Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8166002

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

nearest known ligand 0.41

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 1/20 0.41
CHRM1 known ✓ P11229 4/20 0.39
CHRM3 known ✓ P20309 4/20 0.39
CHRM2 known ✓ P08172 3/20 0.35
CHRM5 P08912 4/20 0.39
BLM P54132 2/20 0.39
POLB P06746 1/20 0.39
ATM Q13315 1/20 0.39
MAPT P10636 1/20 0.39
CHRM4 P08173 3/20 0.35
SMN1; SMN2 Q16637 2/20 0.35
HTR1A P08908 2/20 0.35
CHRNB2 P17787 2/20 0.35
CHRNA7 P36544 2/20 0.35
CHRNA4 P43681 2/20 0.35
CYP2C19 P33261 2/20 0.35
ADRA2A P08913 1/20 0.35
ADRA1A P35348 1/20 0.35
PGR P06401 1/20 0.35
TBXA2R P21731 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
Hydrochloric Acid SCHEMBL525772 0.86 ACHE (0.44) ACHECHRM5CHRM1CHRM3BLM
SCHEMBL33889 0.84 ACHE (0.46) ACHECHRM5CHRM1CHRM3BLM
SCHEMBL8169689 0.84 POLB (0.37) ACHECHRM5CHRM1CHRM3BLM
Bromide SCHEMBL7628216 0.82 ACHE (0.44) ACHECHRM5CHRM1CHRM3BLM
Iodide SCHEMBL8612631 0.82 ACHE (0.44) ACHECHRM5CHRM1CHRM3BLM
Hydrochloric Acid SCHEMBL3963896 0.77 ALDH1A1 (0.44) ACHECHRM5CHRM1CHRM3BLM
Sulfuric Acid SCHEMBL774507 0.77 ACHE (0.40) ACHECHRM5CHRM1CHRM3BLM
SCHEMBL3878819 0.75 TSHR (0.42) ACHECHRM5CHRM1CHRM3CHRM2
Hydrochloric Acid SCHEMBL15419542 0.74 ACHE (0.58) ACHECHRM5CHRM1CHRM3BLM
Iodide SCHEMBL10588908 0.73 TSHR (0.40) ACHELMNAAPEX1ALDH1A1TSHR

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-1815844-B1 Photoprotecting compositions with reduced risk of skin sensitisation DERMATOLOGIQUES D URIAGE LAB (FR) 2015-04-29 EP claimed
US-5741875-A GRAFT POLYMER CONTAINING LIGNIN; HIGH STRENGTH; IMPACT STRENGTH; ACID RESISTANCE; ALKALI RESISTANCE; STABILITY MEISTER JOHN J (US) 1998-04-21 US claimed
US-5424382-A Decomposing lignin grafted with addition polymer MEISTER JOHN J (US) 1995-06-13 US claimed
US-10889674-B2 Method of preparing a grafted copolymer of lignin and/or cellulose BIOFIBER TECH SWEDEN AB (SE) 2021-01-12 US disclosed
US-20190202956-A1 Method of Preparing a Grafted Copolymer of Lignin and/or Cellulose BIOFIBER TECH SWEDEN AB (SE) 2019-07-04 US disclosed
US-6013774-A FREE RADICALLY GRAFT COPOLYMERIZING A SUBSTITUTED ETHENE OR ETHYNE ONTO LIGNIN, THEN MIXING THE GRAFTED LIGNIN WITH A POLYMER MEISTER JOHN J (US) 2000-01-11 US disclosed
US-5852069-A Biodegradable plastics and composites from wood MEISTER JOHN J (US) 1998-12-22 US disclosed
US-5741875-A GRAFT POLYMER CONTAINING LIGNIN; HIGH STRENGTH; IMPACT STRENGTH; ACID RESISTANCE; ALKALI RESISTANCE; STABILITY MEISTER JOHN J (US) 1998-04-21 US disclosed
US-5656708-A ADDING LIGNITE TO THE SOLVENT, ADDING HALIDE SALT, PEROXIDE AND HYDROPHOBIC ETHENE MONOMERS; FREE-RADICAL GRAFT POLYMERIZATION MEISTER JOHN J (US) 1997-08-12 US disclosed
US-5424382-A Decomposing lignin grafted with addition polymer MEISTER JOHN J (US) 1995-06-13 US disclosed
US-5331088-A Molding materials MEISTER JOHN J (US) 1994-07-19 US disclosed