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 SCHEMBL4945487 | 1.00 | KDM3A (0.50) | — | |
| Hydrochloric Acid SCHEMBL24279 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL11058934 | 1.00 | KDM3A (0.50) | — | |
| Hydrochloric Acid SCHEMBL8845531 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL10408499 | 1.00 | KDM3A (0.50) | — | |
| Hydrochloric Acid SCHEMBL10409847 | 1.00 | KDM3A (0.50) | — | |
| Hydrochloric Acid SCHEMBL8855133 | 1.00 | KDM3A (0.50) | — | |
| Hydrochloric Acid SCHEMBL10772341 | 1.00 | KDM3A (0.50) | — | |
| Hydrochloric Acid SCHEMBL6939511 | 1.00 | KDM3A (0.50) | — | |
| Hydrochloric Acid SCHEMBL11606703 | 1.00 | KDM3A (0.50) | — |
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 963 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-121759211-B | Double perovskite-based luminescent material, preparation method thereof and application thereof in luminescent imaging or anti-counterfeiting | 德州学院 | 2026-05-12 | — | — | CN | claimed |
| CN-121102472-B | Cerium-based up-conversion nano enzyme composite material and preparation method thereof | 内蒙古科学技术研究院 | 2026-02-27 | — | — | CN | claimed |
| CN-121573701-A | Rare earth hydroxide micro-nano material with rough surface, and preparation method and application thereof | 复旦大学 | 2026-02-27 | — | — | CN | claimed |
| CN-119823758-A | M(2-x-y-z)Zn(2-x-y-z)NxYbyTmzO3Nanometer photo-thermal material, preparation and application thereof | 湖南赛荧科技有限公司 | 2025-04-15 | — | — | CN | claimed |
| CN-119662256-A | Degradable NaCeF4Up/down conversion luminescent material and its preparation method and application | 山东师范大学 | 2025-03-21 | — | — | CN | claimed |
| US-20250084012-A1 | METHOD FOR REMOVING TERT-BUTOXYCARBONYL GROUP | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2025-03-13 | — | — | US | claimed |
| CN-119331620-B | Perovskite-based composite material for humidity sensor and preparation method and application thereof | 山东伯桢生物科技有限公司 | 2025-02-28 | — | — | CN | claimed |
| CN-119462111-A | Multi-element rare earth silicate/silicon oxygen carbon nano multiphase ceramic and preparation method thereof | 中南大学 | 2025-02-18 | — | — | CN | claimed |
| CN-119433594-A | Lignin derived carbon-alloy-metal oxide heterojunction catalyst and preparation method thereof | 广西大学 | 2025-02-14 | — | — | CN | claimed |
| US-12221410-B2 | Method for preparing pinacolone | HEZE BRANCH, QILU UNIVERSITY OF TECHNOLOGY(SHANDONG ACADEMY OF SCIENCES) (CN) | 2025-02-11 | — | — | US | claimed |
| CN-101274935-A | Amino acid-containing palisade porphyrin compound, preparation thereof and application thereof | INST BIOMEDICAL ENG CAMS (CN) | 2008-10-01 | — | — | CN | claimed |
| CN-100417651-C | Method for catalytic synthesis of lactide from lactic acid | UNIV NORTHWEST NORMAL (CN) | 2008-09-10 | — | — | CN | claimed |
| CN-1721418-A | Method for catalytic synthesis of lactide from lactic acid | UNIV NORTHWEST NORMAL (CN) | 2006-01-18 | — | — | CN | claimed |
| WO-2005054132-A1 | TAGGED POLYMERIC MATERIALS AND METHODS FOR THEIR PREPARATION | ORICA AUSTRALIA PTY LTD (AU) | 2005-06-16 | — | — | WO | claimed |
| EP-1090900-B1 | Method of producing cyclododecanone and cyclododecanol | UBE INDUSTRIES (JP) | 2003-05-07 | — | — | EP | claimed |
| US-6515185-B1 | Cyclododecanone and cyclododecanol are produced each in high yield by reacting a epoxycyclododecane compound with hydrogen in the presence of a solid catalyst containing (a) catalytic component including a platinum group metal, (b) a promoter | UBE INDUSTRIES, LTD. (JP) | 2003-02-04 | — | — | US | claimed |
| EP-1090900-A1 | Method of producing cyclododecanone and cyclododecanol | Ube Industries, Ltd. (JP) | 2001-04-11 | — | — | EP | claimed |
| US-4257967-A | SAID CATALYST COMPRISING REDUCED SILVER, AND YTTRIUM CARBONATE OR A RARE EARTH CARBONATE | TORAY INDUSTRIES, INC. (JP) | 1981-03-24 | — | — | US | claimed |
| US-4211882-A | OXIDIZING P-TOLUALDEHYDE, CATALYST CONSISTING OF A MANGANESE COMPOUND, A COBALT COMPOUND, A BROMINE COMPOUND, AND A NICKEL, IRON, CHROMIUM, OR LANTHANIDE COMPOUND | MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) | 1980-07-08 | — | — | US | claimed |
| US-4126807-A | Gas discharge display device containing source of lanthanum series material in dielectric layer of envelope structure | OWENS-ILLINOIS, INC. (US) | 1978-11-21 | — | — | US | claimed |