SCHEMBL561516

SCHEMBL561516

Nc1ncnc2c1ncn2[C@@H]1OC(CO)(CO)C(O)C1O

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PRMT5 O14744 1/20 0.64
▸ WDR77 Q9BQA1 1/20 0.64
▸ ADORA3 P0DMS8 5/20 0.61
▸ ADORA2A P29274 3/20 0.61
▸ PI4KA P42356 2/20 0.61
▸ PI4K2B Q8TCG2 2/20 0.61
▸ PI4K2A Q9BTU6 2/20 0.61
▸ PI4KB Q9UBF8 2/20 0.61
▸ DPP4 P27487 1/20 0.61
▸ MEN1 O00255 1/20 0.61
▸ SLC28A1 O00337 1/20 0.61
▸ MAP3K7 O43318 1/20 0.61
▸ SLC28A2 O43868 1/20 0.61
▸ GAPDH P04406 1/20 0.61
▸ MAPK1 P28482 1/20 0.61
▸ ADORA2B P29275 1/20 0.61
▸ ADORA1 P30542 1/20 0.61
▸ STAT6 P42226 1/20 0.61
▸ KMT2A Q03164 1/20 0.61
▸ SMN1; SMN2 Q16637 1/20 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
SCHEMBL561515 1.00 PRMT5 (0.64) PRMT5WDR77ADORA3ADORA2API4KA
SCHEMBL561654 1.00 PRMT5 (0.64) PRMT5WDR77ADORA3ADORA2API4KA
SCHEMBL17359784 0.93 PRMT5 (0.59) PRMT5WDR77ADORA3ADORA2API4KA
SCHEMBL31652766 0.93 PRMT5 (0.59) PRMT5WDR77ADORA3ADORA2API4KA
SCHEMBL31652943 0.93 PRMT5 (0.59) PRMT5WDR77ADORA3ADORA2API4KA
SCHEMBL12170653 0.88 ADORA3 (0.56) PRMT5WDR77ADORA3ADORA2API4KA
SCHEMBL17445618 0.86 ADORA3 (0.55) PRMT5WDR77ADORA3ADORA2API4KA
SCHEMBL2318607 0.85 PRMT5 (0.65) PRMT5WDR77ADORA3ADORA2API4KA
SCHEMBL14946260 0.85 PRMT5 (0.65) PRMT5WDR77ADORA3ADORA2API4KA
SCHEMBL6426564 0.85 PRMT5 (0.65) PRMT5WDR77ADORA3ADORA2API4KA

