Bicarbonate

Bicarbonate

SCHEMBL5032083

CCCC[n+]1ccn(C)c1.CCCC[n+]1ccn(C)c1.O=C([O-])[O-]

nearest known ligand 0.41

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GSK3AGSK3BIMPA1

The experimentally established mechanism targets of Bicarbonate. 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
MEN1 O00255 1/20 0.41
HSP90AA1 P07900 1/20 0.41
KMT2A Q03164 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
PABPC1 P11940 1/20 0.37
FDPS P14324 7/20 0.37

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
Bicarbonate SCHEMBL1490993 0.98 MEN1 (0.40) MEN1HSP90AA1KMT2ASMN1; SMN2PABPC1
Acetic Acid SCHEMBL35015 0.95 MEN1 (0.43) MEN1HSP90AA1KMT2ASMN1; SMN2PABPC1
Bicarbonate SCHEMBL2127090 0.95 MEN1 (0.40) MEN1HSP90AA1KMT2ASMN1; SMN2PABPC1
Bicarbonate SCHEMBL28733245 0.93 MEN1 (0.46) MEN1HSP90AA1KMT2ASMN1; SMN2
Propionic Acid SCHEMBL358643 0.93 MEN1 (0.39) MEN1HSP90AA1KMT2ASMN1; SMN2PABPC1
Bicarbonate SCHEMBL28939212 0.93 MEN1 (0.46) MEN1HSP90AA1KMT2ASMN1; SMN2
Bicarbonate SCHEMBL23698434 0.92 MEN1 (0.44) MEN1HSP90AA1KMT2ASMN1; SMN2
Glycolic Acid SCHEMBL18575074 0.92 MEN1 (0.38) MEN1HSP90AA1KMT2ASMN1; SMN2PABPC1
Bicarbonate SCHEMBL6265469 0.92 MEN1 (0.44) MEN1HSP90AA1KMT2ASMN1; SMN2
Succinic Acid SCHEMBL18575091 0.92 CA1 (0.40) MEN1HSP90AA1KMT2ASMN1; SMN2PABPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114317027-A Method for separating naphthenic acid from naphthenic acid-containing oil product by using ionic liquid 中国石油大学(北京) 2022-04-12 CN claimed
CN-112871208-A Application of imidazolium salt ionic liquid catalyst in preparation of battery electrolyte additive 山东卓俊实业有限公司 2021-06-01 CN claimed
CN-112759611-A Preparation method of battery electrolyte additive 山东卓俊实业有限公司 2021-05-07 CN claimed
CN-111321191-A Method for preparing phytosterol ester by enzyme method 山东德普化工科技有限公司 2020-06-23 CN claimed
CN-114317027-B Method for separating naphthenic acid from naphthenic acid-containing oil product by using ionic liquid 中国石油大学(北京) 2023-04-07 CN disclosed
CN-114317027-A Method for separating naphthenic acid from naphthenic acid-containing oil product by using ionic liquid 中国石油大学(北京) 2022-04-12 CN disclosed
CN-113620787-A Synthetic method of fluorine-containing aromatic ether 浙江诺亚氟化工有限公司 2021-11-09 CN disclosed
CN-111807934-B Preparation method of electronic-grade propylene glycol monomethyl ether and product obtained by preparation method 山东海科创新研究院有限公司 2021-02-26 CN disclosed
CN-111807934-A Preparation method of electronic-grade propylene glycol monomethyl ether and product obtained by preparation method 山东海科创新研究院有限公司 2020-10-23 CN disclosed
US-9862675-B1 Method of N-formylating amines with a phosphonic anhydride KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) 2018-01-09 US disclosed
US-8075803-B2 Metathesis of a a quaternary ammonium, phosphonium or sulfonium cation forming a salt of hydrogencarbonate, carbonate, monoalkylcarbonate or monoarylcarbonate; storage stablility PROIONIC GMBH (AT) 2011-12-13 US disclosed
US-20080251759-A1 Method For Producing Ionic Liquids, Ionic Solids Or Mixtures Thereof PROIONIC GMBH (AT) 2008-10-16 US disclosed
WO-2006027069-A1 METHOD FOR PRODUCING HETEROCYCLIC QUATERNARY AMMONIUM AND/OR GUANIDINIUM COMPOUNDS BASF AKTIENGESELLSCHAFT (DE) 2006-03-16 WO disclosed