Salicylic Acid

Salicylic Acid

SCHEMBL299754

O=C(O)c1ccccc1O.[Ti]

nearest known ligand 0.95

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
ALDH1A1 P00352 7/20 0.95
KDM4E B2RXH2 6/20 0.95
HPGD P15428 6/20 0.95
SMN1; SMN2 Q16637 2/20 0.95
CA12 O43570 2/20 0.95
CA1 P00915 2/20 0.95
CA2 P00918 2/20 0.95
CA7 P43166 2/20 0.95
CA9 Q16790 2/20 0.95
CA14 Q9ULX7 2/20 0.95
HMGB1 P09429 1/20 0.95
CA4 P22748 1/20 0.95
CA6 P23280 1/20 0.95
NAPRT Q6XQN6 1/20 0.95
ALOX15 P16050 2/20 0.65
HSD17B10 Q99714 4/20 0.59
MAPT P10636 3/20 0.58
TSHR P16473 2/20 0.58
G6PD P11413 1/20 0.58
CASP7 P55210 1/20 0.58

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 SCHEMBL28028722 1.00 ALDH1A1 (0.95) ALDH1A1KDM4EHPGDSMN1; SMN2CA12
Salicylic Acid SCHEMBL31665922 1.00 ALDH1A1 (0.95) ALDH1A1KDM4EHPGDSMN1; SMN2CA12
Salicylic Acid SCHEMBL10385490 0.97 ALDH1A1 (0.90) ALDH1A1KDM4EHPGDSMN1; SMN2CA12
Salicylic Acid SCHEMBL29606432 0.97 ALDH1A1 (1.00) ALDH1A1KDM4EHPGDSMN1; SMN2CA12
Salicylic Acid SCHEMBL29362663 0.97 ALDH1A1 (1.00) ALDH1A1KDM4EHPGDSMN1; SMN2CA12
Salicylic Acid SCHEMBL29360246 0.97 ALDH1A1 (1.00) ALDH1A1KDM4EHPGDSMN1; SMN2CA12
Salicylic Acid SCHEMBL1509155 0.97 ALDH1A1 (1.00) ALDH1A1KDM4EHPGDSMN1; SMN2CA12
Salicylic Acid SCHEMBL17156443 0.97 ALDH1A1 (1.00) ALDH1A1KDM4EHPGDSMN1; SMN2CA12
Salicylic Acid SCHEMBL8433746 0.97 ALDH1A1 (1.00) ALDH1A1KDM4EHPGDSMN1; SMN2CA12
Salicylic Acid SCHEMBL1967 0.97 ALDH1A1 (1.00) ALDH1A1KDM4EHPGDSMN1; SMN2CA12

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 125 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4444431-A1 SULFATE FREE PERSONAL CLEANSING COMPOSITION COMPRISING EFFECTIVE PRESERVATION The Procter & Gamble Company (US) 2024-10-16 EP claimed
CN-118265516-A Sulfate-free personal cleansing compositions with effective preservation 宝洁公司 2024-06-28 CN claimed
US-20230190606-A1 SULFATE FREE PERSONAL CLEANSING COMPOSITION COMPRISING EFFECTIVE PRESERVATION THE PROCTER & GAMBLE COMPANY 2023-06-22 US claimed
WO-2023108097-A1 SULFATE FREE PERSONAL CLEANSING COMPOSITION COMPRISING EFFECTIVE PRESERVATION THE PROCTER & GAMBLE COMPANY (US) 2023-06-15 WO claimed
US-20080020059-A1 COMPOSITIONS AND METHODS FOR TOPICAL TREATMENT OF SKIN INFECTION CHIOU CONSULTING, INC. (US) 2008-01-24 US claimed
US-20060205615-A1 Additives and lubricant formulations for improved antioxidant properties AFTON CHEMICAL CORPORATION 2006-09-14 US claimed
WO-2005055927-A2 COMPOSITIONS AND METHODS FOR TOPICAL TREATMENT OF SKIN INFECTION CHIOU CONSULTING INC. (US) 2005-06-23 WO claimed
US-20050123620-A1 Compositions and methods for topical treatment of skin infection CHIOU CONSULTING, INC. 2005-06-09 US claimed
EP-4423168-B1 POLYETHER POLYMERIZATION PROCESS DOW GLOBAL TECHNOLOGIES LLC (US) 2025-12-10 EP disclosed
US-12458575-B2 Sulfate free personal cleansing composition comprising effective preservation THE PROCTER & GAMBLE COMPANY (US) 2025-11-04 US disclosed
US-20250241833-A1 SULFUR CO-GRINDING PROCESS THE PROCTER & GAMBLE COMPANY 2025-07-31 US disclosed
CN-119499129-A Personal care composition preservative level optimization 宝洁公司 2025-02-25 CN disclosed
US-12201971-B2 Polyether polymerization process DOW GLOBAL TECHNOLOGIES LLC (US) 2025-01-21 US disclosed
US-20240392068-A1 POLYETHER POLYMERIZATION PROCESS DOW GLOBAL TECHNOLOGIES LLC (US) 2024-11-28 US disclosed
WO-2002022104-A2 TREATED SUBSTRATE WITH IMPROVED TRANSFER EFFICIENCY OF TOPICAL APPLICATION KIMBERLY-CLARK WORLDWIDE, INC. (US) 2002-03-21 WO disclosed
EP-0330697-A4 PREPARATION OF ABO 3? COMPOUNDS FROM MIXED METAL AROMATIC COORDINATION COMPLEXES 1991-06-05 EP disclosed
US-4946810-A Preparation of ABO3 compounds from mixed metal aromatic coordination complexes THE DOW CHEMICAL COMPANY (US) 1990-08-07 US disclosed
US-4880758-A FORMING A POWDER BY DECOMPOSING A COMPLEX OF A METAL A COMPOUND, A METAL B COMPOUND, A SOLVATE, AN ALCOHOL AND A DISUBSTITUTED AROMATIC COMPOUND THE DOW CHEMICAL COMPANY (US) 1989-11-14 US disclosed
EP-0330697-A1 PREPARATION OF ABO 3? COMPOUNDS FROM MIXED METAL AROMATIC COORDINATION COMPLEXES THE DOW CHEMICAL COMPANY (US) 1989-09-06 EP disclosed
WO-1989001922-A1 PREPARATION OF ABO3 COMPOUNDS FROM MIXED METAL AROMATIC COORDINATION COMPLEXES THE DOW CHEMICAL COMPANY (US) 1989-03-09 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 (2 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-20230190606-A1 SULFATE FREE PERSONAL CLEANSING COMPOSITION COMPRISING EFFECTIVE PRESERVATION PRSS3, PLP2, PRSS2 ALDH1A1 3763/4885KDM4E 2496/4885HPGD 2252/4885
US-12458575-B2 Sulfate free personal cleansing composition comprising effective preservation PRSS3, PLP2, PRSS2 ALDH1A1 3763/4885KDM4E 2496/4885HPGD 2252/4885

“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.