Hydrochloric Acid

Hydrochloric Acid

SCHEMBL367303

CCCCCCCCCC(CCC)[n+]1cc[nH]c1.[Cl-]

nearest known ligand 0.34

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
LMNA P02545 2/20 0.34
MAPT P10636 2/20 0.32
MEN1 O00255 1/20 0.32
MAPK1 P28482 1/20 0.32
CASP2 P42575 1/20 0.32
KMT2A Q03164 1/20 0.32
SMN1; SMN2 Q16637 1/20 0.32
HSPD1 P10809 1/20 0.31
RAD52 P43351 1/20 0.31
HSPE1 P61604 1/20 0.31
CYP2D6 P10635 2/20 0.30
SPHK1 Q9NYA1 1/20 0.30
GMNN O75496 1/20 0.30
POLB P06746 1/20 0.30
THPO P40225 1/20 0.30
MTOR P42345 1/20 0.30
BLM P54132 1/20 0.30
KDM4E B2RXH2 1/20 0.30
TP53 P04637 1/20 0.30
CYP1A2 P05177 1/20 0.30

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 SCHEMBL15052946 1.00 LMNA (0.34) LMNAMAPTMEN1MAPK1CASP2
Hydrochloric Acid SCHEMBL368041 1.00 LMNA (0.34) LMNAMAPTMEN1MAPK1CASP2
Hydrochloric Acid SCHEMBL2293581 1.00 LMNA (0.34) LMNAMAPTMEN1MAPK1CASP2
Hydrochloric Acid SCHEMBL367287 1.00 LMNA (0.34) LMNAMAPTMEN1MAPK1CASP2
SCHEMBL367893 0.98 LMNA (0.35) LMNAMAPTCYP2D6SPHK1GMNN
Hydrochloric Acid SCHEMBL365179 0.98 LMNA (0.31) LMNA
Iodide SCHEMBL15008381 0.97 LMNA (0.34) LMNAMAPTSMN1; SMN2CYP2D6SPHK1
Iodide SCHEMBL15008594 0.97 LMNA (0.34) LMNAMAPTSMN1; SMN2CYP2D6SPHK1
Iodide SCHEMBL15053220 0.97 LMNA (0.34) LMNAMAPTSMN1; SMN2CYP2D6SPHK1
Iodide SCHEMBL15008815 0.97 LMNA (0.34) LMNAMAPTSMN1; SMN2CYP2D6SPHK1

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 33 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110185788-A1 IONIC LIQUIDS AS SOLVENTS IN HEADSPACE GAS CHROMATOGRAPHY KOCH PETER 2011-08-04 US claimed
US-20100239524-A1 MICROPARTICLES PREPARED USING AN IONIC LIQUID NOVARTIS AG (CH) 2010-09-23 US claimed
US-7569149-B2 Ionic liquids as solvents in headspace gas chromatography NOVARTIS AG (CH) 2009-08-04 US claimed
US-20050205493-A1 Ionic liquids as solvents in headspace gas chromatography NOVARTIS AG (CH) 2005-09-22 US claimed
US-5994602-A IN THE PRESENCE OF A HYDROCARBYL ALUMINUM OR GALLIUM HALIDE AND A HYDROCARBYL-SUBSTITUTED IMIDAZOLIUM OR PYRIDINIUM HALIDE BP CHEMICALS LIMITED (GB) 1999-11-30 US claimed
EP-0693045-B1 ALKYLATION PROCESS BP CHEM INT LTD (GB) 1997-10-22 EP claimed
EP-0693045-A1 ALKYLATION PROCESS BP CHEM INT LTD (GB) 1996-01-24 EP claimed
WO-1995021872-A1 IONIC LIQUIDS BP CHEMICALS LIMITED (GB) 1995-08-17 WO claimed
WO-1995021806-A1 ALKYLATION PROCESS BP CHEMICALS LIMITED (GB) 1995-08-17 WO claimed
EP-2593403-B1 METHOD FOR PRODUCING A GEL FILM AND FILTRATION MEMBRANE PREPARED WITH THIS METHOD UNIV MONASH (AU) 2020-03-04 EP disclosed
US-10297396-B2 Graphene-based films MONASH UNIVERSITY (AU) 2019-05-21 US disclosed
EP-2615632-B1 MICROSTRUCTURE MANUFACTURING METHOD USING TREATMENT LIQUID FOR INHIBITING PATTERN COLLAPSE IN MICROSTRUCTURES MITSUBISHI GAS CHEMICAL CO (JP) 2019-05-08 EP disclosed
US-9751763-B2 Material and applications therefor MONASH UNIVERSITY (AU) 2017-09-05 US disclosed
US-20160016804-A1 GRAPHENE-BASED FILMS MONASH UNIVERSITY (AU) 2016-01-21 US disclosed
WO-2000041809-A1 IONIC LIQUID CATALYST FOR ALKYLATION BP CHEMICALS LIMITED (GB) 2000-07-20 WO disclosed
US-5994602-A IN THE PRESENCE OF A HYDROCARBYL ALUMINUM OR GALLIUM HALIDE AND A HYDROCARBYL-SUBSTITUTED IMIDAZOLIUM OR PYRIDINIUM HALIDE BP CHEMICALS LIMITED (GB) 1999-11-30 US disclosed
EP-0693045-B1 ALKYLATION PROCESS BP CHEM INT LTD (GB) 1997-10-22 EP disclosed
EP-0693045-A1 ALKYLATION PROCESS BP CHEM INT LTD (GB) 1996-01-24 EP disclosed
WO-1995021806-A1 ALKYLATION PROCESS BP CHEMICALS LIMITED (GB) 1995-08-17 WO disclosed
WO-1995021872-A1 IONIC LIQUIDS BP CHEMICALS LIMITED (GB) 1995-08-17 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 (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-20100239524-A1 MICROPARTICLES PREPARED USING AN IONIC LIQUID FIBP, MIF, CHMP4B LMNA 142/4885MAPT 1567/4885MEN1 1303/4885

“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.