SCHEMBL245091

SCHEMBL245091

CC(C)c1nc(N(C)S(C)(=O)=O)nc(-c2ccc(F)cc2)c1/C=C/[C@@H]1C[C@@H](O)CC(=O)O1

nearest known ligand 0.74

Predicted protein targets (top 1)

geneUniProtsupporting neighboursconfidence
HMGCR P04035 11/20 0.74

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
SCHEMBL13431124 1.00 HMGCR (0.74) HMGCR
SCHEMBL30571418 1.00 HMGCR (0.74) HMGCR
SCHEMBL12897943 1.00 HMGCR (0.74) HMGCR
SCHEMBL18269413 1.00 HMGCR (0.74) HMGCR
SCHEMBL3221050 1.00 HMGCR (0.74) HMGCR
SCHEMBL245092 1.00 HMGCR (0.74) HMGCR
SCHEMBL13625375 1.00 HMGCR (0.74) HMGCR
SCHEMBL14669553 1.00 HMGCR (0.74) HMGCR
SCHEMBL30571404 1.00 HMGCR (0.74) HMGCR
SCHEMBL13764732 1.00 HMGCR (0.74) HMGCR

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 95 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10434067-B2 Composite formulation for oral administration comprising ezetimibe and rosuvastatin HANMI PHARM. CO., LTD. (KR) 2019-10-08 US claimed
US-20160346213-A1 COMPOSITE FORMULATION FOR ORAL ADMINISTRATION COMPRISING EZETIMIBE AND ROSUVASTATIN HANMI PHARM. CO., LTD. (KR) 2016-12-01 US claimed
EP-3089739-A1 COMPOSITE FORMULATION FOR ORAL ADMINISTRATION COMPRISING EZETIMIBE AND ROSUVASTATIN Hanmi Pharm. Co., Ltd. (KR) 2016-11-09 EP claimed
WO-2015102400-A1 COMPOSITE FORMULATION FOR ORAL ADMINISTRATION COMPRISING EZETIMIBE AND ROSUVASTATIN HANMI PHARM. CO., LTD. (KR) 2015-07-09 WO claimed
EP-4710920-A1 PHARMACEUTICAL COMPOSITION COMPRISING COMBINATION OF AMLODIPINE, RAMIPRIL AND ROSUVASTATIN Adamed Pharma S.A. (PL) 2026-03-18 EP disclosed
US-20210169838-A1 Novel class of compounds for the treatment of cardiovascular disease. STICHTING KATHOLIEKE UNIVERSITEIT (NL) 2021-06-10 US disclosed
EP-3454838-B1 PHARMACEUTICAL COMPOSITION ADAMED PHARMA S A (PL) 2020-02-12 EP disclosed
US-20190315696-A1 ROSUVASTATIN CALCIUM AND PROCESS FOR PRODUCING INTERMEDIATE THEREOF API CORPORATION (JP) 2019-10-17 US disclosed
US-10434067-B2 Composite formulation for oral administration comprising ezetimibe and rosuvastatin HANMI PHARM. CO., LTD. (KR) 2019-10-08 US disclosed
WO-2019182276-A1 PHARMACEUTICAL COMBINATION PREPARATION COMPRISING EZETIMIBE AND ROSUVASTATIN HANMI PHARM. CO., LTD. (KR) 2019-09-26 WO disclosed
US-10377722-B2 Rosuvastatin calcium and process for producing intermediate thereof API CORPORATION (JP) 2019-08-13 US disclosed
US-20190038588-A1 NOVEL CLASS OF COMPOUNDS FOR THE TREATMENT OF CARDIOVASCULAR DISEASE STICHTING KATHOLIEKE UNIVERSITEIT (NL) 2019-02-07 US disclosed
US-20070255060-A1 Process for the Manufacture of the Calcium Salt of Rosuvastatin (E)-7-'4-(4-Fluorophenyl)-6-Isopropyl-2-'Methyl (Methylsulfonyl) Amino ! Pyrmidin -5-Yl! (3R, 5S)-3,5-Dihydroxyhept-6-Enoic Acid and Crystalline Intermediates Thereof ASTRAZENECA UK LIMITED (GB) 2007-11-01 US disclosed
