Bromide

Bromide

SCHEMBL29440246

Br.N=c1sc2c(n1CC(=O)c1cccc(Cl)c1)CCCC2

nearest known ligand 0.65

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 20)

geneUniProtsupporting neighboursconfidence
CYP1A1 P04798 2/20 0.65
CYP1B1 Q16678 2/20 0.65
MEN1 O00255 4/20 0.63
KMT2A Q03164 4/20 0.63
MAPT P10636 3/20 0.63
SMN1; SMN2 Q16637 2/20 0.63
MAPK1 P28482 2/20 0.63
ALDH1A1 P00352 2/20 0.63
TP53 P04637 1/20 0.63
CYP3A4 P08684 1/20 0.63
ALOX15 P16050 1/20 0.63
TSHR P16473 1/20 0.63
HSD17B10 Q99714 1/20 0.63
HDAC6 Q9UBN7 1/20 0.63
CXCR3 P49682 1/20 0.48
IDO1 P14902 2/20 0.43
NPC1 O15118 3/20 0.41
POLB P06746 1/20 0.41
RAB9A P51151 1/20 0.41
FLT3 P36888 1/20 0.40

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 SCHEMBL22749448 1.00 CYP1A1 (0.65) CYP1A1CYP1B1MEN1KMT2AMAPT
SCHEMBL22761628 0.99 MEN1 (0.64) CYP1A1CYP1B1MEN1KMT2AMAPT
Bromide SCHEMBL31502672 0.98 CYP1A1 (0.61) CYP1A1CYP1B1MEN1KMT2AMAPT
Bromide SCHEMBL22749447 0.97 MEN1 (0.61) CYP1A1CYP1B1MEN1KMT2AMAPT
Bromide SCHEMBL4796807 0.86 CYP1A1 (0.75) CYP1A1CYP1B1MEN1KMT2AMAPT
Bromide SCHEMBL29440222 0.86 CYP1A1 (0.65) CYP1A1CYP1B1MEN1KMT2AMAPT
Bromide SCHEMBL22749445 0.86 CYP1A1 (0.65) CYP1A1CYP1B1MEN1KMT2AMAPT
Bromide SCHEMBL29440254 0.86 CYP1A1 (0.65) CYP1A1CYP1B1MEN1KMT2AMAPT
Bromide SCHEMBL22749637 0.86 CYP1A1 (0.65) CYP1A1CYP1B1MEN1KMT2AMAPT
Bromide SCHEMBL22749628 0.85 CYP1A1 (0.69) CYP1A1CYP1B1MEN1KMT2AMAPT

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-20220251054-A1 Analogues and Methods of Treating Rett Syndrome UNIV CALIFORNIA (US) 2022-08-11 US disclosed
EP-3976796-A1 PIFITHRIN ANALOGUES AND METHODS OF TREATING RETT SYNDROME The Regents of the University of California (US) 2022-04-06 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-20220251054-A1 Analogues and Methods of Treating Rett Syndrome MECP2, PAX3, PAX2 CYP1A1 4823/4885CYP1B1 4793/4885MEN1 752/4885

“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.