Hydrochloric Acid

Hydrochloric Acid

SCHEMBL636092

[Cl-].c1ccc(-[n+]2ccccc2)cc1

nearest known ligand 0.35

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 4/20 0.33
MAPT P10636 2/20 0.35
HTT P42858 2/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
NPC1 O15118 2/20 0.34
RAB9A P51151 2/20 0.34
BCHE P06276 3/20 0.33
KDM4E B2RXH2 1/20 0.32
MAPK1 P28482 1/20 0.32
NTSR1 P30989 1/20 0.32
NPSR1 Q6W5P4 1/20 0.32
UHRF1 Q96T88 1/20 0.32
SLC22A2 O15244 1/20 0.32
SLC22A1 O15245 1/20 0.32
SLC22A3 O75751 1/20 0.32
SLC6A4 P31645 1/20 0.32
ALDH1A1 P00352 2/20 0.32
CA12 O43570 1/20 0.31
CA1 P00915 1/20 0.31
CA2 P00918 1/20 0.31

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 SCHEMBL30042005 1.00 MAPT (0.35) MAPTHTTSMN1; SMN2NPC1RAB9A
SCHEMBL125499 0.97 MAPT (0.35) MAPTHTTSMN1; SMN2NPC1RAB9A
SCHEMBL28558026 0.94 MAPT (0.34) MAPTHTTSMN1; SMN2NPC1RAB9A
Water SCHEMBL2150507 0.94 ACHE (0.37) MAPTHTTSMN1; SMN2NPC1RAB9A
Fluoride Ion SCHEMBL1502890 0.94 MAPT (0.34) MAPTHTTSMN1; SMN2NPC1RAB9A
Ammonia Solution, Strong SCHEMBL4202272 0.94 MAPT (0.34) MAPTHTTSMN1; SMN2NPC1RAB9A
Bromide SCHEMBL636300 0.94 ACHE (0.37) MAPTHTTSMN1; SMN2NPC1RAB9A
SCHEMBL28817308 0.94 MAPT (0.34) MAPTHTTSMN1; SMN2NPC1RAB9A
Iodide SCHEMBL1502876 0.94 MAPT (0.34) MAPTHTTSMN1; SMN2NPC1RAB9A
SCHEMBL776579 0.87 NPC1 (0.37) MAPTHTTNPC1RAB9AACHE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113567380-A Benzyl chloride pyridinium derivative used as PH indicator and synthetic method thereof 湖北科技学院 2021-10-29 CN claimed
CN-113484317-A Method for preparing PH test paper through benzyl chloride pyridinium derivative 湖北科技学院 2021-10-08 CN claimed
US-11982612-B2 Systems and methods for color-scalable flow cytometry with Raman tags BAYSPEC, INC. (US) 2024-05-14 US disclosed
US-20230333001-A1 SYSTEMS AND METHODS FOR COLOR-SCALABLE FLOW CYTOMETRY WITH RAMAN TAGS BAYSPEC, INC. 2023-10-19 US disclosed
CN-113557313-A Method and apparatus for producing aluminum material 株式会社UACJ 2021-10-26 CN disclosed
EP-2295484-B1 POLYMERIZABLE COMPOSITION FOR POLYTHIOURETHANE OPTICAL MATERIAL, POLYTHIOURETHANE OPTICAL MATERIAL OBTAINED FROM SAME POLYMERIZABLE COMPOSITION, AND POLYMERIZATION CATALYST FOR POLYTHIOURETHANE OPTICAL MATERIAL MITSUI CHEMICALS INC (JP) 2018-01-17 EP disclosed
US-9290656-B2 Polymerizable composition for polythiourethane optical material MITSUI CHEMICALS, INC. (JP) 2016-03-22 US disclosed
US-20160074856-A1 RECOVERY METHOD AND REUSE METHOD OF OXO ACID CATALYST DAICEL CORPORATION (JP) 2016-03-17 US disclosed
EP-2990110-A1 RECOVERY METHOD AND REUSE METHOD OF OXO ACID CATALYST Daicel Corporation (JP) 2016-03-02 EP disclosed
US-20140349969-A1 COMPOUNDS AND METHODS FOR TREATING PAIN AKRON MOLECULES AG (AT) 2014-11-27 US disclosed
US-8642718-B2 Curable composition MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2014-02-04 US disclosed
US-20040024165-A1 Composition for optical material MITSUBISHI GAS CHEMICAL CO., INC. (JP) 2004-02-05 US disclosed
EP-1326095-A1 COMPOSITION FOR OPTICAL MATERIAL MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2003-07-09 EP disclosed
EP-1319966-A1 COMPOSITION FOR OPTICAL MATERIAL MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2003-06-18 EP disclosed
EP-1316819-A1 COMPOSITION FOR OPTICAL MATERIAL MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2003-06-04 EP disclosed
EP-0453197-B1 Amine derivatives ICI PLC (GB) 1994-06-15 EP disclosed
EP-0119831-B1 HEAT BLEACHABLE DYE SYSTEMS MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1988-01-07 EP disclosed
US-4594312-A Photothermographic medium MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1986-06-10 US disclosed
EP-0119831-A2 Heat bleachable dye systems MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1984-09-26 EP disclosed
US-4108882-A QUATERNARY AMMONIUM HALIDE CATALYST DOW CORNING CORPORATION (US) 1978-08-22 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 (2 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-20140349969-A1 COMPOUNDS AND METHODS FOR TREATING PAIN TRPV1, ACHE, OPRL1 ACHE 2/4885MAPT 898/4885HTT 384/4885
US-20160074856-A1 RECOVERY METHOD AND REUSE METHOD OF OXO ACID CATALYST HAO2, HAO1, AOX1 ACHE 177/4885MAPT 4165/4885HTT 1843/4885

“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.