Cilomilast

Cilomilast

SCHEMBL6904030

COc1ccc(C2(C#N)CCC(C(=O)O)CC2)cc1OC1CCCC1.[LiH]

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PDE4APDE4BPDE4CPDE4D

The experimentally established mechanism targets of Cilomilast. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
PDE4B known ✓ Q07343 20/20 0.98
PDE4A known ✓ P27815 19/20 0.98
PDE4C known ✓ Q08493 19/20 0.98
PDE4D known ✓ Q08499 19/20 0.98

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
Cilomilast SCHEMBL13777301 0.99 PDE4B (1.00) PDE4BPDE4APDE4CPDE4D
Cilomilast SCHEMBL26372 0.99 PDE4B (1.00) PDE4BPDE4APDE4CPDE4D
Cilomilast SCHEMBL27515 0.99 PDE4B (1.00) PDE4BPDE4APDE4CPDE4D
Cilomilast SCHEMBL5975855 0.99 PDE4B (1.00) PDE4BPDE4APDE4CPDE4D
Cilomilast SCHEMBL27516 0.99 PDE4B (1.00) PDE4BPDE4APDE4CPDE4D
Cilomilast SCHEMBL29107422 0.98 PDE4B (0.98) PDE4BPDE4APDE4CPDE4D
Cilomilast SCHEMBL7130621 0.98 PDE4B (0.98) PDE4BPDE4APDE4CPDE4D
Cilomilast SCHEMBL7130626 0.98 PDE4B (0.98) PDE4BPDE4APDE4CPDE4D
Cilomilast SCHEMBL7124080 0.96 PDE4B (0.94) PDE4BPDE4APDE4CPDE4D
SCHEMBL28381093 0.95 PDE4B (0.92) PDE4BPDE4APDE4CPDE4D

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20030083507-A1 Treating chronic bronchial asthma by activating adenylate cyclase and inhibiting phosphodiesterase; principal airway smooth muscle relaxation; suppresses cell degranulation; from an oxaspiro-2.5-octane-2,6-dinitrile analog SMITHKLINE BEECHAM CORPORATION 2003-05-01 US claimed
US-20020082440-A1 METHOD FOR PREPARING SUBSTITUTED 4-PHENYL-4-CYANOCYCLOHEXANOIC ACIDS SMITHKLINE BEECHAM CORPORATION 2002-06-27 US claimed
CN-102772411-A Combination of HMG-COA reductase inhibitors, such as roflumilast, roflumilast-N-oxide with a phosphodiesterase 4 inhibitor, rosuvastatin, for the treatment of inflammatory pulmonary diseases NYCOMED GMBH 2012-11-14 CN disclosed
CN-102764440-A Combination of HMG-CoA reductase inhibitors with phosphodiesterase 4 inhibitors for the treatment of inflammatory pulmonary diseases NYCOMED GMBH 2012-11-07 CN disclosed
CN-101484166-B Combination of HMG-CoA reductase inhibitors with phosphodiesterase 4 inhibitors for the treatment of inflammatory pulmonary diseases NYCOMED GMBH 2012-09-05 CN disclosed
CN-101484166-A Combination of HMG-CoA reductase inhibitors with phosphodiesterase 4 inhibitors for the treatment of inflammatory pulmonary diseases NYCOMED GMBH (DE) 2009-07-15 CN disclosed
EP-1043930-A4 METHOD FOR PREPARING SUBSTITUTED 4-PHENYL-4-CYANOCYCLOHEXANOIC ACIDS SMITHKLINE BEECHAM CORP (US) 2004-09-15 EP disclosed
US-20030083507-A1 Treating chronic bronchial asthma by activating adenylate cyclase and inhibiting phosphodiesterase; principal airway smooth muscle relaxation; suppresses cell degranulation; from an oxaspiro-2.5-octane-2,6-dinitrile analog SMITHKLINE BEECHAM CORPORATION 2003-05-01 US disclosed
US-6452022-B1 HEATING ALKALI OR ALKALINE EARTH METAL HALIDE, AND 6-(3-(CYCLOPENTYLOXY)-4-METHOXYPHENYL))-1-OXASPIRO(2.5)OCTANE-2,6 -DICARBONITRILE IN SOLVENT; ADDING STRONG BASE, REMOVING WATER AND SOLVENT SMITHKLINE BEECHAM CORPORATION 2002-09-17 US disclosed
US-20020082440-A1 METHOD FOR PREPARING SUBSTITUTED 4-PHENYL-4-CYANOCYCLOHEXANOIC ACIDS SMITHKLINE BEECHAM CORPORATION 2002-06-27 US disclosed
EP-1043930-A1 METHOD FOR PREPARING SUBSTITUTED 4-PHENYL-4-CYANOCYCLOHEXANOIC ACIDS SMITHKLINE BEECHAM CORPORATION (US) 2000-10-18 EP disclosed
WO-1999018793-A1 METHOD FOR PREPARING SUBSTITUTED 4-PHENYL-4-CYANOCYCLOHEXANOIC ACIDS SMITHKLINE BEECHAM CORPORATION (US) 1999-04-22 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 (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-20030083507-A1 Treating chronic bronchial asthma by activating adenylate cyclase and inhibiting phosphodiesterase; principal airway smooth muscle relaxation; suppresses cell degranulation; from an oxaspiro-2.5-octane-2,6-dinitrile analog PDE3A, PDE3B, PDE2A PDE4B 13/4885PDE4A 10/4885PDE4C 23/4885
US-20020082440-A1 METHOD FOR PREPARING SUBSTITUTED 4-PHENYL-4-CYANOCYCLOHEXANOIC ACIDS PCCA, CA6, CA4 PDE4B 2865/4885PDE4A 2842/4885PDE4C 2892/4885

“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.