Methacrylic Acid

Methacrylic Acid

SCHEMBL873041

C=C(C)C(=O)[O-].CC[N+](C)(C)C.Cl

nearest known ligand 0.36

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
HRH1 known ✓ P35367 1/20 0.35
CA4 P22748 2/20 0.36
BBOX1 O75936 4/20 0.35
MEN1 O00255 1/20 0.35
CYP1A2 P05177 1/20 0.35
KMT2A Q03164 1/20 0.35
CYP2C19 P33261 1/20 0.34
CA1 P00915 2/20 0.33
POLB P06746 1/20 0.33
BLM P54132 1/20 0.33
ATM Q13315 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
SLC22A16 Q86VW1 1/20 0.33
CRAT P43155 1/20 0.31

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 SCHEMBL540788 0.97 CA4 (0.38) CA4BBOX1MEN1CYP1A2HRH1
Methacrylic Acid SCHEMBL873040 0.95 POLB (0.38) CA4BBOX1MEN1CYP1A2HRH1
Methacrylic Acid SCHEMBL28377504 0.85 BBOX1 (0.45) CA4BBOX1CA1TDP1
Methacrylic Acid SCHEMBL4924752 0.85 BBOX1 (0.45) CA4BBOX1CYP2C19CA1TDP1
Methacrylic Acid SCHEMBL6553565 0.85 BBOX1 (0.36) BBOX1MEN1CYP1A2HRH1KMT2A
Methacrylic Acid SCHEMBL17453351 0.83 TDP1 (0.38) CA4BBOX1CA1TDP1
Methacrylic Acid SCHEMBL20917781 0.82 TSHR (0.38) CYP2C19POLBBLMATMTDP1
Tetrylammonium SCHEMBL2347482 0.82 TSHR (0.42) CA4BBOX1CA1ATMTDP1
Methacrylic Acid SCHEMBL8154112 0.82 ALDH1A1 (0.41) BBOX1POLBBLMATMTDP1
Methacrylic Acid SCHEMBL4926692 0.81 ACHE (0.38) CA4BBOX1CYP2C19POLBBLM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119912644-A Amphiphilic sizing agent applicable to glass fiber/resin composite material 宁波维创柔性电子技术有限公司 2025-05-02 CN claimed
CN-119072297-A Microcapsules and methods 联合利华知识产权控股有限公司 2024-12-03 CN claimed
CN-113438939-A Protein microcapsule and preparation method thereof 国际香料和香精公司 2021-09-24 CN claimed
EP-1232190-B1 WATER-IN-OIL POLYMER EMULSION AND METHOD FOR MAKING SAME ARKEMA FRANCE (FR) 2011-07-20 EP claimed
WO-2009063042-A1 THICKENED REDUCING COMPOSITION L'OREAL (FR) 2009-05-22 WO claimed
EP-0940136-B1 Reducing agent from a plurality of components and process for permanent hair waving using it OREAL (FR) 2004-10-13 EP claimed
EP-0930061-B1 Oxidizing agent from a plurality of components and process for permanent hair waving using it OREAL (FR) 2004-02-25 EP claimed
US-6238658-B1 THICKENING POLYMER BEING IN THE FORM OF AN AQUEOUS DISPERSION, AN OILY DISPERSION, OR AS A REVERSE EMULSION, WITH THE PROVISO THAT SAID THICKENING POLYMER IS NOT QUATERNARY HYDROXYETHYLCELLULOSE L'OREAL S.A. (FR) 2001-05-29 US claimed
US-6187302-B1 THIOL-BEARING REDUCING AGENT IN AQUEOUS MEDIUM, AND AT LEAST ONE THICKENING POLYMER IN AQUEOUS MEDIUM, SAID THICKENING POLYMER BEING IN THE FORM OF AN AQUEOUS DISPERSION, AN OILY DISPERSION, OR A REVERSE EMULSION L'OREAL S.A. (FR) 2001-02-13 US claimed
EP-0635265-B1 Controlled release pharmaceutical compositions based on one or more pharmaceutically acceptable salts of gamma hydroxy-butyric acid CT LAB FARM SRL (IT) 2000-02-02 EP claimed
EP-0635265-A1 Controlled release pharmaceutical compositions based on one or more pharmaceutically acceptable salts of gamma hydroxy-butyric acid LABORATORIO FARMACEUTICO C.T. S.r.l. (IT) 1995-01-25 EP claimed
US-12622853-B2 Composition comprising a particular oxidation dye precursor and a particular amino silicone L'OREAL (FR) 2026-05-12 US disclosed
EP-4698156-A1 RECONSTITUTABLE DRY POWDER FORMULATIONS AND METHODS OF USE THEREOF Sanofi Pasteur Inc. (US) 2026-02-25 EP disclosed
US-12558301-B2 Composition comprising a particular oxidation dye precursor and a particular amino silicone L'ORÉAL (FR) 2026-02-24 US disclosed
EP-3825361-B1 ORGANOPOLYSILOXANE EMULSION COMPOSITION SHINETSU CHEMICAL CO (JP) 2025-11-26 EP disclosed
EP-0635265-A1 Controlled release pharmaceutical compositions based on one or more pharmaceutically acceptable salts of gamma hydroxy-butyric acid LABORATORIO FARMACEUTICO C.T. S.r.l. (IT) 1995-01-25 EP disclosed
US-4565635-A GUM, POLYMER, OR BIOGUM MATERIAL AND WATER DONOR MATERIAL MIXTURE RHONE-POULENC SPECIALITES CHIMIQUES (FR) 1986-01-21 US disclosed
US-4548734-A IMPROVED DISPERSABILITY RHONE-POULENC SPECIALITES CHIMIQUES (FR) 1985-10-22 US disclosed
US-4308148-A Preparation of water soluble polymeric flocculants by photopolymerization of hydrophilic monomers RHONE-POULENC INDUSTRIES (FR) 1981-12-29 US disclosed
US-4306955-A Photopolymerized acrylic polymer essentially devoid of residual monomer(s) RHONE-POULENC INDUSTRIES (FR) 1981-12-22 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-12558301-B2 Composition comprising a particular oxidation dye precursor and a particular amino silicone KRT18, PLOD1, PLOD2 HRH1 3000/4885CA4 1590/4885BBOX1 1333/4885
US-12622853-B2 Composition comprising a particular oxidation dye precursor and a particular amino silicone KRT18, SCNN1B, PLOD3 HRH1 159/4885CA4 856/4885BBOX1 572/4885

“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.