Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2905992

C[N+]1(Cc2ccc(CNC(=O)/C=C/c3ccc(Cl)c(Cl)c3)cc2)CCOCC1.[Cl-]

nearest known ligand 0.57

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
ALDH1A1 P00352 1/20 0.57
PYGL P06737 11/20 0.52
HPGD P15428 1/20 0.51
LMNA P02545 2/20 0.49
SMN1; SMN2 Q16637 2/20 0.49
KMT2A Q03164 2/20 0.49
MAPK1 P28482 1/20 0.49
CCR2 P41597 1/20 0.48
MAPT P10636 2/20 0.45
NPC1 O15118 1/20 0.45
RAB9A P51151 1/20 0.45
TDP1 Q9NUW8 1/20 0.45

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 SCHEMBL2905994 1.00 ALDH1A1 (0.57) ALDH1A1PYGLHPGDLMNASMN1; SMN2
SCHEMBL315402 0.99 ALDH1A1 (0.58) ALDH1A1PYGLHPGDLMNASMN1; SMN2
SCHEMBL315403 0.99 ALDH1A1 (0.58) ALDH1A1PYGLHPGDLMNASMN1; SMN2
Iodide SCHEMBL17555178 0.98 ALDH1A1 (0.57) ALDH1A1PYGLHPGDLMNASMN1; SMN2
Iodide SCHEMBL17555180 0.98 ALDH1A1 (0.57) ALDH1A1PYGLHPGDLMNASMN1; SMN2
Hydrochloric Acid SCHEMBL2899956 0.90 ALDH1A1 (0.59) ALDH1A1PYGLHPGDLMNASMN1; SMN2
Hydrochloric Acid SCHEMBL2899954 0.90 ALDH1A1 (0.59) ALDH1A1PYGLHPGDLMNASMN1; SMN2
SCHEMBL13148204 0.89 ALDH1A1 (0.60) ALDH1A1PYGLHPGDLMNASMN1; SMN2
Hydrochloric Acid SCHEMBL2906196 0.88 CCR2 (0.63) ALDH1A1PYGLLMNASMN1; SMN2KMT2A
Hydrochloric Acid SCHEMBL2906194 0.88 CCR2 (0.63) ALDH1A1PYGLLMNASMN1; SMN2KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2212286-A1 SYNTHESIS OF QUATERNARY SALT COMPOUNDS Janssen Pharmaceutica N.V. (BE) 2010-08-04 EP claimed
US-20090112003-A1 SYNTHESIS OF QUATERNARY SALT COMPOUNDS JANSSEN PHARMACEUTICA N.V. (BE) 2009-04-30 US claimed
US-20090112004-A1 SYNTHESIS OF QUATERNARY SALT COMPOUNDS JANSSEN PHARMACEUTICA N.V. (BE) 2009-04-30 US claimed
WO-2009055519-A1 SYNTHESIS OF QUATERNARY SALT COMPOUNDS JANSSEN PHARMACEUTICA, N.V. (BE) 2009-04-30 WO claimed
EP-2212286-A1 SYNTHESIS OF QUATERNARY SALT COMPOUNDS Janssen Pharmaceutica N.V. (BE) 2010-08-04 EP disclosed
WO-2009055519-A1 SYNTHESIS OF QUATERNARY SALT COMPOUNDS JANSSEN PHARMACEUTICA, N.V. (BE) 2009-04-30 WO 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 (2 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-20090112003-A1 SYNTHESIS OF QUATERNARY SALT COMPOUNDS CCR2, CCR1, CCL11 ALDH1A1 1764/4885PYGL 4883/4885HPGD 1716/4885
US-20090112004-A1 SYNTHESIS OF QUATERNARY SALT COMPOUNDS CCR2, CCR1, CCL11 ALDH1A1 1764/4885PYGL 4883/4885HPGD 1716/4885

“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.