Potassium Ion

Potassium Ion

SCHEMBL9616871

Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O[C@H](CO)[C@@H](O)[C@H](O)[C@@H](O)C=O)OP(=O)([O-])[O-])[C@@H](O)[C@H]1O.[K+].[K+]

nearest known ligand 0.63

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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
P2RY1 P47900 9/20 0.63
P2RY11 Q96G91 3/20 0.63
ENPP1 P22413 4/20 0.61
TSHR P16473 1/20 0.61
KDM4E B2RXH2 1/20 0.61
LMNA P02545 1/20 0.61
BLM P54132 1/20 0.61
P2RY2 P41231 3/20 0.59
SRC P12931 2/20 0.59
SMN1; SMN2 Q16637 2/20 0.59
P2RX1 P51575 2/20 0.59
P2RX3 P56373 2/20 0.59
P2RX4 Q99571 1/20 0.59
P2RX2 Q9UBL9 1/20 0.59
ALDH1A1 P00352 1/20 0.59
TRPM2 O94759 2/20 0.58
DNPH1 O43598 1/20 0.58
PRKAB2 O43741 1/20 0.58
LDHA P00338 1/20 0.58
ADRB2 P07550 1/20 0.58

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
SCHEMBL1416581 0.93 P2RY1 (0.64) P2RY1P2RY11ENPP1P2RY2SRC
SCHEMBL5526334 0.93 P2RY1 (0.64) P2RY1P2RY11ENPP1P2RY2SRC
SCHEMBL19260795 0.88 P2RY1 (0.66) P2RY1P2RY11ENPP1TSHRKDM4E
Adenosine Diphosphate SCHEMBL29271907 0.84 P2RY1 (0.61) P2RY1P2RY11ENPP1TSHRKDM4E
SCHEMBL7151766 0.84 P2RY1 (0.64) P2RY1P2RY11ENPP1P2RY2SRC
Adenosine Triphosphate SCHEMBL27553935 0.83 P2RY1 (0.61) P2RY1P2RY11ENPP1TSHRKDM4E
Adenosine Phosphate SCHEMBL2063219 0.83 P2RY1 (0.75) P2RY1P2RY11ENPP1P2RY2SRC
Adenosine Phosphate SCHEMBL28225967 0.82 P2RY1 (0.76) P2RY1P2RY11ENPP1P2RY2SRC
Adenosine Phosphate SCHEMBL5988433 0.82 P2RY1 (0.76) P2RY1P2RY11ENPP1P2RY2SRC
Adenosine Diphosphate SCHEMBL584344 0.82 P2RY1 (0.71) P2RY1P2RY11ENPP1P2RY2SRC

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0423290-A4 METHOD FOR STIMULATING PLANT GROWTH USING SYNTHETICALLY PRODUCED 9-BETA-L(+) ADENOSINE UNIV MICHIGAN STATE (US) 1992-10-21 EP disclosed
EP-0423290-A1 METHOD FOR STIMULATING PLANT GROWTH USING SYNTHETICALLY PRODUCED 9-BETA-L(+) ADENOSINE THE BOARD OF TRUSTEES OF THE MICHIGAN STATE UNIVERSITY (US) 1991-04-24 EP disclosed
US-5009698-A Method for stimulating plant growth using synthetically produced 9-beta-1(+) adenosine BOARD OF TRUSTEES OPERATING MICHIGAN STATE UNIVERSITY (US) 1991-04-23 US disclosed
WO-1990013223-A1 METHOD FOR STIMULATING PLANT GROWTH USING SYNTHETICALLY PRODUCED 9-BETA-L(+) ADENOSINE MICHIGAN STATE UNIVERSITY (US) 1990-11-15 WO disclosed