Bicarbonate

Bicarbonate

SCHEMBL9177243

C=CC(c1ccccc1)[S+](C)C.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 13)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.41
CYP2C19 P33261 1/20 0.41
HPGD P15428 1/20 0.38
CYP2D6 P10635 1/20 0.38
SRC P12931 1/20 0.38
MAPK1 P28482 1/20 0.36
KMT2A Q03164 1/20 0.36
CES2 O00748 1/20 0.35
CES1 P23141 1/20 0.35
AKT1 P31749 1/20 0.35
TDP1 Q9NUW8 1/20 0.34
L3MBTL1 Q9Y468 1/20 0.34
HCAR2 Q8TDS4 1/20 0.34

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
SCHEMBL8962567 0.88 DPP4 (0.40) LMNACYP2C19HPGDKMT2ATDP1
Hydrochloric Acid SCHEMBL1092533 0.86 DPP4 (0.39) LMNACYP2C19HPGDKMT2ATDP1
SCHEMBL1077218 0.80 KDM4E (0.38) LMNAHPGDKMT2ATDP1L3MBTL1
SCHEMBL12770109 0.74 CYP2D6 (0.39) LMNACYP2D6SRCMAPK1KMT2A
Bicarbonate SCHEMBL9180912 0.73 ALPL (0.42) LMNACYP2C19HPGDCYP2D6SRC
Hydrochloric Acid SCHEMBL9359182 0.71 KDM4E (0.36) LMNAKMT2ATDP1L3MBTL1
SCHEMBL776592 0.71 CYP2C19 (0.35) LMNACYP2C19HPGDCYP2D6SRC
Hydrochloric Acid SCHEMBL10446062 0.71 TSHR (0.35) CYP2C19KMT2AL3MBTL1
Acetic Acid SCHEMBL7939756 0.68 ALPL (0.41) LMNACYP2C19HPGDCYP2D6SRC
SCHEMBL11039316 0.67 HPGD (0.46) LMNACYP2C19HPGDCYP2D6SRC

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5464538-A Reverse osmosis membrane THE DOW CHEMICAL COMPANY (US) 1995-11-07 US disclosed
US-5310581-A Photoresists, reacting photolabile onium with a photoreactive nucleophile, modified vinylbenzyl chloride polymer THE DOW CHEMICAL COMPANY (US) 1994-05-10 US disclosed
US-5238747-A Compounds with onium groups cured with compound having nucleophilic groups; photoresists release agents THE DOW CHEMICAL COMPANY (US) 1993-08-24 US disclosed
EP-0220660-B1 SEMI-PERMEABLES MEMBRANES PREPARED VIA REACTION OF CATIONIC GROUPS WITH NUCLEOPHILIC GROUPS THE DOW CHEMICAL COMPANY (US) 1992-03-11 EP disclosed
US-4839203-A COVALENT BONDING PRODUCING A COMPOSITE THE DOW CHEMICAL COMPANY (US) 1989-06-13 US disclosed
US-4797187-A COACERVATION OF CATIONS THE DOW CHEMICAL COMPANY (US) 1989-01-10 US disclosed
US-4704324-A REVERSE OSMOSIS, GAS SEPARATION, ULTRAFILTRATION THE DOW CHEMICAL COMPANY (US) 1987-11-03 US disclosed
WO-1987002682-A1 SEMI-PERMEABLE MEMBRANES PREPARED VIA REACTION OF CATIONIC GROUPS WITH NUCLEOPHILIC GROUPS THE DOW CHEMICAL COMPANY (US) 1987-05-07 WO disclosed
EP-0220660-A2 Semi-permeables membranes prepared via reaction of cationic groups with nucleophilic groups THE DOW CHEMICAL COMPANY (US) 1987-05-06 EP disclosed
US-4469836-A Perfluorocarbon based polymeric coatings having low critical surface tensions THE DOW CHEMICAL COMPANY (US) 1984-09-04 US disclosed