SCHEMBL4025531

SCHEMBL4025531

CCOC(=O)CC(CC(=O)O)OCC

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MGAM O43451 1/20 0.43
GAA P10253 1/20 0.43
SI P14410 1/20 0.43
MGAM2 Q2M2H8 1/20 0.43
ALDH1A1 P00352 6/20 0.40
TRPA1 O75762 1/20 0.40
TSHR P16473 3/20 0.38
CYP3A4 P08684 2/20 0.38
ALOX15 P16050 2/20 0.38
TDP1 Q9NUW8 1/20 0.38
HSD17B10 Q99714 2/20 0.37
CHRM1 P11229 1/20 0.37
ADORA1 P30542 1/20 0.37
CYP1A2 P05177 4/20 0.36
LMNA P02545 5/20 0.35
MAPK1 P28482 4/20 0.35
GMNN O75496 3/20 0.35
MAPT P10636 3/20 0.35
NPSR1 Q6W5P4 3/20 0.35
MEN1 O00255 2/20 0.35

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
SCHEMBL27617039 0.89 MGAM (0.38) MGAMGAASIMGAM2ALDH1A1
SCHEMBL10697367 0.84 GAA (0.43) MGAMGAASIMGAM2ALDH1A1
SCHEMBL8911100 0.83 GAA (0.46) MGAMGAASIMGAM2ALDH1A1
SCHEMBL10134701 0.83 GABRP (0.39) MGAMGAASIMGAM2ALDH1A1
SCHEMBL6156348 0.83 CYP1A2 (0.43) TSHRCYP1A2LMNAMAPK1GMNN
SCHEMBL7736216 0.82 MGAM (0.44) MGAMGAASIMGAM2ALDH1A1
SCHEMBL5175797 0.81 LMNA (0.51) MGAMGAASIMGAM2ALDH1A1
SCHEMBL6036839 0.81 LMNA (0.51) MGAMGAASIMGAM2ALDH1A1
SCHEMBL28274072 0.81 LMNA (0.39) TSHRCYP1A2LMNAMAPK1GMNN
SCHEMBL1268514 0.80 GAA (0.43) MGAMGAASIMGAM2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111518035-A Rosuvastatin tert-butylamine salt and preparation method thereof 安徽鼎旺医药有限公司 2020-08-11 CN claimed
US-8874019-B2 Image forming method KONICA MINOLTA BUSINESS TECHNOLOGIES, INC. (JP) 2014-10-28 US claimed
US-20130202336-A1 IMAGE FORMING METHOD KONICA MINOLTA BUSINESS TECHNOLOGIES, INC. (JP) 2013-08-08 US claimed
CN-106676141-B Enzymatic preparation method of chiral intermediate (S) -3-hydroxy glutaric acid monoester 浙江京新药业股份有限公司 2020-12-08 CN disclosed
CN-111518035-A Rosuvastatin tert-butylamine salt and preparation method thereof 安徽鼎旺医药有限公司 2020-08-11 CN disclosed
US-8874019-B2 Image forming method KONICA MINOLTA BUSINESS TECHNOLOGIES, INC. (JP) 2014-10-28 US disclosed
WO-2014140006-A1 PROCESS FOR ENANTIOSELECTIVE SYNTHESIS OF 3-HYDROXY-GLUTARIC ACID MONOESTERS AND USE THEREOF SANDOZ AG (CH) 2014-09-18 WO disclosed
US-20130202336-A1 IMAGE FORMING METHOD KONICA MINOLTA BUSINESS TECHNOLOGIES, INC. (JP) 2013-08-08 US disclosed
EP-1472228-B1 PROCESS FOR THE MANUFACTURE OF HMG-COA REDUCTASE INHIBITORS NOVARTIS AG (CH) 2009-03-25 EP disclosed
US-20080182873-A1 PROCESS FOR THE MANUFACTURE OF HMG-COA REDUCTASE INHIBITORS ACEMOGLU MURAT 2008-07-31 US disclosed
US-7371865-B2 Process for the manufacture of HMG-CoA reductase inhibitors NOVARTIS PHARMACEUTICALS CORPORATION (US) 2008-05-13 US disclosed
US-20050070605-A1 Process for the manufacture of hmg-coa reductase inhibitors ACEMOGLU MURAT (CH) 2005-03-31 US disclosed
US-20050014954-A1 Pyrrole synthesis CIBA SPECIALTY CHEMICALS CORP. 2005-01-20 US disclosed
EP-1472228-A1 PROCESS FOR THE MANUFACTURE OF HMG-COA REDUCTASE INHIBITORS Novartis AG (CH) 2004-11-03 EP disclosed
EP-1451179-A1 PYRROLE SYNTHESIS Ciba SC Holding AG (CH) 2004-09-01 EP disclosed
WO-2003064392-A1 PROCESS FOR THE MANUFACTURE OF HMG-COA REDUCTASE INHIBITORS NOVARTIS AG (CH) 2003-08-07 WO disclosed
WO-2003044011-A1 PYRROLE SYNTHESIS CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2003-05-30 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 (3 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-20080182873-A1 PROCESS FOR THE MANUFACTURE OF HMG-COA REDUCTASE INHIBITORS HMGCR, COASY, DHCR7 MGAM 917/4885GAA 827/4885SI 514/4885
US-20050014954-A1 Pyrrole synthesis PNPO, PPOX, DHPS MGAM 3146/4885GAA 1947/4885SI 1656/4885
US-20050070605-A1 Process for the manufacture of hmg-coa reductase inhibitors HMGCR, COASY, DHCR7 MGAM 917/4885GAA 827/4885SI 514/4885

“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.