Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4387947

[Cl-].c1ccc([P+](c2ccccc2)(c2ccccc2)C2CCCCC2)cc1

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 20)

geneUniProtsupporting neighboursconfidence
IDO1 P14902 2/20 0.38
GAA P10253 2/20 0.35
L3MBTL1 Q9Y468 1/20 0.35
SLC18A3 Q16572 1/20 0.34
HPGD P15428 1/20 0.34
ALDH1A1 P00352 3/20 0.33
MCOLN3 Q8TDD5 1/20 0.33
HIF1A Q16665 1/20 0.33
EPHX2 P34913 2/20 0.32
CYP1A2 P05177 1/20 0.32
GRM5 P41594 1/20 0.32
KDM4E B2RXH2 1/20 0.32
MEN1 O00255 1/20 0.32
KMT2A Q03164 1/20 0.32
LMNA P02545 1/20 0.32
EPHX1 P07099 1/20 0.32
RAB9A P51151 1/20 0.32
SMN1; SMN2 Q16637 1/20 0.32
PTPRC P08575 1/20 0.32
PTPRF P10586 1/20 0.32

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 SCHEMBL7635385 1.00 IDO1 (0.38) IDO1GAAL3MBTL1SLC18A3HPGD
Hydrochloric Acid SCHEMBL7629171 1.00 IDO1 (0.38) IDO1GAAL3MBTL1SLC18A3HPGD
Bromide SCHEMBL10533526 0.98 IDO1 (0.37) IDO1GAAL3MBTL1SLC18A3HPGD
Hydrochloric Acid SCHEMBL6633309 0.98 GAA (0.36) IDO1GAAL3MBTL1SLC18A3HPGD
SCHEMBL29515524 0.98 IDO1 (0.39) IDO1GAAL3MBTL1SLC18A3HPGD
Bromide SCHEMBL3322091 0.95 IDO1 (0.38) IDO1GAAL3MBTL1SLC18A3HPGD
Bromide SCHEMBL2445980 0.95 IDO1 (0.38) IDO1GAAL3MBTL1SLC18A3HPGD
Iodide SCHEMBL7629435 0.95 IDO1 (0.38) IDO1GAAL3MBTL1SLC18A3HPGD
Iodide SCHEMBL7628894 0.95 IDO1 (0.38) IDO1GAAL3MBTL1SLC18A3HPGD
Bromide SCHEMBL7633092 0.95 IDO1 (0.38) IDO1GAAL3MBTL1SLC18A3HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6316575-B1 MELT TRANSESTERIFICATION OF DIOL COMPOUND AND CARBOANTE COMPOUND USING CATALYST COMPRISING A PHOSPHORUS-CONTAINING BASIC COMPOUND QUATERNARY PHOSPHONIUM SALT TO FORM POLYCARBONATE IDEMITSU KOSAN CO., LTD. (JP) 2001-11-13 US claimed
EP-0329021-B1 Preparation of advanced epoxy resins and dihydric phenols in the presence of phosphonium compounds DOW CHEMICAL CO (US) 1994-01-26 EP claimed
EP-0329021-A2 Preparation of advanced epoxy resins and dihydric phenols in the presence of phosphonium compounds THE DOW CHEMICAL COMPANY (US) 1989-08-23 EP claimed
US-4808692-A Preparation of advanced epoxy resins from epoxy resins and dihydric phenols in the presence of phosphonium compounds THE DOW CHEMICAL COMPANY (US) 1989-02-28 US claimed
US-7629431-B2 Polycarbonate prepolymer for solid phase polymerization and process for producing polycarbonate IDEMITSU KOSAN CO., LTD. (JP) 2009-12-08 US disclosed
US-20080064847-A1 Oxidative carbonylation; molecular weight control IDEMISU KOSAN CO., LTD. (JP) 2008-03-13 US disclosed
EP-0807657-B1 PROCESS FOR PRODUCING POLYCARBONATE IDEMITSU KOSAN CO (JP) 2004-05-19 EP disclosed
US-6476249-B1 Copolycarbonate and process for producing the same IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2002-11-05 US disclosed
US-6462165-B1 REDUCED CONTENT OF IMPURITIES SUCH AS REMAINING MONOMERS AND OLIGOMERS AND HAVING EXCELLENT PHYSICAL PROPERTIES SUCH AS IMPACT STRENGTH, AND ALSO TO OPTICAL MATERIALS AND BLOW MOLDING MATERIALS IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2002-10-08 US disclosed
US-6399738-B1 OXIDATIVE CARBONYLATION OF AROMATIC HYDROXY COMPOUND WITH CARBON MONOXIDE AND OXYGEN IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2002-06-04 US disclosed
EP-0780452-B1 Aqueous paint TOYO SEIKAN KAISHA LTD (JP) 2002-03-06 EP disclosed
US-6316575-B1 MELT TRANSESTERIFICATION OF DIOL COMPOUND AND CARBOANTE COMPOUND USING CATALYST COMPRISING A PHOSPHORUS-CONTAINING BASIC COMPOUND QUATERNARY PHOSPHONIUM SALT TO FORM POLYCARBONATE IDEMITSU KOSAN CO., LTD. (JP) 2001-11-13 US disclosed
EP-0414160-B1 Process for preparing advanced epoxy resins DOW CHEMICAL CO (US) 1996-09-11 EP disclosed
EP-0708077-A1 Diamino compounds and methods for preparing them CHISSO CORPORATION (JP) 1996-04-24 EP disclosed
US-5310854-A Solvent, coatings for beverage cans THE DOW CHEMICAL COMPANY (US) 1994-05-10 US disclosed
EP-0329021-B1 Preparation of advanced epoxy resins and dihydric phenols in the presence of phosphonium compounds DOW CHEMICAL CO (US) 1994-01-26 EP disclosed
US-5206312-A Polysiloxanes hydrosilated with unsaturated aromatic alcohols and siloxy-containing compounds having hydroxy groups to advance polyepoxides and epoxy resins; electronics; coatings; composites THE DOW CHEMICAL COMPANY (US) 1993-04-27 US disclosed
EP-0414160-A2 Process for preparing advanced epoxy resins THE DOW CHEMICAL COMPANY (US) 1991-02-27 EP disclosed
EP-0329021-A2 Preparation of advanced epoxy resins and dihydric phenols in the presence of phosphonium compounds THE DOW CHEMICAL COMPANY (US) 1989-08-23 EP disclosed
US-4808692-A Preparation of advanced epoxy resins from epoxy resins and dihydric phenols in the presence of phosphonium compounds THE DOW CHEMICAL COMPANY (US) 1989-02-28 US disclosed