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 33 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8648054-B2 4′-substituted nucleoside derivatives as inhibitors of HCV RNA replication ROCHE PALO ALTO LLC (US) 2014-02-11 — — US disclosed
US-20130237491-A1 4'-SUBSTITUTED NUCLEOSIDE DERIVATIVES AS INHIBITORS OF HCV RNA REPLICATION ROCHE PALO ALTO LLC (US) 2013-09-12 — — US disclosed
US-20120034184-A1 4'-SUBSTITUTED NUCLEOSIDE DERIVATIVES AS INHIBITORS OF HCV RNA REPLICATION DEVOS RENE ROBERT (GB) 2012-02-09 — — US disclosed
US-8071567-B2 4′-substituted nucleoside derivatives as inhibitors of HCV RNA replication ROCHE PALO ALTO LLC (US) 2011-12-06 — — US disclosed
US-7915232-B2 4′-substituted nucleoside derivatives as inhibitors of HCV RNA replication ROCHE PALO ALTO LLC (US) 2011-03-29 — — US disclosed
US-20100004192-A1 4'-Substituted Nucleoside Derivatives as Inhibitors of HCV RNA Replication MARTIN JOSEPH ARMSTRONG 2010-01-07 — — US disclosed
US-20100003213-A1 4'-SUBSTITUTED NUCLEOSIDE DERIVATIVES AS INHIBITORS OF HCV RNA REPLICATION DEVOS RENE ROBERT 2010-01-07 — — US disclosed
US-7608601-B2 4′-Substituted nucleoside derivatives as inhibitors of HCV RNA replication ROCHE PALO ALTO LLC (US) 2009-10-27 — — US disclosed
US-6784166-B2 FOR THE TREATMENT OF DISEASES MEDIATED BY THE HEPATITIS C VIRUS SYNTEX (U.S.A.) LLC 2004-08-31 — — US disclosed
US-6762170-B1 ANTIINFLAMMATORY AGENTS INHIBIT LEUKOCYTE RECRUITMENT AND ACTIVATION AND ARE AGONISTS OF THE ADENOSINE 2A RECEPTOR; PENDANT ISOXAZOLE; REACTING A 2,6-DIAMINOPURINE WITH A 2-(3-SUBSTITUTED ISOXAZOL-5-YL)TETRAHYDROFURAN-3,4-DIOL SMITHKLINEBEECHAM CORPORATION 2004-07-13 — — US disclosed
EP-1090023-A1 2-(PURIN-9-YL)-TETRAHYDROFURAN-3,4-DIOL DERIVATIVES GLAXO GROUP LIMITED (GB) 2001-04-11 — — EP disclosed
EP-1090022-A1 2-(PURIN-9-YL)-TETRAHYDROFURAN-3,4-DIOL DERIVATIVES GLAXO GROUP LIMITED (GB) 2001-04-11 — — EP disclosed
EP-1051425-A2 2-(PURIN-9-yl)-TETRAHYDROFURAN-3,4-DIOL DERIVATIVES GLAXO GROUP LIMITED (GB) 2000-11-15 — — EP disclosed
WO-1999067265-A1 2-(PURIN-9-YL)-TETRAHYDROFURAN-3,4-DIOL DERIVATIVES GLAXO GROUP LIMITED (GB) 1999-12-29 — — WO disclosed
WO-1999067266-A1 2-(PURIN-9-YL)-TETRAHYDROFURAN-3,4-DIOL DERIVATIVES GLAXO GROUP LIMITED (GB) 1999-12-29 — — WO disclosed
WO-1999067264-A1 2-(PURIN-9-YL)-TETRAHYDROFURAN-3,4-DIOL DERIVATIVES GLAXO GROUP LIMITED (GB) 1999-12-29 — — WO disclosed
WO-1999067263-A1 2-(PURIN-9-YL)-TETRAHYDROFURAN-3,4-DIOL DERIVATIVES GLAXO GROUP LIMITED (GB) 1999-12-29 — — WO disclosed
EP-0948509-A1 2-(PURIN-9-YL)-TETRAHYDROFURAN-3,4-DIOL DERIVATIVES GLAXO GROUP LIMITED (GB) 1999-10-13 — — EP disclosed
WO-1999038877-A2 2-(PURIN-9-yl)-TETRAHYDROFURAN-3,4-DIOL DERIVATIVES GLAXO GROUP LIMITED (GB) 1999-08-05 — — WO disclosed
WO-1998028319-A1 2-(PURIN-9-YL)-TETRAHYDROFURAN-3,4-DIOL DERIVATIVES GLAXO GROUP LIMITED (GB) 1998-07-02 — — 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 (4 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-20100003213-A1 4'-SUBSTITUTED NUCLEOSIDE DERIVATIVES AS INHIBITORS OF HCV RNA REPLICATION NSUN2, RNGTT, RNMT PRMT5 556/4885WDR77 2042/4885ADORA3 583/4885
US-20100004192-A1 4'-Substituted Nucleoside Derivatives as Inhibitors of HCV RNA Replication NSUN2, RNGTT, RNMT PRMT5 556/4885WDR77 2042/4885ADORA3 583/4885
US-20120034184-A1 4'-SUBSTITUTED NUCLEOSIDE DERIVATIVES AS INHIBITORS OF HCV RNA REPLICATION NSUN2, RNGTT, RNMT PRMT5 456/4885WDR77 1692/4885ADORA3 299/4885
US-20130237491-A1 4'-SUBSTITUTED NUCLEOSIDE DERIVATIVES AS INHIBITORS OF HCV RNA REPLICATION NSUN2, RNGTT, RNMT PRMT5 556/4885WDR77 2042/4885ADORA3 583/4885

“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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