Hydrochloric Acid

Hydrochloric Acid

SCHEMBL442699

Cc1cc(C)c(N2C=[N+](c3c(C)cc(C)cc3C)CC2)c(C)c1.[Cl-]

nearest known ligand 0.32

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 6)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.32
POLB P06746 1/20 0.32
MAPT P10636 1/20 0.32
HTT P42858 1/20 0.32
SMN1; SMN2 Q16637 1/20 0.32
NPSR1 Q6W5P4 1/20 0.32

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
SCHEMBL442095 0.98 ALDH1A1 (0.33) ALDH1A1POLBMAPTHTTSMN1; SMN2
Bromide SCHEMBL1608734 0.96 ALDH1A1 (0.32) ALDH1A1POLBMAPTHTTSMN1; SMN2
SCHEMBL819057 0.92
SCHEMBL18287206 0.90
SCHEMBL29603795 0.88 ALDH1A1 (0.34) ALDH1A1POLBMAPTHTTSMN1; SMN2
Hydrochloric Acid SCHEMBL17783834 0.86 L3MBTL1 (0.30)
Bromide SCHEMBL4539689 0.86 ALDH1A1 (0.33) ALDH1A1POLBMAPTHTTSMN1; SMN2
SCHEMBL21722392 0.86 ALDH1A1 (0.33) ALDH1A1POLBMAPTHTTSMN1; SMN2
SCHEMBL29603410 0.86 ALDH1A1 (0.33) ALDH1A1POLBMAPTHTTSMN1; SMN2
Hydrochloric Acid SCHEMBL1609624 0.83

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4026535-B1 BIODEGRADABLE COPOLYMERS FOR COSMETIC USE INTERCOS ITALIANA (IT) 2025-07-09 EP claimed
CN-114573531-B Method for synthesizing FDCA through carbon dioxide oxidation and metal catalysis of HMF 南京先进生物材料与过程装备研究院有限公司 2024-10-18 CN claimed
CN-114149467-B Method for preparing ruthenium-carbene compounds 成都西岭源药业有限公司 2024-04-19 CN claimed
CN-116217352-A Method for preparing cannabigerol and analogues thereof 上海中医药大学 2023-06-06 CN claimed
EP-3452009-B1 BIODEGRADABLE COPOLYMERS FOR COSMETIC USE INTERCOS ITALIANA (IT) 2022-12-07 EP claimed
EP-4026535-A1 BIODEGRADABLE COPOLYMERS FOR COSMETIC USE Intercos S.p.A. (IT) 2022-07-13 EP claimed
CN-114573531-A Method for synthesizing FDCA through carbon dioxide oxidation and metal catalysis HMF 南京先进生物材料与过程装备研究院有限公司 2022-06-03 CN claimed
US-10940106-B2 Biodegradable copolymers for cosmetic use INTERCOS S.P.A. (IT) 2021-03-09 US claimed
US-20190159999-A1 BIODEGRADABLE COPOLYMERS FOR COSMETIC USE INTERCOS S.P.A. (IT) 2019-05-30 US claimed
EP-3452009-A1 BIODEGRADABLE COPOLYMERS FOR COSMETIC USE Intercos S.p.A. (IT) 2019-03-13 EP claimed
US-10053426-B2 Process for the synthesis of metyrapone and alkylated metyrapone analogs ALBEMARLE CORPORATION (US) 2018-08-21 US claimed
US-20170334854-A1 One-Step Process For The Synthesis Of Alkylated Metyrapone Analogs W. R. GRACE & CO.-CONN. 2017-11-23 US claimed
WO-2017191603-A1 BIODEGRADABLE COPOLYMERS FOR COSMETIC USE INTERCOS S.P.A. (IT) 2017-11-09 WO claimed
EP-3237383-A1 ONE-STEP PROCESS FOR THE SYNTHESIS OF ALKYLATED METYRAPONE ANALOGS Albemarle Corporation (US) 2017-11-01 EP claimed
WO-2016105619-A1 ONE-STEP PROCESS FOR THE SYNTHESIS OF ALKYLATED METYRAPONE ANALOGS ALBEMARLE CORPORATION (US) 2016-06-30 WO claimed
WO-2010010559-A1 CONTROLLED HYDROGEN GENERATION, STORAGE AND TRANSPORTATION SOLUTION M.I.H.G. LTD. (IL) 2010-01-28 WO claimed
US-20100021376-A1 CONTROLLED HYDROGEN GENERATION, STORAGE AND TRANSPORTATION SOLUTION SILBERMAN ALEX 2010-01-28 US claimed
EP-4739672-A1 NEW COMPOUNDS Aston University (GB) 2026-05-13 EP disclosed
US-6316380-B1 ONE TRANSITION METAL COMPOUND AND AT LEAST ONE N-HETEROCYCLIC CARBENE OR ITS PROTONATED SALT UNIVERSITY OF NEW ORLEANS RESEARCH & TECHNOLOGY FOUNDATION 2001-11-13 US disclosed
WO-2001066248-A2 C-C AND C-N COUPLING CATALYST COMPRISING TRANSITION METAL AND CARBENE UNIVERSITY OF NEW ORLEANS RESEARCH AND TECHNOLOGY FOUNDATION (US) 2001-09-13 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 (4 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-10940106-B2 Biodegradable copolymers for cosmetic use LAGE3, LMTK2, LSS ALDH1A1 4234/4885POLB 1231/4885MAPT 2423/4885
US-20190159999-A1 BIODEGRADABLE COPOLYMERS FOR COSMETIC USE LAGE3, LMTK2, LSS ALDH1A1 4234/4885POLB 1231/4885MAPT 2423/4885
US-20170334854-A1 One-Step Process For The Synthesis Of Alkylated Metyrapone Analogs MET, MEP1B, ABL1 ALDH1A1 606/4885POLB 719/4885MAPT 3413/4885
US-10053426-B2 Process for the synthesis of metyrapone and alkylated metyrapone analogs MET, ABL1, CMPK1 ALDH1A1 872/4885POLB 911/4885MAPT 3201/4885

“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.