Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2006410

C[n+]1ccccc1Cc1ccccc1.[Cl-]

nearest known ligand 0.44

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 19)

geneUniProtsupporting neighboursconfidence
CALM1 P0DP23 1/20 0.44
KCNH2 Q12809 2/20 0.44
APOBEC3A P31941 1/20 0.41
APOBEC3G Q9HC16 1/20 0.41
TP53 P04637 1/20 0.41
HDAC8 Q9BY41 5/20 0.40
HSD17B10 Q99714 1/20 0.39
LMNA P02545 2/20 0.38
LTA4H P09960 1/20 0.36
KDM4E B2RXH2 2/20 0.35
ALDH1A1 P00352 2/20 0.35
TDP1 Q9NUW8 1/20 0.35
CYP3A4 P08684 1/20 0.35
MAPT P10636 1/20 0.35
HTT P42858 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
MAOB P27338 1/20 0.34
ATM Q13315 1/20 0.34
TAAR1 Q96RJ0 1/20 0.34

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
Bromide SCHEMBL28254649 0.96 CALM1 (0.44) CALM1KCNH2APOBEC3AAPOBEC3GTP53
Hydrochloric Acid SCHEMBL2002518 0.76 HDAC8 (0.44) KCNH2TP53HDAC8HSD17B10KDM4E
Hydrochloric Acid SCHEMBL30330872 0.76 HDAC8 (0.44) KCNH2TP53HDAC8HSD17B10KDM4E
Hydrochloric Acid SCHEMBL31373256 0.75 CALM1 (0.44) CALM1KCNH2APOBEC3AAPOBEC3GTP53
Hydrochloric Acid SCHEMBL10533908 0.75 CALM1 (0.39) CALM1KCNH2APOBEC3AAPOBEC3GTP53
SCHEMBL17130344 0.73 TP53 (0.44) CALM1KCNH2APOBEC3AAPOBEC3GTP53
Hydrochloric Acid SCHEMBL11725090 0.73 KDM4E (0.45) CALM1LMNAKDM4EALDH1A1MAPT
SCHEMBL29729219 0.73
SCHEMBL329433 0.73
SCHEMBL31373271 0.72 CALM1 (0.46) CALM1KCNH2APOBEC3AAPOBEC3GTP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230321604-A1 MEMBRANE-WAFER ASSEMBLY FOR ELECTRODEIONIZATION BOARD OF SUPERVISORS OF LOUISIANA STATE UNIVERSITY AND AGRICULTURAL AND MECHANICAL COLLEGE 2023-10-12 US claimed
US-20230321604-A1 MEMBRANE-WAFER ASSEMBLY FOR ELECTRODEIONIZATION BOARD OF SUPERVISORS OF LOUISIANA STATE UNIVERSITY AND AGRICULTURAL AND MECHANICAL COLLEGE 2023-10-12 US disclosed
US-20230287579-A1 ELECTROCHEMICAL REACTOR FOR UPGRADING METHANE AND SMALL ALKANES TO LONGER ALKANES AND ALKENES UNIV LOUISIANA STATE (US) 2023-09-14 US disclosed
US-11591699-B2 Electrochemical reactor for upgrading methane and small alkanes to longer alkanes and alkenes BOARD OF SUPERVISORS OF LOUISIANA STATE UNIVERSITY (US) 2023-02-28 US disclosed
US-20210164115-A1 ELECTROCHEMICAL REACTOR FOR UPGRADING METHANE AND SMALL ALKANES TO LONGER ALKANES AND ALKENES BOARD OF SUPERVISORS OF LOUISIANA STATE UNIVERSITY AND AGRICULTURAL AND MECHANICAL COLLEGE 2021-06-03 US disclosed
EP-3774029-A1 ELECTROCHEMICAL REACTOR FOR UPGRADING METHANE AND SMALL ALKANES TO LONGER ALKANES AND ALKENES Board of Supervisors of Louisiana State University and Agricultural and Mechanical College (US) 2021-02-17 EP disclosed
CN-108885997-A Method for planarizing semiconductor substrate using silicon-containing composition 日产化学株式会社 2018-11-23 CN disclosed
CN-107427869-A Ash processing is with immobilization of heavy metals agent and uses its grey processing method 栗田工业株式会社 2017-12-01 CN disclosed
CN-103748517-B Silicon-containing resist underlayer film-forming composition having sulfone structure 日产化学工业株式会社 2017-04-19 CN disclosed
US-8182557-B2 Pretreating lignocellulosic (woody biomass) by dissolving in ionic liquid comprising imidazolium or pyridinium salt to form a solution; precipitating with regenerating solvent (water); hydrolysis to form sugar and fermentation to form bioethanol; recycling through evaporation; environmentally friendly NORTH CAROLINA STATE UNIVERSITY (US) 2012-05-22 US disclosed
US-20080190013-A1 USE OF LIGNOCELLULOSICS SOLVATED IN IONIC LIQUIDS FOR PRODUCTION OF BIOFUELS NORTH CAROLINA STATE UNIVERSITY 2008-08-14 US disclosed
US-20080188636-A1 POLYMER DERIVATIVES AND COMPOSITES FROM THE DISSOLUTION OF LIGNOCELLULOSICS IN IONIC LIQUIDS NORTH CAROLINA STATE UNIVERSITY 2008-08-07 US disclosed
US-20080185112-A1 PRODUCT PREPARATION AND RECOVERY FROM THERMOLYSIS OF LIGNOCELLULOSICS IN IONIC LIQUIDS NORTH CAROLINA STATE UNIVERSITY 2008-08-07 US disclosed
EP-1270602-B1 CATALYST FOR VINYL COMPOUND POLYMERIZATION AND PROCESS FOR PRODUCING VINYL POLYMER IDEMITSU KOSAN CO (JP) 2007-10-03 EP disclosed
US-7176266-B2 Catalyst for vinyl compound polymerization and process for producing vinyl polymer IDEMITSU KOSAN CO. LTD. (JP) 2007-02-13 US disclosed
US-6835788-B2 As polymerization catalyst IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2004-12-28 US disclosed
US-20040259720-A1 Catalyst for vinyl compound polymerization and process for producing vinyl polymer IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2004-12-23 US disclosed
US-20030027716-A1 Catalyst for vinyl compounds and process for production of vinyl polymers IDEMITSU KOSAN CO. LTD. (JP) 2003-02-06 US disclosed
EP-1270602-A1 CATALYST FOR VINYL COMPOUND POLYMERIZATION AND PROCESS FOR PRODUCING VINYL POLYMER IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2003-01-02 EP disclosed
EP-1136122-A1 TRANSITION METAL CATALYSTS AND PROCESSES FOR PRODUCING $g(a)-OLEFIN AND VINYL COMPOUND POLYMER IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2001-09-26 EP disclosed