Hydrochloric Acid

Hydrochloric Acid

SCHEMBL330070

CCCCCCCCCCCC[n+]1cccc(C)c1.[Cl-]

nearest known ligand 0.93

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
CHRM2 known ✓ P08172 1/20 0.57
CHRM1 known ✓ P11229 1/20 0.57
ACHE known ✓ P22303 1/20 0.57
SLC6A2 known ✓ P23975 1/20 0.57
SLC6A3 known ✓ Q01959 1/20 0.57
HTT P42858 2/20 0.63
MAPT P10636 2/20 0.60
MEN1 O00255 1/20 0.60
MAPK1 P28482 1/20 0.60
CASP2 P42575 1/20 0.60
KMT2A Q03164 1/20 0.60
SMN1; SMN2 Q16637 1/20 0.60
RAD52 P43351 3/20 0.58
HSPD1 P10809 1/20 0.58
HSPE1 P61604 1/20 0.58
ABCB11 O95342 1/20 0.57
ESR1 P03372 1/20 0.57
PGR P06401 1/20 0.57
HTR1A P08908 1/20 0.57
ADRA2A P08913 1/20 0.57

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 SCHEMBL30330738 1.00 HTT (0.63) HTTMAPTMEN1MAPK1CASP2
Hydrochloric Acid SCHEMBL7613954 1.00 HTT (0.63) HTTMAPTMEN1MAPK1CASP2
Hydrochloric Acid SCHEMBL30330878 1.00 HTT (0.63) HTTMAPTMEN1MAPK1CASP2
Hydrochloric Acid SCHEMBL30330782 1.00 HTT (0.63) HTTMAPTMEN1MAPK1CASP2
Hydrochloric Acid SCHEMBL2760836 1.00 HTT (0.63) HTTMAPTMEN1MAPK1CASP2
Hydrochloric Acid SCHEMBL330507 1.00 HTT (0.63) HTTMAPTMEN1MAPK1CASP2
Hydrochloric Acid SCHEMBL23004283 1.00 HTT (0.63) HTTMAPTMEN1MAPK1CASP2
Hydrochloric Acid SCHEMBL30980158 1.00 HTT (0.63) HTTMAPTMEN1MAPK1CASP2
Hydrochloric Acid SCHEMBL2760949 1.00 HTT (0.63) HTTMAPTMEN1MAPK1CASP2
Hydrochloric Acid SCHEMBL30330328 1.00 HTT (0.63) HTTMAPTMEN1MAPK1CASP2

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 17 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240393290-A1 ELECTROCHEMICAL GAS SENSOR AND ELECTROLYTE FOR AN ELECTROCHEMICAL GAS SENSOR Dräger Safety AG & Co. KGaA (DE) 2024-11-28 US disclosed
CN-117999475-A Electrochemical gas sensor and electrolyte for electrochemical gas sensor 德尔格安全股份两合公司 2024-05-07 CN disclosed
EP-4196779-A1 ELECTROCHEMICAL GAS SENSOR AND ELECTROLYTE FOR AN ELECTROCHEMICAL GAS SENSOR Dräger Safety AG & Co. KGaA (DE) 2023-06-21 EP disclosed
US-11623971-B2 Freestanding ion gel and method for preparing the same Research & Business Foundation Sungkyunkwan University (KR) 2023-04-11 US disclosed
WO-2023046704-A1 ELECTROCHEMICAL GAS SENSOR AND ELECTROLYTE FOR AN ELECTROCHEMICAL GAS SENSOR Dräger Safety AG & Co. KGaA (DE) 2023-03-30 WO disclosed
EP-4155723-A1 ELECTROCHEMICAL GAS SENSOR AND ELECTROLYTE FOR AN ELECTROCHEMICAL GAS SENSOR Dräger Safety AG & Co. KGaA (DE) 2023-03-29 EP disclosed
US-20210054127-A1 FREESTANDING ION GEL AND METHOD FOR PREPARING THE SAME Research & Business Foundation Sungkyunkwan University (KR) 2021-02-25 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-9175012-B2 Method for producing optically active diamine derivative DAIICHI SANKYO COMPANY, LIMITED (JP) 2015-11-03 US disclosed
EP-2407450-B1 Method for producing optically active diamine derivative DAIICHI SANKYO CO LTD (JP) 2015-04-22 EP disclosed
US-20120035369-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE DIAMINE DERIVATIVE DAIICHI SANKYO COMPANY, LIMITED (JP) 2012-02-09 US disclosed
EP-2407450-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE DIAMINE DERIVATIVE Daiichi Sankyo Company, Limited (JP) 2012-01-18 EP disclosed
EP-0468404-B1 Process for preparing di-tert.-butyl dicarbonate SUMITOMO CHEMICAL CO (JP) 1994-11-30 EP disclosed
US-5151542-A Reacting an alkali metal tert-butyl carbonate with methanesulfonyl chloride SUMITOMO CHEMICAL CO., LTD. (JP) 1992-09-29 US disclosed
EP-0468404-A2 Process for preparing di-tert.-butyl dicarbonate SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1992-01-29 EP disclosed
US-4225407-A REDUCIBLE NITROGEN-CONTAINING CATIONS THE DOW CHEMICAL COMPANY (US) 1980-09-30 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-20120035369-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE DIAMINE DERIVATIVE F12, DAO, TFPI CHRM2 3492/4885CHRM1 2449/4885ACHE 539/4885
US-20160074856-A1 RECOVERY METHOD AND REUSE METHOD OF OXO ACID CATALYST HAO2, HAO1, AOX1 CHRM2 1939/4885CHRM1 2568/4885ACHE 177/4885

“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.