Gluconic Acid

Gluconic Acid

SCHEMBL2229853

O=C(O[C@@H](C(=O)[O-])[C@@H](O)[C@H](O)[C@H](O)CO)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.O=C([O-])[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.[Zn+2]

nearest known ligand 0.65

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHESCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9A

The experimentally established mechanism targets of Gluconic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.65
PDE4A P27815 1/20 0.48
USP2 O75604 1/20 0.38
SLCO1B1 Q9Y6L6 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.37
TDP1 Q9NUW8 1/20 0.35

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
Gluconic Acid SCHEMBL3710793 0.97 LMNA (0.65) LMNAPDE4AUSP2SLCO1B1L3MBTL1
Gluconic Acid SCHEMBL826558 0.95 LMNA (0.62) LMNAPDE4AUSP2SLCO1B1L3MBTL1
Gluconic Acid SCHEMBL547729 0.95 LMNA (0.62) LMNAPDE4AUSP2SLCO1B1L3MBTL1
Silver SCHEMBL18889837 0.93 LMNA (0.58) LMNAPDE4AUSP2SLCO1B1L3MBTL1
Gluconic Acid SCHEMBL9142009 0.92 LMNA (0.59) LMNAPDE4AUSP2SLCO1B1L3MBTL1
SCHEMBL9360101 0.92 LMNA (0.56) LMNAPDE4AUSP2SLCO1B1L3MBTL1
SCHEMBL9142871 0.90 PDE4A (0.59) LMNAPDE4AUSP2SLCO1B1L3MBTL1
SCHEMBL9356215 0.90 PDE4A (0.59) LMNAPDE4AUSP2SLCO1B1L3MBTL1
Potassium Ion SCHEMBL30209157 0.90 PDE4A (0.59) LMNAPDE4AUSP2SLCO1B1L3MBTL1
Gluconic Acid SCHEMBL3389955 0.86 LMNA (0.59) LMNAPDE4AUSP2SLCO1B1L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20130150239-A1 AQUEOUS-MISCIBLE OR AQUEOUS-DISPERSIBLE, VOC-FREE BIOCIDAL COMPOSITIONS FOR THE ENHANCED INHIBITION OF GRAM-NEGATIVE BACTERIAL STRAINS, AND METHOD OF PREPARING THE SAME TROY TECHNOLOGY II, INC. 2013-06-13 US disclosed
EP-2531034-A1 AQUEOUS-MISCIBLE OR AQUEOUS-DISPERSIBLE, VOC-FREE BIOCIDAL COMPOSITIONS FOR THE ENHANCED INHIBITION OF GRAM-NEGATIVE BACTERIAL STRAINS, AND METHOD OF PREPARING THE SAME ISP INVESTMENT INC. (US) 2012-12-12 EP disclosed
WO-2011085067-A1 AQUEOUS-MISCIBLE OR AQUEOUS-DISPERSIBLE, VOC-FREE BIOCIDAL COMPOSITIONS FOR THE ENHANCED INHIBITION OF GRAM-NEGATIVE BACTERIAL STRAINS, AND METHOD OF PREPARING THE SAME ISP INVESTMENT INC. (US) 2011-07-14 WO 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-20130150239-A1 AQUEOUS-MISCIBLE OR AQUEOUS-DISPERSIBLE, VOC-FREE BIOCIDAL COMPOSITIONS FOR THE ENHANCED INHIBITION OF GRAM-NEGATIVE BACTERIAL STRAINS, AND METHOD OF PREPARING THE SAME TMBIM6, BAX, DBI LMNA 2091/4885PDE4A 3164/4885USP2 2663/4885

“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.