Potassium Ion

Potassium Ion

SCHEMBL4816016

COC(=O)C=C(C)NC(C(=O)[O-])c1ccc(O)cc1.[K+]

nearest known ligand 0.40

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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
CA12 O43570 3/20 0.40
CA1 P00915 3/20 0.40
CA2 P00918 3/20 0.40
CA7 P43166 3/20 0.40
CA9 Q16790 3/20 0.40
CA14 Q9ULX7 3/20 0.40
TYR P14679 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.38
ESR1 P03372 2/20 0.36
ESR2 Q92731 2/20 0.36
TSHR P16473 2/20 0.36
FOLH1 Q04609 1/20 0.35
MAPT P10636 3/20 0.33
ALDH1A1 P00352 2/20 0.33
MEN1 O00255 2/20 0.33
KMT2A Q03164 2/20 0.33
KDM4E B2RXH2 1/20 0.33
TP53 P04637 1/20 0.33
CYP1A2 P05177 1/20 0.33
CYP2C9 P11712 1/20 0.33

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
Potassium Ion SCHEMBL30367664 1.00 CA12 (0.40) CA12CA1CA2CA7CA9
Potassium Ion SCHEMBL10935064 1.00 CA12 (0.40) CA12CA1CA2CA7CA9
SCHEMBL11226776 0.97 CA1 (0.40) CA12CA1CA2CA7CA9
SCHEMBL9302453 0.97 CA1 (0.40) CA12CA1CA2CA7CA9
Potassium Ion SCHEMBL4825140 0.87 TSHR (0.43) SMN1; SMN2TSHRMAPTALDH1A1MEN1
SCHEMBL6129097 0.87 FOLH1 (0.47) CA12CA1CA2CA7CA9
SCHEMBL5904162 0.87 FOLH1 (0.47) CA12CA1CA2CA7CA9
SCHEMBL5995942 0.87 FOLH1 (0.47) CA12CA1CA2CA7CA9
SCHEMBL2896479 0.87 FOLH1 (0.47) CA12CA1CA2CA7CA9
Potassium Ion SCHEMBL6129087 0.87 CA12 (0.43) CA12CA1CA2CA7CA9

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 37 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7230097-B2 Process for preparation of 7-[α-Amino (4-hydroxyphenyl) acetamido]-3-substituted-3-cephem-4-carboxylic acid LUPIN LTD. (IN) 2007-06-12 US claimed
US-20050113570-A1 Process for preparation of 7-[alpha-amino (4-hydroxyphenyl) acetamido]-3-substituted-3-cephem-4-carboxylic acid LUPIN LTD. (IN) 2005-05-26 US claimed
EP-0439096-A2 Improvements in or relating to beta lactam production BIOCHEMIE GESELLSCHAFT M.B.H. (AT) 1991-07-31 EP claimed
EP-0019345-B1 PROCESS FOR THE PREPARATION OF A (D-ALPHA-AMINO-(P-HYDROXYPHENYL)-ACETAMIDO) GROUP CONTAINING CEPHALOSPORANIC ACID DERIVATIVES GIST-BROCADES N.V. (NL) 1985-06-19 EP claimed
US-4358588-A 7-/D-ALPHA-AMINO/P-HYDROXYPHENYL/ACETAMIDO-3- CEPHEM-4-CARBOXYLIC ACID DERIVATIVES; EFFICIENCY GIST-BROCADES N.V. (NL) 1982-11-09 US claimed
EP-0001133-B1 PROCESS FOR THE PREPARATION OF 6- D-ALPHA-AMINO-(P-HYDROXYPHENYL)-ACETAMIDO PENICILLANIC ACID GIST-BROCADES N.V. (NL) 1982-01-20 EP claimed
EP-0019345-A1 Process for the preparation of a (D-alpha-amino-(p-hydroxyphenyl)-acetamido) group containing cephalosporanic acid derivatives GIST-BROCADES N.V. (NL) 1980-11-26 EP claimed
EP-0001133-A1 Process for the preparation of 6- D-alpha-amino-(p-hydroxyphenyl)-acetamido penicillanic acid GIST-BROCADES N.V. (NL) 1979-03-21 EP claimed
US-4128547-A TERTIARY AMINE CATALYST GIST-BROCADES N.V. (NL) 1978-12-05 US claimed
JP-57188594-A None JP disclosed
US-7427692-B2 Process for preparation of 7-[α-amino (4-hydroxyphenyl) acetamido]-3-substituted-3-cephem-4-carboxylic acid LUPIN LTD. (US) 2008-09-23 US disclosed
US-7355041-B2 Intermediates in cefprozil production SANDOZ GMBH (AU) 2008-04-08 US disclosed
US-7230097-B2 Process for preparation of 7-[α-Amino (4-hydroxyphenyl) acetamido]-3-substituted-3-cephem-4-carboxylic acid LUPIN LTD. (IN) 2007-06-12 US disclosed
US-20060149096-A1 Process for preparation of 7-[a-amino (4-hydroxyphenyl) acetamido]-3-substituted-3-cephem-4-carboxylic acid LUPIN LTD. (IN) 2006-07-06 US disclosed
JP-S57188594-A PREPARATION OF 7-(2-AMINO-2-PHENYLACETAMIDO)CEPHEM DERIVATIVE EISAI CO LTD 1982-11-19 JP disclosed
US-4358588-A 7-/D-ALPHA-AMINO/P-HYDROXYPHENYL/ACETAMIDO-3- CEPHEM-4-CARBOXYLIC ACID DERIVATIVES; EFFICIENCY GIST-BROCADES N.V. (NL) 1982-11-09 US disclosed
EP-0001133-B1 PROCESS FOR THE PREPARATION OF 6- D-ALPHA-AMINO-(P-HYDROXYPHENYL)-ACETAMIDO PENICILLANIC ACID GIST-BROCADES N.V. (NL) 1982-01-20 EP disclosed
EP-0019345-A1 Process for the preparation of a (D-alpha-amino-(p-hydroxyphenyl)-acetamido) group containing cephalosporanic acid derivatives GIST-BROCADES N.V. (NL) 1980-11-26 EP disclosed
EP-0001133-A1 Process for the preparation of 6- D-alpha-amino-(p-hydroxyphenyl)-acetamido penicillanic acid GIST-BROCADES N.V. (NL) 1979-03-21 EP disclosed
US-4128547-A TERTIARY AMINE CATALYST GIST-BROCADES N.V. (NL) 1978-12-05 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-20050113570-A1 Process for preparation of 7-[alpha-amino (4-hydroxyphenyl) acetamido]-3-substituted-3-cephem-4-carboxylic acid IGLV6-57, APC, HBZ CA12 1149/4885CA1 1075/4885CA2 1375/4885
US-20060149096-A1 Process for preparation of 7-[a-amino (4-hydroxyphenyl) acetamido]-3-substituted-3-cephem-4-carboxylic acid IGLV6-57, APC, IL2 CA12 1074/4885CA1 1217/4885CA2 1432/4885

“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.