Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4131844

C=C(C)C(=O)OCC[N+](C)(C)C.C=C(C)C(=O)OCC[N+](C)(C)C.CC=C(C)C(=O)[O-].[Cl-]

nearest known ligand 0.49

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Hydrochloric Acid. 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
CHRM1 known ✓ P11229 6/20 0.49
CHRM3 known ✓ P20309 6/20 0.49
CHRM2 known ✓ P08172 5/20 0.46
ACHE known ✓ P22303 2/20 0.36
CHRM5 P08912 6/20 0.49
CHRM4 P08173 5/20 0.46
CHRNB2 P17787 4/20 0.46
CHRNA4 P43681 4/20 0.46
CHRNA7 P36544 3/20 0.46
SMN1; SMN2 Q16637 2/20 0.46
HTR1A P08908 2/20 0.46
PGR P06401 1/20 0.46
TBXA2R P21731 1/20 0.46
CHRNB4 P30926 1/20 0.46
CHRNA3 P32297 1/20 0.46
CHRNA10 Q9GZZ6 1/20 0.46
CHRNA9 Q9UGM1 1/20 0.46
GALR3 O60755 2/20 0.45
MAPT P10636 1/20 0.44
BLM P54132 1/20 0.44

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
Acrylic Acid SCHEMBL3945710 0.94 CHRM5 (0.44) CHRM5CHRM1CHRM3CHRM2CHRM4
Methacrylic Acid SCHEMBL21931217 0.89 CHRM5 (0.57) CHRM5CHRM1CHRM3CHRM2CHRM4
Methacrylic Acid SCHEMBL2511701 0.89 CHRM5 (0.57) CHRM5CHRM1CHRM3CHRM2CHRM4
Acrylic Acid Ethyl Ester SCHEMBL13519363 0.88 THRB (0.39) CHRM5CHRM1CHRM3CHRM2CHRM4
Methacrylic Acid SCHEMBL16444097 0.87 CHRM5 (0.55) CHRM5CHRM1CHRM3CHRM2CHRM4
Acetic Acid SCHEMBL9619910 0.87 CHRM5 (0.59) CHRM5CHRM1CHRM3CHRM2CHRM4
Hydrochloric Acid SCHEMBL8612391 0.85 THRB (0.42) CHRM5CHRM1CHRM3CHRM2APEX1
Hydrochloric Acid SCHEMBL15954 0.85 CHRM5 (0.65) CHRM5CHRM1CHRM3CHRM2CHRM4
SCHEMBL180003 0.85 CHRM5 (0.65) CHRM5CHRM1CHRM3CHRM2CHRM4
Hydrochloric Acid SCHEMBL30183040 0.85 CHRM5 (0.65) CHRM5CHRM1CHRM3CHRM2CHRM4

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
EP-2079450-A2 METHOD OF PREPARING SOLID DOSAGE FORMS OF MULTI-PHASIC PHARMACEUTICAL COMPOSITIONS Novavax, INC. (US) 2009-07-22 EP claimed
WO-2008063910-A2 METHOD OF PREPARING SOLID DOSAGE FORMS OF MULTI-PHASIC PHARMACEUTICAL COMPOSITIONS NOVAVAX, INC. (US) 2008-05-29 WO claimed
EP-2079450-A2 METHOD OF PREPARING SOLID DOSAGE FORMS OF MULTI-PHASIC PHARMACEUTICAL COMPOSITIONS Novavax, INC. (US) 2009-07-22 EP disclosed
EP-2059518-A2 SALTS OF BENZIMIDAZOLYL PYRIDYL ETHERS AND FORMULATIONS THEREOF Novartis AG (CH) 2009-05-20 EP disclosed
EP-2051702-A1 MULTI-PHASIC PHARMACEUTICAL FORMULATIONS OF POORLY WATER-SOLUBLE DRUGS FOR REDUCED FED/FASTED VARIABILITY AND IMPROVED ORAL BIOAVAILABILITY Novavax, Inc. (US) 2009-04-29 EP disclosed
EP-2046292-A2 FORMULATIONS FOR BENZIMIDAZOLYL PYRIDYL ETHERS Novartis AG (CH) 2009-04-15 EP disclosed
WO-2008091855-A1 MULTI-PHASIC PHARMACEUTICAL FORMULATIONS OF POORLY WATER-SOLUBLE DRUGS FOR REDUCED FED/FASTED VARIABILITY AND IMPROVED ORAL BIOAVAILABILITY NOVAVAX, INC. (US) 2008-07-31 WO disclosed
WO-2008063910-A2 METHOD OF PREPARING SOLID DOSAGE FORMS OF MULTI-PHASIC PHARMACEUTICAL COMPOSITIONS NOVAVAX, INC. (US) 2008-05-29 WO disclosed
WO-2008027523-A2 SALTS OF BENZIMIDAZOLYL PYRIDYL ETHERS AND FORMULATIONS THEREOF NOVARTIS AG (CH) 2008-03-06 WO disclosed
WO-2008011154-A2 FORMULATIONS FOR BENZIMIDAZOLYL PYRIDYL ETHERS NOVARTIS AG (CH) 2008-01-24 WO disclosed