Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8467199

[Cl-].[Cl-].c1ccc(C2=C3CCC4=C(c5ccccc5)C([Zr+2]C2c2ccccc23)c2ccccc24)cc1

nearest known ligand 0.36

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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 14)

geneUniProtsupporting neighboursconfidence
CHRNB2 P17787 1/20 0.34
CHRNA4 P43681 1/20 0.34
ADRA2C P18825 3/20 0.34
PTGS2 P35354 1/20 0.34
HRH1 P35367 1/20 0.34
HTR3A P46098 1/20 0.34
PDE4D Q08499 1/20 0.34
ADRA2A P08913 3/20 0.31
ADRA2B P18089 2/20 0.31
SIGMAR1 Q99720 1/20 0.31
ADRA1D P25100 1/20 0.31
ADRA1A P35348 1/20 0.31
CYP11B2 P19099 1/20 0.31
HTR2C P28335 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 SCHEMBL5616492 0.76 CHRNB2 (0.34) CHRNB2CHRNA4ADRA2CPTGS2HRH1
Hydrochloric Acid SCHEMBL218728 0.75 ADRA2C (0.36) ADRA2CPTGS2HRH1HTR3APDE4D
Hydrochloric Acid SCHEMBL9016935 0.72 ADRA2C (0.34) ADRA2CPTGS2HRH1HTR3APDE4D
Hydrochloric Acid SCHEMBL217506 0.68 ADRA2C (0.33) ADRA2CPTGS2HRH1HTR3APDE4D
Hydrochloric Acid SCHEMBL7938880 0.66 CHRNB2 (0.33) CHRNB2CHRNA4
Hydrochloric Acid SCHEMBL218744 0.64 HTR1A (0.34) CHRNB2CHRNA4ADRA2CADRA2AADRA2B
Hydrochloric Acid SCHEMBL6358953 0.63 CES1 (0.35) ADRA2AADRA1ACYP11B2
Hydrochloric Acid SCHEMBL6911683 0.63 DRD2 (0.38)
SCHEMBL2594422 0.60 ALDH1A1 (0.50) CHRNB2CHRNA4ADRA2CADRA2AADRA2B
SCHEMBL7212942 0.60 ALDH1A1 (0.53) PTGS2SIGMAR1HTR2C

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-5969070-A HOMOGENEOUS COMPOSITION FORMED FROM LINEAR OR BRANCHED CHAIN C3 TO C10 MONOMERS SUCH AS PROPYLENE, 1-BUTENE, 1-PENTENE, 4-METHYL-1-PENTENE, 1-HEXENE AND MIXTURES THEREOF, COMPRISING ALTERNATING ISOTACTIC AND ATACTIC DISASTEREOSEQUENCES THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 1999-10-19 US disclosed
EP-0802935-A4 THERMOPLASTIC ELASTOMERIC STEREOBLOCK OLEFIN POLYMERS METHODS AND METALLOCENE CATALYSTS UNIV LELAND STANFORD JUNIOR (US) 1998-09-30 EP disclosed
EP-0802935-A1 THERMOPLASTIC ELASTOMERIC STEREOBLOCK OLEFIN POLYMERS METHODS AND METALLOCENE CATALYSTS THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 1997-10-29 EP disclosed
US-5594080-A POLYMERIZATION CATALYSIS OF METALLOCENES WITH CYCLOPENTADIENE AND METALS LELAND STANFORD, JR. UNIVERSITY (US) 1997-01-14 US disclosed
WO-1995025757-A1 THERMOPLASTIC ELASTOMERIC STEREOBLOCK OLEFIN POLYMERS METHODS AND METALLOCENE CATALYSTS THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 1995-09-28 WO disclosed