SCHEMBL6906164

SCHEMBL6906164

C#Cc1cn([C@H]2CC(O)[C@@H](CO)O2)c(=O)nc1N

nearest known ligand 0.60

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
DNMT1 P26358 6/20 0.60
ADRB1 P08588 1/20 0.60
DNMT3B Q9UBC3 2/20 0.52
LMNA P02545 3/20 0.48
SMN1; SMN2 Q16637 3/20 0.48
TK1 P04183 2/20 0.48
PNP P00491 1/20 0.47
TP53 P04637 1/20 0.47
HTT P42858 1/20 0.47
PDE4D Q08499 1/20 0.47
PDE3A Q14432 1/20 0.47
RXFP1 Q9HBX9 1/20 0.47
FPR2 P25090 1/20 0.46
ALOX12 P18054 1/20 0.46
ADRA1A P35348 1/20 0.46
TK2 O00142 1/20 0.45

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
SCHEMBL15740192 1.00 DNMT1 (0.60) DNMT1ADRB1DNMT3BLMNASMN1; SMN2
SCHEMBL29070733 1.00 DNMT1 (0.60) DNMT1ADRB1DNMT3BLMNASMN1; SMN2
SCHEMBL5982159 1.00 DNMT1 (0.60) DNMT1ADRB1DNMT3BLMNASMN1; SMN2
SCHEMBL6906161 1.00 DNMT1 (0.60) DNMT1ADRB1DNMT3BLMNASMN1; SMN2
SCHEMBL5982164 1.00 DNMT1 (0.60) DNMT1ADRB1DNMT3BLMNASMN1; SMN2
SCHEMBL5983326 0.89 DNMT1 (0.60) DNMT1ADRB1DNMT3BLMNASMN1; SMN2
SCHEMBL5983324 0.89 DNMT1 (0.60) DNMT1ADRB1DNMT3BLMNASMN1; SMN2
SCHEMBL13293701 0.88 DNMT1 (0.45) DNMT1ADRB1DNMT3BLMNASMN1; SMN2
SCHEMBL10015665 0.87 DNMT1 (0.53) DNMT1ADRB1DNMT3BLMNASMN1; SMN2
SCHEMBL25492471 0.87 DNMT1 (0.57) DNMT1ADRB1DNMT3BLMNASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12612662-B2 DNA repair site detection for personal genomics, epigenomics, and gene therapy SALK INSTITUTE FOR BIOLOGICAL STUDIES (US) 2026-04-28 US claimed
US-20240254545-A1 SPATIOTEMPORALLY RESOLVED TRANSCRIPTOMICS AT SUBCELLULAR RESOLUTION THE BROAD INSTITUTE, INC. (US) 2024-08-01 US claimed
EP-4334471-A1 SPATIOTEMPORALLY RESOLVED TRANSCRIPTOMICS AT SUBCELLULAR RESOLUTION The Broad Institute Inc. (US) 2024-03-13 EP claimed
CN-117616135-A Subcellular resolution space-time resolved transcriptome 布罗德研究所股份有限公司 2024-02-27 CN claimed
US-20230111083-A1 DNA REPAIR SITE DETECTION FOR PERSONAL GENOMICS, EPIGENOMICS, AND GENE THERAPY SALK INSTITUTE FOR BIOLOGICAL STUDIES (US) 2023-04-13 US claimed
WO-2022236011-A1 SPATIOTEMPORALLY RESOLVED TRANSCRIPTOMICS AT SUBCELLULAR RESOLUTION THE BROAD INSTITUTE, INC. (US) 2022-11-10 WO claimed
WO-2021194531-A1 DNA REPAIR SITE DETECTION FOR PERSONAL GENOMICS, EPIGENOMICS, AND GENE THERAPY SALK INSTITUTE FOR BIOLOGICAL STUDIES (US) 2021-09-30 WO claimed
CN-111201327-A Method for detecting one or more DNA ends and uses thereof 音图基因公司 2020-05-26 CN claimed
EP-3186387-B1 METHOD OF DETERMINING THE ACTIVITY OF ENZYMES CONVERTING CYTOSINE DERIVATIVES TO URACIL DERIVATIVES IN CELLS, TISSUES AND ORGANISMS UNIV PALACKEHO (CZ) 2018-10-17 EP claimed
EP-3186387-A1 METHOD OF DETERMINING THE ACTIVITY OF ENZYMES CONVERTING CYTOSINE DERIVATIVES TO URACIL DERIVATIVES IN CELLS, TISSUES AND ORGANISMS Univerzita Palackého v Olomouci (CZ) 2017-07-05 EP claimed
WO-2016029889-A1 METHOD OF DETERMINING THE ACTIVITY OF ENZYMES CONVERTING CYTOSINE DERIVATIVES TO URACIL DERIVATIVES IN CELLS, TISSUES AND ORGANISMS UNIVERZITA PALACKEHO V OLOMOUCI (CZ) 2016-03-03 WO claimed
EP-0923596-A2 LIPOPHILIC OLIGONUCLEOTIDE ANALOGS GILEAD SCIENCES, INC. (US) 1999-06-23 EP claimed
US-5763208-A Oligonucleotides and their analogs capable of passive cell membrane permeation GILEAD SCIENCES, INC. (US) 1998-06-09 US claimed
WO-1998004575-A2 LIPOPHILIC OLIGONUCLEOTIDE ANALOGS GILEAD SCIENCES, INC. (US) 1998-02-05 WO claimed
US-5633360-A CONTAINS AT LEAST TWO NUCLEOSIDE RESIDUES AND INTERNUCLEOTIDE LINKAGES GILEAD SCIENCES, INC. (US) 1997-05-27 US claimed
EP-0573479-A1 CHIMERIC TAR ENZYME CONSTRUCTION FOR HIV THERAPY THE WELLCOME FOUNDATION LIMITED (GB) 1993-12-15 EP claimed
WO-1992015693-A1 CHIMERIC TAR ENZYME CONSTRUCTION FOR HIV THERAPY THE WELLCOME FOUNDATION LIMITED (GB) 1992-09-17 WO claimed
US-12612662-B2 DNA repair site detection for personal genomics, epigenomics, and gene therapy SALK INSTITUTE FOR BIOLOGICAL STUDIES (US) 2026-04-28 US disclosed
EP-0417560-A1 Antiviral compounds THE WELLCOME FOUNDATION LIMITED (GB) 1991-03-20 EP disclosed
EP-0272065-A2 Antiviral compounds THE WELLCOME FOUNDATION LIMITED (GB) 1988-06-22 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 (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-12612662-B2 DNA repair site detection for personal genomics, epigenomics, and gene therapy OGG1, BRCA1, TNNC1 DNMT1 7/4885ADRB1 2522/4885DNMT3B 10/4885

“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.