Potassium Ion

Potassium Ion

SCHEMBL2379644

CN(C)C1(c2ccccc2)CCC(CC(=O)NC(Cc2c[nH]c3ccccc23)C(=O)[O-])CC1.[K+]

nearest known ligand 0.53

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 19)

geneUniProtsupporting neighboursconfidence
OPRL1 P41146 6/20 0.53
OPRM1 P35372 5/20 0.53
ITGB2 P05107 1/20 0.45
ICAM1 P05362 1/20 0.45
ITGAL P20701 1/20 0.45
MEN1 O00255 1/20 0.45
HCRTR1 O43613 1/20 0.45
KMT2A Q03164 1/20 0.45
TACR1 P25103 2/20 0.44
MMP9 P14780 1/20 0.44
MMP8 P22894 1/20 0.44
MMP14 P50281 1/20 0.44
FPR1 P21462 1/20 0.44
FPR2 P25090 1/20 0.44
ALOX15 P16050 1/20 0.44
ECE1 P42892 1/20 0.43
TACR2 P21452 1/20 0.43
ACE P12821 1/20 0.43
P2RY14 Q15391 1/20 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
SCHEMBL3369086 0.92 OPRL1 (0.56) OPRL1OPRM1ITGB2ICAM1ITGAL
SCHEMBL2378945 0.90 KMT2A (0.57) OPRL1OPRM1MEN1HCRTR1KMT2A
SCHEMBL2380119 0.90 KMT2A (0.57) OPRL1OPRM1MEN1HCRTR1KMT2A
Potassium SCHEMBL2378910 0.90 KMT2A (0.56) OPRL1OPRM1MEN1HCRTR1KMT2A
Hydrochloric Acid SCHEMBL302554 0.90 KMT2A (0.56) OPRL1OPRM1MEN1HCRTR1KMT2A
Hydrochloric Acid SCHEMBL2378939 0.90 KMT2A (0.56) OPRL1OPRM1MEN1HCRTR1KMT2A
SCHEMBL2378906 0.90 KMT2A (0.56) OPRL1OPRM1MEN1HCRTR1KMT2A
SCHEMBL2380008 0.88 OPRL1 (0.56) OPRL1OPRM1ITGB2ICAM1ITGAL
SCHEMBL302945 0.87 OPRL1 (0.55) OPRL1OPRM1ITGB2ICAM1ITGAL
Hydrochloric Acid SCHEMBL2379180 0.87 OPRL1 (0.56) OPRL1OPRM1ITGB2ICAM1ITGAL

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-8017630-B2 Cyclohexylacetic acid compounds GRUENENTHAL GMBH (DE) 2011-09-13 US claimed
EP-1751093-B1 SUBSTITUTED CYCLOHEXYLACETIC ACID DERIVATIVES GRUENENTHAL GMBH (DE) 2010-10-06 EP claimed
US-20070129347-A1 Cyclohexylacetic acid compounds GRUENENTHAL GMBH (DE) 2007-06-07 US claimed
US-8017630-B2 Cyclohexylacetic acid compounds GRUENENTHAL GMBH (DE) 2011-09-13 US disclosed
US-20070129347-A1 Cyclohexylacetic acid compounds GRUENENTHAL GMBH (DE) 2007-06-07 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 (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-20070129347-A1 Cyclohexylacetic acid compounds ACACA, HCAR2, PCCA OPRL1 2478/4885OPRM1 3702/4885ITGB2 4847/4885

“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.