Potassium Ion

Potassium Ion

SCHEMBL5607531

CC(=Cc1ccc(O)cc1)C(=O)[O-].[K+]

nearest known ligand 0.59

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 20)

geneUniProtsupporting neighboursconfidence
PTGS2 known ✓ P35354 2/20 0.46
PTGS1 known ✓ P23219 1/20 0.46
ALDH1A1 P00352 3/20 0.59
KDM4E B2RXH2 2/20 0.59
ESR1 P03372 4/20 0.50
ESR2 Q92731 4/20 0.50
TBXAS1 P24557 1/20 0.48
NQO2 P16083 1/20 0.46
AKR1C3 P42330 1/20 0.45
CISD1 Q9NZ45 2/20 0.43
SLC16A3 O15427 1/20 0.43
CYP3A4 P08684 1/20 0.43
HPGD P15428 1/20 0.43
SLC16A1 P53985 1/20 0.43
GPR35 Q9HC97 1/20 0.43
ALDH5A1 P51649 1/20 0.43
ABAT P80404 1/20 0.43
MEN1 O00255 2/20 0.42
KMT2A Q03164 2/20 0.42
TYR P14679 3/20 0.42

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
SCHEMBL5607241 0.98 ALDH1A1 (0.57) ALDH1A1KDM4EESR1ESR2TBXAS1
SCHEMBL8051968 0.83 ALDH1A1 (0.63) ALDH1A1KDM4EESR1ESR2PTGS2
SCHEMBL8051967 0.83 ALDH1A1 (0.63) ALDH1A1KDM4EESR1ESR2PTGS2
SCHEMBL15272115 0.83 ALDH1A1 (0.69) ALDH1A1KDM4EESR1ESR2PTGS2
SCHEMBL15272117 0.83 ALDH1A1 (0.69) ALDH1A1KDM4EESR1ESR2PTGS2
SCHEMBL83883 0.81 AKR1C3 (0.69) ALDH1A1KDM4EESR1ESR2TBXAS1
SCHEMBL83882 0.81 AKR1C3 (0.69) ALDH1A1KDM4EESR1ESR2TBXAS1
SCHEMBL5607459 0.79 AKR1C3 (0.67) ALDH1A1KDM4EESR1ESR2TBXAS1
SCHEMBL5606699 0.79 AKR1C3 (0.67) ALDH1A1KDM4EESR1ESR2TBXAS1
SCHEMBL5607625 0.79 AKR1C3 (0.67) ALDH1A1KDM4EESR1ESR2TBXAS1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070142472-A1 Process for producing optically active 3-(4-hydroxyphenyl)proprionic acids TAKASAGO INTERNATIONAL CORPORATION (JP) 2007-06-21 US disclosed
EP-1687250-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE 3-(4-HYDROXYPHENYL)PROPIONIC ACIDS Takasago International Corporation (JP) 2006-08-09 EP disclosed
WO-2005051882-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE 3-(4-HYDROXYPHENYL)PROPIONIC ACIDS TAKASAGO INTERNATIONAL CORPORATION (JP) 2005-06-09 WO 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 (1 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-20070142472-A1 Process for producing optically active 3-(4-hydroxyphenyl)proprionic acids ALDH1A2, ALDH1A3, GRHPR PTGS2 2308/4885PTGS1 1782/4885ALDH1A1 5/4885

“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.