SCHEMBL4420067

SCHEMBL4420067

Cc1cn([C@H]2CC(O)C(CO)(CO)O2)c(=O)[nH]c1=O

nearest known ligand 0.56

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
TK1 P04183 9/20 0.56
ALB P02768 1/20 0.48
PKM P14618 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
SCHEMBL4420063 1.00 TK1 (0.56) TK1ALBPKM
SCHEMBL24695063 0.94 TK1 (0.53) TK1ALBPKM
SCHEMBL31653281 0.94 TK1 (0.53) TK1ALBPKM
SCHEMBL10159482 0.94 TK1 (0.53) TK1ALBPKM
SCHEMBL5188430 0.93 TK1 (0.52) TK1
SCHEMBL8932107 0.93 TK1 (0.52) TK1ALBPKM
SCHEMBL31653078 0.93 TK1 (0.52) TK1
SCHEMBL25400736 0.93 TK1 (0.52) TK1
SCHEMBL25401466 0.93 TK1 (0.52) TK1
SCHEMBL5188427 0.93 TK1 (0.52) TK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7625872-B2 Branched immunomodulatory compounds and methods of using the same DYNAVAX TECHNOLOGIES CORPORATION (US) 2009-12-01 US disclosed
EP-1625140-A4 BRANCHED IMMUNOMODULATORY COMPOUNDS AND METHODS OF USING THE SAME DYNAVAX TECH CORP (US) 2008-06-18 EP disclosed
EP-1730158-A2 METHODS AND COMPOSITIONS FOR IN VITRO AND IN VIVO USE OF PARALLEL STRANDED HAIRPINS AND TRIPLEX STRUCTURES AS NUCLEIC ACID LIGANDS Cygene, Inc. (US) 2006-12-13 EP disclosed
EP-1625140-A2 BRANCHED IMMUNOMODULATORY COMPOUNDS AND METHODS OF USING THE SAME Dynavax Technologies Corporation (US) 2006-02-15 EP disclosed
WO-2005067437-A2 METHODS AND COMPOSITIONS FOR IN VITRO AND IN VIVO USE OF PARALLEL STRANDED HAIRPINS AND TRIPLEX STRUCTURES AS NUCLEIC ACID LIGANDS CYGENE, INC. (US) 2005-07-28 WO disclosed
US-20050089893-A1 Methods and compositions for in vitro and in vivo use of parallel stranded hairpins and triplex structures as nucleic acid ligands CYGENE, INC. 2005-04-28 US disclosed
WO-2004058159-A2 BRANCHED IMMUNOMODULATORY COMPOUNDS AND METHODS OF USING THE SAME DYNAVAX TECHNOLOGIES CORPORATION (US) 2004-07-15 WO disclosed
US-20040136948-A1 Branched immunomodulatory compounds and methods of using the same DYNAVAX TECHNOLOGIES CORPORATION 2004-07-15 US disclosed
EP-0604409-B1 OLIGONUCLEOTIDE ANALOGS FOR DETECTING AND MODULATING RNA ACTIVITY AND GENE EXPRESSION ISIS PHARMACEUTICALS INC (US) 2004-07-14 EP disclosed
US-6743902-B1 FOR USE IN ANTISENSE THERAPY FOR ENHANCING NUCLEASE RESISTANCE AND CELLULAR UPTAKE VALEANT PHARMACEUTICALS INTERNATIONAL 2004-06-01 US disclosed
EP-1418179-A2 Compositions and methods for detecting and modulating rna activity and gene expression ISIS PHARMACEUTICALS, INC. (US) 2004-05-12 EP disclosed
US-6262241-B1 ANTISENSE COMPOUNDS WHICH CLEAVE PHOSPHORODIESTER BONDS AND IMPROVE PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES OF OLIGONUCLEOTIDES, USEFUL IN DIAGNOSING DISEASES ISIS PHARMACEUTICALS, INC. 2001-07-17 US disclosed
US-6191266-B1 MODIFIED TO COMPRISE SUBSTITUTIONS AT POSITIONS C1', C3', C4' OR C5' OF THE SUGAR MOIETY OF THE NUCLEOSIDE, INCLUDING AN OPTIONAL 3' PHOSPHOROAMIDITE GROUP; USE IN MAKING NUCLEASE RESISTANT OLIGONUCLEOTIDES FOR ANTISENSE THERAPY ICN PHARMACEUTICALS, INC. 2001-02-20 US disclosed
EP-0789706-A4 SUGAR MODIFIED NUCLEOSIDES AND THEIR USE FOR SYNTHESIS OF OLIGONUCLEOTIDES ICN PHARMACEUTICALS (US) 1999-08-11 EP disclosed
US-5712378-A SUGAR MOLECULE IS SUBSTITUTED WITH HYDROCARBON OR SUBSTITUTED HYDROCARBON GROUPS, ANTISENSE AGENTS ICN PHARMACEUTICALS (US) 1998-01-27 US disclosed
EP-0789706-A1 SUGAR MODIFIED NUCLEOSIDES AND THEIR USE FOR SYNTHESIS OF OLIGONUCLEOTIDES ICN PHARMACEUTICALS (US) 1997-08-20 EP disclosed
EP-0604409-A4 COMPOSITIONS AND METHODS FOR DETECTING AND MODULATING RNA ACTIVITY AND GENE EXPRESSION. ISIS PHARMACEUTICALS INC (US) 1996-06-12 EP disclosed
WO-1996014329-A1 SUGAR MODIFIED NUCLEOSIDES AND THEIR USE FOR SYNTHESIS OF OLIGONUCLEOTIDES ICN PHARMACEUTICALS (US) 1996-05-17 WO disclosed
EP-0604409-A1 COMPOSITIONS AND METHODS FOR DETECTING AND MODULATING RNA ACTIVITY AND GENE EXPRESSION ISIS PHARMACEUTICALS, INC. (US) 1994-07-06 EP disclosed
WO-1991010671-A1 COMPOSITIONS AND METHODS FOR DETECTING AND MODULATING RNA ACTIVITY AND GENE EXPRESSION ISIS PHARMACEUTICALS, INC. (US) 1991-07-25 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 (1 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-20040136948-A1 Branched immunomodulatory compounds and methods of using the same IFNG, ICOS, IL2 TK1 2894/4885ALB 2890/4885PKM 2228/4885

“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.