Bromide

Bromide

SCHEMBL5088078

CC[P+](CC)(CC)Cc1ccccc1.[Br-]

nearest known ligand 0.48

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 15)

geneUniProtsupporting neighboursconfidence
TP53 P04637 1/20 0.48
TRPA1 O75762 2/20 0.47
TAAR1 Q96RJ0 4/20 0.44
SIGMAR1 Q99720 4/20 0.44
SLC6A2 P23975 2/20 0.44
MAOA P21397 1/20 0.44
SLC6A4 P31645 1/20 0.44
SLC6A3 Q01959 1/20 0.44
CYP2A6 P11509 1/20 0.44
ADORA2A P29274 1/20 0.44
ADORA1 P30542 1/20 0.44
EPHX1 P07099 1/20 0.42
SLC18A2 Q05940 1/20 0.41
CYP2D6 P10635 1/20 0.41
BDKRB2 P30411 1/20 0.41

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
Water SCHEMBL7721938 0.95 TP53 (0.48) TP53TRPA1TAAR1SIGMAR1SLC6A2
Bromide SCHEMBL5091531 0.95 TP53 (0.48) TP53TRPA1TAAR1SIGMAR1SLC6A2
Fluoride Ion SCHEMBL5246642 0.95 TP53 (0.48) TP53TRPA1TAAR1SIGMAR1SLC6A2
Hydrochloric Acid SCHEMBL2685431 0.95 TP53 (0.48) TP53TRPA1TAAR1SIGMAR1SLC6A2
Bromide SCHEMBL5088593 0.95 TP53 (0.48) TP53TRPA1TAAR1SIGMAR1SLC6A2
Iodide SCHEMBL5086624 0.95 TP53 (0.48) TP53TRPA1TAAR1SIGMAR1SLC6A2
Phosphine SCHEMBL28106805 0.93 TP53 (0.46) TP53TRPA1TAAR1SIGMAR1SLC6A2
Fluoride Ion SCHEMBL65871 0.93 TP53 (0.46) TP53TRPA1TAAR1SIGMAR1SLC6A2
Hydrochloric Acid SCHEMBL2526828 0.90 TP53 (0.48) TP53TRPA1TAAR1SIGMAR1SLC6A2
Fluoride Ion SCHEMBL11373889 0.90 TP53 (0.48) TP53TRPA1TAAR1SIGMAR1SLC6A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118005896-A Method for directly synthesizing polyethylene glycol terephthalate from ethylene oxide 常州大学 2024-05-10 CN claimed
CN-115637020-A Hyperbranched epoxy resin thermosetting resin composition and application thereof 复旦大学 2023-01-24 CN claimed
US-20250326886-A1 POLYMER COMPOSITION, EPOXY RESIN COMPOSITION, CURING AGENT FOR EPOXY RESIN, AND FAST CURING ADHESIVE TORAY FINE CHEMICALS CO., LTD. (JP) 2025-10-23 US disclosed
CN-118005896-A Method for directly synthesizing polyethylene glycol terephthalate from ethylene oxide 常州大学 2024-05-10 CN disclosed
CN-117355557-A Polymer composition, epoxy resin composition, curing agent for epoxy resin, and quick-setting adhesive 东丽精细化工株式会社 2024-01-05 CN disclosed
CN-112010890-B Synthesis method of 3-mercaptopropyl trialkoxysilane 江西晨光新材料股份有限公司 2023-04-07 CN disclosed
CN-115637020-A Hyperbranched epoxy resin thermosetting resin composition and application thereof 复旦大学 2023-01-24 CN disclosed
WO-2022249966-A1 POLYMER COMPOSITION, EPOXY RESIN COMPOSITION, CURING AGENT FOR EPOXY RESIN, AND FAST-CURING ADHESIVE 東レ・ファインケミカル株式会社 2022-12-01 WO disclosed
CN-107540670-B Preparation method of 1- (3-chloropyrazolo [1,5a ] -4,5,6, 7-tetrahydropyridine-2-yl) -5-methylamine pyrazole-4-carbonitrile 湖北相和精密化学有限公司 2021-08-13 CN disclosed
CN-112010890-A Synthesis method of 3-mercaptopropyl trialkoxysilane 江西晨光新材料股份有限公司 2020-12-01 CN disclosed
US-10292390-B2 Inhibition and dispersion of bacterial biofilms with 2-aminobenzimidazole derivatives WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2019-05-21 US disclosed
EP-0502707-B1 Method for production of 3-cyano-3,5,5-trimethyl cyclohexanone NIPPOH CHEMICALS (JP) 1995-10-25 EP disclosed
US-5179221-A METHOD FOR PRODUCTION OF 3-CYANO-3,5,5-TRIMETHYL CYCLOHEXANONE NIPPON CHEMICALS CO., LTD. (JP) 1993-01-12 US disclosed
EP-0502707-A1 Method for production of 3-cyano-3,5,5-trimethyl cyclohexanone NIPPOH CHEMICALS CO., LTD. (JP) 1992-09-09 EP disclosed
EP-0105762-B1 PROCESS FOR PRODUCING ANTHRAQUINONE COMPOUNDS SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1988-03-09 EP disclosed
US-4519947-A SULFONATING 1,4-DIAMINO-2,3-DIHALOGENO-ANTHRAQUINONE SUMITOMO CHEMICAL CO., LTD. (JP) 1985-05-28 US disclosed
EP-0105762-A2 Process for producing anthraquinone compounds SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1984-04-18 EP disclosed
US-4335051-A AQUEOUS ALKALI HYDROXIDE AS ACID ACCEPTOR WHEN REACTING METHANOL W BAYER AKTIENGESELLSCHAFT (DE) 1982-06-15 US disclosed
US-4122288-A Hydrolysis of alkyl substituted dihalobenzene compounds UOP INC. (US) 1978-10-24 US disclosed
US-3992370-A 1,1-Dichloro-1a,1b-dihydrodibenzo(b,f)cycloprop(d)azepine-6(1H)-carboxaldehyde TAKEDA CHEMICAL INDUSTRIES, LTD. (JA) 1976-11-16 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 (1 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-10292390-B2 Inhibition and dispersion of bacterial biofilms with 2-aminobenzimidazole derivatives FLNB, BRI3BP, CCNI TP53 3199/4885TRPA1 4189/4885TAAR1 4519/4885

“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.