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 8)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | LMNA | P02545 | 3/20 | 0.63 |
| ▸ | TKT | P29401 | 12/20 | 0.60 |
| ▸ | HTT | P42858 | 2/20 | 0.59 |
| ▸ | TP53 | P04637 | 1/20 | 0.59 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.54 |
| ▸ | MEN1 | O00255 | 1/20 | 0.52 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.52 |
| ▸ | HSP90AA1 | P07900 | 1/20 | 0.49 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL2900332 | 0.98 | TKT (0.61) | LMNATKTHTTTP53ALDH1A1 | |
| Bromide SCHEMBL7625997 | 0.97 | TKT (0.60) | LMNATKTHTTTP53ALDH1A1 | |
| Hydrochloric Acid SCHEMBL29995247 | 0.97 | TKT (0.60) | LMNATKTHTTTP53ALDH1A1 | |
| Hydrochloric Acid SCHEMBL7617650 | 0.88 | LMNA (0.59) | LMNATKTHTTTP53ALDH1A1 | |
| SCHEMBL18837645 | 0.86 | LMNA (0.56) | LMNATKTHTTTP53ALDH1A1 | |
| SCHEMBL13741341 | 0.85 | TKT (0.67) | LMNATKTHSP90AA1 | |
| Bromide SCHEMBL8984239 | 0.84 | LMNA (0.55) | LMNATKTHTTTP53ALDH1A1 | |
| Fluoride Ion SCHEMBL16038833 | 0.84 | LMNA (0.55) | LMNATKTHTTTP53ALDH1A1 | |
| Iodide SCHEMBL16036467 | 0.84 | LMNA (0.55) | LMNATKTHTTTP53ALDH1A1 | |
| Hydrochloric Acid SCHEMBL4097464 | 0.84 | TKT (0.65) | LMNATKTHSP90AA1 |
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 643 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119701994-A | Ferromanganese-based catalyst for preparing methyl methacrylate and preparation and application thereof | 中国科学院大连化学物理研究所 | 2025-03-28 | — | — | CN | claimed |
| CN-117476368-B | Aluminum electrolytic capacitor with high stability and long service life | 深圳市东联发科技有限公司 | 2024-07-19 | — | — | CN | claimed |
| CN-117476368-A | Aluminum electrolytic capacitor with high stability and long service life | 深圳市东联发科技有限公司 | 2024-01-30 | — | — | CN | claimed |
| CN-117069770-A | Method for synthesizing N-heterocyclic carbene complex by utilizing hydrogen bond | 石河子大学 | 2023-11-17 | — | — | CN | claimed |
| CN-116789577-A | Preparation method of mesotrione compounds | 北京颖泰嘉和生物科技股份有限公司 | 2023-09-22 | — | — | CN | claimed |
| CN-116666117-A | High-pressure high-dissolution electrolyte for aluminum electrolytic cell and preparation method thereof | 南通大学 | 2023-08-29 | — | — | CN | claimed |
| CN-110818689-B | Pincer-shaped polypyridine-polypyrrole silver cluster compound containing five coordination sites as well as preparation method and application thereof | 华侨大学 | 2022-03-25 | — | — | CN | claimed |
| CN-110818689-A | Pincer-shaped polypyridine-polypyrrole silver cluster compound containing five coordination sites as well as preparation method and application thereof | 华侨大学 | 2020-02-21 | — | — | CN | claimed |
| EP-1948598-B1 | PROCESS FOR PREPARATION OF (3R, 5R)-7-[2-(4-FLUOROPHENYL)-5-ISOPROPYL-3-PHENYL-4-[(4-HYDROXY METHYL PHENYL AMINO) CARBONYL]-PYRROL-1-YL]-3,5-DIHYDROXY-HEPTANOIC ACID HEMI CALCIUM SALT | RANBAXY LAB LTD (IN) | 2013-01-09 | — | — | EP | claimed |
| US-7671216-B2 | Process for preparation of (3R,5R)-7-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-[(4-hydroxy methyl phenyl amino) carbonyl]-pyrrol-1-yl]-3,5-dihydroxy-heptanoic acid hemi calcium salt | RANBAXY LABORATORIES LIMITED (IN) | 2010-03-02 | — | — | US | claimed |
| US-5514505-A | SELECTIVE TRANSPARENTIZATION OF PHOTOSENSITIVE MIGRATION MARKING PARTICLES EMBEDDED NEAR THE SURFACE OF A SOFTENABLE LAYER SUPPORTED BY AN ELECTROCONDUCTIVE SUBSTRATE | XEROX CORPORATION (US) | 1996-05-07 | — | — | US | claimed |
| EP-0615854-A1 | Recording sheets containing cationic sulphur compounds | XEROX CORPORATION (US) | 1994-09-21 | — | — | EP | claimed |
| EP-0330172-B1 | Improved process for trans-6-[2-(substituted-pyrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis | WARNER LAMBERT CO (US) | 1994-08-10 | — | — | EP | claimed |
| US-5314747-A | Recording sheets containing cationic sulfur compounds | XEROX CORPORATION (US) | 1994-05-24 | — | — | US | claimed |
| US-5216174-A | Process for trans-6-[12-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis | WARNER-LAMBERT CO. (US) | 1993-06-01 | — | — | US | claimed |
| EP-0267537-B1 | PROCESS FOR THE PREPARATION OF VINYLGLYOXAL DERIVATIVES, VINYLGLYOXAL DERIVATIVES AND THEIR USE | BASF Aktiengesellschaft (DE) | 1992-01-08 | — | — | EP | claimed |
| EP-0448552-A1 | IMPROVED PROCESS FOR $i(TRANS)-6- 2-(SUBSTITUTED-PYRROL-1-YL)ALKYL]PYRAN-2-ONE INHIBITORS OF CHOLESTEROL SYNTHESIS | WARNER-LAMBERT COMPANY (US) | 1991-10-02 | — | — | EP | claimed |
| EP-0330172-A2 | Improved process for trans-6-[2-(substituted-pyrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis | WARNER-LAMBERT COMPANY (US) | 1989-08-30 | — | — | EP | claimed |
| WO-1989007598-A2 | IMPROVED PROCESS FOR TRANS-6-[2-(SUBSTITUTED-PYRROL-1-YL)ALKYL]PYRAN-2-ONE INHIBITORS OF CHOLESTEROL SYNTHESIS | WARNER-LAMBERT COMPANY (US) | 1989-08-24 | — | — | WO | claimed |
| EP-0267537-A2 | Process for the preparation of vinylglyoxal derivatives, vinylglyoxal derivatives and their use | BASF Aktiengesellschaft (DE) | 1988-05-18 | — | — | EP | claimed |