Bromide

Bromide

SCHEMBL8610995

Cc1ccc(C[N+](C)(C)C)cc1.[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
ACHE known ✓ P22303 1/20 0.42
CHRM2 known ✓ P08172 2/20 0.38
CHRM4 known ✓ P08173 1/20 0.38
CHRM5 known ✓ P08912 1/20 0.38
CHRM1 known ✓ P11229 1/20 0.38
CHRM3 known ✓ P20309 1/20 0.38
CHKA known ✓ P35790 1/20 0.35
TDP1 Q9NUW8 2/20 0.54
ALDH1A1 P00352 2/20 0.54
KDM4E B2RXH2 1/20 0.54
IDO1 P14902 2/20 0.46
CYP1A2 P05177 1/20 0.42
CYP2A6 P11509 1/20 0.42
TAAR1 Q96RJ0 1/20 0.42
AGXT P21549 2/20 0.41
CHRNB2 P17787 1/20 0.40
CHRNA4 P43681 1/20 0.40
MEN1 O00255 2/20 0.38
KMT2A Q03164 2/20 0.38
CYP2C9 P11712 1/20 0.38

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
SCHEMBL8167441 0.97 TDP1 (0.56) TDP1ALDH1A1KDM4EIDO1CYP1A2
Water SCHEMBL7624991 0.95 TDP1 (0.54) TDP1ALDH1A1KDM4EIDO1CYP1A2
Hydrochloric Acid SCHEMBL6772823 0.95 TDP1 (0.61) TDP1ALDH1A1KDM4EIDO1CYP1A2
SCHEMBL10455728 0.95 TDP1 (0.54) TDP1ALDH1A1KDM4EIDO1CYP1A2
SCHEMBL10709611 0.95 TDP1 (0.54) TDP1ALDH1A1KDM4EIDO1CYP1A2
SCHEMBL10455727 0.95 TDP1 (0.54) TDP1ALDH1A1KDM4EIDO1CYP1A2
SCHEMBL10453137 0.92 TDP1 (0.52) TDP1ALDH1A1KDM4EIDO1CYP1A2
Hydrochloric Acid SCHEMBL10453138 0.92 TDP1 (0.58) TDP1ALDH1A1KDM4EIDO1CYP1A2
SCHEMBL14094644 0.90 TDP1 (0.50) TDP1ALDH1A1KDM4EIDO1CYP1A2
SCHEMBL4797252 0.86 ALDH1A1 (0.68) TDP1ALDH1A1KDM4ECHRNB2CHRNA4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105198698-A Preparation method of tetrabromo cyclic di-p-xylyene UNIV SOUTHEAST 2015-12-30 CN disclosed
EP-0518352-B1 Process for forming super high-contrast negative images and silver halide photographic material and developer being used therefor DAINIPPON INK & CHEMICALS (JP) 1998-04-22 EP disclosed
US-5460919-A Process of forming super high-contrast negative images and silver halide photographic material and developer being used therefor DAINIPPON INK AND CHEMICALS, INC. (JP) 1995-10-24 US disclosed
US-5372911-A Support having one or more hydrophilic colloidal layers, at least one layer contains pyridinium salt or derivative, quinolinium salt or derivative, or isoquinolinium salt or derivative DAINIPPON INK AND CHEMICALS, INC. (JP) 1994-12-13 US disclosed
EP-0518352-A1 Process for forming super high-contrast negative images and silver halide photographic material and developer being used therefor DAINIPPON INK AND CHEMICALS, INC. (JP) 1992-12-16 EP disclosed