SCHEMBL10049193

SCHEMBL10049193

CC(=O)C[C@H](O)C[C@H](O)/C=C/c1c(C2CC2)nc2ccccc2c1-c1ccc(F)cc1

nearest known ligand 0.87

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ NR4A2 P43354 2/20 0.87
▸ PDE4D Q08499 2/20 0.87
▸ NR1I2 O75469 1/20 0.87
▸ HMGCR P04035 5/20 0.82
▸ RXRA P19793 3/20 0.82
▸ PRKAA2 P54646 1/20 0.51
▸ CYP2C9 P11712 3/20 0.48
▸ SIRT6 Q8N6T7 2/20 0.48
▸ TBXA2R P21731 2/20 0.48
▸ ADRA1A P35348 2/20 0.48
▸ ABCC3 O15438 1/20 0.48
▸ ABCB11 O95342 1/20 0.48
▸ PGR P06401 1/20 0.48
▸ ADORA3 P0DMS8 1/20 0.48
▸ CCKAR P32238 1/20 0.48
▸ PTGS2 P35354 1/20 0.48
▸ SLC10A1 Q14973 1/20 0.48
▸ ESR1 P03372 1/20 0.46
▸ CHRM1 P11229 1/20 0.46
▸ PDE4A P27815 1/20 0.46

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
SCHEMBL14569976 1.00 NR4A2 (0.87) NR4A2PDE4DNR1I2HMGCRRXRA
SCHEMBL14569977 1.00 NR4A2 (0.87) NR4A2PDE4DNR1I2HMGCRRXRA
Pitavastatin SCHEMBL6068297 0.93 PDE4D (1.00) NR4A2PDE4DNR1I2HMGCRRXRA
Pitavastatin SCHEMBL13278902 0.93 PDE4D (1.00) NR4A2PDE4DNR1I2HMGCRRXRA
Pitavastatin SCHEMBL6068293 0.93 PDE4D (1.00) NR4A2PDE4DNR1I2HMGCRRXRA
Pitavastatin SCHEMBL10049191 0.93 PDE4D (1.00) NR4A2PDE4DNR1I2HMGCRRXRA
Pitavastatin SCHEMBL3369 0.93 PDE4D (1.00) NR4A2PDE4DNR1I2HMGCRRXRA
Pitavastatin SCHEMBL1582325 0.93 PDE4D (1.00) NR4A2PDE4DNR1I2HMGCRRXRA
Pitavastatin SCHEMBL2870889 0.93 PDE4D (1.00) NR4A2PDE4DNR1I2HMGCRRXRA
Pitavastatin SCHEMBL13278898 0.93 PDE4D (1.00) NR4A2PDE4DNR1I2HMGCRRXRA

