Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7048253

CC(=O)C[n+]1cccc(C(=O)NCCO)c1.[Cl-]

nearest known ligand 0.45

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 12)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 1/20 0.40
HSP90AA1 P07900 8/20 0.45
BACE1 P56817 3/20 0.44
APOBEC3A P31941 1/20 0.43
APOBEC3G Q9HC16 1/20 0.43
ALDH1A1 P00352 1/20 0.42
RECQL P46063 1/20 0.42
POLB P06746 1/20 0.42
ATM Q13315 1/20 0.40
BCHE P06276 1/20 0.40
LMNA P02545 1/20 0.40
CYP2D6 P10635 1/20 0.40

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
SCHEMBL7506380 0.99 HSP90AA1 (0.43) HSP90AA1BACE1APOBEC3AAPOBEC3GALDH1A1
SCHEMBL7506903 0.83 KMT2A (0.56) HSP90AA1ALDH1A1RECQLPOLBATM
Bromide SCHEMBL7052966 0.82 KMT2A (0.58) ALDH1A1RECQLPOLBATMBCHE
SCHEMBL7509456 0.82 GLA (0.49) HSP90AA1BACE1ALDH1A1RECQLPOLB
SCHEMBL11926114 0.81 HSP90AA1 (0.47) HSP90AA1APOBEC3AAPOBEC3GALDH1A1RECQL
Bromide SCHEMBL7050985 0.81 GLA (0.51) HSP90AA1BACE1ALDH1A1RECQLPOLB
Hydrochloric Acid SCHEMBL7051973 0.81 HSP90AA1 (0.67) HSP90AA1BACE1ALDH1A1LMNACYP2D6
SCHEMBL11926720 0.81 HSP90AA1 (0.44) HSP90AA1BACE1APOBEC3AAPOBEC3GATM
SCHEMBL11927274 0.78 SMYD3 (0.46) HSP90AA1APOBEC3AAPOBEC3GALDH1A1RECQL
SCHEMBL7576220 0.77 KDM4E (0.45) ALDH1A1POLBLMNA

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
EP-1304101-A1 Composition and method for use of pyridinium derivatives in cosmetic and therapeutic applications Torrent Pharmaceuticals Ltd (IN) 2003-04-23 EP claimed
US-20020103228-A1 Composition and method for use of pyridinium derivatives in cosmetic and therapeutic applications TORRENT PHARMACEUTICALS LTD. 2002-08-01 US claimed
EP-1304101-A1 Composition and method for use of pyridinium derivatives in cosmetic and therapeutic applications Torrent Pharmaceuticals Ltd (IN) 2003-04-23 EP disclosed
US-20020103228-A1 Composition and method for use of pyridinium derivatives in cosmetic and therapeutic applications TORRENT PHARMACEUTICALS LTD. 2002-08-01 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-20020103228-A1 Composition and method for use of pyridinium derivatives in cosmetic and therapeutic applications PNPO, PRDX5, PLPBP ACHE 110/4885HSP90AA1 4863/4885BACE1 1232/4885

“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.