Bicarbonate

Bicarbonate

SCHEMBL851219

CC(C)(C)C1CCC(OOC2CCC(C(C)(C)C)CC2)CC1.O=C(O)O

nearest known ligand 0.45

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 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.45
APOBEC3A P31941 1/20 0.44
APOBEC3G Q9HC16 1/20 0.44
HTT P42858 3/20 0.42
SMN1; SMN2 Q16637 2/20 0.42
KDM4E B2RXH2 1/20 0.42
CYP19A1 P11511 1/20 0.41
EPHX1 P07099 1/20 0.41
GAA P10253 1/20 0.41
NPC1 O15118 1/20 0.40
RAB9A P51151 1/20 0.40
GLA P06280 1/20 0.40
LIPA P38571 1/20 0.39
CYP2D6 P10635 1/20 0.38
KCNH2 Q12809 1/20 0.38
HRH3 Q9Y5N1 1/20 0.38
MEN1 O00255 1/20 0.37
KMT2A Q03164 1/20 0.37
EPHX2 P34913 1/20 0.36
HSD11B1 P28845 1/20 0.36

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 SCHEMBL2696873 1.00 MAPT (0.45) MAPTAPOBEC3AAPOBEC3GHTTSMN1; SMN2
SCHEMBL2696875 0.90 MAPT (0.41) MAPTAPOBEC3AAPOBEC3GHTTSMN1; SMN2
SCHEMBL4552150 0.88 MAPT (0.39) MAPTAPOBEC3AAPOBEC3GHTTSMN1; SMN2
SCHEMBL28358599 0.85 MAPT (0.41) MAPTAPOBEC3AAPOBEC3GHTTSMN1; SMN2
Bicarbonate SCHEMBL2763274 0.84 MAPT (0.44) MAPTAPOBEC3AAPOBEC3GHTTSMN1; SMN2
Bicarbonate SCHEMBL679005 0.84 MAPT (0.44) MAPTAPOBEC3AAPOBEC3GHTTSMN1; SMN2
Bicarbonate SCHEMBL35810 0.84 MAPT (0.44) MAPTAPOBEC3AAPOBEC3GHTTSMN1; SMN2
SCHEMBL22733770 0.83 MAPT (0.42) MAPTAPOBEC3AAPOBEC3GHTTSMN1; SMN2
SCHEMBL2380079 0.82 MAPT (0.40) MAPTAPOBEC3AAPOBEC3GHTTSMN1; SMN2
SCHEMBL28199763 0.80 MAPT (0.51) MAPTAPOBEC3AAPOBEC3GHTTSMN1; SMN2

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-12421170-B2 Granulate material and associated coating that is low in odor and emissions, particularly a construction element coating, for example a floor coating, based on a radical polymerization SIDEC NV (BE) 2025-09-23 US claimed
US-20220220031-A1 GRANULATE MATERIAL AND ASSOCIATED COATING THAT IS LOW IN ODOR AND EMISSIONS, PARTICULARLY A CONSTRUCTION ELEMENT COATING, FOR EXAMPLE A FLOOR COATING, BASED ON A RADICAL POLYMERIZATION SIDEC NV (BE) 2022-07-14 US claimed
US-12428559-B2 Curable compositions and methods of making and using the same 3M INNOVATIVE PROPERTIES COMPANY (US) 2025-09-30 US disclosed
US-12421170-B2 Granulate material and associated coating that is low in odor and emissions, particularly a construction element coating, for example a floor coating, based on a radical polymerization SIDEC NV (BE) 2025-09-23 US disclosed
EP-4377367-A1 COMPOSITION INCLUDING MONOMER WITH A CARBOXYLIC ACID GROUP, MONOMER WITH A HYDROXYL GROUP, AN ALKYL MONOMER, AND CROSSLINKER AND RELATED ARTICLE AND METHOD 3M Innovative Properties Company (US) 2024-06-05 EP disclosed
EP-4244267-A1 FREE-RADICALLY POLYMERIZABLE CROSSLINKER, CURABLE COMPOSITION, AND ADHESIVE THEREFROM 3M Innovative Properties Company (US) 2023-09-20 EP disclosed
EP-4244268-A1 FREE-RADICALLY POLYMERIZABLE CROSSLINKER, CURABLE COMPOSITION, AND ADHESIVE THEREFROM 3M Innovative Properties Company (US) 2023-09-20 EP disclosed
WO-2023166342-A1 POLYMERIZABLE COMPOSITIONS INCLUDING A POLYMERIZABLE COMPONENT AND A REDOX INITIATION SYSTEM CONTAINING A PHOTOLABILE REDUCING AGENT, AND A PHOTOLABILE REDUCING AGENT 3M INNOVATIVE PROPERTIES COMPANY (US) 2023-09-07 WO disclosed
US-20230082209-A1 LIGHT AND REDOX CURABLE COMPOSITIONS 3M INNOVATIVE PROPERTIES COMPANY 2023-03-16 US disclosed
WO-2023007401-A1 COMPOSITION INCLUDING MONOMER WITH A CARBOXYLIC ACID GROUP, MONOMER WITH A HYDROXYL GROUP, AN ALKYL MONOMER, AND CROSSLINKER AND RELATED ARTICLE AND METHOD 3M INNOVATIVE PROPERTIES COMPANY (US) 2023-02-02 WO disclosed
US-20220372290-A1 CURABLE COMPOSITIONS AND METHODS OF MAKING AND USING THE SAME 3M INNOVATIVE PROPERTIES COMPANY 2022-11-24 US disclosed
EP-1170815-B1 Battery SONY CORP (JP) 2006-09-27 EP disclosed
US-7074522-B2 Battery SONY CORPORATION (JP) 2006-07-11 US disclosed
CN-1501542-A Lithium secondary battery and a method for preparing the same 三星SDI株式会社 2004-06-02 CN disclosed
US-20020076617-A1 Wherein deterioration is prevented via using a metal foil electroconductive layer other than copper (nickel, chromium), thereby controlling polymerization SONY CORPORATION (JP) 2002-06-20 US disclosed
EP-1170815-A2 Battery SONY CORPORATION (JP) 2002-01-09 EP disclosed
CN-1126137-A Process for preparing colour contrasts on aticles obtained by molding from polymerizable compositions ATOHAAS HOLDING CV (NL) 1996-07-10 CN disclosed
US-4551369-A TOILET SEAT SUPPORT RB KUNSTSTOFFPATENT-VERWERTUNGS AG, WESTBAHNHOFSTRASSE, 11 CH-4500 SOLOTHURN, GERMANY A CORP. OF GERMANY 1985-11-05 US disclosed
EP-0037778-B1 2-(1,4-BENZODIOXANYL)-METHOXY-PROPANOL AMINES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS MEDICINES PIERRE FABRE S.A. (FR) 1983-12-28 EP disclosed
EP-0037778-A1 2-(1,4-Benzodioxanyl)-methoxy-propanol amines, process for their preparation and their use as medicines PIERRE FABRE S.A. (FR) 1981-10-14 EP disclosed