Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7612779

CC(=O)Oc1ccc(C[N+]2(C)C3CCC2CC(O)C3)cc1.[Cl-]

nearest known ligand 0.43

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
▸ CHRM3 known ✓ P20309 2/20 0.37
▸ CHRM2 known ✓ P08172 1/20 0.37
▸ CHRM1 known ✓ P11229 1/20 0.37
▸ SLC6A2 known ✓ P23975 1/20 0.37
▸ SLC6A3 known ✓ Q01959 1/20 0.37
▸ LMNA P02545 2/20 0.38
▸ MEN1 O00255 1/20 0.37
▸ KMT2A Q03164 1/20 0.37
▸ ESR1 P03372 1/20 0.37
▸ PGR P06401 1/20 0.37
▸ ADORA3 P0DMS8 1/20 0.37
▸ AR P10275 1/20 0.37
▸ SMN1; SMN2 Q16637 2/20 0.36
▸ ALDH1A1 P00352 2/20 0.36
▸ MAPT P10636 2/20 0.36
▸ POLB P06746 1/20 0.36
▸ PKM P14618 1/20 0.36
▸ ELANE P08246 1/20 0.35
▸ GLA P06280 1/20 0.35
▸ EPHX2 P34913 1/20 0.34

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 SCHEMBL7614232 0.87 SMN1; SMN2 (0.41) LMNACHRM3KMT2AESR1SMN1; SMN2
SCHEMBL7621356 0.84 LMNA (0.40) LMNACHRM3MEN1KMT2AESR1
SCHEMBL7621358 0.84 LMNA (0.40) LMNACHRM3MEN1KMT2AESR1
Bromide SCHEMBL7620571 0.82 CHRNA7 (0.41) CHRM3CHRM2CHRM1CHRNA7
Bromide SCHEMBL7660614 0.81 CHRM3 (0.35) LMNACHRM3MEN1KMT2ASMN1; SMN2
Bromide SCHEMBL7616454 0.81 CHRM2 (0.42) CHRM3MEN1KMT2ACHRM2CHRM1
Bromide SCHEMBL7617544 0.80 CHRM2 (0.39) CHRM3CHRM2CHRM1CHRNA7
Bromide SCHEMBL7618949 0.80 CHRM2 (0.39) CHRM3CHRM2CHRM1CHRNA7
Bromide SCHEMBL7622878 0.79 PABPC1 (0.46) LMNACHRM3MEN1KMT2ACHRM2
Bromide SCHEMBL11766307 0.76 ALDH1A1 (0.50) LMNAMEN1KMT2ASMN1; SMN2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1150673-A4 MONO-ACYLOXY ARALKYL NEUROMUSCULAR RELAXANTS NEWLAXANT L L C (US) 2002-04-24 — — EP disclosed
EP-1150673-A1 MONO-ACYLOXY ARALKYL NEUROMUSCULAR RELAXANTS Newlaxant, L.L.C. (US) 2001-11-07 — — EP disclosed
WO-2000044377-A1 MONO-ACYLOXY ARALKYL NEUROMUSCULAR RELAXANTS NEWLAXANT, L.L.C. (US) 2000-08-03 — — WO disclosed
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