SCHEMBL6970091

SCHEMBL6970091

COC(=O)CC(=O)CCc1nccs1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 2/20 0.40
PKM P14618 3/20 0.40
ALDH1A1 P00352 1/20 0.40
KMT2A Q03164 2/20 0.39
ALOX15 P16050 1/20 0.37
MAPK1 P28482 1/20 0.37
FDPS P14324 1/20 0.37
SMN1; SMN2 Q16637 2/20 0.37
MEN1 O00255 1/20 0.37
CYP1A2 P05177 1/20 0.37
TSHR P16473 2/20 0.37
CYP2D6 P10635 1/20 0.37
CYP2C19 P33261 1/20 0.37
LMNA P02545 2/20 0.36
HSP90AA1 P07900 1/20 0.36
HSP90B1 P14625 1/20 0.36
NPC1 O15118 2/20 0.36
RAB9A P51151 2/20 0.36
CDK5 Q00535 1/20 0.36
CDK5R1 Q15078 1/20 0.36

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
SCHEMBL291399 0.90 ALDH1A1 (0.44) CYP3A4PKMALDH1A1KMT2AFDPS
SCHEMBL28152645 0.84 TSHR (0.45) CYP3A4PKMALDH1A1KMT2AFDPS
SCHEMBL28011812 0.83 FDPS (0.46) CYP3A4PKMALDH1A1KMT2AFDPS
SCHEMBL12530273 0.80 ALDH1A1 (0.44) CYP3A4PKMALDH1A1KMT2AFDPS
SCHEMBL6959399 0.78 HTT (0.46) CYP3A4PKMALDH1A1KMT2AMAPK1
SCHEMBL6748509 0.78 FDPS (0.41) CYP3A4PKMALDH1A1ALOX15MAPK1
SCHEMBL5900543 0.78 ALDH1A1 (0.49) PKMALDH1A1KMT2AFDPSSMN1; SMN2
Bromide SCHEMBL5529731 0.77 HTT (0.45) CYP3A4PKMALDH1A1KMT2AMAPK1
Hydrochloric Acid SCHEMBL27680689 0.77 HTT (0.45) CYP3A4PKMALDH1A1KMT2AMAPK1
SCHEMBL6296334 0.76 CYP3A4 (0.34) CYP3A4PKMALDH1A1KMT2AALOX15

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6649767-B2 Contacting an enamine compound with a ketonic compound in presence of a base, treating the reaction mixture thus obtained with an acid or combinations of acids PFIZER, INC. 2003-11-18 US disclosed
US-20030176445-A1 Substituted 1,4-dihydropyridine compounds as bradykinin antagonists PFIZER INC. 2003-09-18 US disclosed
US-20030078430-A1 Process for preparing 1,4-dihydropyridine compounds PFIZER INC. 2003-04-24 US disclosed
EP-1106615-B1 Substituted 1,4-dihydropyridine compounds as bradykinin antagonists PFIZER (US) 2003-03-05 EP disclosed
US-6444677-B2 TREATMENT OF INFLAMMATION, CARDIOVASCULAR DISEASE, PAIN, ETC. PFIZER INC. 2002-09-03 US disclosed
US-20020042421-A1 Substituted 1,4-dihydropyridine compounds as bradykinin antagonists OKUMURA YOSHIYUKI (JP) 2002-04-11 US disclosed
US-20010046993-A1 5-memberd heteroaryl substituted 1,4-dihydropyridine compounds as bradykinin antagonists IKEDA TAKAFUMI (JP) 2001-11-29 US disclosed
EP-1110962-A1 Process for preparing 1,4-dihydropyridine compounds PFIZER INC. (US) 2001-06-27 EP disclosed
EP-1106614-A1 5-Membered heteroaryl substituted 1,4-dihydropyridine compounds as bradykinin antagonists PFIZER INC. (US) 2001-06-13 EP disclosed
EP-1106615-A1 Substituted 1,4-dihydropyridine compounds as bradykinin antagonists PFIZER INC. (US) 2001-06-13 EP 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 (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-20030176445-A1 Substituted 1,4-dihydropyridine compounds as bradykinin antagonists BDKRB1, BDKRB2, HRH4 CYP3A4 1099/4885PKM 2320/4885ALDH1A1 2124/4885
US-20030078430-A1 Process for preparing 1,4-dihydropyridine compounds QDPR, HRH1, HRH4 CYP3A4 33/4885PKM 520/4885ALDH1A1 463/4885
US-20010046993-A1 5-memberd heteroaryl substituted 1,4-dihydropyridine compounds as bradykinin antagonists BDKRB1, BDKRB2, CNR2 CYP3A4 1180/4885PKM 1827/4885ALDH1A1 2557/4885
US-20020042421-A1 Substituted 1,4-dihydropyridine compounds as bradykinin antagonists BDKRB1, BDKRB2, HRH4 CYP3A4 938/4885PKM 1798/4885ALDH1A1 1413/4885

“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.