SCHEMBL6397349

SCHEMBL6397349

O=C(Nc1c2ncnc-2ncn1[C@@H]1O[C@H](CO)[C@@H](O)[C@@H]1O)c1ccccc1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 2/20 0.50
ADORA1 P30542 7/20 0.49
ADORA3 P0DMS8 4/20 0.49
ADORA2A P29274 3/20 0.49
SLC29A1 Q99808 3/20 0.49
LMNA P02545 2/20 0.49
ALDH1A1 P00352 1/20 0.49
GLA P06280 1/20 0.49
PMP22 Q01453 1/20 0.49
SMN1; SMN2 Q16637 1/20 0.49
NPC1 O15118 1/20 0.49
NPY1R P25929 1/20 0.49
HTT P42858 1/20 0.49
NPY2R P49146 1/20 0.49
RAB9A P51151 1/20 0.49
RXFP1 Q9HBX9 1/20 0.49
TSHR P16473 1/20 0.49
NFKB1 P19838 1/20 0.49
MAPK1 P28482 1/20 0.49
CYP2C19 P33261 1/20 0.49

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
SCHEMBL29617913 0.79 LMNA (0.72) CYP1A2ADORA1ADORA3ADORA2ASLC29A1
SCHEMBL9945526 0.79 LMNA (0.72) CYP1A2ADORA1ADORA3ADORA2ASLC29A1
SCHEMBL19485512 0.79 LMNA (0.72) CYP1A2ADORA1ADORA3ADORA2ASLC29A1
SCHEMBL6909853 0.79 LMNA (0.72) CYP1A2ADORA1ADORA3ADORA2ASLC29A1
SCHEMBL17889837 0.79 LMNA (0.72) CYP1A2ADORA1ADORA3ADORA2ASLC29A1
SCHEMBL233209 0.79 LMNA (0.72) CYP1A2ADORA1ADORA3ADORA2ASLC29A1
SCHEMBL17301042 0.79 LMNA (0.72) CYP1A2ADORA1ADORA3ADORA2ASLC29A1
SCHEMBL313413 0.79 LMNA (0.72) CYP1A2ADORA1ADORA3ADORA2ASLC29A1
SCHEMBL21953578 0.79 LMNA (0.72) CYP1A2ADORA1ADORA3ADORA2ASLC29A1
SCHEMBL27986516 0.79 LMNA (0.72) CYP1A2ADORA1ADORA3ADORA2ASLC29A1

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-20050059817-A1 Methods for synthesizing nucleosides, nucleoside derivatives and non-nucleoside derivatives SIRNA THERAPEUTICS, INC. (US) 2005-03-17 US disclosed
US-6686463-B2 FEWER SYNTHETIC STEPS; INVOLVES FORMATION OF A 5',4'-BRIDGING SILYL PROTECTING GROUP TO FORM A FUSED SILOXANE ON THE FURAN RING SIRNA THERAPEUTICS, INC. 2004-02-03 US disclosed
US-20020150936-A1 Methods for synthesizing nucleosides, nucleoside derivatives and non-nucleoside derivatives RIBOZYME PHARMACEUTICALS, INC. 2002-10-17 US disclosed
US-20020120129-A1 Methods for synthesizing nucleosides, nucleoside derivatives and non-nucleoside derivatives RIBOZYME PHARMACEUTICALS, INC. 2002-08-29 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 (3 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-20050059817-A1 Methods for synthesizing nucleosides, nucleoside derivatives and non-nucleoside derivatives PNP, NSUN2, NT5C3B CYP1A2 4016/4885ADORA1 652/4885ADORA3 516/4885
US-20020120129-A1 Methods for synthesizing nucleosides, nucleoside derivatives and non-nucleoside derivatives PNP, NSUN2, NT5C3B CYP1A2 3625/4885ADORA1 826/4885ADORA3 636/4885
US-20020150936-A1 Methods for synthesizing nucleosides, nucleoside derivatives and non-nucleoside derivatives PNP, NSUN2, NT5C3B CYP1A2 3869/4885ADORA1 887/4885ADORA3 645/4885

“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.