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 18)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ACHE known ✓ | P22303 | 2/20 | 0.44 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.49 |
| ▸ | BCHE | P06276 | 2/20 | 0.44 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.44 |
| ▸ | HPGD | P15428 | 1/20 | 0.44 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.44 |
| ▸ | ALOX12 | P18054 | 1/20 | 0.44 |
| ▸ | CASP1 | P29466 | 1/20 | 0.44 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.44 |
| ▸ | LMNA | P02545 | 1/20 | 0.44 |
| ▸ | HSP90AA1 | P07900 | 1/20 | 0.43 |
| ▸ | MAOA | P21397 | 1/20 | 0.43 |
| ▸ | TDP1 | Q9NUW8 | 2/20 | 0.42 |
| ▸ | CYP2A6 | P11509 | 1/20 | 0.42 |
| ▸ | HTR2A | P28223 | 1/20 | 0.42 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.42 |
| ▸ | TAAR1 | Q96RJ0 | 1/20 | 0.42 |
| ▸ | LOXL2 | Q9Y4K0 | 1/20 | 0.42 |
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 | |
|---|---|---|---|---|
| SCHEMBL10445050 | 0.98 | CYP2D6 (0.50) | CYP2D6BCHEACHEALDH1A1HPGD | |
| Bromide SCHEMBL5907737 | 0.95 | CYP2D6 (0.49) | CYP2D6BCHEACHE | |
| SCHEMBL7837176 | 0.86 | ALDH1A1 (0.50) | CYP2D6ALDH1A1HPGDALOX15ALOX12 | |
| Hydrochloric Acid SCHEMBL10935706 | 0.85 | ALDH1A1 (0.55) | CYP2D6ACHEALDH1A1HPGDALOX15 | |
| Hydrochloric Acid SCHEMBL19468762 | 0.85 | MAOB (0.56) | CYP2D6LMNAMAOACYP2A6HTR2A | |
| SCHEMBL5282778 | 0.84 | BCHE (0.54) | BCHEACHE | |
| SCHEMBL8758357 | 0.84 | BCHE (0.54) | BCHEACHE | |
| SCHEMBL13838215 | 0.82 | CHKA (0.53) | CYP2D6ACHEALDH1A1HPGDALOX15 | |
| SCHEMBL19504329 | 0.82 | MAOB (0.58) | CYP2D6ALDH1A1HPGDALOX15ALOX12 | |
| SCHEMBL14802084 | 0.80 | BCHE (0.62) | BCHEACHE |
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 38 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-115895622-A | Composition with hydrate inhibition function, preparation method and application | 中国石油化工股份有限公司 | 2023-04-04 | — | — | CN | claimed |
| CN-112794786-A | Method for producing polyfluorobenzene derivative from tetrachloroethylene byproduct | 衢州乾达科技有限公司 | 2021-05-14 | — | — | CN | claimed |
| EP-1015663-A1 | CORROSION INHIBITION THROUGH THE USE OF A QUATERNARY PYRIDINE SALT-HYDROCARBON COMBINATION | Stanchem Inc. (CA) | 2000-07-05 | — | — | EP | claimed |
| WO-1998033953-A1 | CORROSION INHIBITION THROUGH THE USE OF A QUATERNARY PYRIDINE SALT-HYDROCARBON COMBINATION | STANCHEM INC. (CA) | 1998-08-06 | — | — | WO | claimed |
| CN-113341646-B | Organic film forming material, organic film forming method, pattern forming method, and compound | 信越化学工业株式会社 | 2024-12-13 | — | — | CN | disclosed |
| CN-115362216-B | Composition for forming film | 日产化学株式会社 | 2024-07-19 | — | — | CN | disclosed |
| CN-117716295-A | Composition for forming silicon-containing resist underlayer film and silicon-containing resist underlayer film | 日产化学株式会社 | 2024-03-15 | — | — | CN | disclosed |
| CN-117255971-A | Composition for forming silicon-containing resist underlayer film | 日产化学株式会社 | 2023-12-19 | — | — | CN | disclosed |
| CN-115895622-B | Composition with hydrate inhibition function, preparation method and application | 中国石油化工股份有限公司 | 2023-11-17 | — | — | CN | disclosed |
| CN-116761829-A | Organosilicon compound, method for producing same, and curable composition | 信越化学工业株式会社 | 2023-09-15 | — | — | CN | disclosed |
| CN-108885997-B | Planarization method for semiconductor substrate using silicon-containing composition | 日产化学株式会社 | 2023-06-02 | — | — | CN | disclosed |
| CN-115895622-A | Composition with hydrate inhibition function, preparation method and application | 中国石油化工股份有限公司 | 2023-04-04 | — | — | CN | disclosed |
| US-7959765-B2 | Dissolving in liquid; pyrolysis | NORTH CAROLINA STATE UNIVERSTIY (US) | 2011-06-14 | — | — | US | disclosed |
| US-20080190013-A1 | USE OF LIGNOCELLULOSICS SOLVATED IN IONIC LIQUIDS FOR PRODUCTION OF BIOFUELS | NORTH CAROLINA STATE UNIVERSITY | 2008-08-14 | — | — | US | disclosed |
| WO-2008098032-A2 | USE OF LIGNOCELLULOSICS SOLVATED IN IONIC LIQUIDS FOR PRODUCTION OF BIOFUELS | NORTH CAROLINA STATE UNIVERSITY (US) | 2008-08-14 | — | — | WO | disclosed |
| WO-2008098036-A1 | PRODUCT PREPARATION AND RECOVERY FROM THERMOLYSIS OF LIGNOCELLULOSICS IN IONIC LIQUIDS | NORTH CAROLINA STATE UNIVERSITY (US) | 2008-08-14 | — | — | WO | disclosed |
| WO-2008098037-A2 | POLYMER DERIVATIVES AND COMPOSITES FROM THE DISSOLUTION OF LIGNOCELLULOSICS IN IONIC LIQUIDS | NORTH CAROLINA STATE UNIVERSITY (US) | 2008-08-14 | — | — | WO | disclosed |
| US-20080188636-A1 | POLYMER DERIVATIVES AND COMPOSITES FROM THE DISSOLUTION OF LIGNOCELLULOSICS IN IONIC LIQUIDS | NORTH CAROLINA STATE UNIVERSITY | 2008-08-07 | — | — | US | disclosed |
| US-20080185112-A1 | PRODUCT PREPARATION AND RECOVERY FROM THERMOLYSIS OF LIGNOCELLULOSICS IN IONIC LIQUIDS | NORTH CAROLINA STATE UNIVERSITY | 2008-08-07 | — | — | US | disclosed |
| CN-1078174-A | CATALYST OF ALKYLATION OF PARAFFINES | INST FRANCAIS DU PETROLE (FR) | 1993-11-10 | — | — | CN | disclosed |