Glutarate

Glutarate

SCHEMBL106584

O=C([O-])CCCC(=O)[O-].[H+].[K+]

nearest known ligand 0.63

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

AGTR1DHFRGABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTNR3C2PBP2XPTGS1PTGS2VKORC1blablaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAftsImrcAmrcBmrdApbp1apbp1bpbp2apbp2bpbp3polthyA

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

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
CA1 P00915 2/20 0.55
HDAC3 O15379 3/20 0.47
HDAC1 Q13547 3/20 0.47
HDAC2 Q92769 3/20 0.47
HDAC8 Q9BY41 3/20 0.47
FFAR3 O14843 2/20 0.47
FABP3 P05413 6/20 0.44
BBOX1 O75936 3/20 0.44
CA4 P22748 1/20 0.41
HDAC4 P56524 1/20 0.41
HDAC7 Q8WUI4 1/20 0.41
HDAC10 Q969S8 1/20 0.41
HDAC11 Q96DB2 1/20 0.41
HDAC6 Q9UBN7 1/20 0.41
HDAC9 Q9UKV0 1/20 0.41
HDAC5 Q9UQL6 1/20 0.41

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
Glutarate SCHEMBL104914 0.96 CA1 (0.58) CA1HDAC3HDAC1HDAC2HDAC8
Glutarate SCHEMBL1035895 0.96
Adipic Acid SCHEMBL105191 0.93 CA1 (0.55) CA1HDAC3HDAC1HDAC2HDAC8
Glutarate SCHEMBL106177 0.93 CA1 (0.63) CA1HDAC3HDAC1HDAC2HDAC8
Glutarate SCHEMBL107713 0.93 CA1 (0.55) CA1HDAC3HDAC1HDAC2HDAC8
Glutarate SCHEMBL3142994 0.89 CA1 (0.58) CA1HDAC3HDAC1HDAC2HDAC8
Glutarate SCHEMBL5142628 0.89 CA1 (0.58) CA1HDAC3HDAC1HDAC2HDAC8
Glutarate SCHEMBL8745235 0.89 CA1 (0.58) CA1HDAC3HDAC1HDAC2HDAC8
Glutarate SCHEMBL2067310 0.89 CA1 (0.58) CA1HDAC3HDAC1HDAC2HDAC8
Glutarate SCHEMBL5650130 0.89 CA1 (0.58) CA1HDAC3HDAC1HDAC2HDAC8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1312261-B1 Aqueous compositions containing a haloalkynyl compound and a buffer for providing biocidal activity and for stabilising end-use formulations TROY TECHNOLOGY CORP INC (US) 2006-08-30 EP claimed
EP-1312261-A1 Aqueous compositions containing a haloalkynyl compound and a buffer for providing biocidal activity and for stabilising end-use formulations Troy Technology Corporation, Inc. (US) 2003-05-21 EP claimed
EP-0831706-B1 NON-AQUEOUS COMPOSITIONS CONTAINING A HALOALKYNYL COMPOUND AND A BUFFER FOR PROVIDING BIOCIDAL ACTIVITY AND FOR STABILIZING END-USE FORMULATIONS TROY TECHNOLOGY CORP INC (US) 2003-05-02 EP claimed
US-6124350-A PAINT CONTAINING A BIOCIDAL COMPOSITION COMPRISING A HALOPROPYNYL COMPOUND AND A BUFFER TROY TECHNOLOGY CORPORATION, INC. (US) 2000-09-26 US claimed
US-6017955-A A BUFFER STABILIZER FOR ADJUSTING THE PH OF END-USE FORMULATION BETWEEN 3.0 AND 8.0 TO PREVENT DEGRADATION OF PESTICIDE 3-IODO-2-PROPYNYL BUTYL CARBAMATE TROY TECHNOLOGY CORPORATION, INC. (US) 2000-01-25 US claimed
EP-0831706-A1 METHOD OF STABILIZING BIOCIDAL COMPOSITIONS OF HALOALKYNYL COMPOUNDS TROY CHEMICAL CORPORATION (US) 1998-04-01 EP claimed
WO-1996039836-A1 METHOD OF STABILIZING BIOCIDAL COMPOSITIONS OF HALOALKYNYL COMPOUNDS TROY CHEMICAL COMPANY (US) 1996-12-19 WO claimed
CN-116568889-A Anionic glyoxalated polyacrylamides 埃科莱布美国股份有限公司 2023-08-08 CN disclosed
WO-2022110102-A1 ANIONIC GLYOXALATED POLYACRYLAMIDE ECOLAB USA INC. (US) 2022-06-02 WO disclosed
EP-3207093-B1 RESIN COMPOSITIONS AND METHODS FOR MAKING AND USING SAME ECOLAB USA INC (US) 2020-11-25 EP disclosed
US-10144818-B2 Resin compositions and methods for making and using same ECOLAB USA INC. (US) 2018-12-04 US disclosed
EP-2426558-B1 Silicon-containing film-forming composition, silicon-containing film-formed substrate, and patterning process SHINETSU CHEMICAL CO (JP) 2018-10-24 EP disclosed
EP-2500775-B1 PATTERNING PROCESS AND COMPOSITION FOR FORMING SILICON-CONTAINING FILM USABLE THEREFOR SHINETSU CHEMICAL CO (JP) 2018-01-03 EP disclosed
US-20050187356-A1 Glyoxylated polyacrylamide composition strengthening agent GEORGIA-PACIFIC RESINS, INC. (US) 2005-08-25 US disclosed
EP-1312261-A1 Aqueous compositions containing a haloalkynyl compound and a buffer for providing biocidal activity and for stabilising end-use formulations Troy Technology Corporation, Inc. (US) 2003-05-21 EP disclosed
EP-0831706-B1 NON-AQUEOUS COMPOSITIONS CONTAINING A HALOALKYNYL COMPOUND AND A BUFFER FOR PROVIDING BIOCIDAL ACTIVITY AND FOR STABILIZING END-USE FORMULATIONS TROY TECHNOLOGY CORP INC (US) 2003-05-02 EP disclosed
US-6124350-A PAINT CONTAINING A BIOCIDAL COMPOSITION COMPRISING A HALOPROPYNYL COMPOUND AND A BUFFER TROY TECHNOLOGY CORPORATION, INC. (US) 2000-09-26 US disclosed
US-6017955-A A BUFFER STABILIZER FOR ADJUSTING THE PH OF END-USE FORMULATION BETWEEN 3.0 AND 8.0 TO PREVENT DEGRADATION OF PESTICIDE 3-IODO-2-PROPYNYL BUTYL CARBAMATE TROY TECHNOLOGY CORPORATION, INC. (US) 2000-01-25 US disclosed
EP-0831706-A1 METHOD OF STABILIZING BIOCIDAL COMPOSITIONS OF HALOALKYNYL COMPOUNDS TROY CHEMICAL CORPORATION (US) 1998-04-01 EP disclosed
WO-1996039836-A1 METHOD OF STABILIZING BIOCIDAL COMPOSITIONS OF HALOALKYNYL COMPOUNDS TROY CHEMICAL COMPANY (US) 1996-12-19 WO disclosed