Potassium Ion

Potassium Ion

SCHEMBL5124357

O=C([O-])c1cnn2c1CCC2.[K+]

nearest known ligand 0.42

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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 19)

geneUniProtsupporting neighboursconfidence
HTR2A P28223 1/20 0.38
HTR2C P28335 1/20 0.38
CYP11B1 P15538 7/20 0.38
CYP11B2 P19099 7/20 0.38
NTRK1 P04629 1/20 0.35
CDK9 P50750 3/20 0.34
SSTR4 P31391 1/20 0.34
NLRP3 Q96P20 1/20 0.34
MGLL Q99685 1/20 0.33
DRD3 P35462 2/20 0.32
DRD4 P21917 1/20 0.32
KDM4E B2RXH2 1/20 0.31
NPC1 O15118 1/20 0.31
ALDH1A1 P00352 1/20 0.31
HPGD P15428 1/20 0.31
RAB9A P51151 1/20 0.31
KMT2A Q03164 1/20 0.31
HSD17B10 Q99714 1/20 0.31
KDM5B Q9UGL1 1/20 0.31

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
SCHEMBL16814051 0.81 NTRK1 (0.40) HTR2AHTR2CCYP11B1CYP11B2NTRK1
SCHEMBL20207558 0.77 NTRK1 (0.40) HTR2AHTR2CCYP11B1CYP11B2NTRK1
SCHEMBL25172258 0.76 HTR2A (0.43) HTR2AHTR2CCYP11B1CYP11B2CDK9
SCHEMBL4820236 0.73 LMNA (0.48) DRD3DRD4KDM4ENPC1ALDH1A1
SCHEMBL24577981 0.72 CYP11B1 (0.38) HTR2AHTR2CCYP11B1CYP11B2NTRK1
SCHEMBL20223637 0.72 HTR2A (0.43) HTR2AHTR2CNTRK1CDK9SSTR4
SCHEMBL23056002 0.72 HTR2A (0.36) HTR2AHTR2CCYP11B1CYP11B2NTRK1
SCHEMBL24567548 0.69 TSHR (0.50) NTRK1DRD3KDM4EALDH1A1HPGD
Iodide SCHEMBL7949135 0.69 HTR2A (0.39) HTR2AHTR2CNTRK1CDK9SSTR4
SCHEMBL15528465 0.68 LRRK2 (0.40) CYP11B1CYP11B2CDK9SSTR4NLRP3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20080009634-A1 Process for synthesizing beta-lactamase inhibitor intermediates WYETH HOLDINGS CORPORATION (US) 2008-01-10 US disclosed
US-7276611-B2 Process for synthesizing beta-lactamase inhibitor intermediates WYETH HOLDINGS CORPORATION (US) 2007-10-02 US disclosed
EP-1626975-A2 PROCESS FOR SYNTHESIZING ß-LACTAMASE INHIBITOR IN INTERMEDIATES Wyeth Holdings Corporation (US) 2006-02-22 EP disclosed
WO-2004104006-A2 PROCESS FOR SYNTHESIZING β-LACTAMASE INHIBITOR IN INTERMEDIATES WYETH HOLDINGS CORPORATION (US) 2004-12-02 WO disclosed
US-20040242874-A1 Process for synthesizing beta-lactamase inhibitor intermediates WYETH HOLDINGS CORPORATION 2004-12-02 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 (2 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-20080009634-A1 Process for synthesizing beta-lactamase inhibitor intermediates COASY, DCXR, MGAM HTR2A 3395/4885HTR2C 3603/4885CYP11B1 1627/4885
US-20040242874-A1 Process for synthesizing beta-lactamase inhibitor intermediates COASY, DCXR, MGAM HTR2A 3362/4885HTR2C 3537/4885CYP11B1 1650/4885

“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.