Potassium Ion

Potassium Ion

SCHEMBL9929143

CC1=Nc2ccc(S(=O)(=O)[O-])cc2C1(C)CCCS(=O)(=O)[O-].[K+].[K+]

nearest known ligand 0.33

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.

Predicted protein targets (top 2)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.33
TDP1 Q9NUW8 1/20 0.33

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 SCHEMBL30372129 1.00 LMNA (0.33) LMNATDP1
Potassium Ion SCHEMBL560059 0.96 LMNA (0.32) LMNATDP1
Potassium Ion SCHEMBL29713986 0.96 LMNA (0.32) LMNATDP1
SCHEMBL42027 0.94 LMNA (0.35) LMNATDP1
SCHEMBL2721462 0.81 CYP26B1 (0.34) LMNATDP1
SCHEMBL136845 0.81 RXRA (0.31)
SCHEMBL114709 0.81 RXRA (0.31)
Potassium Ion SCHEMBL3791274 0.81 LMNA (0.31) LMNATDP1
Potassium SCHEMBL9929144 0.80 RXRA (0.30)
SCHEMBL9929142 0.80 RXRA (0.30)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11053222-B2 Fluorescent compounds PIERCE BIOTECHNOLOGY, INC. (US) 2021-07-06 US disclosed
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-10000467-B2 Cyanine compounds PIERCE BIOTECHNOLOGY, INC. (US) 2018-06-19 US 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-8889884-B1 Phosphine derivatives of fluorescent compounds PIERCE BIOTECHNOLOGY, INC. (US) 2014-11-18 US 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
EP-2655327-A1 FLUORESCENT COMPOUNDS Pierce Biotechnology, Inc. (US) 2013-10-30 EP disclosed
US-20130251637-A9 FLUORESCENT COMPOUNDS DYOMICS GMBH (DE) 2013-09-26 US disclosed
WO-2013130761-A1 INDOLE DERIVATIVES AS LABELING DYE FOR BIOMOLECULE PIERCE BIOTECHNOLOGY, INC. (US) 2013-09-06 WO 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
WO-2012088007-A1 FLUORESCENT COMPOUNDS PIERCE BIOTECHNOLOGY, INC. (US) 2012-06-28 WO disclosed
US-20120156140-A1 FLUORESCENT COMPOUNDS DYOMICS GMBH (DE) 2012-06-21 US 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 (14 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-20170158858-A9 CYANINE COMPOUNDS NCL, NOP58, NAT10 LMNA 836/4885TDP1 563/4885
US-20180118723-A1 FLUORESCENT COMPOUNDS NCL, FUS, EFTUD2 LMNA 512/4885TDP1 654/4885
US-10351551-B2 Fluorescent compounds NCL, FUS, EFTUD2 LMNA 512/4885TDP1 654/4885
US-20180327387-A1 Cyanine Compounds NCL, NOP58, NAT10 LMNA 836/4885TDP1 563/4885
US-20140255312-A1 CYANINE COMPOUNDS NCL, NOP58, NAT10 LMNA 836/4885TDP1 563/4885
US-20120156140-A1 FLUORESCENT COMPOUNDS NCL, FUS, EFTUD2 LMNA 512/4885TDP1 654/4885
US-10696653-B2 Cyanine compounds NCL, NOP58, NAT10 LMNA 836/4885TDP1 563/4885
US-20130230466-A1 CYANINE COMPOUNDS NCL, NOP58, NAT10 LMNA 836/4885TDP1 563/4885
US-11053222-B2 Fluorescent compounds NCL, FUS, EFTUD2 LMNA 512/4885TDP1 654/4885
US-20130251637-A9 FLUORESCENT COMPOUNDS NCL, FUS, EFTUD2 LMNA 512/4885TDP1 654/4885
US-10000467-B2 Cyanine compounds NCL, NOP58, NAT10 LMNA 836/4885TDP1 563/4885
US-10053447-B2 Fluorescent compounds NCL, FUS, EFTUD2 LMNA 512/4885TDP1 654/4885
US-20120294807-A9 FLUORESCENT COMPOUNDS NCL, FUS, EFTUD2 LMNA 512/4885TDP1 654/4885
US-20140072515-A9 CYANINE COMPOUNDS NCL, NOP58, NAT10 LMNA 836/4885TDP1 563/4885

“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.