Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3943546

FC(F)(F)c1cc(C2=Cc3ccccc3C2[Hf+3])cc(C(F)(F)F)c1.[Cl-].[Cl-].[Cl-]

nearest known ligand 0.35

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 15)

geneUniProtsupporting neighboursconfidence
TACR1 known ✓ P25103 1/20 0.30
CNR1 P21554 1/20 0.35
CNR2 P34972 1/20 0.35
TDP1 Q9NUW8 1/20 0.33
S1PR1 P21453 1/20 0.33
S1PR3 Q99500 1/20 0.33
P2RX1 P51575 2/20 0.32
RXRA P19793 1/20 0.31
RXRB P28702 1/20 0.31
RXRG P48443 1/20 0.31
KIF11 P52732 1/20 0.31
ALDH1A1 P00352 1/20 0.31
TSHR P16473 1/20 0.31
P2RX4 Q99571 1/20 0.30
P2RX7 Q99572 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 SCHEMBL8084823 0.82 CNR1 (0.35) CNR1CNR2TDP1S1PR1S1PR3
Hydrochloric Acid SCHEMBL6290544 0.82 CNR1 (0.35) CNR1CNR2TDP1S1PR1S1PR3
Hydrochloric Acid SCHEMBL3946480 0.81 CNR1 (0.34) CNR1CNR2TDP1S1PR1S1PR3
SCHEMBL6930680 0.80 CNR1 (0.35) CNR1CNR2TDP1P2RX1RXRA
Hydrochloric Acid SCHEMBL7937854 0.80 CNR1 (0.35) CNR1CNR2TDP1S1PR1S1PR3
SCHEMBL7634910 0.79 CNR1 (0.35) CNR1CNR2TDP1S1PR1S1PR3
Hydrochloric Acid SCHEMBL7928681 0.79 CNR1 (0.35) CNR1CNR2TDP1S1PR1S1PR3
SCHEMBL7632084 0.79 CNR1 (0.35) CNR1CNR2TDP1S1PR1S1PR3
Hydrochloric Acid SCHEMBL7639533 0.78 CNR1 (0.35) CNR1CNR2TDP1S1PR1S1PR3
Hydrochloric Acid SCHEMBL7652901 0.77 CNR1 (0.35) CNR1CNR2TDP1S1PR1S1PR3

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
US-7592408-B2 Olefin copolymers containing hydrolytically cleavable linkages and use thereof in degradable products SRI INTERNATIONAL (US) 2009-09-22 US disclosed
US-20080227940-A1 Olefin Copolymers Containing Hydrolytically Cleavable Linkages and Use Thereof In Degradable Products SRI INTERNATIONAL (US) 2008-09-18 US disclosed
US-7399817-B2 Olefin copolymers containing hydrolytically cleavable linkages and use thereof in degradable products SRI INTERNATIONAL (US) 2008-07-15 US disclosed
US-7037992-B2 Olefin copolymers containing hydrolytically cleavable linkages and use thereof in degradable products SRI INTERNATIONAL (US) 2006-05-02 US disclosed
US-20060079654-A1 Olefin copolymers containing hydrolytically cleavable linkages and use thereof in degradable products SRI INTERNATIONAL (US) 2006-04-13 US disclosed
US-20030236371-A1 Olefin copolymers containing hydrolytically cleavable linkages and use thereof in degradable products SRI INTERNATIONAL 2003-12-25 US disclosed
US-6534610-B1 Ethylene copolymer with hydrolyzable component in backbone; prepared by transition metal complex catalyzed addition polymerization SRI INTERNATIONAL 2003-03-18 US disclosed
WO-2001023448-A9 HYDROLYTICALLY DEGRADABLE OLEFIN COPOLYMERS STANFORD RES INST INT (US) 2002-09-26 WO disclosed
EP-1237962-A1 HYDROLYTICALLY DEGRADABLE OLEFIN COPOLYMERS Sri International (US) 2002-09-11 EP disclosed
US-6288184-B1 CATALYTIC COPOLYMERIZATION USING TRANSITION METAL METALLOCENE COMPLEX SRI INTERNATIONAL 2001-09-11 US disclosed
WO-2001023448-A1 HYDROLYTICALLY DEGRADABLE OLEFIN COPOLYMERS SRI INTERNATIONAL (US) 2001-04-05 WO disclosed