Hydrochloric Acid

Hydrochloric Acid

SCHEMBL14675356

C[N+](C)(Cc1ccccc1Cl)Cc1ccccc1Cl.[Cl-]

nearest known ligand 0.60

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
ACHE known ✓ P22303 1/20 0.60
SLC6A2 known ✓ P23975 2/20 0.44
CHRM2 known ✓ P08172 2/20 0.44
CHRM1 known ✓ P11229 1/20 0.44
CHRM3 known ✓ P20309 1/20 0.44
SLC6A3 known ✓ Q01959 1/20 0.42
BCHE P06276 1/20 0.60
IDO1 P14902 3/20 0.48
PNMT P11086 1/20 0.48
TAAR1 Q96RJ0 3/20 0.45
SLC6A4 P31645 2/20 0.44
CYP2D6 P10635 2/20 0.44
KCNH2 Q12809 2/20 0.44
ADRA2C P18825 1/20 0.44
OPRM1 P35372 1/20 0.44
OPRK1 P41145 1/20 0.44
HRH3 Q9Y5N1 1/20 0.44
AOC3 Q16853 1/20 0.42
KMT2A Q03164 1/20 0.41
PKM P14618 1/20 0.41

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 SCHEMBL22264987 0.86 BCHE (0.51) BCHEACHEIDO1PNMTTAAR1
SCHEMBL31658954 0.84 IDO1 (0.50) BCHEACHEIDO1PNMTTAAR1
Hydrochloric Acid SCHEMBL7166508 0.83 ACHE (0.50) BCHEACHEIDO1PNMTTAAR1
Hydrochloric Acid SCHEMBL11140883 0.80 KMT2A (0.61) BCHEACHESLC6A2SLC6A4CHRM2
Hydrochloric Acid SCHEMBL8615986 0.78 CYP2D6 (0.61) BCHEACHEIDO1PNMTTAAR1
SCHEMBL212194 0.76 CYP2D6 (0.63) BCHEACHEIDO1PNMTTAAR1
SCHEMBL9478319 0.74 IDO1 (0.50) BCHEACHEIDO1PNMTTAAR1
Hydrochloric Acid SCHEMBL9663575 0.74 BCHE (0.46) BCHEACHEIDO1PNMTTAAR1
SCHEMBL30633058 0.70
SCHEMBL91282 0.70

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
CN-107011176-B Process for preparing ring-halogenated N, N-dialkylbenzylamines 朗盛德国有限责任公司 2021-07-06 CN disclosed
EP-2739602-B1 METHOD FOR PRODUCING RING-HALOGENATED N,N-DIALKYLBENZYLAMINES LANXESS DEUTSCHLAND GMBH (DE) 2017-08-30 EP disclosed
US-9040751-B2 Method for producing ring-halogenated N,N-dialkylbenzylamines LANXESS DEUTSCHLAND GMBH (US) 2015-05-26 US disclosed
US-20140221691-A1 METHOD FOR PRODUCING RING-HALOGENATED N,N-DIALKYLBENZYLAMINES LANXESS DEUTSCHLAND GMBH (DE) 2014-08-07 US disclosed
EP-2739602-A1 METHOD FOR PRODUCING RING-HALOGENATED N,N-DIALKYLBENZYLAMINES LANXESS Deutschland GmbH (DE) 2014-06-11 EP disclosed
WO-2013017611-A1 METHOD FOR PRODUCING RING-HALOGENATED N,N-DIALKYLBENZYLAMINES LANXESS DEUTSCHLAND GMBH (DE) 2013-02-07 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 (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-20140221691-A1 METHOD FOR PRODUCING RING-HALOGENATED N,N-DIALKYLBENZYLAMINES NPM1, UGT1A6, NNMT ACHE 502/4885SLC6A2 1777/4885CHRM2 1132/4885

“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.