Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2906194

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

nearest known ligand 0.63

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 18)

geneUniProtsupporting neighboursconfidence
CCR2 P41597 1/20 0.63
CCR5 P51681 2/20 0.53
DHODH Q02127 1/20 0.53
MAPK1 P28482 3/20 0.51
LMNA P02545 3/20 0.51
SMN1; SMN2 Q16637 2/20 0.51
MAPT P10636 5/20 0.50
ALDH1A1 P00352 1/20 0.50
GAA P10253 1/20 0.50
TP53 P04637 2/20 0.48
RAB9A P51151 2/20 0.47
PYGL P06737 6/20 0.46
MEN1 O00255 1/20 0.46
KMT2A Q03164 1/20 0.46
NPC1 O15118 1/20 0.45
TDP1 Q9NUW8 1/20 0.45
TRPV1 Q8NER1 1/20 0.44
MCHR1 Q99705 1/20 0.44

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 SCHEMBL2906196 1.00 CCR2 (0.63) CCR2CCR5DHODHMAPK1LMNA
SCHEMBL2696196 0.99 CCR2 (0.64) CCR2CCR5DHODHMAPK1LMNA
SCHEMBL2696192 0.99 CCR2 (0.64) CCR2CCR5DHODHMAPK1LMNA
Iodide SCHEMBL17555090 0.98 CCR2 (0.63) CCR2CCR5DHODHMAPK1LMNA
Iodide SCHEMBL17555092 0.98 CCR2 (0.63) CCR2CCR5DHODHMAPK1LMNA
Hydrochloric Acid SCHEMBL2908323 0.90 CCR5 (0.65) CCR2CCR5DHODHLMNAMAPT
Hydrochloric Acid SCHEMBL2908319 0.90 CCR5 (0.65) CCR2CCR5DHODHLMNAMAPT
SCHEMBL313785 0.89 CCR5 (0.66) CCR2CCR5DHODHLMNAMAPT
SCHEMBL313784 0.89 CCR5 (0.66) CCR2CCR5DHODHLMNAMAPT
Hydrochloric Acid SCHEMBL2905994 0.88 ALDH1A1 (0.57) CCR2MAPK1LMNASMN1; SMN2MAPT

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 CCR2 1/4885CCR5 7/4885DHODH 573/4885
US-20090112004-A1 SYNTHESIS OF QUATERNARY SALT COMPOUNDS CCR2, CCR1, CCL11 CCR2 1/4885CCR5 7/4885DHODH 573/4885

“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.