Bromide

Bromide

SCHEMBL9811054

Br.Br.[SnH2].c1ccc(CCc2ccccc2)cc1

nearest known ligand 0.61

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
SIGMAR1 known ✓ Q99720 1/20 0.50
ALDH1A1 P00352 1/20 0.61
HPGD P15428 1/20 0.61
ALOX15 P16050 1/20 0.61
ALOX12 P18054 1/20 0.61
CASP1 P29466 1/20 0.61
HSD17B10 Q99714 1/20 0.61
MAOA P21397 5/20 0.60
MAOB P27338 4/20 0.60
TDP1 Q9NUW8 2/20 0.58
CYP2A6 P11509 1/20 0.58
HTR2A P28223 1/20 0.58
SMN1; SMN2 Q16637 1/20 0.58
TAAR1 Q96RJ0 1/20 0.58
LOXL2 Q9Y4K0 1/20 0.58
KCNH2 Q12809 2/20 0.55
CALM1 P0DP23 1/20 0.53
FFAR1 O14842 1/20 0.52
CA1 P00915 1/20 0.50
CA2 P00918 1/20 0.50

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 SCHEMBL4538420 0.96 ALDH1A1 (0.65) ALDH1A1HPGDALOX15ALOX12CASP1
Bromide SCHEMBL28646960 0.93 ALDH1A1 (0.61) ALDH1A1HPGDALOX15ALOX12CASP1
Bromide SCHEMBL11532977 0.93 ALDH1A1 (0.61) ALDH1A1HPGDALOX15ALOX12CASP1
Bromide SCHEMBL11283419 0.93 ALDH1A1 (0.61) ALDH1A1HPGDALOX15ALOX12CASP1
Hydrochloric Acid SCHEMBL3787902 0.93 MAOB (0.65) ALDH1A1HPGDALOX15ALOX12CASP1
Bromide SCHEMBL11550987 0.93 ALDH1A1 (0.61) ALDH1A1HPGDALOX15ALOX12CASP1
Bromide SCHEMBL11513180 0.93 ALDH1A1 (0.61) ALDH1A1HPGDALOX15ALOX12CASP1
SCHEMBL9741303 0.93 ALDH1A1 (0.69) ALDH1A1HPGDALOX15ALOX12CASP1
SCHEMBL62125 0.93 ALDH1A1 (0.69) ALDH1A1HPGDALOX15ALOX12CASP1
Benzene SCHEMBL3440179 0.93 ALDH1A1 (0.69) ALDH1A1HPGDALOX15ALOX12CASP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0246414-B1 METHOD OF SUPPRESSING SODIUM POISONING OF CRACKING CATALYSTS DURING FLUID CATALYTIC CRACKING CHEVRON RESEARCH AND TECHNOLOGY COMPANY (US) 1991-06-26 EP disclosed
US-4889617-A PASSIVATION WITH TIN OR TIN COMPOUNDS CHEVRON RESEARCH COMPANY (US) 1989-12-26 US disclosed
EP-0246414-A1 Method of suppressing sodium poisoning of cracking catalysts during fluid catalytic cracking CHEVRON RESEARCH AND TECHNOLOGY COMPANY (US) 1987-11-25 EP disclosed