Hydrochloric Acid

Hydrochloric Acid

SCHEMBL786186

COC(=O)C(C(=O)OCc1ccc2c(c1)OCO2)n1cc[n+](C)c1.[Cl-]

nearest known ligand 0.51

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
CYP3A4 P08684 2/20 0.51
SMN1; SMN2 Q16637 1/20 0.43
NAAA Q02083 1/20 0.43
ACE P12821 1/20 0.42
HSD17B10 Q99714 1/20 0.41
NPC1 O15118 1/20 0.41
RAB9A P51151 1/20 0.41
HPGD P15428 1/20 0.40
HRH4 Q9H3N8 1/20 0.40
EDNRA P25101 1/20 0.40
MAPT P10636 2/20 0.40
FAAH O00519 1/20 0.40
MGLL Q99685 1/20 0.40
GAA P10253 1/20 0.40
ATM Q13315 1/20 0.40
ALDH1A1 P00352 2/20 0.39
TSHR P16473 2/20 0.39
MEN1 O00255 2/20 0.39
KMT2A Q03164 2/20 0.39
PKM P14618 1/20 0.39

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
SCHEMBL786172 0.87 CYP3A4 (0.48) CYP3A4SMN1; SMN2ACENPC1RAB9A
Bromide SCHEMBL786346 0.87 CYP3A4 (0.47) CYP3A4SMN1; SMN2ACENPC1RAB9A
SCHEMBL786531 0.79 ALDH1A1 (0.42) SMN1; SMN2NPC1RAB9AMAPTATM
SCHEMBL786574 0.78 ALDH1A1 (0.41) SMN1; SMN2NPC1RAB9AHPGDMAPT
Bromide SCHEMBL785301 0.78 SMN1; SMN2 (0.45) SMN1; SMN2HSD17B10HPGDMAPTALDH1A1
Bromide SCHEMBL187249 0.77 ALDH1A1 (0.40) SMN1; SMN2NPC1RAB9AHPGDMAPT
SCHEMBL803823 0.77 EDNRA (0.47) HPGDEDNRAGAAALDH1A1KMT2A
SCHEMBL785951 0.76 CYP3A4 (0.47) CYP3A4NPC1RAB9AHPGDEDNRA
SCHEMBL786333 0.76 MEN1 (0.40) CYP3A4MAPTMEN1KMT2A
Bromide SCHEMBL786196 0.76 CYP3A4 (0.46) CYP3A4NPC1RAB9AHPGDEDNRA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8785655-B2 Ionic liquid solvents DUBLIN CITY UNIVERSITY (IE) 2014-07-22 US claimed
US-20120071661-A1 Ionic Liquid Solvents DUBLIN CITY UNIVERSITY (IE) 2012-03-22 US claimed
US-8785655-B2 Ionic liquid solvents DUBLIN CITY UNIVERSITY (IE) 2014-07-22 US disclosed
US-20120071661-A1 Ionic Liquid Solvents DUBLIN CITY UNIVERSITY (IE) 2012-03-22 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20120071661-A1 Ionic Liquid Solvents EBP, PAICS, HACD3 CYP3A4 452/4885SMN1; SMN2 2787/4885NAAA 2049/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.