Adenosine

Adenosine

SCHEMBL1744580

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)OP(=O)(O)OP(=O)(O)O

nearest known ligand 0.82

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 0.80
▸ ADORA3 known ✓ P0DMS8 1/20 0.80
▸ ADORA2A known ✓ P29274 1/20 0.80
▸ ADORA2B known ✓ P29275 1/20 0.80
▸ P2RY2 P41231 4/20 0.82
▸ SMN1; SMN2 Q16637 3/20 0.80
▸ DPP4 P27487 1/20 0.80
▸ MEN1 O00255 1/20 0.80
▸ SLC28A1 O00337 1/20 0.80
▸ MAP3K7 O43318 1/20 0.80
▸ SLC28A2 O43868 1/20 0.80
▸ GAPDH P04406 1/20 0.80
▸ MAPK1 P28482 1/20 0.80
▸ STAT6 P42226 1/20 0.80
▸ PI4KA P42356 1/20 0.80
▸ KMT2A Q03164 1/20 0.80
▸ PI4K2B Q8TCG2 1/20 0.80
▸ DOT1L Q8TEK3 1/20 0.80
▸ SLC29A1 Q99808 1/20 0.80
▸ PI4K2A Q9BTU6 1/20 0.80

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 SCHEMBL29796534 1.00 P2RY2 (0.82) P2RY2ADORA1SMN1; SMN2DPP4MEN1
Vidarabine SCHEMBL7170349 1.00 P2RY2 (0.82) P2RY2ADORA1SMN1; SMN2DPP4MEN1
Adenosine SCHEMBL29397260 1.00 P2RY2 (0.82) P2RY2ADORA1SMN1; SMN2DPP4MEN1
Adenosine SCHEMBL2210868 1.00 P2RY2 (0.82) P2RY2ADORA1SMN1; SMN2DPP4MEN1
Adenosine SCHEMBL459770 0.99 P2RY2 (0.80) P2RY2ADORA1SMN1; SMN2DPP4MEN1
Adenosine SCHEMBL29362201 0.99 P2RY2 (0.80) P2RY2ADORA1SMN1; SMN2DPP4MEN1
Adenosine SCHEMBL28296801 0.99 P2RY2 (0.80) P2RY2ADORA1SMN1; SMN2DPP4MEN1
Adenosine SCHEMBL459996 0.99 P2RY2 (0.80) P2RY2ADORA1SMN1; SMN2DPP4MEN1
Adenosine SCHEMBL28186074 0.99 P2RY2 (0.80) P2RY2ADORA1SMN1; SMN2DPP4MEN1
Adenosine SCHEMBL28240733 0.99 P2RY2 (0.80) P2RY2ADORA1SMN1; SMN2DPP4MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8608922-B2 Biosensor for continuous monitoring of metabolites and proteins and methods of manufacture thereof THE UNIVERSITY OF CONNECTICUT (US) 2013-12-17 — — US claimed
US-20100116691-A1 BIOSENSOR FOR CONTINUOUS MONITORING OF METABOLITES AND PROTEINS AND METHODS OF MANUFACTURE THEREOF UNIVERSITY OF CONNECTICUT (US) 2010-05-13 — — US claimed
EP-0969848-A1 USE OF DIADENOSINE POLYPHOSPHATES FOR REDUCING BLOOD PRESSURE Clemson University (US) 2000-01-12 — — EP claimed
WO-1998030222-A1 USE OF DIADENOSINE POLYPHOSPHATES FOR REDUCING BLOOD PRESSURE CLEMSON UNIVERSITY (US) 1998-07-16 — — WO claimed
JP-62278992-A — — None — — JP disclosed
WO-2026106968-A1 COMPOSITIONS COMPRISING NEMATODE AMINOACYL-TRNA SYNTHETASE AND METHODS OF USING THE SAME THE MEDICAL COLLEGE OF WISCONSIN, INC. (US) 2026-05-21 — — WO disclosed
US-20260022384-A1 ASPARAGINE SYNTHETASE INHIBITORS AND USES THEREOF OSPEDALE SAN RAFFAELE S.R.L. (IT) 2026-01-22 — — US disclosed
WO-2025072741-A1 PRESERVATIVES FOR MOLECULAR SAMPLE ANALYSIS WITH SAMPLE COLLECTION DEVICES BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2025-04-03 — — WO disclosed
US-20250049894-A1 TREATMENT OF NUDT2 MUTATION UNIV GENEVE (CH) 2025-02-13 — — US disclosed
US-12181435-B2 Methionine concentration measurement method KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) 2024-12-31 — — US disclosed
EP-4408431-A1 TREATMENT OF NUDT2 MUTATION Université de Genève (CH) 2024-08-07 — — EP disclosed
US-20230181621-A1 ASPARAGINE SYNTHETASE INHIBITORS AND USES THEREOF OSPEDALE SAN RAFFAELE S.R.L. (IT) 2023-06-15 — — US disclosed
WO-2000003685-A2 NITRILASE HOMOLOGS THOMAS JEFFERSON UNIVERSITY (US) 2000-01-27 — — WO disclosed
EP-0969848-A1 USE OF DIADENOSINE POLYPHOSPHATES FOR REDUCING BLOOD PRESSURE Clemson University (US) 2000-01-12 — — EP disclosed
EP-0969848-A1 USE OF DIADENOSINE POLYPHOSPHATES FOR REDUCING BLOOD PRESSURE Clemson University (US) 2000-01-12 — — EP disclosed
WO-1998030222-A1 USE OF DIADENOSINE POLYPHOSPHATES FOR REDUCING BLOOD PRESSURE CLEMSON UNIVERSITY (US) 1998-07-16 — — WO disclosed
WO-1998030222-A1 USE OF DIADENOSINE POLYPHOSPHATES FOR REDUCING BLOOD PRESSURE CLEMSON UNIVERSITY (US) 1998-07-16 — — WO disclosed
EP-0247819-B1 PROCESS FOR PRODUCING DIADENOSINE TETRAPHOSPHATE AND DERIVATIVES THEREOF UNITIKA LTD. (JP) 1991-07-24 — — EP disclosed
US-4886749-A Process for producing diadenosine tetraphosphate and derivatives thereof UNITIKA LTD. (JP) 1989-12-12 — — US disclosed
JP-S62278992-A PRODUCTION OF DIADENOSINE-TETRAPHOSPHATE OR DERIVATIVE THEREOF UNITIKA LTD 1987-12-03 — — JP 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 (2 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-20230181621-A1 ASPARAGINE SYNTHETASE INHIBITORS AND USES THEREOF ASNS, GLS, GLS2 ADORA1 3853/4885ADORA3 4059/4885ADORA2A 4415/4885
US-20260022384-A1 ASPARAGINE SYNTHETASE INHIBITORS AND USES THEREOF ASNS, AARS1, NARS1 ADORA1 4144/4885ADORA3 4193/4885ADORA2A 4298/4885

“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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