Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6923745

CC1=C(C)C([Zr+2]C2=C(c3cc(C(F)(F)F)cc(C(F)(F)F)c3)CC(C)=C2C)=C(c2ccccc2)C1.[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 20)

geneUniProtsupporting neighboursconfidence
TACR1 known ✓ P25103 8/20 0.33
SLC6A2 known ✓ P23975 1/20 0.31
KIF11 P52732 1/20 0.34
RXRA P19793 4/20 0.33
RXRB P28702 4/20 0.33
CNR1 P21554 1/20 0.32
CNR2 P34972 1/20 0.32
RXRG P48443 3/20 0.32
ATP1A1 P05023 1/20 0.32
ATP1B1 P05026 1/20 0.32
ATP1A3 P13637 1/20 0.32
ATP1B2 P14415 1/20 0.32
ATP1A2 P50993 1/20 0.32
ATP1B3 P54709 1/20 0.32
FXYD2 P54710 1/20 0.32
ATP1A4 Q13733 1/20 0.32
GPBAR1 Q8TDU6 1/20 0.31
MAPT P10636 1/20 0.31
TDP1 Q9NUW8 1/20 0.31
SLC6A4 P31645 1/20 0.31

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 SCHEMBL6290431 0.92 IKBKB (0.33) RXRARXRBRXRG
Hydrochloric Acid SCHEMBL6926682 0.81 KIF11 (0.34) KIF11RXRARXRBTACR1CNR1
Hydrochloric Acid SCHEMBL6930183 0.79 KIF11 (0.37) KIF11SLC6A2
Hydrochloric Acid SCHEMBL6287543 0.72 PTGS2 (0.33) TDP1
Hydrochloric Acid SCHEMBL6289768 0.71 RXRA (0.33) RXRARXRBRXRG
Hydrochloric Acid SCHEMBL8364572 0.68 IKBKB (0.33) RXRARXRBRXRG
Hydrochloric Acid SCHEMBL8367747 0.66
Hydrochloric Acid SCHEMBL8367981 0.66 TACR1 (0.30) TACR1
SCHEMBL2138447 0.66 KIF11 (0.65) KIF11RXRARXRBTACR1CNR1
SCHEMBL4266470 0.66 KIF11 (0.54) KIF11RXRARXRBTACR1RXRG

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 5 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-6479685-B2 POLYMERIZING ETHYLENE AND ANOTHER ALPHA-OLEFIN IN THE PRESENCE OF AN UNBRIDGED, ROTATING, NON-RIGID FLUXIONAL METALLOCENE CATALYST COMPONENT AND A CO-CATALYST THE BOARD OF TRUSTEES OF THE LELAND STANDARD JUNIOR UNIVERSITY 2002-11-12 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
US-6169151-B1 MADE BY POLYMERIZING ETHYLENE AND ALPHA-OLEFIN(S) USING AN UNBRIDGED, ROTATING, NON-RIGID FLUXIONAL METALLOCENE CATALYST AND COCATALYST; CRYSTALLIZABLE ELASTOMERIC COPOLYMER PRODUCT HAS HIGHER MELTING POINT, NARROW COMPOSITION DISTRIBUTION THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY 2001-01-02 US disclosed