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.
⚠ 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 | |
|---|---|---|---|---|
| Bromide SCHEMBL8105621 | 1.00 | — | — | |
| Bromide SCHEMBL28087500 | 1.00 | — | — | |
| Bromide SCHEMBL818580 | 0.82 | — | — | |
| Bromide SCHEMBL818617 | 0.82 | — | — | |
| Bromide SCHEMBL28818081 | 0.82 | — | — | |
| Bromide SCHEMBL816266 | 0.82 | — | — | |
| Bromide SCHEMBL817519 | 0.82 | — | — | |
| Bromide SCHEMBL28423909 | 0.82 | — | — | |
| Bromide SCHEMBL722346 | 0.82 | — | — | |
| SCHEMBL18974 | 0.71 | — | — |
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 911 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-116639725-B | Preparation and application of series alkali metal rare earth chalcohalide and nonlinear optical crystal | TIANJIN UNIVERSITY OF TECHNOLOGY (CN) | 2026-05-26 | — | — | CN | claimed |
| CN-119507054-A | Neodymium-doped lead phenethylamine bromine monocrystal capable of greatly shortening luminescence decay time and application thereof | 西北核技术研究所 | 2025-02-25 | — | — | CN | claimed |
| CN-119433716-A | Trace neodymium doped lead phenethylamine bromine monocrystal capable of simultaneously enhancing light yield and shortening attenuation time and application thereof | 西北核技术研究所 | 2025-02-14 | — | — | CN | claimed |
| CN-117677261-A | Perovskite solar cell and preparation method and application thereof | 中国科学院化学研究所 | 2024-03-08 | — | — | CN | claimed |
| CN-116730869-A | Neodymium-doped lead formamidine-bromine perovskite semiconductor nanocrystalline as well as preparation method and application thereof | 重庆邮电大学 | 2023-09-12 | — | — | CN | claimed |
| CN-116639725-A | Preparation and application of series alkali metal rare earth chalcohalide and nonlinear optical crystal | 天津理工大学 | 2023-08-25 | — | — | CN | claimed |
| EP-3381553-B1 | CATALYST, PRODUCTION METHOD THEREFOR, AND METHOD FOR PRODUCING OPTICALLY ACTIVE ANTI-1,2-NITROALKANOL COMPOUND | MICROBIAL CHEM RES FOUND (JP) | 2023-07-26 | — | — | EP | claimed |
| CN-113772729-B | Based on UCl 3 Framework conductor of type lattice, preparation method and application | 中国科学技术大学 | 2022-09-09 | — | — | CN | claimed |
| CN-113772729-A | Based on UCl3Framework conductor of type lattice, preparation method and application | 中国科学技术大学 | 2021-12-10 | — | — | CN | claimed |
| CN-113281012-A | Artificial light source identification method | 赣州艾科锐检测技术有限公司 | 2021-08-20 | — | — | CN | claimed |
| CN-101307040-A | Method for separating and preparing paclitaxel | DALIAN INST CHEM & PHYSICS (CN) | 2008-11-19 | — | — | CN | claimed |
| US-7442825-B2 | Making nitrile compounds from ethylenically unsaturated compounds | RHODIA POLYAMIDE INTERMEDIATES (FR) | 2008-10-28 | — | — | 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 |
| US-7253298-B2 | Hydrocyanating an unsaturated aliphatic nitrile, or a linear pentenenitrile in a liquid medium with hydrogen cyanide in the presence of a Nickel catalyst with an triaryl phosphite ligand; isomerization | RHODIA POLYAMIDE INTERMEDIATES (FR) | 2007-08-07 | — | — | US | claimed |
| US-20060142609-A1 | Method of producing nitrile compounds from ethylenically-unsaturated compounds | INVISTA NORTH AMERICA SARL | 2006-06-29 | — | — | US | claimed |
| US-20060128980-A1 | Method for making nitrile compounds from ethylenically unsaturated compounds | INVISTA NORTH AMERICA SARL | 2006-06-15 | — | — | US | claimed |
| US-20060100455-A1 | Hydrocyanating an unsaturated aliphatic nitrile, or a linear pentenenitrile in a liquid medium with hydrogen cyanide in the presence of a Nickel catalyst with an triaryl phosphite ligand; isomerization | INVISTA NORTH AMERICA SARL | 2006-05-11 | — | — | US | claimed |
| US-20060052624-A1 | Making nitrile compounds from ethylenically unsaturated compounds | INVISTA NORTH AMERICA SARL | 2006-03-09 | — | — | 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 |