SCHEMBL4528384

SCHEMBL4528384

COC(=O)C[C@H]1COC(C)(C)O1

nearest known ligand 0.46

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
CA2 P00918 2/20 0.46
TMEM97 Q5BJF2 2/20 0.41
SIGMAR1 Q99720 2/20 0.41
ALDH1A1 P00352 1/20 0.38
NPSR1 Q6W5P4 1/20 0.38
PRKCA P17252 2/20 0.36
MIF P14174 4/20 0.35
HDAC6 Q9UBN7 1/20 0.35
NAMPT P43490 3/20 0.34
MGAM O43451 1/20 0.34
GAA P10253 1/20 0.34
SI P14410 1/20 0.34
MGAM2 Q2M2H8 1/20 0.34
L3MBTL1 Q9Y468 1/20 0.33

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
SCHEMBL4526320 1.00 CA2 (0.46) CA2TMEM97SIGMAR1ALDH1A1NPSR1
SCHEMBL8917799 0.85 CA2 (0.41) CA2TMEM97SIGMAR1ALDH1A1NPSR1
SCHEMBL28924707 0.83 CA2 (0.44) CA2TMEM97SIGMAR1ALDH1A1NPSR1
SCHEMBL15786354 0.83 CA2 (0.44) CA2TMEM97SIGMAR1ALDH1A1NPSR1
SCHEMBL25961260 0.83 CA2 (0.44) CA2TMEM97SIGMAR1ALDH1A1NPSR1
SCHEMBL1859536 0.83 CTDSP1 (0.45) CA2TMEM97SIGMAR1ALDH1A1NPSR1
SCHEMBL10314728 0.83 CTDSP1 (0.45) CA2TMEM97SIGMAR1ALDH1A1NPSR1
SCHEMBL10314726 0.83 CTDSP1 (0.45) CA2TMEM97SIGMAR1ALDH1A1NPSR1
SCHEMBL17038984 0.81 CA2 (0.47) CA2TMEM97SIGMAR1ALDH1A1NPSR1
SCHEMBL17038983 0.81 CA2 (0.47) CA2TMEM97SIGMAR1ALDH1A1NPSR1

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 23 patents — showing the first 20. 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
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-1682527-B1 METHOD FOR THE PRODUCTION OF STATINS RATIOPHARM GMBH (DE) 2011-08-24 EP disclosed
US-7504432-B2 Ester derivatives BANYU PHARMACEUTICAL CO., LTD. (JP) 2009-03-17 US disclosed
US-7449485-B2 N-sulfonylurea apoptosis promoters ABBOTT LABORATORIES INC. (US) 2008-11-11 US disclosed
US-7449485-B2 N-sulfonylurea apoptosis promoters ABBOTT LABORATORIES INC. (US) 2008-11-11 US disclosed
US-20080249306-A1 Method for the Production of Statins RATIOPHARM GMBH (DE) 2008-10-09 US disclosed
US-20080249306-A1 Method for the Production of Statins RATIOPHARM GMBH (DE) 2008-10-09 US disclosed
US-20080146572-A1 N-SULFONYLUREA APOPTOSIS PROMOTERS ABBOTT LABORATORIES (US) 2008-06-19 US disclosed
US-20080146572-A1 N-SULFONYLUREA APOPTOSIS PROMOTERS ABBOTT LABORATORIES (US) 2008-06-19 US disclosed
US-20070093660-A1 Method for the production of statins RATIOPHARM GMBH (DE) 2007-04-26 US disclosed
US-20070093660-A1 Method for the production of statins RATIOPHARM GMBH (DE) 2007-04-26 US disclosed
US-7192969-B2 Ester derivatives BANYU PHARMACEUTICAL CO., LTD. (JP) 2007-03-20 US disclosed
CN-1878763-A Process for preparing inhibin RATIOPHARM GMBH (DE) 2006-12-13 CN disclosed
US-20050065211-A1 Ester derivatives MSD K.K. (JP) 2005-03-24 US disclosed
US-6846835-B2 Treating chronic obstructive pulmonary disease, chronic bronchitis, asthma, chronic respiratory tract obstruction, fibroid lung, pulmonary emphysema or rhinitis BANYU PHARMACEUTICAL CO., LTD. (JP) 2005-01-25 US disclosed
US-20030191316-A1 Ester derivatives MSD K.K. (JP) 2003-10-09 US disclosed
EP-1302458-A1 ESTER DERIVATIVES BANYU PHARMACEUTICAL CO., LTD. (JP) 2003-04-16 EP disclosed
EP-1161429-A2 HETEROCYCLIC COMPOUNDS AS ADENOSINE DEAMINASE INHIBITORS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2001-12-12 EP disclosed
WO-2000055155-A2 HETEROCYCLIC COMPOUNDS AS ADENOSINE DEAMINASE INHIBITORS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2000-09-21 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 (5 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-20080146572-A1 N-SULFONYLUREA APOPTOSIS PROMOTERS BAX, BCL2, BAD CA2 2921/4885TMEM97 1996/4885SIGMAR1 2873/4885
US-20070093660-A1 Method for the production of statins HMGCR, CYP11A1, CYP51A1 CA2 887/4885TMEM97 3619/4885SIGMAR1 2859/4885
US-20030191316-A1 Ester derivatives CHRM3, CHRM2, CHRM1 CA2 2104/4885TMEM97 278/4885SIGMAR1 163/4885
US-20050065211-A1 Ester derivatives CHRM3, CHRM2, CHRM1 CA2 1676/4885TMEM97 340/4885SIGMAR1 139/4885
US-20080249306-A1 Method for the Production of Statins HMGCR, COASY, PCSK9 CA2 3154/4885TMEM97 4244/4885SIGMAR1 4258/4885

“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.