Tosifen

Tosifen

SCHEMBL1133723

Cc1ccc(S(=O)(=O)NC(=O)NC(C)Cc2ccccc2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GAA P10253 1/20 1.00
NPC1 O15118 1/20 0.61
RAB9A P51151 1/20 0.61
LMNA P02545 3/20 0.57
F2 P00734 3/20 0.56
PRSS1 P07477 3/20 0.56
PRSS2 P07478 3/20 0.56
PRSS3 P35030 3/20 0.56
ALDH1A1 P00352 1/20 0.53
MMP1 P03956 1/20 0.52
MMP2 P08253 1/20 0.52
MMP9 P14780 1/20 0.52
MMP8 P22894 1/20 0.52
CA2 P00918 1/20 0.51
CA7 P43166 1/20 0.51
NLRP3 Q96P20 1/20 0.51
L3MBTL1 Q9Y468 2/20 0.50
CA12 O43570 1/20 0.50
CYP1A2 P05177 1/20 0.50
CYP3A4 P08684 1/20 0.50

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
Tosifen SCHEMBL29387539 1.00 GAA (1.00) GAANPC1RAB9ALMNAF2
SCHEMBL11755955 0.86 GAA (0.76) GAANPC1RAB9ALMNAALDH1A1
SCHEMBL20335034 0.86 GAA (0.75) GAALMNAF2PRSS1PRSS2
SCHEMBL20335036 0.86 GAA (0.75) GAALMNAF2PRSS1PRSS2
SCHEMBL20335042 0.84 GAA (0.72) GAALMNAF2PRSS1PRSS2
SCHEMBL20335002 0.83 GAA (0.70) GAALMNAF2PRSS1PRSS2
SCHEMBL20335001 0.83 GAA (0.70) GAALMNAF2PRSS1PRSS2
SCHEMBL23467914 0.82 GAA (0.69) GAALMNAALDH1A1CA2CA7
SCHEMBL20335121 0.82 GAA (0.69) GAALMNAF2PRSS1PRSS2
SCHEMBL20335120 0.82 GAA (0.69) GAALMNAF2PRSS1PRSS2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4016291-A CARDIAC DISORDERS INCLUDING ARRHYTHMIA SCHERING CORPORATION (US) 1977-04-05 US claimed
EP-2205639-B1 ANTI-PCSK9 AND METHODS FOR TREATING LIPID AND CHOLESTEROL DISORDERS MERCK SHARP & DOHME (US) 2015-12-23 EP disclosed
US-9089522-B2 Method of reducing total cholesterol level by administering matrilin-2 polypeptide MERCK SHARP & DOHME CORP. (US) 2015-07-28 US disclosed
US-20140161798-A1 ANTI-PCSK9 AND METHODS FOR TREATING LIPID AND CHOLESTEROL DISORDERS MERCK SHARP & DOHME CORP. (US) 2014-06-12 US disclosed
US-8598320-B2 Anti-PCSK9 and methods for treating lipid and cholesterol disorders MERCK SHARP & DOHME CORP. (US) 2013-12-03 US disclosed
US-8257921-B1 NRIP1 regulation of apolipoprotein A1 SCHERING CORPORATION (US) 2012-09-04 US disclosed
WO-2012054438-A1 ANTI-PCSK9 SCHERING CORPORATION (US) 2012-04-26 WO disclosed
CN-102232088-A Anti-PCSK9 and methods for treating lipid and cholesterol disorders SCHERING CORP 2011-11-02 CN disclosed
US-20110150875-A1 EGF-A DOMAIN-MEDIATED MODULATION OF PCKS9 FOR TREATING LIPID DISORDERS MERCK SHARP & DOHME CORP. 2011-06-23 US disclosed
EP-2285399-A2 EGF-A DOMAIN-MEDIATED MODULATION OF PCSK9 FOR TREATING LIPID DISORDERS Schering Corporation (US) 2011-02-23 EP disclosed
US-20110033465-A1 ANTI-PCSK9 AND METHODS FOR TREATING LIPID AND CHOLESTEROL DISORDERS SCHERING CORPORATION (US) 2011-02-10 US disclosed
EP-2205639-A2 ANTI-PCSK9 AND METHODS FOR TREATING LIPID AND CHOLESTEROL DISORDERS SCHERING CORPORATION (US) 2010-07-14 EP disclosed
WO-2009143367-A2 EGF-A DOMAIN-MEDIATED MODULATION OF PCSK9 SCHERING CORPORATION (US) 2009-11-26 WO disclosed
WO-2009055783-A2 ANTI-PCSK9 AND METHODS FOR TREATING LIPID AND CHOLESTEROL DISORDERS SCHERING CORPORATION (US) 2009-04-30 WO disclosed
EP-1385548-B1 COMBINATIONS OF STEROL ABSORPTION INHIBITOR(S) WITH CARDIOVASCULAR AGENT(S) FOR THE TREATMENT OF VASCULAR CONDITIONS SCHERING CORP (US) 2007-05-23 EP disclosed
EP-1541175-A2 Combinations of sterol absorption inhibitor(s) with cardiovascular agent(s) for the treatment of vascular conditions Schering Corporation (US) 2005-06-15 EP disclosed
CN-1582168-A Combinations of sterol absorption inhibitor(s) with cardiovascular agent(s) for the treatment of vascular conditions SCHERING CORP (US) 2005-02-16 CN disclosed
EP-1385548-A2 COMBINATIONS OF STEROL ABSORPTION INHIBITOR(S) WITH CARDIOVASCULAR AGENT(S) FOR THE TREATMENT OF VASCULAR CONDITIONS Schering Corporation (US) 2004-02-04 EP disclosed
WO-2002058731-A2 COMBINATIONS OF STEROL ABSORPTION INHIBITOR(S) WITH CARDIOVASCULAR AGENT(S) FOR THE TREATMENT OF VASCULAR CONDITIONS SCHERING CORPORATION (US) 2002-08-01 WO disclosed
US-4016291-A CARDIAC DISORDERS INCLUDING ARRHYTHMIA SCHERING CORPORATION (US) 1977-04-05 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 (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-20110033465-A1 ANTI-PCSK9 AND METHODS FOR TREATING LIPID AND CHOLESTEROL DISORDERS PCSK9, PCSK7, CETP GAA 196/4885NPC1 16/4885RAB9A 1958/4885
US-20140161798-A1 ANTI-PCSK9 AND METHODS FOR TREATING LIPID AND CHOLESTEROL DISORDERS PCSK9, PCSK7, CETP GAA 196/4885NPC1 16/4885RAB9A 1958/4885

“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.