Cerivastatin

Cerivastatin

SCHEMBL3946004

COCc1c(C(C)C)nc(C(C)C)c(/C=C/[C@@H](O)C[C@@H](O)CC(=O)[O-])c1-c1ccc(F)cc1.COCc1c(C(C)C)nc(C(C)C)c(/C=C/[C@@H](O)C[C@@H](O)CC(=O)[O-])c1-c1ccc(F)cc1.[Na+].[Na+]

nearest known ligand 0.84

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

HMGCR

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

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
HMGCR known ✓ P04035 2/20 0.84
ESR1 P03372 1/20 0.84
CHRM1 P11229 1/20 0.84
TBXA2R P21731 1/20 0.84
PDE4A P27815 1/20 0.84
ADRA1A P35348 1/20 0.84
ABCC3 O15438 1/20 0.57
ABCC4 O15439 1/20 0.57

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
Cerivastatin SCHEMBL15263415 1.00 HMGCR (0.84) HMGCRESR1CHRM1TBXA2RPDE4A
Cerivastatin SCHEMBL31517662 1.00 HMGCR (0.84) HMGCRESR1CHRM1TBXA2RPDE4A
Cerivastatin SCHEMBL28019013 1.00 HMGCR (0.84) HMGCRESR1CHRM1TBXA2RPDE4A
Cerivastatin SCHEMBL41888 1.00 HMGCR (0.84) HMGCRESR1CHRM1TBXA2RPDE4A
Cerivastatin SCHEMBL41887 1.00 HMGCR (0.84) HMGCRESR1CHRM1TBXA2RPDE4A
Cerivastatin SCHEMBL19518120 0.97 HMGCR (0.80) HMGCRESR1CHRM1TBXA2RPDE4A
Cerivastatin SCHEMBL2900117 0.97 HMGCR (0.90) HMGCRESR1CHRM1TBXA2RPDE4A
SCHEMBL6633443 0.94 HMGCR (0.75) HMGCRESR1CHRM1TBXA2RPDE4A
SCHEMBL15686549 0.91 HMGCR (0.86) HMGCRESR1CHRM1TBXA2RPDE4A
SCHEMBL13890391 0.91 HMGCR (0.86) HMGCRESR1CHRM1TBXA2RPDE4A

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
WO-2009021113-A1 METHODS FOR ENHANCING GLUTAHIONE PEROXIDASE ACTIVITY HOLTZMAN, JORDAN, L. (US) 2009-02-12 WO disclosed
US-20060034831-A1 Combination therapy for diabetes, obesity and cardiovascular diseases using GDF-8 inhibitors WYETH 2006-02-16 US disclosed
WO-2005046675-A2 METHODS FOR ENHANCING GLUTATHIONE PEROXIDASE ACTIVITY HOLTZMAN JORDAN (US) 2005-05-26 WO disclosed
US-20020198202-A1 Combination of a PTPase inhibitor and an antilipemic agent WYETH (US) 2002-12-26 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 (2 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-20060034831-A1 Combination therapy for diabetes, obesity and cardiovascular diseases using GDF-8 inhibitors DPP8, IGFBP1, IGFBP5 HMGCR 634/4885ESR1 3100/4885CHRM1 4588/4885
US-20020198202-A1 Combination of a PTPase inhibitor and an antilipemic agent PTPN6, PTPN1, PNLIP HMGCR 53/4885ESR1 3153/4885CHRM1 3044/4885

“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.