SCHEMBL367683

SCHEMBL367683

Nc1nc2c(nnn2[C@H]2CC(O)[C@@H](CO)O2)c(=O)[nH]1

nearest known ligand 0.47

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
▸ PNP P00491 6/20 0.47
▸ TK1 P04183 2/20 0.45
▸ ADRB1 P08588 1/20 0.45
▸ DNMT1 P26358 1/20 0.45
▸ POLA1 P09884 1/20 0.45
▸ POLB P06746 1/20 0.44
▸ LMNA P02545 2/20 0.42
▸ SMN1; SMN2 Q16637 2/20 0.42
▸ TK2 O00142 1/20 0.42
▸ TP53 P04637 1/20 0.41
▸ HTT P42858 1/20 0.41
▸ PDE4D Q08499 1/20 0.41
▸ PDE3A Q14432 1/20 0.41
▸ RXFP1 Q9HBX9 1/20 0.41

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
SCHEMBL4624825 1.00 PNP (0.47) PNPTK1ADRB1DNMT1POLA1
SCHEMBL22399465 0.88 PNP (0.44) PNPTK1POLA1POLB
SCHEMBL29875802 0.84 POLB (0.46) PNPPOLA1POLB
SCHEMBL8185378 0.81 POLB (0.59) PNPPOLA1POLB
SCHEMBL6421906 0.81 POLB (0.59) PNPPOLA1POLB
SCHEMBL26787693 0.81 TK1 (0.46) PNPTK1ADRB1DNMT1POLA1
SCHEMBL655858 0.81 PNP (0.65) PNPTK1ADRB1DNMT1POLB
SCHEMBL21637039 0.81 TK1 (0.46) PNPTK1ADRB1DNMT1POLA1
SCHEMBL655857 0.81 PNP (0.65) PNPTK1ADRB1DNMT1POLB
SCHEMBL21779018 0.80 PNP (0.55) PNPTK1ADRB1DNMT1POLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2361980-A1 Methods and compositions for inhibition of immune responses and autoimmunity Dynavax Technologies Corporation (US) 2011-08-31 — — EP claimed
US-20240150389-A1 MODIFIED GUANINES NUCLERA LTD (GB) 2024-05-09 — — US disclosed
US-20230287034-A1 CYCLIC DINUCLEOTIDES AS STING AGONISTS JANSSEN BIOTECH INC (US) 2023-09-14 — — US disclosed
US-20230257908-A1 MODIFIED DNA-ENCODED CHEMICAL LIBRARY AND METHODS RELATED THERETO TECHNISCHE UNIVERSITAET DORTMUND (DE) 2023-08-17 — — US disclosed
US-11597746-B2 Cyclic dinucleotides as sting agonists JANSSEN BIOTECH, INC. (US) 2023-03-07 — — US disclosed
EP-4127162-A1 MODIFIED DNA-ENCODED CHEMICAL LIBRARY AND METHODS RELATED THERETO Technische Universität Dortmund (DE) 2023-02-08 — — EP disclosed
US-20220389487-A1 Optical Instruments and Systems for Forensic DNA Quantitation ANDE CORPORATION (US) 2022-12-08 — — US disclosed
US-20220315996-A1 Optical Instruments and Systems for Forensic DNA Quantitation ANDE CORPORATION (US) 2022-10-06 — — US disclosed
US-11441173-B2 Optical instruments and systems for forensic DNA quantitation ANDE CORPORATION (US) 2022-09-13 — — US disclosed
WO-2022175685-A1 MODIFIED GUANINES NUCLERA NUCLEICS LTD (GB) 2022-08-25 — — WO disclosed
EP-1307469-A1 NUCLEIC ACID BINDING COMPOUNDS CONTAINING PYRAZOLO[3,4-D]PYRIMIDINE ANALOGUES OF PURIN-2,6-DIAMINE AND THEIR USES BOEHRINGER MANNHEIM GMBH (DE) 2003-05-07 — — EP disclosed
US-6511804-B1 Detecting amplified captured nucleic acids originating from the unknown microorganism; hybridization of the amplified captured nucleic acids to a species-specific nucleic acid sequence; nucleic acid analog SAIGENE CORPORATION 2003-01-28 — — US disclosed
US-20020193314-A1 Process for selectively producing 1-phosphorylated sugar derivative anomer and process for producing nucleoside MITSUI CHEMICALS, INC. (JP) 2002-12-19 — — US disclosed
WO-2002012263-A1 NUCLEIC ACID BINDING COMPOUNDS CONTAINING PYRAZOLO[3,4-D]PYRIMIDINE ANALOGUES OF PURIN-2,6-DIAMINE AND THEIR USES ROCHE DIAGNOSTICS GMBH (DE) 2002-02-14 — — WO disclosed
EP-1178051-A2 PROCESS FOR SELECTIVELY PRODUCING 1-PHOSPHORYLATED SUGAR DERIVATIVE ANOMER AND PROCESS FOR PRODUCING NUCLEOSIDE Mitsui Chemicals, Inc. (JP) 2002-02-06 — — EP disclosed
EP-1064396-A1 A SELECTIVE ASSAY FOR DETERMINING THE IDENTITY OF LIVE MICROORGANISMS IN A MIXED CULTURE Saigene Corporation (US) 2001-01-03 — — EP disclosed
US-6066720-A WITH AT LEAST ONE 8-AZAPURINE BASE; FORMS MORE STABLE HYBRIDIZATION COMPLEXES WITH NUCLEIC ACIDS; FOR ANTISENSE AGENTS, DIAGNOSTIC AGENTS, PROBES, PRIMERS HOECHST AKTIENGESELLSCHAFT (DE) 2000-05-23 — — US disclosed
WO-1999050441-A1 A SELECTIVE ASSAY FOR DETERMINING THE IDENTITY OF LIVE MICROORGANISMS IN A MIXED CULTURE SAIGENE CORPORATION (US) 1999-10-07 — — WO disclosed
US-5789562-A STABLE HYBRIDIZATION COMPLEXES WITH NUCLEI ACIDS HOECHST AKTIENGESELLSCHAFT (DE) 1998-08-04 — — US disclosed
US-4543255-A Carbocyclic analogs of purine 2'-deoxyribofuranosides SOUTHERN RESEARCH INSTITUTE (US) 1985-09-24 — — 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-20230257908-A1 MODIFIED DNA-ENCODED CHEMICAL LIBRARY AND METHODS RELATED THERETO DUT, DCTD, DNMT1 PNP 36/4885TK1 59/4885ADRB1 4622/4885
US-20230287034-A1 CYCLIC DINUCLEOTIDES AS STING AGONISTS STING1, CGAS, IFNAR1 PNP 313/4885TK1 430/4885ADRB1 163/4885
US-20240150389-A1 MODIFIED GUANINES NSUN2, RNMT, RNGTT PNP 72/4885TK1 374/4885ADRB1 3549/4885
US-20020193314-A1 Process for selectively producing 1-phosphorylated sugar derivative anomer and process for producing nucleoside PNP, GALE, MTAP PNP 1/4885TK1 198/4885ADRB1 3648/4885
US-11597746-B2 Cyclic dinucleotides as sting agonists STING1, CGAS, IFNAR1 PNP 319/4885TK1 414/4885ADRB1 186/4885

“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.

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