Bromide

Bromide

SCHEMBL174432

O=C(O)CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]

nearest known ligand 0.96

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 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.96
CYP2D6 P10635 2/20 0.96
CYP2C19 P33261 2/20 0.96
CYP1A2 P05177 1/20 0.96
TSHR P16473 1/20 0.96
HIF1A Q16665 1/20 0.58
CPA3 P15088 1/20 0.48
KEAP1 Q14145 1/20 0.45
NR4A2 P43354 1/20 0.43
MAPK1 P28482 2/20 0.42
FFAR1 O14842 2/20 0.42
HDAC3 O15379 1/20 0.42
ADRA1A P35348 1/20 0.42
HDAC4 P56524 1/20 0.42
SLC6A3 Q01959 1/20 0.42
HDAC1 Q13547 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
HDAC7 Q8WUI4 1/20 0.42
HDAC2 Q92769 1/20 0.42
HDAC10 Q969S8 1/20 0.42

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 SCHEMBL12497328 1.00 ALDH1A1 (0.96) ALDH1A1CYP2D6CYP2C19CYP1A2TSHR
SCHEMBL30793417 0.98 ALDH1A1 (1.00) ALDH1A1CYP2D6CYP2C19CYP1A2TSHR
Bromide SCHEMBL28027685 0.96 ALDH1A1 (0.88) ALDH1A1CYP2D6CYP2C19CYP1A2TSHR
Water SCHEMBL11301878 0.96 ALDH1A1 (0.96) ALDH1A1CYP2D6CYP2C19CYP1A2TSHR
Hydrochloric Acid SCHEMBL845765 0.96 ALDH1A1 (0.96) ALDH1A1CYP2D6CYP2C19CYP1A2TSHR
Bromide SCHEMBL484781 0.88 ALDH1A1 (0.74) ALDH1A1CYP2D6CYP2C19CYP1A2TSHR
Bromide SCHEMBL163452 0.86 ALDH1A1 (0.71) ALDH1A1CYP2D6CYP2C19CYP1A2TSHR
SCHEMBL31204098 0.85 ALDH1A1 (0.77) ALDH1A1CYP2D6CYP2C19CYP1A2TSHR
Bromide SCHEMBL3437057 0.84 TSHR (0.69) ALDH1A1CYP2D6CYP2C19CYP1A2TSHR
Bromide SCHEMBL2854923 0.84 TSHR (0.69) ALDH1A1CYP2D6CYP2C19CYP1A2TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2023159094-A2 PROCESS OF MAKING 3α-HYDROXY-3β-METHOXYMETHYL-21-(1'- IMIDAZOLYL)-5α-PREGNAN-20-ONE PRAXIS PRECISION MEDICINES, INC. (US) 2023-08-24 WO claimed
WO-2023137518-A1 PLATINUM COMPLEXES Western Sydney University (AU) 2023-07-27 WO claimed
US-20220127238-A1 PROCESS FOR THE PREPARATION OF ANGIOTENSIN II RECEPTOR BLOCKERS HETERO LABS LIMITED (IN) 2022-04-28 US claimed
CN-109456250-B Thermal Activation Delayed Fluorescence (TADF) nano probe, preparation method thereof and application thereof in biological imaging 哈尔滨医科大学 2022-03-04 CN claimed
CN-110256757-B Quaternary phosphonium salt composite antibacterial EVA (ethylene-vinyl acetate) insole material and preparation method thereof 广州大学 2021-12-28 CN claimed
CN-112410849-B Preparation method and application of defect black phosphorus alkene carbon nanotube composite material 肇庆市华师大光电产业研究院 2021-12-21 CN claimed
CN-113321747-A Antibacterial component containing quaternary phosphonium salt modified locust bean gum 广州市尚信净化工程有限公司 2021-08-31 CN claimed
CN-111990408-B Nano antibacterial agent, preparation method and application thereof 中国热带农业科学院农产品加工研究所 2021-06-01 CN claimed
CN-112410849-A Preparation method and application of defect black phosphorus alkene carbon nanotube composite material 肇庆市华师大光电产业研究院 2021-02-26 CN claimed
CN-111990408-A Nano antibacterial agent, preparation method and application thereof 中国热带农业科学院农产品加工研究所 2020-11-27 CN claimed
US-12630498-B2 Arylamides and methods of use thereof GENZYME CORPORATION (US) 2026-05-19 US disclosed
EP-4739696-A1 MITOCHONDRIA SPECIFIC TRANSCRIPTION INHIBITOR COMPOUNDS Lunella Biotech, Inc. (CA) 2026-05-13 EP disclosed
EP-4729508-A1 TETRALIN AND TETRAHYDROQUINOLINE COMPOUNDS AS INHIBITORS OF HIF-2ALPHA Arcus Biosciences, Inc. (US) 2026-04-22 EP disclosed
EP-4642784-A1 HETEROCYCLIC AND HETEROARYL COMPOUNDS AS INHIBITORS OF NLRP3 PTC Therapeutics, Inc. (US) 2025-11-05 EP disclosed
US-20250320227-A1 MACROCYCLIC OREXIN RECEPTOR AGONISTS AND USES THEREOF JAZZ PHARMACEUTICALS IRELAND LTD (IE) 2025-10-16 US disclosed
US-4228180-A 7-Oxabicycloheptane and 7-oxabicycloheptene prostaglandin analogs E. R. SQUIBB & SONS, INC. (US) 1980-10-14 US disclosed
US-4165436-A Trans-2,3-didehydro-9-deoxy-9-methylene-PGF compounds THE UPJOHN COMPANY (US) 1979-08-21 US disclosed
US-4052512-A MENSTRUAL REGULATION ONO PHARMACEUTICAL CO., LTD. (JA) 1977-10-04 US disclosed
US-3987087-A ANTI-ULCER, NASAL PATENCY, WOUND HEALING, LABOR INDUCEMENT THE UPJOHN COMPANY (US) 1976-10-19 US disclosed
US-3931296-A Trans-Δ2 -prostaglandins HAYASHI MASAKI 1976-01-06 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 (3 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-20220127238-A1 PROCESS FOR THE PREPARATION OF ANGIOTENSIN II RECEPTOR BLOCKERS AGTR2, AGTR1, ADRB1 ALDH1A1 991/4885CYP2D6 115/4885CYP2C19 72/4885
US-12630498-B2 Arylamides and methods of use thereof CFTR, CLIC1, CLCN2 ALDH1A1 775/4885CYP2D6 246/4885CYP2C19 1312/4885
US-20250320227-A1 MACROCYCLIC OREXIN RECEPTOR AGONISTS AND USES THEREOF HCRTR1, HCRTR2, NPY1R ALDH1A1 1670/4885CYP2D6 2176/4885CYP2C19 1406/4885

“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.