SCHEMBL1096766

SCHEMBL1096766

COc1ccc(C(OC[C@@]23CO[C@@H]([C@H](n4cnc5c(NC(=O)c6ccccc6)ncnc54)O2)[C@@H]3OP(OCCC#N)N(C(C)C)C(C)C)(c2ccccc2)c2ccc(OC)cc2)cc1

nearest known ligand 0.39

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
TYMP P19971 1/20 0.34
PRMT6 Q96LA8 1/20 0.33
ADORA2A P29274 1/20 0.32
ADORA2B P29275 1/20 0.32
GAPDH P04406 1/20 0.32
ADORA3 P0DMS8 1/20 0.32
PRKAG1 P54619 1/20 0.32
PRKAA1 Q13131 1/20 0.32
PRKAB1 Q9Y478 1/20 0.32
P2RY12 Q9H244 1/20 0.31

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
SCHEMBL5558224 1.00 TYMP (0.34) TYMPPRMT6ADORA2AADORA2BGAPDH
SCHEMBL29881527 1.00 TYMP (0.34) TYMPPRMT6ADORA2AADORA2BGAPDH
SCHEMBL25727 0.95 TYMP (0.33) TYMPPRMT6ADORA2AADORA2BGAPDH
SCHEMBL4620914 0.93 CDK5 (0.34) TYMP
SCHEMBL211959 0.91 ADORA2A (0.32) TYMPPRMT6ADORA2AADORA2BADORA3
SCHEMBL29793195 0.91 TYMP (0.33) TYMP
SCHEMBL19825361 0.91 PRMT6 (0.33) PRMT6ADORA2AADORA2BGAPDHADORA3
SCHEMBL19814045 0.91 PRMT6 (0.33) PRMT6ADORA2AADORA2BGAPDHADORA3
SCHEMBL29793002 0.91 TYMP (0.33) TYMP
SCHEMBL210112 0.90 ADORA2B (0.33) PRMT6ADORA2AADORA2BADORA3PRKAG1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210170043-A1 DC-SIGN ANTIBODY CONJUGATES COMPRISING STING AGONISTS CHINOOK THERAPEUTICS, INC. 2021-06-10 US disclosed
US-9885036-B2 Double-stranded polynucleotide DAIICHI SANKYO COMPANY, LIMITED (JP) 2018-02-06 US disclosed
EP-1015469-B2 BI- AND TRI-CYCLIC NUCLEOSIDE, NUCLEOTIDE AND OLIGONUCLEOIDE ANALOGUES EXIQON AS (DK) 2015-11-18 EP disclosed
EP-2305805-B1 DOUBLE-STRANDED POLYNUCLEOTIDE DAIICHI SANKYO CO LTD (JP) 2015-11-11 EP disclosed
US-8153365-B2 Oligonucleotide analogues EXIQON A/S (DK) 2012-04-10 US disclosed
US-8080644-B2 Oligonucleotide analogues EXIQON A/S (DK) 2011-12-20 US disclosed
US-8034909-B2 Oligonucleotide analogues EXIQON A/S (DK) 2011-10-11 US disclosed
US-20110245327-A1 Oligonucleotide Analogues EXIQON A/S (DK) 2011-10-06 US disclosed
EP-2341058-A2 Oligonucleotide Analogues Exiqon A/S (DK) 2011-07-06 EP disclosed
EP-2341057-A2 Oligonucleotide Analogues Exiqon A/S (DK) 2011-07-06 EP disclosed
US-7153954-B2 Method for preparation of LNA phosphoramidites SANTARIS PHARMA A/S (DK) 2006-12-26 US disclosed
US-7034133-B2 Locked Nucleoside Analogues is a biochemical conjugate of nucleotides; as an aptamer in specific binding of antibiotics, drugs, amino acids, peptides, enzymes, saccharides, polysaccharides; heat resistance EXIQON A/S (DK) 2006-04-25 US disclosed
US-20050287566-A1 BICYCLIC LOCKED NUCLEOSIDE ANALOGUES; using an oligomer to isolate, purify, amplify, detect, identify, quantify or capture a natural or synthetic nucleic acid QIAGEN GMBH (DE) 2005-12-29 US disclosed
EP-1557424-A1 Bi-cyclic nucleoside, nucleotide and oligonucleoide analogues Exiqon A/S (DK) 2005-07-27 EP disclosed
EP-1015469-B1 BI- AND TRI-CYCLIC NUCLEOSIDE, NUCLEOTIDE AND OLIGONUCLEOIDE ANALOGUES EXIQON AS (DK) 2005-04-13 EP disclosed
EP-1409497-B1 METHOD FOR PREPARATION OF LNA PHOSPHORAMIDITES SANTARIS PHARMA AS (DK) 2005-01-19 EP disclosed
US-6794499-B2 BICYCLIC LOCKED NUCLEOSIDE ANALOGUES EXIQON A/S (DK) 2004-09-21 US disclosed
US-6670461-B1 Bi-, tri, or polycyclic nucleoside analogues having a \"locked\" structure capable of forming heat resistant nucleobase specific duplexes and triplexes with single and double stranded nucleic acids. EXIQON A/S (DK) 2003-12-30 US disclosed
US-20030134808-A1 Oligonucleotide analogues WENGEL JESPER (DK) 2003-07-17 US disclosed
US-20030032794-A1 Method for preparation of LNA phosphoramidites SANTARIS PHARMA A/S (DK) 2003-02-13 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 (5 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-20030032794-A1 Method for preparation of LNA phosphoramidites NCL, PNP, RNGTT TYMP 9/4885PRMT6 1119/4885ADORA2A 1186/4885
US-20030134808-A1 Oligonucleotide analogues TARBP1, DCLRE1B, ADAR TYMP 23/4885PRMT6 4729/4885ADORA2A 696/4885
US-20210170043-A1 DC-SIGN ANTIBODY CONJUGATES COMPRISING STING AGONISTS STING1, TLR9, TLR3 TYMP 2769/4885PRMT6 2065/4885ADORA2A 693/4885
US-20110245327-A1 Oligonucleotide Analogues POLRMT, POLM, POLN TYMP 19/4885PRMT6 4771/4885ADORA2A 246/4885
US-20050287566-A1 BICYCLIC LOCKED NUCLEOSIDE ANALOGUES; using an oligomer to isolate, purify, amplify, detect, identify, quantify or capture a natural or synthetic nucleic acid POLRMT, POLM, POLN TYMP 61/4885PRMT6 4752/4885ADORA2A 224/4885

“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.