SCHEMBL2215767

SCHEMBL2215767

CC(C)CCCOC(=O)[C@@H](N)Cc1ccccc1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ANPEP P15144 3/20 0.53
RNPEP Q9H4A4 3/20 0.53
DNPEP Q9ULA0 3/20 0.53
ALPI P09923 1/20 0.51
PKM P14618 1/20 0.51
PTGS1 P23219 1/20 0.51
XIAP P98170 1/20 0.51
SLC7A5 Q01650 1/20 0.51
LTA4H P09960 2/20 0.47
LAP3 P28838 3/20 0.46
SLC15A1 P46059 1/20 0.45
SLC6A2 P23975 2/20 0.43
TAAR1 Q96RJ0 2/20 0.43
MAOA P21397 1/20 0.43
SLC6A4 P31645 1/20 0.43
SLC6A3 Q01959 1/20 0.43
SIGMAR1 Q99720 1/20 0.43
CYP2A6 P11509 1/20 0.43
ADORA2A P29274 1/20 0.43
ADORA1 P30542 1/20 0.43

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
SCHEMBL19361331 0.91 ANPEP (0.56) ANPEPRNPEPDNPEPALPIPKM
SCHEMBL2214633 0.89 ANPEP (0.49) ANPEPRNPEPDNPEPALPIPKM
SCHEMBL2214636 0.89 ANPEP (0.49) ANPEPRNPEPDNPEPALPIPKM
SCHEMBL14095409 0.88 ALPI (0.61) ANPEPALPIPKMPTGS1XIAP
SCHEMBL6368998 0.88 ALPI (0.61) ALPIPKMPTGS1XIAPSLC7A5
SCHEMBL15590174 0.86 ALPI (0.59) ALPIPKMPTGS1XIAPSLC7A5
SCHEMBL14095415 0.86 ALPI (0.59) ALPIPKMPTGS1XIAPSLC7A5
SCHEMBL19167232 0.86 ALPI (0.59) ALPIPKMPTGS1XIAPSLC7A5
SCHEMBL26231121 0.86 ALPI (0.59) ALPIPKMPTGS1XIAPSLC7A5
SCHEMBL28695478 0.86 ALPI (0.49) ANPEPRNPEPDNPEPALPIPKM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20130245246-A1 POLYSACCHARIDES COMPRISING CARBOXYL FUNCTIONAL GROUPS SUBSTITUTED BY A HYDROPHOBIC ALCOHOL DERIVATIVE ADOCIA (FR) 2013-09-19 US disclosed
US-8426382-B2 Polysaccharides comprising carboxyl functional groups substituted by a hydrophobic alcohol derivative ADOCIA (FR) 2013-04-23 US disclosed
US-20110178011-A1 Polysaccharide/BMP complexes which are soluble at physiological pH ADOCIA (FR) 2011-07-21 US disclosed
US-20100305035-A1 Polysaccharides comprising carboxyl functional groups substituted by a hydrophobic alcohol derivative ADOCIA (FR) 2010-12-02 US disclosed
US-20100167991-A1 Polysaccharides comprising carboxyl functional groups substituted by a hydrophobic alcohol derivative ADOCIA (FR) 2010-07-01 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 (4 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-20130245246-A1 POLYSACCHARIDES COMPRISING CARBOXYL FUNCTIONAL GROUPS SUBSTITUTED BY A HYDROPHOBIC ALCOHOL DERIVATIVE CD44, B3GAT3, UGCG ANPEP 3272/4885RNPEP 4341/4885DNPEP 3844/4885
US-20100167991-A1 Polysaccharides comprising carboxyl functional groups substituted by a hydrophobic alcohol derivative CD44, ADH1C, ADH5 ANPEP 134/4885RNPEP 1399/4885DNPEP 339/4885
US-20100305035-A1 Polysaccharides comprising carboxyl functional groups substituted by a hydrophobic alcohol derivative CD44, ADH1C, ADH5 ANPEP 134/4885RNPEP 1399/4885DNPEP 339/4885
US-20110178011-A1 Polysaccharide/BMP complexes which are soluble at physiological pH BMP1, BMP2, BMP6 ANPEP 628/4885RNPEP 922/4885DNPEP 1318/4885

“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.