Hydrochloric Acid

Hydrochloric Acid

SCHEMBL376693

Fc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1.[Cl-]

nearest known ligand 0.58

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 17)

geneUniProtsupporting neighboursconfidence
SNCA P37840 2/20 0.58
HIF1A Q16665 1/20 0.44
CYP19A1 P11511 2/20 0.40
PLA2G1B P04054 1/20 0.39
ATG4B Q9Y4P1 1/20 0.39
IDO1 P14902 1/20 0.38
LOXL2 Q9Y4K0 1/20 0.38
ALDH1A1 P00352 3/20 0.38
PPARG P37231 1/20 0.38
PPARA Q07869 1/20 0.38
CYP3A4 P08684 1/20 0.38
TRPA1 O75762 1/20 0.37
MMP2 P08253 1/20 0.37
MMP9 P14780 1/20 0.37
MMP12 P39900 1/20 0.37
RAB9A P51151 1/20 0.36
EPHX1 P07099 1/20 0.36

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
SCHEMBL29751859 0.98 SNCA (0.60) SNCAHIF1ACYP19A1PLA2G1BATG4B
SCHEMBL29392833 0.98 SNCA (0.60) SNCAHIF1ACYP19A1PLA2G1BATG4B
Bromide SCHEMBL1503289 0.96 SNCA (0.61) SNCAHIF1ACYP19A1PLA2G1BATG4B
Iodide SCHEMBL5462695 0.96 SNCA (0.58) SNCAHIF1ACYP19A1PLA2G1BATG4B
SCHEMBL8376764 0.90 SNCA (0.53) SNCAHIF1ACYP19A1PLA2G1BATG4B
SCHEMBL8375928 0.90 SNCA (0.53) SNCAHIF1ACYP19A1PLA2G1BATG4B
SCHEMBL8605747 0.90 SNCA (0.53) SNCAHIF1ACYP19A1PLA2G1BATG4B
Hydrochloric Acid SCHEMBL2446696 0.89 SNCA (0.69) SNCAHIF1AALDH1A1CYP3A4EPHX1
Iodide SCHEMBL9321342 0.84 SNCA (0.69) SNCAHIF1AALDH1A1CYP3A4EPHX1
Bromide SCHEMBL39844 0.84 SNCA (0.73) SNCAHIF1AALDH1A1CYP3A4EPHX1

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 163 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111004239-B Preparation method of ibrutinib precursor 上海柏狮生物科技有限公司 2022-09-13 CN claimed
CN-111004239-A Preparation method of ibrutinib precursor 上海柏狮生物科技有限公司 2020-04-14 CN claimed
EP-4695271-A2 A CYCLIC PEPTIDE FOR TRAPPING INTERLEUKIN-1 BETA Merck Sharp & Dohme LLC (US) 2026-02-18 EP disclosed
WO-2024258943-A1 METHODS OF USING CYCLIC PEPTIDES FOR TRAPPING INTERLEUKIN-1 BETA MERCK SHARP & DOHME LLC (US) 2024-12-19 WO disclosed
WO-2024215820-A2 A CYCLIC PEPTIDE FOR TRAPPING INTERLEUKIN-1 BETA MERCK SHARP & DOHME LLC (US) 2024-10-17 WO disclosed
CN-111004239-B Preparation method of ibrutinib precursor 上海柏狮生物科技有限公司 2022-09-13 CN disclosed
US-10928728-B2 Photoactivable nitrogen bases BASF SE (DE) 2021-02-23 US disclosed
US-10913733-B2 Substituted piperidines thiazolyl acetamides as glycosidase inhibitors and uses thereof ALECTOS THERAPEUTICS INC. (CA) 2021-02-09 US disclosed
US-20210033972-A1 PHOTOACTIVABLE NITROGEN BASES BASF SE (DE) 2021-02-04 US disclosed
EP-3389658-B1 GLYCOSIDASE INHIBITORS AND USES THEREOF MERCK SHARP & DOHME (US) 2020-11-25 EP disclosed
CN-111004239-A Preparation method of ibrutinib precursor 上海柏狮生物科技有限公司 2020-04-14 CN disclosed
US-4866086-A PHENYLTRIAZOLYL OLEFINIC AROMATASE INHIBITORS IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1989-09-12 US disclosed
EP-0311955-A2 Bicyclic peroxide F. HOFFMANN-LA ROCHE AG (CH) 1989-04-19 EP disclosed
US-4806685-A EXERTS VARIOUS EFFECTS ON ENDOCRINOUS SYSTEM OF RATS; INHIBITS GROWTH OF MAMMARY TUMORS GYOGYSZERKUTATO INTEEZET/PHARMACEUTICAL RESEARCH INSTITUTE (HU) 1989-02-21 US disclosed
EP-0299683-A2 Heterocyclic olefinic compounds and their use as aromatase inhibitors IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1989-01-18 EP disclosed
US-4684731-A NEUROLEPTIC, ANTIEMETIC, ANALGESIC HOFFMANN-LA ROCHE INC. (US) 1987-08-04 US disclosed
EP-0037990-B1 PHENYL QUINOLIZIDINES, CORRESPONDING PHARMACEUTICAL PREPARATIONS, THE PREPARATION OF THE ACTIVE COMPOUNDS AND CORRESPONDING STARTING COMPOUNDS F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1984-12-05 EP disclosed
US-4391978-A NEUROLEPTIC AGENTS, ANTIEMETICS, ANALGESICS HOFFMANN-LA ROCHE INC. (US) 1983-07-05 US disclosed
US-4316905-A HYPOTENSIVE AGENTS E. R. SQUIBB & SONS, INC. (US) 1982-02-23 US disclosed
EP-0037990-A1 Phenyl quinolizidines, corresponding pharmaceutical preparations, the preparation of the active compounds and corresponding starting compounds F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1981-10-21 EP 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-20210033972-A1 PHOTOACTIVABLE NITROGEN BASES CBR1, ARNT, NR0B1 SNCA 2054/4885HIF1A 1258/4885CYP19A1 42/4885
US-10928728-B2 Photoactivable nitrogen bases CBR1, NR0B1, NR0B2 SNCA 1887/4885HIF1A 1136/4885CYP19A1 58/4885
US-10913733-B2 Substituted piperidines thiazolyl acetamides as glycosidase inhibitors and uses thereof OGA, ENGASE, GAA SNCA 2723/4885HIF1A 1124/4885CYP19A1 2798/4885

“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.