Bromide

Bromide

SCHEMBL6263418

OCc1cc[n+](Cc2ccccc2)cc1.[Br-]

nearest known ligand 0.71

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 12)

geneUniProtsupporting neighboursconfidence
CHKA known ✓ P35790 9/20 0.71
ACHE known ✓ P22303 2/20 0.46
TSHR P16473 1/20 0.58
ALDH1A1 P00352 4/20 0.56
SMN1; SMN2 Q16637 3/20 0.56
LMNA P02545 2/20 0.56
HTT P42858 2/20 0.56
KDM4E B2RXH2 2/20 0.50
RAB9A P51151 1/20 0.50
MEN1 O00255 1/20 0.46
MAPT P10636 1/20 0.46
KMT2A Q03164 1/20 0.46

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
SCHEMBL6263179 0.98 CHKA (0.68) CHKATSHRALDH1A1SMN1; SMN2LMNA
Hydrochloric Acid SCHEMBL21061013 0.96 CHKA (0.66) CHKATSHRALDH1A1SMN1; SMN2LMNA
Bromide SCHEMBL5206067 0.83 ALDH1A1 (0.62) CHKAALDH1A1SMN1; SMN2LMNAHTT
Bromide SCHEMBL8890844 0.83 CHKA (0.64) CHKAALDH1A1SMN1; SMN2LMNAHTT
SCHEMBL26522365 0.82 TDP1 (0.64) CHKAALDH1A1SMN1; SMN2LMNAHTT
Bromide SCHEMBL8971005 0.82 CHKA (0.58) CHKATSHRALDH1A1SMN1; SMN2LMNA
Bromide SCHEMBL17967626 0.81 CHKA (0.58) CHKAALDH1A1SMN1; SMN2LMNAHTT
Bromide SCHEMBL11693463 0.81 CHKA (0.63) CHKAALDH1A1SMN1; SMN2LMNAHTT
SCHEMBL10326023 0.80 CHKA (0.61) CHKAALDH1A1SMN1; SMN2LMNAHTT
Benzyl Viologen SCHEMBL4079047 0.80 ALDH1A1 (0.71) CHKAALDH1A1SMN1; SMN2LMNAHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250195484-A1 CEREBLON LIGANDS AND USES THEREOF UNIV MICHIGAN (US) 2025-06-19 US disclosed
EP-4554948-A1 TETRAHYDRONAPHTHALENE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS Regents of the University of Michigan (US) 2025-05-21 EP disclosed
WO-2024015409-A1 CHROMAN DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2024-01-18 WO disclosed
WO-2024015408-A1 INDAZOLE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS REGENTS OF THE UNIVESITY OF MICHIGAN (US) 2024-01-18 WO disclosed
WO-2023201012-A1 IKZF2 DEGRADERS AND USES THEREOF REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2023-10-19 WO disclosed
WO-2023183607-A1 CEREBLON LIGANDS AND USES THEREOF REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2023-09-28 WO disclosed
WO-2005076749-A2 A NOVEL PROCESS FOR THE PREPARATION OF 1-BENZYL-4-[(5,6-DIMETHOXY-1-INDANON-2-YL)METHYL]PIPERIDINE JUBILANT ORGANOSYS LIMITED (IN) 2005-08-25 WO 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-20250195484-A1 CEREBLON LIGANDS AND USES THEREOF CRBN, CDR2, CHLSN CHKA 545/4885ACHE 1251/4885TSHR 2521/4885

“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.