SCHEMBL10024048

SCHEMBL10024048

Cc1c(-c2ccc(F)cc2)cc(-c2ccccc2)nc1C(C)C

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SQOR Q9Y6N5 2/20 0.48
TOP1 P11387 2/20 0.48
GCGR P47871 1/20 0.48
HMGCR P04035 2/20 0.47
ADORA2A P29274 1/20 0.47
ADORA1 P30542 1/20 0.47
HPGD P15428 2/20 0.45
MKNK1 Q9BUB5 1/20 0.45
MKNK2 Q9HBH9 1/20 0.45
CYP1A2 P05177 1/20 0.45
CYP2C9 P11712 1/20 0.45
CYP2C19 P33261 1/20 0.45
PTK2B Q14289 1/20 0.45
MAPT P10636 5/20 0.43
KDM4E B2RXH2 3/20 0.43
MEN1 O00255 1/20 0.43
ALDH1A1 P00352 1/20 0.43
KMT2A Q03164 1/20 0.43
TDP1 Q9NUW8 1/20 0.43
L3MBTL1 Q9Y468 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
SCHEMBL10588746 0.84 GCGR (0.52) GCGRHMGCRMAPTKDM4EMEN1
SCHEMBL10345761 0.82 HPGD (0.49) SQORTOP1GCGRHMGCRADORA2A
SCHEMBL8877568 0.82 HMGCR (0.58) GCGRHMGCR
SCHEMBL12102954 0.82 HMGCR (0.48) SQORTOP1HMGCRADORA2AADORA1
SCHEMBL8879993 0.81 HMGCR (0.49) SQORTOP1GCGRHMGCRADORA2A
SCHEMBL8846077 0.81 HMGCR (0.54) SQORTOP1GCGRHMGCRADORA2A
SCHEMBL8878341 0.81 HMGCR (0.57) SQORTOP1HMGCRADORA2AADORA1
SCHEMBL8878013 0.81 SQOR (0.53) SQORTOP1HMGCRADORA2AADORA1
SCHEMBL8225619 0.81 HMGCR (0.54) SQORTOP1GCGRHMGCRADORA2A
SCHEMBL28320987 0.80 GCGR (0.51) GCGR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8148550-B2 selected from fluvastatin, rosuvastatin, cerivastatin, glenvastatin or atorvastatin, by reduction or lactonization of chemical intermediate compounds, then hydrogenation, decyclization and deprotection of hydroxy groups RATIOPHARM GMBH (DE) 2012-04-03 US disclosed
EP-2383260-A2 Process for the preparation of statins Dipharma Francis S.r.l. (IT) 2011-11-02 EP disclosed
US-20080249306-A1 Method for the Production of Statins RATIOPHARM GMBH (DE) 2008-10-09 US disclosed
US-20070093660-A1 Method for the production of statins RATIOPHARM GMBH (DE) 2007-04-26 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 (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-20070093660-A1 Method for the production of statins HMGCR, CYP11A1, CYP51A1 SQOR 168/4885TOP1 993/4885GCGR 2648/4885
US-20080249306-A1 Method for the Production of Statins HMGCR, COASY, PCSK9 SQOR 209/4885TOP1 849/4885GCGR 2133/4885

“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.