Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7058630

Cc1ccc([P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1.[Cl-]

nearest known ligand 0.50

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
ACHE known ✓ P22303 3/20 0.50
LMNA P02545 3/20 0.50
TSHR P16473 2/20 0.50
ALOX12 P18054 1/20 0.50
HPGD P15428 3/20 0.42
TDP1 Q9NUW8 3/20 0.42
CES2 O00748 1/20 0.39
CES1 P23141 1/20 0.39
RAB9A P51151 4/20 0.38
NPC1 O15118 3/20 0.38
L3MBTL1 Q9Y468 3/20 0.38
MEN1 O00255 2/20 0.38
KMT2A Q03164 2/20 0.38
MAPT P10636 1/20 0.38
HKDC1 Q2TB90 1/20 0.38
NPSR1 Q6W5P4 1/20 0.38
HIF1A Q16665 1/20 0.36
SMN1; SMN2 Q16637 4/20 0.35
POLB P06746 2/20 0.35
HTT P42858 1/20 0.35

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
SCHEMBL29404005 0.97 ACHE (0.53) ACHELMNATSHRALOX12HPGD
Iodide SCHEMBL7065210 0.95 LMNA (0.50) ACHELMNATSHRALOX12HPGD
Bromide SCHEMBL7063570 0.95 ACHE (0.50) ACHELMNATSHRALOX12HPGD
Hydrochloric Acid SCHEMBL7932457 0.89 ACHE (0.53) ACHELMNATSHRALOX12TDP1
SCHEMBL7065118 0.88 ACHE (0.43) ACHELMNATSHRALOX12HPGD
SCHEMBL11314306 0.88 ACHE (0.43) ACHELMNATSHRALOX12HPGD
Bromide SCHEMBL9181860 0.86 ACHE (0.50) ACHELMNATSHRALOX12TDP1
SCHEMBL503495 0.84 TSHR (0.40) ACHELMNATSHRALOX12HPGD
Thiocyanic Acid SCHEMBL4447159 0.84 ALDH1A1 (0.43) ACHELMNATSHRALOX12HPGD
SCHEMBL7065117 0.84 ACHE (0.40) ACHELMNATSHRALOX12HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9174918-B2 Process for preparing diaryl oxalate UBE INDUSTRIES, LTD. (JP) 2015-11-03 US disclosed
US-20120296063-A1 PROCESS FOR PREPARING DIARYL OXALATE UBE CORPORATION (JP) 2012-11-22 US disclosed
EP-1013633-B1 Process for producing a diaryl carbonate UBE INDUSTRIES (JP) 2003-05-28 EP disclosed
EP-0832910-B1 Process for producing a polycarbonate UBE INDUSTRIES (JP) 2002-06-26 EP disclosed
EP-0832872-B1 Process for producing diaryl carbonate UBE INDUSTRIES (JP) 2002-01-30 EP disclosed
EP-0795539-B1 Process for producing a diaryl carbonate UBE INDUSTRIES (JP) 2001-10-31 EP disclosed
EP-0834496-B1 Preparation of diaryl carbonate UBE INDUSTRIES (JP) 2001-08-16 EP disclosed
EP-0834495-B1 Process for preparing diaryl carbonate UBE INDUSTRIES (JP) 2000-12-27 EP disclosed
EP-1013633-A1 Process for producing a diaryl carbonate Ube Industries, Ltd. (JP) 2000-06-28 EP disclosed
US-5922827-A Process for producing a polycarbonate UBE INDUSTRIES, LTD. (JP) 1999-07-13 US disclosed
EP-0834496-A1 Preparation of diaryl carbonate UBE INDUSTRIES, LTD. (JP) 1998-04-08 EP disclosed
EP-0832910-A2 Process for producing a polycarbonate UBE INDUSTRIES, LTD. (JP) 1998-04-01 EP disclosed
EP-0832872-A1 Process for producing diaryl carbonate UBE INDUSTRIES, LTD. (JP) 1998-04-01 EP disclosed
US-5731453-A Process for producing a diaryl carbonate UBE INDUSTRIES, LTD. (JP) 1998-03-24 US disclosed
EP-0826658-A1 Catalyst for decarbonylation reaction UBE INDUSTRIES, LTD. (JP) 1998-03-04 EP disclosed
EP-0795539-A1 Process for producing a diaryl carbonate UBE INDUSTRIES LIMITED (JP) 1997-09-17 EP disclosed
US-5648510-A DECARBONYLATION OF OXALATE UBE INDUSTRIES, LTD. (JP) 1997-07-15 US disclosed
EP-0737665-A1 Process for preparation of diaryl carbonate UBE INDUSTRIES, LTD. (JP) 1996-10-16 EP disclosed
US-4324927-A Process for the homologization of methanol RHONE-POULENC INDUSTRIES (FR) 1982-04-13 US disclosed
US-4306091-A CATALYTIC HYDROCARBONYLATION OF METHANOL IN THE PRESENCE OF COBALT, RUTHENIUM AND AN ALKYL HALIDE AND AN IONIC HALIDE RHONE-POULENC INDUSTRIES (FR) 1981-12-15 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-20120296063-A1 PROCESS FOR PREPARING DIARYL OXALATE TH, CYP2E1, ADH1A ACHE 671/4885LMNA 3146/4885TSHR 1038/4885

“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.