Bromide

Bromide

SCHEMBL6909366

Fc1ccc(CC[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1F.[Br-]

nearest known ligand 0.47

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 16)

geneUniProtsupporting neighboursconfidence
CHRM5 known ✓ P08912 1/20 0.33
CHRM1 known ✓ P11229 1/20 0.33
CHRM3 known ✓ P20309 1/20 0.33
HIF1A Q16665 1/20 0.47
HTT P42858 2/20 0.40
ALDH1A1 P00352 2/20 0.38
CYP1A2 P05177 1/20 0.38
CYP2D6 P10635 1/20 0.38
TSHR P16473 1/20 0.38
CYP2C19 P33261 1/20 0.38
SNCA P37840 2/20 0.38
KDM1A O60341 1/20 0.37
DAO P14920 2/20 0.36
FFAR1 O14842 1/20 0.33
FFAR4 Q5NUL3 1/20 0.33
P2RX7 Q99572 1/20 0.33

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 SCHEMBL9351092 0.85 HIF1A (0.42) HIF1AHTTALDH1A1CYP1A2CYP2D6
Bromide SCHEMBL30721146 0.82 SNCA (0.51) HIF1AHTTALDH1A1CYP1A2CYP2D6
Bromide SCHEMBL8015170 0.82 SNCA (0.51) HIF1AHTTALDH1A1CYP1A2CYP2D6
Bromide SCHEMBL26696535 0.81 HIF1A (0.64) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Bromide SCHEMBL7929116 0.81 HIF1A (0.38) HIF1A
Bromide SCHEMBL2768948 0.80 HIF1A (0.52) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Bromide SCHEMBL2767870 0.77 HIF1A (0.64) HIF1AALDH1A1CYP1A2CYP2D6TSHR
SCHEMBL16191225 0.75 HTT (0.51) HTTKDM1ADAOFFAR1
SCHEMBL31526396 0.75 HIF1A (0.67) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Bromide SCHEMBL8030729 0.73 SNCA (0.50) HIF1AHTTALDH1A1CYP2D6SNCA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1149885-B1 Cyclohexane derivatives, liquid crystal compositions comprising the same and liquid crystal display devices CHISSO CORP (JP) 2004-09-22 EP disclosed
US-6500503-B2 Liquid crystal compound containing fluoro substituted benzene ring CHISSO CORPORATION (JP) 2002-12-31 US disclosed
US-20020066888-A1 Cyclohexane derivatives, liquid crystal compositions comprising the same and liquid crystal display devices JNC PETROCHEMICAL CORPORATION (JP) 2002-06-06 US disclosed
EP-1149885-A1 Cyclohexane derivatives, liquid crystal compositions comprising the same and liquid crystal display devices CHISSO CORPORATION (JP) 2001-10-31 EP 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-20020066888-A1 Cyclohexane derivatives, liquid crystal compositions comprising the same and liquid crystal display devices SCO2, KLK1, HCN2 CHRM5 201/4885CHRM1 34/4885CHRM3 194/4885

“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.