Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1123490

CCCCCCCCCCCC[N+](C)(C)Cc1cccc2ccccc12.[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 20)

geneUniProtsupporting neighboursconfidence
CHRM2 known ✓ P08172 1/20 0.43
CHRM1 known ✓ P11229 1/20 0.43
CHRM3 known ✓ P20309 1/20 0.43
SLC6A2 known ✓ P23975 1/20 0.43
SLC6A3 known ✓ Q01959 1/20 0.43
MEN1 O00255 2/20 0.58
KMT2A Q03164 2/20 0.58
MAPK1 P28482 2/20 0.58
SMN1; SMN2 Q16637 2/20 0.58
TP53 P04637 1/20 0.58
HTT P42858 4/20 0.56
DNM1 Q05193 3/20 0.55
PSMD14 O00487 1/20 0.48
HSP90AA1 P07900 1/20 0.48
MMP2 P08253 1/20 0.48
MC4R P32245 1/20 0.48
RAD52 P43351 1/20 0.48
MLNR O43193 1/20 0.43
NR1I2 O75469 1/20 0.43
ESR1 P03372 1/20 0.43

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 SCHEMBL29729671 1.00 MEN1 (0.58) MEN1KMT2AMAPK1SMN1; SMN2TP53
Hydrochloric Acid SCHEMBL30869258 1.00 MEN1 (0.58) MEN1KMT2AMAPK1SMN1; SMN2TP53
Water SCHEMBL8021034 0.98 HTT (0.59) MEN1KMT2AMAPK1SMN1; SMN2TP53
SCHEMBL8083797 0.98 DNM1 (0.57) MEN1KMT2AMAPK1SMN1; SMN2TP53
SCHEMBL6762129 0.98 DNM1 (0.57) MEN1KMT2AMAPK1SMN1; SMN2TP53
Water SCHEMBL11790520 0.97 DNM1 (0.55) MEN1KMT2AMAPK1SMN1; SMN2TP53
Hydrochloric Acid SCHEMBL10445238 0.87 MEN1 (0.49) MEN1KMT2AMAPK1SMN1; SMN2TP53
Hydrochloric Acid SCHEMBL7764453 0.85 KMT2A (0.71) MEN1KMT2AMAPK1SMN1; SMN2TP53
Hydrochloric Acid SCHEMBL8720796 0.85 KMT2A (0.71) MEN1KMT2AMAPK1SMN1; SMN2TP53
Hydrochloric Acid SCHEMBL7760973 0.85 KMT2A (0.71) MEN1KMT2AMAPK1SMN1; SMN2TP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2181596-B1 METHOD OF INHIBITING THE GROWTH OF MICROORGANISM IN AQUEOUS SYSTEMS USING A COMPOSITION COMPRISING LYSOZYME BUCKMAN LABOR INC (US) 2015-07-08 EP claimed
WO-2007100514-A1 HALOPEROXIDASE TREATMENT TO CONTROL ALGAE BUCKMAN LABORATORIES INTERNATIONAL, INC. (US) 2007-09-07 WO claimed
US-20070197388-A1 Haloperoxidase treatment to control algae BUCKMAN LABORATORIES INTERNATIONAL, INC. 2007-08-23 US claimed
US-4311512-A Bactericidal water-soluble complexes POLYCRAFT LABORATORIES, INC., A CORP. OF NJ. 1982-01-19 US claimed
US-3997705-A Method of coagulating a fluoro-elastomer from an aqueous dispersion thereof DYNAMIT NOBEL AKTIENGESELLSCHAFT (DT) 1976-12-14 US claimed
WO-2021252700-A1 USE OF CHLORAMINES AND CATIONIC POLYMERS IN WATER TREATMENT BUCKMAN LABORATORIES INTERNATIONAL, INC. (US) 2021-12-16 WO disclosed
US-20210387876-A1 USE OF CHLORAMINES AND CATIONIC POLYMERS IN WATER TREATMENT BUCKMAN LABORATORIES INTERNATIONAL, INC. (US) 2021-12-16 US disclosed
US-11053641-B2 Modified creping adhesive formulation and creping methods using same BUCKMAN LABORATORIES INTERNATIONAL, INC. (US) 2021-07-06 US disclosed
EP-3768891-A1 MODIFIED CREPING ADHESIVE FORMULATION AND CREPING METHODS USING SAME Buckman Laboratories International, Inc. (US) 2021-01-27 EP disclosed
US-20190292729-A1 Modified Creping Adhesive Formulation And Creping Methods Using Same BUCKMAN LABORATORIES INTERNATIONAL, INC. (US) 2019-09-26 US disclosed
EP-2181596-B1 METHOD OF INHIBITING THE GROWTH OF MICROORGANISM IN AQUEOUS SYSTEMS USING A COMPOSITION COMPRISING LYSOZYME BUCKMAN LABOR INC (US) 2015-07-08 EP disclosed
US-8603453-B2 Antimicrobial polymeric biguanide and acidic co-polymer composition and method of use ARCH UK BIOCIDES LIMITED (GB) 2013-12-10 US disclosed
US-5112871-A ANTI-MICROBIAL BROMO-NITRO COMPOUNDS IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1992-05-12 US disclosed
EP-0478173-A1 Derivatives of 4,5-polymethylene-4-isothiazoline-3 ones and their use as biocides ZENECA LIMITED (GB) 1992-04-01 EP disclosed
WO-1992001380-A1 BIOCIDE COMPOSITION IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1992-02-06 WO disclosed
EP-0457435-A2 Biocide composition and use ZENECA LIMITED (GB) 1991-11-21 EP disclosed
EP-0390394-A2 Composition and use ZENECA LIMITED (GB) 1990-10-03 EP disclosed
EP-0373759-A1 Compound, composition, process and use IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1990-06-20 EP disclosed
US-4311512-A Bactericidal water-soluble complexes POLYCRAFT LABORATORIES, INC., A CORP. OF NJ. 1982-01-19 US disclosed
US-3997705-A Method of coagulating a fluoro-elastomer from an aqueous dispersion thereof DYNAMIT NOBEL AKTIENGESELLSCHAFT (DT) 1976-12-14 US disclosed