Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2907990

C[N+](C)(Cc1ccc(NC(=O)c2sc3ccccc3c2Cl)cc1)C1CCCCC1.[Cl-]

nearest known ligand 0.62

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
MAPK1 P28482 1/20 0.62
MAPT P10636 9/20 0.57
SMN1; SMN2 Q16637 3/20 0.57
TP53 P04637 2/20 0.57
RXFP1 Q9HBX9 2/20 0.57
CCR2 P41597 4/20 0.56
THRB P10828 1/20 0.56
NPC1 O15118 2/20 0.54
RAB9A P51151 2/20 0.54
ALDH1A1 P00352 2/20 0.53
HPGD P15428 1/20 0.53
KDM4E B2RXH2 1/20 0.52
F10 P00742 4/20 0.50
GAA P10253 1/20 0.49
CYP2C9 P11712 1/20 0.49
CYP2C19 P33261 1/20 0.49
OGG1 O15527 1/20 0.48
PPARG P37231 1/20 0.48
NR2E3 Q9Y5X4 1/20 0.48
NCOR2 Q9Y618 1/20 0.48

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
SCHEMBL13148385 0.99 MAPK1 (0.63) MAPK1MAPTSMN1; SMN2TP53RXFP1
Iodide SCHEMBL17555183 0.98 MAPK1 (0.62) MAPK1MAPTSMN1; SMN2TP53RXFP1
Hydrochloric Acid SCHEMBL2906084 0.91 CCR2 (0.63) MAPK1MAPTSMN1; SMN2TP53RXFP1
SCHEMBL2696205 0.90 CCR2 (0.64) MAPK1MAPTSMN1; SMN2TP53RXFP1
Iodide SCHEMBL17555138 0.89 CCR2 (0.63) MAPK1MAPTSMN1; SMN2TP53RXFP1
SCHEMBL314749 0.79 MAPK1 (0.71) MAPK1MAPTSMN1; SMN2TP53RXFP1
Hydrochloric Acid SCHEMBL2906125 0.78 CCR2 (0.56) CCR2F10
Hydrochloric Acid SCHEMBL315423 0.77 CCR2 (0.68) CCR2
SCHEMBL13148384 0.77 CCR2 (0.57) CCR2F10
Hydrochloric Acid SCHEMBL313433 0.77 CCR2 (0.64) CCR2NPC1RAB9A

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-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

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 MAPK1 780/4885MAPT 2532/4885SMN1; SMN2 4702/4885
US-20090112004-A1 SYNTHESIS OF QUATERNARY SALT COMPOUNDS CCR2, CCR1, CCL11 MAPK1 780/4885MAPT 2532/4885SMN1; SMN2 4702/4885

“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.