SCHEMBL5179547

SCHEMBL5179547

CC(=O)CCC(=O)OC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1OC(=O)CCC(C)=O

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AHCY P23526 3/20 0.60
HSP90B1 P14625 1/20 0.56
PRKACA P17612 2/20 0.56
MARS1 P56192 1/20 0.55
ADORA1 P30542 3/20 0.54
P2RY1 P47900 3/20 0.54
SMN1; SMN2 Q16637 2/20 0.54
DNPH1 O43598 1/20 0.54
PRKAB2 O43741 1/20 0.54
TRPM2 O94759 1/20 0.54
LDHA P00338 1/20 0.54
ADRB2 P07550 1/20 0.54
FBP1 P09467 1/20 0.54
SRC P12931 1/20 0.54
P2RY2 P41231 1/20 0.54
PRKAG1 P54619 1/20 0.54
PRKAA2 P54646 1/20 0.54
PDE4D Q08499 1/20 0.54
KCNH2 Q12809 1/20 0.54
PRKAA1 Q13131 1/20 0.54

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
SCHEMBL10587742 0.92 AHCY (0.61) AHCYHSP90B1PRKACAMARS1ADORA1
SCHEMBL1066705 0.91 PRKACA (0.66) AHCYHSP90B1PRKACAMARS1ADORA1
SCHEMBL15293701 0.90 AHCY (0.51) AHCYHSP90B1PRKACAMARS1ADORA1
SCHEMBL15293700 0.90 AHCY (0.51) AHCYHSP90B1PRKACAMARS1ADORA1
SCHEMBL22875576 0.89 EHMT1 (0.60) AHCYHSP90B1PRKACA
SCHEMBL22875787 0.89 EHMT1 (0.60) AHCYHSP90B1PRKACA
SCHEMBL11686718 0.88 AHCY (0.62) AHCYHSP90B1PRKACAMARS1ADORA1
SCHEMBL23982338 0.88 AHCY (0.51) AHCYHSP90B1PRKACAMARS1ADORA1
SCHEMBL15297002 0.87 AHCY (0.49) AHCYHSP90B1PRKACAMARS1ADORA1
SCHEMBL15293696 0.86 AHCY (0.50) AHCYPRKACAMARS1ADORA1P2RY1

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
EP-1379536-A4 BUILDING BLOCKS FOR THE SOLUTION PHASE SYNTHESIS OF OLIGONUCLEOTIDES ISIS PHARMACEUTICALS INC (US) 2007-07-25 EP disclosed
US-20040096947-A1 Building blocks for the solution phase synthesis of oligonucleotides SANGHVI YOGESH S (US) 2004-05-20 US disclosed
EP-1379536-A1 BUILDING BLOCKS FOR THE SOLUTION PHASE SYNTHESIS OF OLIGONUCLEOTIDES ISIS Pharmaceuticals, Inc. (US) 2004-01-14 EP disclosed
US-6677120-B2 PREFERENTIAL DEPROTECTION OF A 3',5'-DI-O- LEVULINYL NUCLEOSIDE; OBTAIN 3',5'-DI-O-LEVULINYL NUCLEOSIDE, INCUBATE WITH LIPASE, RECOVER 3'-O-LEVULINYL AND 5'-O-LEVULINYL NUCLEOSIDE ISIS PHARMACEUTICALS, INC. 2004-01-13 US disclosed
WO-2002079215-A1 BUILDING BLOCKS FOR THE SOLUTION PHASE SYNTHESIS OF OLIGONUCLEOTIDES ISIS PHARMACEUTICALS, INC. (US) 2002-10-10 WO disclosed
US-20020142307-A1 Building blocks for the solution phase synthesis of oligonucleotides IONIS PHARMACEUTICALS, INC. 2002-10-03 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 (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-20040096947-A1 Building blocks for the solution phase synthesis of oligonucleotides RNGTT, TYMS, POLB AHCY 561/4885HSP90B1 4676/4885PRKACA 3176/4885

“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.