Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1854489

CCCCCCCCCCCC[Al+2].[Cl-].[Cl-]

nearest known ligand 0.57

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 9)

geneUniProtsupporting neighboursconfidence
TSHR P16473 4/20 0.57
THRB P10828 1/20 0.57
DNM1 Q05193 6/20 0.43
ALDH1A1 P00352 3/20 0.42
LMNA P02545 2/20 0.42
MEN1 O00255 2/20 0.42
KMT2A Q03164 2/20 0.42
HSD17B10 Q99714 1/20 0.42
SLC22A1 O15245 1/20 0.42

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 SCHEMBL10520281 1.00 TSHR (0.57) TSHRTHRBDNM1ALDH1A1LMNA
Hydrochloric Acid SCHEMBL1538972 1.00 TSHR (0.57) TSHRTHRBDNM1ALDH1A1LMNA
Hydrochloric Acid SCHEMBL1538821 1.00 TSHR (0.57) TSHRTHRBDNM1ALDH1A1LMNA
Hydrochloric Acid SCHEMBL28671040 1.00 TSHR (0.57) TSHRTHRBDNM1ALDH1A1LMNA
Hydrochloric Acid SCHEMBL396600 1.00
Hydrochloric Acid SCHEMBL11435761 1.00 TSHR (0.57) TSHRTHRBDNM1ALDH1A1LMNA
Hydrochloric Acid SCHEMBL6563754 1.00 TSHR (0.57) TSHRTHRBDNM1ALDH1A1LMNA
Hydrochloric Acid SCHEMBL150719 1.00 TSHR (0.57) TSHRTHRBDNM1ALDH1A1LMNA
Hydrochloric Acid SCHEMBL28410687 0.97 TSHR (0.53) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL1232118 0.93 TSHR (0.57) TSHRTHRBDNM1ALDH1A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1976821-B1 DIRECT ALKYLATION OF N-ALKYL-N'-PHENYL-P-PHENYLENEDIAMINE CHEMTURA CORP (US) 2011-05-25 EP claimed
CN-101370766-A Direct alkylation of N-alkyl-N'-phenyl-p-phenylenediamine CHEMTURA CORP (US) 2009-02-18 CN claimed
EP-1976821-A1 DIRECT ALKYLATION OF N-ALKYL-N'-PHENYL-P-PHENYLENEDIAMINE CHEMTURA CORPORATION (US) 2008-10-08 EP claimed
US-7361788-B2 Direct alkylation of N-alkyl-N′-phenyl-p-phenylenediamine CHEMTURA CORPORATION (US) 2008-04-22 US claimed
WO-2007087195-A1 DIRECT ALKYLATION OF N-ALKYL-N'-PHENYL-P-PHENYLENEDIAMINE CHEMTURA CORPORATION (US) 2007-08-02 WO claimed
US-20070173668-A1 Direct alkylation of N-alkyl-N'-phenyl-p-phenylenediamine LANXESS SOLUTIONS US INC. 2007-07-26 US claimed
EP-1976821-B1 DIRECT ALKYLATION OF N-ALKYL-N'-PHENYL-P-PHENYLENEDIAMINE CHEMTURA CORP (US) 2011-05-25 EP disclosed
CN-101370766-A Direct alkylation of N-alkyl-N'-phenyl-p-phenylenediamine CHEMTURA CORP (US) 2009-02-18 CN disclosed
EP-1976821-A1 DIRECT ALKYLATION OF N-ALKYL-N'-PHENYL-P-PHENYLENEDIAMINE CHEMTURA CORPORATION (US) 2008-10-08 EP disclosed
US-7361788-B2 Direct alkylation of N-alkyl-N′-phenyl-p-phenylenediamine CHEMTURA CORPORATION (US) 2008-04-22 US disclosed
WO-2007087195-A1 DIRECT ALKYLATION OF N-ALKYL-N'-PHENYL-P-PHENYLENEDIAMINE CHEMTURA CORPORATION (US) 2007-08-02 WO disclosed
US-20070173668-A1 Direct alkylation of N-alkyl-N'-phenyl-p-phenylenediamine LANXESS SOLUTIONS US INC. 2007-07-26 US disclosed
EP-0968992-A1 Process for producing lanthanide series metal corboxylates and their use for the polymerization of diene monomers Chi Mei Corporation (TW) 2000-01-05 EP disclosed
US-4107418-A OF AN ACRYLIC MONOMER AND ANOTHER UNSATURATED MONOMER; CATALYST COMPRISING AN ORGANOALUMINUM HALIDE AND ORGANIC PEROXIDE MITSUI PETROCHEMICAL INDUSTRIES LTD. (JP) 1978-08-15 US disclosed
US-4092371-A ALKYLATION CATALYSTS INSTITUT FRANCAIS DU PETROLE (FR) 1978-05-30 US disclosed
US-4062805-A Process for manufacturing a catalyst comprising aluminum oxide and boron oxide, the resulting catalyst and the use thereof in alkylation reactions INSTITUT FRANCAIS DU PETROLE (FR) 1977-12-13 US disclosed
US-4054612-A HOMO- OR COPOLYMERIZATION OF BUTADIENE, CATALYTIC SUMITOMO CHEMICAL COMPANY, LIMITED (JA) 1977-10-18 US disclosed
US-4052473-A OF ISOPRENE, NICKEL-ALKYLAMUMIN HALIDE CONTAINING CATALYST SUMITOMO CHEMICAL COMPANY, LIMITED (JA) 1977-10-04 US disclosed
US-4022808-A ZINC-ALUMINUM-TITANIUM-TIN-IRON OR GROUP 5A AS CATALYSTS NIPPON SODA COMPANY LIMITED (JA) 1977-05-10 US disclosed
US-3980727-A TRANSALKYLATING TOLUENE WITH POLY-METHYL BENZENE HYDROCARBONS IN A CATALYST INSTITUT FRANCAIS DU PETROLE, DES CARBURANTS ET LUBRIFIANTS ET ENTREPRISE DE RECHERCHES ET D'ACTIVITIES PETROLIERES ELF (FR) 1976-09-14 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 (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-20070173668-A1 Direct alkylation of N-alkyl-N'-phenyl-p-phenylenediamine PNMT, AAAS, PNN TSHR 4484/4885THRB 4663/4885DNM1 1649/4885

“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.