Bicarbonate

Bicarbonate

SCHEMBL17847277

CC1=CCC(C(C)C)CC1.CC1=CCC(C(C)C)CC1.O=C(O)O.O=C(O)O

nearest known ligand 0.42

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
LMNA P02545 4/20 0.42
NPC1 O15118 1/20 0.38
ALDH1A1 P00352 1/20 0.38
TSHR P16473 1/20 0.38
RAB9A P51151 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
TAS2R46 P59540 6/20 0.33
TAS2R31 P59538 2/20 0.33
TAS2R10 Q9NYW0 2/20 0.33
PTPN1 P18031 2/20 0.33
CYP3A4 P08684 2/20 0.33
ALOX15 P16050 2/20 0.33
HSD11B1 P28845 1/20 0.33
POLB P06746 1/20 0.32
CASP6 P55212 1/20 0.32
CTDSP1 Q9GZU7 1/20 0.32
TDP1 Q9NUW8 1/20 0.32
MEN1 O00255 1/20 0.32
MAPK1 P28482 1/20 0.32
KMT2A Q03164 1/20 0.32

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
Acetic Acid SCHEMBL28183790 0.95 LMNA (0.44) LMNANPC1ALDH1A1TSHRRAB9A
SCHEMBL16796012 0.90 LMNA (0.44) LMNATAS2R46TAS2R31TAS2R10PTPN1
SCHEMBL6882235 0.90 LMNA (0.44) LMNATAS2R46TAS2R31TAS2R10PTPN1
SCHEMBL736990 0.90 LMNA (0.44) LMNATAS2R46TAS2R31TAS2R10PTPN1
SCHEMBL5933973 0.90 LMNA (0.44) LMNATAS2R46TAS2R31TAS2R10PTPN1
SCHEMBL3851126 0.90 LMNA (0.44) LMNATAS2R46TAS2R31TAS2R10PTPN1
SCHEMBL14528164 0.84 LMNA (0.41) LMNANPC1ALDH1A1TSHRRAB9A
SCHEMBL8813386 0.80 LMNA (0.37) LMNATAS2R46TAS2R31TAS2R10PTPN1
SCHEMBL11309572 0.80 LMNA (0.41) LMNANPC1ALDH1A1TSHRRAB9A
SCHEMBL6402023 0.79 LMNA (0.46) LMNANPC1ALDH1A1TSHRRAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3233868-B1 6H-PYRROLO[3,2-B:4,5-B']BIS[1,4]BENZOTHIAZINE-6-CARBOXYLIC ACID ESTERS AS ORGANIC SEMICONDUCTOR MATERIALS FOR USE IN ELECTRONIC DEVICES BASF SE (DE) 2018-11-07 EP disclosed
US-10079346-B2 Heteroaromatic compounds for organic electronics BASF SE (DE) 2018-09-18 US disclosed
US-20170365791-A1 HETEROAROMATIC COMPOUNDS FOR ORGANIC ELECTRONICS BASF SE (DE) 2017-12-21 US disclosed
EP-3233868-A1 6H-PYRROLO[3,2-B:4,5-B']BIS[1,4]BENZOTHIAZINE-6-CARBOXYLIC ACID ESTERS AS ORGANIC SEMICONDUCTOR MATERIALS FOR USE IN ELECTRONIC DEVICES BASF SE (DE) 2017-10-25 EP disclosed
WO-2016096967-A1 6H-PYRROLO[3,2-B:4,5-B']BIS[1,4]BENZOTHIAZINE-6-CARBOXYLIC ACID ESTERS AS ORGANIC SEMICONDUCTOR MATERIALS FOR USE IN ELECTRONIC DEVICES BASF SE (DE) 2016-06-23 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-10079346-B2 Heteroaromatic compounds for organic electronics OR10J3, OR51E2, OXER1 LMNA 3332/4885NPC1 810/4885ALDH1A1 1250/4885
US-20170365791-A1 HETEROAROMATIC COMPOUNDS FOR ORGANIC ELECTRONICS OR10J3, NR0B1, NR0B2 LMNA 2964/4885NPC1 718/4885ALDH1A1 1283/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.