Enoximone

Enoximone

SCHEMBL5153559

CSc1ccc(C(=O)c2[nH]c(=O)[nH]c2C)cc1.CSc1ccc(C(=O)c2[nH]c(=O)[nH]c2C)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PDE3APDE3B

The experimentally established mechanism targets of Enoximone. 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
PDE3B known ✓ Q13370 3/20 1.00
PDE3A known ✓ Q14432 3/20 1.00
PDE4A P27815 11/20 1.00
PDE4B Q07343 11/20 1.00
PDE4C Q08493 11/20 1.00
PDE4D Q08499 11/20 1.00
TSHR P16473 2/20 1.00
CYP1A2 P05177 1/20 1.00
CYP3A4 P08684 1/20 1.00
CYP2C9 P11712 1/20 1.00
HPGD P15428 1/20 1.00
ALOX15 P16050 1/20 1.00
NFKB1 P19838 1/20 1.00
BLM P54132 1/20 1.00
PMP22 Q01453 1/20 1.00
ATM Q13315 1/20 1.00
NPSR1 Q6W5P4 1/20 1.00
HSD17B10 Q99714 1/20 1.00
PLK1 P53350 1/20 0.42
MMP2 P08253 1/20 0.38

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
Enoximone SCHEMBL44049 1.00 PDE4A (1.00) PDE4APDE4BPDE4CPDE4DPDE3B
Enoximone SCHEMBL5702415 0.94 PDE4A (0.89) PDE4APDE4BPDE4CPDE4DPDE3B
Enoximone SCHEMBL28068937 0.85 PDE4A (0.72) PDE4APDE4BPDE4CPDE4DPDE3B
SCHEMBL7442148 0.83 PDE4A (0.70) PDE4APDE4BPDE4CPDE4DPDE3B
SCHEMBL9787151 0.83 PDE4A (0.70) PDE4APDE4BPDE4CPDE4DPDE3B
SCHEMBL5457930 0.81 PDE4A (0.69) PDE4APDE4BPDE4CPDE4DPDE3B
SCHEMBL10635511 0.81 PDE4A (0.69) PDE4APDE4BPDE4CPDE4DPDE3B
SCHEMBL7416132 0.80 PDE4A (0.67) PDE4APDE4BPDE4CPDE4DPDE3B
SCHEMBL11181578 0.80 PDE4A (0.67) PDE4APDE4BPDE4CPDE4DPDE3B
SCHEMBL10924200 0.80 PDE4A (0.67) PDE4APDE4BPDE4CPDE4DPDE3B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1737447-A1 (R)-ENOXIMONE SULFOXIDE AND ITS USE IN THE TREATMENT OF PDE-III MEDIATED DISEASES MYOGEN, INC. (US) 2007-01-03 EP disclosed
EP-1737448-A1 (S) - ENOXIMONE SULFOXIDE AND ITS USE IN THE TREATMENT OF PDE-III MEDIATED DISEASES MYOGEN, INC. (US) 2007-01-03 EP disclosed
EP-1699436-A2 ENOXIMONE FORMULATIONS AND THEIR USE IN THE TREATMENT OF CARDIAC HYPERTROPHY AND HEART FAILURE MYOGEN, INC. (US) 2006-09-13 EP disclosed
WO-2005092332-A1 (S) - ENOXIMONE SULFOXIDE AND ITS USE IN THE TREATMENT OF PDE-III MEDIATED DISEASES MYOGEN, INC. (US) 2005-10-06 WO disclosed
WO-2005092333-A1 (R)-ENOXIMONE SULFOXIDE AND ITS USE IN THE TREATMENT OF PDE-III MEDIATED DISEASES MYOGEN, INC. (US) 2005-10-06 WO disclosed
WO-2005058280-A2 ENOXIMONE FORMULATIONS AND THEIR USE IN THE TREATMENT OF CARDIAC HYPERTROPHY AND HEART FAILURE MYOGEN, INC. (US) 2005-06-30 WO disclosed
EP-1252158-A1 NICOTINAMIDE BENZOFUSED-HETEROCYCLYL DERIVATIVES USEFUL AS SELECTIVE INHIBITORS OF PDE4 ISOZYMES Pfizer Products Inc. (US) 2002-10-30 EP disclosed
WO-2001057036-A1 NICOTINAMIDE BENZOFUSED-HETEROCYCLYL DERIVATIVES USEFUL AS SELECTIVE INHIBITORS OF PDE4 ISOZYMES PFIZER PRODUCTS INC. (US) 2001-08-09 WO disclosed