Rosuvastatin

Rosuvastatin

SCHEMBL41433

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

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

HMGCR

The experimentally established mechanism targets of Rosuvastatin. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
HMGCR known ✓ P04035 4/20 1.00
ALDH1A1 P00352 1/20 1.00
CYP3A4 P08684 1/20 1.00
PDE6D O43924 1/20 1.00
NR1I2 O75469 1/20 1.00
PDE4D Q08499 1/20 1.00
ABCC3 O15438 1/20 0.84
ABCC4 O15439 1/20 0.84
HDAC1 Q13547 1/20 0.83
HDAC2 Q92769 1/20 0.83
HDAC6 Q9UBN7 1/20 0.83
ESR1 P03372 1/20 0.58
CHRM1 P11229 1/20 0.58
TBXA2R P21731 1/20 0.58
PDE4A P27815 1/20 0.58
ADRA1A P35348 1/20 0.58

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
Rosuvastatin SCHEMBL28393539 1.00 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL240432 1.00 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL32686257 1.00 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL2520 1.00 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL3938301 1.00 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL154400 1.00 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL16995485 1.00 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL240433 1.00 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL8268193 1.00 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL29722976 1.00 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2

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

Appears in 10973 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117890509-B Ezetimibe rosuvastatin calcium tablet dissolution curve detection method with distinguishing force 江西施美药业股份有限公司 2026-05-19 CN claimed
CN-122005470-A Preparation method of rosuvastatin calcium tablet 琼海市人民医院 2026-05-12 CN claimed
US-12622895-B2 Anti-neurodegenerative combinations and use for treatment of neurodegenerative diseases ALTO NEUROSCIENCE, INC. (US) 2026-05-12 US claimed
US-20260115142-A1 PHARMACEUTICAL COMPOSITION COMPRISING ROSUVASTATIN AND ACETYLSALICYLIC ACID, PROCESS FOR PREPARING THE SAME, AND USES THEREOF LABORATORIOS SILANES S A DE C V (MX) 2026-04-30 US claimed
EP-4717256-A1 PHARMACEUTICAL COMPOSITION COMPRISING ROSUVASTATIN AND OMEGA-3, PROCESS FOR PREPARING THE SAME, AND USES THEREOF Laboratorios Silanes, S.A. de C.V. (MX) 2026-04-01 EP claimed
EP-4710920-A1 PHARMACEUTICAL COMPOSITION COMPRISING COMBINATION OF AMLODIPINE, RAMIPRIL AND ROSUVASTATIN Adamed Pharma S.A. (PL) 2026-03-18 EP claimed
EP-4678233-A2 PHARMACEUTICAL COMPOSITION COMPRISING HMG-COA REDUCTASE INHIBITORS AND FENOFIBRATE Intas Pharmaceuticals Ltd. (IN) 2026-01-14 EP claimed
US-20250366785-A1 METHODS FOR PROCESSING, ENRICHMENT, DELIVERY, FORMULATION, AND UPTAKE FOR SUPPLEMENTS AND PHARMACEUTICALS VAN DE CASTEELE RUSSELL (US) 2025-12-04 US claimed
US-20250332254-A1 METHODS FOR TREATING PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA REGENERON PHARMA (US) 2025-10-30 US claimed
EP-4636093-A1 TARGETING MAPK-ERK PATHWAY FOR ENHANCING NUCLEIC ACID DELIVERY Paul-Ehrlich-Institut, Bundesinstitut für Impfstoffe und biomedizinische Arzneimittel (DE) 2025-10-22 EP claimed
EP-1465616-A1 TREATMENT OF STATIN SIDE EFFECTS USING URIDINE DERIVATIVES Magral Limited (AU) 2004-10-13 EP claimed
US-20040176615-A1 Processes for preparing calcium salt forms of statins NIDDAM-HILDESHEIM VALERIE (IL) 2004-09-09 US claimed
US-6777552-B2 FROM AN ESTER DERIVATIVE OR PROTECTED ESTER DERIVATIVE OF THE STATIN BY USING CALCIUM HYDROXIDE TEVA PHARMACEUTICAL INDUSTRIES, LTD. (IL) 2004-08-17 US claimed
EP-1425287-A1 PROCESSES FOR PREPARING CALCIUM SALT FORMS OF STATINS TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2004-06-09 EP claimed
WO-2004027075-A2 CHEMOENZYMATIC METHODS FOR THE SYNTHESIS OF STATINS AND STAIN INTERMEDIATES DIVERSA CORPORATION (US) 2004-04-01 WO claimed
US-20030171407-A1 Composition for reducing blood glucose and cholesterol UPSHER-SMITH LABORATORIES, INC. 2003-09-11 US claimed
WO-2003061663-A1 USE OF BENZOTHIAZEPINES HAVING ACTIVITY AS INHIBITORS OF ILEAL BILE ACID TRANSPORT FOR REDUCING CHOLESTEROLOLEMIA ASTRAZENECA AB (SE) 2003-07-31 WO claimed
US-20030114685-A1 Processes for preparing calcium salt forms of statins TEVA PHARMACEUTICAL INDUSTRIES, LTD. (IL) 2003-06-19 US claimed
WO-2003049730-A1 TREATMENT OF STATIN SIDE EFFECTS USING URIDINE DERIVATIVES MAGRAL LIMITED (AU) 2003-06-19 WO claimed
WO-2003016317-A1 PROCESSES FOR PREPARING CALCIUM SALT FORMS OF STATINS TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2003-02-27 WO claimed