SCHEMBL3084982

SCHEMBL3084982

C=C(Br)c1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c(=O)[nH]c1=O

nearest known ligand 0.68

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
PYGM P11217 3/20 0.68
TK2 O00142 2/20 0.63
SLC28A1 O00337 1/20 0.55
SLC28A2 O43868 1/20 0.55
SLC29A1 Q99808 1/20 0.55
SLC28A3 Q9HAS3 1/20 0.55
P2RY2 P41231 4/20 0.50
DNPH1 O43598 1/20 0.48

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
SCHEMBL3080113 1.00 PYGM (0.68) PYGMTK2SLC28A1SLC28A2SLC29A1
SCHEMBL4952189 0.91 PYGM (0.56) PYGMTK2SLC28A1SLC28A2SLC29A1
SCHEMBL3072346 0.90 PYGM (0.55) PYGMTK2P2RY2DNPH1
SCHEMBL3071097 0.90 PYGM (0.55) PYGMTK2SLC28A1SLC28A2SLC29A1
SCHEMBL8775826 0.88 PYGM (0.65) PYGMTK2SLC28A1SLC28A2SLC29A1
SCHEMBL8988015 0.88 PYGM (0.65) PYGMTK2SLC28A1SLC28A2SLC29A1
SCHEMBL9465813 0.88 PYGM (0.65) PYGMTK2SLC28A1SLC28A2SLC29A1
SCHEMBL9465927 0.88 PYGM (0.65) PYGMTK2SLC28A1SLC28A2SLC29A1
SCHEMBL16974933 0.86 PYGM (0.69) PYGMTK2SLC28A1SLC28A2SLC29A1
SCHEMBL16974934 0.86 PYGM (0.69) PYGMTK2SLC28A1SLC28A2SLC29A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2078080-B1 CPG OLIGONUCLEOTIDE ANALOGS CONTAINING HYDROPHOBIC T ANALOGS WITH ENHANCED IMMUNOSTIMULATORY ACTIVITY COLEY PHARM GMBH (DE) 2015-06-17 EP claimed
EP-0217580-A2 Therapeutic nucleosides THE WELLCOME FOUNDATION LIMITED (GB) 1987-04-08 EP claimed
CN-113813386-A Combination tumor immunotherapy 查克美特制药公司 2021-12-21 CN disclosed
CN-107428813-B Combination tumor immunotherapy 查克美特制药公司 2021-08-03 CN disclosed
EP-3835312-A1 COMBINATION TUMOR IMMUNOTHERAPY Checkmate Pharmaceuticals, Inc. (US) 2021-06-16 EP disclosed
US-20210030783-A1 COMPOSITIONS AND METHODS FOR TUMOR IMMUNOTHERAPY CHECKMATE PHARMACEUTICALS, INC. 2021-02-04 US disclosed
EP-3240801-B1 COMBINATION TUMOR IMMUNOTHERAPY CHECKMATE PHARMACEUTICALS INC (US) 2021-01-20 EP disclosed
EP-3752194-A2 COMPOSITIONS AND METHODS FOR TUMOR IMMUNOTHERAPY Checkmate Pharmaceuticals, Inc. (US) 2020-12-23 EP disclosed
US-20200281953-A1 COMBINATION TUMOR IMMUNOTHERAPY CHECKMATE PHARMACEUTICALS, INC. 2020-09-10 US disclosed
US-10682365-B2 Combination tumor immunotherapy CHECKMATE PHARMACEUTICALS, INC. (US) 2020-06-16 US disclosed
WO-2019160866-A2 COMPOSITIONS AND METHODS FOR TUMOR IMMUNOTHERAPY CHECKMATE PHARMACEUTICALS, INC. (US) 2019-08-22 WO disclosed
US-20100227834-A1 NUCLEOSIDES FOR SUPPRESSING OR REDUCING THE DEVELOPMENT OF RESISTANCE IN CYTOSTATIC THERAPY RESprotech GmbH (DE) 2010-09-09 US disclosed
US-20100166780-A1 CpG Oligonucleotide Analogs Containing Hydrophobic T Analogs with Enhanced Immunostimulatory Activity PFIZER INC 2010-07-01 US disclosed
CN-101517082-A CpG oligonucleotide analogs containing hydrophobic T analogs with enhanced immunostimulatory activity COLEY PHARM GMBH (DE) 2009-08-26 CN disclosed
EP-2054406-A1 NUCLEOSIDES FOR SUPPRESSING OR REDUCING THE DEVELOPMENT OF RESISTANCE IN CYTOSTATIC THERAPY RESprotect GmbH (DE) 2009-05-06 EP disclosed
WO-2008017515-A1 NUCLEOSIDES FOR SUPPRESSING OR REDUCING THE DEVELOPMENT OF RESISTANCE IN CYTOSTATIC THERAPY RESPROTECT GMBH (DE) 2008-02-14 WO disclosed
EP-1745061-A1 NOVEL AMPHIPHILIC COMPOUNDS, PREPARATION METHOD THEREOF AND APPLICATIONS OF SAME Universite D'Avignon et Des Pays Du Vaucluse (FR) 2007-01-24 EP disclosed
WO-2005116043-A1 NOVEL AMPHIPHILIC COMPOUNDS, PREPARATION METHOD THEREOF AND APPLICATIONS OF SAME UNIVERSITE D'AVIGNON ET DES PAYS DE VAUCLUSE (FR) 2005-12-08 WO disclosed
US-5064946-A 3-azido-2,3-dideoxy-B-D-erythro-pentofuranosyl derivatives of 4(1H)-pyrimidinones; antiretroviral, anti-AIDS BURROUGHS WELLCOME CO. (US) 1991-11-12 US disclosed
EP-0217580-A2 Therapeutic nucleosides THE WELLCOME FOUNDATION LIMITED (GB) 1987-04-08 EP 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 (2 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-20100166780-A1 CpG Oligonucleotide Analogs Containing Hydrophobic T Analogs with Enhanced Immunostimulatory Activity TLR9, TYMP, STING1 PYGM 3169/4885TK2 58/4885SLC28A1 189/4885
US-20100227834-A1 NUCLEOSIDES FOR SUPPRESSING OR REDUCING THE DEVELOPMENT OF RESISTANCE IN CYTOSTATIC THERAPY TYMP, ENTPD5, NTPCR PYGM 1888/4885TK2 34/4885SLC28A1 52/4885

“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.