Bromide

Bromide

SCHEMBL20874202

CCOC(=O)CNC(=O)[C@H](CSSCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1)NC(=O)CC[C@H](N)C(=O)OCC.[Br-]

nearest known ligand 0.40

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
GLO1 Q04760 3/20 0.40
NOD1 Q9Y239 3/20 0.39
PTGS1 P23219 1/20 0.35
GSTK1 Q9Y2Q3 1/20 0.35
MME P08473 1/20 0.35
ANPEP P15144 1/20 0.35
PPID Q08752 1/20 0.34
F2 P00734 1/20 0.34
F10 P00742 1/20 0.34
ALDH1A1 P00352 2/20 0.34
CYP1A2 P05177 1/20 0.33
CYP3A4 P08684 1/20 0.33
CYP2D6 P10635 1/20 0.33
CYP2C9 P11712 1/20 0.33
CYP2C19 P33261 1/20 0.33
ABCC3 O15438 1/20 0.33
NR1I2 O75469 1/20 0.33
ABCB11 O95342 1/20 0.33
NR3C1 P04150 1/20 0.33
RARG P13631 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 SCHEMBL20874204 1.00 GLO1 (0.40) GLO1NOD1PTGS1GSTK1MME
Bromide SCHEMBL20874250 0.95 NOD1 (0.40) GLO1NOD1PTGS1GSTK1MME
Bromide SCHEMBL20874252 0.95 NOD1 (0.40) GLO1NOD1PTGS1GSTK1MME
Bromide SCHEMBL20874258 0.94 NOD1 (0.41) GLO1NOD1PTGS1GSTK1MME
Bromide SCHEMBL20874287 0.94 NOD1 (0.41) GLO1NOD1PTGS1GSTK1MME
Bromide SCHEMBL20874210 0.93 NOD1 (0.42) GLO1NOD1MMEANPEPPPID
Bromide SCHEMBL20874247 0.93 NOD1 (0.42) GLO1NOD1MMEANPEPPPID
Bromide SCHEMBL20874263 0.93 GLO1 (0.43) GLO1NOD1PTGS1GSTK1PPID
Bromide SCHEMBL20874260 0.93 GLO1 (0.43) GLO1NOD1PTGS1GSTK1PPID
Bromide SCHEMBL20874305 0.90 TLR7 (0.39) GLO1PTGS1GSTK1MMEANPEP

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
EP-3468563-B1 COMPOUNDS FOR DELIVERING GLUTATHIONE TO A TARGET AND METHODS OF MAKING AND USING THE SAME UNIV OREGON STATE (US) 2023-09-13 EP disclosed
US-20190106456-A1 COMPOUNDS FOR DELIVERING GLUTATHIONE TO A TARGET AND METHODS OF MAKING AND USING THE SAME OREGON STATE UNIVERSITY (US) 2019-04-11 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-20190106456-A1 COMPOUNDS FOR DELIVERING GLUTATHIONE TO A TARGET AND METHODS OF MAKING AND USING THE SAME GSR, TXN2, GLS GLO1 106/4885NOD1 3585/4885PTGS1 250/4885

“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.