Adipic Acid

Adipic Acid

SCHEMBL9294379

C1CCCCC1.CO.CO.O=C(O)CCCCC(=O)O

nearest known ligand 0.69

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 0.69
TSHR P16473 5/20 0.65
NFKB1 P19838 1/20 0.65
PMP22 Q01453 1/20 0.65
AKR1B1 P15121 1/20 0.60
SLC22A6 Q4U2R8 2/20 0.59
GPR84 Q9NQS5 8/20 0.57
PPARG P37231 7/20 0.57
PPARD Q03181 7/20 0.57
PPARA Q07869 7/20 0.57
HDAC11 Q96DB2 5/20 0.57
PTPN1 P18031 3/20 0.57
ALDH1A1 P00352 2/20 0.57
TLR2 O60603 2/20 0.57
TDP1 Q9NUW8 2/20 0.57
FABP4 P15090 2/20 0.57
FFAR1 O14842 2/20 0.57
FFAR4 Q5NUL3 2/20 0.57
SLC22A8 Q8TCC7 1/20 0.57
MEN1 O00255 1/20 0.57

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
Octanedioate SCHEMBL28289307 0.97 TSHR (0.71) LMNATSHRNFKB1PMP22AKR1B1
Glutarate SCHEMBL28290689 0.94 SLC22A6 (0.69) LMNATSHRNFKB1PMP22AKR1B1
Adipic Acid SCHEMBL10764903 0.94 LMNA (0.79) LMNATSHRNFKB1PMP22AKR1B1
Adipic Acid SCHEMBL5311340 0.94 LMNA (0.79) LMNATSHRNFKB1PMP22AKR1B1
Adipic Acid SCHEMBL4353087 0.94 LMNA (0.79) LMNATSHRNFKB1PMP22AKR1B1
Adipic Acid SCHEMBL11861116 0.91 LMNA (0.65) LMNATSHRNFKB1PMP22AKR1B1
Adipic Acid SCHEMBL2538446 0.90 LMNA (0.73) LMNATSHRNFKB1PMP22AKR1B1
Adipic Acid SCHEMBL258769 0.90 LMNA (0.73) LMNATSHRNFKB1PMP22AKR1B1
Adipic Acid SCHEMBL8997800 0.90 LMNA (0.73) LMNATSHRNFKB1PMP22AKR1B1
Adipic Acid SCHEMBL2791026 0.90 LMNA (0.73) LMNATSHRNFKB1PMP22AKR1B1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113999488-B Single-component epoxy resin and preparation method thereof 常州大学 2023-12-05 CN claimed
CN-111171285-B Epoxy resin curing agent microcapsule taking polyurethane as shell material and preparation method thereof 常州大学 2022-04-26 CN claimed
CN-113831495-A Polyurethane material with controllable foaming time 苏州意耐实业有限公司 2021-12-24 CN claimed
CN-113999488-B Single-component epoxy resin and preparation method thereof 常州大学 2023-12-05 CN disclosed
CN-113831495-A Polyurethane material with controllable foaming time 苏州意耐实业有限公司 2021-12-24 CN disclosed
CN-113831495-A Polyurethane material with controllable foaming time 苏州意耐实业有限公司 2021-12-24 CN disclosed
US-5330669-A Polyurethane with phosphorus acid group KYOWA HAKKO KOGYO CO., LTD. (US) 1994-07-19 US disclosed
US-5292853-A Magnetic recording media KYOWA HAKKO KOGYO CO., LTD. (US) 1994-03-08 US disclosed
US-5273826-A Polyurethane containing phosphorus groups as binder THE B. F. GOODRICH COMPANY (US) 1993-12-28 US disclosed
EP-0377931-B1 Isocyanate modified blocked sulfonic acid ester as a crosslinking catalyst KING INDUSTRIES INC (US) 1993-11-03 EP disclosed
US-5162162-A Polyurethanes containing phosphorous compounds, epoxides and isocyanates; durability, wear resistance THE B. F. GOODRICH COMPANY (US) 1992-11-10 US disclosed
US-5158830-A Magnetic recording medium comprising a polyurethane resin coating residual groups derived from specified phosphorous containing compounds THE B. F. GOODRICH COMPANY (US) 1992-10-27 US disclosed
US-5102961-A Of hydroxyl, carboxyl or amide containing polymers; improved hardness, flexibility, adhesion and impact strength KING INDUSTRIES (US) 1992-04-07 US disclosed
US-5037934-A Polyurethane resin binder from epoxy, isocyanates, phosphoric acid and polyhydroxy components; durability KYOWA HAKKO KOGYO CO., LTD. (JP) 1991-08-06 US disclosed
EP-0377931-A2 Isocyanate modified blocked sulfonic acid ester as a crosslinking catalyst KING INDUSTRIES, INC. (US) 1990-07-18 EP disclosed
EP-0367667-A2 A new polyurethane resin containing at least one phosphoric acid group and its use in a magnetic coating formulation and a magnetic recording medium KYOWA HAKKO KOGYO CO., LTD. (JP) 1990-05-09 EP disclosed