Hydrochloric Acid

Hydrochloric Acid

SCHEMBL324011

C=C(CCC[N+](C)(C)C)C(=O)O.[Cl-]

nearest known ligand 0.52

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 2/20 0.52
APEX1 P27695 3/20 0.40
NPSR1 Q6W5P4 1/20 0.40
BBOX1 O75936 5/20 0.39
MAPT P10636 1/20 0.39
BLM P54132 1/20 0.39
ENPP2 Q13822 3/20 0.39
TBXAS1 P24557 2/20 0.38
MEN1 O00255 2/20 0.36
NFKB1 P19838 2/20 0.36
KMT2A Q03164 2/20 0.36
LMNA P02545 2/20 0.36
KDM4E B2RXH2 1/20 0.36
SMN1; SMN2 Q16637 1/20 0.36
HSD17B10 Q99714 1/20 0.36
HRH3 Q9Y5N1 1/20 0.36
TSHR P16473 1/20 0.36
RAB9A P51151 1/20 0.36
PMP22 Q01453 1/20 0.36
ALDH1A1 P00352 1/20 0.36

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 SCHEMBL2936558 0.96 ACHE (0.52) ACHEAPEX1NPSR1BBOX1MAPT
Methacrylic Acid SCHEMBL6561454 0.94 ACHE (0.52) ACHEAPEX1NPSR1BBOX1MAPT
Hydrochloric Acid SCHEMBL8222907 0.92 ACHE (0.45) ACHEAPEX1NPSR1BBOX1MAPT
Hydrochloric Acid SCHEMBL8695365 0.92 ACHE (0.45) ACHEAPEX1NPSR1BBOX1MAPT
Hydrochloric Acid SCHEMBL9497105 0.92 APEX1 (0.48) ACHEAPEX1NPSR1ENPP2TBXAS1
Hydrochloric Acid SCHEMBL1703796 0.89 ACHE (0.45) ACHEAPEX1NPSR1BBOX1ENPP2
Methacrylic Acid SCHEMBL159154 0.87 ACHE (0.48) ACHEBBOX1ENPP2SMN1; SMN2ADRA2A
Hydrochloric Acid SCHEMBL6550800 0.86 BLM (0.41) ACHEAPEX1MAPTBLMENPP2
Hydrochloric Acid SCHEMBL7209013 0.85 ACHE (0.39) ACHEBBOX1MAPTBLMENPP2
SCHEMBL7093817 0.84 ACHE (0.41) ACHEAPEX1MAPTBLMLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2358333-B1 COATED COLORING AGENTS HENKEL AG & CO KGAA (DE) 2016-08-17 EP claimed
US-9308176-B2 Less abusable pharmaceutical preparations SUPERNUS PHARMACEUTICALS, INC (US) 2016-04-12 US claimed
US-9144551-B2 Drug formulations having reduced abuse potential SUPERNUS PHARMACEUTICALS, INC. (US) 2015-09-29 US claimed
US-20150150816-A1 DRUG FORMULATIONS HAVING REDUCED ABUSE POTENTIAL SUPERNUS PHARMACEUTICALS, INC. (US) 2015-06-04 US claimed
US-8906413-B2 Drug formulations having reduced abuse potential SUPERNUS PHARMACEUTICALS, INC. (US) 2014-12-09 US claimed
EP-1809259-B1 LESS ABUSABLE PHARMACEUTICAL PREPARATIONS SUPERNUS PHARMACEUTICALS INC (US) 2014-12-03 EP claimed
EP-1624860-B1 DRUG FORMULATIONS HAVING REDUCED ABUSE POTENTIAL SUPERNUS PHARMACEUTICALS INC (US) 2014-02-12 EP claimed
EP-2494961-A1 Drug formulations having reduced abuse potential Supernus Pharmaceuticals, Inc. (US) 2012-09-05 EP claimed
US-20100029853-A1 Controlled architecture copolymers prepared from vinyl phosphonate monomers Rhodia Receherches et Technologies (FR) 2010-02-04 US claimed
US-20090306297-A1 PROCESS FOR PREPARING A COPOLYMER WITH CONTROLLED ARCHITECTURE, OF TELOMER OR BLOCK COPOLYMER TYPE, OBTAINED FROM VINYL PHOSPHONATE MONOMERS, BY IODINE TRANSFER POLYMERIZATION CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2009-12-10 US claimed
WO-2006044805-A2 LESS ABUSABLE PHARMACEUTICAL PREPARATIONS SUPERNUS PHARMACEUTICALS, INC. (US) 2006-04-27 WO claimed
US-20060083690-A1 Less abusable pharmaceutical preparations SUPERNUS PHARMACEUTICALS, INC. 2006-04-20 US claimed
EP-1624860-A2 DRUG FORMULATIONS HAVING REDUCED ABUSE POTENTIAL Shire Laboratories Inc. (US) 2006-02-15 EP claimed
US-6974591-B2 Method for producing a controlled-release preparation WATSON LABORATORIES, INC. (US) 2005-12-13 US claimed
WO-2004100894-A2 DRUG FORMULATIONS HAVING REDUCED ABUSE POTENTIAL SHIRE LABORATORIES, INC. (US) 2004-11-25 WO claimed
EP-1478349-A1 A METHOD FOR RELEASING NANOSIZED PARTICLES OF AN ACTIVE SUBSTANCE FROM A DIFFUSION-CONTROLLED PHARMACEUTICAL COMPOSITION FOR ORAL USE Amarin Development AB (SE) 2004-11-24 EP claimed
US-20040228802-A1 Dosage forms when the drug is properly administered, free of bitter taste, no coloring; when administering not follow the instructions, crushed or extracted and nasally, orally, buccally or sublingually administered, drug will taste bitter, forming color to stain human tissue SUPERNUS PHARMACEUTICALS, INC. 2004-11-18 US claimed
US-20030215513-A1 Method for releasing nanosized particles of an active substance from a diffusion-controlled pharmaceutical composition for oral use AMARIN DEVELOPMENT AB (SE) 2003-11-20 US claimed
WO-2003070225-A1 A METHOD FOR RELEASING NANOSIZED PARTICLES OF AN ACTIVE SUBSTANCE FROM A DIFFUSION-CONTROLLED PHARMACEUTICAL COMPOSITION FOR ORAL USE AMARIN DEVELOPMENT AB (SE) 2003-08-28 WO claimed
US-4758437-A Composition for long acting nicardipine preparation and process of producing the composition YAMANOUCHI PHARMACEUTICAL CO., LTD. (JP) 1988-07-19 US claimed