SCHEMBL1763360

SCHEMBL1763360

O=c1ccn([C@H]2O[C@@H](CO)[C@H](O)[C@@]2(O)F)c(=O)[nH]1

nearest known ligand 0.57

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
SLC29A1 Q99808 2/20 0.57
SLC28A1 O00337 1/20 0.57
SLC28A2 O43868 1/20 0.57
SLC28A3 Q9HAS3 1/20 0.57
POLA1 P09884 1/20 0.48
P2RY2 P41231 3/20 0.47
P2RY4 P51582 1/20 0.47
PDE4D Q08499 1/20 0.46
PDE3A Q14432 1/20 0.46
P2RY14 Q15391 4/20 0.44
P2RY6 Q15077 2/20 0.41
CDA P32320 2/20 0.40

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
SCHEMBL8749574 1.00 SLC29A1 (0.57) SLC29A1SLC28A1SLC28A2SLC28A3POLA1
SCHEMBL233416 1.00 SLC29A1 (0.57) SLC29A1SLC28A1SLC28A2SLC28A3POLA1
SCHEMBL7876363 1.00 SLC29A1 (0.57) SLC29A1SLC28A1SLC28A2SLC28A3POLA1
Hydrochloric Acid SCHEMBL29938288 0.99 SLC29A1 (0.56) SLC29A1SLC28A1SLC28A2SLC28A3POLA1
Phosphoric Acid SCHEMBL20769291 0.95 SLC28A1 (0.53) SLC29A1SLC28A1SLC28A2SLC28A3POLA1
Phosphoric Acid SCHEMBL4575893 0.95 SLC28A1 (0.53) SLC29A1SLC28A1SLC28A2SLC28A3POLA1
Phosphoramidic Acid SCHEMBL17439381 0.93 SLC29A1 (0.51) SLC29A1SLC28A1SLC28A2SLC28A3POLA1
SCHEMBL12170413 0.88 SLC29A1 (0.59) SLC29A1SLC28A1SLC28A2SLC28A3POLA1
SCHEMBL6758716 0.88 SLC29A1 (0.59) SLC29A1SLC28A1SLC28A2SLC28A3POLA1
SCHEMBL94634 0.88 SLC29A1 (0.59) SLC29A1SLC28A1SLC28A2SLC28A3POLA1

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 2 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

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 SLC29A1 72/4885SLC28A1 229/4885SLC28A2 358/4885

“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.