Bicarbonate

Bicarbonate

SCHEMBL5597464

CC(C)(C)C1CCCCC1.CC(C)(C)C1CCCCC1.O=C(O)O.O=C(O)O

nearest known ligand 0.55

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
EPHX1 P07099 5/20 0.55
SMN1; SMN2 Q16637 3/20 0.41
SSTR4 P31391 2/20 0.39
GLA P06280 1/20 0.39
KDM4E B2RXH2 1/20 0.39
HTT P42858 1/20 0.39
LIPA P38571 1/20 0.38
CES2 O00748 1/20 0.38
CES1 P23141 1/20 0.38
CYP2D6 P10635 1/20 0.37
KCNH2 Q12809 1/20 0.37
HRH3 Q9Y5N1 1/20 0.37
KEAP1 Q14145 1/20 0.36
NFE2L2 Q16236 1/20 0.36
APOBEC3A P31941 1/20 0.36
APOBEC3G Q9HC16 1/20 0.36
PDK1 Q15118 1/20 0.35
PDK2 Q15119 1/20 0.35
PDK3 Q15120 1/20 0.35
PDK4 Q16654 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
Bicarbonate SCHEMBL28367894 1.00 EPHX1 (0.55) EPHX1SMN1; SMN2SSTR4GLAKDM4E
Bicarbonate SCHEMBL6036898 1.00 EPHX1 (0.55) EPHX1SMN1; SMN2SSTR4GLAKDM4E
Bicarbonate SCHEMBL8827972 1.00 EPHX1 (0.55) EPHX1SMN1; SMN2SSTR4GLAKDM4E
Bicarbonate SCHEMBL975284 0.97 EPHX1 (0.53) EPHX1SMN1; SMN2SSTR4GLAKDM4E
Bicarbonate SCHEMBL5372441 0.97 EPHX1 (0.53) EPHX1SMN1; SMN2SSTR4GLAKDM4E
Bicarbonate SCHEMBL1125852 0.95 EPHX1 (0.52) EPHX1SMN1; SMN2SSTR4GLAKDM4E
Isobutane SCHEMBL28450845 0.93 EPHX1 (0.50) EPHX1SMN1; SMN2SSTR4GLAKDM4E
Acetic Acid SCHEMBL4353702 0.92 EPHX1 (0.53) EPHX1SMN1; SMN2SSTR4GLAKDM4E
Bicarbonate SCHEMBL28626633 0.91 EPHX1 (0.48) EPHX1SMN1; SMN2SSTR4GLAKDM4E
SCHEMBL23174694 0.86 EPHX1 (0.48) EPHX1SMN1; SMN2SSTR4GLAKDM4E

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 47 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230272137-A1 CROSSLINKABLE FLUOROPOLYMER AND COATING FORMED THEREFROM THE CHEMOURS COMPANY FC, LLC (US) 2023-08-31 US disclosed
US-11674047-B2 Composition for manufacturing passivation layer and passivation layer using the same THE CHEMOURS COMPANY FC, LLC (US) 2023-06-13 US disclosed
EP-4178994-A1 CROSSLINKABLE FLUOROPOLYMER AND COATING FORMED THEREFROM The Chemours Company FC, LLC (US) 2023-05-17 EP disclosed
CN-115161913-A Method for sizing fibers, coated fibers and fiber-reinforced composites 清华大学 2022-10-11 CN disclosed
EP-3411445-B1 FLUOROPOLYMER SOLUTION FOR FORMING A FLUOROPOLYMER COATING CHEMOURS CO FC LLC (US) 2022-07-13 EP disclosed
WO-2022011203-A1 CROSSLINKABLE FLUOROPOLYMER AND COATING FORMED THEREFROM THE CHEMOURS COMPANY FC, LLC (US) 2022-01-13 WO disclosed
EP-3918015-A1 COMPOSITION FOR MANUFACTURING PASSIVATION LAYER AND PASSIVATION LAYER USING THE SAME The Chemours Company FC, LLC (US) 2021-12-08 EP disclosed
WO-2020159974-A1 COMPOSITION FOR MANUFACTURING PASSIVATION LAYER AND PASSIVATION LAYER USING THE SAME THE CHEMOURS COMPANY FC, LLC (US) 2020-08-06 WO disclosed
US-20200239724-A1 COMPOSITION FOR MANUFACTURING PASSIVATION LAYER AND PASSIVATION LAYER USING THE SAME JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT 2020-07-30 US disclosed
US-20200165480-A1 PHOTOCROSSLINKABLE FLUOROPOLYMER COATING COMPOSITION AND COATING LAYER FORMED THEREFROM THE CHEMOURS COMPANY FC, LLC (US) 2020-05-28 US disclosed
EP-0629633-A2 Dinucleotide analogues, intermediates therefor and oligonucleotides derived therefrom CIBA-GEIGY AG (CH) 1994-12-21 EP disclosed
EP-0614906-A1 Mononucleotide analogues and intermediates therefor CIBA-GEIGY AG (CH) 1994-09-14 EP disclosed
EP-0614907-A1 Dinucleotide and oligonucleotide analogues CIBA-GEIGY AG (CH) 1994-09-14 EP disclosed
EP-0614900-A1 Phosphinate esters CIBA-GEIGY AG (CH) 1994-09-14 EP disclosed
EP-0067124-B1 PRODUCTION OF 5,5-DISUBSTITUTED 3-OXO-PENT-4-ENOIC ACIDS, THEIR HALIDES, ESTERS, THIOESTERS AND AMIDES; AND THEIR USE IN ANTIFUNGAL AND ANTIBACTERIAL COMPOSITIONS CIBA-GEIGY AG (CH) 1985-05-02 EP disclosed
US-4472589-A 4-Chloro-4-chloromethyloxetan-2-one CIBA-GEIGY CORPORATION (US) 1984-09-18 US disclosed
US-4398033-A 4-Chloro-4-chloromethyloxetan-2-one and a process for its production CIBA-GEIGY CORPORATION (US) 1983-08-09 US disclosed
US-4384966-A FRICTION AND WEAR RESISTANCE ADDITIVES FOR LUBRICANTS, FIREPROOFING POLYMERS CIBA-GEIGY CORPORATION (US) 1983-05-24 US disclosed
EP-0067124-A1 Production of 5,5-disubstituted 3-oxo-pent-4-enoic acids, their halides, esters, thioesters and amides; and their use in antifungal and antibacterial compositions CIBA-GEIGY AG (CH) 1982-12-15 EP disclosed
US-4363923-A ALGISTATS BACTERICIDES, FUNGICIDES CIBA-GEIGY CORPORATION (US) 1982-12-14 US disclosed