Fluvastatin

Fluvastatin

SCHEMBL41502

CC(C)n1c(/C=C/[C@@H](O)C[C@@H](O)CC(=O)[O-])c(-c2ccc(F)cc2)c2ccccc21.[Na+]

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 Fluvastatin. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HMGCR known ✓ P04035 7/20 0.84
CYP2C9 P11712 4/20 1.00
KDM4E B2RXH2 1/20 1.00
ALDH1A1 P00352 1/20 1.00
LMNA P02545 1/20 1.00
CYP1A2 P05177 1/20 1.00
SMN1; SMN2 Q16637 1/20 1.00
HIF1A Q16665 1/20 1.00
USP2 O75604 1/20 1.00
SIRT6 Q8N6T7 2/20 0.84
ABCC3 O15438 1/20 0.84
ABCB11 O95342 1/20 0.84
PGR P06401 1/20 0.84
ADORA3 P0DMS8 1/20 0.84
RXRA P19793 1/20 0.84
TBXA2R P21731 1/20 0.84
CCKAR P32238 1/20 0.84
ADRA1A P35348 1/20 0.84
PTGS2 P35354 1/20 0.84
NR4A2 P43354 1/20 0.84

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
Fluvastatin SCHEMBL1786786 1.00 CYP2C9 (1.00) CYP2C9KDM4EALDH1A1LMNACYP1A2
Fluvastatin SCHEMBL5056806 1.00 CYP2C9 (1.00) CYP2C9KDM4EALDH1A1LMNACYP1A2
Fluvastatin SCHEMBL29380299 1.00 CYP2C9 (1.00) CYP2C9KDM4EALDH1A1LMNACYP1A2
Fluvastatin SCHEMBL31002987 1.00 CYP2C9 (1.00) CYP2C9KDM4EALDH1A1LMNACYP1A2
Fluvastatin SCHEMBL1147655 1.00 CYP2C9 (1.00) CYP2C9KDM4EALDH1A1LMNACYP1A2
Fluvastatin SCHEMBL556763 1.00 CYP2C9 (1.00) CYP2C9KDM4EALDH1A1LMNACYP1A2
Fluvastatin SCHEMBL6251405 1.00 CYP2C9 (1.00) CYP2C9KDM4EALDH1A1LMNACYP1A2
Fluvastatin SCHEMBL41503 1.00 CYP2C9 (1.00) CYP2C9KDM4EALDH1A1LMNACYP1A2
Fluvastatin SCHEMBL41663 1.00 CYP2C9 (1.00) CYP2C9KDM4EALDH1A1LMNACYP1A2
Fluvastatin SCHEMBL1147661 0.99 CYP2C9 (0.98) CYP2C9KDM4EALDH1A1LMNACYP1A2

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 11952 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250367217-A1 PHARMACEUTICAL COMPOSITIONS FOR COMBINATION THERAPY INTERCEPT PHARMACEUTICALS INC (US) 2025-12-04 US claimed
US-20250367216-A1 PHARMACEUTICAL COMPOSITIONS FOR COMBINATION THERAPY INTERCEPT PHARMACEUTICALS INC (US) 2025-12-04 US claimed
US-20250332254-A1 METHODS FOR TREATING PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA REGENERON PHARMA (US) 2025-10-30 US claimed
US-20250264469-A1 METHODS FOR IMPROVING OUTCOMES FOR HEMATOPOIETIC CELL TRANSPLANT RECIPIENTS AT RISK FOR BRONCHIOLITIS OBLITERANS SYNDROME CHILDREN'S HOSPITAL MEDICAL CENTER 2025-08-21 US claimed
US-20250179219-A1 CYCLODEXTRIN DIMERS, COMPOSITIONS THEREOF, AND USES THEREOF CYCLARITY THERAPEUTICS INC (US) 2025-06-05 US claimed
US-20250051418-A1 VIRAL VECTORS AND USE THEREOF IN ADOPTIVE CELLULAR THERAPY Immatics US, Inc. 2025-02-13 US claimed
US-20240390364-A1 Novel Pyridine Compositions and their use in methods for preventing or treating diseases, disorders and conditions REID CHRISTOPHER BRIAN (US) 2024-11-28 US claimed
US-20240317684-A1 PROCESS FOR PREPARING A CRYSTALLINE FORM OF FLUVASTATIN SODIUM SALT F.I.S. - FABBRICA ITALIANA SINTETICI S.P.A. (IT) 2024-09-26 US claimed
EP-4434967-A1 PROCESS FOR PREPARING A CRYSTALLINE FORM OF FLUVASTATIN SODIUM SALT F.I.S.- Fabbrica Italiana Sintetici S.p.A. (IT) 2024-09-25 EP claimed
CN-118684614-A Process for preparing crystalline form of fluvastatin sodium salt F.I.S.-菲博利佳意大利合成面料股份公司 2024-09-24 CN claimed
CN-1131416-A Hydroxy-substituted azetidinone compounds useful as hypocholesterolemic agents SCHERING CORP (US) 1996-09-18 CN claimed
EP-0457514-B1 Method for preventing, stabilizing or causing regression of atherosclerosis employing a combination of a cholesterol lowering drug and an ace inhibitor SQUIBB & SONS INC (US) 1996-08-21 EP claimed
EP-0671171-A1 Use of HMG COA reductase inhibitor for the manufacture of a medicament for proventing or reducing risks of onset of cardiovascular events BRISTOL-MYERS SQUIBB COMPANY (US) 1995-09-13 EP claimed
WO-1994021230-A1 METHOD AND COMPOSITIONS FOR DISRUPTING THE EPITHELIAL BARRIER FUNCTION CELLEGY PHARMACEUTICALS, INC. (US) 1994-09-29 WO claimed
EP-0508665-A2 Use of ACE inhibitors for lowering serum cholesterol E.R. SQUIBB & SONS, INC. (US) 1992-10-14 EP claimed
EP-0482498-A2 Method for preventing diabetic complications employing a cholesterol lowering drug alone or in combination with an ace inhibitor E.R. SQUIBB & SONS, INC. (US) 1992-04-29 EP claimed
EP-0461548-A2 Method for preventing a second heart attack employing and HMG CoA reductase inhibitor E.R. SQUIBB & SONS, INC. (US) 1991-12-18 EP claimed
EP-0457514-A1 Method for preventing, stabilizing or causing regression of atherosclerosis employing a combination of a cholesterol lowering drug and an ace inhibitor E.R. SQUIBB & SONS, INC. (US) 1991-11-21 EP claimed
EP-0401705-A2 Use of an HMG CoA reductase inhibitor and/or a squalene synthetase inhibitor for treating peripheral atherosclerotic disease E.R. Squibb & Sons, Inc. (US) 1990-12-12 EP claimed
US-4915954-A Dosage form for delivering a drug at two different rates ALZA CORPORATION (US) 1990-04-10 US claimed