Fluvastatin

Fluvastatin

SCHEMBL556754

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

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 1.00
CYP2C9 P11712 4/20 1.00
SIRT6 Q8N6T7 2/20 1.00
NR4A2 P43354 2/20 1.00
PDE4D Q08499 2/20 1.00
TBXA2R P21731 2/20 1.00
ADRA1A P35348 2/20 1.00
ABCC3 O15438 1/20 1.00
ABCB11 O95342 1/20 1.00
PGR P06401 1/20 1.00
ADORA3 P0DMS8 1/20 1.00
RXRA P19793 1/20 1.00
CCKAR P32238 1/20 1.00
PTGS2 P35354 1/20 1.00
SLC10A1 Q14973 1/20 1.00
KDM4E B2RXH2 1/20 0.84
ALDH1A1 P00352 1/20 0.84
LMNA P02545 1/20 0.84
CYP1A2 P05177 1/20 0.84
SMN1; SMN2 Q16637 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 SCHEMBL464787 1.00 HMGCR (1.00) HMGCRCYP2C9SIRT6NR4A2PDE4D
Fluvastatin SCHEMBL2847 1.00 HMGCR (1.00) HMGCRCYP2C9SIRT6NR4A2PDE4D
Fluvastatin SCHEMBL13501651 1.00 HMGCR (1.00) HMGCRCYP2C9SIRT6NR4A2PDE4D
Fluvastatin SCHEMBL628757 1.00 HMGCR (1.00) HMGCRCYP2C9SIRT6NR4A2PDE4D
Fluvastatin SCHEMBL6268460 1.00 HMGCR (1.00) HMGCRCYP2C9SIRT6NR4A2PDE4D
Fluvastatin SCHEMBL23468028 1.00 HMGCR (1.00) HMGCRCYP2C9SIRT6NR4A2PDE4D
Fluvastatin SCHEMBL2848 1.00 HMGCR (1.00) HMGCRCYP2C9SIRT6NR4A2PDE4D
Fluvastatin SCHEMBL678274 1.00 HMGCR (1.00) HMGCRCYP2C9SIRT6NR4A2PDE4D
Fluvastatin SCHEMBL2849 1.00 HMGCR (1.00) HMGCRCYP2C9SIRT6NR4A2PDE4D
Fluvastatin SCHEMBL4295454 1.00 HMGCR (1.00) HMGCRCYP2C9SIRT6NR4A2PDE4D

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111110854-A Composition comprising a histamine release-promoting substance and an inhibitory compound 黄泳华 2020-05-08 CN claimed
CN-111068064-A Composition comprising fatty acid or derivative thereof and dihydroxyheptanoic acid derivative 黄泳华 2020-04-28 CN claimed
EP-4566597-A1 STATINS USEFUL IN THE TREATMENT OF SPLACHNIC VASCULAR DYSFUNCTIONS Hospital Clínic de Barcelona (ES) 2025-06-11 EP disclosed
CN-111110854-A Composition comprising a histamine release-promoting substance and an inhibitory compound 黄泳华 2020-05-08 CN disclosed
CN-111068064-A Composition comprising fatty acid or derivative thereof and dihydroxyheptanoic acid derivative 黄泳华 2020-04-28 CN disclosed
EP-3256131-A1 ANALOGS OF 3,5-DIHYDROXYPENTANOATE FOR BONE FORMATION Kaohsiung Medical University (TW) 2017-12-20 EP disclosed
US-9713614-B2 Combination of HMG-CoA reductase inhibitors with phosphodiesterase 4 inhibitors for the treatment of inflammatory pulmonary diseases ASTRAZENECA AB (SE) 2017-07-25 US disclosed
WO-2016130181-A1 ANALOGS OF 3,5-DIHYDROXYPENTANOATE FOR BONE FORMATION KAOHSIUNG MEDICAL UNIVERSITY (TW) 2016-08-18 WO disclosed
US-9345671-B2 Adiponectin production enhancer DAIICHI SANKYO COMPANY, LIMITED (JP) 2016-05-24 US disclosed
US-9315447-B2 Compositions and methods for the treatment of inflammation A.T. Resolve Sarl (CH) 2016-04-19 US disclosed
EP-2419399-B1 COMPOSITIONS AND METHODS FOR THE TREATMENT OF INFLAMMATION C T RESOLVE SARL (CH) 2016-03-23 EP disclosed
EP-1515717-A1 CALCIUM SALTS OF INDOLE DERIVED STATINS Novartis AG (CH) 2005-03-23 EP disclosed
US-20040248813-A1 Compounds and methods for the modulation of cd154 CBR INSTITUTE FOR BIOMEDICAL RESEARCH, INC. 2004-12-09 US disclosed
EP-1478640-A1 PROCESS FOR THE MANUFACTURE OF HMG-COA REDUCTASE INHIBITORY MEVALONIC ACID DERIVATIVES Novartis AG (CH) 2004-11-24 EP disclosed
EP-1472228-A1 PROCESS FOR THE MANUFACTURE OF HMG-COA REDUCTASE INHIBITORS Novartis AG (CH) 2004-11-03 EP disclosed
US-20040063628-A1 Active agent delivery systems and methods for protecting and administering active agents NEW RIVER PHARMACEUTICALS INC. 2004-04-01 US disclosed
WO-2003106435-A1 FUSED-RING PYRIMIDIN-4(3H)-ONE DERIVATIVES, PROCESSES FOR THE PREPARATION AND USES THEREOF SANKYO COMPANY, LIMITED (JP) 2003-12-24 WO disclosed
WO-2003105837-A1 CALCIUM SALTS OF INDOLE DERIVED STATINS NOVARTIS AG (CH) 2003-12-24 WO disclosed
WO-2003070717-A1 PROCESS FOR THE MANUFACTURE OF HMG-COA REDUCTASE INHIBITORY MEVALONIC ACID DERIVATIVES NOVARTIS AG (CH) 2003-08-28 WO disclosed
WO-2003064392-A1 PROCESS FOR THE MANUFACTURE OF HMG-COA REDUCTASE INHIBITORS NOVARTIS AG (CH) 2003-08-07 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-20040063628-A1 Active agent delivery systems and methods for protecting and administering active agents HDGF, CTSA, IAPP HMGCR 2422/4885CYP2C9 4779/4885SIRT6 2082/4885

“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.