Adenosine

Adenosine

SCHEMBL531208

Cc1cn([C@H]2C[C@H](O)[C@@H](CO)O2)c(=O)[nH]c1=O.Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O

nearest known ligand 0.76

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADORA1ADORA2AADORA2BADORA3

The experimentally established mechanism targets of Adenosine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ADORA3 known ✓ P0DMS8 3/20 0.61
ADORA2A known ✓ P29274 1/20 0.61
ADORA2B known ✓ P29275 1/20 0.61
ADORA1 known ✓ P30542 1/20 0.61
DTYMK P23919 4/20 0.76
DNMT1 P26358 7/20 0.62
DNMT3B Q9UBC3 4/20 0.62
FPR2 P25090 3/20 0.62
DPP4 P27487 1/20 0.61
MEN1 O00255 1/20 0.61
SLC28A1 O00337 1/20 0.61
MAP3K7 O43318 1/20 0.61
SLC28A2 O43868 1/20 0.61
GAPDH P04406 1/20 0.61
MAPK1 P28482 1/20 0.61
STAT6 P42226 1/20 0.61
PI4KA P42356 1/20 0.61
KMT2A Q03164 1/20 0.61
SMN1; SMN2 Q16637 1/20 0.61
PI4K2B Q8TCG2 1/20 0.61

