Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7930573

CCOC(=O)c1ccc([P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1.[Cl-]

nearest known ligand 0.58

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
NAMPT known ✓ P43490 1/20 0.49
MEN1 O00255 5/20 0.58
KMT2A Q03164 5/20 0.58
SMN1; SMN2 Q16637 4/20 0.57
ALDH1A1 P00352 3/20 0.57
CA12 O43570 1/20 0.56
CA1 P00915 1/20 0.56
CA2 P00918 1/20 0.56
ESR1 P03372 1/20 0.56
CA7 P43166 1/20 0.56
CA9 Q16790 1/20 0.56
ESR2 Q92731 1/20 0.56
CA14 Q9ULX7 1/20 0.56
RAB9A P51151 4/20 0.55
NPC1 O15118 3/20 0.55
GAA P10253 2/20 0.55
LMNA P02545 2/20 0.54
CYP1A2 P05177 1/20 0.54
CYP3A4 P08684 1/20 0.54
MAOA P21397 1/20 0.54

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
Benzene SCHEMBL27873122 0.84 CA1 (0.76) MEN1KMT2ASMN1; SMN2ALDH1A1CA12
Ethyl Benzoate SCHEMBL11021859 0.82 LMNA (0.66) MEN1KMT2ASMN1; SMN2ALDH1A1CA12
Ethyl Benzoate SCHEMBL11149423 0.82 LMNA (0.66) MEN1KMT2ASMN1; SMN2ALDH1A1CA12
Ethyl Benzoate SCHEMBL11441694 0.82 LMNA (0.66) MEN1KMT2ASMN1; SMN2ALDH1A1CA12
Ethyl Benzoate SCHEMBL10340354 0.82 LMNA (0.66) MEN1KMT2ASMN1; SMN2ALDH1A1CA12
Ethyl Benzoate SCHEMBL11047082 0.82 LMNA (0.66) MEN1KMT2ASMN1; SMN2ALDH1A1CA12
Ethyl Benzoate SCHEMBL25388294 0.82 LMNA (0.70) MEN1KMT2ASMN1; SMN2ALDH1A1CA12
Ethyl Benzoate SCHEMBL2762273 0.82 LMNA (0.70) MEN1KMT2ASMN1; SMN2ALDH1A1CA12
Ethyl Benzoate SCHEMBL55674 0.82 LMNA (0.70) MEN1KMT2ASMN1; SMN2ALDH1A1CA12
Hydrochloric Acid SCHEMBL9519563 0.81 TSHR (0.64) MEN1KMT2ASMN1; SMN2ALDH1A1CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
US-5892089-A FROM DIARYL OXALATE IN LIQUID PHASE BY DECARBONYLATION USING ORGANIC PHOSHORUS COMPOUND CATALYST UBE INDUSTRIES, LTD. (JP) 1999-04-06 US disclosed
US-5892091-A PHOSPHOROUS CATALYSTS AND HALOGEN ATOMS UBE INDUSTRIES, LTD. (JP) 1999-04-06 US disclosed
EP-0737665-B1 Process for preparation of diaryl carbonate UBE INDUSTRIES (JP) 1998-10-21 EP disclosed
US-5792883-A Preparation of diaryl carbonate UBE INDUSTRIES, LTD. (JP) 1998-08-11 US disclosed
EP-0834496-A1 Preparation of diaryl carbonate UBE INDUSTRIES, LTD. (JP) 1998-04-08 EP disclosed
EP-0834495-A1 Process for preparing diaryl carbonate UBE INDUSTRIES, LTD. (JP) 1998-04-08 EP disclosed
EP-0826658-A1 Catalyst for decarbonylation reaction UBE INDUSTRIES, LTD. (JP) 1998-03-04 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