Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2701710

C=CC(=O)C(C)[N+](C)(C)CC1CO1.[Cl-]

nearest known ligand 0.32

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 6)

geneUniProtsupporting neighboursconfidence
CHRM2 known ✓ P08172 4/20 0.32
CHRM3 known ✓ P20309 4/20 0.32
CHRM1 known ✓ P11229 2/20 0.30
CHRM5 P08912 4/20 0.32
CHRM4 P08173 3/20 0.32
ALDH1A1 P00352 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 SCHEMBL27759126 0.80 CHRM2 (0.36) CHRM2CHRM5CHRM3CHRM4ALDH1A1
Hydrochloric Acid SCHEMBL28219697 0.77 TSHR (0.34) ALDH1A1
Hydrochloric Acid SCHEMBL27792028 0.73 TSHR (0.34) ALDH1A1
Hydrochloric Acid SCHEMBL1304769 0.72 TSHR (0.35)
Hydrochloric Acid SCHEMBL27759135 0.71 CHRM2 (0.39) CHRM2CHRM5CHRM3CHRM4CHRM1
Hydrochloric Acid SCHEMBL28736100 0.70 TSHR (0.32) ALDH1A1
Hydrochloric Acid SCHEMBL27919664 0.70 BLM (0.38)
Iodide SCHEMBL28038909 0.70 TSHR (0.34) ALDH1A1
Hydrochloric Acid SCHEMBL422092 0.68 TSHR (0.36) ALDH1A1
Hydrochloric Acid SCHEMBL2701711 0.68 PRKD3 (0.34) CHRM2CHRM5CHRM3CHRM4ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1545876-B1 LIQUID UNCROSSLINKED MICHAEL ADDITION OLIGOMERS PREPARED IN THE PRESENCE OF A CATALYST HAVING BOTH AN EPOXY MOIETY AND A QUATERNARY SALT ASHLAND LICENSING & INTELLECTU (US) 2012-05-09 EP disclosed
EP-1545876-A4 LIQUID UNCROSSLINKED MICHAEL ADDITION OLIGOMERS PREPARED IN THE PRESENCE OF A CATALYST HAVING BOTH AN EPOXY MOIETY AND A QUATERNARY SALT ASHLAND LICENSING & INTELLECTU (US) 2008-10-01 EP disclosed
CN-100377874-C Liquid uncrosslinked michael addition oligomers prepared in the presence of a catalyst having both an epoxy moiety and a quaternary salt ASHLAND INC (US) 2008-04-02 CN disclosed
CN-1708401-A Liquid uncrosslinked michael addition oligomers prepared in the presence of a catalyst having both an epoxy moiety and a quaternary salt ASHLAND INC (US) 2005-12-14 CN disclosed
EP-1545876-A2 LIQUID UNCROSSLINKED MICHAEL ADDITION OLIGOMERS PREPARED IN THE PRESENCE OF A CATALYST HAVING BOTH AN EPOXY MOIETY AND A QUATERNARY SALT ASHLAND INC. (US) 2005-06-29 EP disclosed
WO-2004029118-A2 LIQUID UNCROSSLINKED MICHAEL ADDITION OLIGOMERS PREPARED IN THE PRESENCE OF A CATALYST HAVING BOTH AN EPOXY MOIETY AND A QUATERNARY SALT ASHLAND INC. (US) 2004-04-08 WO disclosed
US-6706414-B1 Liquid uncrosslinked Michael addition oligomers prepared in the presence of a catalyst having both an epoxy moiety and a quaternary salt ASHLAND INC. 2004-03-16 US disclosed