Hydrochloric Acid

Hydrochloric Acid

SCHEMBL14778403

C[n+]1ccn(CCCCCCCCCO)c1.[Cl-]

nearest known ligand 0.66

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 16)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 3/20 0.66
MEN1 O00255 2/20 0.66
HSP90AA1 P07900 2/20 0.66
KMT2A Q03164 2/20 0.66
APAF1 O14727 1/20 0.66
NPC1 O15118 1/20 0.66
PLA2G1B P04054 1/20 0.66
MAPT P10636 1/20 0.66
MAPK1 P28482 1/20 0.66
HTT P42858 1/20 0.66
RAB9A P51151 1/20 0.66
NPSR1 Q6W5P4 1/20 0.66
ATG4B Q9Y4P1 1/20 0.66
FDPS P14324 13/20 0.37
LMNA P02545 1/20 0.36
PON1 P27169 1/20 0.33

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
Hydrochloric Acid SCHEMBL14777598 1.00 SMN1; SMN2 (0.66) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
Hydrochloric Acid SCHEMBL14777932 1.00 SMN1; SMN2 (0.66) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
SCHEMBL18507042 0.98 SMN1; SMN2 (0.68) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
SCHEMBL21490444 0.98 SMN1; SMN2 (0.68) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
Hydrochloric Acid SCHEMBL6115662 0.98 SMN1; SMN2 (0.62) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
SCHEMBL23271637 0.98 SMN1; SMN2 (0.68) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
Iodide SCHEMBL14778060 0.96 SMN1; SMN2 (0.66) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
Bromide SCHEMBL14778818 0.96 SMN1; SMN2 (0.71) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
Bromide SCHEMBL14777595 0.96 SMN1; SMN2 (0.71) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
Bromide SCHEMBL14779135 0.96 SMN1; SMN2 (0.71) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8658842-B2 Process for producing ethylene glycol catalyzed by ionic liquid INSTITUTE OF PROCESS ENGINEERING, CHINESE ACADEMY OF SCIENCES (CN) 2014-02-25 US disclosed
US-20130072727-A1 PROCESS FOR PRODUCING ETHYLENE GLYCOL CATALYZED BY IONIC LIQUID INSTITUTE OF PROCESS ENGINEERING, CHINESE ACADEMY OF SCIENCES (CN) 2013-03-21 US 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-20130072727-A1 PROCESS FOR PRODUCING ETHYLENE GLYCOL CATALYZED BY IONIC LIQUID AGL, ALKBH3, ELL SMN1; SMN2 3065/4885MEN1 4002/4885HSP90AA1 3161/4885

“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.