Hydrochloric Acid

Hydrochloric Acid

SCHEMBL556929

CCCn1cc[n+](C)c1.[Cl-]

nearest known ligand 0.73

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 5/20 0.39
PON1 P27169 3/20 0.37
LMNA P02545 1/20 0.37

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
SCHEMBL17139699 0.98 SMN1; SMN2 (0.68) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
SCHEMBL293656 0.98
Iodide SCHEMBL180142 0.95 SMN1; SMN2 (0.66) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
Fluoride Ion SCHEMBL1898574 0.95 SMN1; SMN2 (0.66) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
Bromide SCHEMBL557293 0.95 SMN1; SMN2 (0.71) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
Fluoride SCHEMBL28444338 0.95 SMN1; SMN2 (0.66) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
Water SCHEMBL28929074 0.95 SMN1; SMN2 (0.66) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
Iodide SCHEMBL3774573 0.95 SMN1; SMN2 (0.66) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
Hydrochloric Acid SCHEMBL8018852 0.92 MEN1 (0.73) SMN1; SMN2MEN1HSP90AA1KMT2AAPAF1
SCHEMBL25362454 0.90 SMN1; SMN2 (0.59) 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 334 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250188048-A1 METHOD FOR PREPARING 2,5-FURANDICARBOXYLIC ACID COMPOUND JIANGSU CELLURANICS NEW MATERIAL TECHNOLOGY CO., LTD. (CN) 2025-06-12 US claimed
CN-119350702-A Preparation method of spectrum-adjustable flexible cellulose-based aerogel material 南京工业大学 2025-01-24 CN claimed
EP-4477651-A1 METHOD FOR PREPARING 2,5-FURANDICARBOXYLIC ACID COMPOUND Jiangsu Celluranics New Material Technology Co., Ltd. (CN) 2024-12-18 EP claimed
CN-119049824-A Magnetorheological shear thickening fluid with flame retardant and anti-sedimentation effects and preparation method thereof 中国科学技术大学 2024-11-29 CN claimed
CN-112624131-B Preparation method of monodisperse large-particle-size silicon dioxide microspheres 深圳先进电子材料国际创新研究院 2022-09-06 CN claimed
CN-112791010-B Chestnut shell aerogel and preparation method and application thereof 华南理工大学 2022-05-24 CN claimed
CN-114420896-A High-rate lithium battery negative electrode piece and preparation method and application thereof 中国科学院上海硅酸盐研究所 2022-04-29 CN claimed
CN-109651114-B Method for synthesizing alkyl aromatic aldehyde 中国石油化工股份有限公司 2022-04-05 CN claimed
CN-109647528-B Catalyst for synthesizing alkyl aromatic aldehyde 中国石油化工股份有限公司 2022-04-05 CN claimed
CN-109651112-B Method for synthesizing alkyl aromatic aldehyde by alkyl aromatic hydrocarbon carbonylation 中国石油化工股份有限公司 2022-04-01 CN claimed
US-20050205493-A1 Ionic liquids as solvents in headspace gas chromatography NOVARTIS AG (CH) 2005-09-22 US claimed
EP-1311472-B1 METHOD FOR PREPARING ALKOXYAMINES FROM NITROXIDES ATOFINA (FR) 2004-10-20 EP claimed
US-6700007-B2 IN A BIPHASIC MEDIUM, BY MIXING AN IONIC LIQUID SUCH AS AN ALKYLIMIDAZOLIUM HALIDE, AN ORGANIC SOLVENT, A TRANSITION METAL SALT, A METAL LIGAND, A HALOHYDROCARBON AND A NITROXIDE ATOFINA (FR) 2004-03-02 US claimed
US-6579343-B2 Contacting gas with a liquid ionic compound comprising a nitrogen-containing heterocyclic cation UNIVERSITY OF NOTRE DAME DU LAC 2003-06-17 US claimed
US-20030050507-A1 Method for prepararing alkoxyamines from nitroxides ATOFINA (FR) 2003-03-13 US claimed
US-20020189444-A1 Purification of gas with liquid ionic compounds NATIONAL SCIENCE FOUNDATION 2002-12-19 US claimed
WO-2000040673-A1 INDUSTRIAL PROCESS AND CATALYSTS THE SECRETARY OF STATE FOR DEFENCE (GB) 2000-07-13 WO 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-0791643-A1 Lubricating oils BP Chemicals Limited (GB) 1997-08-27 EP claimed

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-20030050507-A1 Method for prepararing alkoxyamines from nitroxides ZYX, ZFX, PNMT SMN1; SMN2 3622/4885MEN1 4242/4885HSP90AA1 4154/4885
US-20250188048-A1 METHOD FOR PREPARING 2,5-FURANDICARBOXYLIC ACID COMPOUND HPD, DPYD, PGD SMN1; SMN2 4474/4885MEN1 4667/4885HSP90AA1 3762/4885

“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.