Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5485232

N#[N+]c1cccc(Cl)c1.[Cl-]

nearest known ligand 0.44

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
TSHR P16473 3/20 0.41
ALDH1A1 P00352 3/20 0.41
MGLL Q99685 1/20 0.38
NOTUM Q6P988 2/20 0.37
PNMT P11086 1/20 0.37
CHRM5 P08912 1/20 0.35
TDP1 Q9NUW8 2/20 0.35
SMN1; SMN2 Q16637 2/20 0.35
MEN1 O00255 2/20 0.35
MAPT P10636 2/20 0.35
KMT2A Q03164 2/20 0.35
CYP3A4 P08684 1/20 0.35
ALOX15 P16050 1/20 0.35
HSD17B10 Q99714 1/20 0.35
CISD1 Q9NZ45 1/20 0.35
TAAR1 Q96RJ0 1/20 0.34
PARP1 P09874 1/20 0.34
NPC1 O15118 1/20 0.34
TP53 P04637 1/20 0.34
NFKB1 P19838 1/20 0.34

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
SCHEMBL11574020 0.98
SCHEMBL1504016 0.89 TSHR (0.37) TSHRALDH1A1MGLLNOTUMPNMT
SCHEMBL27637793 0.87 TSHR (0.35) TSHRALDH1A1MGLLNOTUMPNMT
Hydrochloric Acid SCHEMBL11203807 0.82
SCHEMBL2915809 0.73
Hydrochloric Acid SCHEMBL31299764 0.71 CA12 (0.50) TSHRALDH1A1TDP1KMT2ACYP3A4
Hydrochloric Acid SCHEMBL10986928 0.71 ACHE (0.50) TSHRALDH1A1MGLLTDP1SMN1; SMN2
SCHEMBL826242 0.71 TSHR (0.50) TSHRALDH1A1CYP3A4HSD17B10TP53
SCHEMBL31448035 0.70 AR (0.47) ALDH1A1SMN1; SMN2MEN1MAPTKMT2A
SCHEMBL9343117 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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114874155-A Benzyl thiazolamine compounds and preparation method and anti-tumor application thereof 华南理工大学 2022-08-09 CN claimed
JP-57139146-A None JP disclosed
CN-114874155-B Benzyl thiazole amine compound, preparation method and anti-tumor application thereof 华南理工大学 2024-02-06 CN disclosed
CN-114874155-A Benzyl thiazolamine compounds and preparation method and anti-tumor application thereof 华南理工大学 2022-08-09 CN disclosed
WO-2017089470-A1 PROCESS FOR THE SYNTHESIS OF ARYLDIAZONIUM SALTS USING NITROGEN OXIDES IN OXYGEN-CONTAINING GAS STREAMS, ESPECIALLY FROM INDUSTRIAL WASTE GASES Friedrich-Alexander-Universität Erlangen-Nürnberg (DE) 2017-06-01 WO disclosed
EP-3173401-A1 PROCESS FOR THE SYNTHESIS OF ARYLDIAZONIUM SALTS USING NITROGEN OXIDES IN OXYGEN-CONTAINING GAS STREAMS, ESPECIALLY FROM INDUSTRIAL WASTE GASES Friedrich-Alexander-Universität Erlangen-Nürnberg (DE) 2017-05-31 EP disclosed
US-20100196319-A1 4, 5-RING ANNULATED INDOLE DERIVATIVES FOR TREATING OR PREVENTING OF HCV AND RELATED VIRAL INFECTIONS SCHERING CORPORATION (US) 2010-08-05 US disclosed
US-20070185178-A1 Triazole compounds and their use as metabotropic glutamate receptor antagonists AATRAZENECA AB (SE) 2007-08-09 US disclosed
EP-1720860-A1 TRIAZOLE COMPOUNDS AND THEIR USE AS METABOTROPIC GLUTAMATE RECEPTOR ANTAGONISTS AstraZeneca AB (SE) 2006-11-15 EP disclosed
US-20060019997-A1 Triazole compounds and their use as metabotropic glutamate receptor antagonists ASTRAZENECA AB 2006-01-26 US disclosed
US-5468857-A Phenylmethoxypropenoic esters IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1995-11-21 US disclosed
EP-0307103-B1 Fungicides ZENECA LTD (GB) 1994-09-21 EP disclosed
US-5334748-A A methyl 2-aryl heterofunctional phenoxyphenyl-3-methoxy-propenoate compound; treating the plant diseases IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1994-08-02 US disclosed
CN-1021009-C FUNGICIDES ICI PLC (GB) 1993-06-02 CN disclosed
US-4515940-A REACTING ARYLDIAZONIUM SALTS WITH ALKALI OR ALKALINE EARTH METAL SULFITES HOECHST AKTIENGESELLSCHAFT (DE) 1985-05-07 US disclosed
EP-0068338-B1 Process for preparing phenyldiazosulphonates HOECHST AKTIENGESELLSCHAFT (DE) 1984-12-12 EP disclosed
EP-0068338-A1 Process for preparing phenyldiazosulphonates HOECHST AKTIENGESELLSCHAFT (DE) 1983-01-05 EP disclosed
JP-S57139146-A STABILIZATION OF DIAZONIUM SALT TYPE AZOIC DYE SHOWA KAKO KK 1982-08-27 JP disclosed
US-4145362-A DIAZOTIZATION OF ARYLAMINE IN PRESENCE OF ALKANOIC ACID, COPPER HALIDE CATALYST S.A. P R B EN NEERLANDAIS PRB N.V. (BE) 1979-03-20 US disclosed
US-4046763-A INTERMEDIATE FOR ULTRAVIOLET LIGHT ABSORBERS MCNEIL LABORATORIES, INCORPORATED (US) 1977-09-06 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 (3 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-20100196319-A1 4, 5-RING ANNULATED INDOLE DERIVATIVES FOR TREATING OR PREVENTING OF HCV AND RELATED VIRAL INFECTIONS ZC3HAV1, IDO1, ZC3HAV1L TSHR 1385/4885ALDH1A1 410/4885MGLL 2879/4885
US-20060019997-A1 Triazole compounds and their use as metabotropic glutamate receptor antagonists GRM3, GRIN3A, GRM1 TSHR 377/4885ALDH1A1 3228/4885MGLL 4027/4885
US-20070185178-A1 Triazole compounds and their use as metabotropic glutamate receptor antagonists GRM5, GRM3, GRIK5 TSHR 483/4885ALDH1A1 3599/4885MGLL 2849/4885

“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.