Hydrochloric Acid

Hydrochloric Acid

SCHEMBL961160

CCCC[n+]1ccn(CC)c1.[Cl-]

nearest known ligand 0.41

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 18)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 3/20 0.41
KMT2A Q03164 3/20 0.41
SMN1; SMN2 Q16637 3/20 0.41
HSP90AA1 P07900 2/20 0.41
FDPS P14324 2/20 0.41
MAPT P10636 2/20 0.39
MAPK1 P28482 2/20 0.39
CASP2 P42575 1/20 0.39
HSPD1 P10809 1/20 0.38
RAD52 P43351 1/20 0.38
HSPE1 P61604 1/20 0.38
APAF1 O14727 1/20 0.38
NPC1 O15118 1/20 0.38
PLA2G1B P04054 1/20 0.38
HTT P42858 1/20 0.38
RAB9A P51151 1/20 0.38
NPSR1 Q6W5P4 1/20 0.38
ATG4B Q9Y4P1 1/20 0.38

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
SCHEMBL372519 0.98 MEN1 (0.42) MEN1KMT2ASMN1; SMN2HSP90AA1FDPS
Iodide SCHEMBL1758290 0.96 SMN1; SMN2 (0.41) MEN1KMT2ASMN1; SMN2HSP90AA1FDPS
Bromide SCHEMBL5168946 0.96 MEN1 (0.45) MEN1KMT2ASMN1; SMN2HSP90AA1FDPS
Fluoride Ion SCHEMBL5172541 0.96 MEN1 (0.41) MEN1KMT2ASMN1; SMN2HSP90AA1FDPS
Hydrochloric Acid SCHEMBL962124 0.94 MEN1 (0.47) MEN1KMT2ASMN1; SMN2HSP90AA1MAPT
Hydrochloric Acid SCHEMBL25413444 0.92 MEN1 (0.50) MEN1KMT2ASMN1; SMN2HSP90AA1MAPT
Hydrochloric Acid SCHEMBL25415803 0.92 MEN1 (0.50) MEN1KMT2ASMN1; SMN2HSP90AA1MAPT
Hydrochloric Acid SCHEMBL22026956 0.92 MEN1 (0.50) MEN1KMT2ASMN1; SMN2HSP90AA1MAPT
Hydrochloric Acid SCHEMBL25415755 0.92 MEN1 (0.50) MEN1KMT2ASMN1; SMN2HSP90AA1MAPT
Hydrochloric Acid SCHEMBL960532 0.92 MEN1 (0.50) MEN1KMT2ASMN1; SMN2HSP90AA1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109651114-B Method for synthesizing alkyl aromatic aldehyde 中国石油化工股份有限公司 2022-04-05 CN claimed
CN-109647528-B Catalyst for synthesizing alkyl aromatic aldehyde 中国石油化工股份有限公司 2022-04-05 CN claimed
CN-109651112-B Method for synthesizing alkyl aromatic aldehyde by alkyl aromatic hydrocarbon carbonylation 中国石油化工股份有限公司 2022-04-01 CN claimed
CN-107847867-B Composite membranes having improved performance and/or durability and methods of use thereof 3M创新有限公司 2021-06-25 CN claimed
CN-108409581-B Preparation method of dinonyl-substituted diphenylamine antioxidant 江苏飞亚化学工业有限责任公司 2020-07-14 CN claimed
US-20200164319-A1 COMPOSITE MEMBRANES WITH IMPROVED PERFORMANCE AND/OR DURABILITY AND METHODS OF USE 3M INNOVATIVE PROPERTIES COMPANY 2020-05-28 US claimed
US-20200030748-A1 COMPOSITE MEMBRANES WITH IMPROVED PERFORMANCE AND/OR DURABILITY AND METHODS OF USE 3M INNOVATIVE PROPERTIES COMPANY 2020-01-30 US claimed
CN-110665017-A Preparation method of sensitizer for targeting tumor to combine CT imaging and photothermal therapy 上海纳米技术及应用国家工程研究中心有限公司 2020-01-10 CN claimed
CN-110559439-A Preparation method of photo-thermal and photodynamic cooperative therapeutic agent 上海纳米技术及应用国家工程研究中心有限公司 2019-12-13 CN claimed
US-10478778-B2 Composite membranes with improved performance and/or durability and methods of use 3M INNOVATIVE PROPERTIES COMPANY (US) 2019-11-19 US claimed
US-20120207525-A1 RESISTANCE HEATING COMPOSITION AND HEATING COMPOSITE, HEATING APPARATUS, AND FUSING APPARATUS, INCLUDING RESISTANCE HEATING COMPOSITION SAMSUNG ELECTRONICS CO., LTD. (KR) 2012-08-16 US claimed
US-7943543-B1 Ionic liquid-solid-polymer mixed matrix membranes for gas separations UOP LLC (US) 2011-05-17 US claimed
US-20110000782-A1 ALUMINUM RECOVERY PROCESS THE UNIVERSITY OF ALABAMA (US) 2011-01-06 US claimed
WO-2009102419-A2 ALUMINUM RECOVERY PROCESS THE UNIVERSITY OF ALABAMA (US) 2009-08-20 WO claimed
EP-1663921-B1 METHOD FOR PRODUCING HALOALKANES FROM ALCOHOLS BASF AG (DE) 2007-05-02 EP claimed
US-20070055084-A1 Method for producing haloalkanes from alcohols BASF AKTIENGESELLSCHAFT (DE) 2007-03-08 US claimed
WO-2003051894-A1 PREPARATION OF IONIC LIQUIDS CYTEC CANADA INC. (CA) 2003-06-26 WO claimed
US-6579343-B2 Contacting gas with a liquid ionic compound comprising a nitrogen-containing heterocyclic cation UNIVERSITY OF NOTRE DAME DU LAC 2003-06-17 US claimed
US-20020189444-A1 Purification of gas with liquid ionic compounds NATIONAL SCIENCE FOUNDATION 2002-12-19 US claimed
EP-0693045-B1 ALKYLATION PROCESS BP CHEM INT LTD (GB) 1997-10-22 EP claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 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-20070055084-A1 Method for producing haloalkanes from alcohols ADH1C, HDHD5, ADH5 MEN1 4351/4885KMT2A 735/4885SMN1; SMN2 4795/4885

“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.