Potassium Ion

Potassium Ion

SCHEMBL8104536

CCC(CC(=O)c1ccccc1)C(=O)[O-].[K+]

nearest known ligand 0.59

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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
TSHR P16473 1/20 0.59
KMT2A Q03164 3/20 0.58
MEN1 O00255 2/20 0.58
NPC1 O15118 1/20 0.58
L3MBTL1 Q9Y468 3/20 0.45
SMN1; SMN2 Q16637 3/20 0.45
ALDH1A1 P00352 3/20 0.45
MAPT P10636 2/20 0.45
HPGD P15428 2/20 0.45
LMNA P02545 1/20 0.45
POLB P06746 1/20 0.44
HTT P42858 1/20 0.44
NPSR1 Q6W5P4 1/20 0.44
CES1 P23141 2/20 0.44
MAPK1 P28482 2/20 0.44
KDM4E B2RXH2 1/20 0.44
CYP3A4 P08684 1/20 0.44
ALOX15 P16050 1/20 0.44
TDP1 Q9NUW8 1/20 0.44
PTPN1 P18031 2/20 0.43

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
Lithium Ion SCHEMBL8120162 0.97 TSHR (0.59) TSHRKMT2AMEN1NPC1L3MBTL1
SCHEMBL28458528 0.97 TSHR (0.59) TSHRKMT2AMEN1NPC1L3MBTL1
SCHEMBL3693703 0.84 TSHR (0.78) TSHRKMT2AMEN1NPC1L3MBTL1
SCHEMBL25645644 0.82 TSHR (0.63) TSHRKMT2AMEN1NPC1L3MBTL1
Potassium Ion SCHEMBL8104538 0.76 MMP2 (0.55) TSHRKMT2AMEN1NPC1L3MBTL1
SCHEMBL755941 0.76 TSHR (0.59) TSHRKMT2AMEN1NPC1L3MBTL1
SCHEMBL8114355 0.75 L3MBTL1 (0.60) TSHRKMT2AMEN1NPC1L3MBTL1
SCHEMBL9225409 0.74 TSHR (0.57) TSHRKMT2AMEN1NPC1L3MBTL1
SCHEMBL11768086 0.74 TSHR (0.57) TSHRKMT2AMEN1NPC1L3MBTL1
Hydrochloric Acid SCHEMBL29091991 0.74 TSHR (0.57) TSHRKMT2AMEN1NPC1L3MBTL1

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-6126855-A Reaction products of lyotropic liquid crystal salt complexes ELLIOTT STANLEY B (US) 2000-10-03 US disclosed
US-5833877-A DIAGMAGNETIC COMPLEX; SUPERCONDUCTORS ELLIOTT STANLEY B (US) 1998-11-10 US disclosed
US-5595683-A COMPLEX OF METAL SALT OF BENZOYLPROPIONIC ACID, LATTICE MODIFIER, CYCLIZATION, HUMIDITY SENSORS ELLIOTT STANLEY B (US) 1997-01-21 US disclosed
US-5443753-A Reaction products of lyotropic liquid crystal salt complexes ELLIOTT STANLEY B (US) 1995-08-22 US disclosed
US-5354499-A Reaction products of lyotropic liquid crystal salt complexes ELLIOTT STANLEY B (US) 1994-10-11 US disclosed
US-5354496-A Lyotropic liquid crystal salt/inorganic compound complexation products ELLIOTT STANLEY B (US) 1994-10-11 US disclosed