Rosuvastatin

Rosuvastatin

SCHEMBL247384

CC(C)NC(C)C.CC(C)c1nc(N(C)S(C)(=O)=O)nc(-c2ccc(F)cc2)c1C=C[C@@H](O)C[C@@H](O)CC(=O)O

nearest known ligand 0.92

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 3/20 0.92
ALDH1A1 P00352 1/20 0.92
CYP3A4 P08684 1/20 0.92
PDE6D O43924 1/20 0.92
NR1I2 O75469 1/20 0.92
PDE4D Q08499 1/20 0.92
HDAC1 Q13547 1/20 0.79
HDAC2 Q92769 1/20 0.79
HDAC6 Q9UBN7 1/20 0.79
ABCC3 O15438 1/20 0.78
ABCC4 O15439 1/20 0.78
ESR1 P03372 1/20 0.54
CHRM1 P11229 1/20 0.54
TBXA2R P21731 1/20 0.54
PDE4A P27815 1/20 0.54
ADRA1A P35348 1/20 0.54

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 SCHEMBL29722976 0.96 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL32686257 0.96 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL240433 0.96 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL154400 0.96 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL2520 0.96 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL3938301 0.96 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL8268193 0.96 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL41433 0.96 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL16995485 0.96 HMGCR (1.00) HMGCRALDH1A1CYP3A4PDE6DNR1I2
Rosuvastatin SCHEMBL240432 0.96 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

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8476432-B2 Process for the preparation of HMG-COA reductase inhibitors and intermediates thereof YUHAN CORPORATION (KR) 2013-07-02 US disclosed
EP-2588474-A2 PROCESS FOR THE PREPARATION OF HMG-COA REDUCTASE INHIBITORS AND INTERMEDIATES THEREOF Yuhan Corporation (KR) 2013-05-08 EP disclosed
US-20130096303-A1 PROCESS FOR THE PREPARATION OF HMG-COA REDUCTASE INHIBITORS AND INTERMEDIATES THEREOF YUHAN CORPORATION (KR) 2013-04-18 US disclosed
WO-2012002741-A2 PROCESS FOR THE PREPARATION OF HMG-COA REDUCTASE INHIBITORS AND INTERMEDIATES THEREOF YUHAN CORPORATION (KR) 2012-01-05 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 (1 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-20130096303-A1 PROCESS FOR THE PREPARATION OF HMG-COA REDUCTASE INHIBITORS AND INTERMEDIATES THEREOF HMGCR, COASY, PCSK9 HMGCR 1/4885ALDH1A1 2644/4885CYP3A4 67/4885

“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.