Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4367840

C=CC[n+]1ccn(CCC)c1.[Cl-]

nearest known ligand 0.42

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 15)

geneUniProtsupporting neighboursconfidence
FDPS P14324 16/20 0.42
MEN1 O00255 2/20 0.39
HSP90AA1 P07900 2/20 0.39
KMT2A Q03164 2/20 0.39
SMN1; SMN2 Q16637 2/20 0.39
APAF1 O14727 1/20 0.35
NPC1 O15118 1/20 0.35
PLA2G1B P04054 1/20 0.35
MAPT P10636 1/20 0.35
MAPK1 P28482 1/20 0.35
HTT P42858 1/20 0.35
RAB9A P51151 1/20 0.35
NPSR1 Q6W5P4 1/20 0.35
ATG4B Q9Y4P1 1/20 0.35
PON1 P27169 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
SCHEMBL3304991 0.98 FDPS (0.43) FDPSMEN1HSP90AA1KMT2ASMN1; SMN2
Iodide SCHEMBL4363776 0.96 FDPS (0.42) FDPSMEN1HSP90AA1KMT2ASMN1; SMN2
Bromide SCHEMBL28977684 0.96 FDPS (0.42) FDPSMEN1HSP90AA1KMT2ASMN1; SMN2
SCHEMBL28921008 0.92 FDPS (0.40) FDPSMEN1HSP90AA1KMT2ASMN1; SMN2
Hydrochloric Acid SCHEMBL3803548 0.90 MEN1 (0.47) FDPSMEN1HSP90AA1KMT2ASMN1; SMN2
Thiocyanic Acid SCHEMBL28711222 0.89 FDPS (0.38) FDPSMEN1HSP90AA1KMT2ASMN1; SMN2
SCHEMBL1931515 0.88 MEN1 (0.48) FDPSMEN1HSP90AA1KMT2ASMN1; SMN2
Hydrochloric Acid SCHEMBL2900815 0.87 MEN1 (0.55) FDPSMEN1HSP90AA1KMT2ASMN1; SMN2
SCHEMBL20840133 0.87 MEN1 (0.33) FDPSMEN1HSP90AA1KMT2ASMN1; SMN2
SCHEMBL1680334 0.86 MEN1 (0.54) FDPSMEN1HSP90AA1KMT2ASMN1; 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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120118462-A Preparation method and application of ZnO QDs/Ga@ amphiphilic thin-wall cellulose composite material 昆明理工大学 2025-06-10 CN disclosed
EP-1721900-B1 NOVEL IMIDAZOLIUM COMPOUND KANTO KAGAKU (JP) 2014-06-11 EP disclosed
US-7517999-B2 needs no complicated operations for dissolution and has excellent handleability and a high ionic conductivity, electrolytes; 1-butyl-3-allylimidazolium bromide KANTO KAGAKU KABUSHIKI KAISHA (JP) 2009-04-14 US disclosed
US-20070191612-A1 Needs no complicated operations for dissolution and has excellent handleability and a high ionic conductivity, electrolytes; 1-butyl-3-allylimidazolium bromide HIROYUKI OHNO (JP) 2007-08-16 US disclosed
EP-1721900-A1 NOVEL IMIDAZOLIUM COMPOUND Kanto Kagaku Kabushiki Kaisha (JP) 2006-11-15 EP 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 (1 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-20070191612-A1 Needs no complicated operations for dissolution and has excellent handleability and a high ionic conductivity, electrolytes; 1-butyl-3-allylimidazolium bromide SLC26A3, KCNJ11, SLC26A4 FDPS 4229/4885MEN1 636/4885HSP90AA1 3528/4885

“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.