Pitavastatin

Pitavastatin

SCHEMBL1582328

O=C(O)CC(O)CC(O)C=Cc1c(C2CC2)nc2ccccc2c1-c1ccc(F)cc1

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 Pitavastatin. 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 5/20 0.85
PDE4D Q08499 3/20 1.00
NR4A2 P43354 2/20 1.00
NR1I2 O75469 2/20 1.00
RXRA P19793 3/20 0.85
CYP2C9 P11712 4/20 0.54
SIRT6 Q8N6T7 2/20 0.54
TBXA2R P21731 2/20 0.54
ADRA1A P35348 2/20 0.54
ABCC3 O15438 1/20 0.54
ABCB11 O95342 1/20 0.54
PGR P06401 1/20 0.54
ADORA3 P0DMS8 1/20 0.54
CCKAR P32238 1/20 0.54
PTGS2 P35354 1/20 0.54
SLC10A1 Q14973 1/20 0.54
PRKAA2 P54646 1/20 0.53
ESR1 P03372 1/20 0.51
CHRM1 P11229 1/20 0.51
PDE4A P27815 1/20 0.51

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
Pitavastatin SCHEMBL1582325 1.00 PDE4D (1.00) PDE4DNR4A2NR1I2HMGCRRXRA
Pitavastatin SCHEMBL6068297 1.00 PDE4D (1.00) PDE4DNR4A2NR1I2HMGCRRXRA
Pitavastatin SCHEMBL2878734 1.00 PDE4D (1.00) PDE4DNR4A2NR1I2HMGCRRXRA
Pitavastatin SCHEMBL13278896 1.00 PDE4D (1.00) PDE4DNR4A2NR1I2HMGCRRXRA
Pitavastatin SCHEMBL6068293 1.00 PDE4D (1.00) PDE4DNR4A2NR1I2HMGCRRXRA
Pitavastatin SCHEMBL2878610 1.00 PDE4D (1.00) PDE4DNR4A2NR1I2HMGCRRXRA
Pitavastatin SCHEMBL13278902 1.00 PDE4D (1.00) PDE4DNR4A2NR1I2HMGCRRXRA
Pitavastatin SCHEMBL13278898 1.00 PDE4D (1.00) PDE4DNR4A2NR1I2HMGCRRXRA
Pitavastatin SCHEMBL2878736 1.00 PDE4D (1.00) PDE4DNR4A2NR1I2HMGCRRXRA
Pitavastatin SCHEMBL3369 1.00 PDE4D (1.00) PDE4DNR4A2NR1I2HMGCRRXRA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1623978-B1 METHOD FOR PRODUCING ETHYL (3R, 5S, 6E)-7-[2-CYCLOPROPYL-4-( 4-FLUOROPHENYL)QUINOLINE-3-YL]-3,5-DIHYDROXY-6-HEPTENOATE DAICEL CHEM (JP) 2010-08-11 EP claimed
EP-1391455-B1 PROCESS FOR PREPARATION OF A QUINOLINECARBALDEHYDE DAICEL CHEM (JP) 2010-04-14 EP claimed
US-7193086-B2 Process for preparation of a quinolinecarbaldehyde NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2007-03-20 US claimed
US-20040147750-A1 Process for preparation of a quinolinecarbaldehyde DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2004-07-29 US claimed
EP-1391455-A1 PROCESS FOR PREPARATION OF A QUINOLINECARBALDEHYDE Daicel Chemical Industries, Ltd. (JP) 2004-02-25 EP claimed
EP-0747341-B1 PROCESS FOR PRODUCING OPTICALLY ACTIVE MEVALONOLACTONE COMPOUNDS DAICEL CHEM (JP) 2002-05-22 EP claimed
EP-4072552-A1 CHEMOTHERAPEUTIC DRUG IMPLANT Extruded Pharmaceuticals Ltd (GB) 2022-10-19 EP disclosed
WO-2015024925-A1 MODULATORS OF THE UNCONVENTIONAL SECRETORY PATHWAY FOR USE IN THE TREATMENT OF ALEXANDER DISEASE RHEINISCHE FRIEDRICH-WILHELMS UNIVERSITÄT BONN (DE) 2015-02-26 WO disclosed
EP-2751081-A1 POLYMORPHIC FORM OF PITAVASTATIN CALCIUM Farma GRS, d.o.o. (SI) 2014-07-09 EP disclosed
WO-2013037838-A1 POLYMORPHIC FORM OF PITAVASTATIN CALCIUM FARMA GRS, D.O.O. (SI) 2013-03-21 WO disclosed
CN-102321019-A The crystalline form of quinoline compound and working method thereof NISSAN CHEMICAL IND LTD 2012-01-18 CN disclosed
EP-1375485-B1 METHOD FOR PREPARING 7-QUINOLINYL-3,5-DIHYDROXYHEPT-6-ENOATE NISSAN CHEMICAL IND LTD (JP) 2011-04-20 EP disclosed
CN-1946384-B Statins for the treatment of ocular hypertension and glaucoma ALCON INC 2011-04-20 CN disclosed
WO-2005046725-A1 NOVEL COMBINATION CONTAINING A STIMULATOR OF SOLUBLE GUANYLATE CYCLASE AND A LIPID-LOWERING SUBSTANCE BAYER HEALTHCARE AG (DE) 2005-05-26 WO disclosed
US-20050014947-A1 Method for preparing a 7-quinolinyl-3, 5-dihydroxyhept-6-enoate NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2005-01-20 US disclosed
US-20040147750-A1 Process for preparation of a quinolinecarbaldehyde DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2004-07-29 US disclosed
EP-1391455-A1 PROCESS FOR PREPARATION OF A QUINOLINECARBALDEHYDE Daicel Chemical Industries, Ltd. (JP) 2004-02-25 EP disclosed
EP-1375485-A1 METHOD FOR PREPARING 7-QUINOLINYL-3,5-DIHYDROXYHEPT-6-ENOATE Nissan Chemical Industries, Ltd. (JP) 2004-01-02 EP disclosed
EP-0747341-B1 PROCESS FOR PRODUCING OPTICALLY ACTIVE MEVALONOLACTONE COMPOUNDS DAICEL CHEM (JP) 2002-05-22 EP disclosed
EP-0747341-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE MEVALONOLACTONE COMPOUND DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1996-12-11 EP 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-20050014947-A1 Method for preparing a 7-quinolinyl-3, 5-dihydroxyhept-6-enoate QDPR, DHCR7, GHRHR HMGCR 584/4885PDE4D 747/4885NR4A2 1857/4885
US-20040147750-A1 Process for preparation of a quinolinecarbaldehyde OGDH, DOHH, CBR3 HMGCR 430/4885PDE4D 1723/4885NR4A2 4276/4885

“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.