US-20070255060-A1 Process for the Manufacture of the Calcium Salt of Rosuvastatin (E)-7-'4-(4-Fluorophenyl)-6-Isopropyl-2-'Methyl (Methylsulfonyl) Amino ! Pyrmidin -5-Yl! (3R, 5S)-3,5-Dihydroxyhept-6-Enoic Acid and Crystalline Intermediates Thereof ASTRAZENECA UK LIMITED (GB) 2007-11-01 US disclosed
US-20070155765-A1 Method of preparation of the hemi-calcium salt of (e)-7-[4-(4fluorophenyl)-6-isopropyl-2-[methyl(methylsulfonvl)aminolpyrimidin-5-yl](3r,5s)-3,5-, dihvdroxy-6-heptenoic acid ZENTIVA, A.S. (CZ) 2007-07-05 US disclosed
US-7199126-B2 Compositions and treatments for inhibiting kinase and/or HMG-CoA reductase PHARMIX CORPORATION (US) 2007-04-03 US disclosed
US-7183285-B2 Compositions and treatments for inhibiting kinase and/or HMG-CoA reductase PHARMIX CORP. (US) 2007-02-27 US disclosed
US-20070015779-A1 COMPOSITIONS AND TREATMENTS FOR INHIBITING KINASE AND/OR HMG-COA REDUCTASE NUMERATE, INC. 2007-01-18 US disclosed
US-7163945-B2 Compositions and treatments for inhibiting kinase and/or HMG-CoA reductase PHARMIX CORP. (US) 2007-01-16 US disclosed
US-20070004758-A1 COMPOSITIONS AND TREATMENTS FOR INHIBITING KINASE AND/OR HMG-COA REDUCTASE NUMERATE, INC. 2007-01-04 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 (8 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-20190038588-A1 NOVEL CLASS OF COMPOUNDS FOR THE TREATMENT OF CARDIOVASCULAR DISEASE FABP3, TNNI3, TNNT2 HMGCR 18/4885
US-20070255060-A1 Process for the Manufacture of the Calcium Salt of Rosuvastatin (E)-7-'4-(4-Fluorophenyl)-6-Isopropyl-2-'Methyl (Methylsulfonyl) Amino ! Pyrmidin -5-Yl! (3R, 5S)-3,5-Dihydroxyhept-6-Enoic Acid and Crystalline Intermediates Thereof HMGCR, DHCR7, FADS2 HMGCR 1/4885
US-20070004758-A1 COMPOSITIONS AND TREATMENTS FOR INHIBITING KINASE AND/OR HMG-COA REDUCTASE HMGCR, HMGB3, HMGB2 HMGCR 1/4885
US-20210169838-A1 Novel class of compounds for the treatment of cardiovascular disease. FABP3, TNNI3, TNNT2 HMGCR 16/4885
US-10377722-B2 Rosuvastatin calcium and process for producing intermediate thereof HMGCR, COASY, PCSK9 HMGCR 1/4885
US-20190315696-A1 ROSUVASTATIN CALCIUM AND PROCESS FOR PRODUCING INTERMEDIATE THEREOF HMGCR, COASY, PCSK9 HMGCR 1/4885
US-20070015779-A1 COMPOSITIONS AND TREATMENTS FOR INHIBITING KINASE AND/OR HMG-COA REDUCTASE HMGCR, HMGB3, HMGB2 HMGCR 1/4885
US-20070155765-A1 Method of preparation of the hemi-calcium salt of (e)-7-[4-(4fluorophenyl)-6-isopropyl-2-[methyl(methylsulfonvl)aminolpyrimidin-5-yl](3r,5s)-3,5-, dihvdroxy-6-heptenoic acid HRH4, HRH3, CACNA1E HMGCR 7/4885

“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.