SCHEMBL1097616

SCHEMBL1097616

CC1(C)O[C@@H]2[C@H](O1)[C@@H](CO)O[C@H]2n1cnc2c(NC(=O)c3ccccc3)ncnc21

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PI4KA P42356 1/20 0.62
PI4K2B Q8TCG2 1/20 0.62
PI4K2A Q9BTU6 1/20 0.62
PI4KB Q9UBF8 1/20 0.62
P2RY12 Q9H244 1/20 0.55
ADORA1 P30542 4/20 0.52
ADORA3 P0DMS8 3/20 0.51
SLC29A1 Q99808 2/20 0.51
TP53 P04637 1/20 0.51
TDP1 Q9NUW8 1/20 0.51
LMNA P02545 2/20 0.51
NFKB1 P19838 2/20 0.51
THPO P40225 2/20 0.51
ADORA2A P29274 2/20 0.51
ALDH1A1 P00352 1/20 0.51
GLA P06280 1/20 0.51
PMP22 Q01453 1/20 0.51
SMN1; SMN2 Q16637 1/20 0.51
NPC1 O15118 1/20 0.51
NPY1R P25929 1/20 0.51

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
SCHEMBL22402681 1.00 PI4KA (0.62) PI4KAPI4K2BPI4K2API4KBP2RY12
SCHEMBL22601403 1.00 PI4KA (0.62) PI4KAPI4K2BPI4K2API4KBP2RY12
SCHEMBL29444514 1.00 PI4KA (0.62) PI4KAPI4K2BPI4K2API4KBP2RY12
SCHEMBL30827092 1.00 PI4KA (0.62) PI4KAPI4K2BPI4K2API4KBP2RY12
SCHEMBL16378775 1.00 PI4KA (0.62) PI4KAPI4K2BPI4K2API4KBP2RY12
SCHEMBL26361736 1.00 PI4KA (0.62) PI4KAPI4K2BPI4K2API4KBP2RY12
SCHEMBL1795484 1.00 PI4KA (0.62) PI4KAPI4K2BPI4K2API4KBP2RY12
SCHEMBL21504639 0.93 PI4KA (0.52) PI4KAPI4K2BPI4K2API4KBP2RY12
SCHEMBL26937492 0.93 PI4KA (0.52) PI4KAPI4K2BPI4K2API4KBP2RY12
SCHEMBL26361740 0.93 PI4KA (0.52) PI4KAPI4K2BPI4K2API4KBP2RY12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240325426-A1 POLYNUCLEOTIDE AND PHARMACEUTICAL COMPOSITION KYOWA KIRIN CO., LTD. (JP) 2024-10-03 US disclosed
US-12077558-B2 Phosphorus (V)-based reagents, processes for the preparation thereof, and their use in making stereo-defined organophosphorus (V) compounds BRISTOL-MYERS SQUIBB COMPANY (US) 2024-09-03 US disclosed
EP-4365288-A1 POLYNUCLEOTIDE AND MEDICINAL COMPOSITION Kyowa Kirin Co., Ltd. (JP) 2024-05-08 EP disclosed
US-20240124511-A1 COMPOSITIONS AND METHODS OF MODULATING THE IMMUNE RESPONSE BY ACTIVATING ALPHA PROTEIN KINASE 1 TIANJIN HONGKE BAISHI QIXIN VENTURE CAPITAL PARTNERSHIP (LIMITED PARTNERSHIP) (CN) 2024-04-18 US disclosed
US-11840551-B2 Compositions and methods of modulating the immune response by activating alpha protein kinase 1 SHANGHAI YAO YUAN BIOTECHNOLOGY CO., LTD. (CN) 2023-12-12 US disclosed
US-11773131-B2 Compositions and methods of modulating the immune response by activating alpha protein kinase 1 SHANGHAI YAO YUAN BIOTECHNOLOGY CO., LTD. (CN) 2023-10-03 US disclosed
US-20230242569-A1 PHOSPHOROUS (V)-BASED REAGENTS, PROCESSES FOR THE PREPARATION THEREOF, AND THEIR USE IN MAKING STEREO-DEFINED ORGANOPHOSHOROUS (V) COMPOUNDS THE SCRIPPS RESEARCH INSTITUTE 2023-08-03 US disclosed
US-20230242569-A1 PHOSPHOROUS (V)-BASED REAGENTS, PROCESSES FOR THE PREPARATION THEREOF, AND THEIR USE IN MAKING STEREO-DEFINED ORGANOPHOSHOROUS (V) COMPOUNDS THE SCRIPPS RESEARCH INSTITUTE 2023-08-03 US disclosed
