Salicylic Acid

Salicylic Acid

SCHEMBL668244

CCCC[P+](CCCC)(CCCC)CCCC.O=C(O)c1ccccc1O.O=C([O-])c1ccccc1O

nearest known ligand 0.53

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHE

The experimentally established mechanism targets of Salicylic 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
KDM4E B2RXH2 6/20 0.53
ALDH1A1 P00352 6/20 0.53
HPGD P15428 3/20 0.53
CA12 O43570 3/20 0.51
CA9 Q16790 3/20 0.51
CA2 P00918 2/20 0.51
SMN1; SMN2 Q16637 2/20 0.51
CA1 P00915 1/20 0.51
HMGB1 P09429 1/20 0.51
CA4 P22748 1/20 0.51
CA6 P23280 1/20 0.51
CA7 P43166 1/20 0.51
NAPRT Q6XQN6 1/20 0.51
CA14 Q9ULX7 1/20 0.51
LMNA P02545 2/20 0.48
NAAA Q02083 1/20 0.43
MEN1 O00255 1/20 0.43
RECQL P46063 1/20 0.43
KMT2A Q03164 1/20 0.43
GAA P10253 3/20 0.42

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
Salicylic Acid SCHEMBL666959 0.94 KDM4E (0.59) KDM4EALDH1A1HPGDCA12CA9
Salicylic Acid SCHEMBL3468302 0.89 ALDH1A1 (0.50) KDM4EALDH1A1HPGDCA12CA9
Salicylic Acid SCHEMBL17710452 0.87 ALDH1A1 (0.54) KDM4EALDH1A1HPGDSMN1; SMN2LMNA
Phthalic Acid SCHEMBL5048545 0.85 ALDH1A1 (0.47) KDM4EALDH1A1HPGDCA2SMN1; SMN2
Cinnamic Acid SCHEMBL669104 0.83 MAPT (0.48) KDM4EALDH1A1HPGDSMN1; SMN2LMNA
Tetrabuthylammonium SCHEMBL11218875 0.83 KDM4E (0.53) KDM4EALDH1A1HPGDCA12CA9
Tributylmethylammonium SCHEMBL668411 0.82 KDM4E (0.51) KDM4EALDH1A1HPGDCA12CA9
Salicylic Acid SCHEMBL8621859 0.81 ALDH1A1 (0.72) KDM4EALDH1A1HPGDCA12CA9
Salicylic Acid SCHEMBL294304 0.81 ALDH1A1 (0.72) KDM4EALDH1A1HPGDCA12CA9
Salicylic Acid SCHEMBL28753449 0.81 ALDH1A1 (0.44) KDM4EALDH1A1HPGDSMN1; SMN2LMNA

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-9278134-B2 Dual functioning ionic liquids and salts thereof THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ALABAMA (US) 2016-03-08 US disclosed
US-20120046244-A1 DUAL FUNCTIONING IONIC LIQUIDS AND SALTS THEREOF THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ALABAMA (US) 2012-02-23 US disclosed
WO-2010078300-A1 DUAL FUNCTIONING IONIC LIQUIDS AND SALTS THEREOF THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ALABAMA (US) 2010-07-08 WO 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-20120046244-A1 DUAL FUNCTIONING IONIC LIQUIDS AND SALTS THEREOF SLC6A6, SLC10A2, CLK2 KDM4E 4730/4885ALDH1A1 3146/4885HPGD 1301/4885

“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.