SCHEMBL2087026

SCHEMBL2087026

NC(=O)c1cnc(N)c(N)c1

nearest known ligand 0.50

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
▸ NNMT P40261 7/20 0.50
▸ SMN1; SMN2 Q16637 1/20 0.50
▸ CHEK2 O96017 8/20 0.42
▸ MKNK1 Q9BUB5 2/20 0.42
▸ FYN P06241 1/20 0.42
▸ MAP4K4 O95819 1/20 0.41
▸ PSMD14 O00487 1/20 0.41
▸ STAMBP O95630 1/20 0.41
▸ COPS5 Q92905 1/20 0.41
▸ HPGDS O60760 1/20 0.40
▸ MKNK2 Q9HBH9 1/20 0.40
▸ CHEK1 O14757 1/20 0.39

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
SCHEMBL7216707 0.83 ALDH1A1 (0.50) MAP4K4
SCHEMBL30884164 0.83 ALDH1A1 (0.50) MAP4K4
SCHEMBL30566473 0.79 NNMT (0.47) NNMTSMN1; SMN2MKNK1PSMD14STAMBP
SCHEMBL13824870 0.79 NNMT (0.47) NNMTSMN1; SMN2MKNK1PSMD14STAMBP
SCHEMBL23203545 0.79 NNMT (0.47) NNMTSMN1; SMN2CHEK2MKNK1FYN
SCHEMBL28509281 0.79 NNMT (0.47) NNMTSMN1; SMN2CHEK2MKNK1FYN
SCHEMBL17490781 0.79 NOS3 (0.52) NNMTSMN1; SMN2CHEK2MKNK1FYN
SCHEMBL5904298 0.79 HTT (0.52) NNMTSMN1; SMN2CHEK2MKNK1FYN
SCHEMBL12716074 0.79 NNMT (0.43) NNMTSMN1; SMN2MKNK1FYNPSMD14
SCHEMBL31705858 0.76 KDM4E (0.51) SMN1; SMN2PSMD14

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110059941-A1 2-PHENYL SUBSTITUTED IMIDAZOL [4,5B] PYRIDINE/PYRAZINE AND PURINE DERIVATIVES AS GLUCOKINASE MODULATORS ASTRAZENECA AB (SE) 2011-03-10 — — US disclosed
US-7728008-B2 N-linked heterocyclic antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions BRISTOL-MYERS SQUIBB COMPANY (US) 2010-06-01 — — US disclosed
US-20090247755-A1 Process for Preparing a Substituted Imidazopyridine Compound ELMAN BJORN 2009-10-01 — — US disclosed
US-20090247755-A1 Process for Preparing a Substituted Imidazopyridine Compound ELMAN BJORN 2009-10-01 — — US disclosed
US-20090247755-A1 Process for Preparing a Substituted Imidazopyridine Compound ELMAN BJORN 2009-10-01 — — US disclosed
EP-1891069-A1 2-PHENYL SUBSTITUTED IMIDAZOL [4,5B]PYRIDINE/ PYRAZINE AND PURINE DERIVATIVES AS GLUCOKINASE MODULATORS AstraZeneca AB (SE) 2008-02-27 — — EP disclosed
WO-2006125958-A1 2-PHENYL SUBSTITUTED IMIDAZOL [4 , 5B] PYRIDINE/ PYRAZINE AND PURINE DERIVATIVES AS GLUCOKINASE MODULATORS ASTRAZENECA AB (SE) 2006-11-30 — — WO disclosed
CN-1255404-C Process for preparing substituted imidazopyridine compounds ASTRAZENECA AB (SE) 2006-05-10 — — CN disclosed
US-20060063797-A1 Process for preparing a substituted imidazopyridine compound ELMAN BJORN 2006-03-23 — — US disclosed
EP-1073657-B1 IMIDAZO PYRIDINE DERIVATIVES WHICH INHIBIT GASTRIC ACID SECRETION ASTRAZENECA AB (SE) 2005-12-07 — — EP disclosed
CN-1452621-A Process for preparing substd. imidazopyridine compound ASTRAZENECA AB (SE) 2003-10-29 — — CN disclosed
EP-1317455-A1 PROCESS FOR PREPARING A SUBSTITUTED IMIDAZOPYRIDINE COMPOUND AstraZeneca AB (SE) 2003-06-11 — — EP disclosed
WO-2002020523-A1 PROCESS FOR PREPARING A SUBSTITUTED IMIDAZOPYRIDINE COMPOUND ASTRAZENECA AB (SE) 2002-03-14 — — WO disclosed
US-6313137-B1 FOR THERAPY AND PROPHYLAXIS OF GASTROINTESTINAL INFLAMMATORY DISEASES ASTRAZENECA AB (SE) 2001-11-06 — — US disclosed
CN-1307577-A Imidazo pyridine derivatives which inhibit gastric acid secretion ASTRA ZENECA AKTIEBOLAG (SE) 2001-08-08 — — CN disclosed
EP-1073657-A1 IMIDAZO PYRIDINE DERIVATIVES WHICH INHIBIT GASTRIC ACID SECRETION AstraZeneca AB (SE) 2001-02-07 — — EP disclosed
WO-1999055706-A9 IMIDAZO PYRIDINE DERIVATIVES WHICH INHIBIT GASTRIC ACID SECRETION ASTRA AB (SE) 2000-03-16 — — WO disclosed
WO-1999055706-A1 IMIDAZO PYRIDINE DERIVATIVES WHICH INHIBIT GASTRIC ACID SECRETION ASTRAZENECA AB (SE) 1999-11-04 — — WO disclosed
US-5863916-A 8-aza, 6-aza and 6,8-diaza-1,4-dihydroquinoxaline-2,3-diones and the use thereof as antagonists for the glycine/NMDA receptor STATE OF OREGON, ACTING BY AND THROUGH THE OREGON STATE BOARD OF HIGHER-EDUCATION, ACTING FOR AND ON BEHALF OF THE OREGON HEALTH SCIENCES UNIVERSITY AND THE UNIVERSITY OF OREGON (US) 1999-01-26 — — US disclosed
US-5620978-A 8-aza, 6-aza and 6,8-diaza-1,4-dihydroquinoxaline-2,3-diones and the use thereof as antagonists for the glycine/NMDA receptor STATE OF OREGON, ACTING BY AND THROUGH THE OREGON STATE BOARD OF HIGHER EDUCATION, ACTING FOR AND ON BEHALF OF THE OREGON HEALTH SCIENCES UNIVERSITY AND THE UNIVERSITY OF OREGON, EUGENE OREGON (US) 1997-04-15 — — 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-20060063797-A1 Process for preparing a substituted imidazopyridine compound NISCH, CYP1B1, CYP1A2 NNMT 3678/4885SMN1; SMN2 2455/4885CHEK2 454/4885
US-20090247755-A1 Process for Preparing a Substituted Imidazopyridine Compound NISCH, CYP1A2, CYP1B1 NNMT 3712/4885SMN1; SMN2 2481/4885CHEK2 404/4885
US-20110059941-A1 2-PHENYL SUBSTITUTED IMIDAZOL [4,5B] PYRIDINE/PYRAZINE AND PURINE DERIVATIVES AS GLUCOKINASE MODULATORS GCK, PDXK, GCKR NNMT 2328/4885SMN1; SMN2 3734/4885CHEK2 1779/4885

“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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