Adipic Acid

Adipic Acid

SCHEMBL105756

O=C([O-])CCCCC(=O)O.[Na+]

nearest known ligand 0.65

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC18A2SLC6A2SLC6A3

The experimentally established mechanism targets of Adipic Acid. 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
LMNA P02545 2/20 0.65
TSHR P16473 4/20 0.61
NFKB1 P19838 2/20 0.61
PMP22 Q01453 1/20 0.61
SLC22A6 Q4U2R8 2/20 0.56
CA1 P00915 1/20 0.55
GPR84 Q9NQS5 4/20 0.50
FFAR1 O14842 2/20 0.50
FFAR4 Q5NUL3 2/20 0.50
AKR1B1 P15121 1/20 0.50
CYP2D6 P10635 1/20 0.50
FOLH1 Q04609 1/20 0.50
PPARG P37231 4/20 0.48
PPARD Q03181 4/20 0.48
PPARA Q07869 4/20 0.48
HDAC11 Q96DB2 3/20 0.48
ALDH1A1 P00352 2/20 0.48
TDP1 Q9NUW8 2/20 0.48
SLC22A8 Q8TCC7 1/20 0.48
TLR2 O60603 1/20 0.48

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
Adipic Acid SCHEMBL21489542 1.00 LMNA (0.65) LMNATSHRNFKB1PMP22SLC22A6
Octanedioate SCHEMBL9642090 0.97 TSHR (0.67) LMNATSHRNFKB1PMP22SLC22A6
Azelaic Acid SCHEMBL4094376 0.97 TSHR (0.67) LMNATSHRNFKB1PMP22SLC22A6
Sebacic Acid SCHEMBL6135890 0.97 TSHR (0.67) LMNATSHRNFKB1PMP22SLC22A6
Pimelic Acid SCHEMBL30384892 0.97 TSHR (0.67) LMNATSHRNFKB1PMP22SLC22A6
Adipic Acid SCHEMBL105192 0.94 LMNA (0.65) LMNATSHRNFKB1PMP22SLC22A6
Adipic Acid SCHEMBL105952 0.94 LMNA (0.65) LMNATSHRNFKB1PMP22SLC22A6
Adipic Acid SCHEMBL30776749 0.94 LMNA (0.65) LMNATSHRNFKB1PMP22SLC22A6
Glutarate SCHEMBL106178 0.94 SLC22A6 (0.65) LMNATSHRNFKB1PMP22SLC22A6
Adipic Acid SCHEMBL23780654 0.92 LMNA (0.61) LMNATSHRNFKB1PMP22SLC22A6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024175174-A1 STABILIZING COMPOSITION FOR HALOGEN-CONTAINING POLYMERS REAGENS S.P.A. (IT) 2024-08-29 WO claimed
WO-2024175568-A1 STABILIZING COMPOSITION FOR HALOGEN-CONTAINING POLYMERS REAGEN S.P.A. (IT) 2024-08-29 WO claimed
EP-3850040-B1 A STABILIZED CHLORINATED POLYVINYLCHLORIDE AND AN ARTICLE MADE THEREFROM REAGENS SPA (IT) 2023-04-19 EP claimed
CN-112955500-B Stabilized chlorinated polyvinyl chloride and articles made therefrom 利晶股份公司 2022-11-08 CN claimed
EP-3850040-A1 A STABILIZED CHLORINATED POLYVINYLCHLORIDE AND AN ARTICLE MADE THEREFROM Reagens S.p.A. (IT) 2021-07-21 EP claimed
CN-112955500-A Stabilized chlorinated polyvinyl chloride and articles made therefrom 利晶股份公司 2021-06-11 CN claimed
WO-2020053157-A1 A STABILIZED CHLORINATED POLYVINYLCHLORIDE AND AN ARTICLE MADE THEREFROM REAGENS S.P.A. (IT) 2020-03-19 WO claimed
EP-2475000-B1 PROCESSING AGENT COMPOSITION FOR SEMICONDUCTOR SURFACE AND METHOD FOR PROCESSING SEMICONDUCTOR SURFACE USING SAME WAKO PURE CHEM IND LTD (JP) 2015-07-01 EP claimed
US-9034810-B2 Processing agent composition for semiconductor surface and method for processing semiconductor surface using same WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) 2015-05-19 US claimed
US-20120259138-A1 METHODS AND SYSTEMS OF PRODUCING DICARBOXYLIC ACIDS BioAmber International S.à.r.I. (LU) 2012-10-11 US claimed
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
EP-0492803-B1 Stabilized halogen containing polymer compositions ATOCHEM NORTH AMERICA ELF (US) 1996-06-12 EP claimed
US-4268694-A HYDROLYSIS OF TETRAHALOCYCLOHEXANONE FISONS LIMITED (GB) 1981-05-19 US claimed
US-4200586-A Inhibiting the carbon-carbon double bond isomerization of substituted or unsubstituted hydrocarbon compounds PHILLIPS PETROLEUM COMPANY (US) 1980-04-29 US claimed