALDH1A1 (0.66) ALDH1A1MAPTNPC1SMN1; SMN2RAB9A
SCHEMBL2636529 0.87 ALDH1A1 (0.66) ALDH1A1MAPTNPC1SMN1; SMN2RAB9A
SCHEMBL3057301 0.84 ALDH1A1 (0.46) ALDH1A1MAPTNPC1SMN1; SMN2RAB9A
SCHEMBL12092306 0.81 HSD11B1 (0.62) ALDH1A1MAPTNPC1SMN1; SMN2RAB9A
SCHEMBL4134141 0.80 MEN1 (0.44) ALDH1A1MAPTNPC1SMN1; SMN2RAB9A
SCHEMBL28269605 0.79 ALDH1A1 (0.75) ALDH1A1MAPTNPC1SMN1; SMN2RAB9A
SCHEMBL3063864 0.79 MAPT (0.65) ALDH1A1MAPTSMN1; SMN2RAB9AHTT
SCHEMBL31462930 0.75 ALDH1A1 (0.42) ALDH1A1MEN1KMT2ALMNANPSR1
SCHEMBL3325905 0.75 ALDH1A1 (0.61) ALDH1A1MAPTNPC1SMN1; SMN2RAB9A
SCHEMBL23859795 0.74 ALDH1A1 (0.41) ALDH1A1MEN1KMT2ALMNANPSR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070249670-A1 Glycogen Phosphorylase Inhibitor Compounds and Pharmaceutical Compositions Thereof SMITHKLINE BEECHAM CORPORATION (US) 2007-10-25 US disclosed
EP-1812383-A1 GLYCOGEN PHOSPHORYLASE INHIBITOR COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS THEREOF Smithkline Beecham Corporation (US) 2007-08-01 EP disclosed
WO-2006052722-A1 GLYCOGEN PHOSPHORYLASE INHIBITOR COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS THEREOF SMITHKLINE BEECHAM CORPORATION (US) 2006-05-18 WO disclosed
US-5214042-A Use of 5-phenyl-2-furan esters, amides and ketones as neuroprotective agents NORWICH EATON PHARMACEUTICALS, INC. (US) 1993-05-25 US disclosed
US-5118708-A USE OF 5-PHENYL-2-FURAN ESTERS, AMIDES AND KETONES AS NEUROPROTECTIVE AGENTS NORWICH EATON PHARMACEUTICALS, INC. (US) 1992-06-02 US disclosed
US-5023272-A Use of 5-phenyl-2-furan esters and amides as antiepileptic agents NORWICH EATON PHARMACEUTICALS, INC. (US) 1991-06-11 US disclosed
EP-0404231-A1 The use of 5-phenyl-2 furan esters and amides as antiepileptic agents Norwich Eaton Pharmaceuticals, Inc. (US) 1990-12-27 EP disclosed
EP-0404233-A2 Novel use of 5-phenyl-2-furan esters, amides and ketones as neuroprotective agents Norwich Eaton Pharmaceuticals, Inc. (US) 1990-12-27 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-20070249670-A1 Glycogen Phosphorylase Inhibitor Compounds and Pharmaceutical Compositions Thereof PYGM, PYGL, GYS1 ALDH1A1 2212/4885MAPT 1171/4885NPC1 1701/4885

“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.