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
Adenosine SCHEMBL6863617 1.00 DTYMK (0.76) DTYMKDNMT1DNMT3BFPR2ADORA3
Adenosine SCHEMBL8846731 0.94 DTYMK (0.69) DTYMKDNMT1DNMT3BFPR2ADORA3
Deoxyadenosine SCHEMBL20819422 0.93 DTYMK (0.67) DTYMKDNMT1DNMT3BFPR2SMN1; SMN2
Adenosine SCHEMBL23835231 0.92 DTYMK (0.66) DTYMKDNMT1DNMT3BFPR2ADORA3
Adenosine SCHEMBL7101792 0.92 DTYMK (0.66) DTYMKDNMT1DNMT3BFPR2ADORA3
Adenosine SCHEMBL1549514 0.92 DTYMK (0.66) DTYMKDNMT1DNMT3BFPR2ADORA3
Adenosine SCHEMBL3194871 0.89 DTYMK (0.91) DTYMKSMN1; SMN2
Adenosine SCHEMBL574772 0.89 DTYMK (0.63) DTYMKADORA3DPP4MEN1SLC28A1
Adenosine SCHEMBL9710357 0.89 DTYMK (0.66) DTYMKDNMT1DNMT3BFPR2ADORA3
Adenosine SCHEMBL10496357 0.89 DTYMK (0.69) DTYMKDNMT1DNMT3BFPR2ADORA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11732286-B2 T5 exonuclease-based method to identify DNA topoisomerase inhibitors THE FLORIDA INTERNATIONAL UNIVERSITY BOARD OF TRUSTEES (US) 2023-08-22 US claimed
US-20220170070-A1 T5 EXONUCLEASE-BASED METHOD TO IDENTIFY DNA TOPOISOMERASE INHIBITORS THE FLORIDA INTERNATIONAL UNIVERSITY BOARD OF TRUSTEES (US) 2022-06-02 US claimed
US-20220119858-A1 T5 EXONUCLEASE-BASED METHOD TO IDENTIFY DNA TOPOISOMERASE INHIBITORS THE FLORIDA INTERNATIONAL UNIVERSITY BOARD OF TRUSTEES (US) 2022-04-21 US claimed
US-11268129-B1 T5 exonuclease-based method to identify DNA topoisomerase inhibitors THE FLORIDA INTERNATIONAL UNIVERSITY BOARD OF TRUSTEES (US) 2022-03-08 US claimed
US-10150987-B2 Labeled circular DNA molecules for analysis of DNA topology, and topoisomerases and for drug screening THE FLORIDA INTERNATIONAL UNIVERSITY BOARD OF TRUSTEES (US) 2018-12-11 US claimed
US-20180135112-A1 LABELED CIRCULAR DNA MOLECULES FOR ANALYSIS OF DNA TOPOLOGY, AND TOPOISOMERASES AND FOR DRUG SCREENING THE FLORIDA INTERNATIONAL UNIVERSITY BOARD OF TRUSTEES (US) 2018-05-17 US claimed
US-9890416-B2 Labeled circular DNA molecules for analysis of DNA topology, and topoisomerases and for drug screening THE FLORIDA INTERNATIONAL UNIVERSITY BOARD OF TRUSTEES (US) 2018-02-13 US claimed
EP-2432314-B1 MOUSE MODELS CARRYING A KNOCK-OUT MUTATION OF THE QPCTL-GENE PROBIODRUG AG (DE) 2017-12-20 EP claimed
US-20170096701-A1 LABELED CIRCULAR DNA MOLECULES FOR ANALYSIS OF DNA TOPOLOGY, AND TOPOISOMERASES AND FOR DRUG SCREENING THE FLORIDA INTERNATIONAL UNIVERSITY BOARD OF TRUSTEES (US) 2017-04-06 US claimed
US-20130183765-A1 Ultraviolet and High-Performance Liquid Chromatography Methods for the Evaluation of Sunscreen Efficacy Sena Research Incorporated (US) 2013-07-18 US claimed
WO-2012037158-A2 ULTRAVIOLET AND HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY METHODS FOR THE EVALUATION OF SUNSCREEN EFFICACY SENA RESEARCH, INCORPORATED (US) 2012-03-22 WO claimed
EP-4330384-A1 ENZYME COMPOSITION WITH AT LEAST TWO DIFFERENT THERMOSTABLE POLYPEPTIDES HAVING TYPE II DNA METHYLTRANSFERASE ACTIVITY Blucon Biotech GmbH (DE) 2024-03-06 EP disclosed
CN-117441014-A Enzyme composition having at least two different thermostable polypeptides having type II DNA methyltransferase activity 布鲁克生物科技公司 2024-01-23 CN disclosed
US-20230364057-A1 BACTERIAL DNA GYRASE INHIBITORS AND METHODS OF USE THEREOF UNIVERSITY OF CENTRAL FLORIDA RESEARCH FOUNDATION, INC. 2023-11-16 US disclosed
US-11732286-B2 T5 exonuclease-based method to identify DNA topoisomerase inhibitors THE FLORIDA INTERNATIONAL UNIVERSITY BOARD OF TRUSTEES (US) 2023-08-22 US disclosed
US-6270962-B1 DECREASING INCIDENCE OF DNA(DEOXYRIBO NUCLEIC ACID) POLYMERASE STOPS OR PAUSING OCCURRING IN A REACTION MIXTURE CONTAINING A DNA POLYMERASE BY ADDING NITROGEN CONTAINING ORGANIC COMPOUNDS (E.G: BETAINE, TRIMETHYLAMINE N-OXIDE, ETC) THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2001-08-07 US disclosed
WO-2001003686-A2 INHIBITORS OF STAPHYLOCOCCUS SARA PROTEIN AND THEIR USE IN TREATING STAPHYLOCOCCAL INFECTIONS BOARD OF TRUSTEES OF THE UNIVERSITY OF ARKANSAS (US) 2001-01-18 WO disclosed
EP-0742838-A4 METHODS FOR THE ELIMINATION OF DNA SEQUENCING ARTIFACTS UNIV CALIFORNIA (US) 2000-01-05 EP disclosed
EP-0742838-A1 METHODS FOR THE ELIMINATION OF DNA SEQUENCING ARTIFACTS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1996-11-20 EP disclosed
WO-1995020682-A1 METHODS FOR THE ELIMINATION OF DNA SEQUENCING ARTIFACTS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1995-08-03 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-20230364057-A1 BACTERIAL DNA GYRASE INHIBITORS AND METHODS OF USE THEREOF TOP1, DNA2, TOP2A ADORA3 3677/4885ADORA2A 3990/4885ADORA2B 4337/4885

“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.