2'-B-Methyl-Guanosine

2'-B-Methyl-Guanosine

SCHEMBL939849

C[C@@]1(O)[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(O)nc(N)nc21

nearest known ligand 0.69

Full drug profile on Sugi Atlas →

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
ADORA2A P29274 9/20 0.69
ADA P00813 1/20 0.60
ADORA3 P0DMS8 11/20 0.55
ADORA1 P30542 8/20 0.55
ADORA2B P29275 4/20 0.55
ALOX15 P16050 1/20 0.55
CYP2C19 P33261 1/20 0.48
SLC29A1 Q99808 2/20 0.45

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
2'-B-Methyl-Guanosine SCHEMBL11888942 1.00 ADORA2A (0.69) ADORA2AADAADORA3ADORA1ADORA2B
2'-B-Methyl-Guanosine SCHEMBL10316549 1.00 ADORA2A (0.69) ADORA2AADAADORA3ADORA1ADORA2B
SCHEMBL10137892 0.90 ADORA2A (0.80) ADORA2AADAADORA3ADORA1ADORA2B
SCHEMBL14589609 0.90 ADORA2A (0.80) ADORA2AADAADORA3ADORA1ADORA2B
SCHEMBL873738 0.90 ADORA2A (0.80) ADORA2AADAADORA3ADORA1ADORA2B
SCHEMBL474849 0.90 ADORA2A (0.80) ADORA2AADAADORA3ADORA1ADORA2B
SCHEMBL10169502 0.90 ADORA2A (0.80) ADORA2AADAADORA3ADORA1ADORA2B
SCHEMBL15908433 0.90 ADORA2A (0.80) ADORA2AADAADORA3ADORA1ADORA2B
SCHEMBL1552038 0.88 ADORA2A (0.53) ADORA2AADAADORA3ADORA1ADORA2B
SCHEMBL1552034 0.88 ADORA2A (0.53) ADORA2AADAADORA3ADORA1ADORA2B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1476169-A4 METHODS OF INHIBITING ORTHOPOXVIRUS REPLICATION WITH NUCLEOSIDE COMPOUNDS MERCK & CO INC (US) 2009-06-03 EP claimed
US-7323453-B2 Methods of inhibiting orthopoxvirus replication with nucleoside compounds MERCK & CO., INC. (US) 2008-01-29 US claimed
US-20050164960-A1 Methods of inhibiting orthopoxvirus replication with nucleoside compounds MERCK SHARP & DOHME CORP. 2005-07-28 US claimed
EP-1476169-A1 METHODS OF INHIBITING ORTHOPOXVIRUS REPLICATION WITH NUCLEOSIDE COMPOUNDS Merck & Co., Inc. (US) 2004-11-17 EP claimed
WO-2003068244-A1 METHODS OF INHIBITING ORTHOPOXVIRUS REPLICATION WITH NUCLEOSIDE COMPOUNDS MERCK & CO., INC. (US) 2003-08-21 WO claimed
EP-2937350-B9 1' -substituted carba-nucleoside analogs for antiviral treatment GILEAD SCIENCES INC (US) 2022-08-17 EP disclosed
EP-2697241-B1 1'-SUBSTITUTED PYRIMIDINE N-NUCLEOSIDE ANALOGS FOR ANTIVIRAL TREATMENT GILEAD SCIENCES INC (US) 2019-06-12 EP disclosed
EP-3150608-B1 2' -FLUORO SUBSTITUTED CARBA-NUCLEOSIDE ANALOGS FOR ANTIVIRAL TREATMENT GILEAD SCIENCES INC (US) 2019-04-10 EP disclosed
US-RE46762-E1 1′-substituted carba-nucleoside analogs for antiviral treatment GILEAD SCIENCES, INC (US) 2018-03-27 US disclosed
EP-2937350-B1 1' -substituted carba-nucleoside analogs for antiviral treatment GILEAD SCIENCES INC (US) 2018-01-10 EP disclosed
EP-3219713-A1 INHIBITORS OF FLAVIVIRIDAE VIRUSES Gilead Sciences, Inc. (US) 2017-09-20 EP disclosed
EP-2523950-B1 INHIBITORS OF FLAVIVIRIDAE VIRUSES GILEAD SCIENCES INC (US) 2017-03-15 EP disclosed
US-20100021425-A1 1'-SUBSTITUTED CARBA-NUCLEOSIDE ANALOGS FOR ANTIVIRAL TREATMENT GILEAD SCIENCES, INC. (US) 2010-01-28 US disclosed
US-20090317361-A1 CARBA-NUCLEOSIDE ANALOGS FOR ANTIVIRAL TREATMENT GILEAD SCIENCES, INC. (US) 2009-12-24 US disclosed
EP-2132216-A1 NOVEL NUCLEOSIDE ANALOGS FOR TREATMENT OF VIRAL INFECTIONS Novartis Pharma AG. (CH) 2009-12-16 EP disclosed
WO-2009132123-A1 CARBA-NUCLEOSIDE ANALOGS FOR ANTIVIRAL TREATMENT GILEAD SCIENCES, INC. (US) 2009-10-29 WO disclosed
WO-2009132135-A1 1' -SUBSTITUTED CARBA-NUCLEOSIDE ANALOGS FOR ANTIVIRAL TREATMENT GILEAD SCIENCES, INC. (US) 2009-10-29 WO disclosed
WO-2008095993-A1 NOVEL NUCLEOSIDE ANALOGS FOR TREATMENT OF VIRAL INFECTIONS NOVARTIS AG (CH) 2008-08-14 WO disclosed
US-7323453-B2 Methods of inhibiting orthopoxvirus replication with nucleoside compounds MERCK & CO., INC. (US) 2008-01-29 US disclosed
US-20050164960-A1 Methods of inhibiting orthopoxvirus replication with nucleoside compounds MERCK SHARP & DOHME CORP. 2005-07-28 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-20100021425-A1 1'-SUBSTITUTED CARBA-NUCLEOSIDE ANALOGS FOR ANTIVIRAL TREATMENT PNP, MTAP, SLC29A1 ADORA2A 93/4885ADA 31/4885ADORA3 139/4885
US-20090317361-A1 CARBA-NUCLEOSIDE ANALOGS FOR ANTIVIRAL TREATMENT CDA, PNP, MTAP ADORA2A 41/4885ADA 6/4885ADORA3 50/4885
US-20050164960-A1 Methods of inhibiting orthopoxvirus replication with nucleoside compounds ITPA, PNP, NUDT1 ADORA2A 192/4885ADA 43/4885ADORA3 225/4885

“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.