Gluconic Acid

Gluconic Acid

SCHEMBL5142632

O=C(O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.O=S(=O)([O-])[O-].[Na+].[Na+]

nearest known ligand 0.76

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9A

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 11)

geneUniProtsupporting neighboursconfidence
PDE4A P27815 1/20 0.76
LMNA P02545 2/20 0.64
USP2 O75604 1/20 0.48
SLCO1B1 Q9Y6L6 1/20 0.48
L3MBTL1 Q9Y468 1/20 0.44
TDP1 Q9NUW8 1/20 0.42
TSHR P16473 2/20 0.42
CYP2C9 P11712 1/20 0.42
TP53 P04637 1/20 0.39
OR51E2 Q9H255 1/20 0.34
KDM4E B2RXH2 2/20 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
Gluconic Acid SCHEMBL29053550 0.96 PDE4A (0.76) PDE4ALMNAUSP2SLCO1B1L3MBTL1
Gluconic Acid SCHEMBL16370767 0.96 PDE4A (0.76) PDE4ALMNAUSP2SLCO1B1L3MBTL1
Gluconic Acid SCHEMBL28402789 0.88 LMNA (0.84) PDE4ALMNAUSP2SLCO1B1L3MBTL1
Gluconic Acid SCHEMBL28658431 0.88 PDE4A (0.83) PDE4ALMNAUSP2SLCO1B1L3MBTL1
Gluconic Acid SCHEMBL20919813 0.88 PDE4A (0.83) PDE4ALMNAUSP2SLCO1B1L3MBTL1
Gluconic Acid SCHEMBL9775275 0.88 PDE4A (0.83) PDE4ALMNAUSP2SLCO1B1L3MBTL1
Gluconic Acid SCHEMBL4896915 0.88 PDE4A (0.83) PDE4ALMNAUSP2SLCO1B1L3MBTL1
Gluconic Acid SCHEMBL28705777 0.87 PDE4A (0.91) PDE4ALMNAUSP2SLCO1B1L3MBTL1
Gluconic Acid SCHEMBL28120184 0.87 PDE4A (0.91) PDE4ALMNAUSP2SLCO1B1L3MBTL1
Gluconic Acid SCHEMBL262276 0.87 PDE4A (0.91) PDE4ALMNAUSP2SLCO1B1L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111187146-B Process for producing 2-methyl-3-buten-2-ol 浙大宁波理工学院 2023-06-23 CN disclosed
CN-111187146-A Method for producing 2-methyl-3-buten-2-ol 浙江大学宁波理工学院 2020-05-22 CN disclosed
EP-1752428-B1 Method for reducing chromium (VI) in cement GCP APPLIED TECH INC (US) 2017-03-15 EP disclosed
WO-2007021617-A2 DOSAGE EFFICIENT, STORAGE STABLE COMPOSITIONS FOR REDUCING CHROMIUM (VI) IN CEMENT W.R. GRACE & CO.-CONN. (US) 2007-02-22 WO disclosed
US-20070034118-A1 Dosage efficient, storage stable compositions for reducing chromium (VI) in cement W. R. GRACE & CO.-CONN. 2007-02-15 US disclosed
EP-1752428-A2 Dosage efficient, storage stable compositions for reducing chromium (VI) in cement W.R. GRACE & CO.-CONN. (US) 2007-02-14 EP disclosed