Potassium Ion

Potassium Ion

SCHEMBL9929223

CC1=Nc2ccc3c(S(=O)(=O)[O-])cc(S(=O)(=O)[O-])cc3c2C1(C)CCCS(=O)(=O)[O-].[K+].[K+].[K+]

nearest known ligand 0.00

Full drug profile on Sugi Atlas →

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.

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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 SCHEMBL4886117 0.85 FOLH1 (0.35)
Potassium Ion SCHEMBL14695214 0.81 MEN1 (0.43)
Potassium Ion SCHEMBL30372129 0.80 LMNA (0.33)
Potassium Ion SCHEMBL9929143 0.80 LMNA (0.33)
SCHEMBL133416 0.79 FOLH1 (0.32)
SCHEMBL9929222 0.78 FOLH1 (0.32)
Potassium Ion SCHEMBL560059 0.77 LMNA (0.32)
Potassium Ion SCHEMBL29713986 0.77 LMNA (0.32)
SCHEMBL42027 0.74 LMNA (0.35)
SCHEMBL30203159 0.73 POLB (0.35)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10696653-B2 Cyanine compounds PIERCE BIOTECHNOLOGY, INC. (US) 2020-06-30 US disclosed
US-10351551-B2 Fluorescent compounds PIERCE BIOTECHNOLOGY, INC. (US) 2019-07-16 US disclosed
EP-3081564-B1 INDOLE DERIVATIVES AS LABELING DYE FOR BIOMOLECULE PIERCE BIOTECHNOLOGY INC (US) 2019-07-10 EP disclosed
US-20180327387-A1 Cyanine Compounds PIERCE BIOTECHNOLOGY, INC. (US) 2018-11-15 US disclosed
US-10053447-B2 Fluorescent compounds PIERCE BIOTECHNOLOGY, INC (US) 2018-08-21 US disclosed
EP-3029027-B1 FLUORESCENT COMPOUNDS PIERCE BIOTECHNOLOGY INC (US) 2018-06-27 EP disclosed
US-20180118723-A1 FLUORESCENT COMPOUNDS PIERCE BIOTECHNOLOGY, INC. (US) 2018-05-03 US disclosed
US-20170158858-A9 CYANINE COMPOUNDS PIERCE BIOTECHNOLOGY, INC. 2017-06-08 US disclosed
US-20170114038-A9 CYANINE COMPOUNDS PIERCE BIOTECHNOLOGY, INC. 2017-04-27 US disclosed
EP-3081564-A1 INDOLE DERIVATIVES AS LABELING DYE FOR BIOMOLECULE Pierce Biotechnology, Inc. (US) 2016-10-19 EP disclosed
US-20160168383-A1 CYANINE COMPOUNDS HERMANSON GREG (US) 2016-06-16 US disclosed
EP-2804860-B1 INDOLE DERIVATIVES AS LABELING DYE FOR BIOMOLECULE PIERCE BIOTECHNOLOGY INC (US) 2016-06-15 EP disclosed
EP-3029027-A1 FLUORESCENT COMPOUNDS Pierce Biotechnology, Inc. (US) 2016-06-08 EP disclosed
EP-2655327-B1 FLUORESCENT COMPOUNDS PIERCE BIOTECHNOLOGY INC (US) 2016-02-24 EP disclosed
US-20140255312-A1 CYANINE COMPOUNDS PIERCE BIOTECHNOLOGY, INC. 2014-09-11 US disclosed
US-20140072515-A9 CYANINE COMPOUNDS PIERCE BIOTECHNOLOGY, INC. 2014-03-13 US disclosed
US-20130251637-A9 FLUORESCENT COMPOUNDS DYOMICS GMBH (DE) 2013-09-26 US disclosed
US-20130230466-A1 CYANINE COMPOUNDS HERMANSON GREG (US) 2013-09-05 US disclosed
US-20120294807-A9 FLUORESCENT COMPOUNDS DYOMICS GMBH (DE) 2012-11-22 US disclosed
US-20120156140-A1 FLUORESCENT COMPOUNDS DYOMICS GMBH (DE) 2012-06-21 US disclosed