Potassium Ion

Potassium Ion

SCHEMBL4826211

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

nearest known ligand 0.43

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
AGTR1 known ✓ P30556 1/20 0.33
CA12 O43570 3/20 0.43
CA1 P00915 3/20 0.43
CA2 P00918 3/20 0.43
CA9 Q16790 3/20 0.43
CA7 P43166 2/20 0.43
CA14 Q9ULX7 2/20 0.43
ESR2 Q92731 3/20 0.39
ESR1 P03372 3/20 0.38
MIF P14174 2/20 0.36
MAPT P10636 6/20 0.36
LMNA P02545 5/20 0.36
MDM2 Q00987 2/20 0.36
MDM4 O15151 1/20 0.36
KMT2A Q03164 3/20 0.36
KDM4E B2RXH2 3/20 0.35
GAA P10253 1/20 0.35
FOLH1 Q04609 1/20 0.34
NPSR1 Q6W5P4 3/20 0.34
POLB P06746 1/20 0.34

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 SCHEMBL6129087 1.00 CA12 (0.43) CA12CA1CA2CA9CA7
Potassium Ion SCHEMBL31198116 1.00 CA12 (0.43) CA12CA1CA2CA9CA7
SCHEMBL9302196 0.97 CA12 (0.43) CA12CA1CA2CA9CA7
Potassium Ion SCHEMBL29349588 0.88 MAPT (0.48) MAPTLMNAMDM2MDM4KMT2A
SCHEMBL3987755 0.88 FOLH1 (0.46) CA12CA1CA2CA9CA7
SCHEMBL3987754 0.88 FOLH1 (0.46) CA12CA1CA2CA9CA7
Potassium Ion SCHEMBL8624951 0.88 MAPT (0.48) MAPTLMNAMDM2MDM4KMT2A
Potassium Ion SCHEMBL6155599 0.88 MAPT (0.48) MAPTLMNAMDM2MDM4KMT2A
Potassium Ion SCHEMBL4816016 0.87 CA12 (0.40) CA12CA1CA2CA9CA7
Potassium Ion SCHEMBL30367664 0.87 CA12 (0.40) CA12CA1CA2CA9CA7

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 28 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
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
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 disclosed
EP-0523585-B1 Improvements in or relating to beta lactam production SANDOZ AG (CH) 2005-02-02 EP disclosed
US-20040192909-A1 Intermediates in cephalosporin production SANDOZ GMBH (AT) 2004-09-30 US disclosed
EP-1414827-A2 INTERMEDIATES IN CEPHALOSPORIN PRODUCTION SANDOZ GMBH (AT) 2004-05-06 EP disclosed
US-5338868-A Reacting glycine derivative with trifluoro methane sulfonic acid derivative at low temperature CHINOIN GYOGYSZER- ES VEGYESZETI TERMEKEK GYARA RT. (HU) 1994-08-16 US disclosed
EP-0523585-A2 Improvements in or relating to beta lactam production BIOCHEMIE Gesellschaft m.b.H. (AT) 1993-01-20 EP disclosed
EP-0439096-A2 Improvements in or relating to beta lactam production BIOCHEMIE GESELLSCHAFT M.B.H. (AT) 1991-07-31 EP disclosed
EP-0127541-B1 SALTS OF AMINO-BETA-LACTAMIC ACIDS AND PROCESS FOR THE PREPARATION THEREOF GEMA S.A. (ES) 1990-08-01 EP disclosed
US-4659814-A Salts of amino-beta-lactamic acids and process for the preparation thereof GEMA, S.A. (ES) 1987-04-21 US disclosed
EP-0127541-A2 Salts of amino-beta-lactamic acids and process for the preparation thereof GEMA S.A. (ES) 1984-12-05 EP 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-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 (3 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 AGTR1 2071/4885CA12 1149/4885CA1 1075/4885
US-20060149096-A1 Process for preparation of 7-[a-amino (4-hydroxyphenyl) acetamido]-3-substituted-3-cephem-4-carboxylic acid IGLV6-57, APC, IL2 AGTR1 1901/4885CA12 1074/4885CA1 1217/4885
US-20040192909-A1 Intermediates in cephalosporin production MRPL21, PEPD, CUTA AGTR1 1835/4885CA12 1598/4885CA1 1996/4885

“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.