SCHEMBL7023950

SCHEMBL7023950

CCOC(=O)/C=C\C1OC(C)O1

nearest known ligand 0.47

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
HCAR2 Q8TDS4 2/20 0.47
MAPT P10636 4/20 0.40
L3MBTL1 Q9Y468 3/20 0.39
CA12 O43570 1/20 0.38
CA1 P00915 1/20 0.38
CA2 P00918 1/20 0.38
CA7 P43166 1/20 0.38
CA9 Q16790 1/20 0.38
CA14 Q9ULX7 1/20 0.38
NPSR1 Q6W5P4 1/20 0.37
TDP1 Q9NUW8 1/20 0.36
ALDH1A1 P00352 2/20 0.36
TTR P02766 1/20 0.35
DPP4 P27487 1/20 0.35
ATM Q13315 1/20 0.34
LMNA P02545 1/20 0.33
MDM2 Q00987 1/20 0.33
CYP3A4 P08684 1/20 0.33

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
SCHEMBL8242959 1.00 HCAR2 (0.47) HCAR2MAPTL3MBTL1CA12CA1
SCHEMBL13285790 0.88 HCAR2 (0.43) HCAR2MAPTL3MBTL1CA12CA1
SCHEMBL8179462 0.84 MAPT (0.59) HCAR2MAPTL3MBTL1CA12CA1
SCHEMBL19637533 0.79 HCAR2 (0.48) HCAR2MAPTL3MBTL1CA12CA1
SCHEMBL13182144 0.75 ALDH1A1 (0.40) ALDH1A1LMNA
Diethyl Maleate SCHEMBL2015896 0.72 HCAR2 (0.80) HCAR2MAPTCA12CA1CA2
Diethyl Maleate SCHEMBL43033 0.72 HCAR2 (0.80) HCAR2MAPTCA12CA1CA2
Diethyl Maleate SCHEMBL2015895 0.72 HCAR2 (0.80) HCAR2MAPTCA12CA1CA2
Diethyl Maleate SCHEMBL42602 0.72 HCAR2 (0.80) HCAR2MAPTCA12CA1CA2
Diethyl Maleate SCHEMBL60423 0.72 HCAR2 (0.80) HCAR2MAPTCA12CA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8183019-B2 (3R,4R)-3-hydroxy-4-hydroxymethylpyrrolidine or (3S,4S)-3-hydroxy-4-hydroxymethylpyrrolidine; enzyme-catalysed enantioselective hydrolysis of a racemic 3,4-trans-disubstituted pyrrolidinone; for purine nucleoside phosphorylase (PNP) inhibitors INDUSTRIAL RESEARCH LIMITED (NZ) 2012-05-22 US disclosed
US-20080280334-A1 Method for Preparing 3-Hydroxy-4-Hydroxymethyl-Pyrrolidine Compounds ALBERT EINSTEIN COLLEGE OF MEDICINE 2008-11-13 US disclosed
WO-2007048225-A1 A 4-OXO-1- (3-SUBSTITUTED PHENYL) -1, 4-DIHYDRO-1, 8-NAPHTHYRIDINE-3-CARBOXAMIDE PHOSPHODIESTERASE-4-INHIBITOR AND A METHOD OF PREPARING SAME MERCK FROSST CANADA LTD. (CA) 2007-05-03 WO disclosed
WO-2007050576-A2 A METHOD OF PREPARING A 4-OXO-1- (3 SUBSTITUTED PHENYL) -1, 4-DIHYDRO-1, 8-NAPHTHYRIDINE-3- CARBOXAMIDE PHOSPHODIESTERASE-4 INHIBITOR MERCK & CO., INC. (US) 2007-05-03 WO 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-20080280334-A1 Method for Preparing 3-Hydroxy-4-Hydroxymethyl-Pyrrolidine Compounds HPD, DHPS, CYP3A5 HCAR2 1091/4885MAPT 4323/4885L3MBTL1 4459/4885

“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.