Sonedenoson

Sonedenoson

SCHEMBL1094599

Nc1nc(OCCc2ccc(Cl)cc2)nc2c1ncn2[C@@H]1O[C@H](CO)C(O)C1O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADORA2A

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

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
ADORA2A known ✓ P29274 17/20 1.00
ADORA2B P29275 14/20 1.00
ADORA1 P30542 7/20 1.00
ADORA3 P0DMS8 6/20 0.85

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
Sonedenoson SCHEMBL24838606 1.00 ADORA2A (1.00) ADORA2AADORA2BADORA1ADORA3
Sonedenoson SCHEMBL13010610 1.00 ADORA2A (1.00) ADORA2AADORA2BADORA1ADORA3
Sonedenoson SCHEMBL29379294 1.00 ADORA2A (1.00) ADORA2AADORA2BADORA1ADORA3
Sonedenoson SCHEMBL23898701 1.00 ADORA2A (1.00) ADORA2AADORA2BADORA1ADORA3
Sonedenoson SCHEMBL1094594 1.00 ADORA2A (1.00) ADORA2AADORA2BADORA1ADORA3
SCHEMBL8111704 0.93 ADORA2A (0.88) ADORA2AADORA2BADORA1ADORA3
SCHEMBL8111713 0.93 ADORA2A (0.88) ADORA2AADORA2BADORA1ADORA3
SCHEMBL14903077 0.92 ADORA2A (0.85) ADORA2AADORA2BADORA1ADORA3
SCHEMBL8111385 0.92 ADORA2A (0.86) ADORA2AADORA2BADORA1ADORA3
SCHEMBL2294338 0.92 ADORA2A (1.00) ADORA2AADORA2BADORA1ADORA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2491928-A2 Therapeutic agent for vitiligo and method of accelerating pigmentation The University of Tokyo (JP) 2012-08-29 EP claimed
US-8153781-B2 Dendrimer conjugates of agonists and antagonists of the GPCR superfamily THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2012-04-10 US claimed
US-20110144027-A1 PHARMACEUTICAL COMPOSITIONS FOR PROMOTING WOUND HEALING KING PHARMACEUTICALS RESEARCH AND DEVELOPMENT, INC. 2011-06-16 US claimed
US-20100324279-A1 CRYSTAL FORMS OF 2-[2-(4-CHLOROPHENYL)ETHOXY]ADENOSINE KING PHARMACEUTICALS RESEARCH AND DEVELOPMENT INC 2010-12-23 US claimed
EP-2225255-A1 CRYSTAL FORMS OF 2-[2-(4-CHLOROPHENYL)ETHOXY]ADENOSINE King Pharmaceuticals Research and Development Inc. (US) 2010-09-08 EP claimed
US-20100222275-A1 THERAPEUTIC AGENT FOR VITILIGO AND METHOD OF ACCELERATING PIGMENTATION MARUHO CO., LTD (JP) 2010-09-02 US claimed
EP-2198887-A1 THERAPEUTIC AGENT FOR LEUKODERMA AND METHOD FOR ACCELERATION OF PIGMENTATION The University of Tokyo (JP) 2010-06-23 EP claimed
EP-2170401-A1 DENDRIMER CONJUGATES OF AGONISTS AND ANTAGONISTS OF THE GPCR SUPERFAMILY Government of the United States of America, Represented by the Secretary, Department of Health and Human Services (US) 2010-04-07 EP claimed
WO-2009085909-A1 CRYSTAL FORMS OF 2-[2-(4-CHLOROPHENYL)ETHOXY]ADENOSINE KING PHARMACEUTICALS RESEARCH AND DEVELOPMENT, INC. (US) 2009-07-09 WO claimed
US-20090012035-A1 DENDRIMER CONJUGATES OF AGONISTS AND ANTAGONISTS OF THE GPCR SUPERFAMILY GOVERNMENT OF THE UNITED STATES OF AMERICA, REPRESENTED BY THE SECRETARY, DEPA (US) 2009-01-08 US claimed
WO-2009006046-A1 DENDRIMER CONJUGATES OF AGONISTS AND ANTAGONISTS OF THE GPCR SUPERFAMILY GOVERNMENT OF THE UNITED STATES OF AMERICA, REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2009-01-08 WO claimed
EP-2001489-A2 PHARMACEUTICAL COMPOSITIONS FOR PROMOTING WOUND HEALING King Pharmaceuticals Research and Development Inc. (US) 2008-12-17 EP claimed
US-7342003-B2 Synthesis of 2-aralkyloxyadenosines, 2-alkoxyadenosines, and their analogs KING PHARMACEUTICALS RESEARCH AND DEVELOPMENT, INC. (US) 2008-03-11 US claimed
WO-2007123740-A2 PHARMACEUTICAL COMPOSITIONS FOR PROMOTING WOUND HEALING KING PHARMACEUTICALS RESEARCH AND DEVELOPMENT, INC. (US) 2007-11-01 WO claimed
EP-1446413-A4 SYNTHESIS OF 2-ARALKOXY ADENOSINES AND 2-ALKOXYADENOSINES KING PHARMACEUTICALS RES & DEV (US) 2007-10-17 EP claimed
US-20070232561-A1 Pharmaceutical compositions for promoting wound healing KING PHARMACEUTICALS RESEARCH AND DEVELOPMENT, INC. 2007-10-04 US claimed
US-6951932-B2 Synthesis of 2-aralkoxyadenosines and 2-alkoxyadenosines KING PHARMACEUTICALS RESEARCH & DEVELOPMENT, INC. (US) 2005-10-04 US claimed
EP-1446413-A1 SYNTHESIS OF 2-ARALKOXY ADENOSINES AND 2-ALKOXYADENOSINES King Pharmaceuticals Research and Development Inc. (US) 2004-08-18 EP claimed
US-20030199686-A1 Synthesis of 2-aralkoxyadenosines and 2-alkoxyadenosines KING PHARMACEUTICALS RESEARCH AND DEVELOPMENT, INC. 2003-10-23 US claimed
WO-2003035662-A1 SYNTHESIS OF 2-ARALKOXY ADENOSINES AND 2-ALKOXYADENOSINES KING PHARMACEUTICALS RESEARCH & DEVELOPMENT, INC. (US) 2003-05-01 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 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-20030199686-A1 Synthesis of 2-aralkoxyadenosines and 2-alkoxyadenosines AMPD2, ADAR, ADA ADORA2A 16/4885ADORA2B 58/4885ADORA1 69/4885
US-20100222275-A1 THERAPEUTIC AGENT FOR VITILIGO AND METHOD OF ACCELERATING PIGMENTATION TYR, PRKACG, MC1R ADORA2A 1496/4885ADORA2B 2309/4885ADORA1 2423/4885
US-20090012035-A1 DENDRIMER CONJUGATES OF AGONISTS AND ANTAGONISTS OF THE GPCR SUPERFAMILY ADORA1, ADORA2A, ADORA3 ADORA2A 2/4885ADORA2B 9/4885ADORA1 1/4885
US-20100324279-A1 CRYSTAL FORMS OF 2-[2-(4-CHLOROPHENYL)ETHOXY]ADENOSINE ADORA2A, ADORA1, ADORA3 ADORA2A 1/4885ADORA2B 4/4885ADORA1 2/4885

“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.