Known targets — ChEMBL curated mechanism
ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3APH1AAPH1BCHRM2CHRM3EZH2GRIN2AHTR1AHTR1BHTR1DHTR1FHTR3ANCSTNP2RY12PSEN1PSEN2PSENENSIGMAR1SLC6A2SLC6A3SLC6A4
The experimentally established mechanism targets of Bromide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
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 | |
|---|---|---|---|---|
| SCHEMBL2402385 | 0.93 | — | — | |
| Hydrochloric Acid SCHEMBL395005 | 0.86 | — | — | |
| Iodide SCHEMBL394769 | 0.86 | — | — | |
| Bromide SCHEMBL643183 | 0.68 | — | — | |
| Isobutane SCHEMBL28999947 | 0.68 | — | — | |
| Isobutane SCHEMBL28999929 | 0.68 | ALDH1A1 (0.43) | — | |
| Isobutane SCHEMBL3368265 | 0.68 | — | — | |
| SCHEMBL954969 | 0.67 | — | — | |
| SCHEMBL953793 | 0.67 | — | — | |
| SCHEMBL955306 | 0.67 | — | — |
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 228 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-115724739-A | Resorcinol carboxylate metal complex, eutectic crystal or salt, and preparation method and application thereof | 山东特珐曼药业有限公司 | 2023-03-03 | — | — | CN | claimed |
| CN-115626897-A | Preparation method of 5-amino-4, 6-diisopropyl pyrimidine | 常州佳德医药科技有限公司 | 2023-01-20 | — | — | CN | claimed |
| EP-3162786-B1 | METHOD FOR PRODUCING 4-ISOPROPYL-3-METHYLPHENOL | OSAKA KASEI CO LTD (JP) | 2019-08-28 | — | — | EP | claimed |
| US-10252964-B2 | Producing method for 4-isopropyl-3-methylphenol | OSAKA KASEI CO., LTD. (JP) | 2019-04-09 | — | — | US | claimed |
| US-20170129836-A1 | PRODUCING METHOD FOR 4-ISOPROPYL-3-METHYLPHENOL | OSAKA KASEI CO., LTD. (JP) | 2017-05-11 | — | — | US | claimed |
| EP-3162786-A1 | METHOD FOR PRODUCING 4-ISOPROPYL-3-METHYLPHENOL | Osaka Kasei Co., Ltd. (JP) | 2017-05-03 | — | — | EP | claimed |
| US-20260022118-A1 | HETEROCYCLIC COMPOUNDS AS NRAS INHIBITORS | UNIV TEXAS (US) | 2026-01-22 | — | — | US | disclosed |
| US-20250381187-A1 | KRAS G12C INHIBITORS AND METHODS OF USING THE SAME | AMGEN INC. (US) | 2025-12-18 | — | — | US | disclosed |
| US-12440491-B2 | KRAS G12C inhibitors and methods of using the same | AMGEN INC. (US) | 2025-10-14 | — | — | US | disclosed |
| US-12404241-B2 | Substituted 3-((3-aminophenyl)amino)piperidine-2,6-dione compounds, compositions thereof, and methods of treatment therewith | CELGENE CORPORATION (US) | 2025-09-02 | — | — | US | disclosed |
| EP-3268129-B1 | OLEFIN OLIGOMERISATION PROCESS WITH A CATALYST COMPRISING A CHROMIUM COMPLEX WITH A PHOSPHACYCLE-CONTAINING LIGAND | DOW GLOBAL TECHNOLOGIES LLC (US) | 2025-06-18 | — | — | EP | disclosed |
| CN-119654322-A | TYK2 inhibitors | 渤健马萨诸塞州股份有限公司 | 2025-03-18 | — | — | CN | disclosed |
| CN-119219606-A | Substituted 3- ((3-aminophenyl) amino) piperidine-2, 6-dione compounds, compositions thereof, and methods of treatment using the same | 细胞基因公司 | 2024-12-31 | — | — | CN | disclosed |
| EP-2035436-A1 | FUSED THIAZOLE DERIVATIVES AS KINASE INHIBITORS | UCB Pharma S.A. (BE) | 2009-03-18 | — | — | EP | disclosed |
| WO-2009029592-A1 | HETEROBICYCLIC-SUBSTITUTED QUINOLONES USEFUL AS NITRIC OXIDE SYNTHASE INHIBITORS | KALYPSYS, INC. (US) | 2009-03-05 | — | — | WO | disclosed |
| WO-2008001076-A1 | FUSED THIAZOLE DERIVATIVES AS KINASE INHIBITORS | UCB PHARMA S.A. (BE) | 2008-01-03 | — | — | WO | disclosed |
| US-20070203159-A1 | Purine compounds | UNIVERSITETET I OLSO (NO) | 2007-08-30 | — | — | US | disclosed |
| EP-0013082-B1 | PROCESS FOR PRODUCING STEROID COMPOUNDS HAVING AN OXOGROUP IN THE SIDE CHAIN | TEIJIN LIMITED (JP) | 1982-12-15 | — | — | EP | disclosed |
| US-4298537-A | Process for producing steroid compounds having an oxo group in the side chain | TEIJIN LIMITED (JP) | 1981-11-03 | — | — | US | disclosed |
| EP-0013082-A1 | Process for producing steroid compounds having an oxogroup in the side chain | TEIJIN LIMITED (JP) | 1980-07-09 | — | — | EP | disclosed |