SCHEMBL1318516

SCHEMBL1318516

CC(=O)OCO[C@@H]1[C@@H]2O[Si](C(C)C)(C(C)C)O[Si](C(C)C)(C(C)C)OC[C@H]2O[C@H]1n1ccc(=O)[nH]c1=O

nearest known ligand 0.41

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
▸ TDP1 Q9NUW8 2/20 0.41
▸ P2RY2 P41231 3/20 0.33
▸ SLC28A1 O00337 1/20 0.33
▸ SLC28A2 O43868 1/20 0.33
▸ SLC29A1 Q99808 1/20 0.33
▸ SLC28A3 Q9HAS3 1/20 0.33
▸ P2RY6 Q15077 1/20 0.33
▸ P2RY14 Q15391 3/20 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
SCHEMBL1317537 0.93 TDP1 (0.36) TDP1P2RY2SLC28A1SLC28A2SLC29A1
SCHEMBL1316980 0.93 TDP1 (0.36) TDP1P2RY2SLC28A1SLC28A2SLC29A1
SCHEMBL1319978 0.91 TDP1 (0.35) TDP1P2RY2SLC28A1SLC28A2SLC29A1
SCHEMBL26780258 0.90 TDP1 (0.41) TDP1P2RY2SLC28A1SLC28A2SLC29A1
SCHEMBL706579 0.90 TDP1 (0.41) TDP1P2RY2SLC28A1SLC28A2SLC29A1
SCHEMBL25608882 0.87 TDP1 (0.35) TDP1P2RY2SLC28A1SLC28A2SLC29A1
SCHEMBL29707946 0.87 TDP1 (0.35) TDP1P2RY2SLC28A1SLC28A2SLC29A1
SCHEMBL16243030 0.86 SLC28A1 (0.33) TDP1P2RY2SLC28A1SLC28A2SLC29A1
SCHEMBL12212785 0.86 TDP1 (0.36) TDP1P2RY2SLC28A1SLC28A2SLC29A1
SCHEMBL15261259 0.86 TDP1 (0.33) TDP1P2RY2SLC28A1SLC28A2SLC29A1

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-8536318-B2 Chemical RNA synthesis method CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2013-09-17 — — US disclosed
EP-2303905-B1 CHEMICAL RNA SYNTHESIS METHOD CENTRE NAT RECH SCIENT (FR) 2012-11-28 — — EP disclosed
US-20110275793-A1 Chemical RNA Synthesis Method CHEMGENES CORPORATION 2011-11-10 — — US disclosed
EP-2303905-A1 CHEMICAL RNA SYNTHESIS METHOD Centre National de la Recherche Scientifique (FR) 2011-04-06 — — EP disclosed
WO-2009144418-A1 CHEMICAL RNA SYNTHESIS METHOD CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2009-12-03 — — 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-20110275793-A1 Chemical RNA Synthesis Method NSUN3, POLR2E, POLR2H TDP1 2936/4885P2RY2 3875/4885SLC28A1 3400/4885

“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.

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