Bromide

Bromide

SCHEMBL4048814

O=C(C[S+]1CCCC1)c1cccc2ccccc12.[Br-]

nearest known ligand 0.54

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
PTPN1 P18031 1/20 0.54
ALDH1A1 P00352 5/20 0.48
MAPT P10636 4/20 0.48
HPGD P15428 3/20 0.48
LMNA P02545 3/20 0.48
POLB P06746 3/20 0.48
KDM4E B2RXH2 3/20 0.48
MEN1 O00255 2/20 0.48
GMNN O75496 2/20 0.48
MAPK1 P28482 2/20 0.48
BLM P54132 2/20 0.48
PMP22 Q01453 2/20 0.48
KMT2A Q03164 2/20 0.48
NPSR1 Q6W5P4 2/20 0.48
CMKLR1 Q99788 2/20 0.48
TDP1 Q9NUW8 2/20 0.48
TP53 P04637 1/20 0.48
CYP1A2 P05177 1/20 0.48
CYP3A4 P08684 1/20 0.48
CYP2D6 P10635 1/20 0.48

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
SCHEMBL3871190 0.98 PTPN1 (0.56) PTPN1ALDH1A1MAPTHPGDLMNA
Trifluoromethanesulfonic Acid SCHEMBL3872598 0.86 PTPN1 (0.43) PTPN1ALDH1A1MAPTHPGDLMNA
Trifluoromethanesulfonic Acid SCHEMBL29625806 0.86 PTPN1 (0.43) PTPN1ALDH1A1MAPTHPGDLMNA
SCHEMBL7044332 0.86 PTPN1 (0.43) PTPN1ALDH1A1MAPTHPGDLMNA
SCHEMBL3881528 0.84 PTPN1 (0.42) PTPN1ALDH1A1MAPTHPGDLMNA
Hydrochloric Acid SCHEMBL3921075 0.82 ALDH1A1 (0.52) PTPN1ALDH1A1MAPTHPGDLMNA
SCHEMBL3877973 0.80 AR (0.40) PTPN1ALDH1A1MAPTHPGDLMNA
SCHEMBL3877031 0.80 PTPN1 (0.39) PTPN1ALDH1A1MAPTHPGDLMNA
SCHEMBL3879944 0.79 PTPN1 (0.38) PTPN1ALDH1A1MAPTHPGDLMNA
SCHEMBL3870778 0.78 SMN1; SMN2 (0.37) PTPN1ALDH1A1MAPTHPGDLMNA

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-7531686-B2 Salt suitable for an acid generator and a chemically amplified resist composition containing the same SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2009-05-12 US disclosed
US-20070100158-A1 Salt suitable for an acid generator and a chemically amplified resist composition containing the same SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2007-05-03 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-20070100158-A1 Salt suitable for an acid generator and a chemically amplified resist composition containing the same SLC26A3, RFC1, RFC2 PTPN1 1482/4885ALDH1A1 1641/4885MAPT 4784/4885

“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.