Bromide

Bromide

SCHEMBL131195

CCCCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]

nearest known ligand 0.58

Full drug profile on Sugi Atlas →

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 10)

geneUniProtsupporting neighboursconfidence
HIF1A Q16665 1/20 0.58
ALDH1A1 P00352 1/20 0.45
CYP1A2 P05177 1/20 0.45
CYP2D6 P10635 1/20 0.45
TSHR P16473 1/20 0.45
CYP2C19 P33261 1/20 0.45
TRAP1 Q12931 2/20 0.44
CHRNA7 P36544 9/20 0.44
BDKRB2 P30411 1/20 0.41
DNM1 Q05193 1/20 0.39

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.

Compoundsimilaritytop predictedshared targets
Bromide SCHEMBL635580 0.98 HIF1A (0.56) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Bromide SCHEMBL2979400 0.98 HIF1A (0.56) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Bromide SCHEMBL678415 0.98 HIF1A (0.56) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Bromide SCHEMBL362235 0.98 HIF1A (0.56) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Bromide SCHEMBL164301 0.98 HIF1A (0.56) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Bromide SCHEMBL7759526 0.98 HIF1A (0.56) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Bromide SCHEMBL1866839 0.98 HIF1A (0.56) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Bromide SCHEMBL286882 0.98 HIF1A (0.56) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Bromide SCHEMBL8775234 0.98 HIF1A (0.56) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Bromide SCHEMBL2446607 0.98 HIF1A (0.56) HIF1AALDH1A1CYP1A2CYP2D6TSHR

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 348 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115894562-B Zero-dimensional hybridization cuprous halide material with photoluminescence and radiation luminescence properties, and preparation method and application thereof 济宁学院 2024-08-20 CN claimed
CN-118209650-A Method for extracting and determining succinate dehydrogenase inhibitor based on magnetic eutectic solvent-liquid microextraction-high performance liquid chromatography 山西农业大学 2024-06-18 CN claimed
CN-115894562-A Zero-dimensional hybridized cuprous halide material with excellent photoluminescence and radiation luminescence properties and preparation method and application thereof 济宁学院 2023-04-04 CN claimed
CN-114634528-A Efficient narrow-band green light emitting metal halide and preparation method and application thereof 华南理工大学 2022-06-17 CN claimed
CN-114214031-A Flame-retardant polyphenyl ether adhesive and preparation method and application thereof 四川大学 2022-03-22 CN claimed
CN-110283304-B Dithienobenzene diimide-based conjugated polymer and preparation method and application thereof 南京邮电大学 2021-12-28 CN claimed
CN-110143968-B Dithienophenyldiimide derivative and preparation method and application thereof 南京邮电大学 2020-12-01 CN claimed
CN-111943820-A Method for simply and efficiently synthesizing alpha, beta-unsaturated aldehyde without synthesis gas 四川大学 2020-11-17 CN claimed
CN-111825537-A Method for efficiently synthesizing alpha, beta-unsaturated aldehyde without synthesis gas 四川大学 2020-10-27 CN claimed
CN-110283304-A A kind of Dithiophene acene imidodicarbonic diamide base conjugated polymer and the preparation method and application thereof 南京邮电大学 2019-09-27 CN claimed
US-20170129874-A1 NOVEL IMPROVED PROCESS FOR PREPARING A TRIAZOLE ANTIFUNGAL AGENT VIRUPAKSHA ORGANICS LTD (IN) 2017-05-11 US claimed
US-7709168-B2 Phosphonium containing charge transport layer photoconductors XEROX CORPORATION (US) 2010-05-04 US claimed
US-20090092914-A1 PHOSPHONIUM CONTAINING PHOTOGENERATING LAYER PHOTOCONDUCTORS XEROX CORPORATION (US) 2009-04-09 US claimed
US-20090092915-A1 PHOSPHONIUM CONTAINING CHARGE TRANSPORT LAYER PHOTOCONDUCTORS XEROX CORPORATION (US) 2009-04-09 US claimed
US-6248161-B1 Preparation of permanent color inks from water-soluble colorants using specific phosphonium salts HEWLETT-PACKARD COMPANY 2001-06-19 US claimed
WO-1996007707-A1 EPOXY RESIN POWDER COATING COMPOSITION SHELL INTERNATIONALE RESEARCH MAATSCHAPPIJ B.V. (NL) 1996-03-14 WO claimed
EP-0181568-A2 Anti-inflammatory/anti-allergic compounds RHONE-POULENC RORER PHARMACEUTICALS INC. (US) 1986-05-21 EP claimed
US-20260144251-A1 ANTIMICROBIAL NANOCLAYS COMPRISING CATIONIC ANTIMICROBIALS, METHOD OF PREPARATION AND USES THEREOF POLYAMYNA NANOTECH INC. (CA) 2026-05-28 US disclosed
US-3987073-A SYNTHESIS OF TRIDECADIENOIC ESTERS ZOECON CORPORATION (US) 1976-10-19 US disclosed
US-3953532-A 4,8-Tridecadien-1-ol,4 cis,8 cis,trans ZOECON CORPORATION (US) 1976-04-27 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20260144251-A1 ANTIMICROBIAL NANOCLAYS COMPRISING CATIONIC ANTIMICROBIALS, METHOD OF PREPARATION AND USES THEREOF KLF10, SLC11A2, SLC7A11 HIF1A 3809/4885ALDH1A1 4757/4885CYP1A2 4682/4885
US-20170129874-A1 NOVEL IMPROVED PROCESS FOR PREPARING A TRIAZOLE ANTIFUNGAL AGENT ERG28, CYP51A1, CYP4F11 HIF1A 1790/4885ALDH1A1 3171/4885CYP1A2 24/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.