Potassium Ion

Potassium Ion

SCHEMBL4869310

Cc1cc2c(F)c(Oc3ncnn4cc([O-])c(C)c34)ccc2[nH]1.[K+]

nearest known ligand 0.76

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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 20)

geneUniProtsupporting neighboursconfidence
▸ KDR P35968 15/20 0.76
▸ CYP3A4 P08684 12/20 0.68
▸ FGFR1 P11362 5/20 0.68
▸ KCNH2 Q12809 3/20 0.68
▸ STK10 O94804 2/20 0.68
▸ MAP4K4 O95819 2/20 0.68
▸ RET P07949 2/20 0.68
▸ PDGFRB P09619 2/20 0.68
▸ DDR1 Q08345 2/20 0.68
▸ SLK Q9H2G2 2/20 0.68
▸ EPHB6 O15197 1/20 0.68
▸ RIPK2 O43353 1/20 0.68
▸ ABL1 P00519 1/20 0.68
▸ EGFR P00533 1/20 0.68
▸ LCK P06239 1/20 0.68
▸ CSF1R P07333 1/20 0.68
▸ HCK P08631 1/20 0.68
▸ KIT P10721 1/20 0.68
▸ SRC P12931 1/20 0.68
▸ PDGFRA P16234 1/20 0.68

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
SCHEMBL12020489 0.89 KDR (0.81) KDRCYP3A4FGFR1KCNH2STK10
SCHEMBL1226910 0.87 KDR (1.00) KDRCYP3A4FGFR1KCNH2STK10
SCHEMBL1227665 0.84 KDR (0.77) KDRCYP3A4FGFR1KCNH2STK10
SCHEMBL1226894 0.83 KDR (0.83) KDRCYP3A4FGFR1KCNH2STK10
SCHEMBL14140810 0.83 KDR (0.77) KDRCYP3A4FGFR1KCNH2STK10
SCHEMBL1227648 0.83 KDR (0.75) KDRCYP3A4FGFR1KCNH2STK10
SCHEMBL1227548 0.83 KDR (0.77) KDRCYP3A4FGFR1KCNH2STK10
SCHEMBL4281456 0.82 KDR (0.71) KDRCYP3A4FGFR1KCNH2STK10
SCHEMBL1227552 0.82 KDR (0.77) KDRCYP3A4FGFR1KCNH2STK10
SCHEMBL12899428 0.82 KDR (0.79) KDRCYP3A4FGFR1KCNH2STK10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7393667-B2 Stereoselective reduction process for the preparation of pyrrolotriazine compounds BRISTOL-MYERS SQUIBB COMPANY (US) 2008-07-01 — — US disclosed
US-20060286646-A1 STEREOSELECTIVE REDUCTION PROCESS FOR THE PREPARATION OF PYRROLOTRIAZINE COMPOUNDS BRISTOL-MYERS SQUIBB COMPANY (US) 2006-12-21 — — 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 (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-20060286646-A1 STEREOSELECTIVE REDUCTION PROCESS FOR THE PREPARATION OF PYRROLOTRIAZINE COMPOUNDS ADH1C, ADH5, ADH1A KDR 4188/4885CYP3A4 76/4885FGFR1 2346/4885

“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.

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