Adipic Acid

Adipic Acid

SCHEMBL25482

O=C(O)CCCCC(=O)O.O=C(O)CCCCC(=O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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 3/20 1.00
TSHR P16473 4/20 0.92
NFKB1 P19838 2/20 0.92
PMP22 Q01453 1/20 0.92
SLC22A6 Q4U2R8 2/20 0.83
GPR84 Q9NQS5 4/20 0.69
FFAR1 O14842 2/20 0.69
FFAR4 Q5NUL3 2/20 0.69
AKR1B1 P15121 1/20 0.69
CYP2D6 P10635 1/20 0.69
FOLH1 Q04609 1/20 0.69
ALKBH5 Q6P6C2 1/20 0.67
SUCNR1 Q9BXA5 1/20 0.67
EGLN1 Q9GZT9 1/20 0.67
CAMK2A Q9UQM7 1/20 0.67
PPARG P37231 5/20 0.65
PPARD Q03181 5/20 0.65
PPARA Q07869 5/20 0.65
HDAC11 Q96DB2 4/20 0.65
ALDH1A1 P00352 2/20 0.65

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 SCHEMBL8407905 1.00 LMNA (1.00) LMNATSHRNFKB1PMP22SLC22A6
Adipic Acid SCHEMBL1330953 1.00 LMNA (1.00) LMNATSHRNFKB1PMP22SLC22A6
Adipic Acid SCHEMBL9092384 1.00 LMNA (1.00) LMNATSHRNFKB1PMP22SLC22A6
Adipic Acid SCHEMBL28337915 1.00 LMNA (1.00) LMNATSHRNFKB1PMP22SLC22A6
Adipic Acid SCHEMBL2244299 1.00 LMNA (1.00) LMNATSHRNFKB1PMP22SLC22A6
Adipic Acid SCHEMBL28191616 1.00 LMNA (1.00) LMNATSHRNFKB1PMP22SLC22A6
Adipic Acid SCHEMBL28191617 1.00 LMNA (1.00) LMNATSHRNFKB1PMP22SLC22A6
Adipic Acid SCHEMBL4930 1.00 LMNA (1.00) LMNATSHRNFKB1PMP22SLC22A6
Adipic Acid SCHEMBL8941691 1.00 LMNA (1.00) LMNATSHRNFKB1PMP22SLC22A6
SCHEMBL25186232 0.96 TSHR (1.00) 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 170 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119816502-A Crystalline forms of TYK2 inhibitors 温缇克斯生物科学公司 2025-04-11 CN claimed
CN-106046321-B A kind of feature curing agent and its method for preparing bisphenol A type epoxy resin 西北师范大学 2018-02-13 CN claimed
CN-205700146-U Adipic acid nitrogen oxide in tail gas removing means 平顶山市普恩科技有限公司 2016-11-23 CN claimed
CN-106046321-A Functional curing agent and method for preparing bisphenol A type epoxy resin thereof 西北师范大学 2016-10-26 CN claimed
US-20110136989-A1 POLYETHERAMIDE COMPOSITIONS AKZO NOBEL N.V. (NL) 2011-06-09 US claimed
US-7704308-B2 Method of highlighting with a reversible highlighting mixture, highlighting kit, and highlighted complex SANFORD, L.P. (US) 2010-04-27 US claimed
EP-1841828-B1 METHOD OF HIGHLIGHTING WITH A REVERSIBLE HIGHLIGHTING MIXTURE, HIGHLIGHTING KIT, AND HIGHLIGHTED COMPLEX SANFORD LP (US) 2009-01-14 EP claimed
CN-101210091-A Halogen-containing polymer composition with thermal stability and thermal stabilizer thereof FORMOSAN RUBBER GROUP INC (CN) 2008-07-02 CN claimed
EP-1841828-A1 METHOD OF HIGHLIGHTING WITH A REVERSIBLE HIGHLIGHTING MIXTURE, HIGHLIGHTING KIT, AND HIGHLIGHTED COMPLEX Sanford, L.P. (US) 2007-10-10 EP claimed
US-7163575-B2 Water-based, resin-free and solvent-free eradicable ball-pen inks SANFORD, L.P. (US) 2007-01-16 US claimed
WO-2006068723-A1 METHOD OF HIGHLIGHTING WITH A REVERSIBLE HIGHLIGHTING MIXTURE, HIGHLIGHTING KIT, AND HIGHLIGHTED COMPLEX SANFORD L.P. (US) 2006-06-29 WO claimed
WO-2006019672-A1 ERADICABLE BALL-PEN INKS SANFORD L.P. (US) 2006-02-23 WO claimed
US-20060032398-A1 Water-based, resin-free and solvent-free eradicable ball-pen inks SANFORD, L.P. 2006-02-16 US claimed
US-20050158471-A1 Method of highlighting with a reversible highlighting mixture, highlighting kit, and highlighted complex SANFORD, L.P. 2005-07-21 US claimed
EP-3346011-B1 HOST CELLS FOR PREPARING ADIPATE (ESTER OR THIOESTER) GENOMATICA INC (US) 2026-05-20 EP disclosed
EP-4705418-A1 HIGH PERFORMANCE GEAR OIL AND RELATED METHODS ExxonMobil Technology and Engineering Company (US) 2026-03-11 EP disclosed
US-20250382643-A1 GENETICALLY MODIFIED MICROORGANISM FOR PRODUCING 3-HYDROXYADIPIC ACID AND/OR Alpha-HYDROXYADIPIC ACID, AND METHOD FOR PRODUCING CHEMICAL PRODUCT TORAY INDUSTRIES, INC. (JP) 2025-12-18 US disclosed
US-4731384-A ADJUVANTS, ANTIINFLAMMATORY AGENTS TROPONWERKE GMBH & CO, KG (DE) 1988-03-15 US disclosed
EP-0230510-A2 Amine oxide process and composition ETHYL CORPORATION (US) 1987-08-05 EP disclosed
US-4532347-A Maintaining high concentration gradient for solute across membrane with extracting solvent by converting permeated solute to another compound, improving separation VAREN TECHNOLOGY (US) 1985-07-30 US disclosed