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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Hydrochloric Acid SCHEMBL7124477 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL3116792 | 0.93 | — | — | |
| Hydrochloric Acid SCHEMBL3680046 | 0.91 | — | — | |
| Hydrochloric Acid SCHEMBL3679765 | 0.90 | — | — | |
| Hydrochloric Acid SCHEMBL3126482 | 0.89 | — | — | |
| Hydrochloric Acid SCHEMBL3682025 | 0.84 | ALDH1A1 (0.30) | — | |
| Hydrochloric Acid SCHEMBL3123293 | 0.83 | ALDH1A1 (0.32) | — | |
| Hydrochloric Acid SCHEMBL3814873 | 0.81 | ALDH1A1 (0.34) | — | |
| Hydrochloric Acid SCHEMBL3109018 | 0.81 | — | — | |
| Hydrochloric Acid SCHEMBL3112737 | 0.80 | — | — |
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 18 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20250129019-A1 | CONTINUOUS PRODUCTION OF AQUEOUS ORGANIC PEROXIDE EMULSIONS | NOURYON CHEMICALS INTERNATIONAL B.V. (NL) | 2025-04-24 | — | — | US | claimed |
| EP-4541788-A1 | CONTINUOUS PRODUCTION OF AQUEOUS ORGANIC PEROXIDE EMULSIONS | Nouryon Chemicals International B.V. (NL) | 2025-04-23 | — | — | EP | claimed |
| US-20250129019-A1 | CONTINUOUS PRODUCTION OF AQUEOUS ORGANIC PEROXIDE EMULSIONS | NOURYON CHEMICALS INTERNATIONAL B.V. (NL) | 2025-04-24 | — | — | US | disclosed |
| EP-4541788-A1 | CONTINUOUS PRODUCTION OF AQUEOUS ORGANIC PEROXIDE EMULSIONS | Nouryon Chemicals International B.V. (NL) | 2025-04-23 | — | — | EP | disclosed |
| CN-115340644-B | Initiator for polymer polyol and method for preparing polymer polyol | 万华化学集团股份有限公司 | 2024-05-03 | — | — | CN | disclosed |
| EP-1195393-B1 | Process for preparing ethylene interpolymers and ethylene interpolymers obtained therefrom | WESTLAKE LONGVIEW CORP (US) | 2010-04-07 | — | — | EP | disclosed |
| EP-1195392-B1 | Process for preparing ethylene interpolymers and ethylene interpolymers obtained therefrom | EASTMAN CHEM CO (US) | 2006-07-19 | — | — | EP | disclosed |
| EP-1092730-B1 | PROCESS FOR PRODUCING OLEFIN POLYMER AND OLEFIN POLYMER | MITSUI CHEMICALS INC (JP) | 2005-03-23 | — | — | EP | disclosed |
| US-20040122192-A1 | Polar group-containing olefin copolymer, process for preparing the same, thermoplastic resin composition containing the copolymer, and uses thereof | MITSUI CHEMICALS, INC. | 2004-06-24 | — | — | US | disclosed |
| US-6608156-B1 | And optionally carbon monoxide; high pressure, free radical initiator; melting peak temperatures (Tm) equal to or greater than 50 degrees C.; olefin hetero monomer is allyl; vinyl ethylene carbonate, 3,4-diacetoxy-1-butene, 3-butene-1,2-diol | EASTMAN CHEMICAL COMPANY | 2003-08-19 | — | — | US | disclosed |
| US-6608157-B1 | And optionally carbon monoxide; high pressure, free radicalinitiator; melting peak temperatures (Tm) equal to or greaterthan 50 degrees C.; olefin hetero monomer is allyl; vinylethylene carbonate, 3,4-diacetoxy-1-butene, | EASTMAN CHEMICAL COMPANY | 2003-08-19 | — | — | US | disclosed |
| US-6583237-B1 | Silyl-terminated olefin polymers; catalyst is transition metal cyclopentadiene compound, organoaluminum oxycompound, compounds that form an ion pair, organoaluminum compound, organosilicon compound, a dialkylzinc compound, and hydrogen | MITSUI CHEMICALS, INC. (JP) | 2003-06-24 | — | — | US | disclosed |
| US-6472491-B1 | PREPARING INTERPOLYMERS COMPRISING ETHYLENE AND AT LEAST TWO MONOMER UNITS SELECTED FROM HETEROATOM SUBSTITUTED OLEFIN MONOMER UNITS DERIVED FROM A COMPOUND WITH HETEROATOMS SELECTED FROM OXYGEN, NITROGEN, AND SULFUR, WHICH ARE BOUND TO | EASTMAN CHEMICAL COMPANY | 2002-10-29 | — | — | US | disclosed |
| EP-1195392-A2 | Process for preparing ethylene interpolymers and ethylene interpolymers obtained therefrom | EASTMAN CHEMICAL COMPANY (US) | 2002-04-10 | — | — | EP | disclosed |
| EP-1195393-A2 | Process for preparing ethylene interpolymers and ethylene interpolymers obtained therefrom | EASTMAN CHEMICAL COMPANY (US) | 2002-04-10 | — | — | EP | disclosed |
| US-6297333-B1 | METALLOCENE TRANSITION METAL COMPOUND HAVING AN INDENYL GROUP AND A FLUORENYL GROUP AS LIGANDS, SPECIFIC SUBSTITUENT ON A SPECIFIC POSITION OF THE INDENYL GROUP GIVES HIGH MOLECULAR WEIGHT AND HIGH ACTIVITY | MITSUI CHEMICALS INC (JP) | 2001-10-02 | — | — | US | disclosed |
| US-6004897-A | TRANSITION METAL INDENE-FLUORINE COMPLEX COORDINATION CATALYST WITH ORGANOALUMINUM AND ALUMOXANE COMPOUNDS | MITSUI CHEMICALS, INC. (JP) | 1999-12-21 | — | — | US | disclosed |
| EP-0754698-A2 | An olefin polymerization catalyst and a process for preparing olefin polymer | MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) | 1997-01-22 | — | — | EP | disclosed |