SCHEMBL8906323

SCHEMBL8906323

Cc1nc2ncnc(O)c2[nH]1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AKT2 P31751 1/20 0.44
NUDT1 P36639 3/20 0.41
ADORA3 P0DMS8 2/20 0.37
KIT P10721 1/20 0.37
ADORA2A P29274 2/20 0.36
ADORA1 P30542 2/20 0.36
SMN1; SMN2 Q16637 1/20 0.35
JAK2 O60674 1/20 0.34
JAK1 P23458 1/20 0.34
TYK2 P29597 1/20 0.34
JAK3 P52333 1/20 0.34
PI4KA P42356 2/20 0.33
PI4K2B Q8TCG2 2/20 0.33
PI4K2A Q9BTU6 2/20 0.33
PI4KB Q9UBF8 2/20 0.33
CHEK1 O14757 1/20 0.32
AURKA O14965 1/20 0.32
PDPK1 O15530 1/20 0.32
CHEK2 O96017 1/20 0.32
HSP90AA1 P07900 1/20 0.32

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
SCHEMBL2639251 0.81 ADORA2A (0.37) NUDT1ADORA2AADORA1PI4KAPI4K2B
SCHEMBL9010833 0.78 ADORA2A (0.35) NUDT1ADORA2AADORA1PI4KAPI4K2B
SCHEMBL5667619 0.78 ADORA2A (0.43) NUDT1ADORA2AADORA1PI4KAPI4K2B
SCHEMBL612166 0.78 ADORA2A (0.35) NUDT1ADORA2AADORA1PI4KAPI4K2B
SCHEMBL16513158 0.78 ADORA2A (0.35) NUDT1ADORA2AADORA1PI4KAPI4K2B
SCHEMBL932299 0.78 ADORA2A (0.35) NUDT1ADORA2AADORA1PI4KAPI4K2B
SCHEMBL7168415 0.78 ADORA2A (0.35) NUDT1ADORA2AADORA1PI4KAPI4K2B
SCHEMBL94915 0.78 ADORA2A (0.35) NUDT1ADORA2AADORA1PI4KAPI4K2B
SCHEMBL7072636 0.76 AKT2 (0.42) AKT2NUDT1ADORA3KITADORA2A
Water SCHEMBL3986355 0.76 ADORA2A (0.34) NUDT1ADORA2AADORA1PI4KAPI4K2B

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 16 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3401683-A1 DIAGNOSING METABOLIC DISEASE BY THE USE OF A BIOMARKER Eberhard Karls Universität Tübingen Medizinische Fakultät (DE) 2018-11-14 EP claimed
US-20230272401-A1 COMPOSITIONS FOR FLCN GENE MODULATION AND METHODS THEREOF Genetic Intelligence, Inc 2023-08-31 US disclosed
US-20230167447-A1 Compositions for FNIP1/FNIP2 Gene Modulation and Methods Thereof GENETIC INTELLIGENCE INC (US) 2023-06-01 US disclosed
EP-4165185-A2 COMPOSITIONS FOR FLCN GENE MODULATION AND METHODS THEREOF Genetic Intelligence, Inc, New York, NY (US) 2023-04-19 EP disclosed
WO-2021252903-A2 COMPOSITIONS FOR FLCN GENE MODULATION AND METHODS THEREOF GENETIC INTELLIGENCE, INC, NEW YORK, NY (US) 2021-12-16 WO disclosed
US-10668027-B1 Method of treating Acanthamoeba infection using allopurinol UNIVERSITY OF SOUTH FLORIDA (US) 2020-06-02 US disclosed
EP-3401683-A1 DIAGNOSING METABOLIC DISEASE BY THE USE OF A BIOMARKER Eberhard Karls Universität Tübingen Medizinische Fakultät (DE) 2018-11-14 EP disclosed
WO-2016043661-A1 MODIFIED PEPTIDE NUCLEIC ACIDS AND THEIR USE NANYANG TECHNOLOGICAL UNIVERSITY (SG) 2016-03-24 WO disclosed
US-7608600-B2 Treating hepatitis C virus infections; antivirals have low toxicity to the host; inhibit Flaviviridae polymerase IDENIX PHARMACEUTICALS, INC. (US) 2009-10-27 US disclosed
US-7365057-B2 Treating hepatitis C virus infections; antivirals have low toxicity to the host; inhibit Flaviviridae polymerase IDENIX PHARMACEUTICALS, INC. (US) 2008-04-29 US disclosed
US-7192936-B2 Use treating hepatitis C infection optionally with other viricides such as interferons or ribavirin; low toxicity to the host; use of cytosine-based nucleotides or nucleosides having a 2'-trifluoromethyl-ribose moiety which forms a 5'-phosphate or hydroxy moiety in vivo IDENIX PHARMACEUTICALS, INC. (US) 2007-03-20 US disclosed
US-5698685-A Morpholino-subunit combinatorial library and method ANTIVIRALS INC. (US) 1997-12-16 US disclosed
US-5506337-A Morpholino-subunit combinatorial library and method ANTIVIRALS INC. (US) 1996-04-09 US disclosed
WO-1995031459-A1 MORPHOLINO-SUBUNIT COMBINATORIAL LIBRARY AND METHOD ANTIVIRALS INC. (US) 1995-11-23 WO disclosed
EP-0502690-A2 Cyclopropane derivative Ajinomoto Co., Inc. (JP) 1992-09-09 EP disclosed
EP-0391592-A1 Process for the enzymatic synthesis of nucleosides THE TEXAS A & M UNIVERSITY SYSTEM (US) 1990-10-10 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 (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-20230167447-A1 Compositions for FNIP1/FNIP2 Gene Modulation and Methods Thereof FNIP1, FN1, TNNC1 AKT2 3399/4885NUDT1 3137/4885ADORA3 4455/4885
US-20230272401-A1 COMPOSITIONS FOR FLCN GENE MODULATION AND METHODS THEREOF TARDBP, FUS, RBM17 AKT2 4102/4885NUDT1 2858/4885ADORA3 4554/4885
US-10668027-B1 Method of treating Acanthamoeba infection using allopurinol XDH, DPM1, GUSB AKT2 4190/4885NUDT1 67/4885ADORA3 2318/4885

“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.