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 16)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ACHE known ✓ | P22303 | 9/20 | 0.50 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.50 |
| ▸ | APOBEC3A | P31941 | 1/20 | 0.48 |
| ▸ | APOBEC3G | Q9HC16 | 1/20 | 0.48 |
| ▸ | ALDH1A1 | P00352 | 4/20 | 0.38 |
| ▸ | CA1 | P00915 | 1/20 | 0.38 |
| ▸ | CA2 | P00918 | 1/20 | 0.38 |
| ▸ | CA7 | P43166 | 1/20 | 0.38 |
| ▸ | CA9 | Q16790 | 1/20 | 0.38 |
| ▸ | TSHR | P16473 | 3/20 | 0.35 |
| ▸ | LMNA | P02545 | 2/20 | 0.35 |
| ▸ | ALOX12 | P18054 | 1/20 | 0.35 |
| ▸ | IDO1 | P14902 | 1/20 | 0.33 |
| ▸ | CES2 | O00748 | 1/20 | 0.33 |
| ▸ | CES1 | P23141 | 1/20 | 0.33 |
| ▸ | CYP2A6 | P11509 | 1/20 | 0.33 |
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 | |
|---|---|---|---|---|
| SCHEMBL841700 | 0.97 | ACHE (0.53) | ACHETDP1APOBEC3AAPOBEC3GALDH1A1 | |
| SCHEMBL27385711 | 0.94 | ACHE (0.50) | ACHETDP1APOBEC3AAPOBEC3GALDH1A1 | |
| Bromide SCHEMBL8612056 | 0.94 | ACHE (0.50) | ACHETDP1APOBEC3AAPOBEC3GALDH1A1 | |
| Iodide SCHEMBL8506434 | 0.94 | APOBEC3A (0.55) | ACHETDP1APOBEC3AAPOBEC3GALDH1A1 | |
| Water SCHEMBL11594553 | 0.94 | ACHE (0.50) | ACHETDP1APOBEC3AAPOBEC3GALDH1A1 | |
| SCHEMBL13548402 | 0.88 | ACHE (0.44) | ACHETDP1APOBEC3AAPOBEC3GALDH1A1 | |
| Hydrochloric Acid SCHEMBL6368015 | 0.87 | APOBEC3A (0.59) | ACHETDP1APOBEC3AAPOBEC3GALDH1A1 | |
| SCHEMBL2489383 | 0.83 | APOBEC3A (0.62) | ACHEAPOBEC3AAPOBEC3GCA9 | |
| Hydrochloric Acid SCHEMBL29010537 | 0.81 | ACHE (0.50) | ACHETDP1ALDH1A1CA1CA2 | |
| Iodide SCHEMBL6373433 | 0.79 | APOBEC3A (0.69) | ACHEAPOBEC3AAPOBEC3GCA9 |
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 40 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2014025352-A1 | FLAME RETARDANT NYLON | EMPIRE TECHNOLOGY DEVELOPMENT LLC (US) | 2014-02-13 | — | — | WO | disclosed |
| US-8206673-B2 | Method of preparing boron-nitrogen compounds | WILDCAT DISCOVERY TECHNOLOGIES (US) | 2012-06-26 | — | — | US | disclosed |
| US-20110064640-A1 | METHOD OF PREPARING BORON-NITROGEN COMPOUNDS | WILDCAT DISCOVERY TECHNOLOGIES (US) | 2011-03-17 | — | — | US | disclosed |
| EP-0269884-B1 | CATALYZED ALKYLATION OF HALOPYRIDINATES IN THE ABSENCE OF ADDED ORGANIC SOLVENTS | DOWELANCO (US) | 1991-09-25 | — | — | EP | disclosed |
| EP-0277292-B1 | ORGANIC SOLVENT-FREE PROCESS FOR PREPARING PYRIMIDINYL ORGANOPHOSPHATES | THE DOW CHEMICAL COMPANY (US) | 1991-05-08 | — | — | EP | disclosed |
| EP-0277292-A1 | Organic solvent-free process for preparing pyrimidinyl organophosphates | THE DOW CHEMICAL COMPANY (US) | 1988-08-10 | — | — | EP | disclosed |
| EP-0269884-A1 | Catalyzed alkylation of halopyridinates in the absence of added organic solvents | DOWELANCO (US) | 1988-06-08 | — | — | EP | disclosed |
| US-4701531-A | Catalyzed alkylation of halopyridinates in the absence of added organic solvents | THE DOW CHEMICAL COMPANY (US) | 1987-10-20 | — | — | US | disclosed |
| US-4699634-A | SEMIPERMEABLE MEMBRANES | THE STANDARD OIL COMPANY (US) | 1987-10-13 | — | — | US | disclosed |
| US-4546189-A | Preparation of cyano(6-(substituted phenoxy)-2-pyridinyl)methyl esters of 3-(2,2-dihaloethenyl)-2,2-dimethylcyclopropane carboxylic acids | THE DOW CHEMICAL COMPANY (US) | 1985-10-08 | — | — | US | disclosed |
| US-4028439-A | QUATERNARY AMMONIUM SALT AND IMIDAZOLE CATALYSTS | THE DOW CHEMICAL COMPANY (US) | 1977-06-07 | — | — | US | disclosed |
| US-4016225-A | WITH QUATERNARY AMMONIUM SALT AND 1,4-DIAZABICYCLO(2.2.2)OCTANE CATALYST | THE DOW CHEMICAL COMPANY (US) | 1977-04-05 | — | — | US | disclosed |
| US-4014891-A | FROM AN ALKALI METAL ARYL MERCAPTIDE AND BROMOCHLOROMETHANE IN A QUATERNARY AMMONIUM SALT | THE DOW CHEMICAL COMPANY (US) | 1977-03-29 | — | — | US | disclosed |
| US-4007197-A | QUATERNARY AMMONIUM OR PHOSPHONIUM SALT AND TERTIARY AMINE CATALYST | THE DOW CHEMICAL COMPANY (US) | 1977-02-08 | — | — | US | disclosed |
| US-4001293-A | Process for production of γ-halonitriles | THE DOW CHEMICAL COMPANY (US) | 1977-01-04 | — | — | US | disclosed |
| US-3996259-A | QUATERNARY AMMONIUM OR PHOSPHONIUM SALT | THE DOW CHEMICAL COMPANY (US) | 1976-12-07 | — | — | US | disclosed |
| US-3992159-A | Process for purification by cryogenic sublimation | BELL TELEPHONE LABORATORIES, INCORPORATED (US) | 1976-11-16 | — | — | US | disclosed |
| US-3974199-A | Process for production of cyclopropylcyanide | THE DOW CHEMICAL COMPANY (US) | 1976-08-10 | — | — | US | disclosed |
| US-3972887-A | QUATERNARY AMMONIUM SALT CATALYST | THE DOW CHEMICAL COMPANY (US) | 1976-08-03 | — | — | US | disclosed |
| US-3969360-A | Catalyzed alkylation of halopyridinates | THE DOW CHEMICAL COMPANY (US) | 1976-07-13 | — | — | US | disclosed |