Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6567666

CCCC[N+]1(CCCC)CCOCC1.[Cl-]

nearest known ligand 0.38

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 7)

geneUniProtsupporting neighboursconfidence
CDC25A P30304 1/20 0.36
CTDSP1 Q9GZU7 1/20 0.36
LMNA P02545 1/20 0.33
TSHR P16473 1/20 0.33
THRB P10828 1/20 0.33
HPGD P15428 1/20 0.30
ALOX15 P16050 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
SCHEMBL1962073 0.98 CDC25A (0.37) CDC25ACTDSP1LMNATSHRTHRB
Iodide SCHEMBL10751393 0.95 CTDSP1 (0.39) CDC25ACTDSP1LMNATSHRTHRB
SCHEMBL9936179 0.95 CDC25A (0.36) CDC25ACTDSP1LMNATSHRTHRB
Water SCHEMBL11593967 0.95 CDC25A (0.36) CDC25ACTDSP1LMNATSHRTHRB
SCHEMBL9935048 0.95 CDC25A (0.36) CDC25ACTDSP1LMNATSHRTHRB
SCHEMBL12638482 0.93 CDC25A (0.38) CDC25ACTDSP1LMNATSHRTHRB
SCHEMBL3308384 0.93 CTDSP1 (0.41) CDC25ACTDSP1LMNATSHRTHRB
Bromide SCHEMBL829698 0.91 CTDSP1 (0.41) CDC25ACTDSP1LMNATSHRTHRB
Hydrochloric Acid SCHEMBL11781908 0.91 CDC25A (0.41) CDC25ACTDSP1TSHRTHRB
SCHEMBL8965122 0.91 CDC25A (0.41) CDC25ACTDSP1TSHRTHRB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6806371-B2 BY MEANS OF PHASE TRANSFER CATALYSIS DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO KG (AT) 2004-10-19 US disclosed
EP-1405847-A1 Process to prepare substituted pyridine-N-oxide compounds DSM Fine Chemicals Austria Nfg GmbH & Co KG (AT) 2004-04-07 EP disclosed
US-20040063957-A1 Preparation of substituted pyridine N-oxide compounds DSM FINE CHEMICALS AUSTRIA NFG GMBH & COKG (AT) 2004-04-01 US disclosed
EP-0269884-B1 CATALYZED ALKYLATION OF HALOPYRIDINATES IN THE ABSENCE OF ADDED ORGANIC SOLVENTS DOWELANCO (US) 1991-09-25 EP disclosed
EP-0277292-B1 ORGANIC SOLVENT-FREE PROCESS FOR PREPARING PYRIMIDINYL ORGANOPHOSPHATES THE DOW CHEMICAL COMPANY (US) 1991-05-08 EP disclosed
EP-0277292-A1 Organic solvent-free process for preparing pyrimidinyl organophosphates THE DOW CHEMICAL COMPANY (US) 1988-08-10 EP disclosed
EP-0269884-A1 Catalyzed alkylation of halopyridinates in the absence of added organic solvents DOWELANCO (US) 1988-06-08 EP disclosed
US-4701531-A Catalyzed alkylation of halopyridinates in the absence of added organic solvents THE DOW CHEMICAL COMPANY (US) 1987-10-20 US disclosed
US-4699634-A SEMIPERMEABLE MEMBRANES THE STANDARD OIL COMPANY (US) 1987-10-13 US disclosed
US-4546189-A Preparation of cyano(6-(substituted phenoxy)-2-pyridinyl)methyl esters of 3-(2,2-dihaloethenyl)-2,2-dimethylcyclopropane carboxylic acids THE DOW CHEMICAL COMPANY (US) 1985-10-08 US disclosed
US-4092312-A CATALYST SYSTEM OF A QUATERNARY AMMONIUM SALT AND 1,4-DIAZABICYCLO(2.2.2)OCTANE THE DOW CHEMICAL COMPANY (US) 1978-05-30 US disclosed
US-4086253-A 3,3',5,5'-Tetra-substituted diphenoquinone from 2,6-disubstituted phenol by phase-transfer catalysis THE DOW CHEMICAL COMPANY (US) 1978-04-25 US disclosed
US-4061682-A QUATERNARY AMMONIUM OR PHOSPHONIUM SALT THE DOW CHEMICAL COMPANY (US) 1977-12-06 US disclosed
US-4028439-A QUATERNARY AMMONIUM SALT AND IMIDAZOLE CATALYSTS THE DOW CHEMICAL COMPANY (US) 1977-06-07 US disclosed
US-4016225-A WITH QUATERNARY AMMONIUM SALT AND 1,4-DIAZABICYCLO(2.2.2)OCTANE CATALYST THE DOW CHEMICAL COMPANY (US) 1977-04-05 US disclosed
US-4007197-A QUATERNARY AMMONIUM OR PHOSPHONIUM SALT AND TERTIARY AMINE CATALYST THE DOW CHEMICAL COMPANY (US) 1977-02-08 US disclosed
US-4001293-A Process for production of γ-halonitriles THE DOW CHEMICAL COMPANY (US) 1977-01-04 US disclosed
US-3996259-A QUATERNARY AMMONIUM OR PHOSPHONIUM SALT THE DOW CHEMICAL COMPANY (US) 1976-12-07 US disclosed
US-3974199-A Process for production of cyclopropylcyanide THE DOW CHEMICAL COMPANY (US) 1976-08-10 US disclosed
US-3972887-A QUATERNARY AMMONIUM SALT CATALYST THE DOW CHEMICAL COMPANY (US) 1976-08-03 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-20040063957-A1 Preparation of substituted pyridine N-oxide compounds HRH2, SCO2, CBR1 CDC25A 762/4885CTDSP1 2163/4885LMNA 2031/4885

“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.