Bromide

Bromide

SCHEMBL1882151

CCCCCn1cc[n+](-c2c(C)cc(C)cc2C)c1.[Br-]

nearest known ligand 0.51

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
▸ NPC1 O15118 4/20 0.51
▸ HTT P42858 4/20 0.51
▸ RAB9A P51151 4/20 0.51
▸ HSP90AA1 P07900 3/20 0.51
▸ SMN1; SMN2 Q16637 3/20 0.51
▸ MEN1 O00255 2/20 0.51
▸ KMT2A Q03164 2/20 0.51
▸ MAPT P10636 2/20 0.51
▸ MAPK1 P28482 2/20 0.51
▸ NPSR1 Q6W5P4 2/20 0.51
▸ APAF1 O14727 1/20 0.51
▸ PLA2G1B P04054 1/20 0.51
▸ ATG4B Q9Y4P1 1/20 0.51
▸ PON1 P27169 1/20 0.42
▸ FDPS P14324 12/20 0.36
▸ LMNA P02545 2/20 0.36
▸ ALDH1A1 P00352 1/20 0.36
▸ PABPC1 P11940 1/20 0.36
▸ APOBEC3A P31941 1/20 0.36
▸ APOBEC3G Q9HC16 1/20 0.36

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 SCHEMBL1885380 0.98 NPC1 (0.54) NPC1HTTRAB9AHSP90AA1SMN1; SMN2
Bromide SCHEMBL1884396 0.98 NPC1 (0.54) NPC1HTTRAB9AHSP90AA1SMN1; SMN2
Bromide SCHEMBL1885921 0.98 NPC1 (0.54) NPC1HTTRAB9AHSP90AA1SMN1; SMN2
Bromide SCHEMBL1879504 0.98 NPC1 (0.54) NPC1HTTRAB9AHSP90AA1SMN1; SMN2
Bromide SCHEMBL1881356 0.98 NPC1 (0.54) NPC1HTTRAB9AHSP90AA1SMN1; SMN2
SCHEMBL23698417 0.97 NPC1 (0.51) NPC1HTTRAB9AHSP90AA1SMN1; SMN2
SCHEMBL23698381 0.97 NPC1 (0.51) NPC1HTTRAB9AHSP90AA1SMN1; SMN2
SCHEMBL21834759 0.97 NPC1 (0.51) NPC1HTTRAB9AHSP90AA1SMN1; SMN2
SCHEMBL21834756 0.97 NPC1 (0.51) NPC1HTTRAB9AHSP90AA1SMN1; SMN2
SCHEMBL23698569 0.97 NPC1 (0.51) NPC1HTTRAB9AHSP90AA1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9260397-B2 Salts comprising aryl-alkyl-substituted imidazolium and triazolium cations and the use thereof TECHNISCHE UNIVERSITAET DRESDEN (DE) 2016-02-16 — — US disclosed
US-20110105761-A1 Salts Comprising Aryl-Alkyl-Substituted Imidazolium and Triazolium Cations and the Use Thereof TECHNISCHE UNIVERSITAET DRESDEN (DE) 2011-05-05 — — 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-20110105761-A1 Salts Comprising Aryl-Alkyl-Substituted Imidazolium and Triazolium Cations and the Use Thereof RDX, HAX1, CHRM2 NPC1 1145/4885HTT 1484/4885RAB9A 3824/4885

“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.

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