Adipic Acid

Adipic Acid

SCHEMBL21489542

O=C(O)CCCCC(=O)O.O=C([O-])CCCCC(=O)[O-].[Na+].[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 SCHEMBL105756 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 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11938109-B2 Methods for the preparation of a levothyroxine solution EMP LEVO US B.V. (NL) 2024-03-26 US claimed
US-20210353577-A1 METHODS FOR THE PREPARATION OF A LEVOTHYROXINE SOLUTION EMP LEVO US B.V. (NL) 2021-11-18 US claimed
US-20190321316-A1 METHODS FOR THE PREPARATION OF A LEVOTHYROXINE SOLUTION EMP LEVO US B.V. (NL) 2019-10-24 US claimed
US-11938109-B2 Methods for the preparation of a levothyroxine solution EMP LEVO US B.V. (NL) 2024-03-26 US disclosed
US-20210353577-A1 METHODS FOR THE PREPARATION OF A LEVOTHYROXINE SOLUTION EMP LEVO US B.V. (NL) 2021-11-18 US disclosed
US-20190321316-A1 METHODS FOR THE PREPARATION OF A LEVOTHYROXINE SOLUTION EMP LEVO US B.V. (NL) 2019-10-24 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 (3 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-11938109-B2 Methods for the preparation of a levothyroxine solution TPO, TSHR, TRHDE LMNA 3650/4885TSHR 2/4885NFKB1 2823/4885
US-20190321316-A1 METHODS FOR THE PREPARATION OF A LEVOTHYROXINE SOLUTION TPO, TSHR, TRHDE LMNA 3650/4885TSHR 2/4885NFKB1 2823/4885
US-20210353577-A1 METHODS FOR THE PREPARATION OF A LEVOTHYROXINE SOLUTION TPO, TSHR, TRHDE LMNA 3650/4885TSHR 2/4885NFKB1 2823/4885

“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.