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 SCHEMBL1370750 | 0.89 | — | — | |
| Hydrochloric Acid SCHEMBL7860335 | 0.89 | — | — | |
| Iodide SCHEMBL28208265 | 0.89 | — | — | |
| Hydrochloric Acid SCHEMBL19715271 | 0.89 | — | — | |
| Hydrochloric Acid SCHEMBL6249807 | 0.89 | — | — | |
| SCHEMBL15333 | 0.88 | — | — | |
| SCHEMBL10425917 | 0.88 | FDPS (0.31) | — | |
| Tert-Butylamine SCHEMBL8521741 | 0.82 | — | — | |
| SCHEMBL6128086 | 0.82 | — | — | |
| SCHEMBL2194227 | 0.82 | — | — |
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 19 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-111714451-B | Anti-angiogenesis micelle for preventing scar generation and preparation method thereof | 瑞希(重庆)生物科技有限公司 | 2022-11-29 | — | — | CN | claimed |
| CN-111714451-A | Anti-angiogenesis micelle for preventing scar generation and preparation method thereof | 瑞希(重庆)生物科技有限公司 | 2020-09-29 | — | — | CN | claimed |
| CN-107759776-B | Conjugated polypyrimidine compound, method for preparing compound through multi-component tandem polymerization and application of compound | 华南理工大学 | 2020-04-28 | — | — | CN | claimed |
| CN-111714451-B | Anti-angiogenesis micelle for preventing scar generation and preparation method thereof | 瑞希(重庆)生物科技有限公司 | 2022-11-29 | — | — | CN | disclosed |
| CN-111714451-A | Anti-angiogenesis micelle for preventing scar generation and preparation method thereof | 瑞希(重庆)生物科技有限公司 | 2020-09-29 | — | — | CN | disclosed |
| CN-107759776-B | Conjugated polypyrimidine compound, method for preparing compound through multi-component tandem polymerization and application of compound | 华南理工大学 | 2020-04-28 | — | — | CN | disclosed |
| US-7217851-B1 | Synthesis of butadiynes | UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE AIR FORCE (US) | 2007-05-15 | — | — | US | disclosed |
| US-6891072-B2 | Process for production of dimers or aromatic monohydroxyl compounds | KABUSHIKI KAISHA UENO SEIYAKU OYO KENKYUJO (JP) | 2005-05-10 | — | — | US | disclosed |
| US-6849742-B2 | Binaphthol derivative and process for producing the same | KABUSHIKI KAISHA UENO SEIYAKU OYO KENKYUJO (JP) | 2005-02-01 | — | — | US | disclosed |
| US-20040143141-A1 | Process for production of dimers of aromatic monohydroxyl compounds | THEODORE BARGMAN CO | 2004-07-22 | — | — | US | disclosed |
| US-20040063963-A1 | Binaphthol derivative and process for producing the same | KABUSHIKI KAISHA UENO SEIYAKU OYO KENKYUJO (JP) | 2004-04-01 | — | — | US | disclosed |
| EP-1380564-A1 | BINAPHTOL DERIVATIVE AND PROCESS FOR PRODUCING THE SAME | Kabushiki Kaisha Ueno Seiyaku Oyo Kenkyujo (JP) | 2004-01-14 | — | — | EP | disclosed |
| EP-1380558-A1 | PROCESS FOR PRODUCTION OF DIMERS OF AROMATIC MONOHYDROXYL COMPOUNDS | Kabushiki Kaisha Ueno Seiyaku Oyo Kenkyujo (JP) | 2004-01-14 | — | — | EP | disclosed |
| US-5985446-A | Acetylenic carbon allotrope | LAGOW RICHARD J (US) | 1999-11-16 | — | — | US | disclosed |
| EP-0821702-A4 | AN ACETYLENIC CARBON ALLOTROPE | LAGOW RICHARD J (US) | 1998-04-29 | — | — | EP | disclosed |
| US-5716708-A | Acetylenic carbon allotrope | LAGOW RICHARD J (US) | 1998-02-10 | — | — | US | disclosed |
| EP-0821702-A1 | AN ACETYLENIC CARBON ALLOTROPE | Lagow, Richard J. (US) | 1998-02-04 | — | — | EP | disclosed |
| WO-1996022314-A1 | AN ACETYLENIC CARBON ALLOTROPE | LAGOW RICHARD J (US) | 1996-07-25 | — | — | WO | disclosed |
| US-5153106-A | A mixture of a dye capable of absorbing radiation energy and thermochromic aryl diacetylene component; photopolymerization | ISP INVESTMENTS INC. (US) | 1992-10-06 | — | — | US | disclosed |