Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5315399

COc1ccc(CN)c(OC)c1.[Cl-].[H+]

nearest known ligand 0.59

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
APLNR P35414 1/20 0.59
ADRA1A P35348 2/20 0.53
TAAR1 Q96RJ0 1/20 0.53
CA12 O43570 1/20 0.52
CA1 P00915 1/20 0.52
CA2 P00918 1/20 0.52
CA7 P43166 1/20 0.52
CA9 Q16790 1/20 0.52
CA14 Q9ULX7 1/20 0.52
ALDH1A1 P00352 4/20 0.50
CYP3A4 P08684 1/20 0.50
IDO1 P14902 2/20 0.49
HTR2B P41595 1/20 0.47
MELK Q14680 1/20 0.46
ADRA2A P08913 1/20 0.46
HTR2A P28223 1/20 0.46
MAPT P10636 2/20 0.46
MEN1 O00255 1/20 0.46
THRB P10828 1/20 0.46
KMT2A Q03164 1/20 0.46

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
SCHEMBL29350908 0.96 APLNR (0.63) APLNRADRA1ATAAR1CA12CA1
SCHEMBL153750 0.96 APLNR (0.63) APLNRADRA1ATAAR1CA12CA1
Hydrochloric Acid SCHEMBL1197172 0.94 APLNR (0.61) APLNRADRA1ATAAR1CA12CA1
Methyl Alcohol SCHEMBL28318211 0.92 APLNR (0.59) APLNRADRA1ATAAR1CA12CA1
Methylene Chloride SCHEMBL28212226 0.91 APLNR (0.58) APLNRADRA1ATAAR1CA12CA1
SCHEMBL10644538 0.87 TDP1 (0.55) APLNRADRA1ATAAR1CA12CA1
SCHEMBL10643461 0.87 APLNR (0.54) APLNRADRA1ATAAR1CA12CA1
SCHEMBL29042697 0.86 APLNR (0.53) APLNRADRA1ATAAR1CA12CA1
Piperazine SCHEMBL16716811 0.86 APLNR (0.53) APLNRADRA1ATAAR1CA12CA1
SCHEMBL2878154 0.83 CA2 (0.56) APLNRADRA1ATAAR1CA12CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2007056208-A2 N-ARYLALKYL-THIENOPYRIMIDIN-4-AMINES AND ANALOGS AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS AND THE USE THEREOF CYTOVIA, INC. (US) 2007-05-18 WO disclosed
US-20070099941-A1 N-arylalkyl-thienopyrimidin-4-amines and analogs as activators of caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. (US) 2007-05-03 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-20070099941-A1 N-arylalkyl-thienopyrimidin-4-amines and analogs as activators of caspases and inducers of apoptosis and the use thereof CASP10, CASP3, CASP4 APLNR 496/4885ADRA1A 867/4885TAAR1 871/4885

“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.