Adenosine

Adenosine

SCHEMBL459769

Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O.Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O.O=P(O)(O)O.O=P(O)(O)O.O=P(O)(O)O.O=P(O)(O)O

nearest known ligand 0.89

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
ADORA1 known ✓ P30542 3/20 0.89
ADORA3 known ✓ P0DMS8 3/20 0.89
ADORA2A known ✓ P29274 1/20 0.89
ADORA2B known ✓ P29275 1/20 0.89
SMN1; SMN2 Q16637 3/20 0.89
DPP4 P27487 1/20 0.89
MEN1 O00255 1/20 0.89
SLC28A1 O00337 1/20 0.89
MAP3K7 O43318 1/20 0.89
SLC28A2 O43868 1/20 0.89
GAPDH P04406 1/20 0.89
MAPK1 P28482 1/20 0.89
STAT6 P42226 1/20 0.89
PI4KA P42356 1/20 0.89
KMT2A Q03164 1/20 0.89
PI4K2B Q8TCG2 1/20 0.89
DOT1L Q8TEK3 1/20 0.89
SLC29A1 Q99808 1/20 0.89
PI4K2A Q9BTU6 1/20 0.89
SLC28A3 Q9HAS3 1/20 0.89

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 SCHEMBL6242700 1.00 ADORA1 (0.89) ADORA1SMN1; SMN2ADORA3DPP4MEN1
Adenosine SCHEMBL9171507 1.00 ADORA1 (0.89) ADORA1SMN1; SMN2ADORA3DPP4MEN1
Adenosine SCHEMBL3046213 1.00 ADORA1 (0.89) ADORA1SMN1; SMN2ADORA3DPP4MEN1
Adenosine SCHEMBL3031964 1.00 ADORA1 (0.89) ADORA1SMN1; SMN2ADORA3DPP4MEN1
Adenosine SCHEMBL1746637 1.00 ADORA1 (0.89) ADORA1SMN1; SMN2ADORA3DPP4MEN1
Adenosine SCHEMBL50788 1.00 ADORA1 (0.89) ADORA1SMN1; SMN2ADORA3DPP4MEN1
Adenosine SCHEMBL468212 1.00 ADORA1 (0.89) ADORA1SMN1; SMN2ADORA3DPP4MEN1
Adenosine SCHEMBL1744578 1.00 ADORA1 (0.89) ADORA1SMN1; SMN2ADORA3DPP4MEN1
Vidarabine SCHEMBL7103173 1.00 ADORA1 (0.89) ADORA1SMN1; SMN2ADORA3DPP4MEN1
Adenosine SCHEMBL9147194 1.00 ADORA1 (0.89) ADORA1SMN1; SMN2ADORA3DPP4MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4600370-A1 NUDE.1 AS A DECAPPING ENZYME FOR COFACTOR- AND \"CANONICALLY\"-CAPPED RNA SPECIES Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2025-08-13 EP claimed
US-20250049894-A1 TREATMENT OF NUDT2 MUTATION UNIV GENEVE (CH) 2025-02-13 US claimed
EP-4408431-A1 TREATMENT OF NUDT2 MUTATION Université de Genève (CH) 2024-08-07 EP claimed
EP-4389214-A2 USE OF TRIMETHOXYBENZYL ACETYLSINAPATE, ADVANTAGEOUSLY IN COMBINATION WITH AT LEAST ONE SUNSCREEN, FOR PROTECTING THE SKIN Thorel, Jean-Noël (FR) 2024-06-26 EP claimed
EP-3466419-B1 USE OF TRIMETHOXYBENZYL ACETYLSINAPATE, ADVANTAGEOUSLY IN COMBINATION WITH AT LEAST ONE SUNSCREEN, FOR PROTECTING THE SKIN THOREL JEAN NOEL (FR) 2024-05-08 EP claimed
CN-117070547-A Application of modified APaH gene in improving expression activity of exogenous gene 齐鲁工业大学(山东省科学院) 2023-11-17 CN claimed
WO-2023052411-A1 TREATMENT OF NUDT2 MUTATION UNIVERSITÉ DE GENÈVE (CH) 2023-04-06 WO claimed
EP-3466419-A1 USE OF TRIMETHOXYBENZYL ACETYLSINAPATE, ADVANTAGEOUSLY IN COMBINATION WITH AT LEAST ONE SUNSCREEN, FOR PROTECTING THE SKIN Thorel, Jean-Noël (FR) 2019-04-10 EP claimed
EP-1581177-B1 CUTANEOUS METABOLIC BIO-ACTIVATOR THOREL JEAN NOEL (FR) 2018-04-11 EP claimed
US-20150369817-A1 PLATELET BIOMARKERS IN CANCER DIAGNOSIS NEOPROTEOMICS AB (SE) 2015-12-24 US claimed
EP-0969848-A1 USE OF DIADENOSINE POLYPHOSPHATES FOR REDUCING BLOOD PRESSURE Clemson University (US) 2000-01-12 EP claimed
WO-1999043326-A1 USE OF A CARDIAC PURINOCEPTOR TO EFFECT CELLULAR GLUCOSE UPTAKE THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 1999-09-02 WO claimed
EP-0721955-B1 Diadenosine tetraphosphate tetrasodium salt dodecahydrate crystals UNITIKA LTD (JP) 1999-04-07 EP claimed
WO-1998030222-A1 USE OF DIADENOSINE POLYPHOSPHATES FOR REDUCING BLOOD PRESSURE CLEMSON UNIVERSITY (US) 1998-07-16 WO claimed
EP-0566140-B1 Method for producing dinucleoside polyphosphate, nucleoside polyphosphate or derivatives thereof UNITIKA LTD (JP) 1998-07-01 EP claimed
US-5306629-A Two-stage reaction using two enzymes: adenosine-5-triphosphate sulfurylase and diadenosine tetraphosphate phosphorylase as catalysts, and adenosine-5-triphosphate, polyphosphate and a sulfate as substrates UNITIKA LTD. (JP) 1994-04-26 US claimed
EP-0566140-A2 Method for producing dinucleoside polyphosphate, nucleoside polyphosphate or derivatives thereof UNITIKA LTD. (JP) 1993-10-20 EP claimed
EP-0247819-B1 PROCESS FOR PRODUCING DIADENOSINE TETRAPHOSPHATE AND DERIVATIVES THEREOF UNITIKA LTD. (JP) 1991-07-24 EP claimed
US-4886749-A Process for producing diadenosine tetraphosphate and derivatives thereof UNITIKA LTD. (JP) 1989-12-12 US claimed
EP-0247819-A2 Process for producing diadenosine tetraphosphate and derivatives thereof UNITIKA LTD. (JP) 1987-12-02 EP claimed