Bromide

Bromide

SCHEMBL5087902

Br.CCCCC(CCCC)C(N)(CCCC)CCCC

nearest known ligand 0.35

Full drug profile on Sugi Atlas →

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.

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
FDPS P14324 3/20 0.35
ALDH1A1 P00352 2/20 0.34
TDP1 Q9NUW8 1/20 0.34
DNM1 Q05193 2/20 0.33
OPRM1 P35372 1/20 0.32
CA1 P00915 1/20 0.31
CA2 P00918 1/20 0.31

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
SCHEMBL302193 0.98 FDPS (0.37) FDPSALDH1A1TDP1DNM1OPRM1
Bromide SCHEMBL3126204 0.96 FDPS (0.33) FDPSALDH1A1TDP1DNM1OPRM1
Bromide SCHEMBL3916851 0.96 FDPS (0.41) FDPSALDH1A1TDP1DNM1OPRM1
Fluoride SCHEMBL8161717 0.95 FDPS (0.35) FDPSALDH1A1TDP1DNM1OPRM1
Hydrochloric Acid SCHEMBL5088126 0.95 FDPS (0.35) FDPSALDH1A1TDP1DNM1OPRM1
Water SCHEMBL28462530 0.95 FDPS (0.35) FDPSALDH1A1TDP1DNM1OPRM1
Iodide SCHEMBL5091363 0.95 FDPS (0.35) FDPSALDH1A1TDP1DNM1OPRM1
Bromide SCHEMBL5091596 0.94 FDPS (0.44) FDPSDNM1OPRM1CA2
Bromide SCHEMBL5085195 0.94 FDPS (0.44) FDPSDNM1OPRM1CA2
Bromide SCHEMBL5138211 0.94 FDPS (0.44) FDPSDNM1OPRM1CA2

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 7 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107417686-B Method for synthesizing avibactam sodium 北京化工大学 2020-04-28 CN claimed
CN-118146068-A Method for preparing (substituted) benzyl alcohol/aldehyde by rapid phase transfer hydrolysis of benzyl chloride 南京工业大学 2024-06-07 CN disclosed
CN-115073459-A Continuous flow synthesis method of avibactam sodium intermediate 江西国药有限责任公司 2022-09-20 CN disclosed
CN-107840347-B Titanium-silicon molecular sieve and preparation method and application thereof 中国石油化工股份有限公司 2020-08-18 CN disclosed
CN-107840344-B Titanium-silicon molecular sieve and preparation method and application thereof 中国石油化工股份有限公司 2020-08-18 CN disclosed
CN-107417686-B Method for synthesizing avibactam sodium 北京化工大学 2020-04-28 CN disclosed
US-20080214386-A1 Stability; easily separated from solution; surface treatment of catalyst with Group seven compound; reacting epoxide with carbon dioxide NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 2008-09-04 US disclosed