Potassium Ion

Potassium Ion

SCHEMBL2474101

CCCCCCC(C)S(=O)(=O)[O-].[K+]

nearest known ligand 0.50

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Known targets — ChEMBL curated mechanism

AGTR1DHFRGABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTNR3C2PBP2XPTGS1PTGS2VKORC1blablaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAftsImrcAmrcBmrdApbp1apbp1bpbp2apbp2bpbp3polthyA

The experimentally established mechanism targets of Potassium Ion. 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
TP53 P04637 1/20 0.50
OPRM1 P35372 1/20 0.44
CA1 P00915 2/20 0.42
SPHK1 Q9NYA1 1/20 0.42
NR1I2 O75469 1/20 0.41
RECQL P46063 2/20 0.41
GLA P06280 1/20 0.41
HPGD P15428 1/20 0.41
TSHR P16473 1/20 0.41
MAPK1 P28482 1/20 0.41
EPHX2 P34913 1/20 0.41
BLM P54132 1/20 0.41
CA2 P00918 2/20 0.39
ADH1B P00325 1/20 0.39
ADH1C P00326 1/20 0.39
ADH1A P07327 1/20 0.39
ADH4 P08319 1/20 0.39
ADH7 P40394 1/20 0.39
LAP3 P28838 1/20 0.39
ACE2 Q9BYF1 1/20 0.38

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
Potassium Ion SCHEMBL9659113 1.00 TP53 (0.50) TP53OPRM1CA1SPHK1NR1I2
Potassium Ion SCHEMBL8585180 1.00 TP53 (0.50) TP53OPRM1CA1SPHK1NR1I2
SCHEMBL3924982 0.96 TP53 (0.50) TP53OPRM1CA1SPHK1NR1I2
SCHEMBL27503908 0.96 TP53 (0.50) TP53OPRM1CA1SPHK1NR1I2
SCHEMBL7629661 0.96 TP53 (0.50) TP53OPRM1CA1SPHK1NR1I2
SCHEMBL9019654 0.96 TP53 (0.50) TP53OPRM1CA1SPHK1NR1I2
SCHEMBL6691126 0.96 TP53 (0.50) TP53OPRM1CA1SPHK1NR1I2
SCHEMBL8677767 0.93 TP53 (0.52) TP53OPRM1CA1SPHK1NR1I2
SCHEMBL27767212 0.86 TP53 (0.43) TP53OPRM1CA1NR1I2RECQL
SCHEMBL29178075 0.85 FAAH (0.46) TP53EPHX2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111691217-B Method for recovering free starch in papermaking white water 瑞辰星生物技术(广州)有限公司 2022-06-21 CN disclosed
CN-111691224-B Modified starch and preparation method and application thereof 瑞辰星生物技术(广州)有限公司 2022-05-31 CN disclosed
CN-111691223-B Process for making paper 瑞辰星生物技术(广州)有限公司 2022-05-13 CN disclosed
CN-111691217-A Method for recovering free starch in papermaking white water 瑞辰星生物技术(广州)有限公司 2020-09-22 CN disclosed
CN-111691224-A Modified starch and preparation method and application thereof 瑞辰星生物技术(广州)有限公司 2020-09-22 CN disclosed
CN-111691223-A Method for making paper 瑞辰星生物技术(广州)有限公司 2020-09-22 CN disclosed
EP-2370527-B1 ADDITIVES FOR ENHANCING THE ANTISTATIC PROPERTIES OF CONDUCTIVE POLYMER-BASED COATINGS ESSILOR INT (FR) 2012-10-24 EP disclosed
US-20110248223-A1 Additives for Enhancing the Antistatic Properties of Conductive Polymer-Based Coatings ESSILOR INTERNATIONAL (COMPAGNIE GENERALE D'OPTIQUE) (FR) 2011-10-13 US disclosed
EP-2370527-A1 ADDITIVES FOR ENHANCING THE ANTISTATIC PROPERTIES OF CONDUCTIVE POLYMER-BASED COATINGS Essilor International (Compagnie Générale D'Optique) (FR) 2011-10-05 EP disclosed
WO-2010076314-A1 ADDITIVES FOR ENHANCING THE ANTISTATIC PROPERTIES OF CONDUCTIVE POLYMER-BASED COATINGS ESSILOR INTERNATIONAL (COMPAGNIE GENERALE D'OPTIQUE) (FR) 2010-07-08 WO disclosed