Adipic Acid

Adipic Acid

SCHEMBL437560

CCCC(O)OC(=O)CCC(=O)O.O=C(O)CCCC(=O)O.O=C(O)CCCCC(=O)O

nearest known ligand 0.47

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
FFAR4 Q5NUL3 2/20 0.47
FFAR1 O14842 2/20 0.47
ALDH1A1 P00352 3/20 0.46
AKR1B1 P15121 1/20 0.45
GPR84 Q9NQS5 7/20 0.44
PPARG P37231 7/20 0.44
PPARD Q03181 7/20 0.44
PPARA Q07869 7/20 0.44
HDAC11 Q96DB2 5/20 0.44
TSHR P16473 5/20 0.44
PTPN1 P18031 3/20 0.44
TLR2 O60603 2/20 0.44
TDP1 Q9NUW8 2/20 0.44
FABP4 P15090 2/20 0.44
SLC22A6 Q4U2R8 1/20 0.44
SLC22A8 Q8TCC7 1/20 0.44
MEN1 O00255 1/20 0.44
ESR1 P03372 1/20 0.44
ALOX15 P16050 1/20 0.44
PDE4A P27815 1/20 0.44

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
SCHEMBL114259 0.93 FFAR4 (0.50) FFAR4FFAR1ALDH1A1AKR1B1GPR84
SCHEMBL8153854 0.93 TSHR (0.48) FFAR4FFAR1ALDH1A1AKR1B1GPR84
SCHEMBL2141472 0.93 HDAC1 (0.41) FFAR4FFAR1ALDH1A1AKR1B1GPR84
SCHEMBL5475791 0.91 FFAR4 (0.53) FFAR4FFAR1ALDH1A1AKR1B1GPR84
Ethylene Glycol SCHEMBL4914065 0.88 FFAR4 (0.46) FFAR4FFAR1ALDH1A1AKR1B1GPR84
SCHEMBL2839365 0.86 FFAR4 (0.46) FFAR4FFAR1ALDH1A1AKR1B1GPR84
SCHEMBL5712400 0.85 LMNA (0.48) ALDH1A1TSHRTDP1MEN1KMT2A
SCHEMBL11652184 0.85 LMNA (0.53) ALDH1A1TSHRTDP1MEN1KMT2A
SCHEMBL2706936 0.85 LMNA (0.42) ALDH1A1TSHRTDP1LMNA
SCHEMBL4667879 0.84 FFAR4 (0.53) FFAR4FFAR1ALDH1A1AKR1B1GPR84

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8541057-B2 Cyclohexane oxidation process byproduct derivatives and methods for using the same INVISTA NORTH AMERICA S.A R.L. (US) 2013-09-24 US disclosed
US-20120101009-A1 CYCLOHEXANE OXIDATION PROCESS BYPRODUCT STREAM DERIVATIVES AND METHODS FOR USING THE SAME INVISTA NORTH AMERICA S.A.R.L. (US) 2012-04-26 US disclosed
US-20120064252-A1 CYCLOHEXANE OXIDATION PROCESS BYPRODUCT DERIVATIVES AND METHODS FOR USING THE SAME INVISTA NORTH AMERICA S.A.R.L. (US) 2012-03-15 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20120101009-A1 CYCLOHEXANE OXIDATION PROCESS BYPRODUCT STREAM DERIVATIVES AND METHODS FOR USING THE SAME DECR1, SIGMAR1, NOP2 FFAR4 84/4885FFAR1 6/4885ALDH1A1 2087/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.