SCHEMBL958369

SCHEMBL958369

CCOC(=O)CCc1ccc(C)nc1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CYP4F2 P78329 2/20 0.61
▸ CYP4A11 Q02928 2/20 0.61
▸ CYP4Z1 Q86W10 3/20 0.52
▸ TSHR P16473 1/20 0.50
▸ SMN1; SMN2 Q16637 1/20 0.50
▸ JAK2 O60674 1/20 0.45
▸ JAK1 P23458 1/20 0.45
▸ TYK2 P29597 1/20 0.45
▸ JAK3 P52333 1/20 0.45
▸ SYK P43405 1/20 0.45
▸ PDE3B Q13370 1/20 0.44
▸ PDE3A Q14432 1/20 0.44
▸ P2RY12 Q9H244 1/20 0.44
▸ CYP4F11 Q9HBI6 1/20 0.44
▸ CYP4F12 Q9HCS2 1/20 0.44
▸ MAPT P10636 1/20 0.43
▸ HRH3 Q9Y5N1 1/20 0.42
▸ TDP1 Q9NUW8 1/20 0.42
▸ POLB P06746 1/20 0.42
▸ P4HTM Q9NXG6 1/20 0.41

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
SCHEMBL3676514 0.86 CYP4F2 (0.59) CYP4F2CYP4A11CYP4Z1JAK2JAK1
SCHEMBL4734773 0.85 TSHR (0.51) CYP4F2CYP4A11CYP4Z1TSHRSMN1; SMN2
SCHEMBL30605730 0.84 CYP4F2 (0.58) CYP4F2CYP4A11CYP4Z1JAK2JAK1
SCHEMBL8663044 0.84 CYP4F2 (0.58) CYP4F2CYP4A11CYP4Z1JAK2JAK1
SCHEMBL4590909 0.84 CYP4F2 (0.58) CYP4F2CYP4A11CYP4Z1JAK2JAK1
SCHEMBL4903126 0.84 CYP4F2 (0.58) CYP4F2CYP4A11CYP4Z1SMN1; SMN2JAK2
SCHEMBL29089598 0.84 CYP4F2 (0.58) CYP4F2CYP4A11CYP4Z1JAK2JAK1
SCHEMBL10663309 0.84 TSHR (0.45) CYP4F2CYP4A11CYP4Z1TSHRSMN1; SMN2
SCHEMBL2503936 0.83 CYP4Z1 (0.50) CYP4F2CYP4A11CYP4Z1TSHRSMN1; SMN2
SCHEMBL6307266 0.83 CYP4F2 (0.56) CYP4F2CYP4A11CYP4Z1JAK2JAK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0070185-B1 PREPARATION OF LOWER ALKYL 2-FORMYL-3-(6-METHYL-3-PYRIDINYL)-PROPIONATES SMITHKLINE BECKMAN CORPORATION (US) 1985-04-10 — — EP claimed
US-8173820-B2 Compounds which potentiate the AMPA receptor and uses thereof in medicine GLAXO GROUP LIMITED (GB) 2012-05-08 — — US disclosed
US-20110021578-A1 Compounds which Potentiate the AMPA Receptor and Uses Thereof in Medicine GLAXO GROUP LIMITED (GB) 2011-01-27 — — US disclosed
EP-2222632-A1 COMPOUNDS WHICH POTENTIATE THE AMPA RECEPTOR AND USES THEREOF IN MEDICINE Glaxo Group Limited (GB) 2010-09-01 — — EP disclosed
WO-2009080637-A1 COMPOUNDS WHICH POTENTIATE THE AMPA RECEPTOR AND USES THEREOF IN MEDICINE GLAXO GROUP LIMITED (GB) 2009-07-02 — — WO disclosed
US-7196080-B2 Respiratory system disordeers; chronic obstructive pulminary disease ASTELLAS PHARMA INC. (JP) 2007-03-27 — — US disclosed
US-5763461-A ANTIPICORNAVIRAL AGENTS SANOFI (FR) 1998-06-09 — — US disclosed
US-5618821-A VIRICIDES, PICORNAVIRUS SANOFI, S.A. (FR) 1997-04-08 — — US disclosed
WO-1995031438-A1 THERAPEUTIC PHENOXYALKYLHETEROCYCLES SANOFI WINTHROP, INC. (US) 1995-11-23 — — WO disclosed
EP-0206294-B1 ALKYL ESTERS OF 3-HYDROXY-3-(2-METHYL-5-PYRIDYL)-PROPIONIC ACID LONZA AG (CH) 1990-05-16 — — EP disclosed
EP-0017680-A1 Pyrimidone derivatives, process for preparing them and pharmaceutical compositions containing them SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1980-10-29 — — EP disclosed
US-4227000-A Intermediates in the process for making histamine antagonists SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1980-10-07 — — US disclosed
EP-0015138-A1 Pyrimidone derivatives, processes for their preparation and pharmaceutical compositions containing them SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1980-09-03 — — EP disclosed
US-4216318-A HISTAMINE HZ-ANTAGONISTS, ISOCYTOSINES SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1980-08-05 — — US disclosed
EP-0013071-A1 Pyrimidinone derivatives, processes for preparing them and pharmaceutical compositions containing them SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1980-07-09 — — EP disclosed
WO-1980000966-A1 NEW HISTAMINE H2-ANTAGONISTS SMITH KLINE FRENCH LAB (GB) 1980-05-15 — — WO disclosed
EP-0007232-A1 Iso(thio)ureas, processes for their preparation and compositions containing them SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1980-01-23 — — EP disclosed
EP-0004793-A2 2-nitro aminopyrimidone derivatives, a process for their preparation and their use to prepare 2-aminopyrimidone derivatives which have histamine H2-antagonist activity SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1979-10-17 — — EP disclosed
EP-0003677-A2 Pyrimidones, processes for their preparation and pharmaceutical compositions containing them SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1979-08-22 — — EP disclosed
US-4154834-A HETEROCYCLIC-(THIO)ALKYLAMINO SUBSTITUTED-4-PYRIMIDONE OR -THIONES SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1979-05-15 — — 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 (1 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-20110021578-A1 Compounds which Potentiate the AMPA Receptor and Uses Thereof in Medicine GRIN1, GRM1, GRM2 CYP4F2 662/4885CYP4A11 640/4885CYP4Z1 1159/4885

“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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