US-11613554-B2 Phosphorous (V)-based reagents, processes for the preparation thereof, and their use in making stereo-defined organophoshorous (V) compounds BRISTOL-MYERS SQUIBB COMPANY (US) 2023-03-28 US disclosed
US-20230073999-A1 POLYNUCLEOTIDE AND PHARMACEUTICAL COMPOSITION NATIONAL UNIVERSITY CORPORATION TOKAI NATIONAL HIGHER EDUCATION AND RESEARCH SYSTEM (JP) 2023-03-09 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-1545555-A2 COMPOSITIONS AND METHODS FOR TREATING EPITHELIAL AND RETINAL TISSUE DISEASES Inspire Pharmaceuticals, Inc. (US) 2005-06-29 EP disclosed
EP-1015469-B1 BI- AND TRI-CYCLIC NUCLEOSIDE, NUCLEOTIDE AND OLIGONUCLEOIDE ANALOGUES EXIQON AS (DK) 2005-04-13 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
WO-2003072067-A2 COMPOSITIONS AND METHODS FOR TREATING EPITHELIAL AND RETINAL TISSUE DISEASES INSPIRE PHARMACEUTICALS, INC. (US) 2003-09-04 WO disclosed
US-20030134808-A1 Oligonucleotide analogues WENGEL JESPER (DK) 2003-07-17 US disclosed
EP-0422638-A1 Novel inosine/guanosine derivatives MERRELL DOW PHARMACEUTICALS INC. (US) 1991-04-17 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 (9 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-20240325426-A1 POLYNUCLEOTIDE AND PHARMACEUTICAL COMPOSITION RNGTT, RNMT, NT5C PI4KA 2805/4885PI4K2B 2788/4885PI4K2A 2326/4885
US-20230242569-A1 PHOSPHOROUS (V)-BASED REAGENTS, PROCESSES FOR THE PREPARATION THEREOF, AND THEIR USE IN MAKING STEREO-DEFINED ORGANOPHOSHOROUS (V) COMPOUNDS PPIP5K2, INPP5B, PTMS PI4KA 93/4885PI4K2B 110/4885PI4K2A 113/4885
US-20030134808-A1 Oligonucleotide analogues TARBP1, DCLRE1B, ADAR PI4KA 3880/4885PI4K2B 4159/4885PI4K2A 3812/4885
US-12077558-B2 Phosphorus (V)-based reagents, processes for the preparation thereof, and their use in making stereo-defined organophosphorus (V) compounds PPIP5K2, PLCB3, PLCG2 PI4KA 41/4885PI4K2B 58/4885PI4K2A 62/4885
US-11840551-B2 Compositions and methods of modulating the immune response by activating alpha protein kinase 1 PHKA1, PHKA2, PRKCA PI4KA 123/4885PI4K2B 194/4885PI4K2A 147/4885
US-20240124511-A1 COMPOSITIONS AND METHODS OF MODULATING THE IMMUNE RESPONSE BY ACTIVATING ALPHA PROTEIN KINASE 1 PHKA1, PHKA2, PRKCA PI4KA 123/4885PI4K2B 194/4885PI4K2A 147/4885
US-11613554-B2 Phosphorous (V)-based reagents, processes for the preparation thereof, and their use in making stereo-defined organophoshorous (V) compounds PPIP5K2, INPP5B, PTMS PI4KA 93/4885PI4K2B 110/4885PI4K2A 113/4885
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 PI4KA 2324/4885PI4K2B 3143/4885PI4K2A 2558/4885
US-11773131-B2 Compositions and methods of modulating the immune response by activating alpha protein kinase 1 PHKA1, PHKA2, PRKCA PI4KA 123/4885PI4K2B 194/4885PI4K2A 147/4885

“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.