SCHEMBL4034464

SCHEMBL4034464

CCOC(=O)c1cc([C@H]2CCCN(C(=O)OCc3ccc(C(F)(F)F)cc3)C2)ccc1C

nearest known ligand 0.51

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
BCL9 O00512 9/20 0.51
CTNNB1 P35222 9/20 0.51
PROKR1 Q8TCW9 2/20 0.44
PDE4B Q07343 2/20 0.42
KDM4E B2RXH2 1/20 0.41
ALDH1A1 P00352 1/20 0.41
TRPC3 Q13507 1/20 0.40
TRPC7 Q9HCX4 1/20 0.40
GPBAR1 Q8TDU6 1/20 0.39
CETP P11597 1/20 0.39
ATM Q13315 1/20 0.38

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
SCHEMBL4034468 1.00 BCL9 (0.51) BCL9CTNNB1PROKR1PDE4BKDM4E
SCHEMBL4028589 0.91 BCL9 (0.54) BCL9CTNNB1PROKR1PDE4BGPBAR1
SCHEMBL4033307 0.91 BCL9 (0.54) BCL9CTNNB1PROKR1PDE4BGPBAR1
SCHEMBL4028580 0.91 BCL9 (0.54) BCL9CTNNB1PROKR1PDE4BGPBAR1
SCHEMBL6193930 0.86 BCL9 (0.50) BCL9CTNNB1PROKR1PDE4BGPBAR1
SCHEMBL6193937 0.86 BCL9 (0.50) BCL9CTNNB1PROKR1PDE4BGPBAR1
SCHEMBL4030825 0.85 BCL9 (0.54) BCL9CTNNB1PROKR1PDE4BCETP
SCHEMBL4029702 0.84 BCL9 (0.48) BCL9CTNNB1PROKR1PDE4BKDM4E
SCHEMBL27635071 0.84 BCL9 (0.48) BCL9CTNNB1PROKR1PDE4BKDM4E
SCHEMBL4029916 0.84 BCL9 (0.47) BCL9CTNNB1PROKR1PDE4BKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1567493-B1 PHENYL SUBSTITUTED PIPERIDINE COMPOUNDS FOR USE AS PPAR ACTIVATORS PFIZER PROD INC (US) 2009-03-18 EP disclosed
CN-100439337-C Phenyl substituted piperidine compounds for use as PPAR activators PFIZER PROD INC (US) 2008-12-03 CN disclosed
US-20070191429-A1 PPAR ACTIVATORS PFIZER INC. (US) 2007-08-16 US disclosed
US-7199243-B2 Piperidine compounds useful as PPAR activators PFIZER INC. (US) 2007-04-03 US disclosed
CN-1717389-A Phenyl substituted piperidine compounds for use as PPAR activators PFIZER PROD INC (US) 2006-01-04 CN disclosed
EP-1567493-A1 PHENYL SUBSTITUTED PIPERIDINE COMPOUNDS FOR USE AS PPAR ACTIVATORS Pfizer Products Inc. (US) 2005-08-31 EP disclosed
US-20040157885-A1 PPAR activators PFIZER INC 2004-08-12 US disclosed
WO-2004048334-A1 PHENYL SUBSTITUTED PIPERIDINE COMPOUNDS FOR USE AS PPAR ACTIVATORS PFIZER PRODUCTS INC. (US) 2004-06-10 WO 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 (2 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-20070191429-A1 PPAR ACTIVATORS PPARA, PPARG, PPARD BCL9 2684/4885CTNNB1 2280/4885PROKR1 949/4885
US-20040157885-A1 PPAR activators PPARA, PPARG, PPARD BCL9 2684/4885CTNNB1 2280/4885PROKR1 949/4885

“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.