Adipic Acid

Adipic Acid

SCHEMBL8071355

CC(C)=NO.CC(C)=NO.O=C(O)CCCCC(=O)O

nearest known ligand 0.61

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 0.61
TSHR P16473 5/20 0.58
NFKB1 P19838 1/20 0.58
PMP22 Q01453 1/20 0.58
AKR1B1 P15121 1/20 0.55
SLC22A6 Q4U2R8 2/20 0.53
GPR84 Q9NQS5 8/20 0.52
PPARG P37231 7/20 0.52
PPARD Q03181 7/20 0.52
PPARA Q07869 7/20 0.52
HDAC11 Q96DB2 5/20 0.52
PTPN1 P18031 3/20 0.52
ALDH1A1 P00352 2/20 0.52
TLR2 O60603 2/20 0.52
TDP1 Q9NUW8 2/20 0.52
FABP4 P15090 2/20 0.52
SLC22A8 Q8TCC7 1/20 0.52
MEN1 O00255 1/20 0.52
ESR1 P03372 1/20 0.52
ALOX15 P16050 1/20 0.52

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
SCHEMBL30543592 0.84 LMNA (0.55) LMNATSHRNFKB1PMP22AKR1B1
Adipic Acid SCHEMBL28824681 0.82 LMNA (0.79) LMNATSHRNFKB1PMP22AKR1B1
Adipic Acid SCHEMBL7894497 0.82 LMNA (0.79) LMNATSHRNFKB1PMP22AKR1B1
Adipic Acid SCHEMBL743697 0.82 LMNA (0.79) LMNATSHRNFKB1PMP22AKR1B1
Adipic Acid SCHEMBL28289311 0.82 LMNA (0.79) LMNATSHRNFKB1PMP22AKR1B1
Sebacic Acid SCHEMBL3065275 0.79 TSHR (0.80) LMNATSHRNFKB1PMP22AKR1B1
Adipic Acid SCHEMBL614869 0.79 LMNA (0.73) LMNATSHRNFKB1PMP22AKR1B1
Sebacic Acid SCHEMBL15111284 0.79 TSHR (0.80) LMNATSHRNFKB1PMP22AKR1B1
Azelaic Acid SCHEMBL1539243 0.79 TSHR (0.80) LMNATSHRNFKB1PMP22AKR1B1
Octanedioate SCHEMBL15111383 0.79 TSHR (0.80) 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 2 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1021515-A1 USE OF OXIME ESTERS AS ACTIVATORS FOR INORGANIC PER-COMPOUNDS BASF AKTIENGESELLSCHAFT (DE) 2000-07-26 EP disclosed
WO-1997017420-A1 USE OF OXIME ESTERS AS ACTIVATORS FOR INORGANIC PER-COMPOUNDS BASF AKTIENGESELLSCHAFT (DE) 1997-05-15 WO disclosed