SCHEMBL6403262

SCHEMBL6403262

CO[C@@H]1[C@@H]2O[Si](C(C)(C)C)(C(C)(C)C)OC[C@H]2O[C@H]1n1cnc2c(N)nc(NC(=O)C(C)C)nc21

nearest known ligand 0.41

Predicted protein targets (top 5)

geneUniProtsupporting neighboursconfidence
▸ ADORA2A P29274 9/20 0.38
▸ ADORA3 P0DMS8 8/20 0.38
▸ ADORA1 P30542 6/20 0.38
▸ STING1 Q86WV6 3/20 0.36
▸ SARS1 P49591 1/20 0.35

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
SCHEMBL1582239 0.92 CDK5 (0.38) ADORA2AADORA3ADORA1
SCHEMBL6362480 0.87 ADORA2A (0.37) ADORA2AADORA3ADORA1STING1SARS1
SCHEMBL7197488 0.87 ADORA2A (0.37) ADORA2AADORA3ADORA1STING1SARS1
SCHEMBL1582124 0.84 HINT1 (0.39) ADORA2AADORA3STING1
SCHEMBL27419759 0.79 ADORA2A (0.36) ADORA2AADORA3ADORA1STING1SARS1
SCHEMBL6402479 0.73 STING1 (0.49) ADORA3STING1
SCHEMBL20547879 0.72 STING1 (0.35) STING1
SCHEMBL22559797 0.72 ADORA2A (0.34) ADORA2AADORA3ADORA1SARS1
SCHEMBL16392689 0.72 ADORA2A (0.34) ADORA2AADORA3ADORA1SARS1
SCHEMBL8939101 0.72 STING1 (0.38) ADORA2AADORA3STING1

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 ADORA2A 287/4885ADORA3 516/4885ADORA1 652/4885
US-20020120129-A1 Methods for synthesizing nucleosides, nucleoside derivatives and non-nucleoside derivatives PNP, NSUN2, NT5C3B ADORA2A 278/4885ADORA3 636/4885ADORA1 826/4885
US-20020150936-A1 Methods for synthesizing nucleosides, nucleoside derivatives and non-nucleoside derivatives PNP, NSUN2, NT5C3B ADORA2A 310/4885ADORA3 645/4885ADORA1 887/4885

“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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