Hydrochloric Acid

Hydrochloric Acid

SCHEMBL394062

CCCC[N+](CC)(CC)CC.[Cl-]

nearest known ligand 0.72

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
DNM1 Q05193 5/20 0.72
SLC22A1 O15245 3/20 0.69
SLC22A2 O15244 1/20 0.59
TSHR P16473 2/20 0.53
ALDH1A1 P00352 1/20 0.53
TP53 P04637 1/20 0.53
CYP3A4 P08684 1/20 0.53
ALOX15 P16050 1/20 0.53
ALOX12 P18054 1/20 0.53
SMN1; SMN2 Q16637 1/20 0.53
HIF1A Q16665 1/20 0.53
HSD17B10 Q99714 1/20 0.53
KDM4E B2RXH2 1/20 0.50
PMP22 Q01453 1/20 0.50
ATM Q13315 1/20 0.50
NFKB1 P19838 1/20 0.44
KCNA1 Q09470 1/20 0.44

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
SCHEMBL1239368 0.97 DNM1 (0.77) DNM1SLC22A1SLC22A2TSHRALDH1A1
SCHEMBL17800111 0.93 DNM1 (0.72) DNM1SLC22A1SLC22A2TSHRALDH1A1
Fluoride Ion SCHEMBL31559159 0.93 DNM1 (0.72) DNM1SLC22A1SLC22A2TSHRALDH1A1
Hydrochloric Acid SCHEMBL4131094 0.93 SLC22A1 (0.69) DNM1SLC22A1SLC22A2TSHRALDH1A1
Hydrochloric Acid SCHEMBL5084823 0.93 SLC22A1 (0.69) DNM1SLC22A1SLC22A2TSHRALDH1A1
Bromide SCHEMBL622840 0.93 DNM1 (0.78) DNM1SLC22A1SLC22A2TSHRALDH1A1
Bromide SCHEMBL10701064 0.93 DNM1 (0.72) DNM1SLC22A1SLC22A2TSHRALDH1A1
Iodide SCHEMBL5088044 0.93 DNM1 (0.72) DNM1SLC22A1SLC22A2TSHRALDH1A1
Water SCHEMBL999491 0.93 DNM1 (0.72) DNM1SLC22A1SLC22A2TSHRALDH1A1
Hydrochloric Acid SCHEMBL2468750 0.90 DNM1 (0.88) DNM1SLC22A1SLC22A2TSHRALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120158951-A High-purity cellulose and preparation method thereof 浙江理工大学 2025-06-17 CN claimed
CN-119976882-A Method for synthesizing hierarchical pore molecular sieve 中国石油大学(华东) 2025-05-13 CN claimed
EP-3912969-B1 METHOD FOR DIRECT CONVERSION OF CARBON DIOXIDE TO DIALKYL CARBONATES USING ETHYLENE OXIDE AS FEEDSTOCK E3TEC SERVICE LLC (US) 2022-11-30 EP claimed
CN-108840311-B Hydrogen sulfide liquid-phase oxidation removal method using eutectic solvent as medium 南京大学 2022-04-22 CN claimed
CN-112608258-A Method for synthesizing 4,4' -dichlorodiphenyl sulfone by sulfoxide oxidation method 江苏傲伦达科技实业股份有限公司 2021-04-06 CN claimed
CN-112041306-A Method for producing a fuel additive 英国石油国际有限公司 2020-12-04 CN claimed
CN-111936474-A Method for preparing fuel additive 英国石油国际有限公司 2020-11-13 CN claimed
EP-3732172-A1 METHODS FOR PREPARING FUEL ADDITIVES BP Oil International Limited (GB) 2020-11-04 EP claimed
EP-3732171-A1 METHODS FOR PREPARING FUEL ADDITIVES BP Oil International Limited (GB) 2020-11-04 EP claimed
EP-3732173-A1 METHODS FOR PREPARING FUEL ADDITIVES BP Oil International Limited (GB) 2020-11-04 EP claimed
CN-111788188-A Method for producing a fuel additive 英国石油国际有限公司 2020-10-16 CN claimed
CN-111269363-A Liquid-absorbing polymer and its preparing process 仲恺农业工程学院 2020-06-12 CN claimed
US-4299989-A Preparation of ketones UOP INC. (US) 1981-11-10 US claimed
JP-2124901-A None JP disclosed
EP-4667473-A2 PROCESS FOR PREPARING 2-EXO-(2-METHYLBENZYLOXY)-1-METHYL-4-ISOPROPYL-7-OXABICYCLO[2.2.1]HEPTANE BASF Agro B.V. (NL) 2025-12-24 EP disclosed
EP-3583106-B1 PROCESS FOR PREPARING 2-EXO-(2-METHYLBENZYLOXY)-1-METHYL-4-ISOPROPYL-7-OXABICYCLO[2.2.1]HEPTANE BASF AGRO BV (NL) 2025-10-22 EP disclosed
US-4334079-A Synthesis of substituted benzyl esters ELI LILLY AND COMPANY (US) 1982-06-08 US disclosed
US-4299989-A Preparation of ketones UOP INC. (US) 1981-11-10 US disclosed
US-4027016-A Everninomicin antibacterial derivatives, electrochemical method for their manufacture, method for their use as antibacterial agents, and pharmaceutical compositions useful therefor SCHERING CORPORATION (US) 1977-05-31 US disclosed
US-3998708-A Electrochemical process for preparing hydroxylaminoeverninomicins SCHERING CORPORATION (US) 1976-12-21 US disclosed