SCHEMBL1763062

SCHEMBL1763062

COc1nc(N)nc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)[C@@H](O)[C@@H]1O

nearest known ligand 0.69

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ P2RY1 P47900 6/20 0.69
▸ P2RX3 P56373 3/20 0.69
▸ ENPP1 P22413 2/20 0.69
▸ P2RX1 P51575 2/20 0.69
▸ P2RX4 Q99571 2/20 0.69
▸ P2RY11 Q96G91 2/20 0.69
▸ P2RY6 Q15077 1/20 0.69
▸ P2RY12 Q9H244 2/20 0.68
▸ RNASEL Q05823 4/20 0.65
▸ P2RY2 P41231 2/20 0.63
▸ P2RX2 Q9UBL9 2/20 0.63
▸ SRC P12931 1/20 0.63
▸ ALDH1A1 P00352 1/20 0.63
▸ SMN1; SMN2 Q16637 1/20 0.63
▸ GPR17 Q13304 2/20 0.61
▸ NT5E P21589 2/20 0.61

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
SCHEMBL1527226 1.00 P2RY1 (0.69) P2RY1P2RX3ENPP1P2RX1P2RX4
SCHEMBL29471281 1.00 P2RY1 (0.69) P2RY1P2RX3ENPP1P2RX1P2RX4
SCHEMBL14948878 1.00 P2RY1 (0.69) P2RY1P2RX3ENPP1P2RX1P2RX4
SCHEMBL15038285 0.92 P2RY1 (0.60) P2RY1P2RX3ENPP1P2RX1P2RX4
SCHEMBL31029199 0.92 P2RY1 (0.68) P2RY1P2RX3ENPP1P2RX1P2RX4
SCHEMBL15305340 0.92 CA5A (0.67) P2RY1P2RX3ENPP1P2RY11P2RY12
SCHEMBL14946172 0.90 RNASEL (0.71) P2RY1P2RX3ENPP1P2RX1P2RX4
SCHEMBL6880958 0.90 P2RY1 (0.65) P2RY1P2RX3ENPP1P2RX1P2RX4
SCHEMBL13857854 0.89 P2RY1 (0.79) P2RY1P2RX3ENPP1P2RX1P2RX4
SCHEMBL3502237 0.89 P2RY1 (0.79) P2RY1P2RX3ENPP1P2RX1P2RX4

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-8614312-B2 Method for preparing nucleotides and related analogues by synthesis on soluble substrate, and biological tools thus prepared CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2013-12-24 — — US disclosed
US-20110118454-A1 METHOD FOR PREPARING NUCLEOTIDES AND RELATED ANALOGUES BY SYNTHESIS ON SOLUBLE SUBSTRATE, AND BIOLOGICAL TOOLS THUS PREPARED CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2011-05-19 — — US disclosed
EP-2265624-A1 METHOD FOR PREPARING NUCLEOTIDES AND RELATED ANALOGUES BY SYNTHESIS ON SOLUBLE SUBSTRATE, AND BIOLOGICAL TOOLS THUS PREPARED Centre National de la Recherche Scientifique (FR) 2010-12-29 — — EP disclosed
WO-2009115694-A1 METHOD FOR PREPARING NUCLEOTIDES AND RELATED ANALOGUES BY SYNTHESIS ON SOLUBLE SUBSTRATE, AND BIOLOGICAL TOOLS THUS PREPARED CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2009-09-24 — — 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-20110118454-A1 METHOD FOR PREPARING NUCLEOTIDES AND RELATED ANALOGUES BY SYNTHESIS ON SOLUBLE SUBSTRATE, AND BIOLOGICAL TOOLS THUS PREPARED PNP, NUDT1, DUT P2RY1 218/4885P2RX3 539/4885ENPP1 19/4885

“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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