Bromide

Bromide

SCHEMBL10606554

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

nearest known ligand 0.33

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 2)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.33
DNM1 Q05193 1/20 0.30

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 SCHEMBL30477 0.95 TSHR (0.36) TSHRDNM1
Bromide SCHEMBL302580 0.95 TSHR (0.36) TSHRDNM1
SCHEMBL29563566 0.89
SCHEMBL9752174 0.84 TSHR (0.36) TSHR
Hydrochloric Acid SCHEMBL127178 0.84 TSHR (0.36) TSHR
Fluoride Ion SCHEMBL941760 0.84 TSHR (0.36) TSHR
Iodide SCHEMBL3863164 0.84 TSHR (0.38) TSHR
Water SCHEMBL107107 0.84 TSHR (0.36) TSHR
SCHEMBL7178147 0.84
SCHEMBL2862407 0.80 TSHR (0.33) TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0208265-B1 1-Oxa-3,8-diaza-4-oxo-spiro[4,5]decane compounds and process for their preparation HOECHST AKTIENGESELLSCHAFT (DE) 1989-08-23 EP disclosed