Methacrylic Acid

Methacrylic Acid

SCHEMBL1788554

C=C(C)C(=O)O.C=C(C)C(=O)O.CCCCCCC(C)(O)O

nearest known ligand 0.48

Full drug profile on Sugi Atlas →

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.43
FDPS P14324 8/20 0.41
GGPS1 O95749 5/20 0.41
CES2 O00748 1/20 0.40
THRB P10828 1/20 0.40
FNTA P49354 1/20 0.40
FNTB P49356 1/20 0.40
PGGT1B P53609 1/20 0.40
ALDH1A1 P00352 1/20 0.39
SLC22A6 Q4U2R8 1/20 0.39
SLC22A8 Q8TCC7 1/20 0.39
GPR84 Q9NQS5 1/20 0.39

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
Methacrylic Acid SCHEMBL9063427 0.98 TSHR (0.40) TSHRFDPSGGPS1CES2THRB
Methacrylic Acid SCHEMBL1299928 0.84 TSHR (0.41) TSHRFDPSGGPS1CES2THRB
Dodecane SCHEMBL17222843 0.83 TSHR (0.56) TSHRTHRBFNTAFNTBPGGT1B
Decane SCHEMBL20943079 0.83 TSHR (0.56) TSHRTHRBFNTAFNTBPGGT1B
Octane SCHEMBL9639081 0.83 TSHR (0.56) TSHRTHRBFNTAFNTBPGGT1B
Octane SCHEMBL2702853 0.83 TSHR (0.56) TSHRTHRBFNTAFNTBPGGT1B
Methacrylic Acid SCHEMBL8469735 0.83 TSHR (0.56) TSHRTHRBFNTAFNTBPGGT1B
Decane SCHEMBL2509675 0.83 TSHR (0.56) TSHRTHRBFNTAFNTBPGGT1B
Dodecane SCHEMBL821201 0.83 TSHR (0.56) TSHRTHRBFNTAFNTBPGGT1B
Decane SCHEMBL4879362 0.83 TSHR (0.56) TSHRTHRBFNTAFNTBPGGT1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6627720-B2 Monoethylenically unsaturated monomers are polymerized with at least one multiethylenically unsaturated monomer at high temperatures by free radical polymerization in a continuous reactor, without formation of highly crosslinked gels JOHNSON POLYMER, LLC 2003-09-30 US claimed
US-6265511-B1 BLEND OF DIVINYL MONOMER AND MONOETHYLENICALLY UNSATURATED MONOMER S. C. JOHNSON COMMERICAL MARKETS, INC. 2001-07-24 US claimed
CN-113347950-A Ophthalmic lenses, pharmaceutical compositions and uses thereof 红婴生物科技股份有限公司 2021-09-03 CN disclosed
US-20120287201-A1 PROCESS FOR PREPARING A DISPERSION OF A PARTICULATE SOLID FUJIFILM IMAGING COLORANTS LIMITED (GB) 2012-11-15 US disclosed
US-8258231-B2 Process for preparing a dispersion of a particulate solid FUJIFILM IMAGING COLORANTS LIMITED (GB) 2012-09-04 US disclosed
US-20110123716-A1 Process for Preparing a Dispersion of a Particulate Solid FUJIFILM IMAGING COLORANTS LIMITED (GB) 2011-05-26 US disclosed
US-20040048987-A1 Process for producing hyperbranched polymers CAMPBELL J DAVID (NL) 2004-03-11 US disclosed
US-6627720-B2 Monoethylenically unsaturated monomers are polymerized with at least one multiethylenically unsaturated monomer at high temperatures by free radical polymerization in a continuous reactor, without formation of highly crosslinked gels JOHNSON POLYMER, LLC 2003-09-30 US disclosed
EP-1001998-B1 PROCESS FOR PRODUCING HYPERBRANCHED POLYMERS JOHNSON S C COMM MARKETS INC (US) 2002-11-06 EP disclosed
US-20010039316-A1 Hyperbranched polymers BASF CORPORATION 2001-11-08 US disclosed
US-6265511-B1 BLEND OF DIVINYL MONOMER AND MONOETHYLENICALLY UNSATURATED MONOMER S. C. JOHNSON COMMERICAL MARKETS, INC. 2001-07-24 US disclosed
EP-1001998-A1 PROCESS FOR PRODUCING HYPERBRANCHED POLYMERS S.C. Johnson Commercial Markets, Inc. (US) 2000-05-24 EP disclosed
US-5986020-A HEATING MONOMER MIXTURE AND FREE RADICAL CATALYST WITH MULTI UNSATURATED COMPOUNDS BASF CORPORATION 1999-11-16 US disclosed
WO-1999007754-A1 PROCESS FOR PRODUCING HYPERBRANCHED POLYMERS S.C. JOHNSON COMMERCIAL MARKETS, INC. (US) 1999-02-18 WO disclosed