SCHEMBL3302845

SCHEMBL3302845

COC(=O)CCCC(=O)c1cccc(OC)c1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CES2 O00748 1/20 0.56
CES1 P23141 1/20 0.56
CTNNB1 P35222 2/20 0.54
WNT3A P56704 2/20 0.54
NPC1 O15118 3/20 0.53
RAB9A P51151 2/20 0.53
POLB P06746 1/20 0.53
BLM P54132 1/20 0.53
SMN1; SMN2 Q16637 1/20 0.53
ALDH1A1 P00352 1/20 0.53
MAPT P10636 1/20 0.53
TDP1 Q9NUW8 1/20 0.53
PARP1 P09874 1/20 0.53
KMT2A Q03164 2/20 0.52
HTR1A P08908 1/20 0.52
ADRA2A P08913 1/20 0.52
DRD1 P21728 1/20 0.52
SLC6A2 P23975 1/20 0.52
SLC6A4 P31645 1/20 0.52
ADRA1A P35348 1/20 0.52

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
SCHEMBL4889161 0.97 CES2 (0.56) CES2CES1CTNNB1WNT3ANPC1
SCHEMBL30416977 0.91 CTNNB1 (0.60) CES2CES1CTNNB1WNT3ANPC1
SCHEMBL3588375 0.91 CTNNB1 (0.60) CES2CES1CTNNB1WNT3ANPC1
SCHEMBL28188567 0.86 PDE4B (0.67) CES2CES1CTNNB1WNT3ANPC1
SCHEMBL7389569 0.85 CES2 (0.56) CES2CES1CTNNB1WNT3ANPC1
SCHEMBL4638591 0.84 CES2 (0.59) CES2CES1CTNNB1WNT3ANPC1
SCHEMBL28133957 0.84 PARP1 (0.53) CES2CES1CTNNB1WNT3ANPC1
SCHEMBL2130116 0.84 CES2 (0.62) CES2CES1CTNNB1WNT3ANPC1
SCHEMBL30626936 0.84 CES2 (0.62) CES2CES1CTNNB1WNT3ANPC1
SCHEMBL4884872 0.83 PDE4B (0.62) CES2CES1CTNNB1WNT3ANPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-104250236-B γ hydrocarbon oxygen sulfonylmethyl gamma butyrolactone, the synthetic method of δ hydrocarbon oxygen sulfonylmethyl δ valerolactone 大连大学 2017-03-01 CN disclosed
US-8236818-B2 Substituted imidazopyridine derivatives as melanocortin-4 receptor antagonists SANTHERA PHARMACEUTICALS (SCHWEIZ) AG (CH) 2012-08-07 US disclosed
US-20100093697-A1 Substituted Imidazopyridine Derivatives As Melanocortin-4 Receptor Antagonists SANTHERA PHARMACEUTICALS (SCHWEIZ) AG (CH) 2010-04-15 US disclosed
EP-2144907-A1 SUBSTITUTED IMIDAZOPYRIDINE DERIVATIVES AS MELANOCORTIN-4 RECEPTOR ANTAGONISTS Santhera Pharmaceuticals (Schweiz) AG (CH) 2010-01-20 EP disclosed
WO-2008116665-A1 SUBSTITUTED IMIDAZOPYRIDINE DERIVATIVES AS MELANOCORTIN-4 RECEPTOR ANTAGONISTS SANTHERA PHARMACEUTICALS (SCHWEIZ) AG (CH) 2008-10-02 WO disclosed
EP-1974729-A1 Substituted imidazopyridine derivates as melanocortin- 4 receptor antagonists Santhera Pharmaceuticals (Schweiz) AG (CH) 2008-10-01 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-20100093697-A1 Substituted Imidazopyridine Derivatives As Melanocortin-4 Receptor Antagonists MC4R, MC3R, MC5R CES2 4645/4885CES1 4666/4885CTNNB1 3076/4885

“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.