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 16 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9517233-B2 Local cochlear application of statins for stimulating neurite regrowth in the cochlea NORTHWESTERN UNIVERSITY (US) 2016-12-13 — — US disclosed
US-20160022663-A1 LOCAL COCHLEAR APPLICATION OF STATINS FOR STIMULATING NEURITE REGROWTH IN THE COCHLEA THE GOVERNMENT OF THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE NAVY 2016-01-28 — — US disclosed
US-20160015819-A1 FATTY ACID CONJUGATES OF STATIN AND FXR AGONISTS: COMPOSITIONS AND METHODS OF USE CATABASIS PHARMACEUTICALS, INC. (US) 2016-01-21 — — US disclosed
US-9084826-B2 Fatty acid conjugates of statin and FXR agonists; compositions and method of uses CATABASIS PHARMACEUTICALS, INC. (US) 2015-07-21 — — US disclosed
US-20140127295-A1 COMPOSITIONS, PROCESS OF PREPARATION OF SAID COMPOSITIONS AND METHOD OF TREATING INFLAMMATORY DISEASES Cellworks Group, Inc (US) 2014-05-08 — — US disclosed
US-8487105-B2 Process for preparing pitavastatin, intermediates and pharmaceuctically acceptable salts thereof MSN LABORATORIES LIMITED (IN) 2013-07-16 — — US disclosed
US-20130072688-A1 METHOD FOR PREPARING AN INTERMEDIATE OF PITAVASTATIN OR OF THE SALT THEREOF H.L. GENOMICS (KR) 2013-03-21 — — US disclosed
US-20120016129-A1 Process for Preparing Pitavastatin, Intermediates and Pharmaceuctically Acceptable Salts Thereof MSN LABORATORIES LIMITED (IN) 2012-01-19 — — US disclosed
US-20090275752-A1 Novel Process for Statins and its Pharmaceutically Acceptable Salts Thereof MSN LABORATORIES LIMITED (IN) 2009-11-05 — — US disclosed
US-20080312462-A1 Process for the manufacture of HMG-CoA reductase inhibitory mevalonic acid derivatives SEDELMEIER GOTTFRIED 2008-12-18 — — US disclosed
US-20080182873-A1 PROCESS FOR THE MANUFACTURE OF HMG-COA REDUCTASE INHIBITORS ACEMOGLU MURAT 2008-07-31 — — US disclosed
US-7371865-B2 Process for the manufacture of HMG-CoA reductase inhibitors NOVARTIS PHARMACEUTICALS CORPORATION (US) 2008-05-13 — — US disclosed
US-7335757-B2 Carbonyl reductase, gene encoding the same, and process for producing optically active alcohols using the same MITSUBISHI CHEMICAL CORPORATION (JP) 2008-02-26 — — US disclosed
US-20070155970-A1 PROCESS FOR THE MANUFACTURE OF HMG-COA REDUCTASE INHIBITORY MEVALONIC ACID DERIVATIVES SEDELMEIER GOTTFRIED 2007-07-05 — — US disclosed
US-7208623-B2 Process for the manufacture of HMG-CoA reductase inhibitory mevalonic acid derivatives NOVARTIS AG (CH) 2007-04-24 — — US disclosed
US-7193086-B2 Process for preparation of a quinolinecarbaldehyde NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2007-03-20 — — 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 (9 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-20080312462-A1 Process for the manufacture of HMG-CoA reductase inhibitory mevalonic acid derivatives HMGCR, COASY, DHCR7 NR4A2 4293/4885PDE4D 3066/4885NR1I2 626/4885
US-20080182873-A1 PROCESS FOR THE MANUFACTURE OF HMG-COA REDUCTASE INHIBITORS HMGCR, COASY, DHCR7 NR4A2 3561/4885PDE4D 3207/4885NR1I2 493/4885
US-20120016129-A1 Process for Preparing Pitavastatin, Intermediates and Pharmaceuctically Acceptable Salts Thereof PCSK9, HMGCR, HDLBP NR4A2 3911/4885PDE4D 579/4885NR1I2 3388/4885
US-20070155970-A1 PROCESS FOR THE MANUFACTURE OF HMG-COA REDUCTASE INHIBITORY MEVALONIC ACID DERIVATIVES HMGCR, COASY, DHCR7 NR4A2 4188/4885PDE4D 2938/4885NR1I2 997/4885
US-20130072688-A1 METHOD FOR PREPARING AN INTERMEDIATE OF PITAVASTATIN OR OF THE SALT THEREOF DPP4, REN, DPP7 NR4A2 3647/4885PDE4D 200/4885NR1I2 4730/4885
US-20140127295-A1 COMPOSITIONS, PROCESS OF PREPARATION OF SAID COMPOSITIONS AND METHOD OF TREATING INFLAMMATORY DISEASES TNF, C5, C9 NR4A2 3354/4885PDE4D 646/4885NR1I2 3664/4885
US-20160022663-A1 LOCAL COCHLEAR APPLICATION OF STATINS FOR STIMULATING NEURITE REGROWTH IN THE COCHLEA NGF, BDNF, NLN NR4A2 2373/4885PDE4D 214/4885NR1I2 3837/4885
US-20160015819-A1 FATTY ACID CONJUGATES OF STATIN AND FXR AGONISTS: COMPOSITIONS AND METHODS OF USE SLC10A1, NR1H4, FXR1 NR4A2 831/4885PDE4D 2176/4885NR1I2 160/4885
US-20090275752-A1 Novel Process for Statins and its Pharmaceutically Acceptable Salts Thereof HMGCR, NPC1L1, PCSK9 NR4A2 4110/4885PDE4D 1145/4885NR1I2 437/4885

“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.

Send feedback