Hydrochloric Acid

Hydrochloric Acid

SCHEMBL852092

[BH4-].[Ce].[Cl-].[Na+].[Na+]

nearest known ligand 0.00

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.

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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.

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3705472-B1 METHOD FOR PRODUCING PROSTAGLANDIN DERIVATIVE AGC INC (JP) 2023-06-21 EP disclosed
WO-2023073574-A1 PROCESS FOR THE PREPARATION OF PIPERIDINE CARBOXAMIDES SALT FORMS AND THEREOF CELLIX BIO PRIVATE LIMITED (IN) 2023-05-04 WO disclosed
US-11377413-B2 Method for producing prostaglandin derivative AGC Inc. (JP) 2022-07-05 US disclosed
CN-111263750-B Process for producing prostaglandin derivative AGC株式会社 2022-02-25 CN disclosed
EP-3705472-A1 METHOD FOR PRODUCING PROSTAGLANDIN DERIVATIVE AGC Inc. (JP) 2020-09-09 EP disclosed
US-20200239397-A1 METHOD FOR PRODUCING PROSTAGLANDIN DERIVATIVE AGC Inc. (JP) 2020-07-30 US disclosed
CN-111263750-A Process for producing prostaglandin derivative AGC株式会社 2020-06-09 CN disclosed
CN-104788485-B The method for preparing antiviral agent 百时美-施贵宝爱尔兰控股公司 2017-10-03 CN disclosed
EP-1644384-B1 PROCESS AND INTERMEDIATES FOR THE SYNTHESIS OF ENTECAVIR BRISTOL MYERS SQUIBB CO (US) 2012-10-31 EP disclosed
EP-2433941-A1 Process for isolating the antiviral agent [1S-(1alpha, 3alpha, 4beta)]-2-amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)-2-methylenecyclopentyl]-6H-purin-6-one Bristol-Myers Squibb Company (US) 2012-03-28 EP disclosed
US-20040192912-A1 Process for preparing the antiviral agent [1S-(1alpha,3 alpha,4beta)]-2-amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)-2-methylenecyclopentyl]-6H-purin-6-one BRISTOL-MYERS SQUIBB COMPANY 2004-09-30 US disclosed
WO-2004052310-A2 PROCESS AND INTERMEDIATES FOR SYNTHESIS ENTECAVIR BRISTOL-MYERS SQUIBB COMPANY (US) 2004-06-24 WO disclosed
US-6191279-B1 8-HYDROXY-2,2,6,7-TETRAMETHYL-7,8,9,10-TETRAHYDRO-2H,6H-DIPYRANO (2,3-F:2,3-H)QUINOLIN-10-ONE, FOR EXAMPLE; SCREENING FOR ANTI-HIV ACTIVITY; BETTER SOLUBILITY, METABOLIC STABILITY COUNCIL OF SCIENCE & INDUSTRIAL RESEARCH 2001-02-20 US disclosed
US-5420310-A Anticoagulants, antiulcer, antiatherosclerosis agents formed in multistage reaction TORAY INDUSTRIES, INC. (JP) 1995-05-30 US disclosed
EP-0381959-B1 Cyclohexaneacetamide derivatives HOFFMANN LA ROCHE (CH) 1995-05-03 EP disclosed
EP-0463162-B1 PREPARATION OF 5,6,7-TRINOR-4,8-INTER-m-PHENYLENE PGI 2 DERIVATIVES TORAY INDUSTRIES (JP) 1994-05-11 EP disclosed
US-5202447-A Stereospecific TORAY INDUSTRIES, INC. (JP) 1993-04-13 US disclosed
EP-0463162-A1 PREPARATION OF 5,6,7-TRINOR-4,8-INTER-m-PHENYLENE PGI 2 DERIVATIVES TORAY INDUSTRIES, INC. (JP) 1992-01-02 EP disclosed
US-5015653-A Posess Cognitive Enhancement And Antiamnestic Activity HOFFMANN-LA ROCHE INC. (US) 1991-05-14 US disclosed
EP-0381959-A1 Cyclohexaneacetamide derivatives F. HOFFMANN-LA ROCHE AG (CH) 1990-08-16 EP disclosed