Bromide

Bromide

SCHEMBL3616347

Cc1ccc(C(=O)C[n+]2ccccc2)cc1.[Br-]

nearest known ligand 0.70

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 14)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 4/20 0.70
LMNA P02545 5/20 0.68
ALDH1A1 P00352 5/20 0.68
SMN1; SMN2 Q16637 2/20 0.68
HTT P42858 1/20 0.68
PABPC1 P11940 2/20 0.65
KMT2A Q03164 4/20 0.64
ATM Q13315 1/20 0.64
MAPT P10636 2/20 0.63
MEN1 O00255 3/20 0.56
RAB9A P51151 3/20 0.56
POLB P06746 1/20 0.55
NPC1 O15118 1/20 0.55
GLA P06280 1/20 0.52

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
SCHEMBL841434 0.98 ALDH1A1 (0.69) KDM4ELMNAALDH1A1SMN1; SMN2HTT
Iodide SCHEMBL20704647 0.96 PABPC1 (0.70) KDM4ELMNAALDH1A1SMN1; SMN2HTT
Hydrochloric Acid SCHEMBL5907533 0.96 ALDH1A1 (0.72) KDM4ELMNAALDH1A1SMN1; SMN2HTT
SCHEMBL8660257 0.92 KDM4E (0.64) KDM4ELMNAALDH1A1SMN1; SMN2HTT
SCHEMBL8660261 0.89 ALDH1A1 (0.59) KDM4ELMNAALDH1A1SMN1; SMN2HTT
SCHEMBL8968159 0.88 KDM4E (0.63) KDM4ELMNAALDH1A1SMN1; SMN2HTT
Bromide SCHEMBL31501128 0.86 LMNA (0.74) KDM4ELMNAALDH1A1SMN1; SMN2HTT
Bromide SCHEMBL27941533 0.85 KDM4E (0.79) KDM4ELMNAALDH1A1SMN1; SMN2HTT
Bromide SCHEMBL698678 0.85 KDM4E (0.79) KDM4ELMNAALDH1A1SMN1; SMN2HTT
SCHEMBL765905 0.83 KDM4E (0.76) KDM4ELMNAALDH1A1SMN1; SMN2HTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7816352-B2 antiapoptosis agents such as 1-[2-Methoxyimino-2-(4-pyrrolidin-1-yl-phenyl)-ethyl]-quinolinium bromide, used for cytoprotection or for side effect reduction of anticarcinogenic agents THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2010-10-19 US disclosed
US-20080280903-A1 Apoptosis Inhibitors NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2008-11-13 US disclosed
WO-2006099301-A2 APOPTOSIS INHIBITORS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2006-09-21 WO disclosed
EP-0681225-B1 Electrostatic toner comprising phenacyl compounds BASF AG (DE) 1998-11-18 EP disclosed
US-5541032-A CHARGE STABILIZERS WHICH ARE INSENSITIVE TO MOISTURE, HEAT RESISTANT AND PRODUCE CRISP, UNIFORM VISIBLE IMAGES OF HIGH COLOR INTENSITY BASF AKTIENGESELLSCHAFT (DE) 1996-07-30 US disclosed
EP-0681225-A1 Electrostatic toner comprising phenacyl compounds BASF AKTIENGESELLSCHAFT (DE) 1995-11-08 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-20080280903-A1 Apoptosis Inhibitors BAD, MCL1, AIFM1 KDM4E 3580/4885LMNA 1596/4885ALDH1A1 2244/4885

“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.