Salicylic Acid

Salicylic Acid

SCHEMBL3497364

CC1CN(C)C(C)N1C.O=C(O)c1ccccc1O

nearest known ligand 0.53

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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 12/20 0.53
ALDH1A1 P00352 12/20 0.53
HPGD P15428 9/20 0.53
SMN1; SMN2 Q16637 3/20 0.53
CA12 O43570 1/20 0.53
CA1 P00915 1/20 0.53
CA2 P00918 1/20 0.53
HMGB1 P09429 1/20 0.53
CA4 P22748 1/20 0.53
CA6 P23280 1/20 0.53
CA7 P43166 1/20 0.53
CA9 Q16790 1/20 0.53
NAPRT Q6XQN6 1/20 0.53
CA14 Q9ULX7 1/20 0.53
MEN1 O00255 3/20 0.41
KMT2A Q03164 3/20 0.41
USP2 O75604 1/20 0.41
MAPT P10636 1/20 0.41
HSD17B10 Q99714 5/20 0.40
LMNA P02545 4/20 0.40

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
Phthalic Acid SCHEMBL29350307 0.91 ALDH1A1 (0.47) KDM4EALDH1A1MAPTALOX15BRD4
Phthalic Acid SCHEMBL3845259 0.91 ALDH1A1 (0.47) KDM4EALDH1A1MAPTALOX15BRD4
Phthalic Acid SCHEMBL930633 0.91 ALDH1A1 (0.47) KDM4EALDH1A1MAPTALOX15BRD4
Phthalic Acid SCHEMBL29661852 0.91 ALDH1A1 (0.47) KDM4EALDH1A1MAPTALOX15BRD4
Anthranilic Acid SCHEMBL2260329 0.84 KDM4E (0.42) KDM4EALDH1A1HPGDMAPTHSD17B10
Salicylic Acid SCHEMBL3493607 0.83 ALDH1A1 (0.47) KDM4EALDH1A1HPGDSMN1; SMN2CA12
SCHEMBL4362753 0.79 KDM4E (0.41) KDM4EALDH1A1HPGDSMN1; SMN2NAPRT
SCHEMBL4357999 0.78 MMP2 (0.40) KDM4EALDH1A1SMN1; SMN2MEN1KMT2A
SCHEMBL4360831 0.75 CSNK2A1 (0.42) ALDH1A1HPGDMEN1KMT2ALMNA
Salicylic Acid SCHEMBL7079199 0.75 ALDH1A1 (0.95) KDM4EALDH1A1HPGDSMN1; 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 8 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2698802-B1 Electrolytic capacitor PANASONIC IP MAN CO LTD (JP) 2018-05-16 EP disclosed
EP-1808875-B1 ELECTROLYTE FOR ELECTROLYTIC CAPACITOR AND ELECTROLYTIC CAPACITOR UTILIZING THE SAME PANASONIC IP MAN CO LTD (JP) 2017-11-08 EP disclosed
EP-2698802-A1 Electrolytic capacitor comprising a separtor comprising a conductive polymer containing a p-dopant on its surface Panasonic Corporation (JP) 2014-02-19 EP disclosed
US-7859828-B2 supresses increase in the ESR (equivalent series resistance) with the elapse of time in an electrolytic capacitor is suppressed PANASONIC CORPORATION (JP) 2010-12-28 US disclosed
CN-101057306-B Electrolyte for electrolytic capacitor and electrolytic capacitor utilizing the same MATSUSHITA ELECTRIC INDUSTRIAL CO LTD 2010-09-08 CN disclosed
US-20080316679-A1 Electrolytic Solution for Electrolytic Capacitor, and Electrolytic Capacitor Using the Same PANASONIC CORPORATION (JP) 2008-12-25 US disclosed
CN-101057306-A Electrolyte for electrolytic capacitor and electrolytic capacitor utilizing the same MATSUSHITA ELECTRIC INDUSTRIAL CO LTD (JP) 2007-10-17 CN disclosed
EP-1808875-A1 ELECTROLYTE FOR ELECTROLYTIC CAPACITOR AND ELECTROLYTIC CAPACITOR UTILIZING THE SAME MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) 2007-07-18 EP disclosed