Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7045853

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

nearest known ligand 0.30

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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 2)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 1/20 0.30
BBOX1 O75936 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 SCHEMBL142822 0.91 ACHE (0.33) ACHEBBOX1
SCHEMBL361078 0.87 ACHE (0.34) ACHEBBOX1
Hydrochloric Acid SCHEMBL27740878 0.87 BBOX1 (0.31) BBOX1
Water SCHEMBL5407242 0.84 ACHE (0.33) ACHEBBOX1
Iodide SCHEMBL28293289 0.84 ACHE (0.33) ACHEBBOX1
Bromide SCHEMBL4276591 0.84 ACHE (0.37) ACHEBBOX1
Fluoride Ion SCHEMBL6689085 0.84 ACHE (0.33) ACHEBBOX1
Ammonia Solution, Strong SCHEMBL6558011 0.84 ACHE (0.33) ACHEBBOX1
SCHEMBL5447792 0.81 ACHE (0.31) ACHEBBOX1
SCHEMBL8019334 0.81 ACHE (0.31) ACHEBBOX1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6646083-B2 Such as diallyldimethylammonium chloride crosslinked with 1,3-bis(N,N-diallylpiperid-1-ium-4-yl) propane dichloride; thermal stability; use as polymer catalyst for producing glycols from oxiranes; ion exchange catalyst NIPPON SHOKUBAI CO., LTD. (JP) 2003-11-11 US disclosed
US-20030130510-A1 Process for producing N-hydroxyalkyl compound, and tris (2-hydroxyethyl) isocyanurate composition NIPPON SHOKUBAI CO., LTD. 2003-07-10 US disclosed
EP-1323706-A1 Process for producing N-hydroxyalkyl compound, and tris(2-hydroxyethyl) isocyanurate composition Nippon Shokubai Co., Ltd. (JP) 2003-07-02 EP disclosed
US-20020028887-A1 Crosslinked polymer, method for manufacturing it and use thereof NIPPON SHOKUBAI CO., LTD. (JP) 2002-03-07 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-20030130510-A1 Process for producing N-hydroxyalkyl compound, and tris (2-hydroxyethyl) isocyanurate composition HAAO, ALKBH3, FTO ACHE 1208/4885BBOX1 755/4885

“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.