Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6927670

CC1C(c2ccccc2)=C(C2=C(c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C([Hf+2])c3ccccc32)c2ccccc21.[Cl-].[Cl-]

nearest known ligand 0.34

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 13)

geneUniProtsupporting neighboursconfidence
TACR1 known ✓ P25103 8/20 0.34
ATP1A1 P05023 1/20 0.31
ATP1B1 P05026 1/20 0.31
ATP1A3 P13637 1/20 0.31
ATP1B2 P14415 1/20 0.31
ATP1A2 P50993 1/20 0.31
ATP1B3 P54709 1/20 0.31
FXYD2 P54710 1/20 0.31
ATP1A4 Q13733 1/20 0.31
GPBAR1 Q8TDU6 3/20 0.31
HTR1A P08908 1/20 0.31
HTR7 P34969 1/20 0.31
KIF11 P52732 1/20 0.30

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 SCHEMBL6927007 1.00 TACR1 (0.34) TACR1ATP1A1ATP1B1ATP1A3ATP1B2
Hydrochloric Acid SCHEMBL7526331 0.96 HTR1A (0.32) TACR1ATP1A1ATP1B1ATP1A3ATP1B2
Hydrochloric Acid SCHEMBL6923694 0.89 RXRA (0.32)
Hydrochloric Acid SCHEMBL6927081 0.86
Hydrochloric Acid SCHEMBL6930149 0.86 TACR1 (0.37) TACR1ATP1A1ATP1B1ATP1A3ATP1B2
Hydrochloric Acid SCHEMBL6924045 0.86 TACR1 (0.37) TACR1ATP1A1ATP1B1ATP1A3ATP1B2
Hydrochloric Acid SCHEMBL7133093 0.81 TACR1 (0.34) TACR1ATP1A1ATP1B1ATP1A3ATP1B2
SCHEMBL7939157 0.80 TACR1 (0.34) TACR1HTR1AHTR7
SCHEMBL7939166 0.77 HTR1A (0.31) TACR1HTR1AHTR7
Hydrochloric Acid SCHEMBL8366096 0.77 TACR1 (0.35) TACR1GPBAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6518378-B2 Using an unbridged cyclopentadienyl metallocene catalyst capable of interconverting between states with different copolymerization characteristics THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY 2003-02-11 US disclosed
US-20020115805-A1 Methods of production of ethylene copolymers having narrow composition distributions and high melting temperatures THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY 2002-08-22 US disclosed
US-20010049425-A1 High-melting polyolefin copolymer elastomers, catalysts and methods of synthesis BP CORPORATION NORTH AMERICA INC. 2001-12-06 US disclosed
US-20010034426-A1 High-melting polyolefin copolymer elastomers, catalysts and methods of synthesis BP CORPORATION NORTH AMERICA INC. 2001-10-25 US disclosed
EP-1062257-A1 ETHYLENE COPOLYMERS WITH NARROW COMPOSITION DISTRIBUTION AND HIGH MELTING TEMPERATURES, AND METHODS OF PRODUCTION THEREOF THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2000-12-27 EP disclosed
WO-2000040625-A1 ETHYLENE COPOLYMERS WITH NARROW COMPOSITION DISTRIBUTION AND HIGH MELTING TEMPERATURES, AND METHODS OF PRODUCTION THEREOF THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2000-07-13 WO disclosed