Known targets — ChEMBL curated mechanism
ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1
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.
Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CHRM2 known ✓ | P08172 | 1/20 | 0.37 |
| ▸ | CHRM1 known ✓ | P11229 | 1/20 | 0.37 |
| ▸ | CHRM3 known ✓ | P20309 | 1/20 | 0.37 |
| ▸ | DNM1 | Q05193 | 2/20 | 0.44 |
| ▸ | SMN1; SMN2 | Q16637 | 3/20 | 0.40 |
| ▸ | MAPK1 | P28482 | 2/20 | 0.40 |
| ▸ | MEN1 | O00255 | 2/20 | 0.40 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.40 |
| ▸ | TP53 | P04637 | 1/20 | 0.40 |
| ▸ | HTT | P42858 | 3/20 | 0.40 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.40 |
| ▸ | LMNA | P02545 | 1/20 | 0.40 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.40 |
| ▸ | HIF1A | Q16665 | 1/20 | 0.40 |
| ▸ | TSHR | P16473 | 1/20 | 0.37 |
| ▸ | APOBEC3A | P31941 | 1/20 | 0.37 |
| ▸ | APOBEC3G | Q9HC16 | 1/20 | 0.37 |
| ▸ | MLNR | O43193 | 1/20 | 0.37 |
| ▸ | NR1I2 | O75469 | 1/20 | 0.37 |
| ▸ | ESR1 | P03372 | 1/20 | 0.37 |
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 | |
|---|---|---|---|---|
| SCHEMBL2679442 | 0.98 | DNM1 (0.42) | DNM1SMN1; SMN2MAPK1MEN1KMT2A | |
| Iodide SCHEMBL1502864 | 0.95 | APOBEC3A (0.42) | DNM1SMN1; SMN2MAPK1MEN1KMT2A | |
| Fluoride Ion SCHEMBL1502872 | 0.95 | DNM1 (0.41) | DNM1SMN1; SMN2MAPK1MEN1KMT2A | |
| Water SCHEMBL187783 | 0.95 | DNM1 (0.41) | DNM1SMN1; SMN2MAPK1MEN1KMT2A | |
| Hydrochloric Acid SCHEMBL635867 | 0.95 | SMN1; SMN2 (0.44) | DNM1SMN1; SMN2MAPK1MEN1KMT2A | |
| Bromide SCHEMBL5086652 | 0.93 | DNM1 (0.52) | DNM1SMN1; SMN2MAPK1MEN1KMT2A | |
| Bromide SCHEMBL5087942 | 0.91 | DNM1 (0.55) | DNM1SMN1; SMN2MAPK1MEN1KMT2A | |
| Bromide SCHEMBL5092887 | 0.91 | DNM1 (0.55) | DNM1SMN1; SMN2MAPK1MEN1KMT2A | |
| Bromide SCHEMBL5088300 | 0.91 | DNM1 (0.55) | DNM1SMN1; SMN2MAPK1MEN1KMT2A | |
| Bromide SCHEMBL5091383 | 0.91 | DNM1 (0.55) | DNM1SMN1; SMN2MAPK1MEN1KMT2A |
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 112 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-115490991-B | High-performance crystal dropping glue and application thereof | 无锡嘉联电子材料有限公司 | 2024-10-29 | — | — | CN | claimed |
| CN-113999492-A | UV-resistant aging-resistant high-performance LED epoxy resin composition and preparation method thereof | 无锡嘉联电子材料有限公司 | 2022-02-01 | — | — | CN | claimed |
| EP-1006374-B1 | Process for producing a resin having a large refractive index | MITSUBISHI GAS CHEMICAL CO (JP) | 2009-01-07 | — | — | EP | claimed |
| WO-2024146848-A1 | CURABLE MATERIALS BASED ON CYCLIC THIOETHER COMPOUNDS, AND USES THEREOF | DELO INDUSTRIE KLEBSTOFFE GMBH & CO. KGAA (DE) | 2024-07-11 | — | — | WO | disclosed |
| CN-110343365-B | High CTI epoxy resin for copper-clad plate and preparation method thereof | 建滔(广州)高新材料有限公司 | 2022-03-18 | — | — | CN | disclosed |
| CN-113999492-A | UV-resistant aging-resistant high-performance LED epoxy resin composition and preparation method thereof | 无锡嘉联电子材料有限公司 | 2022-02-01 | — | — | CN | disclosed |
| EP-2735581-B1 | COMPOSITION AND POLYMER | ASAHI CHEMICAL IND (JP) | 2021-07-14 | — | — | EP | disclosed |
| EP-2799455-B1 | Resin composition for optical member and optical member obtained from the same | MITSUBISHI GAS CHEMICAL CO (JP) | 2018-03-28 | — | — | EP | disclosed |
| EP-2295484-B1 | POLYMERIZABLE COMPOSITION FOR POLYTHIOURETHANE OPTICAL MATERIAL, POLYTHIOURETHANE OPTICAL MATERIAL OBTAINED FROM SAME POLYMERIZABLE COMPOSITION, AND POLYMERIZATION CATALYST FOR POLYTHIOURETHANE OPTICAL MATERIAL | MITSUI CHEMICALS INC (JP) | 2018-01-17 | — | — | EP | disclosed |
| US-9738757-B2 | Composition and polymer | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2017-08-22 | — | — | US | disclosed |
| EP-2700636-B1 | PROCESS FOR PREPARING EPISULFIDE COMPOUNDS | ASAHI CHEMICAL IND (JP) | 2017-08-02 | — | — | EP | disclosed |
| US-6201061-B1 | CURING A RESIN FOR OPTICAL USE | MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) | 2001-03-13 | — | — | US | disclosed |
| EP-1046931-A2 | Composition for optical materials | MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) | 2000-10-25 | — | — | EP | disclosed |
| US-6130307-A | POLY(THIO)URETHANES | MITSUBISHI GAS CHEMICAL CO., INC. (JP) | 2000-10-10 | — | — | US | disclosed |
| EP-1006374-A2 | Process for producing a resin having a large refractive index | MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) | 2000-06-07 | — | — | EP | disclosed |
| EP-0950905-A2 | Process for producing a novel resin for optical materials having excellent color tone and transparency | MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) | 1999-10-20 | — | — | EP | disclosed |
| EP-0936233-A2 | Composition for a resin | MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) | 1999-08-18 | — | — | EP | disclosed |
| EP-0278257-B1 | 4-TERT.-BUTYL-1,2-BENZENEDITHIOL, COMPLEX COMPOUNDS DERIVED THEREFROM, AND A METHOD OF PRODUCING THE SAME | SEITETSU KAGAKU CO., LTD. (JP) | 1992-05-13 | — | — | EP | disclosed |
| US-4835317-A | 4-tert.-butyl-1,2-benzenedithiol, complex compounds derived therefrom, and a method of producing the same | SEITETSU KAGAKU CO., LTD. (JP) | 1989-05-30 | — | — | US | disclosed |
| EP-0278257-A1 | 4-Tert.-butyl-1,2-benzenedithiol, complex compounds derived therefrom, and a method of producing the same | SEITETSU KAGAKU CO., LTD. (JP) | 1988-08-17 | — | — | EP | disclosed |