Perflubutane

Perflubutane

SCHEMBL4458683

FC(F)(F)C(F)(F)C(F)(F)C(F)(F)F.O=S(=O)(O)O

nearest known ligand 0.50

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Perflubutane. 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
CA2 P00918 9/20 0.50
CA1 P00915 8/20 0.50
MMP1 P03956 5/20 0.50
MMP2 P08253 5/20 0.50
MMP9 P14780 5/20 0.50
MMP8 P22894 5/20 0.50
MMP13 P45452 5/20 0.50
CA5A P35218 2/20 0.46
CA5B Q9Y2D0 2/20 0.46
F2 P00734 4/20 0.44
PRSS1 P07477 4/20 0.44
PRSS2 P07478 4/20 0.44
PRSS3 P35030 4/20 0.44
THRB P10828 1/20 0.43
TSHR P16473 2/20 0.40
TDP1 Q9NUW8 1/20 0.40
ALDH1A1 P00352 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.38
LMNA P02545 1/20 0.37
CA7 P43166 2/20 0.33

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
Perflubutane SCHEMBL7865494 0.96 CA2 (0.48) CA2CA1MMP1MMP2MMP9
Sulfuric Acid SCHEMBL19348238 0.96 CA2 (0.52) CA2CA1MMP1MMP2MMP9
Perflubutane SCHEMBL10729483 0.96 CA2 (0.48) CA2CA1MMP1MMP2MMP9
Perflubutane SCHEMBL1302828 0.96 CA2 (0.48) CA2CA1MMP1MMP2MMP9
Sulfuric Acid SCHEMBL2819379 0.96 CA2 (0.52) CA2CA1MMP1MMP2MMP9
Sulfuric Acid SCHEMBL1303190 0.93 CA2 (0.50) CA2CA1MMP1MMP2MMP9
Sulfuric Acid SCHEMBL19690369 0.93 CA2 (0.50) CA2CA1MMP1MMP2MMP9
Perflutren SCHEMBL3944011 0.92 CA5A (0.46) CA2CA1MMP1MMP2MMP9
Perflubutane SCHEMBL6557063 0.89 TSHR (0.57) CA2CA1MMP1MMP2MMP9
Sulfuric Acid SCHEMBL28980726 0.87 CA2 (0.42) CA2CA1MMP1MMP2MMP9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2525972-B1 FLAME-PROTECTED ARTICLE HAVING A HIGH LEVEL OF TRANSMISSION COVESTRO DEUTSCHLAND AG (DE) 2016-11-02 EP claimed
EP-2785782-B1 UV-STABILIZED, GLASS-FIBER REINFORCED, FLAME-RETARDANT POLYCARBONATES FOR THE EE AND IT SECTOR COVESTRO DEUTSCHLAND AG (DE) 2016-11-02 EP claimed
EP-2785783-B1 ETHYLENE-PROPYLENE-MALEIC ACID ANHYDRIDE COPOLYMER AS IMPACT MODIFIER IN GLASS-FIBER REINFORCED, FLAME-RETARDANT POLYCARBONATES FOR THE EE SECTOR COVESTRO DEUTSCHLAND AG (DE) 2016-09-28 EP claimed
EP-1910386-B1 DIARYL ALKYLPHOSPHONATES AND METHOD FOR PREPARING SAME FRX POLYMERS INC (US) 2015-09-02 EP claimed
US-7569717-B2 Diaryl alkylphosphonates and method for preparing same FRX POLYMERS, LLC (US) 2009-08-04 US claimed
EP-1910386-A2 DIARYL ALKYLPHOSPHONATES AND METHOD FOR PREPARING SAME Triton Systems Inc. (US) 2008-04-16 EP claimed
US-20070021626-A1 forming methyldiphenyl phosphonate through reaction of phosphorous trichloride and methanol in presence of an alkylation catalyst methyl iodide; high yield; industrial scale, cost efficiency; free of phosphorus contaminants FRX POLYMERS, INC. 2007-01-25 US claimed
WO-2007011998-A2 DIARYL ALKYLPHOSPHONATES AND METHOD FOR PREPARING SAME TRITON SYSTEMS, INC. (US) 2007-01-25 WO claimed
EP-0664570-B1 Primary or secondary electrochemical generator having an electrode comprising nanometer size particles RENATA AG (CH) 1998-04-08 EP claimed
US-5569561-A Primary or secondary electrochemical generator having a nanoparticulate electrode RENATA A.G. (CH) 1996-10-29 US claimed
EP-0664570-A1 Primary or secondary electrochemical generator having an electrode comprising nanometer size particles Renata AG (CH) 1995-07-26 EP claimed
CN-120201999-A Antimicrobial compositions AHV国际有限公司 2025-06-24 CN disclosed
EP-1910386-B1 DIARYL ALKYLPHOSPHONATES AND METHOD FOR PREPARING SAME FRX POLYMERS INC (US) 2015-09-02 EP disclosed
CN-101501048-B Diaryl alkylphosphonates and method for preparing same FRX POLYMERS LLC 2012-11-28 CN disclosed
CN-101501048-A Diaryl alkylphosphonates and method for preparing same FRX POLYMERS LLC (US) 2009-08-05 CN disclosed
EP-1910386-A2 DIARYL ALKYLPHOSPHONATES AND METHOD FOR PREPARING SAME Triton Systems Inc. (US) 2008-04-16 EP disclosed
US-20070021626-A1 forming methyldiphenyl phosphonate through reaction of phosphorous trichloride and methanol in presence of an alkylation catalyst methyl iodide; high yield; industrial scale, cost efficiency; free of phosphorus contaminants FRX POLYMERS, INC. 2007-01-25 US disclosed
WO-2007011998-A2 DIARYL ALKYLPHOSPHONATES AND METHOD FOR PREPARING SAME TRITON SYSTEMS, INC. (US) 2007-01-25 WO disclosed
EP-0664570-B1 Primary or secondary electrochemical generator having an electrode comprising nanometer size particles RENATA AG (CH) 1998-04-08 EP disclosed
EP-0664570-A1 Primary or secondary electrochemical generator having an electrode comprising nanometer size particles Renata AG (CH) 1995-07-26 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 (1 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-20070021626-A1 forming methyldiphenyl phosphonate through reaction of phosphorous trichloride and methanol in presence of an alkylation catalyst methyl iodide; high yield; industrial scale, cost efficiency; free of phosphorus contaminants PHOSPHO1, PPIP5K2, IPMK CA2 2048/4885CA1 3005/4885MMP1 3696/4885

“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.