SCHEMBL1243083

SCHEMBL1243083

CCCn1c(=O)n(C2CC2)c(=O)c2[nH]c(-c3ccc(N(CC)C(=O)c4ccc(C(F)(F)F)nc4)nc3)nc21

nearest known ligand 0.47

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
ADORA2B P29275 18/20 0.47
ADORA2A P29274 13/20 0.47
ADORA3 P0DMS8 9/20 0.47
ADORA1 P30542 6/20 0.47
KDM4E B2RXH2 1/20 0.43
MEN1 O00255 1/20 0.43
ALDH1A1 P00352 1/20 0.43
GLA P06280 1/20 0.43
HPGD P15428 1/20 0.43
TSHR P16473 1/20 0.43
KMT2A Q03164 1/20 0.43
HSD17B10 Q99714 1/20 0.43

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
SCHEMBL1242266 0.95 ADORA2B (0.47) ADORA2BADORA2AADORA3ADORA1KDM4E
SCHEMBL1242614 0.94 ADORA2B (0.46) ADORA2BADORA2AADORA3ADORA1KDM4E
SCHEMBL1242640 0.93 ADORA2B (0.45) ADORA2BADORA2AADORA3ADORA1KDM4E
SCHEMBL1243258 0.93 ADORA2B (0.47) ADORA2BADORA2AADORA3ADORA1KDM4E
SCHEMBL30741230 0.93 ADORA2B (0.47) ADORA2BADORA2AADORA3ADORA1KDM4E
SCHEMBL1243733 0.93 ADORA2B (0.44) ADORA2BADORA2AADORA3ADORA1KDM4E
SCHEMBL1242635 0.93 ADORA2B (0.45) ADORA2BADORA2AADORA3ADORA1KDM4E
SCHEMBL1240743 0.92 ADORA2B (0.43) ADORA2BADORA2AADORA3ADORA1KDM4E
SCHEMBL1242534 0.92 ADORA2B (0.44) ADORA2BADORA2AADORA3ADORA1KDM4E
SCHEMBL1240908 0.92 ADORA2B (0.55) ADORA2BADORA2AADORA3ADORA1KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9221821-B2 Methods for the synthesis of 1,3-substituted aminouracils and other xanthine-related compounds Forest Laboratories Holdings, Limited (BM) 2015-12-29 US disclosed
US-9221821-B2 Methods for the synthesis of 1,3-substituted aminouracils and other xanthine-related compounds Forest Laboratories Holdings, Limited (BM) 2015-12-29 US disclosed
EP-2029143-B1 SUBSTITUTED 8-[6-AMINO-3-PYRIDYL]XANTHINES DOGWOOD PHARMACEUTICALS INC (US) 2015-07-08 EP disclosed
EP-2029143-B1 SUBSTITUTED 8-[6-AMINO-3-PYRIDYL]XANTHINES DOGWOOD PHARMACEUTICALS INC (US) 2015-07-08 EP disclosed
US-8258142-B2 Substituted 8-[6-amino-3-pyridyl]xanthines DOGWOOD PHARMACEUTICALS, INC. (US) 2012-09-04 US disclosed
US-8258142-B2 Substituted 8-[6-amino-3-pyridyl]xanthines DOGWOOD PHARMACEUTICALS, INC. (US) 2012-09-04 US disclosed
US-8258142-B2 Substituted 8-[6-amino-3-pyridyl]xanthines DOGWOOD PHARMACEUTICALS, INC. (US) 2012-09-04 US disclosed
US-8193200-B2 administering a substituted 8-(3-pyridyl)-xanthine; ulcerative colitis; Crohn's disease UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2012-06-05 US disclosed
US-8193200-B2 administering a substituted 8-(3-pyridyl)-xanthine; ulcerative colitis; Crohn's disease UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2012-06-05 US disclosed
US-8193200-B2 administering a substituted 8-(3-pyridyl)-xanthine; ulcerative colitis; Crohn's disease UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2012-06-05 US disclosed
US-20110082139-A1 SUBSTITUTED 8-[6-AMINO-3-PYRIDYL]XANTHINES ALLERGAN SALES, LLC 2011-04-07 US disclosed
US-7884100-B2 Substituted 8-[6-amino-3-pyridyl]xanthines PGXHEALTH, LLC (US) 2011-02-08 US disclosed
US-7884100-B2 Substituted 8-[6-amino-3-pyridyl]xanthines PGXHEALTH, LLC (US) 2011-02-08 US disclosed
US-7884100-B2 Substituted 8-[6-amino-3-pyridyl]xanthines PGXHEALTH, LLC (US) 2011-02-08 US disclosed
US-20080176845-A1 Antagonists of A2B adenosine receptors for treatment of inflammatory bowel disease EMORY UNIVERSITY 2008-07-24 US disclosed
US-20080176845-A1 Antagonists of A2B adenosine receptors for treatment of inflammatory bowel disease EMORY UNIVERSITY 2008-07-24 US disclosed
US-20080176845-A1 Antagonists of A2B adenosine receptors for treatment of inflammatory bowel disease EMORY UNIVERSITY 2008-07-24 US disclosed
US-20080004292-A1 Substituted 8-[6-amino-3-pyridyl]xanthines ALLERGAN SALES, LLC 2008-01-03 US disclosed
US-20080004292-A1 Substituted 8-[6-amino-3-pyridyl]xanthines ALLERGAN SALES, LLC 2008-01-03 US disclosed
US-20080004292-A1 Substituted 8-[6-amino-3-pyridyl]xanthines ALLERGAN SALES, LLC 2008-01-03 US 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 (3 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-20110082139-A1 SUBSTITUTED 8-[6-AMINO-3-PYRIDYL]XANTHINES ADORA2B, ADORA2A, ADORA3 ADORA2B 1/4885ADORA2A 2/4885ADORA3 3/4885
US-20080004292-A1 Substituted 8-[6-amino-3-pyridyl]xanthines ADORA2B, ADORA2A, ADORA3 ADORA2B 1/4885ADORA2A 2/4885ADORA3 3/4885
US-20080176845-A1 Antagonists of A2B adenosine receptors for treatment of inflammatory bowel disease ADORA2B, ADORA2A, ADORA1 ADORA2B 1/4885ADORA2A 2/4885ADORA3 4/4885

“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.